id|nct_id|document_id|document_type|url|comment
104685|NCT04488107|ICH topic S9|ICH topic S9 - nonclinical evaluation for anticancer pharmaceuticals. 2009|https://database.ich.org/sites/default/files/S9_Guideline.pdf|
104686|NCT04488107|IBRANCE® (palbociclib) capsule|label for IBRANCE® (palbociclib) capsules|https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/207103s000lbl.pdf|
104687|NCT04488107|IBRANCE® (palbociclib) tablets|label for IBRANCE® (palbociclib) tablets,|https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212436lbl.pdf|
104688|NCT04488107|KISQALI® (ribociclib) tablets|Label for KISQALI® (ribociclib) tablets|https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/209092s005lbl.pdf|
104689|NCT04488107|ICH Topic E6 (R1)|ICH Topic E6 (R1) Guideline for Good Clinical Practice|https://www.ema.europa.eu/en/documents/scientific-guideline/ich-e6-r1-guideline-good-clinical-practice_en.pdf|
104690|NCT04488107|ICH Topic E9|ICH Topic E9 Statistical Principles for Clinical Trials|https://www.ema.europa.eu/en/documents/scientific-guideline/ich-e-9-statistical-principles-clinical-trials-step-5_en.pdf|
104691|NCT04487964|EgyptianBiomedicalRN|Study Protocol|https://drive.google.com/file/d/1JF9GMByaEHNRiKMssyEchmPTV_V5dRp_/view?usp=sharing|this link describ the study protocol
104692|NCT04469439|REDCap|Individual Participant Data Set|https://redcap.ucdenver.edu/|Study data will be collected and managed using REDCap (Research Electronic Data Capture). REDCap is a secure web application designed to support data capture for research studies, providing user-friendly web-based case report forms, real-time data entry validation (e.g. for data types and range checks), audit trails and an indirectly identified data export mechanism to common statistical packages.
104693|NCT04464369|LPDSItopride study|Study Protocol|http://www.targid.eu|
104694|NCT04457921|Mary Colleen Simonelli|Study Protocol|http://pubmed.ncbi.nlm.nih.gov/30102886/|web site is provided
104695|NCT04445727|vitamin c|Clinical Study Report|http://www.bonusan.es/vademecum/vitamina_c1000_complejo_de_ascorbatos.html|
104696|NCT04437693||Clinical Study Report|https://www.worldometers.info/coronavirus/|https://www.worldometers.info/coronavirus/
104697|NCT04437693||Clinical Study Report|https://www.who.int/docs/default-source/coronaviruse/who-china-joint-mission-on-covid-19-final-report.pdf|https://www.who.int/docs/default-source/coronaviruse/who-china-joint-mission-on-covid-19-final-report.pdf
104698|NCT04437693||Clinical Study Report|https://www.cdc.gov/coronavirus/2019-ncov/need-extra-precautions/groups-at-higher-risk.html|https://www.cdc.gov/coronavirus/2019-ncov/need-extra-precautions/groups-at-higher-risk.html
104699|NCT04434508|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|elnakeebayman@yahoo.com
104700|NCT04419571|285260|Individual Participant Data Set|https://www.myresearchproject.org.uk/|Data collection template available on IRAS (Integrated Research Application System) registration
104701|NCT04419571|285260|Statistical Analysis Plan|https://www.myresearchproject.org.uk/|Statistical analysis plan as part of protocol available on IRAS (Integrated Research Application System) registration
104702|NCT04419571|285260|Study Protocol|https://www.myresearchproject.org.uk/|Protocol available on IRAS (Integrated Research Application System) registration
104703|NCT04415333||De-identified data set|https://library.unc.edu/scholarly-communications/open-access/carolina-digital-repository-cdr/|Data will be accessible at the above Carolina Data Repository for the UNC library system.
104704|NCT04413747|guest_1|Study Protocol|http://giardinostlucia.it|
104705|NCT04413747|guest_2|Informed Consent Form|http://giardinostlucia.it|
104706|NCT04413747|guest_3|Individual Participant Data Set|http://giardinostlucia.it|
104707|NCT04411355|10128359|National Thesis Center|https://tez.yok.gov.tr/UlusalTezMerkezi|thesis Number: 494582
104708|NCT04411290||Principal investigator data|https://scholar.google.com.tr/citations?user=6bFlCZwAAAAJ&hl=tr|
104709|NCT04405713|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|elnakeebayman@yahoo.com
104710|NCT04404907||Clinical Study Report|http://doi.org/10.3886/ICPSR37603.v1|Mustanski, Brian. Multilevel Influences on HIV and Substance Use in a YMSM Cohort (RADAR) - Visit #1, Chicago Metropolitan Area, 2015-2018. Inter-university Consortium for Political and Social Research [distributor], 2020-03-19.
104711|NCT04401722|Ayman El Nakeeb|Study Protocol|http://www.mans.edu.eg/en/|through elnakeebayman@yahoo.com
104712|NCT04392869|clinicaltrialsCRAFT|Summary and comparison of mindfulness based programs|https://drive.ugr.es/index.php/s/ytdazx47iReHMeu|This is not a comprehensive description of any of the programs, but rather a schematic outline with the most salient similarities and differences between them.
104713|NCT04392869|clinicaltrialsCRAFT|Human Subjects Review|https://drive.ugr.es/index.php/s/DGKxnBhZfm058DA|Human Subjects Review approval and its translation into English
104714|NCT04392869|clinicaltrialsCRAFT|Informed Consent Form|https://drive.ugr.es/index.php/s/10ptY8LrAdwdWTj|This document contains the welcome email, the informed consent form and the demographic survey. Please, bear in mind that this is the English version of the text in Spanish uploaded to the LimeSurvey platform.
104715|NCT04392869|clinicaltrialsCRAFT|Official CRAFTftiugr logo|https://drive.ugr.es/index.php/s/zHklhje0InjZAF7|This is the official logo of the project. It represents a way of communication that goes beyond words. Earphones are a special reference to interpreters.
104716|NCT04391933|CPR|Informed Consent Form|https://komite.regionsyddanmark.dk/wm258128|
104717|NCT04374240|ISRCTN06254734|ISRCTN Registry|http://www.isrctn.com/ISRCTN06254734|
104718|NCT04357327||Scientific paper|https://www.sciencedirect.com/science/article/pii/S0163445320302139|Recently, we published a study that demonstrates that saliva is a promising diagnostic tool to detect SARS-CoV-2. We analyzed salivary samples of 25 patients affected by COVID-19 and all of them proved positive at rRT-PCR analysis.
104719|NCT04352400|GPR (PI)|Individual Participant Data Set|https://ncov.medsci.ox.ac.uk|The link https://ncov.medsci.ox.ac.uk allows connection to EDCap database, a secure web platform for building and managing online databases and surveys. Data collection will use the WHO Case Record Form.
104720|NCT04347148||Study Protocol|http://www.ptvonline.it/cei_temp.asp|
104721|NCT04340804||Study Protocol|https://osf.io/k369t/|
104722|NCT04340804||Statistical Analysis Plan|https://osf.io/k369t/|
104723|NCT04340804||Informed Consent Form|https://osf.io/k369t/|
104724|NCT04340804||Individual Participant Data Set|https://osf.io/k369t/|When results will be published
104725|NCT04340791||Study Protocol|https://osf.io/kq9c8/|
104726|NCT04340791||Statistical Analysis Plan|https://osf.io/kq9c8/|
104727|NCT04340791||Informed Consent Form|https://osf.io/kq9c8/|
104728|NCT04340791||Individual Participant Data Set|https://osf.io/kq9c8/|When results will be published
104729|NCT04338568||Clinical Study Report|https://www.castoredc.com/|
104730|NCT04337762||Study Website|https://www.beatcovidtrial.com/|
104731|NCT04335422||Device website|https://www.hocoma.com/solutions/armeo-spring/|
104732|NCT04335422||references|https://www.ncbi.nlm.nih.gov/pubmed/28540536|
104733|NCT04329871||Individual Participant Data Set|http://Metabolic-institute.com|
104734|NCT04322123||Study Protocol|https://www.medrxiv.org/content/10.1101/2020.05.19.20106997v1|Preprint of the Protocol
104735|NCT04312334||Individual Participant Data Set|https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-015-0532-z|Our data will be suitable for sharing in anonymised form.Potential users will learn about the data on the websites of the collaborating institutes, and links to the relevant data repositories will be available on those websites.The link will contain information on how to apply to use the data. We aim to offer controlled access to study data. Potential users of the data will be invited to register and provide information on their aims and proposed analyses of the data. The PI and Co-Is will decide whether to grant release of the data based on these requests. Our intended policy will be to make data available to researchers, within 2 years of completion of the study. This is to make maximum use of data collected using public funding while protecting the intellectual property rights of the study team.Restrictions or delays to sharing, with planned actions to limit such restrictions We would like to retain exclusive use for 2 years
104736|NCT04303299|Thai government data|Data references|https://ddc.moph.go.th|
104737|NCT04303299||News|https://world.kbs.co.kr/service/news_view.htm?lang=e&Seq_Code=151108|
104738|NCT04303299||Reference News|https://world.kbs.co.kr/service/news_view.htm?lang=e&Seq_Code=151108|
104739|NCT04283773||Study Protocol|https://www.sciencedirect.com/science/article/pii/S1110036214000211|Treatment outcomes of female germ cell tumors: The Egyptian National Cancer Institute experience. Journal of the Egyptian National Cancer Institute
104740|NCT04283773||Study Protocol|https://journals.lww.com/greenjournal/Fulltext/2006/05000/Malignant_Germ_Cell_Tumors_of_the_Ovary.19.aspx|Incidence and Survival Rates for Female Malignant Germ Cell Tumors
104741|NCT04283773||Study Protocol|https://pubs.rsna.org/doi/full/10.1148/radiographics.21.2.g01mr09475|Ovarian Teratomas: Tumor Types and Imaging Characteristics
104742|NCT04283773||Study Protocol|https://synapse.koreamed.org/DOIx.php?id=10.3802/jgo.2012.23.2.125|Early diagnosis of malignant-transformed ovarian mature cystic teratoma: fat-suppressed MRI findings
104743|NCT04270500||Study Protocol|https://1drv.ms/w/s!Aon5a6DA8kPHg0ZhMYuGTm8DJpGL|
104744|NCT04270500||Informed Consent Form|https://1drv.ms/w/s!Aon5a6DA8kPHg0rxq5uWmY7Hp66L|
104745|NCT04270500||Individual Participant Data Set|https://1drv.ms/w/s!Aon5a6DA8kPHg0z2GYrZyv3ne09p|
104746|NCT04262752||Study Protocol|https://mowoot-my.sharepoint.com/:f:/g/personal/it_mowoot_onmicrosoft_com/Et7crRPr0OtJvA81kVAmfb0BVO5aB7mj_FGRtcDVmPV0WQ?e=Mib3DN|"Accessible under request for password to ihf@mowoot.com with the subject IPS info request"
104747|NCT04262752||Informed Consent Form|https://mowoot-my.sharepoint.com/:f:/g/personal/it_mowoot_onmicrosoft_com/Et7crRPr0OtJvA81kVAmfb0BVO5aB7mj_FGRtcDVmPV0WQ?e=Mib3DN|"Accessible under request for password to ihf@mowoot.com with the subject IPS info request"
104748|NCT04230785||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/?term=Differential+long+noncoding+RNA+expressions+in+peripheral+blood+mononuclear+cells+for+detection+of+acute+ischemic+stroke|
104749|NCT04221009||Informed Consent Form|https://arc.research.usf.edu/Prod/sd/Doc/0/DDRU7K2KMHLK9ECT12FPTMA60B/3S78A88933BKN7869JO1NSMT62.pdf|
104750|NCT04221009||Study Protocol|https://arc.research.usf.edu/Prod/sd/Doc/0/06USV5NTK2VKJ06CUK3TQJR578/Protocol%20v01%202019-10-24.docx|
104751|NCT04214405||Clinical Study Report|https://www.ncbi.nlm.nih.gov|Birgfeld CB, Mundinger GS, Gruss JS. Evidence-based medicine: Evaluation and treatment of zygoma fractures. Plast Reconstr Surg 2017;139(1): 168e-80e.[http://dx.doi.org/10.1097/PRS.0000000000002852] [PMID: 28027253]
104752|NCT04213079||Study Protocol|http://mdds.nyc/|
104753|NCT04210765||Individual Participant Data Set|https://dremrahkovalak.com/wp-content/uploads/2019/12/registration.pdf|unfinished
104754|NCT04205721||Individual Participant Data Set|http://dataverse.unc.edu/dataverse/cpc|Search for South Africa Impact Evaluation
104755|NCT04201977||Individual Participant Data Set|https://www.ufsm.br/cursos/pos-graduacao/santa-maria/ppgrf/|We are organizing the availability of data on the website of the Postgraduate Program in Functional Rehabilitation after publication.
104756|NCT04200794||Individual Participant Data Set|https://yareta.unige.ch|The data of this study are deposited on a YARETA, a FAIR digital solution for long-term preservation of research data for all Geneva Universities (https://yareta.unige.ch). DOI: 10.26037/yareta:dhglarpzdfcgzefx4pky7sua3m
104757|NCT04199338||web-site link|http://peritondiyalizim.com/login.php|
104758|NCT04183842||Protocol, Validation of Ethic Comitee, Informed consent form, D2 test of attention, Hangover severity scale, Randomization chart|https://hidrive.ionos.com/share/bv7z7738u3|Password will be provided by Administrator. Please ask for it at : bommelaer@shadeline.com
104759|NCT04171557||Statistical Analysis Plan|http://aktivsundhed.dk/images/docs/SAPMRL.pdf|Pre-defined statistical analysis plan. Published on Centre for Physical Activity Research prior to commencing the analyses.
104760|NCT04164186|NSCLC Radiomics Interobserver|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC-Radiomics-Interobserver1|
104761|NCT04164186|NSCLC Radiomics|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC-Radiomics|
104762|NCT04164186|NSCLC Radiogenomics|Individual Participant Data Set|https://wiki.cancerimagingarchive.net/display/Public/NSCLC+Radiogenomics|
104763|NCT04160403||Study Protocol|https://www.ncbi.nlm.nih.gov/|
104764|NCT04160169|doi:10.15139/S3/XEXQXO|Individual Participant Data Set|https://dataverse.unc.edu/dataset.xhtml?persistentId=doi:10.15139/S3/XEXQXO|
104765|NCT04153916|0266-19-TLV|Study Protocol|http://www.neurotrigger.info|Upon completion of the study, results will be published and the study data will be available from the PI
104766|NCT04140383||Clinical Study Report|http://rdcu.be/bUabz|
104767|NCT04139174||Clinical Study Report|https://www.ajodo.org/article/0002-9416(82)90428-6/pdf|this is the guiding study document reference
105023|NCT03184948||Statistical Analysis Plan|http://ketkisheth.weebly.com/|
104768|NCT04132778||Study Protocol|https://ki.box.com/s/fdmbyp38heozwgmlwdtxe2drsbncjx9g|
104769|NCT04132778||Statistical Analysis Plan|https://ki.box.com/s/fdmbyp38heozwgmlwdtxe2drsbncjx9g|
104770|NCT04132323||Study Protocol|https://www.venousregistry.org/index.php?f=1&id=97|
104771|NCT04126785|CAAE 96882818.3.0000.5398|Brazil Research Ethics Committees|http://plataformabrasil.saude.gov.br/|
104772|NCT04119284||Informed Consent Form|http://irbnet.org|The Informed consent form can be obtained while the patient is seen for scoliosis at Nemours-AIDHC.
104773|NCT04110704|IRAS 261294|Study Protocol|http://preview-kcl.cloud.contensis.com/Preview/1/research/project?id=478a6e61-4446-4a12-945e-c41a3879371d|
104774|NCT04109963|Not yet available|Individual Participant Data Set|https://dataverse.scholarsportal.info/dataverse/calgary|The dataset with individual de-identified participant data will be hosted on the University of Calgary PRISM dataverse once the main results results are published. The identifier will be assigned when the dataset is uploaded.
104775|NCT04106648||Pubmed|http://www.ncbi.nlm.nih.gov/pubmed/|
104776|NCT04106622||Pubmed|https://www.ncbi.nlm.nih.gov/pubmed/|
104777|NCT04100629||Study Protocol|https://drive.google.com/open?id=1vNjwT5j9Y32e7vdayZAMBp-3PvJWCiSK|
104778|NCT04087239||Individual Participant Data Set|http://www.redcap.uzchs.ac.zw/redcap|Data being entered, now verification of enrolment case report forms
104779|NCT04068129||Individual Participant Data Set|http://www.abcd-vision.org/references/index.html|
104780|NCT04067518||Individual Participant Data Set|https://clinicaltrials.servier.com/|
104781|NCT04067518||Study Protocol|https://clinicaltrials.servier.com/|
104782|NCT04067518||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
104783|NCT04067518||Informed Consent Form|https://clinicaltrials.servier.com/|
104784|NCT04067518||Clinical Study Report|https://clinicaltrials.servier.com/|
104785|NCT04067518||study-level clinical trial data|https://clinicaltrials.servier.com/|
104786|NCT04067375||Information website|http://hipstudie.nl/|Information for participating caregivers, participants or other interested parties.
104787|NCT04067375||Study Protocol|http://hipstudie.nl/wp-content/uploads/2016/11/Studieprotocol-HIP-studie.pdf|
104788|NCT04067375||Informed Consent Form|http://hipstudie.nl/wp-content/uploads/2016/12/VoorbeeldAanvraag-HIPstudie.pdf|Digital form
104789|NCT04067375||Informed Consent Form|http://hipstudie.nl/wp-content/uploads/2017/01/2701-001_Formulier_27a_V1-7.pdf|Paper form
104790|NCT04067375||Approval Medical Ethical Committee|http://hipstudie.nl/wp-content/uploads/2017/03/Uitslag-CME-Verklaring-geen-bezwaar.pdf|
104791|NCT04056663|CONNECARE|Framework|http://www.connecare.eu|The ambition of the CONNECARE consortium is to co-design, develop, deploy, and evaluate a novel smart, adaptive integrated care system for chronic care management
104792|NCT04048954||ASCO CONGRESS 2018|https://ascopubs.org/doi/abs/10.1200/JCO.2018.36.15_suppl.6500|
104793|NCT04044118||Individual Participant Data Set|https://github.com/HuaZou/NonobeseBP/tree/master/datset/phenotype.csv|cohort description including sex, weigt, weight, age
104794|NCT04044118||Analytic Code|https://github.com/HuaZou/NonobeseBP/|The Rmd files are used for this study in each directory
104795|NCT04044118||gut microbiota and amino acids profiles|https://github.com/HuaZou/NonobeseBP/tree/master/datset/profile|the relative abundance profie of gut micorbiota and the concertration profiles of blood amino acids profile
104796|NCT04025034||Informed Consent Form|http://microsoftwindows.com|Navigator
104797|NCT04024644|10.1016/j.joms.2011.09.034|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22177812|
104798|NCT04024644|10.1016/j.joms.2011.09.034|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/31149009|
104799|NCT04020003|mengxinke|Individual Participant Data Set|http://www.chictr.org.cn|
104800|NCT04018547||Individual Participant Data Set|http://www.oxitone.com|De-identified data for primary and secondary outcome measures
104801|NCT04009070||Individual Participant Data Set|https://www.clinicalkey.com/#!/content/playContent/1-s2.0-S2213260016303058?returnurl=https:%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS2213260016303058%3Fshowall%3Dtrue&referrer=https:%2F%2Fwww.ncbi.nlm.nih.|
104802|NCT03997916||Individual Participant Data Set|http://redcap.uhhospitals.org/redcap|
104803|NCT03992469||Individual Participant Data Set|https://vivli.org/|
104804|NCT03990714|Proyect|Study Protocol|https://drive.google.com/file/d/1EEFxi3XpaRW12IAzVctIrrOSo6EKi70_/view?usp=sharing|A project that compares both surgical techniques in the treatment of right colon cancer and assess which is associated with a lower postoperative morbidity
104805|NCT03980028||Individual Participant Data Set|https://www.iuct-oncopole.fr/recherches-necessitant-une-reutilisation-de-donnees|All the information is provided on this web page in accordance with the RGPD regulations
104806|NCT03974633||Individual Participant Data Set|https://docs.google.com/spreadsheets/d/1dEjSUmhIkqAOvh30WaJ0svs6jrdEGDyU5FXHeBuTOF8/edit?usp=sharing|
104807|NCT03956628||stay safe programme|http://www.staysafe.ie|data can be accessed by approaching the above specified cite as it has programme that was used in the study.
104808|NCT03955380||Bibliografic References|http://ipb.hhu.de/publikationen-ipb.html|"Leithold et al., Pharm Res. 33, 328-336 (2016).~van Groen et al., Sci Rep 7, 16275 (2017).~Schemmert et al., Mol Neurobiol 56, 2211 (2019).~Kutzsche et al., Molecules 22, 1693 (2017).~Schemmert et al., Neurobiol Dis 124, 36 (2019)."
104809|NCT03944460||Bibliografic References|http://www.ipb.hhu.de/publikationen-ipb.html|"Leithold et al., Pharm Res. 33, 328-336 (2016).~van Groen et al., Sci Rep 7, 16275 (2017).~Schemmert et al., Mol Neurobiol 56, 2211 (2019).~Kutzsche et al., Molecules 22, 1693 (2017).~Schemmert et al., Neurobiol Dis 124, 36 (2019)."
104810|NCT03941470|IRB17200056|Study Protocol|http://Email:ethics_committee12@yahoo.com|
104811|NCT03928665||DDLS - reference|https://www.sign.ac.uk/assets/sign144_disc_chart_colour.pdf|
104812|NCT03912948||Web site for patient information on studies bases on patients data (RGPD)|https://www.iuct-oncopole.fr/recherches-necessitant-une-reutilisation-de-donnees|
104813|NCT03909672||Study Protocol|http://facisa.ufrn.br|
104814|NCT03906864||Publication|http://www.annals.edu.sg/pdf/42VolNo11Nov2013/V42N11p579.pdf|
104815|NCT03904082||Clinical Study Report|http://doi.org/10.1016/j.jclinane.2018.06.033|
104816|NCT03900299||Study Protocol|http://www.med.alexu.edu.eg/ethics-committee/|
105024|NCT03182582||Study Protocol|https://eprotocol.stanford.edu/|
104817|NCT03877705|Pubmed|Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/m/pubmed/30455769/?i=6&from=xylitol%20review|
104818|NCT03869892||Individual Participant Data Set|https://clinicaltrials.servier.com/|
104819|NCT03869892||Study Protocol|https://clinicaltrials.servier.com/|
104820|NCT03869892||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
104821|NCT03869892||Informed Consent Form|https://clinicaltrials.servier.com/|
104822|NCT03869892||Clinical Study Report|https://clinicaltrials.servier.com/|
104823|NCT03869892||study-level clinical trial data|https://clinicaltrials.servier.com/|
104824|NCT03856502||Individual Participant Data Set|https://hrcak.srce.hr/106014|
104825|NCT03856502||Individual Participant Data Set|https://hrcak.srce.hr/143046|
104826|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889771|
104827|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889781|
104828|NCT03856502||Individual Participant Data Set|https://www.bib.irb.hr/889773|
104829|NCT03849755||Study Protocol|https://drive.google.com/file/d/10iRR1OAoqjuQ6ot9Yt2e-ATlgDqHDtn6/view?usp=sharing|
104830|NCT03833557||Individual Participant Data Set|http://scholar.cu.edu.eg|
104831|NCT03827278||Informed Consent Form|http://oldweb.gxmuyfy.cn/gxmufy1/1fy/browse/browse6.asp?id=10080|
104832|NCT03825406||Study Protocol|http://va.gov|Type Study Protocol To request an electronic copy send email to Anthony.bavry@va.gov or debra.robertson1@va.gov
104833|NCT03825406||Individual Participant Data Set|http://va.gov|De-identified data set for primary and secondary outcomes measures To request an electronic copy send email to Anthony.bavry@va.gov or Debra.robertson1@va.gov
104834|NCT03819348||Informed Consent Form|http://oldweb.gxmuyfy.cn/gxmufy1/1fy/browse/browse6.asp?id=10080|
104835|NCT03816618||Individual Participant Data Set|https://www.nice.org.uk/guidance/CG10|National Institute for Health and Clinical Excellence. Type 2 diabetes; prevention and management of foot problems
104836|NCT03799029||Study Protocol|http://www.unifr.ch/psycho/staff/martin-soelch-chantal|No web site is provided yet
104837|NCT03793101||Clinical Study Report|http://eyemed.pl|
104838|NCT03789448||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-017-2128-8|
104839|NCT03783117||Clinical Study Report|https://www.facebook.com/Cardiovasculartherapy/?modal=admin_todo_tour|After the clinical trials are completed, the clinical study report will be provided upon request via rtao@temple.edu.
104840|NCT03762486||Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/pubmed/citmatch|
104841|NCT03761511|NICOFA|Study Protocol|https://ukaachen.sharepoint.com/:b:/s/NICOFA/ESUAT8h1fTBHlTcsdu48LrQBbvvAABdsy81bvQ4Egq696g?e=8Xliis|
104842|NCT03755154||Individual Participant Data Set|https://clinicaltrials.servier.com/|
104843|NCT03755154||Study Protocol|https://clinicaltrials.servier.com/|
104844|NCT03755154||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
104845|NCT03755154||Informed Consent Form|https://clinicaltrials.servier.com/|
104846|NCT03755154||Clinical Study Report|https://clinicaltrials.servier.com/|
104847|NCT03755154||Study-level clinical trial data|https://clinicaltrials.servier.com/|
104848|NCT03750019|10.5255/UKDA-SN-853370|Individual Participant Data Set|http://dx.doi.org/10.5255/UKDA-SN-853370|
104849|NCT03750019|10.17605/OSF.IO/WYCKJ|Study Protocol|https://doi.org/10.17605/OSF.IO/WYCKJ|
104850|NCT03745183||Study Protocol|https://drive.google.com/open?id=1ial1puH4ar075LyGcoWIrU1AXclt3FO-|
104851|NCT03745183||Tables 1-5|https://drive.google.com/open?id=1pmZyUhTfoOPWRDJgEFjMsa_K9bvQ_Lon|
104852|NCT03745183||Figure 1. Flow chart of the study procedure|https://drive.google.com/open?id=1MpUGMeNkzeOlThYZ_Zur4xTgt5cOvQNN|
104853|NCT03745183||Informed Consent Form|https://drive.google.com/open?id=1kV91jvmtUDi_BA2paf-iszXb7bCnKHZO|
104854|NCT03745183||Individual Participant Data Set|https://drive.google.com/open?id=1n3y-FDFc63KGyGfbkNBlpLJ-6HE9BBUZ|
104855|NCT03745183||Appendix E. Illustrated checklist for the T'boli|https://drive.google.com/open?id=1t2b-wyQsJaTEy6qqJCiL4Opg-Hdvdxzj|
104856|NCT03745183||Appendix F. Illustrated instruction on Senna alata decoction preparation|https://drive.google.com/open?id=17hMRr2-GhROnq7Gdw0Skd1KFApCpCgzy|
104857|NCT03743311||the SF36 scale questioner|https://clinmedjournals.org/articles/jmdt/jmdt-2-023-figure-1.pdf|The scale the SF36 scale questioner can be sent by email.
104858|NCT03739450|602d|Individual Participant Data Set|https://www.tbindsc.org/StaticFiles/SOP/602d%20-%20External%20Use%20TBIMS%20National%20Database%20Notification.pdf|
104859|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Baothman+OA%2C+Zamzami+MA%2C+Taher+I%2C+ABugaker+J%2C+Abu-Farhca+MA.+The+role+of+Gut+Microbiota+in+the+development+of+obesity+and+diabetes|
104860|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Barengolts+E.+Vitamin+D+and+prebiotics+may+benefit+the+intestinal+microbacteria+and+improve+glucose+homeostasis+in+prediabetes+and+type+2+diabetes.|
104861|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Capdor+J%2C+Foster+M%2C+Petocz+P%2C+Samman+S.+Zinc+and+glycemic+control%3A+a+meta-analysis+of+randomised+placebo+controlled+supplementation+trials+in+humans.|
104862|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Fruit+and+vegetable+intake+and+the+association+with+glucose+parameters%3A+a+cross-sectional+analysis+of+the+Let%27s+Prevent+Diabetes+Study|
104863|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/15008827|
104864|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Foster+M%2C+Petocz+P%2C+Samman+S.+Inflammation+markers+predict+zinc+transporter+gene+expression+in+women+with+type+2+diabetes+mellitus|
104865|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Gokhale+NH%2C+Acharya+AB%2C+Patil+VS%2C+Trivedi+DJ%2C+Thakur+SL.+(2013)+A+short-term+evaluation+of+the+relationship+between+plasma+ascorbic+acid+levels+and+periodontal+disease+in+systemically+healthy+and+type+2+diabetes+mellitus+subjects|
104866|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Jansen+J%2C+Rosenkranz+E%2C+Overbeck+S%2C+Warmuth+S%2C+Mocchegiani+E%2C+Giacconi+R%2C+Weiskirchen+R%2C+Karges+W%2C+Rink+L.+Disturbed+zinc+homeostasis+in+diabetic+patients+by+in+vitro+and+in+vivo+analysis+of+insulinomimetic+activity+of+zinc|
104867|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/20606205|
104868|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/22699609|
104869|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Kayaniyil+S%2C+Vieth+R%2C+Retnakaran+R%2C+Knight+JA%2C+Qi+Y%2C+Gerstein+HC%2C+et+al.+Association+of+vitamin+D+with+insulin+resistance+and+beta-cell+dysfunction+in+subjects+at+risk+for+type+2+diabetes.+Diabetes+care|
104870|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Ley%2C+R.+E.%2C+Lozupone%2C+C.+A.%2C+Hamady%2C+M.%2C+Knight%2C+R.+%26+Gordon%2C+J.+I.+Worlds+within+worlds%3A+evolution+of+the+vertebrate+gut+microbiota|
104871|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Mandl+J%2C+Szarka+A%2C+Bángheyl.+(2009)+Vitamin+C%3A+update+on+physiology+and+pharmacology.+B+J+Pharmacol|
104872|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Efficacy+of+supplementary+vitamins+C+and+E+on+anxiety%2C+depression+and+stress+in+type+2+diabetic+patients%3A+a+randomized%2C+single-blind%2C+placebo-controlled+trial|
104873|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Effect+of+vitamin+C+supplementation+on+postprandial+oxidative+stress+and+lipid+profile+in+type+2+diabetic+patients.|
104874|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/9794114|
104875|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Rafighi%2C+Z.%2C+Shiva+A.%2C+Arab%2C+S.+and+Mohd+Yousof%2C+R.+(2013)+Association+of+dietary+vitamin+C+and+E+intake+and+antioxidant+enzymes+in+type+2+diabetes+mellitus+patients|
104876|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Zinc+as+a+potential+coadjuvant+in+therapy+for+type+2+diabetes.|
104877|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Sarmento+RA%2C+Silva+FM%2C+Sbruzzi+G%2C+Schaan+BD%2C+Almeida+JC.+Antioxidant+micronutrients+and+cardiovascular+risk+in+patients+with+diabetes%3A+a+systematic+review|
104878|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/25284151|
104879|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/27915988|
104880|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Insulino-mimetic+and+anti-diabetic+effects+of+zinc|
104881|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/28615382|
104882|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/12502486|
104883|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/22375253|
104884|NCT03734445||scientific article|http://www.ncbi.nlm.nih.gov/pubmed/?term=Iman+M+Ibrahim%2C+and+Manal+M+Alkady.+Role+of+Vitamin+D+on+glycemic+control+and+oxidative+stress+in+type+2+diabetes+mellitus|
104885|NCT03733470|Data Distribution|Individual Participant Data Set|http://www.i-clic.uihc.uiowa.edu/|
104886|NCT03731416||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/27283920|
104887|NCT03723382|StateData001|Clinical Study Report|http://www.strokesregistry.com/data-in-graphs/|These are measures for national stroke measures in State Pool of data
104888|NCT03715166||Individual Participant Data Set|https://clinicaltrials.servier.com/|
104889|NCT03715166||Study Protocol|https://clinicaltrials.servier.com/|
104890|NCT03715166||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
104891|NCT03715166||Informed Consent Form|https://clinicaltrials.servier.com/|
104892|NCT03715166||Clinical Study Report|https://clinicaltrials.servier.com/|
104893|NCT03715166||study-level clinical trial data|https://clinicaltrials.servier.com/|
104894|NCT03715153||Individual Participant Data Set|https://clinicaltrials.servier.com/|
104895|NCT03715153||Study Protocol|https://clinicaltrials.servier.com/|
104896|NCT03715153||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
104897|NCT03715153||Informed Consent Form|https://clinicaltrials.servier.com/|
104898|NCT03715153||Clinical Study Report|https://clinicaltrials.servier.com/|
104899|NCT03715153||study-level clinical trial data]|https://clinicaltrials.servier.com/|
104900|NCT03701113|2018_04_05_EHS|Study Protocol|http://www.ul.ie/ehs/research-ethics|Contact The EHS Research Ethics Contact Point of the Education and Health Sciences Research Ethics Committee, Room E1003, University of Limerick, Limerick, Ireland
104901|NCT03696901|Xydalba|Study Protocol|https://awbdb.bfarm.de/ords/f?p=101:STARTSEITE::::::|BfArM AWB Datenbank
104902|NCT03692286||Individual Participant Data Set|https://drive.google.com/open?id=1rZXDbSgsneWDO4xGz8KGkklEHHw2YYIX|
104903|NCT03686436||Study Protocol|https://www.clinicaltrials.gov|
104904|NCT03681574|study protocol|Study Protocol|https://www.justbeamit.com/k7ciq|study protocol
104905|NCT03681574|data set|Individual Participant Data Set|https://www.justbeamit.com/nwxjr|individual participant data set
104906|NCT03681574|informed consent form|Informed Consent Form|https://www.justbeamit.com/n2c2d|consert form
104907|NCT03681574|statistical plan|Statistical Analysis Plan|https://www.justbeamit.com/43kxq|statistical plan
104908|NCT03673397||Individual Participant Data Set|https://doi.org/10.7910/DVN/WASN36|
104909|NCT03672695||Individual Participant Data Set|https://clinicaltrials.servier.com/|
104910|NCT03672695||Study Protocol|https://clinicaltrials.servier.com/|
104911|NCT03672695||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
104912|NCT03672695||Informed Consent Form|https://clinicaltrials.servier.com/|
104913|NCT03672695||Clinical Study Report|https://clinicaltrials.servier.com/|
104914|NCT03672435||Individual Participant Data Set|http://www.abcd-vision.org/OCR/OCR%20proparacaine%20de-identified.pdf|deidentified OCR topical anesthetic recovery outcomes
104915|NCT03668067||Individual Participant Data Set|http://www.abcd-vision.org/references/2WIN%20Bus%20de-identified%209-6-18.pdf|Public de-identified ongoing
104916|NCT03662165||Individual Participant Data Set|https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/UULS6T|
104917|NCT03641729||Study Protocol|http://aline.priori.fioritto@gmail.com|More information contact the principal investigator
104918|NCT03630744||web page|http://fluidday.com|
104919|NCT03626220||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/27013473|
104920|NCT03612674||Analytic Code|http://www.epiclin.it|
104921|NCT03602833||Summary of Product Characteristics|https://www.medicines.org.uk/emc/product/8453|
104922|NCT03602001||Study Protocol|https://osf.io/btzhw/|The study protocol was pre-registered prior to starting recruitment on the Open Science Framework and is available via this link. IPD underlying publications will also be available here.
104923|NCT03582969||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/25938992|
104924|NCT03582215||Individual Participant Data Set|https://jamanetwork.com/journals/jama/fullarticle/2733085|Deidentified participant data for Part 1 is accessible under Supplement 3
104925|NCT03582215||Individual Participant Data Set|https://jamanetwork.com/journals/jama/fullarticle/2759002|Deidentified participant data for Part 2 is accessible under Supplement 3
104926|NCT03579303|123|Individual Participant Data Set|http://bethesda.org?data-id=123|De-identified data for primary and secondary outcome measures
104927|NCT03567629||Individual Participant Data Set|https://en.wikipedia.org/wiki/United_States_National_Library_of_Medicine|
104928|NCT03556917||Statistical Analysis Plan|http://www.unopar.com.br/|
104929|NCT03553264||Study Protocol|https://www.comitatoeticolazio1.it/comitato-etico-lazio-1/segreteria-tecnico-scientifica|
104930|NCT03543904||Pilot study|http://doi.org/10.1016/j.jpedsurg.2019.10.058|Preserving pulmonary function and functional capacity in children undergoing open abdominal surgery: A one group pretest-posttest, quasiexperimental pilot trial
104931|NCT03543904|Version 1|Individual Participant Data Set|http://dx.doi.org/10.17632/skkt9tsjd3.1|"Effect of Pre-operative physiotherapy education and Post-operative physiotherapy in children with abdominal surgery, Mendeley Data, v1 http://dx.doi.org/10.17632/skkt9tsjd3.1"
104932|NCT03543904||Clinical Study Report|http://doi.org/10.1016/j.jpedsurg.2020.04.007|A randomized clinical trial in improving pulmonary function and functional capacity in paediatric open abdominal surgery
104933|NCT03532815||Study Protocol|https://sites.google.com/view/lifestyle-intervention-/home|
104934|NCT03521492||Individual Participant Data Set|https://files.fm/u/x9zfbndg|
104935|NCT03495635|osf.io/8ukfv|Individual Participant Data Set|https://osf.io/|
104936|NCT03494712||Individual Participant Data Set|https://clinicaltrials.servier.com/|
104937|NCT03494712||Study Protocol|https://clinicaltrials.servier.com/|
104938|NCT03494712||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
104939|NCT03494712||Informed Consent Form|https://clinicaltrials.servier.com/|
104940|NCT03494712||Clinical Study Report|https://clinicaltrials.servier.com/|
104941|NCT03494712||study-level clinical trial data|https://clinicaltrials.servier.com/|
104942|NCT03470298|ABC123|Individual Participant Data Set|http://doi.org/10.1093/humrep/dew053|
104943|NCT03459976|10.1002/jcla.22223|Individual Participant Data Set|https://www.scopus.com/record/display.uri?eid=2-s2.0-85017447906&origin=resultslist&sort=plf-f&src=s&st1=DJ-1%3b+HE4%3b+PARK7%3b+endometrial+cancer&st2=&sid=c9b2b927dbc42cc33a01eb39e68b0a6d&sot=b&sdt=b&sl=51&s=TITLE-ABS-KEY%28DJ-1%3b+HE4%3b+PARK7%3b+endometrial+cancer%29&relpos=0&citeCnt=0&searchTerm=|DJ-1; HE4; PARK7; endometrial cancer
104944|NCT03449992||Individual Participant Data Set|https://doi.org/10.6084/m9.figshare.5873190.v1|
104945|NCT03436095||Clinical Study Report|http://www.szrch.com/|
104946|NCT03434782|60622416.1.0000.0018|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
104947|NCT03427138|C2495|Individual Participant Data Set|http://ndar.nih.gov|
104948|NCT03413566||Individual Participant Data Set|https://www.siv.no/seksjon/CP-registeret_/Documents/CPRN-registration_at_5_years.pdf|Cerebral Palsy Registry of Norway - registration form at 5 years of age
104949|NCT03413566||Informed Consent Form|https://www.siv.no/seksjon/CP-registeret_/Documents/Samtykker-og-skjemaer/Samtykke_CPRNogCPOP_130206_engelsk.pdf|Cerebral Palsy Registry of Norway - consent form
104950|NCT03411161||Individual Participant Data Set|https://clinicaltrials.servier.com/|
104951|NCT03411161||Study Protocol|https://clinicaltrials.servier.com/|
104952|NCT03411161||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
104953|NCT03411161||Informed Consent Form|https://clinicaltrials.servier.com/|
104954|NCT03411161||Clinical Study Report|https://clinicaltrials.servier.com/|
104955|NCT03411161||study-level clinical trial data|https://clinicaltrials.servier.com/|
104956|NCT03408275||Individual Participant Data Set|http://www.bristol.ac.uk/alspac/|ALSPAC data available to researchers on application through the website
104957|NCT03407391||Individual Participant Data Set|http://www.bristol.ac.uk/alspac/|ALSPAC data is available for use by researchers on application through the website
104958|NCT03391583||Individual Participant Data Set|http://project-redcap.org/|"The Applied Health Research Centre (AHRC), an academic research organization based at St Michael's Hospital, will use software called REDCap to create the web-based electronic CRF (eCRF).~Authorized personnel receive a username and password which is unique, and database access is controlled by the DCC in collaboration with the Principal Investigator."
104959|NCT03361943||Individual Participant Data Set|https://www.cdc.gov/nchs/nhanes/nhanes_questionnaires.htm|NHANES provides de-identified data for public use that can be readily downloaded. This study did not use any restricted data.
104960|NCT03347734||Clinical Study Report|https://en.wikipedia.org/wiki/Bates_method|
104961|NCT03336827||Study design|http://pdf.lu/YtWd|
104962|NCT03336827||List of questionnaires|http://pdf.lu/TJ4c|
104963|NCT03336827||Informed Consent Form|http://pdf.lu/dN2P|
104964|NCT03336827||Informed Consent Form|http://pdf.lu/07Xz|
104965|NCT03331120|Neck pain,Ambulatory,Orthotic|Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-019-3337-0|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-019-3337-0
104966|NCT03324321||Funder|http://dunhillmedical.org.uk/|Dunhill RTF Grant (RTF97/0117)
104967|NCT03315234|NCT03150680|Clinical Study Report|https://clinicaltrials.gov/ct2/show/NCT03150680|"GESS trial [ClinicalTrials.gov Identifier: NCT03150680] was designed exclusively based on the protocol of the study Correlation of Genetic Polymorphisms and Clinical Parameters With the Complexity of Coronary Artery Disease [CIP_PhD Rampidis Georgios_1.1]"
104968|NCT03311048|Sistema Nacional de Informação|Informed Consent Form|http://portal2.saude.gov.br/sisnep/pesquisador|
104969|NCT03306394||Individual Participant Data Set|https://clinicaltrials.servier.com/|
104970|NCT03306394||Study Protocol|https://clinicaltrials.servier.com/|
104971|NCT03306394||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
104972|NCT03306394||Informed Consent Form|https://clinicaltrials.servier.com/|
104973|NCT03306394||Clinical Study Report|https://clinicaltrials.servier.com/|
104974|NCT03306394||study-level clinical trial data|https://clinicaltrials.servier.com/|
104975|NCT03289130||Individual Participant Data Set|https://pcap.bioinf.unc.edu/|
104976|NCT03286517||Any information required can be provided|http://www.qau.edu.pk/profile.php?id=802001|Prof. Muhammad Shahab will provide the information upon request.
104977|NCT03284073|NCT01844362|Study Protocol|http://clinicaltrials.gov|
104978|NCT03276611||Statistical Analysis Plan|http://www.ncbi.nlm.nih.gov/|
104979|NCT03274882||Individual Participant Data Set|https://clinicaltrials.servier.com/|
104980|NCT03274882||Study Protocol|https://clinicaltrials.servier.com/|
104981|NCT03274882||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
104982|NCT03274882||Informed Consent Form|https://clinicaltrials.servier.com/|
104983|NCT03274882||Clinical Study Report|https://clinicaltrials.servier.com/|
104984|NCT03274882||Study-level clinical trial data|https://clinicaltrials.servier.com/|
104985|NCT03273465||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/25938992|
104986|NCT03272282|prospective auther of journals|Study Protocol|http://www.iiste.org/journals/|All the journals articles are amiable online to the reader all over the world without financially legal barriers
104987|NCT03266926||Study Protocol|https://www.scribd.com/document/344597619/Study-Protocol|
104988|NCT03266926||Informed Consent Form|https://www.scribd.com/document/344597523/Consent-Form|
104989|NCT03266926||Individual Participant Data Set|https://www.scribd.com/document/344597573/Data-Collection-Spreadsheet|
104990|NCT03266926||Participant Documents|https://www.scribd.com/document/344597424/Participant-Documents|
104991|NCT03257202|HS-17-00319|Study Protocol|http://istar.usc.edu|
104992|NCT03257202|HS-17-00319|Informed Consent Form|http://istar.usc.edu|
104993|NCT03253887||Study Protocol|https://www.cdc.gov/hicpac/bsi/bsi-guidelines-2011.html|Guidelines for the Prevention of Intravascular Catheter-Related Infections, 2011
104994|NCT03253887||Study Protocol|https://www.cdc.gov/nhsn/pdfs/pscmanual/4psc_clabscurrent.pdf|Bloodstream Infection Event (Central Line-Associated Bloodstream Infection and non-central line-associated Bloodstream Infection)
104995|NCT03253887||Study Protocol|https://www.cdc.gov/nhsn/pdfs/pscmanual/17pscnosinfdef_current.pdf|CDC/NHSN Surveillance Definitions for Specific Types of Infections
104996|NCT03249168||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/26705527|
104997|NCT03246035|CODIM-MBM-17-052|Study Protocol|http://www.ladydavis.ca/en/jonathanafilalo|Pilot study protocol
104998|NCT03246035|CODIM-MBM-17-052|Informed Consent Form|http://www.ladydavis.ca/en/jonathanafilalo|Patient consent Caregiver consent French and English available
104999|NCT03238742|2|Clinical Review& Education|http://www.ncbi.nlm.nih.gov/pubmed/26903338|Singer M, Deutschman CS, Seymour CW, Shankar-Hari M, Annane D, Bauer M, Bellomo R, Bernard GR, Chiche JD, Coopersmith CM, Hotchkiss RS, Levy MM, Marshall JC, Martin GS, Opal SM, Rubenfeld GD, van der Poll T, Vincent JL, Angus DC.The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). JAMA. 2016;315(8):801-10.
105000|NCT03237949|NCT02571244|Study Protocol|https://clinicaltrials.gov|This protocol is an extension of a previous research:Telephone Counseling and Text Messaging for Supporting Post-discharge Quit Attempts Among Hospitalized Smokers in Brazil, a feasibility study.
105001|NCT03228316||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/27208713|
105002|NCT03222765||Study Protocol|http://www.epredice.eu|Study Protocol Version 5.0
105003|NCT03214068||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282811/|
105004|NCT03207321||Individual Participant Data Set|http://apcaps.lshtm.ac.uk/|
105005|NCT03206541||Suplemental Data|https://www.nejm.org/doi/suppl/10.1056/NEJMoa1605564/suppl_file/nejmoa1605564_appendix.pdf|This data set contains detailed information on a cohort of 68 cases with Guillain-Barre syndrome that was analyzed as part of NEAS. The NEAS forms used to collect clinical information are available at the end of the document.
105006|NCT03205020||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/25118503|
105007|NCT03202433||Clinical Study Report|http://www.researchgate.net/publication/287542931_Psychological_coping_with_invasive_and_painful_medical_procedures_in_the_treatment_of_childhood_and_adolescent_cancer_The_cognitive-behavioural_approach|
105008|NCT03202433||Clinical Practice Guide|http://www.criscancer.org|
105009|NCT03200561|201308036MIND|Clinical trial approval|https://drive.google.com/file/d/0B0dfeciPPNsQVjg1N0ktcXJxYm8/view?usp=sharing|
105010|NCT03196960||Scoring Sheet|https://docs.google.com/document/d/1pqYbMe4S-W-vgYRHzd1d4Is7s6ZbMt_MGDlWtndRRdM/edit?usp=sharing|Mobilization Quantification Score
105011|NCT03196479||Textbook|http://accessmedicine.mhmedical.com/book.aspx?bookID=564|Butterworth JF, Mackey DC, Wasnick JD. Morgan & Mikhail's Clinical Anesthesiology. 5th ed. New York: McGraw Hill Education, 2013.
105012|NCT03194984|27045285|Metanalysis, systematic review|https://www.ncbi.nlm.nih.gov/pubmed/?term=27045285|
105013|NCT03194984|21740236|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=21740236|
105014|NCT03194984|21488723|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=21488723|
105015|NCT03194984|27007348|Informed Consent Form|https://www.ncbi.nlm.nih.gov/pubmed/?term=27007348|
105016|NCT03192163||Survey|http://j.mp/2qdz7P2|This is the RedCap survey that subjects will take.
105017|NCT03192020||Study Protocol|http://bmjopen.bmj.com/content/8/3/e019054|Protocol in BMJ Open access
105018|NCT03191227||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/22984148|Cohort profile
105019|NCT03189797||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed|
105020|NCT03189238||Informed Consent Form|http://cvvd.org/research|"Link for the informed consent is in the section titled PLATELET RICH PLASMA (PRP) INJECTIONS FOR THE TREATMENT OF FEMALE ORGASMIC DISORDER."
105021|NCT03188016||PhD thesis explaining origin of the musical improvisation approach to be trialed|http://arro.anglia.ac.uk/314588/|NB In the thesis the staff interacting with the young people with intellectual disability were not following principles of Intensive Interaction, although some had been trained in that approach and spontaneously applied some elements of it. All cases were studied solely by way of reviewing video recordings after a lapse of 1 - 2 years.
105022|NCT03185104||Study Protocol|https://1drv.ms/w/s!AlX91p3wWjCtlEgV-_cCb_yGU4Uo|Study protocol can be downloaded from this web site.
105025|NCT03181711||Study Protocol|http://mah.se|can be requested by mail Karin.Ridell@mah.se
105026|NCT03180775|0566-16-RMB|Study Protocol|https://drive.google.com/file/d/0B3pwT5OrV8jZRlR0cUd5SG9aQnM/view?usp=sharing|
105027|NCT03180775|0566-16-RMB|Data sheet-Dietary supplements|https://drive.google.com/drive/folders/0B3pwT5OrV8jZalBEYjhlTlZ5bnc?usp=sharing|The data sheet from each one of the amino acids that will be administered to the participants as dietary supplements are included in this file.
105028|NCT03180203|Study Intensive Care|Study Protocol|https://www.catharinaziekenhuis.nl/contact.html|Contact can be made to request the study protocol (Dutch)
105029|NCT03179280||Poster at an international meeting|http://2011.ispad.org/materials/final_program.pdf|
105030|NCT03177967||Study Protocol|https://www.oppegard.kommune.no/helse/psykisk-helsetjeneste-|The study protocol is unfortunately only available in Norwegian at the time being.
105031|NCT03177772|dtp38|Study Protocol|https://osf.io/dtp38/|Open Science Framework. we are registered
105032|NCT03176446|1.941.369|Approval of the ethics committee|http://plataformabrasil.saude.gov.br|
105033|NCT03173209|Calm Moments Cards program|intervention materials|http://www.everymomentcounts.org|Calm Moments Cards program
105034|NCT03172468||Informed Consent Form|https://box.medunigraz.at/s/QuTYym3xsqXybWI|
105035|NCT03172468||Study Protocol|https://box.medunigraz.at/s/YbufqAn3DBI1f4Q|
105036|NCT03167671|ISBN-10: 1886039224|Book|https://www.amazon.com/Prescription-Drug-Abuse-Epidemic-Understanding/dp/1886039224|
105037|NCT03167671||NAtional statistical Report|https://www.bls.gov/news.release/pdf/osh2.pdf|year 2015
105038|NCT03167580||Study Protocol|https://sites.google.com/view/relaxtrial/study-details-and-documents/protocol|
105039|NCT03162744||Consensus conference report|https://www.has-sante.fr/portail/upload/docs/application/pdf/suicilong.pdf|
105040|NCT03160456|IPG598|"NICE guidance Hypoglossal Nerve Stimulation"|https://www.nice.org.uk/guidance/ipg598|National Institute for Health and Care Excellence
105041|NCT03160040|MINOCIN® (minocycline)|Package Insert|http://www.themedicinescompany.com/products/us-marketed-products|"MINOCIN® (minocycline) for Injection 100 mg/vial. United States Prescribing Information.~The Medicines Company; Parsippany, New Jersey. April 2015"
105042|NCT03159403|ORBACTIV® (oritavancin)|Package Insert|http://www.themedicinescompany.com/products/us-marketed-products|ORBACTIV® (oritavancin). United States Prescribing Information. The Medicines Company; Parsippany, New Jersey. October 2016
105043|NCT03151694||Peer-Reviewed Article|http://onlinelibrary.wiley.com/doi/10.1111/jcpp.12646/full|
105044|NCT03151694||Peer-Reviewed Article|http://jamanetwork.com/journals/jamapediatrics/fullarticle/2529982|
105045|NCT03151694||Peer-Reviewed Article|http://jamanetwork.com/journals/jamapediatrics/fullarticle/2529983|
105046|NCT03151694||Peer-Reviewed Article|http://www.sciencedirect.com/science/article/pii/S0149763416303281|
105047|NCT03150264||Study Protocol|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161575/|
105048|NCT03142451||Study Protocol|http://foamix.co.il/|
105049|NCT03141970|CTRI/2015/06/005939|Study Protocol|http://ctri.nic.in/Clinicaltrials/login.php|Contains details of registration of clinical trial prior to recruiting patients in India, at website of Clinical Trials Registry of India
105050|NCT03141281|https://osf.io/dp8n5/|Statistical Analysis Plan|https://osf.io/kq8yz/register/565fb3678c5e4a66b5582f67|Open Science Foundation registration of Data Analysis Plan
105051|NCT03141216||Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|"Search for buscar pesquisas aprovadas and fill the the blanks with research title and investigator's full name"
105052|NCT03139591||Textbook|https://books.google.co.id/books/about/Laryngeal_Mask_Anesthesia.html?id=XBJsAAAAMAAJ&redir_esc=y|Problems. In: Brimacombe JR. Laryngeal Mask Anesthesia principles and practice. London: Saunders Ltd, 2004;551-71.
105053|NCT03136705|STU00089165|Study Protocol|https://irb.northwestern.edu/contact|
105054|NCT03136705|STU00089165|Informed Consent Form|https://irb.northwestern.edu/contact|
105055|NCT03136042||references|https://www.ncbi.nlm.nih.gov/pubmed/|GINA. Global Strategy for Asthma Management and Prevention NHLBI/WHO Workshop Report 2012. 2012 ISAAC. Worldwide variations in the prevalence of asthma symptoms: the International Study of Asthma and Allergies in Childhood (ISAAC). Eur Respir J 1998; 12:315-335 Solé D, Wandalsen GF, Camelo-Nunes IC, et al. Prevalence of symptoms of asthma, rhinitis, and atopic eczema among Brazilian children and adolescents identified by the International Study of Asthma and Allergies in Childhood (ISAAC) - Phase 3. J Pediatr (Rio J) 2006; 82:341-346 Barnabé V, Saraiva B, Stelmach R, et al. Chest physiotherapy does not induce bronchospasm in stable asthma. Physiotherapy 2003; 89:714-719 ATS. Standardization of Spirometry - American Thoracic Society. Am J Respir Crit Care Med 1995; 152:1107-1136 Saraiva-Romanholo BM, Barnabe V, Carvalho AL, et al. Comparison of three methods for differential cell count in induced sputum. Chest 2003; 124:1060-1066
105056|NCT03134924||Informed Consent Form|https://miami.box.com/s/bpncfa8380gph02cxk3c69g90de0pgt2|
105057|NCT03134612||Textbook|https://sydney.edu.au/medicine/pmri/pdf/Acute-pain-management-scientific-evidence-third-edition.pdf|Assessment and measurement of pain and its treatment. In: Macintyre PE SD, Schug SA, Visser EJ, Walker SM, editors. Acute pain management: scientific evidence. Melbourne: Australian and New Zealand College of Anaesthetists and Faculty of Pain Medicine; 2010.p. 35-43
105058|NCT03134612||Textbook|http://accessanesthesiology.mhmedical.com/book.aspx?bookID=413|Candido KD, Winnie AP. Intravenous regional block for upper & lower extremity surgery. In: Hadzic A, editor. Textbook of regional anesthesia and acute pain management. New York: McGraw-Hill; 2007. p. 565-78
105059|NCT03134612||Textbook|http://accessmedicine.mhmedical.com/book.aspx?bookID=564|Butterworth JF, Wasnick JD. Adjuncts to anesthesia. In: Butterworth JF, Wasnick JD, editors. Morgan & Mikhail's Clinical Anesthesiology. New York: McGraw-Hill; 2013. p. 277-93
105060|NCT03134612||Textbook|http://accessmedicine.mhmedical.com/book.aspx?bookid=1613|Sanders-Bush E HL. 5-Hydroxytryptamine (Serotonin) and Dopamin. In: Brunton L CB, Knollman B, editors. Goodman and Giman's The Pharmacological Basis of Therapeutics. New York: McGraw-Hill; 2011
105061|NCT03134560||Textbook|https://books.google.co.id/books/about/Pediatric_Anesthesia.html?id=RYe4GBD6LrQC&redir_esc=y|Hannallah RS , Verghese ST. Peripheral vascular access. In: Bissonnette B, Anderson BJ, Bosenberg A, Engelhardt T, Mason LJ, Tobias JD, editors. Pediatric Anesthesia. Connecticut: People's Medical Publishing House USA, 2011.p. 1097-102.
105103|NCT03075046||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|
105062|NCT03134287||Textbook|http://onlinelibrary.wiley.com/doi/10.1111/j.1742-6723.2004.00655.x/full|Samuels LE, Roberts JR, Hedges JR. Nasogastric and Feeding Tube Placement, In: Clinical Procedures in Emergency Medicine. 4th ed. WB Saunders; 2004. p784-804.
105063|NCT03134287||Textbook|https://books.google.co.id/books?id=ooH1nH81_h4C&pg=PR4&lpg=PR4&dq=Irwin+and+Rippe%27s+Intensive+Care+Medicine+2008&source=bl&ots=43X9QRBshe&sig=Y3ycuRyss2vYHzN3q0WFtrSdPRM&hl=en&sa=X&ved=0ahUKEwjk_6TIo8LTAhWMvY8KHSvTDo8Q6AEIRzAG#v=onepage&q=Irwin%20and%20Rippe's%20Intensive%20Care%20Medicine%202008&f=false|Irwin RS, Rippe JM. Irwin and Rippe's Intensive Care Medicine: Endoscopic Placement of Feeding Tubes. 6th ed. Lippincott Williams & Wilkins; 2008. p145-150.
105064|NCT03134287||Textbook|https://books.google.co.id/books/about/The_ICU_Book.html?id=OWEmVx9MS74C&redir_esc=y|Marino PL. Enteral Tube Feeding. In: The ICU Book. 3rd ed. Lippincott Williams & Wilkins; 2007. p842-855.
105065|NCT03134235||Individual Participant Data Set|https://drive.google.com/file/d/0B3HECjLwDFbeLTctV3pic0pXUDA/view?usp=sharing|Demographics, anthropometrics, biochemical and nutrient intake data.
105066|NCT03134235||Study Protocol|https://drive.google.com/file/d/0B3HECjLwDFbeYVhRYnVPVkZRbHc/view?usp=sharing|
105067|NCT03134235||Statistical Analysis Plan|https://drive.google.com/file/d/0B3HECjLwDFbedGczRlRTMGtVRVk/view?usp=sharing|
105068|NCT03134235||Informed Consent Form|https://drive.google.com/file/d/0B3HECjLwDFbeNjNMZXhGSmY3dTQ/view?usp=sharing|
105069|NCT03128190||Individual Participant Data Set|http://lattes.cnpq.br/0310250742582348|
105070|NCT03128190||Individual Participant Data Set|http://lattes.cnpq.br/1823080587913061|
105071|NCT03126253||Report of the survey along with sampling plan|https://dhsprogram.com/pubs/pdf/fr265/fr265.pdf|
105072|NCT03125265||Study Protocol|http://bmjopen.bmj.com/content/5/3/e006897.long|
105073|NCT03122808||Study Protocol|https://drive.google.com/file/d/0B9G2TfsoMdfsdnlyd2p0M2dYcVk/view?usp=sharing|
105074|NCT03121027||Individual Participant Data Set|https://dhsprogram.com/pubs/pdf/fr265/fr265.pdf|Detail about sampling and BDHS 2011 report
105075|NCT03119298||application for ethical approval|https://www.uni-trier.de/index.php?id=55894&L=2|The application for ethical approval (German version) includes the study protocol, statistical analysis plan and informed consent form. To request an electronic copy send an email to spaderna@uni-trier.de.
105076|NCT03119025||Clinical Study Report|https://doi.org/10.1007/s12026-017-8967-2|Chernykh E., Leplina O., Oleynik E., Tikhonova M., Tyrinova T., Starostina N., Ostanin A. Immunotherapy with interferon-α-induced dendritic cells for chronic HCV infection (the results of pilot clinical trial) // Immunologic Research.- 2017
105077|NCT03118219||Study Protocol|https://www.klinikum.uni-heidelberg.de/personen/apl-prof-dr-sc-hum-tewes-wischmann-2809/|Study Data can be requested per mail to Tewes Wischmann
105078|NCT03117725|31098|Study Protocol|https://ezdrug.mfds.go.kr|
105079|NCT03117322||Informed Consent Form|https://drive.google.com/file/d/0B2DsNKWyL7bfNUo4NkVPd3V0aHc/view?usp=sharing|Just a google drive link to download the informed consent form in pdf.
105080|NCT03116672|UABC|Clinical Study Report|http://www.uabc.mx|Clinical trial that evaluate drug and placebo
105081|NCT03116672|protocol guide|Individual Participant Data Set|http://www.uabc.mx|Clinical Guide
105082|NCT03114072||Study Protocol|https://helseforskning.etikkom.no/prosjekterirek/prosjektregister/prosjekt?p_document_id=742253&p_parent_id=755398&_ikbLanguageCode=n|This is a brief description of the Project published at the web site of The Regional Ethics Committee (REC West).
105083|NCT03112317|REC West (2016-2193)|Study Protocol|https://helseforskning.etikkom.no/komiteerogmoter/vest/sekretariat?region=10796&p_dim=34985&_ikbLanguageCode=us|Study protocol is available on request to Regional Committees for Medical and Health Research Ethics.
105084|NCT03111290||Summary Data Set|http://dx.doi.org/10.5281/zenodo.45811|Dataset supporting Alagapan et al. 2016 PLoS Biology
105085|NCT03111186|HS-15-00706|Study Protocol|http://istar.usc.edu|
105086|NCT03111186|HS-15-00706|Informed Consent Form|http://istar.usc.edu|
105087|NCT03110471||Publications|http://orcid.org/0000-0002-5691-2987|Prof Sue Jordan- publication list
105088|NCT03105713|2016/1102|Study Protocol|https://helseforskning.etikkom.no/komiteerogmoter/vest/sekretariat?p_dim=34985&region=10796|Study protocol in English and other relevant information on this study can be accessed by e-mail to Arvid.Haugen@helse-bergen.no
105089|NCT03105362||Study Protocol|http://www.childrenshospital.org/research-and-innovation/research/research-administration/office-of-clinical-investigation|For further details contact Lissette Jimenez, MD Email: lissette.jimenez@childrens.harvard.edu
105090|NCT03104972||similar protocol|http://www.ncbi.nlm.nih.gov/pubmed/27339019|Looi CY, Cohen Kadosh R. Brain stimulation, mathematical, and numerical training: Contribution of core and noncore skills. Prog Brain Res. 2016;227:353-88. doi: 10.1016/bs.pbr.2016.04.009.
105091|NCT03102775||first report (Norwegian)|http://www.hioa.no/Om-HiOA/Senter-for-velferds-og-arbeidslivsforskning/AFI/Publikasjoner-AFI/Helhetlig-oppfoelging-av-lavinntektsfamilier|
105092|NCT03098173||Study Protocol|http://www.todai-shoukakan.com/cont4/29.html|
105093|NCT03091231|mpUS2016|Study Protocol|http://www.martini-klinik.de|to request an electronic copy send an email to a.renter@uke.de
105094|NCT03091114||Study Protocol|https://uni-wh.de/fileadmin/user_upload/03_G/07_Humanmedizin/05_Institute/IFOM/IFF-PROFAK_Protocol.pdf|
105095|NCT03091075|APP-17-01020|Study Protocol|http://istar.usc.edu|
105096|NCT03091075|APP-17-01020|Informed Consent Form|http://istar.usc.edu|
105097|NCT03088501|PMID: PMC5065083|Protocol of the birth cohort|https://bmcpregnancychildbirth.biomedcentral.com/articles/10.1186/s12884-016-1088-4|The proposed randomized controlled trial is nested within the MAASTHI Birth cohort in order to improve the follow-up rates.
105098|NCT03085576||Clinical Study Report|http://www.stcccv-tunisie.com/files/Nature%20AF%20%20STCCCV-2018.pdf|Study results (presentation)
105099|NCT03083795||Study Protocol|https://docs.google.com/document/d/1r7Lx_wrrZ9PrTMHU5VcGd2n4UnEhx0EuMotejIr_bh8/edit?usp=sharing|Study protocol
105100|NCT03083795||Informed Consent Form|https://docs.google.com/a/bcdiabetes.ca/document/d/13w8Jyd6TrHWTNjUD-n90OCaHqZGzYQ2vGdk1Z3-F8Kc/edit?usp=sharing|Informed consent form
105101|NCT03077464||preliminary results|http://hdl.handle.net/2097/19148|Rodicheva master's thesis document with preliminary analyses
105102|NCT03075332|plataforma brasil|Ethics committee project|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|all project
105477|NCT02527629||Study results|https://pubmed.ncbi.nlm.nih.gov/32386409/|
105104|NCT03074695|Pro00079368|Informed Consent Form|https://eirb.mc.duke.edu/|
105105|NCT03070470|ECGCIPA|Individual Participant Data Set|https://physionet.org/physiobank/database/ecgcipa/|ECG effects of ranolazine, verapamil, lopinavir+ritonavir, chloroquine, dofetilide, diltiazem, and dofetilide+diltiazem in a small sample size clinical study. The ECGCIPA database contains multi-channel ECG recordings, pharmacokinetic, and clinical data of 60 subjects participating in the CiPA ECG validation study.
105106|NCT03070470||Study Protocol|https://ascpt.onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fcpt.896&file=cpt896-sup-0001-suppinfo1.pdf|Study protocol included in the supporting information of the study design and rationale manuscript (Vicente et al. Clin Pharmacol Ther 2018, doi: 10.1002/cpt.896)
105107|NCT03070470||Statistical Analysis Plan|https://ascpt.onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fcpt.896&file=cpt896-sup-0003-suppinfo3.pdf|Statistical Analysis Plan (SAP) included in the supporting information of the study design and rationale manuscript (Vicente et al. Clin Pharm Ther 2018, doi: 10.1002/cpt.896)
105108|NCT03070470||Study Results Report|https://ascpt.onlinelibrary.wiley.com/doi/epdf/10.1002/cpt.1303|Report with full baseline characteristics, adverse events frequencies by treatment, and Consolidated Standards of Reporting Trials (CONSORT) flow diagram, as well as detailed results for multiple ECG biomarkers, as described in the statistical analysis plan is available as Supplementary Materials S1 in the study results manuscript (Vicente et al. Clin Pharmacol Ther 2018 Nov 17. doi: 10.1002/cpt.1303. [Epub ahead of print])
105109|NCT03070106||The Institute of Functional Medicine Consensus Statement|https://www.functionalmedicine.org/AboutFM/Initiatives/ClevelandClinic/|Functional Medicine Diagnostic and Treatment Approach to Type 2 Diabetes Mellitus and Cardio-Metabolic Syndrome
105110|NCT03068299|63133316.4.0000.5504|Ethics Acceptance letter|http://plataformabrasil.saude.gov.br/login.jsf|Enter with number CAAE box (63133316.4.0000.5504) and access the official document of ethics acceptance letter of study.
105111|NCT03068000||Individual Participant Data Set|https://www.ncbi.nlm.nih.gov/pubmed/21874720|The study by Bala and Drid (2010) was used for the sample calculation of the participants.
105112|NCT03067259|10.1016/j.neuint.2005.10.007|Study Protocol|http://www.sciencedirect.com/science/article/pii/S0197018605002500|
105113|NCT03060421||Study Protocol|http://www.parkerinst.dk|
105114|NCT03058211|PI16/00486|Study Protocol|http://www.iispv.cat|Protocol in Spanish language
105115|NCT03058211|PI16/00486|Informed Consent Form|http://www.iispv.cat|Informed consent form in Spanish language
105116|NCT03057886|56202616.9.0000.0083|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|There you may find the project and all step to get the approval
105117|NCT03053128||Individual Participant Data Set|http://www.medresman.org|
105118|NCT03052374||Informed Consent Form|http://childstudies.ca/contact|
105119|NCT03052374||Study Protocol|http://childstudies.ca/contact|
105120|NCT03052374||Statistical Analysis Plan|http://childstudies.ca/contact|
105121|NCT03049917|Current FIT Protocol|Study Protocol|http://depts.washington.edu/gwach/wp-content/uploads/2012/10/2.18.18-FIT-Protocol_V4.0_clean_.pdf|
105122|NCT03047122|P110006|U.S. Food and Drug Administration. somo-v Automated Breast Ultrasound System|http://www.accessdata.fda.gov/cdrh_docs/pdf11/P110006b.pdf|
105123|NCT03045458||Clinical Study Report|http://mc.manuscriptcentral.com/jperio|
105124|NCT03045172||Informed Consent Form|http://www.cvvd.org/research|"Click the link titled NEW STUDY FOR LICHEN SCLEROSUS- PLATELET RICH PLASMA (PRP)- Open to new participants to open the informed consent."
105125|NCT03044899||Study Protocol|http://www.asos.org.za/|ASOS Protocol version 1.0
105126|NCT03044171|57655916.3.0000.0018|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
105127|NCT03038061||Informed Consent Form|http://ventilation.fbmi.cvut.cz/wp-content/uploads/2017/01/Informed-Consent-Form.pdf|Informed Consent
105128|NCT03037814|26161601|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/26161601|
105129|NCT03037814|19953810|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/19953810|
105130|NCT03037814|12542617|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/12542617|
105131|NCT03034850||Study Protocol|https://drive.google.com/open?id=0B0qo2hDQpXhncWZFZkNfZXhZMjVuUGcxc0IzZll5TEtjaXdn|
105132|NCT03034850|eudract/B-nr B37120154199|Advice Ethical Committee|https://drive.google.com/open?id=0B0qo2hDQpXhnU3AzRHY0d1NtVmlsSmx1cFhKOGtKLTVscno0|
105133|NCT03032692||Study Protocol|https://drive.google.com/file/d/0B2kmuI2zObfcMVhZYWhpdm9fRUE/view?usp=sharing|
105134|NCT03030352||Pilot Study of the How-to trial|http://link.springer.com/article/10.1007/s10826-013-9751-0|
105135|NCT03029195||Study Protocol|http://dent.alexu.edu.eg/|
105136|NCT03029078||Study Protocol|https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-003048-11/FR|
105137|NCT03019835||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/7880668|
105138|NCT03019133|201609843|Informed Consent Form|http://hawkirb.research.uiowa.edu|
105139|NCT03016676||Study Protocol|http://www.ijpbs.net/abstract.php?article=5240|
105140|NCT03013725||Study Protocol|http://husk.b.uib.no/prototest/|Protocol
105141|NCT03012802||Study Protocol|http://www.grupogerm.es/power|
105142|NCT03012802||Statistical Analysis Plan|http://www.grupogerm.es/power|
105143|NCT03012802||Clinical Study Report|http://www.grupogerm.es/power|
105144|NCT03011385||Study Protocol|https://drive.google.com/file/d/0BzlMP61UQ1tGYlRDYTlZN2NOTXM/view?usp=sharing|The file includes the protocol of data collection and intervention sessions
105145|NCT03009370||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/26806685|
105146|NCT02995941||Study Protocol|https://drive.google.com/file/d/0BzDEuj8l-dI1QkZSRUtyZGJ0RG8/view?usp=sharing|
105147|NCT02995941||Individual Participant Data Set|https://drive.google.com/file/d/0BzDEuj8l-dI1VEppLWVOb2Jhd00/view?usp=sharing|Patient Group Data Forms
105148|NCT02995941||Individual Participant Data Set|https://drive.google.com/file/d/0BzDEuj8l-dI1cHJFWkpKQmEweEU/view?usp=sharing|Rater Group Data Form
105149|NCT02993627|18039384|Clinical Study Report|http://lipidworld.biomedcentral.com/articles/10.1186/1476-511X-6-33/|
105150|NCT02993627||Clinical Study Report|https://www.scopus.com/inward/record.uri?eid=2-s2.0-70449559397&partnerID=40&md5=d8d36fa95497bf9e358abf2acbfa3923|
105151|NCT02991781|neurofeedback-auth|Individual Participant Data Set|http://ckan.smokefreebrain.eu/|
105152|NCT02990988||Survey Report|https://www.hhs.gov/oidp/topics/blood-tissue-safety/surveys/national-blood-collection-and-utilization-survey/index.html|
105153|NCT02988076|CNSR012 Protocol|Study Protocol|http://myndanalytics.com|Please email snavarre@myndanalytics.com for approved version of the protocol
105154|NCT02988076|CNSR012 ICD|Informed Consent Form|http://myndanalytics.com|Please email snavarre@myndanalytics.com for approved version of ICD
105155|NCT02985697|DEXProtocol|Study Protocol|https://drive.google.com/open?id=0BwBFaEmsvS0PYnlzVDUyMGREWFk|Protocol for the study; includes introduction, design, and references/citations.
105156|NCT02983916||Clinical Study Report|https://doi.org/10.1038/s41395-018-0158-9|
105157|NCT02982967||Individual Participant Data Set|https://figshare.com/s/8f238bd02ca631cfe5fd|
105158|NCT02979366||Individual Participant Data Set|https://clinicaltrials.servier.com/|
105159|NCT02979366||Study Protocol|https://clinicaltrials.servier.com/|
105160|NCT02979366||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
105161|NCT02979366||Informed Consent Form|https://clinicaltrials.servier.com/|
105162|NCT02979366||Clinical Study Report|https://clinicaltrials.servier.com/|
105163|NCT02979366||Study-level clinical trial data|https://clinicaltrials.servier.com/|
105164|NCT02968966||Synopsis|http://www.medizin.uni-tuebingen.de/kinder/de/abteilungen/cpcs/projekte/|
105165|NCT02964767||Epidemiological report|http://www.who.int|
105166|NCT02964767||Clinical Study Report|http://www.Wiley.com|
105167|NCT02960750|4382156|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382156/?report=classic|
105168|NCT02960750|4323230|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323230/?report=classic|
105169|NCT02960750|4266209|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266209/|
105170|NCT02948881|BON103593|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105171|NCT02948881|BON103593|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105172|NCT02948881|BON103593|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105173|NCT02948881|BON103593|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105174|NCT02948881|BON103593|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105175|NCT02948881|BON103593|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105176|NCT02948881|BON103593|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105177|NCT02947802||Study Instrument (Online Survey)|https://hbs.qualtrics.com/SE/?SID=SV_1LdkKR5P4DyCevH|This is the online survey participants will complete.
105178|NCT02944292||Study Protocol|https://drive.google.com/open?id=0B-XpW352z4ZJMFdseHNwTWI2clU|
105179|NCT02941159||Study Protocol|http://www.tdrc.org.zm|Data documents can be requested from at info@tdrc.org.zm using the above given website contact page
105180|NCT02940678|10.6084/m9.figshare.4042572.v1|Study Protocol|https://dx.doi.org/10.6084/m9.figshare.4042572.v1|
105181|NCT02938884||Study Protocol|https://oncore.umn.edu/login/|
105182|NCT02931422|FIT-Pilot|Study Protocol|https://catalyst.uw.edu/workspace/jslyker/55146/|Anyone with a gmail account should be able to access this PDF. Please contact the study investigators to request a copy of the protocol if you are unable to access this link.
105183|NCT02929134|NTDSC 056.2 Sri Lanka|Study Protocol|http://www.ntdsupport.org/|Contact NTDSupport@taskforce.org
105184|NCT02929121|NTDSC 056.1 India|Study Protocol|http://www.ntdsupport.org/|Contact NTDSupport@taskforce.org
105185|NCT02928796||Ethics Approval|https://drive.google.com/file/d/0BwB78Ersj1NcNTIydG9PYnNrSnc/view?usp=sharing|Ethical approval from Clinical Research Ethics Committee, University College Cork
105186|NCT02928796||Study Protocol|https://drive.google.com/file/d/0BwB78Ersj1NcNzI3MHA2eHZ1U28/view?usp=sharing|"Ethical applications to Clinical Research Ethics Committee, University College Cork.~Includes Study Protocol, including references and CV of Chief Investigator Prof Anthony G Gallagher."
105187|NCT02928783||Individual Participant Data Set|http://1drv.ms/u/s!AoPKs7skMI1VhFodaJODFrvEJ9kc|Data set
105188|NCT02927496|NTDSC 056.3 Mali|Study Protocol|http://www.ntdsupport.org/|Contact NTDSupport@taskforce.org
105189|NCT02926820||Study Protocol|http://www.yorku.ca/ctill|The lead investigator, Dr. Christine Till, can be contacted by email (ctill@yorku.ca) for a copy of the Informed Consent Form or study protocol.
105190|NCT02924961|PMID: 22055272|Clinical Study Report|http://www.sciencedirect.com/science/article/pii/S0268003311002816|First publication on subset (first 20 patients) of this study
105191|NCT02924961|PMID: 29448880|Clinical Study Report|https://www.tandfonline.com/doi/pdf/10.1080/17453674.2018.1429108|6-year analysis paper
105192|NCT02922075||Individual Participant Data Set|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|"Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets.~All data can be downloaded from the website, if there are any questions please feel free to contact us."
105193|NCT02922075||Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets. All data can be downloaded from the website, if there are any questions please feel free to contact us.
105194|NCT02922075||Statistical Analysis Plan|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets. All data can be downloaded from the website, if there are any questions please feel free to contact us.
105244|NCT02870946||Study Protocol|https://1drv.ms/b/s!AsGKR7DfCSXas3VgxZsCQh7c29IR|Additional file of study protocol
105298|NCT02777736||Study Protocol|http://www.lymphoma.cz/docs/studies/dlbcl/CLSG-CNS-01_en.pdf|
105195|NCT02922075||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets. All data can be downloaded from the website, if there are any questions please feel free to contact us.
105196|NCT02922075||Clinical Study Report|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets. All data can be downloaded from the website, if there are any questions please feel free to contact us.
105197|NCT02922075||Analytic Code|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|Public title: Stability of the architecture of the hard and soft tissue after immediate tooth replacement with implants in fresh grafted sockets. All data can be downloaded from the website, if there are any questions please feel free to contact us.
105198|NCT02920697||Individual Participant Data Set|https://clinicaltrials.servier.com/|
105199|NCT02920697||Study Protocol|https://clinicaltrials.servier.com/|
105200|NCT02920697||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
105201|NCT02920697||Informed Consent Form|https://clinicaltrials.servier.com/|
105202|NCT02920697||study-level clinical trial data|https://clinicaltrials.servier.com/|
105203|NCT02920697||Clinical Study Report|https://clinicaltrials.servier.com/|
105204|NCT02920541||Individual Participant Data Set|https://clinicaltrials.servier.com/|
105205|NCT02920541||Study Protocol|https://clinicaltrials.servier.com/|
105206|NCT02920541||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
105207|NCT02920541||Informed Consent Form|https://clinicaltrials.servier.com/|
105208|NCT02920541||study-level clinical trial data|https://clinicaltrials.servier.com/|
105209|NCT02920541||Clinical Study Report|https://clinicaltrials.servier.com/|
105210|NCT02918916||Tables. Training program, Phototherapy parameters, Time point of outcomes|https://pt.scribd.com/document/325401697/Documents-ClinicalTrials-ID-2015-25219-0|
105211|NCT02917278||Meeting abstract|https://www.asn-online.org/api/download/?file=/education/kidneyweek/archives/KW16Abstracts.pdf|Abstract presented as a poster at the ASN Kidney Week 2016 (TH-PO762)
105212|NCT02916992|NL50605.091.14|Study Protocol|https://www.toetsingonline.nl/to/ccmo_search.nsf/Searchform?OpenForm|ABR form (Algemeen Beoordelings en Registratie formulier; document of dutch board of human research (Centrale Commissie Mensgebonden Onderzoek)
105213|NCT02916758||Individual Participant Data Set|http://grad.kean.edu/ot/faculty|Please contact cmulry@kean.edu to request the data set
105214|NCT02914301|FWA00005945|Informed Consent Form|https://files.acrobat.com/a/preview/c262292c-6de1-4f73-bae3-689555b8c77f|
105215|NCT02914301|Post-Partum Survey|Individual Participant Data Set|https://files.acrobat.com/a/preview/5ec925dd-52ad-4b07-b6fc-2084d2f751d5|
105216|NCT02914301|Prenatal Participant Data -22|Individual Participant Data Set|https://files.acrobat.com/a/preview/984213bb-ccef-419b-8f56-87336004ec5a|
105217|NCT02909712||Assessment report: Eurartesim - dihydroartemisinin / piperaquine phosphate EMEA/H/C/1199|http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Public_assessment_report/human/001199/WC500118116.pdf|
105218|NCT02907489||Study Protocol|https://www.scribd.com/document/328018560/Protocol-Omaia-Repaired-Autosaved|
105219|NCT02905604||Study Protocol|https://lakemedelsverket.se/english/product/Medical-devices/Clinical-Investigations/|Updated investigational plan can be requested from the Swedish medical products agency
105220|NCT02904824||Clinical Study Report|http://www.dynasolutions.com|CRO data base
105221|NCT02899858|140503|Study Protocol|https://www4.vanderbilt.edu/irb/|
105222|NCT02898246||application for ethical approval|https://www.uni-trier.de/index.php?id=55894&L=2|The application for ethical approval (German version) includes the study protocol, statistical analysis plan and informed consent form. To request an electronic copy send an email to spaderna@uni-trier.de.
105223|NCT02896686||Study Protocol|https://cirurgiahj23.wordpress.com|
105224|NCT02893735||Clinical Study Report|https://live.blueskybroadcast.com/bsb/client/_new_default.asp?action=SEARCH&Client=404900|
105225|NCT02889458|BrCA.risk.001|Study Protocol|http://www.hkuctr.com/Study/Show/b122235f3995420a97d570a85d03b542|
105226|NCT02887300||Clinical Study Report|https://www.rcpi.ie/research/hospital-doctors-wellbeing/|
105227|NCT02887014||Appendix. Verbal instructions depending on participants' randomization|https://docs.google.com/document/d/1zXjjsaT73xrnsDaGpmhIXzpNgQiJaOLvs9BNB4ZHyFk/edit?usp=sharing|
105228|NCT02885298||Study Protocol|https://drive.google.com/drive/folders/0B5w-TjIZHObhSWxqbElCUmxINnc|Study protocol can be provided via email if requested. Please email turnjose@iu.edu
105229|NCT02882880|Study Protocol|Study Protocol|http://lucohybridosa.com/?post_type=wpdmpro&p=3683&preview=true|
105230|NCT02882880|Statistical Analysis Plan|Statistical Analysis Plan|http://lucohybridosa.com/?post_type=wpdmpro&p=3683&preview=true|
105231|NCT02882880|Informed Consent|Informed Consent Form|http://lucohybridosa.com/wp-content/uploads/2016/08/INFORMED-CONSENT.pdf|
105232|NCT02882880|Study Report|Clinical Study Report|http://lucohybridosa.com/wp-content/uploads/2016/08/CLINICAL-STUDY-REPORT.pdf|
105233|NCT02879747||Study Protocol|http://www.gpgrc.gu.se|"The document will be found under Trials and then GH-dose/Maintenance study"
105234|NCT02879747||Statistical Analysis Plan|http://www.gpgrc.gu.se|"The document will be found under Trials and then GH-dose/Maintenance study"
105235|NCT02877810||Study Protocol|http://www.ucdmc.ucdavis.edu/children/clinical_services/pediatric_telemedicine/Telemed_Research.html|Any study documents may be requested directly from Jamie Kissee at jkissee@ucdavis.edu
105236|NCT02877615||Study Protocol|https://clinicaltrials.servier.com/|
105237|NCT02877615||Individual Participant Data Set|https://clinicaltrials.servier.com/|
105238|NCT02877615||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
105239|NCT02877615||Informed Consent Form|https://clinicaltrials.servier.com/|
105240|NCT02877615||Clinical Study Report|https://clinicaltrials.servier.com/|
105241|NCT02877615||Study-level clinical trial data|https://clinicaltrials.servier.com/|
105242|NCT02872376||Study Protocol|https://sites.google.com/site/ridartstudy/|
105243|NCT02872376||Informed Consent Form|https://sites.google.com/site/ridartstudy/|
105245|NCT02870426||Individual Participant Data Set|http://www.stgeorges.nhs.uk|The project documents will be available directly from the research team. Please e-mail Dr Florence Hogg fhogg@sgul.ac.uk
105246|NCT02855476||Study Protocol|http://hdclarity.net/study-information/|
105247|NCT02855476||Informed Consent Form|http://hdclarity.net/study-information/|Draft informed consent form, not yet approved by an Institutional Review Board for clinical use
105248|NCT02854007||Study Protocol|http://reparaqalystudy.com/publicprotocol.php|
105249|NCT02853799||Study Protocol|http://journals.lww.com/annalsofsurgery/pages/articleviewer.aspx?year=2016&issue=03000&article=00007&type=abstract|"2. Chowdhury, Abeed H., et al. Effects of Bolus and Continuous Nasogastric Feeding on Gastric Emptying, Small Bowel Water Content, Superior Mesenteric Artery Blood Flow, and Plasma Hormone Concentrations in Healthy Adults: A Randomized Crossover Study. Annals of Surgery (2014)."
105250|NCT02853747||Study Protocol|https://dsbg.unibas.ch/forschung/|Homepage DSBG Research
105251|NCT02848443||Individual Participant Data Set|https://clinicaltrials.servier.com/|
105252|NCT02848443||Study Protocol|https://clinicaltrials.servier.com/|
105253|NCT02848443||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
105254|NCT02848443||Informed Consent Form|https://clinicaltrials.servier.com/|
105255|NCT02848443||Clinical Study Report|https://clinicaltrials.servier.com/|
105256|NCT02848443||study-level clinical trial data|https://clinicaltrials.servier.com/|
105257|NCT02848053||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/?term=Chinese+Herbal+Medicine+Tianqi+Reduces+Progression+From+Impaired+Glucose+Tolerance+to+Diabetes%3A+A+Double-Blind%2C+Randomized%2C+Placebo-Controlled%2C+Multicenter+Trial|This is the original study, the registration study is the follow-up study aimed at Tianqi capsule
105258|NCT02842671||Study Protocol|http://irb.psu.edu|
105259|NCT02842671||Informed Consent Form|http://irb.psu.edu|for participants
105260|NCT02842671||Accommodation Survey|http://irb.psu.edu|
105261|NCT02842671||Patient Satisfaction Survey|http://irb.psu.edu|
105262|NCT02842671||Medical Student Survey|http://irb.psu.edu|
105263|NCT02842671||Summary Explanation of Research|http://irb.psu.edu|for medical students
105264|NCT02841488||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf|
105265|NCT02839564||Study Protocol|http://gmail.com|Study data can be requested by mailing to mjmolegraaf@gmail.com
105266|NCT02836769||Study Protocol|http://www.implementationscience.com/content/10/1/6|Publication of the initial project protocol
105267|NCT02836769||Clinical Study Report|http://link.springer.com/article/10.1007%2Fs00520-015-3021-1|Publication based on findings from focus groups used to create the intervention in this study
105268|NCT02836002||Individual Participant Data Set|https://datadryad.org//resource/doi:10.5061/dryad.60h41|
105269|NCT02833129||Study Protocol|http://arxiv.org/abs/1607.01756|
105270|NCT02829567||Informed Consent Form|https://drive.google.com/file/d/0B_GXNZ4CbxyGVWxrcG1RV1ozZTA/view?usp=sharing|
105271|NCT02829359||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/28122361|Oncotarget. 2017 Feb 28;8(9):15047-15056. doi: 10.18632/oncotarget.14789.
105272|NCT02827396||Study Protocol|http://www.sjog.mw|Contact the author
105273|NCT02827396||Individual Participant Data Set|http://www.sjog.mw|Contact author
105274|NCT02826850||Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf#|
105275|NCT02826850||Informed Consent Form|http://aplicacao.saude.gov.br/plataformabrasil/visao/pesquisador/gerirPesquisa/gerirPesquisaAgrupador.jsf#|
105276|NCT02812888||Individual Participant Data Set|https://www.opendrive.com/|"Using network platform: https://www.opendrive.com/ username: 18361811955@163.com password: woaini1314 The repository and management of the data can be obtained via Public Folder."
105277|NCT02809612||Study Protocol|http://www.kbh.uu.se|
105278|NCT02808442||Individual Participant Data Set|https://clinicaltrials.servier.com/|
105279|NCT02808442||Study Protocol|https://clinicaltrials.servier.com/|
105280|NCT02808442||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
105281|NCT02808442||Informed Consent Form|https://clinicaltrials.servier.com/|
105282|NCT02808442||Clinical Study Report|https://clinicaltrials.servier.com/|
105283|NCT02808442||Study-level clinical trial data|https://clinicaltrials.servier.com/|
105284|NCT02804958|INTERSTELLAR-Stature|Clinical Study Report|http://www.ajconline.org/article/S0002-9149(16)30568-9/fulltext|Relation of Stature to Outcomes in Korean Patients Undergoing Primary Percutaneous Coronary Intervention for Acute ST-Elevation Myocardial Infarction
105285|NCT02800720||Embedded Qualitative Study|http://link.springer.com/article/10.1007/s12671-015-0458-8|
105286|NCT02798900||Statistical Analysis Plan|https://uredu-my.sharepoint.com/personal/rosy_cardenas_urosario_edu_co/_layouts/15/guestaccess.aspx?guestaccesstoken=QcFnsRtAu0sL3C3BykRoRmzup56%2fKS1U50PYsgfCPaQ%3d&docid=180e16d39085f4beda2f90ff3f40398ad|
105287|NCT02798900||Informed Consent Form|https://uredu-my.sharepoint.com/personal/rosy_cardenas_urosario_edu_co/_layouts/15/guestaccess.aspx?guestaccesstoken=22KPPvsG5ChMhU6k%2bwtjMT9u%2b72A2ABD0JwYpY0D7p8%3d&docid=1b012eb2a38df4685b5d63e2429ba5bcf|
105288|NCT02798640||Informed Consent Form|https://mega.nz/#!C5U1HZwI!7XB2jar-JDElrnYOZTbwg0RD5T1WPQEv3HkzT0XPXz8|
105289|NCT02798640||Clinical Investigation plan|https://mega.nz/#!3gEnFCDK!DK911mpjGBw_bAKdfsR4F2RgzCQG7mYR3oBqrVkRtpA|
105290|NCT02798640||Clinical Study Report|https://mega.nz/#!S1tThKrL!gaWPII28P3I0BLBrLD9iZJYRqb2R1x-uZT5djgV4ML8|
105291|NCT02795052||Clinical Study Report|http://mdstemcells.com/nest/|http://mdstemcells.com/nest/
105292|NCT02789085||Reference|http://www.psy.unsw.edu.au/research/research-tools/depression-anxiety-stress-scales-dass|UNSW Australia SoP. Depression & Anxiety Stress Scales (DASS): UNSW Australia; 2011
105293|NCT02786264||Statistical Analysis Plan|https://docs.google.com/document/d/1SUzYG_9aKT5sSkPXEmhvRTqvhXRflQLBiXJe59inDh4/edit?usp=sharing|
105294|NCT02785562||Study Protocol|http://www.g-f-p-c.org|The login can be obtained directly on gfpc site.
105295|NCT02779647||Study Protocol|http://scielo.isciii.es/pdf/nh/v28n3/22original18.pdf|
105296|NCT02779647||Study Protocol|http://scielo.isciii.es/pdf/nh/v28n3/23original19.pdf|
105297|NCT02777996||Study Protocol|http://www.ispo.it|In Italian, available under request
105299|NCT02774122|22633033|Individual Participant Data Set|http://www.sciencedirect.com/science/article/pii/S0140673612604693|
105300|NCT02771652||Detailed intervention description|https://www.sport.fau.de/files/2016/05/ms-intakt-e-training-intervention-description.pdf|Detailed description of the processes of the e-training intervention (english language)
105301|NCT02771652||Clinical Study Report|https://www.sport.fau.de/files/2015/05/ms-intakt-abschlussbericht-19_05_2015.pdf|Final report for funding foundation (german)
105302|NCT02761967||Study Protocol|http://www.nutricionhospitalaria.es/wp-content/uploads/2016/02/27_AE_10155_Aguilar_esp.pdf|
105303|NCT02761967||Sistematic review|http://revista.nutricionhospitalaria.net/index.php/nh/article/view/514/312|
105304|NCT02758483|63683417.1.0000.5257|Study Protocol|http://aplicacao.saude.gov.br/plataformabrasil/login.jsf|
105305|NCT02755818||Informed Consent Form|https://www.irbnet.org/release/study/overview.do?ctx_id=0&spk_id=855867|for a copy of Approved Consent Form-please contact Study Coordinator -Tjien Dwyer at tlthio@ucdavis.edu
105306|NCT02754401||statistic of the government|http://www.bzaek.de/fileadmin/PDFs/GOZ-Analyse/yb12-13_goz-analyse-12.pdf|24. Bundeszahnärztekammer (2013) Statistisches Jahrbuch 2012/2013. BZÄK, Berlin 160-169.
105307|NCT02753270||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/18426039|
105308|NCT02753270||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/19952380|
105309|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/20922783|
105310|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/?term=In+vitro+effects+of+detergent+sclerosants+on+coagulation%2C+platelets+and+microparticles.|
105311|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/21725957|
105312|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/16226898|
105313|NCT02753270||Literature Review|http://www.ncbi.nlm.nih.gov/pubmed/11231246|
105314|NCT02751086||Study Protocol, study information, news|http://www.imigastric.com|"The study is open to other interested Institutions.~Correspondance to:~Jacopo Desiderio, MD djdesi85@hotmail.it"
105315|NCT02748603||Report on National Journal|http://www.giornaledicardiologia.it/r.php?v=1015&a=11055&l=15130&f=allegati/01015_2012_01/fulltext/06.De%20Servi%20(47-49).pdf|De Servi S, Klugmann S: Qualità e appropriatezza dell'angioplastica coronarica in Lombardia: qualche riflessione sui dati di attivita' del registro della Società Italiana di Cardiologia Invasiva SICI-GISE) . G. Ital Cardiol 2012; 13: 47-9
105316|NCT02747875|Pr 7364|Study Protocol|http://www.irbear.org|The Effect of Methadone vs. Fentanyl Administration on Postoperative Pain Control in Pediatric Patients Undergoing Cardiac Surgery. A Randomized, Double-Blinded Controlled Trial
105317|NCT02747017||Study Protocol|http://insight.ccbr.umn.edu/official_documents/CDIFF/protocol_documents/I7-Protocol.pdf|
105318|NCT02746952||Individual Participant Data Set|https://clinicaltrials.servier.com/|
105319|NCT02746952||Study Protocol|https://clinicaltrials.servier.com/|
105320|NCT02746952||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
105321|NCT02746952||Informed Consent Form|https://clinicaltrials.servier.com/|
105322|NCT02746952||Clinical Study Report|https://clinicaltrials.servier.com/|
105323|NCT02746952||Study-level clinical trial data|https://clinicaltrials.servier.com/|
105324|NCT02744521|Study protocol|Study Protocol|https://sites.google.com/site/relevantdocuments2016|I shared this protocol on Google Plus.
105325|NCT02744144||Statistical Analysis Plan|http://ki.se/en/people/andalg|
105326|NCT02744092|AFT-28|Study Protocol|https://www.allianceforclinicaltrialsinoncology.org/main/public/standard.xhtml?path=%2FPublic%2FAFT|Email the study team at CANVAS@AllianceFoundationTrials.org.
105327|NCT02743221||Individual Participant Data Set|http://clinicaltrials.servier.com/|
105328|NCT02743221||Study Protocol|https://clinicaltrials.servier.com/|
105329|NCT02743221||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
105330|NCT02743221||Informed Consent Form|https://clinicaltrials.servier.com/|
105331|NCT02743221||Clinical Study Report|https://clinicaltrials.servier.com/|
105332|NCT02743221||study-level clinical trial data|https://clinicaltrials.servier.com/|
105333|NCT02740309|Sala Institute|Sala Institute for Child & Family Centered Care|http://nyulangone.org/locations/hassenfeld-childrens-hospital/sala-institute-for-child-family-centered-care|
105334|NCT02738463||Individual Participant Data Set|http://www.ncbi.nlm.nih.gov/pubmed|
105335|NCT02735083||Individual Participant Data Set|https://clinicaltrials.servier.com/|
105336|NCT02735083||Study Protocol|https://clinicaltrials.servier.com/|
105337|NCT02735083||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
105338|NCT02735083||Informed Consent Form|https://clinicaltrials.servier.com/|
105339|NCT02735083||Clinical Study Report|https://clinicaltrials.servier.com/|
105340|NCT02735083||Study-level clinical trial data|https://clinicaltrials.servier.com/|
105341|NCT02732145|ISBN:978-1-63484-507-6|Chapter/Commentary|https://novapublishers.com/shop/cryosurgery-and-colposcopy-practices-outcomes-and-potential-complications/|"Harni V, Babic D, Barisic D. Three Rings Vulvoscopy - A New Approach to the Vulva. In: Cryosurgery and Colposcopy: Practices, Outcomes and Potential Complications, Editor: Lillian Watson. Publisher: Nova Science Publishers Inc, NewYork, USA, 2016."
105342|NCT02731820||Study Protocol|http://www.ior.it/en/ricerca-e-innovazione/ethical-committee|Study protocol is available on request
105343|NCT02731820|doi: 10.3390/nu10091293|Clinical Study Report|http://www.mdpi.com/2072-6643/10/9/1293/pdf|
105344|NCT02729831||outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Hip Osteoarthritis Decision Quality Instrument
105345|NCT02729831||outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Knee Osteoarthritis Decision Quality Instrument
105346|NCT02726776||Study Protocol|https://cloud.scientificnet.org/index.php/s/7vKbCJ1vs0UOYNN|Unfortunately available only in German
105347|NCT02726776||Informed Consent Form|https://cloud.scientificnet.org/index.php/s/9RXyWhRxEgUgbTd|Unfortunately available only in German or Italian
105348|NCT02726464||Patient Brochure|http://www.lightintegra.com/prism-study|
105349|NCT02724826||Clinical Study Report|http://resolver.ebscohost.com/openurl?sid=Entrez%3aPubMed&id=pmid%3a18090079&site=ftf-live|
105476|NCT02531503||Clinical Study Report|http://www.jacionline.org/article/S0091-6749(15)01766-2/abstract|
105350|NCT02718261|NCT02467621|Study Protocol|https://clinicaltrials.gov/ct2/show/NCT02467621?term=SUP-ICU&rank=1|SUP-ICU Website
105351|NCT02714907||Study Protocol|http://cortrium.com|In Danish language
105352|NCT02713438||Study Protocol|https://goo.gl/zqU1tI|The handbook with the protocol for experimenters (in Polish)
105353|NCT02712255||Study Protocol|https://goo.gl/O1mn1t|The handbook with the protocol for experimenters (in Polish)
105354|NCT02711891|Loperamide|Study Protocol|http://www.rush.edu/clinical-trials-rush-university-medical-center|Contact the Rush Office of Research Affairs for all materials 312 942-5498
105355|NCT02711891|Loperamide|Informed Consent Form|http://www.rush.edu/clinical-trials-rush-university-medical-center|Contact the Rush Office of Research Affairs for all materials 312 942-5498
105356|NCT02706938|Informed Consent Form|Informed Consent Form|https://drive.google.com/file/d/0B6Uam9x9PtiiZzRVZE5wQmhIV1E/view?usp=sharing|Informed Consent Form
105357|NCT02706938|Basic Data Formulary|Basic Data Formulary|https://drive.google.com/file/d/0B6Uam9x9PtiiVS1GUWl6Q0pFWWs/view?usp=sharing|Formulary for gathering basic variables of each participant
105358|NCT02706938|SF-36 questionnaire|SF-36 questionnaire|https://drive.google.com/file/d/0B6Uam9x9PtiiVFVTY2dUVDA2UkE/view?usp=sharing|Questionnaire for assessing secondary outcome
105359|NCT02706938|RDQ questionnaire|RDQ questionnaire|https://drive.google.com/file/d/0B6Uam9x9PtiieExLaGJyZDVVV00/view?usp=sharing|Questionnaire for assessing primary outcome
105360|NCT02706938|Instruction for the patient|Instructions for the patient|https://drive.google.com/file/d/0B6Uam9x9PtiiMVJDbVhLVFY1bnc/view?usp=sharing|Written instructions for the patient about how to use wooden prisms.
105361|NCT02706938|Clinical Trial Protocol|Study Protocol|https://drive.google.com/open?id=0B6Uam9x9PtiiV2xUcDBKU3RHYU0|
105362|NCT02705690||Analytic Code|https://bitbucket.org/samjewell/stannah-iphone-accelerometer/src|
105363|NCT02701218|ENT-2558-03601|Study Protocol|http://ros.med.cmu.ac.th/Security/SignIn.aspx|Research administration section website
105364|NCT02700490|10.17863/CAM.43399|Complete Data Set|https://doi.org/10.17863/CAM.43399|
105365|NCT02700087|Consent form cycle 3|Informed Consent Form|https://eprotocol.stanford.edu/irb/ControlServlet?updateFlag=Y|
105366|NCT02699957|Data Collection Form|Individual Participant Data Set|http://cvquality.acc.org/en/NCDR-Home/Data-Collection.aspx|
105367|NCT02699957|Data Dictionary|Individual Participant Data Set|http://cvquality.acc.org/en/NCDR-Home/Data-Collection.aspx|Element definitions and coding instructions.
105368|NCT02699736||Study Protocol|http://www.chip.dk/Ongoing-Studies/EuroSIDA/Study-documents|
105369|NCT02698098||Study Protocol|http://dx.doi.org/10.7910/DVN/RO34OK|
105370|NCT02698098||Individual Participant Data Set|http://dx.doi.org/10.7910/DVN/RO34OK|
105371|NCT02698098||Analytic Code|http://dx.doi.org/10.7910/DVN/RO34OK|
105372|NCT02697058||Individual Participant Data Set|https://clinicaltrials.servier.com/|
105373|NCT02697058||Study Protocol|https://clinicaltrials.servier.com/|
105374|NCT02697058||Statistical Analysis Plan|https://clinicaltrials.servier.com/|
105375|NCT02697058||Informed Consent Form|https://clinicaltrials.servier.com/|
105376|NCT02697058||Clinical Study Report|https://clinicaltrials.servier.com/|
105377|NCT02697058||study-level clinical trial data|https://clinicaltrials.servier.com/|
105378|NCT02696850|SNOT-22|Questionnaire|https://otm.wustl.edu/for-industry/tools/#SNOT|
105379|NCT02696850|CGI scale|Questionnaire|https://www.psywellness.com.sg/docs/CGI.pdf|
105380|NCT02696603||Data description|http://www.nature.com/articles/sdata201611|Here we present data from mPower, a clinical observational study about Parkinson disease conducted purely through an iPhone app interface. The study interrogated aspects of this movement disorder through surveys and frequent sensor-based recordings from participants with and without Parkinson disease. Benefitting from large enrollment and repeated measurements on many individuals, these data may help establish baseline variability of real-world activity measurement collected via mobile phones, and ultimately may lead to quantification of the ebbs-and-flows of Parkinson symptoms. App source code for these data collection modules are available through an open source license for use in studies of other conditions. We hope that releasing data contributed by engaged research participants will seed a new community of analysts working collaboratively on understanding mobile health data to advance human health.
105381|NCT02696174||Study Protocol|https://www.flipdrive.com/site/login|Username: HMI Password: insurance Total protocol FILE named protocol.pdf
105382|NCT02696174||Informed Consent Form|https://www.flipdrive.com/site/login|Username: HMI Password: insurance Patient Information Sheet and Consent forms in English and Bahasa Malaysia
105383|NCT02696174||Questionnaires|https://www.flipdrive.com/site/login|Username: HMI Password: insurance All questionnaires (English) uploaded
105384|NCT02695394||Supporting information: Methods and Results|https://onlinelibrary.wiley.com/doi/10.1111/ene.14269|
105385|NCT02694016||Study Protocol|https://drive.google.com/file/d/0B8f6XnAry76dUERObVRWUjhGZzg/view?usp=sharing|English protocol description file
105386|NCT02694016||Informed Consent Form|https://drive.google.com/file/d/0B8f6XnAry76dYW04ZDNld3VNV2c/view?usp=sharing|Finnish language consent form
105387|NCT02694016||Patient information in Finnish|https://drive.google.com/file/d/0B8f6XnAry76dTGEtenRaUENSUTg/view?usp=sharing|Patient information in Finnish
105388|NCT02693626|15OCCSULiaoYanhui|Study Protocol|http://pan.baidu.com/disk/home#list/path=%2F|Please send me email: tangliaoyanhui@163.com if you cannot open it.
105389|NCT02692495|10.17632/8bk6h6bmkr.1|Individual Participant Data Set|https://data.mendeley.com/datasets/8bk6h6bmkr/1|
105390|NCT02692495||Clinical Study Report|http://www.aurametrix.com/nct02692495|
105391|NCT02692495|10.1101/139014|Preprint|http://biorxiv.org/content/early/2017/05/19/139014|Study results
105392|NCT02691585||Study Protocol|http://rguhs.ac.in/|
105393|NCT02691312||FDA 501(k)|https://www.accessdata.fda.gov/cdrh_docs/pdf10/K101935.pdf|
105394|NCT02690896||Study-related materials|http://psychology.cos.ucf.edu/older/|Please contact the UCF OLDeR Lab for any questions regarding the study and/or study materials.
105395|NCT02689973||Study Protocol|http://goo.gl/100EuU|An abbreviated version of the study protocol
105396|NCT02689804||Publication|http://dx.doi.org/10.1016/j.contraception.2017.01.004|Results Reference: Yes
105397|NCT02688218|STUDY00015452|Study Protocol|http://eirb.ohsu.edu|Institutionally reviewed and accepted protocol for this study.
105398|NCT02685839||Clinical Study Report|https://drive.google.com/file/d/0B2qKUXYO2VcCQkJYbVpvZERWZ2tOdkc2LW4tTHYtNkYxd0NF/view?usp=sharing|
105399|NCT02685839||Clinical Study Report|https://drive.google.com/file/d/0B2qKUXYO2VcCTTMxQlZMeWZId3Vvd3F5RnFJa28wZm1ka3Z3/view?usp=sharing|
105400|NCT02685839||Clinical Study Report|https://drive.google.com/file/d/0B2qKUXYO2VcCODdSaE1TM05TOE9Pc1RnR0Z2NGw1d3FjdzBJ/view?usp=sharing|
105401|NCT02685839||Clinical Study Report|https://drive.google.com/file/d/0B2qKUXYO2VcCOGg2bnNDbkNEOUd3Mlg5MEhEdnVydHVaNk1V/view?usp=sharing|
105402|NCT02685839||Clinical Study Report|http://goo.gl/FilVtL|
105403|NCT02685839||Clinical Study Report|https://drive.google.com/file/d/0B2qKUXYO2VcCdnlCVzRJUFlqcURZYzJ3VkJYNjlnaXcwU3F3/view?usp=sharing|
105404|NCT02683811||Study Protocol|http://www.diariodellasalute.it|Study protocol (Italian version) can be requested by contacting the project manager (lmarinaro@aslcn2.it)
105405|NCT02683811||program materials and tools|http://www.diariodellasalute.it|The Italian version of program materials and tools (teachers' manual, students' booklet and parents' booklet) can be freely accessed and downloaded from project web site.
105406|NCT02682147|Data Distribution|Individual Participant Data Set|http://www.i-clic.uihc.uiowa.edu/|
105407|NCT02680067||Arthritis Research & Therapy Publication|http://arthritis-research.biomedcentral.com/articles/10.1186/s13075-016-1092-0|Lymphatic imaging to assess rheumatoid flare: mechanistic insights and biomarker potential.
105408|NCT02679872||Study Protocol|http://www.regionh.dk/CAMES|Possible to request full protocol, inclusive full reference list, in pdf from first investigator Kirsten Gjeraa, MD, email: kirsten.gjeraa@regionh.dk
105409|NCT02679690||Informed Consent Form|http://www.osiris.pitt.edu|
105410|NCT02677766|TOEFFI15_14|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/30250407|"Titolo dello studio: Terapia occupazionale nei pazienti complessi : studio pilota.~Codice protocollo TOEFFI15_14 Data di rilascio: 16/09/15"
105411|NCT02677675||Study Protocol|http://www.nmrr.gov.my|
105412|NCT02676479||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/4037016|
105413|NCT02675972||Clinical Study Report|https://academic.oup.com/ajh/article-abstract/30/5/524/2997211/Predictive-Significance-of-Day-to-Day-Blood?redirectedFrom=fulltext|
105414|NCT02675933|Satisfaction survey|Satisfaction Survey|https://drive.google.com/file/d/0B_NqlF7oW2UNVjY1VlQ3MmtjR1E/view?usp=sharing|Please email if there are any issues downloading from google drive at ceyee@seton.org
105415|NCT02675933|Questionnaire|Questionnaire|https://drive.google.com/file/d/0B_NqlF7oW2UNdVFBXzhDRkxpdlU/view?usp=sharing|Please email me if there are any issues downloading from google drive at ceyee@seton.org
105416|NCT02674659||informed consent, research proposal, good clinical practice certificate, questioner (in one folder)|https://drive.google.com/folderview?id=0Bzz_LouDZWOkU1FoTWh1bC1HNmM&usp=sharing|informed consent, research proposal, good clinical practice certificate, World health organization quality of life questioner (in one folder)
105417|NCT02672631||Study Protocol|http://clinical-mri.com/mr-neurography-diagnostic-criteria-to-determine-lesions-of-peripheral-nerves/|
105418|NCT02671786||Pilot Study Research Paper|http://www.worldwidejournals.com/ijar/file.php?val=April_2015_1427896145__152.pdf|
105419|NCT02670629|Fx radio distal|Individual Participant Data Set|https://drive.google.com/open?id=0Bwd7ib0yn_zqMnBVZnY2NFFJTzA|Excel document with all the information regarding the patients included in this research protocol
105420|NCT02664935||Trial Website|http://www.birmingham.ac.uk/research/activity/mds/trials/crctu/trials/matrix/index.aspx|
105421|NCT02664935|ISRCTN38344105|ISRCTN Registry|http://www.isrctn.com/ISRCTN38344105|
105422|NCT02662231||Study Protocol|http://globalsurg.org/globalsurg-2-protocol/|GlobalSurg-II Study Protocol: available in multiple languages
105423|NCT02656667|22116795|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed|Vivodtzev I, Debigaré R, Gagnon P, and al. Vivodtzev I, Debigaré R, Gagnon P, Mainguy V, Saey D, Dubé A, Paré MÈ, Bélanger M, Maltais F. Functional and muscular effects of neuromuscular electrical stimulation in patients with severe COPD: a randomized clinical trial. Chest. 2012 Mar;141(3):716-25.
105424|NCT02656667|24418570|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed|Vieira PJ, Chiappa AM, Cipriano G Jr, Umpierre D, Arena R, Chiappa GR. Neuromuscular electrical stimulation improves clinical and physiological function in COPD patients.Respir Med. 2014 Apr;108(4):609-20.
105425|NCT02656667|23440837|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed|Maddocks M, Gao W, Higginson IJ, Wilcock A.Neuromuscular electrical stimulation for muscle weakness in adults with advanced disease. Cochrane Database Syst Rev. 2013 Jan 31;1.
105426|NCT02656667|16806873|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed|Ozalevli S, Ozden A, Itil O, Akkoclu A. Comparison of the Sit-to-Stand Test with 6 min walk test in patients with chronic obstructive pulmonary disease. Respir Med 2007;101(2):286-93.
105427|NCT02647554||Study Protocol|http://pan.baidu.com/s/1eQJUJDK|
105428|NCT02640963||Study Protocol|http://www.tandfonline.com/doi/abs/10.1080/01924788.2013.816832|Activities, Adaptations & Ageing Journal Article Article can be requested via email contact with tim@agefitsolutions.com.au
105429|NCT02640144||Study Protocol|http://www.nr-ortho.com|Original study protocol is written in Hebrew. protocol is available at the Ziv Medical Center, Institutional Review Board (IRB) , or in direct request via the website address posted above.
105430|NCT02638051|10.3892/mco.2017.1221|Clinical Study Report|https://www.spandidos-publications.com/mco/6/5/723?articleTypes=ARTICLE&articleTypes=REVIEW&fileTypes=LETTER_TO_THE_EDITOR&fileTypes=MANUSCRIPT&fileTypes=TABLE&fileTypes=IMAGE&fileTypes=LANG_EDIT|Pang CLK, Zhang X, Wang Z, Ou J, Lu Y, Chen P, Zhao C, Wang X, Zhang H, Roussakow SV. Local modulated electro-hyperthermia in combination with traditional Chinese medicine vs. intraperitoneal chemoinfusion for the treatment of peritoneal carcinomatosis with malignant ascites: A phase II randomized trial. Mol Clin Oncol. 2017;6:723-32,
105431|NCT02637206|200920|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105432|NCT02637206|200920|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105433|NCT02637206|200920|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105434|NCT02637206|200920|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105435|NCT02637206|200920|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105436|NCT02637206|200920|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105437|NCT02637206|200920|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105438|NCT02636205|25014045|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/25014045|
105439|NCT02636205|21261965|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/?term=The+Armeo+Spring+as+training+tool+to+improve+upper+limb+functionality+in+multiple+sclerosis%3A+a+pilot+study|
105440|NCT02632422||Informed Consent Form|http://trumbower-lab.com/contact.html|Requests for study informed consent may be made using the lab's contact form.
105441|NCT02627469||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed?otool=karolib|"The study is reported in the paper:~Effect of 12-month weekly professional oral hygiene care on the composition of the oral flora in dentate, dependent elderly residents: A prospective study.~Wikström M, Kareem KL, Almståhl A, Palmgren E, Lingström P, Wårdh I.~Gerodontology. 2017 Jun;34(2):240-248"
105442|NCT02626520||Study Protocol|https://docs.google.com/viewer?a=v&pid=sites&srcid=ZGVmYXVsdGRvbWFpbnxyZWFsd29ybGRvbmNvbG9neXxneDo2OGI0ZDgxMzdkZDIxYWJh|
105443|NCT02625402||Outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Hip Osteoarthritis Decision Quality Instrument
105444|NCT02625402||Outcome measure|https://mghdecisionsciences.org/tools-training/decision-quality-instruments/|Knee Osteoarthritis Decision Quality Instrument
105445|NCT02621554||Statistical Analysis Plan|https://drive.google.com/open?id=0Bx6LS4H2DroFNnVaQWlTakh5dEU|
105446|NCT02621554||Statistical Analysis Plan|https://drive.google.com/open?id=0Bx6LS4H2DroFazRhT1hZVm41RzA|05.01.2017 updated because of an amendment of ethnic proposal.
105447|NCT02619942||Study Protocol|http://www.trialsjournal.com/content/17/1/582|
105448|NCT02615002||Study website|http://www.recognitionstudy.com|
105449|NCT02614443|10.1186/s40814-016-0068-9|Study Protocol|https://pilotfeasibilitystudies.biomedcentral.com/articles/10.1186/s40814-016-0068-9|
105450|NCT02605395|201528|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105451|NCT02605395|201528|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105452|NCT02605395|201528|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105453|NCT02605395|201528|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105454|NCT02592655||Primary Outcome Ultrasound Images|https://doi.org/10.5281/zenodo.236263|NCT02592655 Primary Outcome Tourniquet Study
105455|NCT02592655||Individual Participant Data Set|https://doi.org/10.5281/zenodo.237773|NCT02592655 Individual level data set
105456|NCT02592655||Informed Consent Form|https://doi.org/10.5281/zenodo.245150|Informed consent form containing description of study and procedures.
105457|NCT02581410|201198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105458|NCT02581410|201198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105459|NCT02581410|201198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105460|NCT02581410|201198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105461|NCT02581410|201198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105462|NCT02581410|201198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105463|NCT02581410|201198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105464|NCT02578953|204646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105465|NCT02578953|204646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105466|NCT02578953|204646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105467|NCT02549027||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1064-003&kw=1064-003&tab=access|
105468|NCT02549014||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1064-001&kw=1064-001&tab=access|
105469|NCT02542813|201558|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105470|NCT02542813|201558|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105471|NCT02542813|201558|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105472|NCT02542813|201558|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105473|NCT02542813|201558|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105474|NCT02542813|201558|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105475|NCT02542813|201558|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105478|NCT02525224|DOI: 10.1111/jocd.12295|Clinical Study Report|http://onlinelibrary.wiley.com/doi/10.1111/jocd.12295/full|
105479|NCT02524665|114553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105480|NCT02524665|114553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105481|NCT02524665|114553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105482|NCT02524665|114553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105483|NCT02524665|114553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105484|NCT02524665|114553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105485|NCT02509104|201897|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105486|NCT02509104|201897|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105487|NCT02509104|201897|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105488|NCT02509104|201897|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105489|NCT02509104|201897|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105490|NCT02509104|201897|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105491|NCT02509104|201897|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105492|NCT02502734|107112|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105493|NCT02502734|107112|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105494|NCT02502734|107112|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105495|NCT02502734|107112|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105496|NCT02502734|107112|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105497|NCT02502734|107112|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105498|NCT02502734|107112|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105499|NCT02496221|201834|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105500|NCT02496221|201834|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105501|NCT02496221|201834|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105502|NCT02496221|201834|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105503|NCT02496221|201834|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105504|NCT02496221|201834|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105505|NCT02496221|201834|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105506|NCT02486016||AAPS presented poster|https://www.aaps.org/search?executeSearch=true&SearchTerm=published+posters&l=1|Shin SH, Yu M, Thomas S, Hammell DC, Ghosh, P, Raney SG, Hassan HH, Stinchcomb AL. Evaluation of level A in vitro/in vivo correlations (IVIVC) for nicotine and fentanyl transdermal delivery systems with transient heat exposure by using multiple approaches. Poster presentation at the 2017 AAPS Annual Meeting and Exposition; November 12-15, 2017; San Diego, CA
105507|NCT02480933|https://doi.org/10.3892/mco.20|Study Protocol|http://www.spandidos-publications.com/mco|feasibility of the protocol paper
105508|NCT02477046||Statistical Analysis Plan|https://idmod.sharepoint.com/projects/_layouts/15/guestaccess.aspx?guestaccesstoken=3%2bxJO%2bcBwXx6PfMuzCQmu8ESB0X7mhLPtowTTLaYTmY%3d&docid=02ab39752ccb14c10bdfd61c0a731e6ff&rev=1|
105509|NCT02476578||Study Protocol|https://goo.gl/B6j1oF|LIMIT HEBREW PROTOCOL Version 3 (Final)
105510|NCT02470949|27094920|Published Manuscript|http://www.sciencedirect.com/science/article/pii/S0031938416301603|
105511|NCT02467933|449|Study Protocol|https://www.socialscienceregistry.org/trials/729|Study protocol archived on American Economic Association Social Science Registry page.
105512|NCT02467933|448|Statistical Analysis Plan|https://www.socialscienceregistry.org/trials/729|"Pre-specified analysis plan archived on American Economic Association Social Science Registry page.~Final version prior to unblinding: Version 2.0 (March 5, 2016)"
105513|NCT02446613|204509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105514|NCT02446613|204509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105515|NCT02446613|204509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105516|NCT02446613|204509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105517|NCT02446613|204509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105518|NCT02446613|204509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105519|NCT02446613|204509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105520|NCT02446496|201529|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105521|NCT02446496|201529|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105522|NCT02446496|201529|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105523|NCT02446496|201529|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105524|NCT02446496|201529|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105525|NCT02446496|201529|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105526|NCT02446483|201527|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105527|NCT02446483|201527|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105528|NCT02446483|201527|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105529|NCT02446483|201527|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105530|NCT02446483|201527|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105531|NCT02439827||Study Protocol|https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-015-2543-2|Study design paper
105532|NCT02439827||Individual Participant Data Set|http://www.scielo.br/scielo.php?pid=S1980-00372016000200207&script=sci_arttext|Instrument validation study
105533|NCT02439827||Individual Participant Data Set|http://www.sciencedirect.com/science/article/pii/S0091743517300129?np=y&npKey=9c20ac447db45d3921238d85220bcf0edbabb56a32ce49ef571691741a9e21ed|Intervention results
105534|NCT02437253||Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=28119823|
105535|NCT02437175||Methodology paper|https://www.dovepress.com/articles.php?article_id=25534|
105536|NCT02416180|201909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105537|NCT02416180|201909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105538|NCT02416180|201909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105539|NCT02416180|201909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105540|NCT02416180|201909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105541|NCT02416180|201909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105542|NCT02415933||Study Protocol|https://knowledge.uchicago.edu/handle/11417/69|
105543|NCT02404012||Website|https://ngletsum.wixsite.com/nito|
105544|NCT02397915|201474|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105545|NCT02397915|201474|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105546|NCT02397915|201474|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105547|NCT02397915|201474|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105548|NCT02397915|201474|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105549|NCT02397915|201474|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105550|NCT02397915|201474|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105551|NCT02393586||Link to Pubmed (Final publication)|https://www.ncbi.nlm.nih.gov/pubmed/28333342|
105552|NCT02384122|27619827|Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/27619827|
105553|NCT02378402|ClinicalTrials.gov/NCT02378402|Clinical Study Report|http://jcmr-online.biomedcentral.com/articles/10.1186/s12968-016-0228-3|
105554|NCT02371603|200229|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105555|NCT02371603|200229|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105556|NCT02371603|200229|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105557|NCT02371603|200229|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105558|NCT02371603|200229|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105559|NCT02371603|200229|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105560|NCT02369341|201959|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105561|NCT02369341|201959|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105562|NCT02369341|201959|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105563|NCT02369341|201959|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105564|NCT02369341|201959|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105565|NCT02369341|201959|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105566|NCT02369341|201959|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105567|NCT02369120||Study Protocol|http://www.biomedcentral.com/1472-6947/15/97|
105568|NCT02356770|PMID: 27310522|1. Publication|https://www.ncbi.nlm.nih.gov/pubmed/27310522|A first publication was published concerning the primary outcome of the transmucosal measurements.
105569|NCT02356770|PMID: 28107560|2. publicaton|https://www.ncbi.nlm.nih.gov/pubmed/28107560|2. publication concerning the volumetric changes of the soft tissue
105570|NCT02348372|115385|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105571|NCT02348372|115385|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105572|NCT02348372|115385|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105573|NCT02348372|115385|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105574|NCT02348372|115385|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105575|NCT02348372|115385|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105576|NCT02348372|115385|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105577|NCT02345161|116853|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105578|NCT02345161|116853|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105579|NCT02345161|116853|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105580|NCT02345161|116853|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105581|NCT02345161|116853|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105582|NCT02345161|116853|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105583|NCT02345161|116853|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105584|NCT02328170||Clinical Study Report|http://www.jacionline.org/article/S0091-6749(16)32038-3/fulltext|
105585|NCT02322671|200107|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105586|NCT02322671|200107|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105587|NCT02322671|200107|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105588|NCT02322671|200107|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105589|NCT02322671|200107|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105590|NCT02322671|200107|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105591|NCT02322671|200107|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105592|NCT02319031|PMID: 26822022|Primary Publication|http://www.ncbi.nlm.nih.gov/pubmed/26822022|
105593|NCT02306096|GSE60789|RNA-seq Processed Gene Expression Data and Annotations|https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE60789|SuperSeries: GSE60789 SubSeries: GSE60785, GSE60788
105594|NCT02294084||Clinical Study Report|https://www.health-holland.com/project/2015/effect-of-antidiabetic-drug-on-brown-adipose-tissue-bat-in-overweight-men|A simplified summary of the main results of the study can be found when following the link. In addition, the results are described in a paper that will be published by Diabetologia later this year.
105595|NCT02292004|10.1177/2325967116672176|Clinical Study Report|http://ojs.sagepub.com/content/4/11/2325967116672176?cpetoc|This is the paper publishing the three-month results of the BEAR I study.
105596|NCT02291575||Clinical Study Report|http://science.sciencemag.org/content/354/6308/aaf7384|Published article
105597|NCT02289560||Clinical Study Report|https://www.accessdata.fda.gov/cdrh_docs/pdf15/p150038c.pdf|
105598|NCT02281318|200862|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105599|NCT02281318|200862|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105600|NCT02281318|200862|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105601|NCT02281318|200862|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105602|NCT02281318|200862|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105603|NCT02281318|200862|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105604|NCT02281318|200862|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105605|NCT02272946||Clinical Study Report|https://drive.google.com/open?id=1n47RTe3nB2_aPQTCXkkTfYodX-gnWKLE|The link above shows the current enrollment table of the Canakinumab study as of March 2, 2020. Of note, 40 participants have been enrolled in the study.
105606|NCT02272946||IL-1B inhibition [by way of Canakinumab] Reduces Atherosclerotic Inflammation in HIV Infection - Journal of the American College of Cardiology|https://drive.google.com/open?id=1bWGEW1WwDj6dSAtTwBe0GwExiN94WCum|The link above is the research publication written by Dr. Hsue (Primary Investigator) about how IL-1B inhibition [by way of Canakinumab] reduces atherosclerotic inflammation in the setting of HIV.
105607|NCT02262689|201402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105608|NCT02262689|201402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105609|NCT02262689|201402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105610|NCT02262689|201402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105611|NCT02262689|201402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105612|NCT02262689|201402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105613|NCT02262689|201402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105614|NCT02257398|115775|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105615|NCT02257398|115775|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105616|NCT02257398|115775|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105617|NCT02257398|115775|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105618|NCT02257398|115775|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105619|NCT02257398|115775|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105620|NCT02257398|115775|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105621|NCT02257385|116961|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105622|NCT02257385|116961|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105623|NCT02257385|116961|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105624|NCT02257385|116961|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105625|NCT02257385|116961|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105626|NCT02257385|116961|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105627|NCT02257385|116961|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105628|NCT02257372|201314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105629|NCT02257372|201314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105630|NCT02257372|201314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105631|NCT02257372|201314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105632|NCT02257372|201314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105633|NCT02257372|201314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105634|NCT02257372|201314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105635|NCT02256865||Statistical Analysis Plan|https://research.labiomed.org/redcap/redcap_v7.2.2/FileRepository/file_download.php?pid=174&id=19887|Data Analysis Plan available by request to PI
105636|NCT02256514|PMCID: PMC4649454|Abstract of 75-patient Phase II study|http://doi.org/10.1186/2051-1426-3-S2-P200|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4649454/pdf/2051-1426-3-S2-P200.pdf
105637|NCT02254447|201713|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105638|NCT02254447|201713|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105639|NCT02254447|201713|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105640|NCT02254447|201713|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105641|NCT02254447|201713|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105642|NCT02254447|201713|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105643|NCT02254447|201713|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105644|NCT02252081||we have no results yet|https://www.mc.vanderbilt.edu|Study is currently enrolling
105645|NCT02243904||Study Protocol|http://www.tandfonline.com/doi/full/10.3109/08037051.2014.996409|
105646|NCT02242643|201234|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105647|NCT02242643|201234|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105648|NCT02242643|201234|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105649|NCT02242643|201234|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105650|NCT02242643|201234|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105651|NCT02242643|201234|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105652|NCT02242643|201234|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105653|NCT02240472||Study Protocol|http://senomac.se/Home/study%20protocol.html|Study protocol and patient information (English)
105654|NCT02236611|201315|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105655|NCT02236611|201315|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105656|NCT02236611|201315|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105657|NCT02236611|201315|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105658|NCT02236611|201315|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105659|NCT02236611|201315|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105660|NCT02236611|201315|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105661|NCT02234479||Abstract|http://www.redjournal.org/article/S0360-3016(15)02475-X/abstract|
105662|NCT02224521|112071|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105663|NCT02224521|112071|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105664|NCT02224521|112071|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105665|NCT02224521|112071|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105666|NCT02224521|112071|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105667|NCT02224521|112071|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105668|NCT02224521|112071|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105669|NCT02224469|k9f10|Individual Participant Data Set|http://datadryad.org/resource/doi:10.5061/dryad.k9f10|
105670|NCT02218697|117276|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105671|NCT02218697|117276|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105672|NCT02218697|117276|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105673|NCT02218697|117276|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105674|NCT02218697|117276|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105675|NCT02218697|117276|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105676|NCT02218697|117276|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105677|NCT02214017|doi: 10.1177/1357633X15608984|publication|https://www.ncbi.nlm.nih.gov/pubmed/26468213|
105678|NCT02207829|201316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105679|NCT02207829|201316|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105680|NCT02207829|201316|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105681|NCT02207829|201316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105682|NCT02207829|201316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105683|NCT02207829|201316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105684|NCT02207829|201316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105685|NCT02202161|201351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105686|NCT02202161|201351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105687|NCT02202161|201351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105688|NCT02202161|201351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105689|NCT02202161|201351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105690|NCT02202161|201351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105691|NCT02202161|201351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105692|NCT02197598|2014-000413-31|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-000413-31/results|
105693|NCT02197481|PMID:25925431|Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/25925431|
105694|NCT02197468||Clinical Study Report|https://www.frontiersin.org/articles/10.3389/fped.2018.00347/full|Publication from this study
105695|NCT02184637|200951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105696|NCT02184637|200951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105697|NCT02184637|200951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105698|NCT02184637|200951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105699|NCT02184637|200951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105700|NCT02184637|200951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105701|NCT02184637|200951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105702|NCT02184624|200301|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105703|NCT02184624|200301|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105704|NCT02184624|200301|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105705|NCT02184624|200301|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105706|NCT02184624|200301|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105707|NCT02184624|200301|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105708|NCT02184624|200301|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105709|NCT02184585|117057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105710|NCT02184585|117057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106584|NCT01717287||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-248&kw=0518-248&tab=access|
105711|NCT02184585|117057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105712|NCT02184585|117057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105713|NCT02184585|117057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105714|NCT02184585|117057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105715|NCT02184585|117057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105716|NCT02180828||Clinical Study Report|http://onlinelibrary.wiley.com/doi/10.1111/myc.12485/epdf|The efficacy and safety of clotrimazole vaginal tablet vs. oral fluconazole in treating severe vulvovaginal candidiasis
105717|NCT02173470||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/26857421|Ultra low-dose chest ct with iterative reconstructions as an alternative to conventional chest x-ray prior to heart surgery (CRICKET study): Rationale and design of a multicenter randomized trial.
105718|NCT02169583|201022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105719|NCT02169583|201022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105720|NCT02169583|201022|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105721|NCT02169583|201022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105722|NCT02169583|201022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105723|NCT02169583|201022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105724|NCT02169583|201022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105725|NCT02155400||Individual Participant Data Set|https://zenodo.org/record/51218#.VzFDBEfieL0|De-identified datasets supporting our findings
105726|NCT02153242|A449|Poster Contribution|http://content.onlinejacc.org/article.aspx?articleid=2198078#Methods:|
105727|NCT02152605|201211|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105728|NCT02152605|201211|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105729|NCT02152605|201211|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105730|NCT02152605|201211|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105731|NCT02152605|201211|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105732|NCT02152605|201211|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105733|NCT02152605|201211|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105734|NCT02145468|116197|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105735|NCT02145468|116197|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105736|NCT02145468|116197|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105737|NCT02145468|116197|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105738|NCT02145468|116197|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105739|NCT02145468|116197|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105740|NCT02145468|116197|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105741|NCT02141217|117044|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105742|NCT02141217|117044|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105743|NCT02141217|117044|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105744|NCT02141217|117044|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105745|NCT02141217|117044|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105746|NCT02141217|117044|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105747|NCT02135848|114272|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105748|NCT02135848|114272|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105749|NCT02135848|114272|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105750|NCT02135848|114272|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105751|NCT02135848|114272|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105752|NCT02135848|114272|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105753|NCT02135848|114272|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105754|NCT02135354||Study Protocol|https://www.researchgate.net/project/Azithromycin-for-acute-COPD-exacerbations-with-hospitalisation-The-BACE-trial|
105755|NCT02135354||Statistical Analysis Plan|https://www.researchgate.net/project/Azithromycin-for-acute-COPD-exacerbations-with-hospitalisation-The-BACE-trial|
105756|NCT02134483||Article|https://www.ncbi.nlm.nih.gov/pubmed/26375142|
105757|NCT02132936||Clinical Study Report|http://www.leo-pharma.com/Home/Research-and-Development/Clinical-trial-disclosure/Clinical-trial-summaries-and-reports.aspx|Clinical Trials at LEO Pharma
105758|NCT02124798|200339|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105759|NCT02124798|200339|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105760|NCT02124798|200339|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105761|NCT02124798|200339|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105762|NCT02124798|200339|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105763|NCT02124798|200339|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105764|NCT02124798|200339|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105765|NCT02119286|200110|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105766|NCT02119286|200110|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105767|NCT02119286|200110|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105768|NCT02119286|200110|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105769|NCT02119286|200110|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105770|NCT02119286|200110|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105771|NCT02119286|200110|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105772|NCT02105974|200820|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105773|NCT02105974|200820|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105774|NCT02105974|200820|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105775|NCT02105974|200820|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105776|NCT02105974|200820|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105777|NCT02105974|200820|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105778|NCT02105974|200820|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105779|NCT02100644|200776|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105780|NCT02100644|200776|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105781|NCT02100644|200776|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105782|NCT02100644|200776|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105783|NCT02100644|200776|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105784|NCT02095405||Published article|http://onlinelibrary.wiley.com/doi/10.1111/jce.12504/full|DOI: 10.1111/jce.12504
105785|NCT02094937|201135|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105786|NCT02094937|201135|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105787|NCT02094937|201135|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105788|NCT02094937|201135|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105789|NCT02094937|201135|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105790|NCT02094924|200957|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105791|NCT02094924|200957|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105792|NCT02094924|200957|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105793|NCT02094924|200957|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105794|NCT02094924|200957|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105795|NCT02094924|200957|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105796|NCT02094924|200957|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105797|NCT02084316|CTN0056|Study Protocol|http://ctndisseminationlibrary.org/protocols/ctn0056.htm|
105798|NCT02075619|200561|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105799|NCT02075619|200561|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105800|NCT02075619|200561|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105801|NCT02075619|200561|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105802|NCT02075619|200561|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105803|NCT02075619|200561|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105804|NCT02075619|200561|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105805|NCT02071680||Published article|http://www.heartrhythmjournal.com/article/S1547-5271(16)30735-4/fulltext|DOI: http://dx.doi.org/10.1016/j.hrthm.2016.08.038
105806|NCT02069002||Study Protocol|http://bmjopen.bmj.com/content/6/6/e011003.full.pdf+html|
105807|NCT02064504|201010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105808|NCT02064504|201010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105809|NCT02064504|201010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105810|NCT02064504|201010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105811|NCT02064504|201010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105812|NCT02064504|201010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105813|NCT02064504|201010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105814|NCT02064465|200697|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105815|NCT02064465|200697|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105816|NCT02064465|200697|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105817|NCT02064465|200697|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105818|NCT02064465|200697|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105819|NCT02064465|200697|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105820|NCT02064465|200697|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105821|NCT02060344|HCHS-SOL|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/hchssol/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
105822|NCT02060344||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hchssol/|
105823|NCT02060344||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/hchssol/|
105824|NCT02058628|200398|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105825|NCT02058628|200398|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105826|NCT02058628|200398|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107505|NCT01407276||CSR Synopsis Links|http://www.merck.com/clinical-trials/study.html?id=3102-009&kw=3102-009&tab=access|
105827|NCT02058628|200398|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105828|NCT02058628|200398|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105829|NCT02058628|200398|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105830|NCT02058628|200398|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105831|NCT02052661|106793|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105832|NCT02052661|106793|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105833|NCT02052661|106793|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105834|NCT02052661|106793|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105835|NCT02052661|106793|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105836|NCT02052661|106793|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105837|NCT02052661|106793|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105838|NCT02045953|201092|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105839|NCT02045953|201092|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105840|NCT02045953|201092|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105841|NCT02045953|201092|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105842|NCT02045953|201092|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105843|NCT02045953|201092|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105844|NCT02045953|201092|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105845|NCT02045849|117349|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105846|NCT02045849|117349|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105847|NCT02045849|117349|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105848|NCT02045849|117349|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105849|NCT02045849|117349|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105850|NCT02045849|117349|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105851|NCT02045849|117349|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105852|NCT02045797|116704|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105853|NCT02045797|116704|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105854|NCT02045797|116704|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105855|NCT02045797|116704|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105856|NCT02045797|116704|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105857|NCT02045797|116704|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105858|NCT02045797|116704|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105859|NCT02035540||Study results|http://pubmed.ncbi.nlm.nih.gov/30879050/|
105860|NCT02033668|116891|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105861|NCT02033668|116891|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105862|NCT02033668|116891|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105863|NCT02033668|116891|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105864|NCT02033668|116891|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105865|NCT02033668|116891|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105866|NCT02033668|116891|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105867|NCT02028065||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8616-101&kw=8616-101&tab=access|
105868|NCT02019719|116099|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105869|NCT02019719|116099|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105870|NCT02019719|116099|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105871|NCT02019719|116099|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105872|NCT02019719|116099|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105873|NCT02019719|116099|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105874|NCT02019719|116099|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105875|NCT02016963|HGS1021-C1069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105876|NCT02016963|HGS1021-C1069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105877|NCT02016963|HGS1021-C1069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105878|NCT02016963|HGS1021-C1069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105879|NCT02016963|HGS1021-C1069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105880|NCT02016963|HGS1021-C1069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105881|NCT02016963|HGS1021-C1069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105882|NCT02014480|116132|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105883|NCT02014480|116132|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105884|NCT02014480|116132|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105885|NCT02014480|116132|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105886|NCT02014480|116132|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105887|NCT02014480|116132|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105888|NCT02014480|116132|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105889|NCT02011490||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8616-105&kw=8616-105&tab=access|
105890|NCT02006602|201011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105891|NCT02006602|201011|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105892|NCT02006602|201011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105893|NCT02006602|201011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105894|NCT02006602|201011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105895|NCT02006602|201011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105896|NCT02006602|201011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105897|NCT02006589|200956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105898|NCT02006589|200956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105899|NCT02006589|200956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105900|NCT02006589|200956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105901|NCT02006589|200956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105902|NCT02006589|200956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105903|NCT02006589|200956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107546|NCT01385189||Clinical Study Report|http://smhs.gwu.edu/mitm-crg/clinical-trials|
105904|NCT02006537|117023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105905|NCT02006537|117023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105906|NCT02006537|117023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105907|NCT02006537|117023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105908|NCT02006537|117023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105909|NCT02006537|117023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105910|NCT02006537|117023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105911|NCT02004886||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0893-005&kw=0893-005&tab=access|
105912|NCT02003274||Individual Participant Data Set|http://www.ncbi.nlm.nih.gov|
105913|NCT02000804|117326|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105914|NCT02000804|117326|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105915|NCT02000804|117326|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105916|NCT02000804|117326|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105917|NCT02000804|117326|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105918|NCT02000804|117326|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105919|NCT02000804|117326|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105920|NCT02000765|115774|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105921|NCT02000765|115774|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105922|NCT02000765|115774|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105923|NCT02000765|115774|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105924|NCT02000765|115774|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105925|NCT02000765|115774|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105926|NCT02000765|115774|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105927|NCT02000453|200208|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105928|NCT02000453|200208|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105929|NCT02000453|200208|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105930|NCT02000453|200208|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105931|NCT02000453|200208|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105932|NCT02000453|200208|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105933|NCT02000453|200208|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105934|NCT01999842|201072|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105935|NCT01999842|201072|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105936|NCT01999842|201072|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105937|NCT01999842|201072|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105938|NCT01999842|201072|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105939|NCT01999842|201072|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105940|NCT01999842|201072|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105941|NCT01999530||Publication|https://www.ncbi.nlm.nih.gov/pubmed/28233334|
105942|NCT01999309||Study Protocol|http://www.sciencedirect.com/science/article/pii/S2214647415000859|Simvastatin augmentation for recent-onset psychotic disorder: A study protocol (open access)
105943|NCT01996995||Study Protocol|http://trialsjournal.biomedcentral.com/articles/10.1186/s13063-015-0622-4|
105944|NCT01996540||study publication|https://www.ncbi.nlm.nih.gov/pubmed/27472648|"Maltoni M et al Systematic versus on-demand early palliative care: results from a multicentre, randomised clinical trial.~Eur J Cancer 2016 Sep;65:61-8"
105945|NCT01996540||study publication|https://www.ncbi.nlm.nih.gov/pubmed/27821313|"Maltoni M et al Systematic versus on-demand early palliative care: A randomised clinical trial assessing quality of care and treatment aggressiveness near the end of life.~Eur J Cancer 2016 Dec;69:110-118."
105946|NCT01996540||study publication|https://doi.org/10.1007/s00520-018-4517-2|"Scarpi E. et al~Systematic vs. on-demand early palliative care in gastric cancer patients:~a randomized clinical trial assessing patient and healthcare service outcomes"
105947|NCT01989884||Clinical Study Report|https://doi.org/10.1007/s11060-019-03116-z|
105948|NCT01984775|117191|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105949|NCT01984775|117191|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105950|NCT01984775|117191|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105951|NCT01984775|117191|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105952|NCT01984775|117191|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105953|NCT01984775|117191|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105954|NCT01984086|200921|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105955|NCT01984086|200921|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105956|NCT01984086|200921|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105957|NCT01984086|200921|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105958|NCT01984086|200921|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105959|NCT01984086|200921|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105960|NCT01984086|200921|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105961|NCT01980940||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0663-168&kw=0663-168&tab=access|
105962|NCT01979250||Manuscript|http://www.ncbi.nlm.nih.gov/pubmed/27273977|To acces the results, please go to the above mentioned manuscript.
105963|NCT01978327|200592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105964|NCT01978327|200592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105965|NCT01978327|200592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105966|NCT01978327|200592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105967|NCT01978327|200592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105968|NCT01978327|200592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105969|NCT01978327|200592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105970|NCT01978145|115646|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105971|NCT01978145|115646|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105972|NCT01978145|115646|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105973|NCT01978145|115646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105974|NCT01978145|115646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105975|NCT01978145|115646|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105976|NCT01978145|115646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105977|NCT01978119|115645|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105978|NCT01978119|115645|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105979|NCT01978119|115645|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105980|NCT01978119|115645|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105981|NCT01978119|115645|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105982|NCT01978119|115645|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105983|NCT01977768|immunotherapy of TB|Clinical Study Report|https://www.researchgate.net/project/Immunotherapy-of-tuberculosis|QUARTERLY UPDATE
105984|NCT01974999|SDY1094|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1094|Participant level data and additional relevant materials are available to the public in the Immunology Database and Analysis Portal (ImmPort), a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. Data analysis tools are also available to researchers.
105985|NCT01974999|SDY1094|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1094|ImmPort study identifier is SDY1094.
105986|NCT01974999|SDY1094|Study summary, -design, -summary of participant assessments, -interventions, -medications, -demographics, -lab tests, -study files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1094|ImmPort study identifier is SDY1094.
105987|NCT01974895|200806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105988|NCT01974895|200806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105989|NCT01974895|200806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105990|NCT01974895|200806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105991|NCT01974895|200806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105992|NCT01974895|200806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105993|NCT01974895|200806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105994|NCT01973777||Clinical Study Report|http://www.contraceptionjournal.org/article/S0010-7824%2815%2930125-6/abstract|
105995|NCT01972425||Study Protocol|https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-016-1442-x|
105996|NCT01969708|PB2016-103333|Study Protocol|https://ntrl.ntis.gov/NTRL/|SCORE2 Protocol Version 3.0 (the Identifier for the appendices is PB2016-103334)
105997|NCT01962467|200284|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105998|NCT01962467|200284|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
105999|NCT01962467|200284|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106000|NCT01962467|200284|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106001|NCT01962467|200284|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106002|NCT01962467|200284|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106003|NCT01962467|200284|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106004|NCT01961479||Study Protocol|http://trialsjournal.biomedcentral.com/articles/10.1186/1745-6215-15-472|Kues, J. N., Janda, C., Kleinstaeuber, M., & Weise, C. (2014). Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial. Trials, 15(1), 472. doi:10.1186/1745-6215-15-472
106005|NCT01961479||Study Protocol|http://www.karger.de/ProdukteDB/miscArchiv/000/439/336/000439336_sm_Eversion.pdf|Janda, C., Kues, J. N., Kleinstaeuber, M., & Weise, C. (2015). A Therapeutic Approach to Premenstrual Syndrome (PMS): Modularized Treatment Program. Verhaltenstherapie, 25. doi:10.1159/000439336
106006|NCT01961479||Questionnaire Validation|http://www.tandfonline.com/doi/abs/10.1080/03630242.2015.1118734?journalCode=wwah20|Kues, J. N., Janda, C., Kleinstäuber, M., & Weise, C. (2015). How to Measure the Impact of Premenstrual Symptoms? Development and Validation of the German PMS-Impact Questionnaire. Women & Health, null-null. doi:10.1080/03630242.2015.1118734
106007|NCT01957202|200286|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106008|NCT01957202|200286|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106009|NCT01957202|200286|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106010|NCT01957202|200286|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106011|NCT01957202|200286|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106012|NCT01957202|200286|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106013|NCT01957202|200286|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106014|NCT01957189|200254|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106015|NCT01957189|200254|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106016|NCT01957189|200254|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106017|NCT01957189|200254|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106018|NCT01957189|200254|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106019|NCT01957189|200254|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106020|NCT01957189|200254|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106021|NCT01957163|200109|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106022|NCT01957163|200109|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106023|NCT01957163|200109|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106024|NCT01957163|200109|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106025|NCT01957163|200109|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106026|NCT01957163|200109|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106027|NCT01957163|200109|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106028|NCT01956487|116371|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106029|NCT01956487|116371|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106030|NCT01956487|116371|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106031|NCT01956487|116371|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106032|NCT01956487|116371|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106033|NCT01956487|116371|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106034|NCT01956487|116371|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106035|NCT01954264|200187|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106036|NCT01954264|200187|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106037|NCT01954264|200187|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106038|NCT01954264|200187|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106039|NCT01954264|200187|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106040|NCT01954264|200187|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106041|NCT01954251|117036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106042|NCT01954251|117036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106043|NCT01954251|117036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106044|NCT01954251|117036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106045|NCT01954251|117036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106046|NCT01954251|117036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106047|NCT01954251|117036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106048|NCT01953549||Statistical Analysis Plan|https://doi.org/10.6084/m9.figshare.5375026.v1|Statistical Analysis Plan of PHYS-Stroke Trial. If download path is offline please contact torsten.rackoll@charite.de
106049|NCT01949051|200285|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106050|NCT01949051|200285|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106051|NCT01949051|200285|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106052|NCT01949051|200285|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106053|NCT01949051|200285|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106054|NCT01949051|200285|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106055|NCT01949051|200285|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106056|NCT01948739||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/27065787|
106057|NCT01948739||Study Protocol|https://www.ncbi.nlm.nih.gov/pubmed/25570900|
106058|NCT01934231|117150|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106059|NCT01934231|117150|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106060|NCT01934231|117150|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106061|NCT01934231|117150|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106062|NCT01934231|117150|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106063|NCT01934231|117150|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106064|NCT01934231|117150|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106065|NCT01934205|116666|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106066|NCT01934205|116666|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106067|NCT01934205|116666|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106068|NCT01934205|116666|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106069|NCT01934205|116666|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106070|NCT01934205|116666|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106071|NCT01934205|116666|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106072|NCT01934153|117157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106073|NCT01934153|117157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106074|NCT01934153|117157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106075|NCT01934153|117157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106076|NCT01934153|117157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106077|NCT01934153|117157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106078|NCT01934153|117157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106079|NCT01934127|115415|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106080|NCT01934127|115415|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106081|NCT01934127|115415|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106082|NCT01934127|115415|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106083|NCT01934127|115415|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106084|NCT01934127|115415|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106085|NCT01930773||Study Protocol|http://www.ncbi.nlm.nih.gov/pubmed/26365936|"Study design and rationale for Optimal aNtiplatelet pharmacotherapy guided by bedSIDE genetic or functional TESTing in elective percutaneous coronary intervention patients (ONSIDE TEST): a prospective, open-label, randomised parallel-group multicentre trial (NCT01930773).~Kołtowski Ł, Aradi D, Huczek Z, Tomaniak M, Sibbing D, Filipiak KJ, Kochman J, Balsam P, Opolski G.~Kardiol Pol. 2016;74(4):372-9. doi: 10.5603/KP.a2015.0172."
106086|NCT01930773||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/28281736|"Optimal aNtiplatelet pharmacotherapy guided by bedSIDE genetic or functional TESTing in elective PCI patients: A pilot study: ONSIDE TEST pilot.~Koltowski L, Tomaniak M, Aradi D, Huczek Z, Filipiak KJ, Kochman J, Gajda S, Balsam P, Opolski G.~Cardiol J. 2017 Mar 10. doi: 10.5603/CJ.a2017.0026. [Epub ahead of print]"
106087|NCT01930058||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8876-003&kw=8876-003|
106088|NCT01930045||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-295&kw=0518-295&tab=access|
106089|NCT01929863|200185|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106090|NCT01929863|200185|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106091|NCT01929863|200185|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106092|NCT01929863|200185|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106093|NCT01929863|200185|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106094|NCT01929863|200185|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106095|NCT01929863|200185|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106096|NCT01929330|117342|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106097|NCT01929330|117342|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106098|NCT01929330|117342|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106099|NCT01929330|117342|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106100|NCT01929330|117342|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106101|NCT01929330|117342|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106102|NCT01929330|117342|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106103|NCT01929317|116991|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106104|NCT01929317|116991|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106105|NCT01928927||Grading table|https://rsc.tech-res.com/clinical-research-sites/safety-reporting/daids-grading-tables|
106106|NCT01928914|114582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106107|NCT01928914|114582|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106108|NCT01928914|114582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106109|NCT01928914|114582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106110|NCT01928914|114582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106111|NCT01928914|114582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106112|NCT01928914|114582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106113|NCT01926015||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V260-060&kw=V260-060&tab=access|
106114|NCT01924858|117155|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106115|NCT01924858|117155|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106116|NCT01924858|117155|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106117|NCT01924858|117155|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106118|NCT01924858|117155|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106119|NCT01924858|117155|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106120|NCT01924858|117155|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106121|NCT01920867||Clinical Study Report|http://mdstemcells.com/scots-ii/|http://mdstemcells.com/scots-ii/
106122|NCT01918033||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4117-200&kw=4117-200&tab=access|
106123|NCT01916980||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4117-202&kw=4117-202&tab=access|
106124|NCT01916967||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4117-201&kw=4117-201&tab=access|
106125|NCT01916720|480848/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106126|NCT01916720|480848/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106127|NCT01916720|480848/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106128|NCT01916720|480848/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106129|NCT01916720|480848/010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106130|NCT01916720|480848/010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106131|NCT01916720|480848/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106132|NCT01916226|200165|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106133|NCT01916226|200165|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106134|NCT01916226|200165|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106135|NCT01916226|200165|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106136|NCT01916226|200165|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106137|NCT01916226|200165|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106138|NCT01916226|200165|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106139|NCT01915940|FSV5-002 Manuscript|Study Manuscript|http://www.aaojournal.org/article/S0161-6420(16)30203-2/abstract|peer-reviewed publication of primary results from FSV5-002 study
106140|NCT01911559|9433361|Clinical Study Report|http://www.biomedsearch.com/nih/Effectiveness-Standing-Frame-Constipation-in/24838311.html|Rivi, Elena & Filippi, Mariacristina & Fornasari, Elisa & Mascia, Maria Teresa & Ferrari, Adriano & Costi, Stefania. (2014). Effectiveness of Standing Frame on Constipation in Children with Cerebral Palsy: A Single-Subject Study. Occupational therapy international.
106141|NCT01906034|DOI:10.1159/000442087|Academic Journal Paper|https://www.karger.com/Article/FullText/442087|
106142|NCT01904903||Manuscript|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534513/|
106143|NCT01899768|117270|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106144|NCT01899768|117270|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106145|NCT01899768|117270|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106146|NCT01899768|117270|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106147|NCT01899768|117270|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106148|NCT01899768|117270|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106149|NCT01899768|117270|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106150|NCT01899755|116987|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106151|NCT01899755|116987|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106152|NCT01899755|116987|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106153|NCT01899755|116987|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106154|NCT01899755|116987|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106155|NCT01899755|116987|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106156|NCT01899755|116987|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106157|NCT01899742|116960|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106158|NCT01899742|116960|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106159|NCT01899742|116960|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106160|NCT01899742|116960|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106161|NCT01899742|116960|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106162|NCT01899742|116960|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106163|NCT01899742|116960|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106164|NCT01899703|117213|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106165|NCT01899703|117213|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106166|NCT01899703|117213|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106167|NCT01899703|117213|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106168|NCT01899703|117213|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106169|NCT01899703|117213|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106170|NCT01899703|117213|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106171|NCT01899638|115380|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106172|NCT01899638|115380|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106173|NCT01899638|115380|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106174|NCT01899638|115380|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106175|NCT01899638|115380|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106176|NCT01899638|115380|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106177|NCT01899638|115380|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106178|NCT01894386|200587|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106179|NCT01894386|200587|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106180|NCT01894386|200587|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106181|NCT01894386|200587|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106182|NCT01894386|200587|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106183|NCT01894386|200587|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106184|NCT01894386|200587|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106185|NCT01894360|117100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106186|NCT01894360|117100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106187|NCT01894360|117100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106188|NCT01894360|117100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106189|NCT01894360|117100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106190|NCT01894360|117100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106191|NCT01894360|117100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106192|NCT01893203|25109244|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/|
106193|NCT01890863|200260|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106194|NCT01890863|200260|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106195|NCT01890863|200260|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106196|NCT01890863|200260|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106197|NCT01890863|200260|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106198|NCT01890863|200260|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106199|NCT01890863|200260|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106200|NCT01887171|10.15825/1995-1191-2015-3-24|Clinical Study Report|http://journal.transpl.ru/vtio/article/view/561/488|
106201|NCT01887171|10.21614/jtmr-21-2-82|Clinical Study Report|http://www.jtmr.ro/article/portal-and-arterial-flushing-with-htk-and-tacrolimus-can-attenuate-the-incidence-of-early-liver-allograft-dysfunction|
106202|NCT01879423|115207|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106203|NCT01879423|115207|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106204|NCT01879423|115207|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106205|NCT01879423|115207|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106206|NCT01879423|115207|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106207|NCT01879423|115207|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106208|NCT01879423|115207|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106209|NCT01879410|114951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106210|NCT01879410|114951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106211|NCT01879410|114951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106212|NCT01879410|114951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106213|NCT01879410|114951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106214|NCT01879410|114951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106215|NCT01879410|114951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106216|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/25735317|"Passardi A et al. Effectiveness of bevacizumab added to gold standard chemotherapy in metastatic colorectal cancer: final results of first-line from the ITACa randomized clinical trial.~Ann Oncol 2015 Jun;26(6):1201-7"
106217|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/26244985|"Passardi A et al. Impact of Pre-Treatment Lactate Dehydrogenase Levels on Prognosis and Bevacizumab Efficacy in Patients with Metastatic Colorectal Cancer.~PLoS One 2015; 10(8): e0134732"
106218|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/27120807|"Passardi A et al. Inflammatory indexes as predictors of prognosis and bevacizumab efficacy in patients with metastatic colorectal cancer.~Oncotarget 2016 May 31;7(22):33210-9"
106219|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/26259598|"Ulivi P et al. eNOS polymorphisms as predictors of efficacy of bevacizumab-based chemotherapy in metastatic colorectal cancer: data from a randomized clinical trial.~J Transl Med 2015;11(3): 258"
106220|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/26848624|"Casadei Gardini A et al. Prognostic role of serum concentrations of high-sensitivity C-reactive protein in patients with metastatic colorectal cancer: results from the ITACa trial.~Oncotarget 2016 Mar 1;7(9):10193-202"
106221|NCT01878422||study publication|https://www.ncbi.nlm.nih.gov/pubmed/28465540|"Marisi G et al Circulating VEGF and eNOS variations as predictors of outcome in metastatic colorectal cancer patients receiving bevacizumab.~Sci Rep 2017 May 2;7(1):1293"
106222|NCT01874548||Clinical Study Report|http://onlinelibrary.wiley.com/doi/10.1002/jmri.25386/abstract;jsessionid=86852D9FCBC14AF375566F8E7E214CB0.f01t04|
106223|NCT01874067|35110|Clinical Study Report|http://usir.salford.ac.uk/35110/|Conference Abstract: Hammond, A, Prior, Y, Jones, V, Dooley, M, Hough, Y and Jacklin, A 2015, 'A pre-post test pilot trial of compression gloves in early inflammatory and rheumatoid arthritis' , Rheumatology, 54 (S1) , i111-112
106224|NCT01873950|doi:10.13026/C2HP45|ECG, PK and clinical information database|https://physionet.org/physiobank/database/ecgrdvq/|This publicly available database contains raw and annotated ECG signals, PK measures as well as clinical information of this study.
106225|NCT01873339|115678|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106226|NCT01873339|115678|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106227|NCT01873339|115678|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106228|NCT01873339|115678|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106229|NCT01873339|115678|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106230|NCT01873339|115678|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106231|NCT01873339|115678|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106232|NCT01870115||Publication|http://www.aging-us.com/article/101158|
106233|NCT01868035|393229/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106234|NCT01868035|393229/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106235|NCT01868035|393229/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106236|NCT01868035|393229/007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106237|NCT01868035|393229/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106238|NCT01868035|393229/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106239|NCT01868035|393229/007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106240|NCT01867996|116073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106241|NCT01867996|116073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106242|NCT01867996|116073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106243|NCT01867996|116073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106244|NCT01867996|116073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106245|NCT01867996|116073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106246|NCT01867996|116073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106247|NCT01866319||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3475-006&kw=3475-006&tab=access|
106248|NCT01863667||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=3102-027&kw=3102-027&tab=access|
106249|NCT01857895|200016|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106250|NCT01857895|200016|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106251|NCT01857895|200016|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106252|NCT01857895|200016|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106253|NCT01857895|200016|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106254|NCT01857895|200016|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106255|NCT01857895|200016|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106256|NCT01857869|117014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106257|NCT01857869|117014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106258|NCT01857869|117014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106259|NCT01857869|117014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106260|NCT01857869|117014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106261|NCT01857869|117014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106262|NCT01857869|117014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106263|NCT01857063||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0476-519&kw=0476-519&tab=access|
106264|NCT01853878|116389|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106265|NCT01853878|116389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106266|NCT01853878|116389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106267|NCT01853878|116389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106268|NCT01853878|116389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106269|NCT01853878|116389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106270|NCT01853878|116389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106271|NCT01852812||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0476-520&kw=0476-520&tab=access|
106272|NCT01852565|115679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106273|NCT01852565|115679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106274|NCT01852565|115679|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106275|NCT01852565|115679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106276|NCT01852565|115679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106277|NCT01852565|115679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106278|NCT01852565|115679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106279|NCT01849822||Publication|http://www.vis.caltech.edu/papers|"Hand Shape Representation in Parietal Reach Region. The Journal of Neuroscience."
106280|NCT01849822||Publication|http://www.vis.caltech.edu/papers|"Decoding motor imagery from the posterior parietal cortex of a tetraplegic human. Science"
106281|NCT01849016|Version 7.0 - 5/31/2016|Statistical Analysis Plan|http://www2.hematologie-amc.nl/nac_studie|
106282|NCT01847872||Study Protocol|http://cdn.mrc.gm/downloads/SCC_1327_Protocol_v7_31_Mar_2014.pdf|
106283|NCT01847417|116498|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107547|NCT01385033||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3328-002&kw=3328-002&tab=access|
106284|NCT01847417|116498|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106285|NCT01847417|116498|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106286|NCT01847417|116498|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106287|NCT01847417|116498|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106288|NCT01847417|116498|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106289|NCT01847404|116480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106290|NCT01847404|116480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106291|NCT01847404|116480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106292|NCT01847404|116480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106293|NCT01847404|116480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106294|NCT01847404|116480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106295|NCT01842620|117219|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106296|NCT01842620|117219|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106297|NCT01842620|117219|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106298|NCT01842620|117219|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106299|NCT01842620|117219|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106300|NCT01842620|117219|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106301|NCT01842620|117219|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106302|NCT01842607|115661|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106303|NCT01842607|115661|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106304|NCT01842607|115661|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106305|NCT01842607|115661|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106306|NCT01842607|115661|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106307|NCT01842607|115661|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106308|NCT01842607|115661|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106309|NCT01841697||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-026&kw=3102-026&tab=access|
106310|NCT01837667||publication|http://clincancerres.aacrjournals.org/cgi/content/abstract/1078-0432.CCR-16-2299|"Safety, tolerability, and preliminary activity of LB-100, an inhibitor of protein phosphatase 2A, in patients with relapsed solid tumors has been published by Clinical Cancer Research"
106311|NCT01837316|116592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106312|NCT01837316|116592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106313|NCT01837316|116592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106314|NCT01837316|116592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106315|NCT01837316|116592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106316|NCT01837316|116592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106317|NCT01837316|116592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106318|NCT01831791|114264|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106319|NCT01831791|114264|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106320|NCT01831791|114264|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106321|NCT01831791|114264|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106322|NCT01831791|114264|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106323|NCT01831791|114264|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106324|NCT01831791|114264|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106325|NCT01829360||Treatment & Testing Scripts|http://doi.org/10.23641/asha.9745181|See item S4 and S7.
106326|NCT01829360||Published report of findings|http://doi.org/10.1044/2019_LSHSS-VOIA-18-0131|This article is open access
106327|NCT01827904||Clinical Study Report|https://www.accessdata.fda.gov/cdrh_docs/pdf15/p150038c.pdf|
106328|NCT01827839|116796|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106329|NCT01827839|116796|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106330|NCT01827839|116796|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106331|NCT01827839|116796|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106332|NCT01827839|116796|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106333|NCT01827839|116796|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106334|NCT01827839|116796|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106335|NCT01827631|116416|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106336|NCT01827631|116416|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106337|NCT01827631|116416|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106338|NCT01827631|116416|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106339|NCT01827631|116416|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106340|NCT01827631|116416|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106341|NCT01827631|116416|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106342|NCT01825213|PMID: 25181365|Peer reviewed article|http://ieeexplore.ieee.org/document/6887313/?arnumber=6887313|
106343|NCT01822899|116134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106344|NCT01822899|116134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106345|NCT01822899|116134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106346|NCT01822899|116134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106347|NCT01822899|116134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106348|NCT01822899|116134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106349|NCT01822899|116134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106350|NCT01822639|116798|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106351|NCT01822639|116798|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106352|NCT01822639|116798|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106353|NCT01822639|116798|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106354|NCT01822639|116798|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106355|NCT01822639|116798|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106356|NCT01822639|116798|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106357|NCT01818024|116343|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106358|NCT01818024|116343|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106359|NCT01818024|116343|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106360|NCT01818024|116343|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106361|NCT01818024|116343|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106362|NCT01818024|116343|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106363|NCT01818024|116343|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106364|NCT01818011|116266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106365|NCT01818011|116266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106366|NCT01818011|116266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106367|NCT01818011|116266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106368|NCT01818011|116266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106369|NCT01818011|116266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106370|NCT01818011|116266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106371|NCT01817777|116086|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106372|NCT01817777|116086|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106373|NCT01817777|116086|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106374|NCT01817777|116086|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106375|NCT01817777|116086|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106376|NCT01817777|116086|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106377|NCT01817777|116086|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106378|NCT01817764|114930|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106379|NCT01817764|114930|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106380|NCT01817764|114930|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106381|NCT01817764|114930|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106382|NCT01817764|114930|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106383|NCT01817764|114930|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106384|NCT01817764|114930|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106385|NCT01815268|doi: 10.1177/1740774515625976|Study Protocol|http://ctj.sagepub.com/content/early/2016/02/10/1740774515625976.abstract|"We have published our study design and rationale in Clinical Trials Journal. Citation is below.~Stefan Gravenstein, Roshani Dahal, Pedro L Gozalo, H Edward Davidson, Lisa F Han, Monica Taljaard, and Vincent Mor. A cluster randomized controlled trial comparing relative effectiveness of two licensed influenza vaccines in US nursing homes: Design and rationale. Clin Trials 1740774515625976, first published on February 11, 2016 doi:10.1177/1740774515625976"
106386|NCT01814722||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-266&kw=0518-266&tab=access|
106387|NCT01812382|117151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106388|NCT01812382|117151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106389|NCT01812382|117151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106390|NCT01812382|117151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106391|NCT01812382|117151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106392|NCT01812382|117151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106393|NCT01812382|117151|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106394|NCT01808482|116702|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106395|NCT01808482|116702|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106396|NCT01808482|116702|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106397|NCT01808482|116702|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106398|NCT01808482|116702|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106399|NCT01808482|116702|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106400|NCT01808482|116702|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106401|NCT01808365|114991|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106402|NCT01808365|114991|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106403|NCT01808365|114991|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106404|NCT01808365|114991|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106405|NCT01808365|114991|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106406|NCT01808365|114991|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106407|NCT01808365|114991|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106408|NCT01808339|117156|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106409|NCT01808339|117156|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106410|NCT01808339|117156|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106411|NCT01808339|117156|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106412|NCT01808339|117156|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106413|NCT01808339|117156|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106414|NCT01808339|117156|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106415|NCT01808261|104615|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106416|NCT01808261|104615|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106417|NCT01808261|104615|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106418|NCT01808261|104615|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106419|NCT01808261|104615|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106420|NCT01808261|104615|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106421|NCT01808261|104615|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106422|NCT01805752|doi: 10.1016/S2352-3018(16)000|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/27126487|Aliyu MH, Blevins M, Audet CM, Kalish M, Gebi UI, Onwujekwe O, Lindegren ML, Shepherd BE, Wester CW, Vermund SH. Integrated prevention of mother-to-child HIV transmission services, antiretroviral therapy initiation, and maternal and infant retention in care in rural north-central Nigeria: a cluster-randomised controlled trial. Lancet HIV. 2016 May;3(5):e202-11. doi: 10.1016/S2352-3018(16)00018-7. PubMed PMID: 27126487; PubMed Central PMCID: PMC4852280.
106423|NCT01802931|117016|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106424|NCT01802931|117016|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106425|NCT01802931|117016|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106426|NCT01802931|117016|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106427|NCT01802931|117016|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106428|NCT01802931|117016|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106429|NCT01802931|117016|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106430|NCT01797926|116799|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106431|NCT01797926|116799|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106432|NCT01797926|116799|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106433|NCT01797926|116799|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106434|NCT01797926|116799|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106435|NCT01797926|116799|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106436|NCT01797926|116799|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106437|NCT01792817||Publication|http://onlinelibrary.wiley.com/doi/10.1111/head.12896/full|Non-Invasive Vagus Nerve Stimulation for the ACute Treatment of Cluster Headache: Findings From the Randomized, Double-Blind, Sham-Controlled ACT1 Study Stephen D. Silberstein, MD; Laszlo L. Mechtler, MD; David B. Kudrow, MD; Anne H. Calhoun, MD; Candace McClure, PhD; Joel R. Saper, MD; Eric J. Liebler; Emily Rubenstein Engel, MD; Stewart J. Tepper, MD; on Behalf of the ACT1 Study Group
106438|NCT01792674||Clinical Study Report|http://ncbi.nlm.nih.gov/pmc/articles/PMC4611309/pdf/bmjopen-2015-008344.pdf|Sørensen JL, van der Vleuten C, Rosthøj S, Østergaard D, LeBlanc V, Johansen M, Ekelund K, Starkopf L, Lindschou J, Gluud C, Weikop P, Ottesen B.Simulation-based multiprofessional obstetric anaesthesia training conducted in situ versus off-site leads to similar individual and team outcomes: a randomised educational trial. BMJ Open 2015;5: e008344
106439|NCT01792674||Qualitative study based on the study population from randomised trial.|http://ncbi.nlm.nih.gov/pmc/articles/PMC4608174/pdf/bmjopen-2015-008345.pdf|Sørensen JL, Navne LE, Martin HM, Ottesen B, Albrectsen CK, Pedersen BW. Clarifying the learning experiences of healthcare professionals with in situ versus off site simulation-based medical education: a qualitative study. BMJ Open 2015;5:e008345
106440|NCT01782664|116679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106441|NCT01782664|116679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106442|NCT01782664|116679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106443|NCT01782664|116679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106444|NCT01782664|116679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106445|NCT01782664|116679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106446|NCT01782664|116679|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106447|NCT01781949||Study Protocol|http://www.denveremresearch.org/hiv-studies|"Version 2.5 of the protocol is available by clicking on the Click Here link under the description of The HIV TESTED Trial."
106448|NCT01777334|117115|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106449|NCT01777334|117115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106450|NCT01777334|117115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106451|NCT01777334|117115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106452|NCT01777334|117115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106453|NCT01777334|117115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106454|NCT01777334|117115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106455|NCT01777321|116760|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106456|NCT01777321|116760|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106457|NCT01777321|116760|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106458|NCT01777321|116760|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106459|NCT01777321|116760|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106460|NCT01777321|116760|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106461|NCT01777321|116760|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106462|NCT01777282|116170|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106463|NCT01777282|116170|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106464|NCT01777282|116170|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106465|NCT01777282|116170|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106466|NCT01777282|116170|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106467|NCT01777282|116170|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106468|NCT01777256|115919|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106469|NCT01777256|115919|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106470|NCT01777256|115919|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106471|NCT01777256|115919|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106472|NCT01777256|115919|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106473|NCT01777256|115919|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106474|NCT01777256|115919|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106475|NCT01772199|116477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106476|NCT01772199|116477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106477|NCT01772199|116477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106478|NCT01772199|116477|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106479|NCT01772199|116477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106480|NCT01772199|116477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106481|NCT01772199|116477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106482|NCT01772147|116136|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106483|NCT01772147|116136|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106484|NCT01772147|116136|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106485|NCT01772147|116136|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106486|NCT01772147|116136|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106487|NCT01772147|116136|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106488|NCT01772147|116136|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106489|NCT01772134|116135|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106490|NCT01772134|116135|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106491|NCT01772134|116135|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106492|NCT01772134|116135|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106493|NCT01772134|116135|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106494|NCT01772134|116135|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106495|NCT01772134|116135|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106496|NCT01767688||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-031&kw=3102-031&tab=access|
106497|NCT01762878|116617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106498|NCT01762878|116617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106499|NCT01762878|116617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106500|NCT01762878|116617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106501|NCT01762878|116617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106502|NCT01762878|116617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106503|NCT01762878|116617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106504|NCT01762813||Study Protocol|http://translational-medicine.biomedcentral.com/articles/10.1186/s12967-016-0951-4|
106505|NCT01762774|114068|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106506|NCT01762774|114068|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106507|NCT01762774|114068|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106508|NCT01762774|114068|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106509|NCT01762774|114068|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106510|NCT01762774|114068|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106511|NCT01762774|114068|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106512|NCT01760356|PMID: 25142246|Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25142246|Tacrolimus pharmacodynamics and pharmacogenetics along the calcineurin pathway in human lymphocytes.
106513|NCT01760356|PMID: 29054923|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/29054923|Activity of the Calcineurin Pathway in Patients on the Liver Transplantation Waiting List: Factors of Variability and Response to Tacrolimus Inhibition.
106514|NCT01756495|116628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106515|NCT01756495|116628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106516|NCT01756495|116628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106517|NCT01756495|116628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106518|NCT01756495|116628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106519|NCT01756495|116628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106520|NCT01756495|116628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106521|NCT01751113|116572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106522|NCT01751113|116572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106523|NCT01751113|116572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106524|NCT01751113|116572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106525|NCT01751113|116572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106526|NCT01751074|115677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106527|NCT01751074|115677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106528|NCT01751074|115677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106529|NCT01751074|115677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106530|NCT01751074|115677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106531|NCT01751074|115677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106532|NCT01751074|115677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106533|NCT01744301|CSR Study Report Synopsis|Study Protocol|http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7112&studyid=674&filename=D9612N00017_Seizure_Study_report_synopsis_FINAL_redacted.pdf|D9612N00017_Seizure_Study_report_synopsis_FINAL_redacted
106534|NCT01742234|SDY292|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY292|ImmPort study identifier is SDY292
106535|NCT01742234|SDY292|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY292|ImmPort study identifier is SDY292. The study protocol is available in the Design tab section.
106536|NCT01741025||publication 6 month results|https://www.ncbi.nlm.nih.gov/pubmed/27179664|
106537|NCT01741025||publication 6 month results|https://www.ncbi.nlm.nih.gov/pubmed/27629371|
106538|NCT01738867|116753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106539|NCT01738867|116753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106540|NCT01738867|116753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106541|NCT01738867|116753|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106542|NCT01738867|116753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106543|NCT01738867|116753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106544|NCT01738867|116753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106545|NCT01734239||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V110-018&kw=V110-018&tab=access|
106546|NCT01733758|113121|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106547|NCT01733758|113121|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106548|NCT01733758|113121|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106549|NCT01733758|113121|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106550|NCT01733758|113121|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106551|NCT01733758|113121|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106552|NCT01733758|113121|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106553|NCT01727609||Study Protocol|https://www.npeu.ox.ac.uk/downloads/files/sift/protocols/SIFT%20Protocol%20V5.1%20-%2004%20Feb%202016.pdf|
106554|NCT01725685|116524|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106555|NCT01725685|116524|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106556|NCT01725685|116524|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106557|NCT01725685|116524|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106558|NCT01725685|116524|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106559|NCT01725685|116524|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106560|NCT01725685|116524|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106561|NCT01725672|116806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106562|NCT01725672|116806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106563|NCT01725672|116806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106564|NCT01725672|116806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106565|NCT01725672|116806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106566|NCT01725672|116806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106567|NCT01725672|116806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106568|NCT01725126|116623|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106569|NCT01725126|116623|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106570|NCT01725126|116623|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106571|NCT01725126|116623|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106572|NCT01725126|116623|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106573|NCT01725126|116623|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106574|NCT01725126|116623|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106575|NCT01722903||Publication|http://www.ncbi.nlm.nih.gov/pubmed/25807199|
106576|NCT01721317|116878|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106577|NCT01721317|116878|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106578|NCT01721317|116878|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106579|NCT01721317|116878|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106580|NCT01721317|116878|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106581|NCT01721317|116878|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106582|NCT01721317|116878|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106583|NCT01717950||Clinical Study Report|https://smhs.gwu.edu/mitm-crg/|
106585|NCT01716520|116133|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106586|NCT01716520|116133|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106587|NCT01716520|116133|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106588|NCT01716520|116133|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106589|NCT01716520|116133|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106590|NCT01716520|116133|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106591|NCT01716520|116133|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106592|NCT01711736|116926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106593|NCT01711736|116926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106594|NCT01711736|116926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106595|NCT01711736|116926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106596|NCT01711736|116926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106597|NCT01711736|116926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106598|NCT01711723|115676|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106599|NCT01711723|115676|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106600|NCT01711723|115676|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106601|NCT01711723|115676|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106602|NCT01711723|115676|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106603|NCT01711723|115676|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106604|NCT01711723|115676|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106605|NCT01711463|115199|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106606|NCT01711463|115199|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106607|NCT01711463|115199|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106608|NCT01711463|115199|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106609|NCT01711463|115199|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106610|NCT01711463|115199|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106611|NCT01711463|115199|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106612|NCT01706328|116974|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106613|NCT01706328|116974|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106614|NCT01706328|116974|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106615|NCT01706328|116974|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106616|NCT01706328|116974|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106617|NCT01706328|116974|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106618|NCT01706328|116974|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106619|NCT01706315|116778|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106620|NCT01706315|116778|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106621|NCT01706315|116778|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106622|NCT01706315|116778|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106623|NCT01706315|116778|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106624|NCT01706315|116778|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106625|NCT01706315|116778|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106626|NCT01706263|114551|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106627|NCT01706263|114551|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106628|NCT01706263|114551|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106629|NCT01706263|114551|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106630|NCT01706263|114551|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106631|NCT01706263|114551|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106632|NCT01706250|114550|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106633|NCT01706250|114550|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106634|NCT01706250|114550|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106635|NCT01706250|114550|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106636|NCT01706250|114550|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106637|NCT01704261||CSR Synopsis Links|http://www.merck.com/clinical-trials/study.html?id=3102-022&kw=3102-022&tab=access|
106638|NCT01703221||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-020&kw=3102-020&tab=access|
106639|NCT01702493|117041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106640|NCT01702493|117041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106641|NCT01702493|117041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106642|NCT01702493|117041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106643|NCT01702493|117041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106644|NCT01702493|117041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106645|NCT01702493|117041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106646|NCT01702467|116698|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106647|NCT01702467|116698|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106648|NCT01702467|116698|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106649|NCT01702467|116698|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106650|NCT01702467|116698|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106651|NCT01702467|116698|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106652|NCT01702467|116698|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106653|NCT01702454|116023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106654|NCT01702454|116023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106655|NCT01702454|116023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106656|NCT01702454|116023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106657|NCT01702454|116023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106658|NCT01702454|116023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106659|NCT01702454|116023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106660|NCT01702376|113789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106661|NCT01702376|113789|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106662|NCT01702376|113789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106663|NCT01702376|113789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106664|NCT01702376|113789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106665|NCT01702376|113789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106666|NCT01702376|113789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106667|NCT01702363|115361|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106668|NCT01702363|115361|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106669|NCT01702363|115361|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106670|NCT01702363|115361|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106671|NCT01702363|115361|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106672|NCT01702363|115361|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106673|NCT01702363|115361|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106674|NCT01702298||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431D-312&kw=0431D-312&tab=access|
106675|NCT01697592||CSR Snyopsis|http://www.merck.com/clinical-trials/study.html?id=3102-015&kw=3102-015&tab=access|
106676|NCT01697085||Clinical Study Report|http://www.maturitas.org/article/S0378-5122%2814%2900239-4/abstract?cc=y=|
106677|NCT01696604|116715|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106678|NCT01696604|116715|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106679|NCT01696604|116715|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106680|NCT01696604|116715|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106681|NCT01696604|116715|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106682|NCT01696604|116715|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106683|NCT01696604|116715|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106684|NCT01691885|116601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106685|NCT01691885|116601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106686|NCT01691885|116601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106687|NCT01691885|116601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106688|NCT01691885|116601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106689|NCT01691885|116601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106690|NCT01691885|116601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106691|NCT01691547|116415|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106692|NCT01691547|116415|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106693|NCT01691547|116415|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106694|NCT01691547|116415|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106695|NCT01691547|116415|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106696|NCT01691547|116415|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106697|NCT01691547|116415|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106698|NCT01691521|115588|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106699|NCT01691521|115588|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106700|NCT01691521|115588|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106701|NCT01691521|115588|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106702|NCT01691521|115588|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106703|NCT01691521|115588|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106704|NCT01691521|115588|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106705|NCT01691508|115575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106706|NCT01691508|115575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106707|NCT01691508|115575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106708|NCT01691508|115575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106709|NCT01691508|115575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106710|NCT01691508|115575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106711|NCT01691508|115575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106712|NCT01691482|114956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106713|NCT01691482|114956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106714|NCT01691482|114956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106715|NCT01691482|114956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106716|NCT01691482|114956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106717|NCT01691482|114956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106718|NCT01691482|114956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106719|NCT01686633|116863|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106720|NCT01686633|116863|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106721|NCT01686633|116863|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106722|NCT01686633|116863|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106723|NCT01686633|116863|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106724|NCT01686633|116863|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106725|NCT01686633|116863|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106726|NCT01681004|INSITE|Individual Participant Data Set|http://yoda.yale.edu/|
106727|NCT01678820||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431D-266&kw=0431D-266&tab=access|
106728|NCT01678131||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-048&kw=7009-048&tab=access|
106729|NCT01673620||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0476A-484&kw=0476A-484&tab=access|
106730|NCT01673555|116008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106731|NCT01673555|116008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106732|NCT01673555|116008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106733|NCT01673555|116008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106734|NCT01673555|116008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106735|NCT01673555|116008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106736|NCT01673555|116008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106737|NCT01673529|115246|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106738|NCT01673529|115246|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106739|NCT01673529|115246|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106740|NCT01673529|115246|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106741|NCT01673529|115246|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106742|NCT01673529|115246|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106743|NCT01673529|115246|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106744|NCT01672892|NCT01672892-D1|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
106745|NCT01669083|116741|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106746|NCT01669083|116741|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106747|NCT01669083|116741|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106748|NCT01669083|116741|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106749|NCT01669083|116741|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106750|NCT01669083|116741|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106751|NCT01669083|116741|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106752|NCT01669070|115441|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106753|NCT01669070|115441|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106754|NCT01669070|115441|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106755|NCT01669070|115441|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106756|NCT01669070|115441|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106757|NCT01669070|115441|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106758|NCT01669070|115441|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106759|NCT01668654|113388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106760|NCT01668654|113388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106761|NCT01668654|113388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106762|NCT01668654|113388|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106763|NCT01668654|113388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106764|NCT01668654|113388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106765|NCT01668654|113388|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106766|NCT01667107||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5592-105&kw=5592-105&tab=access|
106767|NCT01663714|104514|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106768|NCT01663714|104514|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106769|NCT01663714|104514|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106770|NCT01663714|104514|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106771|NCT01663714|104514|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106772|NCT01663714|104514|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106773|NCT01663714|104514|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106774|NCT01663389|112167|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106775|NCT01663389|112167|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106776|NCT01663389|112167|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106777|NCT01663389|112167|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106778|NCT01663389|112167|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106779|NCT01663389|112167|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106780|NCT01663389|112167|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106781|NCT01656434||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06448&kw=P06448&tab=access|
106782|NCT01656408||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8150-002&kw=8150-002&tab=access|
106783|NCT01656317|DOI: 10.2340/16501977-2121|Article|https://www.ncbi.nlm.nih.gov/pubmed/27494170|"Impact of early mobilization and rehabilitation on global functional outcome one year after aneurysmal subarachnoid hemorrhage.~Karic T1,2, Røe C1,3, Nordenmark TH1, Becker F4,3, Sorteberg W2, Sorteberg A2,3."
106784|NCT01656317|DOI: 10.3171/2015.12.JNS151744|Article|https://www.ncbi.nlm.nih.gov/pubmed/27058204|"J Neurosurg. 2017 Feb;126(2):518-526. doi: 10.3171/2015.12.JNS151744. Epub 2016 Apr 8.~Effect of early mobilization and rehabilitation on complications in aneurysmal subarachnoid hemorrhage.~Karic T1,2, Røe C1,3, Nordenmark TH1, Becker F4,3, Sorteberg W2, Sorteberg A2,3."
106785|NCT01656317|10.3109/09638288.2014.966162|Article|https://www.ncbi.nlm.nih.gov/pubmed/25264735|"Disabil Rehabil. 2015;37(16):1446-54. doi: 10.3109/09638288.2014.966162. Epub 2014 Sep 29.~Early rehabilitation in patients with acute aneurysmal subarachnoid hemorrhage.~Karic T1, Sorteberg A, Haug Nordenmark T, Becker F, Roe C."
106786|NCT01651949||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-003&kw=V503-003&tab=access|
106787|NCT01648283||Publication|https://www.ncbi.nlm.nih.gov/pubmed?term=%22Anesthesiology%22[Jour]%20AND%202015[pdat]%20AND%20Kharasch[author]%20AND%20methadone%20cyp2b6&cmd=correctspelling|Study results published Anesthesiology. 2015 Nov;123(5):1142-53. doi: 10.1097/ALN.0000000000000867
106788|NCT01648231|116797|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106789|NCT01648231|116797|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106790|NCT01648231|116797|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106791|NCT01648231|116797|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106792|NCT01648231|116797|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106793|NCT01648231|116797|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106794|NCT01648231|116797|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106795|NCT01648192|116681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106796|NCT01648192|116681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106797|NCT01648192|116681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106798|NCT01648192|116681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106799|NCT01648192|116681|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106800|NCT01648192|116681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106801|NCT01648192|116681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106802|NCT01648179|116595|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106803|NCT01648179|116595|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106804|NCT01648179|116595|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106805|NCT01648179|116595|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106806|NCT01648179|116595|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106807|NCT01648179|116595|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106808|NCT01648179|116595|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106809|NCT01648153|116378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106810|NCT01648153|116378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106811|NCT01648153|116378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106812|NCT01648153|116378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106813|NCT01648153|116378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106814|NCT01648153|116378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106815|NCT01648153|116378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106816|NCT01648140|115879|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106817|NCT01648140|115879|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106818|NCT01648140|115879|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106819|NCT01648140|115879|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106820|NCT01648140|115879|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106821|NCT01648140|115879|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106822|NCT01648101|114855|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106823|NCT01648101|114855|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106824|NCT01648101|114855|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106825|NCT01648101|114855|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106826|NCT01648101|114855|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106827|NCT01648101|114855|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106828|NCT01648101|114855|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106829|NCT01644643|D4280C00006|Study Protocol|http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=1452&filename=Clinical%20Study%20Protocol_3%20Redacted%20amended.pdf|D4280C00006 Clinical Study Protocol
106830|NCT01644643|D4280C00006|Study Protocol|http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=1452&filename=Clinical%20Study%20Protocol%20Amendment%202%20Redacted%20amended.pdf|D4280C00006 Clinical Study Protocol Amendment 2 Redacted amended
106831|NCT01644643|D4280C00006|Study Protocol|http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=1452&filename=Clinical%20Study%20Protocol%20Amendment%203%20Redacted%20amended.pdf|D4280C00006 Clinical Study Protocol Amendment 3 Redacted amended
106832|NCT01641692|116402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106833|NCT01641692|116402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106834|NCT01641692|116402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106835|NCT01641692|116402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106836|NCT01641692|116402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106837|NCT01641692|116402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106838|NCT01641692|116402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106839|NCT01640990|115387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106840|NCT01640990|115387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106841|NCT01640990|115387|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106842|NCT01640990|115387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106843|NCT01640990|115387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106844|NCT01640990|115387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106845|NCT01640990|115387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106846|NCT01639092|25596179|Pubmed|http://www.ncbi.nlm.nih.gov/pubmed/25596179|Publication for the primary study results
106847|NCT01639066|25800784|pubmed|http://www.ncbi.nlm.nih.gov/pubmed/25800784|Publication for the primary study results
106848|NCT01636960||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P08556&kw=P08556&tab=access|
106849|NCT01636947||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0869-225&kw=0869-225&tab=access|
106850|NCT01636713|114634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106851|NCT01636713|114634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106852|NCT01636713|114634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106853|NCT01636713|114634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106854|NCT01636713|114634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106855|NCT01636713|114634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106856|NCT01636713|114634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106857|NCT01630135|116364|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106858|NCT01630135|116364|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106859|NCT01630135|116364|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106860|NCT01630135|116364|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106861|NCT01627587|115893|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106862|NCT01627587|115893|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106863|NCT01627587|115893|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106864|NCT01627587|115893|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106865|NCT01627587|115893|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106866|NCT01627587|115893|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106867|NCT01627587|115893|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106868|NCT01627340|115918|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106869|NCT01627340|115918|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106870|NCT01627340|115918|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106871|NCT01627340|115918|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106872|NCT01627340|115918|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106873|NCT01627340|115918|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106874|NCT01627327|115805|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106875|NCT01627327|115805|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106876|NCT01627327|115805|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106877|NCT01627327|115805|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106878|NCT01627327|115805|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106879|NCT01627327|115805|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106880|NCT01627327|115805|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106881|NCT01626820|116664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106882|NCT01626820|116664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106883|NCT01626820|116664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106884|NCT01626820|116664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106885|NCT01626820|116664|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106886|NCT01626820|116664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106887|NCT01626820|116664|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106888|NCT01622231|116365|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106889|NCT01622231|116365|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106890|NCT01622231|116365|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106891|NCT01622231|116365|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106892|NCT01617187||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05688&kw=P05688&tab=access|
106893|NCT01615796|115198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106894|NCT01615796|115198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106895|NCT01615796|115198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106896|NCT01615796|115198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106897|NCT01615796|115198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106898|NCT01615796|115198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106899|NCT01615796|115198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106900|NCT01614769||CSR Snyposis Link|http://www.merck.com/clinical-trials/study.html?id=0000-253&kw=0000-253&tab=access|
106901|NCT01611883||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06541&kw=P06541&tab=access|
106902|NCT01610388|113376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106903|NCT01610388|113376|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106904|NCT01610388|113376|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106905|NCT01610388|113376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106906|NCT01610388|113376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106907|NCT01610388|113376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106908|NCT01610388|113376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106909|NCT01608477||Study Protocol|http://dx.doi.org/10.1111/jan.12519|Building research initiative group: chronic illness management and adherence in transplantation (BRIGHT) study: study protocol
106910|NCT01607385|116511|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106911|NCT01607385|116511|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106912|NCT01607385|116511|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106913|NCT01607385|116511|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106914|NCT01607385|116511|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106915|NCT01607385|116511|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106916|NCT01607385|116511|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106917|NCT01607372|116392|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106918|NCT01607372|116392|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106919|NCT01607372|116392|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106920|NCT01607372|116392|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106921|NCT01607372|116392|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106922|NCT01607372|116392|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106923|NCT01607372|116392|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106924|NCT01607086|111649|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106925|NCT01607086|111649|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106926|NCT01607086|111649|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106927|NCT01607086|111649|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106928|NCT01607086|111649|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106929|NCT01607086|111649|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106930|NCT01607086|111649|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106931|NCT01606800||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8908B-059&kw=8908B-059&tab=access|
106932|NCT01602900|116038|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106933|NCT01602900|116038|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106934|NCT01602900|116038|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106935|NCT01602900|116038|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106936|NCT01602900|116038|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106937|NCT01602900|116038|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106938|NCT01602900|116038|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106939|NCT01602562|116100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106940|NCT01602562|116100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106941|NCT01602562|116100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106942|NCT01602562|116100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106943|NCT01600586||Publication|http://pediatrics.aappublications.org/content/133/3/462.short|
106944|NCT01600092||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V260-035&kw=V260-035&tab=access|
106945|NCT01598298||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
106946|NCT01594749||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0517-031&kw=0517-031&tab=access|
106947|NCT01590810||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8150-001&kw=8150-001&tab=access|
106948|NCT01590797||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-254&kw=0431-254&tab=access|
106949|NCT01590771||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-253&kw=0431-253&tab=access|
106950|NCT01587924|116582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106951|NCT01587924|116582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106952|NCT01587924|116582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106953|NCT01587924|116582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106954|NCT01587924|116582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106955|NCT01587924|116582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106956|NCT01587924|116582|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106957|NCT01587898|116581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106958|NCT01587898|116581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106959|NCT01587898|116581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106960|NCT01587898|116581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106961|NCT01587898|116581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106962|NCT01587898|116581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106963|NCT01587898|116581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106964|NCT01587716|115658|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106965|NCT01587716|115658|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106966|NCT01587716|115658|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106967|NCT01587716|115658|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106968|NCT01587716|115658|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106969|NCT01587716|115658|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106970|NCT01587716|115658|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106971|NCT01583036|116216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106972|NCT01583036|116216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106973|NCT01583036|116216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106974|NCT01583036|116216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106975|NCT01583036|116216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106976|NCT01583036|116216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106977|NCT01583036|116216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106978|NCT01577732|115389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106979|NCT01577732|115389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106980|NCT01577732|115389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106981|NCT01577732|115389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106982|NCT01577732|115389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106983|NCT01577732|115389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106984|NCT01577693|115148|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106985|NCT01577693|115148|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106986|NCT01577693|115148|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106987|NCT01577693|115148|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106988|NCT01577693|115148|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106989|NCT01577693|115148|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106990|NCT01577693|115148|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106991|NCT01577680|114637|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106992|NCT01577680|114637|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106993|NCT01577680|114637|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106994|NCT01577680|114637|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106995|NCT01577680|114637|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106996|NCT01577680|114637|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106997|NCT01577680|114637|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106998|NCT01573819|115719|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
106999|NCT01573819|115719|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107000|NCT01573819|115719|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107001|NCT01573819|115719|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107002|NCT01573819|115719|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107003|NCT01573819|115719|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107004|NCT01573819|115719|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107005|NCT01573767|106853|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107006|NCT01573767|106853|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107007|NCT01573767|106853|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107008|NCT01573767|106853|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107009|NCT01573767|106853|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107010|NCT01573767|106853|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107011|NCT01573767|106853|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107012|NCT01573624|115938|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107013|NCT01573624|115938|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107014|NCT01573624|115938|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107015|NCT01573624|115938|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107016|NCT01573624|115938|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107017|NCT01573624|115938|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107018|NCT01573624|115938|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107019|NCT01573000|104515|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107020|NCT01573000|104515|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107021|NCT01573000|104515|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107022|NCT01573000|104515|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107023|NCT01573000|104515|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107024|NCT01573000|104515|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107025|NCT01573000|104515|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107026|NCT01571999|114636|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107027|NCT01571999|114636|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107028|NCT01571999|114636|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107029|NCT01571999|114636|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107030|NCT01571999|114636|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107031|NCT01571999|114636|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107032|NCT01571999|114636|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107033|NCT01570218||Clinical Study Report|https://doi.org/10.1177/1534735418757349|Alcântara-Silva TR, Freitas-Junior R, Freitas NMA, de Paula Junior W, da Silva DJ, Machado GDP, Ribeiro MKA, Carneiro JP, Soares LR. Music Therapy Reduces Radiotherapy-Induced Fatigue in Patients With Breast or Gynecological Cancer: A Randomized Trial. Integr Cancer Ther. 2018 Apr 1:1534735418757349. doi: 10.1177/1534735418757349.
107034|NCT01563575||Country Article|http://clinhp.org/ifile/Vol4_Issue1_p15_21.pdf|Czech Republic
107035|NCT01563575||Country Article|http://www.clinhp.org/ifile/Vol5_Issue1_p11_p17.pdf|Taiwan
107036|NCT01563042|114594|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107037|NCT01563042|114594|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107038|NCT01563042|114594|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107039|NCT01563042|114594|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107040|NCT01563042|114594|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107041|NCT01563042|114594|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107042|NCT01563042|114594|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107043|NCT01563029|106855|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107044|NCT01563029|106855|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107045|NCT01563029|106855|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107046|NCT01563029|106855|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107047|NCT01563029|106855|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107048|NCT01563029|106855|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107049|NCT01563029|106855|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107050|NCT01557504||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-296&kw=0431A-296&tab=access|
107051|NCT01552681|SDY823|Study Protocol|http://www.immport.org/immport-open/public/home/home|ImmPort study identifier is SDY823.
107052|NCT01552681|SDY823|Complete set of descriptive data and results|http://www.immport.org/immport-open/public/home/home|ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. This archive is in support of the NIH mission to share data with the public.
107053|NCT01551771|115802|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107054|NCT01551771|115802|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107055|NCT01551771|115802|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107056|NCT01551771|115802|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107057|NCT01551771|115802|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107058|NCT01551771|115802|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107059|NCT01551771|115802|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107060|NCT01551758|115151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107061|NCT01551758|115151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107062|NCT01551758|115151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107063|NCT01551758|115151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107064|NCT01551758|115151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107065|NCT01551758|115151|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107066|NCT01551758|115151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107067|NCT01545570|114403|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107068|NCT01545570|114403|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107069|NCT01545570|114403|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107070|NCT01545570|114403|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107071|NCT01545570|114403|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107072|NCT01545570|114403|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107073|NCT01545570|114403|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107074|NCT01545388||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-136&kw=0431A-136&tab=access|
107075|NCT01536561|104728|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107076|NCT01536561|104728|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107077|NCT01536561|104728|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107078|NCT01536561|104728|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107079|NCT01536561|104728|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107080|NCT01536561|104728|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107081|NCT01536561|104728|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107082|NCT01536405||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V221-027&kw=V221-027&tab=access|
107083|NCT01534351||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0906A-149&kw=0906A-149&tab=access|
107084|NCT01527123|115959|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107085|NCT01527123|115959|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107086|NCT01527123|115959|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107087|NCT01527123|115959|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107088|NCT01527123|115959|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107089|NCT01527123|115959|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107090|NCT01527110|115215|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107091|NCT01527110|115215|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107092|NCT01527110|115215|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107093|NCT01527110|115215|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107094|NCT01527110|115215|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107095|NCT01527110|115215|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107096|NCT01524835|SDY294|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY294|ImmPort study identifier is SDY294
107097|NCT01524835|SDY294|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY294|ImmPort study identifier is SDY294. The study protocol is available in the Design tab section.
107098|NCT01524835|SDY294|Study summary, -design, -demographics, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY294|ImmPort study identifier is SDY294
107099|NCT01521390|115487|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107100|NCT01521390|115487|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107101|NCT01521390|115487|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107102|NCT01521390|115487|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107103|NCT01521390|115487|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107104|NCT01521390|115487|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107105|NCT01521390|115487|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107106|NCT01521377|114635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107107|NCT01521377|114635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107108|NCT01521377|114635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107109|NCT01521377|114635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107110|NCT01521377|114635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107111|NCT01521377|114635|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107112|NCT01521377|114635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107113|NCT01516632||Informed Consent Form|http://innovativepublichealth.org/projects/sms-usa-4/|All study materials (e.g., consent form, assessments) can be downloaded from the project website
107114|NCT01516450|116119|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107115|NCT01516450|116119|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107116|NCT01516450|116119|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107117|NCT01516450|116119|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107118|NCT01516450|116119|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107119|NCT01516450|116119|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107120|NCT01516450|116119|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107121|NCT01506895|115403|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107122|NCT01506895|115403|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107123|NCT01506895|115403|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107124|NCT01506895|115403|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107125|NCT01506895|115403|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107126|NCT01506895|115403|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107127|NCT01506895|115403|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107128|NCT01502371||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04223&kw=P04223&tab=access|
107129|NCT01499446|FFA20001|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107130|NCT01499446|FFA20001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107131|NCT01499446|FFA20001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107132|NCT01499446|FFA20001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107133|NCT01499446|FFA20001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107134|NCT01499446|FFA20001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107135|NCT01499446|FFA20001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107136|NCT01499290|D4280C00001 Revised CSP|Study Protocol|http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=1448&filename=RECLAIM%201%20(D4280C00001)%20Protocol.pdf|RECLAIM 1 (D4280C00001) Revised Clinical Study Protocol
107137|NCT01498679|113719|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107138|NCT01498679|113719|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107139|NCT01498679|113719|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107140|NCT01498679|113719|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107141|NCT01498679|113719|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107142|NCT01498679|113719|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107143|NCT01498679|113719|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107144|NCT01498653|113714|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107145|NCT01498653|113714|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107146|NCT01498653|113714|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107147|NCT01498653|113714|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107148|NCT01498653|113714|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107149|NCT01498653|113714|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107150|NCT01498653|113714|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107151|NCT01495026|115708|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107152|NCT01495026|115708|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107153|NCT01495026|115708|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107154|NCT01495026|115708|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107155|NCT01495026|115708|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107156|NCT01495026|115708|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107157|NCT01495026|115708|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107158|NCT01495013|115317|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107159|NCT01495013|115317|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107160|NCT01495013|115317|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107161|NCT01495013|115317|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107162|NCT01495013|115317|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107163|NCT01495013|115317|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107164|NCT01494636|115419|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107165|NCT01494636|115419|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107166|NCT01494636|115419|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107167|NCT01494636|115419|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107168|NCT01494636|115419|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107169|NCT01494636|115419|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107170|NCT01494636|115419|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107171|NCT01494610|114334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107172|NCT01494610|114334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107173|NCT01494610|114334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107174|NCT01494610|114334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107175|NCT01494610|114334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107176|NCT01494610|114334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107177|NCT01494610|114334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107178|NCT01494584|113284|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107179|NCT01494584|113284|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107180|NCT01494584|113284|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107181|NCT01494584|113284|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107182|NCT01494584|113284|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107183|NCT01494584|113284|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107184|NCT01494584|113284|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107185|NCT01494532|111569|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107186|NCT01494532|111569|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107187|NCT01494532|111569|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107188|NCT01494532|111569|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107189|NCT01494532|111569|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107190|NCT01494532|111569|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107191|NCT01491815||Study Protocol|http://www.biomedcentral.com/search?query=glinatsi&searchType=publisherSearch|Publication of the protocol. Glinatsi et al. Trials (2017) 18:161
107192|NCT01485445|115440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107193|NCT01485445|115440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107194|NCT01485445|115440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107195|NCT01485445|115440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107196|NCT01485445|115440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107197|NCT01485445|115440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107198|NCT01485445|115440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107199|NCT01485172|111662|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107200|NCT01485172|111662|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107201|NCT01485172|111662|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107202|NCT01485172|111662|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107203|NCT01485172|111662|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107204|NCT01485172|111662|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107205|NCT01484496|112341|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107206|NCT01484496|112341|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107207|NCT01484496|112341|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107208|NCT01484496|112341|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107209|NCT01484496|112341|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107210|NCT01484496|112341|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107211|NCT01484496|112341|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107212|NCT01480609|115214|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107213|NCT01480609|115214|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107214|NCT01480609|115214|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107215|NCT01480609|115214|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107216|NCT01480609|115214|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107217|NCT01480609|115214|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107218|NCT01480609|115214|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107219|NCT01480271|114450|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107220|NCT01480271|114450|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107221|NCT01480271|114450|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107222|NCT01480271|114450|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107223|NCT01480271|114450|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107224|NCT01480271|114450|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107225|NCT01480271|114450|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107226|NCT01477853||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431E-211&kw=0431E-211&tab=access|
107227|NCT01476098|114693|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107228|NCT01476098|114693|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107229|NCT01476098|114693|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107230|NCT01476098|114693|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107231|NCT01476098|114693|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107232|NCT01476098|114693|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107233|NCT01476098|114693|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107234|NCT01476046|110951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107235|NCT01476046|110951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107236|NCT01476046|110951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107237|NCT01476046|110951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107238|NCT01476046|110951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107239|NCT01476046|110951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107240|NCT01476046|110951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107241|NCT01475734|108372|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107242|NCT01475734|108372|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107243|NCT01475734|108372|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107244|NCT01475734|108372|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107245|NCT01475734|108372|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107246|NCT01475734|108372|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107247|NCT01475734|108372|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107248|NCT01475721|115359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107249|NCT01475721|115359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107250|NCT01475721|115359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107251|NCT01475721|115359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107252|NCT01475721|115359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107253|NCT01475721|115359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107254|NCT01475721|115359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107255|NCT01472341||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0000-113&kw=0000-113&tab=access|
107256|NCT01471678|115707|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107257|NCT01471678|115707|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107258|NCT01471678|115707|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107259|NCT01471678|115707|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107260|NCT01471678|115707|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107261|NCT01471678|115707|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107262|NCT01471678|115707|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107263|NCT01471665|115134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107264|NCT01471665|115134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107265|NCT01471665|115134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107266|NCT01471665|115134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107267|NCT01471665|115134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107268|NCT01471665|115134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107269|NCT01471665|115134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107270|NCT01471327|115705|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107271|NCT01471327|115705|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107272|NCT01471327|115705|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107273|NCT01471327|115705|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107274|NCT01471327|115705|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107275|NCT01471327|115705|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107276|NCT01471327|115705|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107277|NCT01469299||Publication|https://www.ncbi.nlm.nih.gov/pubmed/24269069|6-Month Report: Guske et al. A New Method for Defining Balance: Promising Short-term outcomes of Sensor-Guided TKA. J Arthroplasty. 2014 May;29(5):955-60
107278|NCT01469299||Publication|https://www.ncbi.nlm.nih.gov/pubmed/25210632|1-year Report: Gustke et al. Primary TKA patients with Quantifiably Balanced Soft-Tissue Achieve Significant Clinical Gains Sooner than Unbalanced Patients. Adv Orthop. 2014:628695
107279|NCT01466322|114919|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107280|NCT01466322|114919|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107281|NCT01466322|114919|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107282|NCT01466322|114919|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107283|NCT01466322|114919|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107284|NCT01466322|114919|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107285|NCT01466322|114919|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107286|NCT01462669|115860|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107287|NCT01462669|115860|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107288|NCT01462669|115860|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107289|NCT01462669|115860|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107290|NCT01462669|115860|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107291|NCT01462669|115860|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107292|NCT01462669|115860|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107293|NCT01462617|115117|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107294|NCT01462617|115117|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107295|NCT01462617|115117|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107296|NCT01462617|115117|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107297|NCT01462617|115117|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107298|NCT01462617|115117|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107299|NCT01462617|115117|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107300|NCT01462357|115411|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107301|NCT01462357|115411|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107302|NCT01462357|115411|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107303|NCT01462357|115411|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107304|NCT01462357|115411|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107305|NCT01462357|115411|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107306|NCT01462344|115358|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107307|NCT01462344|115358|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107308|NCT01462344|115358|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107309|NCT01462344|115358|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107310|NCT01462344|115358|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107311|NCT01462344|115358|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107312|NCT01462344|115358|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107313|NCT01462266||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-260&kw=0431-260&tab=access|
107314|NCT01457560|217744/060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107315|NCT01457560|217744/060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107316|NCT01457560|217744/060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107317|NCT01457560|217744/060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107318|NCT01457560|217744/060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107319|NCT01457547|217744/094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107320|NCT01457547|217744/094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107321|NCT01457547|217744/094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107322|NCT01457547|217744/094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107323|NCT01457547|217744/094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107324|NCT01457547|217744/094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107325|NCT01453725||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P07642&kw=8259-006&tab=access|
107326|NCT01453491|115951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107327|NCT01453491|115951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107328|NCT01453491|115951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107329|NCT01453491|115951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107330|NCT01453491|115951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107331|NCT01453491|115951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107332|NCT01453491|115951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107333|NCT01453478|115550|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107334|NCT01453478|115550|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107335|NCT01453478|115550|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107336|NCT01453478|115550|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107337|NCT01453478|115550|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107338|NCT01453478|115550|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107339|NCT01453478|115550|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107340|NCT01453296|112776|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107341|NCT01453296|112776|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107342|NCT01453296|112776|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107343|NCT01453296|112776|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107344|NCT01453296|112776|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107345|NCT01453296|112776|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107346|NCT01453296|112776|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107347|NCT01453023|112777|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107348|NCT01453023|112777|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107349|NCT01453023|112777|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107350|NCT01453023|112777|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107351|NCT01453023|112777|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107352|NCT01453023|112777|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107353|NCT01453023|112777|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107354|NCT01451437||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=P07649&kw=P07649&tab=access|
107355|NCT01449799|113423|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107356|NCT01449799|113423|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107357|NCT01449799|113423|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107358|NCT01449799|113423|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107359|NCT01449799|113423|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107360|NCT01449799|113423|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107361|NCT01449799|113423|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107362|NCT01446237|115576|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107363|NCT01446237|115576|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107364|NCT01446237|115576|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107365|NCT01446237|115576|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107366|NCT01446237|115576|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107367|NCT01446237|115576|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107368|NCT01446237|115576|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107369|NCT01440595||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5172-012&kw=5172-012&tab=access|
107370|NCT01440387|115418|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107371|NCT01440387|115418|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107372|NCT01440387|115418|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107373|NCT01440387|115418|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107374|NCT01440387|115418|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107375|NCT01440387|115418|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107376|NCT01439308|111925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107377|NCT01439308|111925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107378|NCT01439308|111925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107379|NCT01439308|111925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107380|NCT01439308|111925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107381|NCT01439308|111925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107382|NCT01439308|111925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107383|NCT01436110|115285|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107384|NCT01436110|115285|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107385|NCT01436110|115285|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107386|NCT01436110|115285|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107387|NCT01436110|115285|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107388|NCT01436110|115285|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107389|NCT01436110|115285|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107390|NCT01436071|115283|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107391|NCT01436071|115283|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107392|NCT01436071|115283|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107393|NCT01436071|115283|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107394|NCT01436071|115283|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107395|NCT01436071|115283|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107396|NCT01436071|115283|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107397|NCT01435993|114840|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107398|NCT01435993|114840|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107399|NCT01435993|114840|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107400|NCT01435993|114840|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107401|NCT01435993|114840|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107402|NCT01435993|114840|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107403|NCT01435993|114840|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107404|NCT01431976|115377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107405|NCT01431976|115377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107406|NCT01431976|115377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107407|NCT01431976|115377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107408|NCT01431976|115377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107409|NCT01431963|115376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107410|NCT01431963|115376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107411|NCT01431963|115376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107412|NCT01431963|115376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107413|NCT01431963|115376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107414|NCT01431950|114496|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107415|NCT01431950|114496|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107416|NCT01431950|114496|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107417|NCT01431950|114496|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107418|NCT01431950|114496|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107419|NCT01431950|114496|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107420|NCT01431950|114496|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107421|NCT01431937|114347|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107422|NCT01431937|114347|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107423|NCT01431937|114347|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107424|NCT01431937|114347|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107425|NCT01431937|114347|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107426|NCT01431937|114347|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107427|NCT01431937|114347|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107428|NCT01431521||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4074-008&kw=4074-008&tab=access|
107429|NCT01428479|115070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107430|NCT01428479|115070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107431|NCT01428479|115070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107432|NCT01428479|115070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107433|NCT01428479|115070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107434|NCT01428479|115070|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107435|NCT01428466|114849|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107436|NCT01428466|114849|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107437|NCT01428466|114849|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107438|NCT01428466|114849|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107439|NCT01428453|114458|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107440|NCT01428453|114458|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107441|NCT01428453|114458|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107442|NCT01428453|114458|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107443|NCT01428453|114458|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107444|NCT01428453|114458|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107445|NCT01428453|114458|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107446|NCT01426776|PMID: 24938583|published article|https://pubmed.ncbi.nlm.nih.gov/24938583|We found central sleep apnea was eliminated after cardiac valve replacement surgery, however, there was no change in obstructive sleep apnea.
107447|NCT01425203||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P08160&kw=P08160&tab=access|
107448|NCT01425190||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P07614&kw=P07614&tab=access|
107449|NCT01424514|114974|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107450|NCT01424514|114974|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107451|NCT01424514|114974|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107452|NCT01424514|114974|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107453|NCT01424514|114974|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107454|NCT01424514|114974|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107455|NCT01424514|114974|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107456|NCT01424436|113043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107457|NCT01424436|113043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107458|NCT01424436|113043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107459|NCT01424436|113043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107460|NCT01424436|113043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107461|NCT01424436|113043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107462|NCT01424436|113043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107463|NCT01424397|111924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107464|NCT01424397|111924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107465|NCT01424397|111924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107466|NCT01424397|111924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107467|NCT01424397|111924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107468|NCT01424397|111924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107469|NCT01424397|111924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107470|NCT01424384|105012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107471|NCT01424384|105012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107472|NCT01424384|105012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107473|NCT01424384|105012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107474|NCT01424384|105012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107475|NCT01424384|105012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107476|NCT01424384|105012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107477|NCT01421277||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-076&kw=0974-076&tab=access|
107478|NCT01416571|112691|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107479|NCT01416571|112691|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107480|NCT01416571|112691|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107481|NCT01416571|112691|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107482|NCT01416571|112691|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107483|NCT01416571|112691|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107484|NCT01416376|115830|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107485|NCT01416376|115830|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107486|NCT01416376|115830|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107487|NCT01416376|115830|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107488|NCT01416376|115830|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107489|NCT01416376|115830|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107490|NCT01416324|114985|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107491|NCT01416324|114985|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107492|NCT01416324|114985|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107493|NCT01416324|114985|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107494|NCT01416324|114985|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107495|NCT01416324|114985|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107496|NCT01416324|114985|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107497|NCT01414192||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0653A-204&kw=0653A-204&tab=access|
107498|NCT01411111|112362|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107499|NCT01411111|112362|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107500|NCT01411111|112362|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107501|NCT01411111|112362|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107502|NCT01411111|112362|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107503|NCT01411111|112362|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107504|NCT01411111|112362|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107506|NCT01406262|107085|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107507|NCT01406262|107085|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107508|NCT01406262|107085|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107509|NCT01406262|107085|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107510|NCT01406262|107085|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107511|NCT01406262|107085|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107512|NCT01406262|107085|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107513|NCT01405937||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-044&kw=7009-044&tab=access|
107514|NCT01405924||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0517-030&kw=0517-030&tab=access|
107515|NCT01405859||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983677/|Final Study Results, Published in Tremor and Other Hyperkinetic Disorders
107516|NCT01405560||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-045&kw=7009-045&tab=access|
107517|NCT01400906|114748|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107518|NCT01400906|114748|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107519|NCT01400906|114748|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107520|NCT01400906|114748|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107521|NCT01400906|114748|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107522|NCT01400906|114748|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107523|NCT01400906|114748|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107524|NCT01395888|115247|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107525|NCT01395888|115247|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107526|NCT01395888|115247|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107527|NCT01395888|115247|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107528|NCT01395888|115247|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107529|NCT01395888|115247|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107530|NCT01395888|115247|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107531|NCT01391065||Published article|https://doi.org/10.1016/j.ijrobp.2019.10.037|
107532|NCT01387230|115408|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107533|NCT01387230|115408|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107534|NCT01387230|115408|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107535|NCT01387230|115408|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107536|NCT01387230|115408|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107537|NCT01387230|115408|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107538|NCT01387230|115408|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107539|NCT01387217|114070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107540|NCT01387217|114070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107541|NCT01387217|114070|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107542|NCT01387217|114070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107543|NCT01387217|114070|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107544|NCT01387217|114070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107545|NCT01387217|114070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107548|NCT01381575|114700|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107549|NCT01381575|114700|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107550|NCT01381575|114700|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107551|NCT01381575|114700|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107552|NCT01381575|114700|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107553|NCT01381575|114700|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107554|NCT01381536|114243|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107555|NCT01381536|114243|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107556|NCT01381536|114243|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107557|NCT01381536|114243|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107558|NCT01381536|114243|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107559|NCT01381536|114243|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107560|NCT01381445|113435|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107561|NCT01381445|113435|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107562|NCT01381445|113435|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107563|NCT01381445|113435|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107564|NCT01381445|113435|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107565|NCT01381445|113435|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107566|NCT01381445|113435|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107567|NCT01379937|115115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107568|NCT01379937|115115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107569|NCT01379937|115115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107570|NCT01379937|115115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107571|NCT01379937|115115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107572|NCT01379937|115115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107573|NCT01377480||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05267&kw=P05267&tab=access|
107574|NCT01376388|115362|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107575|NCT01376388|115362|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107576|NCT01376388|115362|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107577|NCT01376388|115362|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107578|NCT01376323|114728|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107579|NCT01376323|114728|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107580|NCT01376323|114728|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107581|NCT01376323|114728|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107582|NCT01376323|114728|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107583|NCT01376323|114728|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107584|NCT01376323|114728|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107585|NCT01376245|113684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107586|NCT01376245|113684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107587|NCT01376245|113684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107588|NCT01376245|113684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107589|NCT01376245|113684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107590|NCT01376245|113684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107591|NCT01376245|113684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107592|NCT01376232|113634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107593|NCT01376232|113634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107594|NCT01376232|113634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107595|NCT01376232|113634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107596|NCT01376232|113634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107597|NCT01376232|113634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107598|NCT01376232|113634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107599|NCT01376167|112582|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107600|NCT01376167|112582|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107601|NCT01376167|112582|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107602|NCT01376167|112582|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107603|NCT01376167|112582|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107604|NCT01376167|112582|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107605|NCT01372410|115321|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107606|NCT01372410|115321|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107607|NCT01372410|115321|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107608|NCT01372410|115321|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107609|NCT01372410|115321|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107610|NCT01372410|115321|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107611|NCT01372410|115321|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107612|NCT01372137|doi: 10.1111/bph.13433|Manuscript|http://onlinelibrary.wiley.com/doi/10.1111/bph.13433/abstract;jsessionid=E657A6C9667BB70DE92E5B69B86B1D3F.f01t01|
107613|NCT01371812|114660|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107614|NCT01371812|114660|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107615|NCT01371812|114660|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107616|NCT01371812|114660|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107617|NCT01371812|114660|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107618|NCT01371812|114660|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107619|NCT01371812|114660|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107620|NCT01371799|113746|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107621|NCT01371799|113746|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107622|NCT01371799|113746|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107623|NCT01371799|113746|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107624|NCT01371799|113746|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107625|NCT01371799|113746|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107626|NCT01371682|112771|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107627|NCT01371682|112771|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107628|NCT01371682|112771|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107629|NCT01371682|112771|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107630|NCT01371682|112771|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107631|NCT01371682|112771|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107632|NCT01371682|112771|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107633|NCT01370694||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=8808-001&kw=8808-001&tab=access|
107634|NCT01370642||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-043&kw=7009-043&tab=access|
107635|NCT01370616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0826-061&kw=0826-061&tab=access|
107636|NCT01367743||Statistical Analysis Plan|http://cic-p-nancy.fr/wp-content/uploads/2019/01/revUS_SAP_OPTIMA_CC_KD_NG.pdf|
107637|NCT01366846|LEAP-On (ITN049AD)|Individual Participant Data Set|https://www.itntrialshare.org/|
107638|NCT01366846|LEAP-On (ITN049AD)|Study protocol synopsis; datasets and figures from published NEJM 2016 article|https://www.itntrialshare.org/|
107639|NCT01366573|115256|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107640|NCT01366573|115256|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107641|NCT01366573|115256|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107642|NCT01366573|115256|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107643|NCT01366573|115256|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107644|NCT01366573|115256|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107645|NCT01366573|115256|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107646|NCT01366560|114639|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107647|NCT01366560|114639|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107648|NCT01366560|114639|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107649|NCT01366560|114639|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107650|NCT01366560|114639|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107651|NCT01366560|114639|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107652|NCT01366560|114639|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107653|NCT01366534|114460|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107654|NCT01366534|114460|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107655|NCT01366534|114460|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107656|NCT01366534|114460|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107657|NCT01366534|114460|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107658|NCT01366534|114460|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107659|NCT01366521|114092|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107660|NCT01366521|114092|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107661|NCT01366521|114092|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107662|NCT01366521|114092|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107663|NCT01366521|114092|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107664|NCT01366521|114092|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107665|NCT01366521|114092|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107666|NCT01362530||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0869-208&kw=0869-208&tab=access|
107667|NCT01362322|114778|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107668|NCT01362322|114778|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107669|NCT01362322|114778|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107670|NCT01362322|114778|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107671|NCT01362322|114778|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107672|NCT01362322|114778|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107673|NCT01362257|112014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107674|NCT01362257|112014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107675|NCT01362257|112014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107676|NCT01362257|112014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107677|NCT01362257|112014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107678|NCT01362257|112014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107679|NCT01362257|112014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107680|NCT01362244|111782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107681|NCT01362244|111782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107682|NCT01362244|111782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107683|NCT01362244|111782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107684|NCT01362244|111782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107685|NCT01362244|111782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107686|NCT01362244|111782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107687|NCT01360398|114378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107688|NCT01360398|114378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107689|NCT01360398|114378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107690|NCT01360398|114378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107691|NCT01360398|114378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107692|NCT01360398|114378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107693|NCT01360398|114378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107694|NCT01358825|115375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107695|NCT01358825|115375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107696|NCT01358825|115375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107697|NCT01358825|115375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107698|NCT01358825|115375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107699|NCT01358825|115375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107700|NCT01358825|115375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107701|NCT01357889|114856|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107702|NCT01357889|114856|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107703|NCT01357889|114856|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107704|NCT01357889|114856|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107705|NCT01357889|114856|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107706|NCT01357889|114856|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107707|NCT01357889|114856|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107708|NCT01357850|112670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107709|NCT01357850|112670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107710|NCT01357850|112670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107711|NCT01357850|112670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107712|NCT01357850|112670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107713|NCT01357850|112670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107714|NCT01357850|112670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107715|NCT01357135||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-201&kw=0431-201&tab=access|
107716|NCT01357070|DOI:10.4172/2472-1921.100060|Clinical Study Report|https://clinical-nutrition.imedpub.com/consumption-of-broccoli-sprouts-attenuatesintracellular-p38-map-kinase-and-reactiveoxygen-species-proinflammatory-activationin-hum.php?aid=21325|RESULTS REPORT
107717|NCT01353898||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=1972-003&kw=1972-003&tab=access|
107718|NCT01353768|115008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107719|NCT01353768|115008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107720|NCT01353768|115008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107721|NCT01353768|115008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107722|NCT01353768|115008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107723|NCT01353768|115008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107724|NCT01353768|115008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107725|NCT01353742|114957|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107726|NCT01353742|114957|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107727|NCT01353742|114957|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107728|NCT01353742|114957|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107729|NCT01353742|114957|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107730|NCT01353742|114957|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107731|NCT01353742|114957|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107732|NCT01353729|114346|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107733|NCT01353729|114346|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107734|NCT01353729|114346|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107735|NCT01353729|114346|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107736|NCT01353729|114346|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107737|NCT01353729|114346|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107738|NCT01353729|114346|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107739|NCT01353703|111157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107740|NCT01353703|111157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107741|NCT01353703|111157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107742|NCT01353703|111157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107743|NCT01353703|111157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107744|NCT01353703|111157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107745|NCT01350934||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0217A-264&kw=0217A-264&tab=access|
107746|NCT01350219|PMC5689778|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/?term=stem+cell+educator+type+1+diabetes%2C+platelets|Yong Zhao*, Zhaoshun Jiang, Elias Delgado, Heng Li, Huimin Zhou, Wei Hu, Marcos Perez-Basterrechea, Anna Janostakova, Qidong Tan, Jing Wang, Mao Mao, Zhaohui Yin, Ye Zhang, Ying Li, Quanhai Li, Jing Zhou, Yunxiang Li, Eva Martinez Revuelta, Jose Maria García-Gala, Honglan Wang, Silvia Perez-López, Maria Alvarez-Viejo, Edelmiro Menendez, Thomas Moss, Edward Guindi, Jesus Otero. Platelets-derived mitochondria display embryonic stem cell markers and improve pancreatic islet β-cell function in humans. STEM CELLS Translational Medicine. July 7, 2017. DOI: 10.1002/sctm.17-0078.
107747|NCT01347255||Clinical Study Report|http://www.leo-pharma.com/Home/Research-and-Development/Clinical-trial-disclosure/Clinical-trial-summaries-and-reports.aspx|Clinical Trials at LEO Pharma
107748|NCT01342913|113107|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107749|NCT01342913|113107|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107750|NCT01342913|113107|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107751|NCT01342913|113107|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107752|NCT01342913|113107|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107753|NCT01342913|113107|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107754|NCT01342913|113107|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107755|NCT01340911|115444|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107756|NCT01340911|115444|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107757|NCT01340911|115444|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107758|NCT01340911|115444|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107759|NCT01340911|115444|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107760|NCT01340911|115444|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107761|NCT01338779|ImmPort Study ID: SDY546|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY546|
107762|NCT01338779|ImmPort Study ID: SDY546|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY546|
107763|NCT01338779|ImmPort Study ID: SDY546|Study summary,-design, demographics,mechanistic assays,-study files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY546|
107764|NCT01338779|Study ID: FACTOR/ITN507ST|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN507STAJT/Study%20Data/begin.view|FACTOR/ITN507ST is the Study Identifier in the ITN TrialShare Clinical Trials Research Portal.
107765|NCT01338779|Study ID: FACTOR/ITN507ST|Original articles w/data and reports; abstracts et al.|http://www.itntrialshare.org/project/Studies/ITN507STAJT/Study%20Data/begin.view|FACTOR/ITN507ST is the Study Identifier in the ITN TrialShare Clinical Trials Research Portal.
107766|NCT01337674||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4618-010&kw=4618-010&tab=access|
107767|NCT01336608|113108|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107768|NCT01336608|113108|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107769|NCT01336608|113108|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107770|NCT01336608|113108|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107771|NCT01336608|113108|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107772|NCT01336608|113108|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107773|NCT01336608|113108|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107774|NCT01335997||CSR Synsopsi Link|http://www.merck.com/clinical-trials/study.html?id=0524B-143&kw=0524B-143&tab=access|
107812|NCT01328444|114417|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107775|NCT01335139|ITN043AD|Individual Participant Data Set|https://www.itntrialshare.org/project/Studies/ITN043ADJAMA/Study%20Data/begin.view|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.Creating an account for ITN TrialShare is free and allows for searching studies of interest.
107776|NCT01335139|ITN043AD|Synopsis, Adverse Events, -Data and Reports, -Schedule of Assessments|https://www.itntrialshare.org/project/Studies/ITN043ADJAMA/Study%20Data/begin.view|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.Creating an account for ITN TrialShare is free and allows for searching studies of interest.
107777|NCT01333813|112688|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107778|NCT01333813|112688|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107779|NCT01333813|112688|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107780|NCT01333813|112688|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107781|NCT01333813|112688|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107782|NCT01333813|112688|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107783|NCT01332552|115040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107784|NCT01332552|115040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107785|NCT01332552|115040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107786|NCT01332552|115040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107787|NCT01332552|115040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107788|NCT01332552|115040|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107789|NCT01332552|115040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107790|NCT01332513|114552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107791|NCT01332513|114552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107792|NCT01332513|114552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107793|NCT01332513|114552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107794|NCT01332513|114552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107795|NCT01332513|114552|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107796|NCT01332513|114552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107797|NCT01332292|102942|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107798|NCT01332292|102942|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107799|NCT01332292|102942|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107800|NCT01332292|102942|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107801|NCT01332292|102942|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107802|NCT01332292|102942|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107803|NCT01332292|102942|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107804|NCT01330485||Individual Participant Data Set|https://osf.io/426pd|
107805|NCT01330485||All study files|https://osf.io/uhwnb|
107806|NCT01328444|114417|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107807|NCT01328444|114417|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107808|NCT01328444|114417|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107809|NCT01328444|114417|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107810|NCT01328444|114417|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107811|NCT01328444|114417|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107813|NCT01324362|SAM40065|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107814|NCT01324362|SAM40065|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107815|NCT01324362|SAM40065|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107816|NCT01324362|SAM40065|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107817|NCT01324362|SAM40065|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107818|NCT01324362|SAM40065|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107819|NCT01324362|SAM40065|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107820|NCT01323972|113398|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107821|NCT01323972|113398|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107822|NCT01323972|113398|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107823|NCT01323972|113398|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107824|NCT01323972|113398|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107825|NCT01323972|113398|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107826|NCT01323959|113060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107827|NCT01323959|113060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107828|NCT01323959|113060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107829|NCT01323959|113060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107830|NCT01323959|113060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107831|NCT01323959|113060|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107832|NCT01323946|109825|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107833|NCT01323946|109825|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107834|NCT01323946|109825|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107835|NCT01323946|109825|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107836|NCT01323946|109825|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107837|NCT01323946|109825|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107838|NCT01323946|109825|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107839|NCT01323673|115054|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107840|NCT01323673|115054|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107841|NCT01323673|115054|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107842|NCT01323673|115054|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107843|NCT01323673|115054|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107844|NCT01323673|115054|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107845|NCT01323673|115054|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107846|NCT01323660|114418|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107847|NCT01323660|114418|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107848|NCT01323660|114418|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107849|NCT01323660|114418|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107850|NCT01323660|114418|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107851|NCT01323660|114418|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107852|NCT01323660|114418|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107853|NCT01323647|114306|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107854|NCT01323647|114306|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107855|NCT01323647|114306|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107856|NCT01323647|114306|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107857|NCT01323647|114306|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107858|NCT01323647|114306|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107859|NCT01323634|113109|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107860|NCT01323634|113109|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107861|NCT01323634|113109|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107862|NCT01323634|113109|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107863|NCT01323634|113109|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107864|NCT01323634|113109|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107865|NCT01323634|113109|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107866|NCT01323621|112352|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107867|NCT01323621|112352|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107868|NCT01323621|112352|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107869|NCT01323621|112352|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107870|NCT01323621|112352|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107871|NCT01323621|112352|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107872|NCT01323621|112352|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107873|NCT01319019|115032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107874|NCT01319019|115032|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107875|NCT01319019|115032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107876|NCT01319019|115032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107877|NCT01319019|115032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107878|NCT01319019|115032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107879|NCT01319019|115032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107880|NCT01319006|114703|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107881|NCT01319006|114703|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107882|NCT01319006|114703|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107883|NCT01319006|114703|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107884|NCT01319006|114703|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107885|NCT01319006|114703|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107886|NCT01319006|114703|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107887|NCT01318980|114604|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107888|NCT01318980|114604|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107889|NCT01318980|114604|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107890|NCT01318980|114604|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107891|NCT01318980|114604|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107892|NCT01318980|114604|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107893|NCT01318980|114604|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107894|NCT01316913|113374|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107895|NCT01316913|113374|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107896|NCT01316913|113374|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107897|NCT01316913|113374|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107898|NCT01316913|113374|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107899|NCT01316913|113374|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107900|NCT01316913|113374|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107901|NCT01316900|113360|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107902|NCT01316900|113360|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107903|NCT01316900|113360|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107904|NCT01316900|113360|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107905|NCT01316900|113360|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107906|NCT01316900|113360|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107907|NCT01316900|113360|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107908|NCT01316887|113359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107909|NCT01316887|113359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107910|NCT01316887|113359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107911|NCT01316887|113359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107912|NCT01316887|113359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107913|NCT01316887|113359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107914|NCT01316887|113359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107915|NCT01315847||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-067&kw=0974-067&tab=access|
107916|NCT01313676|113782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107917|NCT01313676|113782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107918|NCT01313676|113782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107919|NCT01313676|113782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107920|NCT01313676|113782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107921|NCT01313676|113782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107922|NCT01313676|113782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107923|NCT01313650|113373|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107924|NCT01313650|113373|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107925|NCT01313650|113373|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107926|NCT01313650|113373|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108005|NCT01277822||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0954F-399&kw=0954F-399&tab=access|
107927|NCT01313650|113373|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107928|NCT01313650|113373|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107929|NCT01313650|113373|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107930|NCT01313637|113361|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107931|NCT01313637|113361|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107932|NCT01313637|113361|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107933|NCT01313637|113361|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107934|NCT01313637|113361|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107935|NCT01313637|113361|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107936|NCT01313637|113361|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107937|NCT01310413|114464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107938|NCT01310413|114464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107939|NCT01310413|114464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107940|NCT01310413|114464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107941|NCT01310413|114464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107942|NCT01310413|114464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107943|NCT01302834|NCT01302834|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive
107944|NCT01300455||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-036&kw=4305-036&tab=access|
107945|NCT01299610|113434|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107946|NCT01299610|113434|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107947|NCT01299610|113434|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107948|NCT01299610|113434|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107949|NCT01299610|113434|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107950|NCT01299610|113434|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107951|NCT01299610|113434|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107952|NCT01299597|109652|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107953|NCT01299597|109652|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107954|NCT01299597|109652|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107955|NCT01299597|109652|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107956|NCT01299597|109652|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107957|NCT01299597|109652|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107958|NCT01299597|109652|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107959|NCT01299558|102934|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107960|NCT01299558|102934|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107961|NCT01299558|102934|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107962|NCT01299558|102934|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107963|NCT01299558|102934|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107964|NCT01299558|102934|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107965|NCT01299558|102934|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107966|NCT01295372|2010-022181-28|EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2010-022181-28/result|
107967|NCT01295320|114825|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107968|NCT01295320|114825|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107969|NCT01295320|114825|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107970|NCT01295320|114825|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107971|NCT01295320|114825|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107972|NCT01295320|114825|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107973|NCT01295320|114825|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107974|NCT01294709||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-014&kw=0974-014&tab=access|
107975|NCT01294696||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0663-140&kw=0663-140&tab=access|
107976|NCT01294683||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-118&kw=0524B-118&tab=access|
107977|NCT01294605|263855/034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107978|NCT01294605|263855/034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107979|NCT01294605|263855/034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107980|NCT01294605|263855/034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107981|NCT01294605|263855/034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107982|NCT01294605|263855/034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107983|NCT01294566|114422|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107984|NCT01294566|114422|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107985|NCT01294566|114422|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107986|NCT01294566|114422|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107987|NCT01294566|114422|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107988|NCT01294566|114422|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107989|NCT01294566|114422|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107990|NCT01293006||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-032&kw=4305-032&tab=access|
107991|NCT01287065|114624|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107992|NCT01287065|114624|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107993|NCT01287065|114624|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107994|NCT01287065|114624|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107995|NCT01287065|114624|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107996|NCT01287065|114624|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107997|NCT01287065|114624|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107998|NCT01286831|106181|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
107999|NCT01286831|106181|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108000|NCT01286831|106181|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108001|NCT01286831|106181|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108002|NCT01286831|106181|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108003|NCT01286831|106181|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108004|NCT01286831|106181|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108006|NCT01277705|711866/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108007|NCT01277705|711866/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108008|NCT01277705|711866/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108009|NCT01277705|711866/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108010|NCT01277705|711866/003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108011|NCT01277705|711866/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108012|NCT01277211||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06450&kw=P06450&tab=access|
108013|NCT01277042|114590|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108014|NCT01277042|114590|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108015|NCT01277042|114590|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108016|NCT01277042|114590|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108017|NCT01277042|114590|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108018|NCT01277042|114590|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108019|NCT01274559||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0524A-133&kw=0524A-133&tab=access|
108020|NCT01270139|doi: 10.13140/2.1.3109.5847|Study Protocol|https://www.researchgate.net/publication/273623828_Protocol_v31_of_NANOM-FIM_trial|The protocol of the trial (v. 3.1.) was released in ResearchGate in March 2015.
108021|NCT01270139|doi: 10.17632/rkz98ttjrd.1|Study Protocol|https://data.mendeley.com/datasets/rkz98ttjrd/1|This is a protocol of NANOM-FIM trial released in Mendeley Datasets.
108022|NCT01270139|doi: 10.17632/5hzb3249hn.1|Individual Participant Data Set|https://data.mendeley.com/datasets/5hzb3249hn/1|There is Atomic Force Microscopy data from random patients.
108023|NCT01270139|doi: 10.13140/RG.2.1.4913|Protocol and Proposal of the Research Project|https://www.researchgate.net/publication/286927115_Development_of_bioresorbable_scaffolds_and_nanotechnologies_for_reversal_of_atherosclerosis_DREAM|This is a set of documents of the related DREAM project funded by the FP7/ European Commission. The DREAM study was a collaborative project at the loop between Erasmus MC (Rotterdam, The Netherlands) and Ural Institute of Cardiology (Yekaterinburg, Russia) including NANOM-FIM trial.
108024|NCT01267071|114136|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108025|NCT01267071|114136|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108026|NCT01267071|114136|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108027|NCT01267071|114136|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108028|NCT01267071|114136|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108029|NCT01267071|114136|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108030|NCT01267071|114136|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108031|NCT01267006|114922|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108032|NCT01267006|114922|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108033|NCT01267006|114922|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108034|NCT01267006|114922|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108035|NCT01267006|114922|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108036|NCT01267006|114922|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108037|NCT01267006|114922|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108038|NCT01266980|113970|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108039|NCT01266980|113970|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108040|NCT01266980|113970|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108041|NCT01266980|113970|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108042|NCT01266980|113970|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108043|NCT01266980|113970|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108044|NCT01266980|113970|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108045|NCT01266941|111789|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108046|NCT01266941|111789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108047|NCT01266941|111789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108048|NCT01266941|111789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108049|NCT01266941|111789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108050|NCT01266941|111789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108051|NCT01266941|111789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108052|NCT01262911|115083|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108053|NCT01262911|115083|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108054|NCT01262911|115083|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108055|NCT01262911|115083|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108056|NCT01262911|115083|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108057|NCT01262911|115083|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108058|NCT01262911|115083|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108059|NCT01262872|114174|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108060|NCT01262872|114174|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108061|NCT01262872|114174|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108062|NCT01262872|114174|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108063|NCT01262872|114174|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108064|NCT01262872|114174|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108065|NCT01258608|200149|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108066|NCT01258608|200149|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108067|NCT01258608|200149|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108068|NCT01258608|200149|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108069|NCT01258608|200149|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108070|NCT01258608|200149|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108071|NCT01258530|115096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108072|NCT01258530|115096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108073|NCT01258530|115096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108074|NCT01258530|115096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108075|NCT01258530|115096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108076|NCT01258530|115096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108077|NCT01258530|115096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108078|NCT01254643||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-008&kw=V503-008&tab=access|
108079|NCT01254604||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=2452-002&kw=2452-002&tab=access|
108080|NCT01254071|114694|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108081|NCT01254071|114694|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108082|NCT01254071|114694|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108083|NCT01254071|114694|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108084|NCT01254071|114694|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108085|NCT01254071|114694|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108086|NCT01254071|114694|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108087|NCT01254032|114169|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108088|NCT01254032|114169|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108089|NCT01254032|114169|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108090|NCT01254032|114169|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108091|NCT01254032|114169|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108092|NCT01248975|114387|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108093|NCT01248975|114387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108094|NCT01248975|114387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108095|NCT01248975|114387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108096|NCT01248975|114387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108097|NCT01248975|114387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108098|NCT01248975|114387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108099|NCT01245933||general information|http://www.asconet.net|
108100|NCT01245764||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-046&kw=V501-046&tab=access|
108101|NCT01245738||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0000-204&kw=0000-204&tab=access|
108102|NCT01245426|114749|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108103|NCT01245426|114749|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108104|NCT01245426|114749|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108105|NCT01245426|114749|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108106|NCT01245426|114749|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108107|NCT01245426|114749|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108108|NCT01245426|114749|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108109|NCT01245140|117221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108110|NCT01245140|117221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108111|NCT01245140|117221|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108112|NCT01245140|117221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108113|NCT01245140|117221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108114|NCT01245140|117221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108115|NCT01245140|117221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108116|NCT01244984|113989|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108117|NCT01244984|113989|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108118|NCT01244984|113989|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108119|NCT01244984|113989|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108120|NCT01244984|113989|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108121|NCT01244984|113989|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108122|NCT01244984|113989|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108123|NCT01244815||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06107&kw=P06107&tab=access|
108124|NCT01236040|114371|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108125|NCT01236040|114371|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108126|NCT01236040|114371|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108127|NCT01236040|114371|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108128|NCT01236040|114371|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108129|NCT01236040|114371|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108130|NCT01235975|113807|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108131|NCT01235975|113807|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108132|NCT01235975|113807|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108133|NCT01235975|113807|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108134|NCT01235975|113807|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108135|NCT01235975|113807|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108136|NCT01235949|112921|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108137|NCT01235949|112921|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108138|NCT01235949|112921|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108139|NCT01235949|112921|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108140|NCT01235949|112921|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108141|NCT01235949|112921|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108142|NCT01235728||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-022&kw=0873-022&tab=access|
108143|NCT01231620|114373|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108144|NCT01231620|114373|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108145|NCT01231620|114373|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108146|NCT01231620|114373|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108147|NCT01231620|114373|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108148|NCT01231620|114373|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108149|NCT01231620|114373|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108150|NCT01231607|114263|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108151|NCT01231607|114263|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108152|NCT01231607|114263|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108153|NCT01231607|114263|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108154|NCT01231607|114263|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108155|NCT01231607|114263|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108156|NCT01231607|114263|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108157|NCT01225731||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05495&kw=P05495&tab=access|
108158|NCT01224821|104731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108159|NCT01224821|104731|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108160|NCT01224821|104731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108161|NCT01224821|104731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108162|NCT01224821|104731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108163|NCT01224821|104731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108164|NCT01224821|104731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108165|NCT01222078|113390|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108166|NCT01222078|113390|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108167|NCT01222078|113390|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108168|NCT01222078|113390|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108169|NCT01222078|113390|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108170|NCT01222078|113390|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108171|NCT01222078|113390|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108172|NCT01218308|114541|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108173|NCT01218308|114541|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108174|NCT01218308|114541|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108175|NCT01218308|114541|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108176|NCT01218308|114541|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108177|NCT01218308|114541|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108178|NCT01218308|114541|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108179|NCT01218126|113006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108180|NCT01218126|113006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108181|NCT01218126|113006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108182|NCT01218126|113006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108183|NCT01218126|113006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108184|NCT01218126|113006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108185|NCT01218126|113006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108186|NCT01217073||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-006&kw=3102-006&tab=access|
108187|NCT01213849|102932|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108188|NCT01213849|102932|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108189|NCT01213849|102932|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108190|NCT01213849|102932|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108191|NCT01213849|102932|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108192|NCT01213849|102932|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108193|NCT01213849|102932|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108194|NCT01212094||Paper describing the results of interim analysis|http://onlinelibrary.wiley.com/doi/10.1002/acn3.293/full|
108195|NCT01210651||Individual Participant Data Set|http://prathikanti.com/studydata/|The individual participant dataset includes de-identified demographic/clinical information obtained from all randomized participants at screening, as well as primary and secondary outcome measures obtained over the course of the 8-week intervention period.
108196|NCT01209104|113722|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108197|NCT01209104|113722|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108198|NCT01209104|113722|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108199|NCT01209104|113722|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108200|NCT01209104|113722|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108201|NCT01209104|113722|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108202|NCT01209104|113722|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108203|NCT01209078|113414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108204|NCT01209078|113414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108205|NCT01209078|113414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108206|NCT01209078|113414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108207|NCT01209078|113414|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108208|NCT01209078|113414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108209|NCT01209078|113414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108210|NCT01209052|112483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108211|NCT01209052|112483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108212|NCT01209052|112483|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108213|NCT01209052|112483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108214|NCT01209052|112483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108215|NCT01209052|112483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108216|NCT01209052|112483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108217|NCT01209026|102936|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108218|NCT01209026|102936|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108219|NCT01209026|102936|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108220|NCT01209026|102936|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108221|NCT01209026|102936|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108222|NCT01209026|102936|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108223|NCT01209026|102936|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108224|NCT01208207||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0663-108&kw=0663-108&tab=access|
108225|NCT01208181||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0663-107&kw=0663-107&tab=access|
108226|NCT01207765||Biology of Blood and Marrow Transplant , Volume 21 , Issue 2 , S199|http://www.bbmt.org/article/S1083-8791(14)01012-X/abstract|Published Abstract
108227|NCT01204671|114269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108228|NCT01204671|114269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108229|NCT01204671|114269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108230|NCT01204671|114269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108231|NCT01204671|114269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108232|NCT01204671|114269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108233|NCT01204671|114269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108234|NCT01198769|114351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108235|NCT01198769|114351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108236|NCT01198769|114351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108237|NCT01198769|114351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108238|NCT01198769|114351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108239|NCT01198769|114351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108240|NCT01198769|114351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108241|NCT01198756|113314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108242|NCT01198756|113314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108243|NCT01198756|113314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108244|NCT01198756|113314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108245|NCT01198756|113314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108246|NCT01198756|113314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108247|NCT01198756|113314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108248|NCT01196988|113275|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108249|NCT01196988|113275|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108250|NCT01196988|113275|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108251|NCT01196988|113275|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108252|NCT01196988|113275|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108253|NCT01196988|113275|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108254|NCT01196988|113275|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108255|NCT01196975|112963|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108256|NCT01196975|112963|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108257|NCT01196975|112963|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108258|NCT01196975|112963|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108259|NCT01196975|112963|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108260|NCT01196975|112963|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108261|NCT01196975|112963|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108262|NCT01196026|114451|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108263|NCT01196026|114451|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108264|NCT01196026|114451|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108265|NCT01196026|114451|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108266|NCT01196026|114451|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108267|NCT01196026|114451|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108268|NCT01195792|111850|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108269|NCT01195792|111850|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108270|NCT01195792|111850|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108271|NCT01195792|111850|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108272|NCT01195792|111850|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108273|NCT01195792|111850|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108274|NCT01195792|111850|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108275|NCT01195779|114294|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108276|NCT01195779|114294|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108277|NCT01195779|114294|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108278|NCT01195779|114294|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108279|NCT01195779|114294|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108280|NCT01195779|114294|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108281|NCT01192776||Publication|http://www.ncbi.nlm.nih.gov/pubmed/25536254|
108282|NCT01192191|114156|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108283|NCT01192191|114156|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108284|NCT01192191|114156|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108285|NCT01192191|114156|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108286|NCT01192191|114156|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108287|NCT01192191|114156|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108288|NCT01192191|114156|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108289|NCT01192178|113872|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108290|NCT01192178|113872|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108291|NCT01192178|113872|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108292|NCT01192178|113872|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108293|NCT01192178|113872|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108294|NCT01192178|113872|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108295|NCT01192178|113872|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108296|NCT01190215|114452|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108297|NCT01190215|114452|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108298|NCT01190215|114452|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108299|NCT01190215|114452|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108300|NCT01190215|114452|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108301|NCT01190215|114452|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108302|NCT01183468|RETAIN ITN041AI|Individual Participant Data Set|https://www.itntrialshare.org/project/Studies/ITN041AIPUBLIC/Study%20Data/begin.view?pageId=study.DATA_ANALYSIS|RETAIN ITN041AI is the Study Identifier in the Immune Tolerance Network (ITN) TrialShare Clinical Trials Research Portal
108303|NCT01181895|112060|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108304|NCT01181895|112060|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108305|NCT01181895|112060|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108306|NCT01181895|112060|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108307|NCT01181895|112060|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108308|NCT01181895|112060|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108309|NCT01181895|112060|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108310|NCT01177826|111426|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108311|NCT01177826|111426|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108312|NCT01177826|111426|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108313|NCT01177826|111426|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108314|NCT01177826|111426|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108315|NCT01177826|111426|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108316|NCT01177384||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431-130&kw=0431-130&tab=access|
108317|NCT01176565|Protocol|Study Protocol|https://drive.google.com/file/d/0B4XP2p9l3yybYk1sX2pBYm1LSFh1cEZndHoySkVQZUxJN2Jz/view?usp=sharing|
108318|NCT01175083|114056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108319|NCT01175083|114056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108320|NCT01175083|114056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108321|NCT01175083|114056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108322|NCT01175083|114056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108323|NCT01175083|114056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108324|NCT01175083|114056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108325|NCT01171989|113978|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108326|NCT01171989|113978|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108327|NCT01171989|113978|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108328|NCT01171989|113978|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108329|NCT01171989|113978|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108330|NCT01171989|113978|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108331|NCT01171989|113978|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108332|NCT01171963|113808|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108333|NCT01171963|113808|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108334|NCT01171963|113808|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108335|NCT01171963|113808|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108336|NCT01171963|113808|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108337|NCT01171963|113808|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108338|NCT01171963|113808|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108339|NCT01168167|01168167|Study Protocol|https://clinicaltrials.gov/ct2/show/NCT01168167|
108340|NCT01165320||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0991-074&kw=0991-074&tab=access|
108341|NCT01165242|114249|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108342|NCT01165242|114249|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108343|NCT01165242|114249|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108344|NCT01165242|114249|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108345|NCT01165242|114249|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108346|NCT01165242|114249|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108347|NCT01165203|112673|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108348|NCT01165203|112673|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108349|NCT01165203|112673|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108350|NCT01165203|112673|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108351|NCT01165203|112673|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108466|NCT01148472|2004-005069-39|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2004-005069-39/results|
108352|NCT01165203|112673|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108353|NCT01165203|112673|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108354|NCT01165138|106827|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108355|NCT01165138|106827|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108356|NCT01165138|106827|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108357|NCT01165138|106827|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108358|NCT01165138|106827|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108359|NCT01165138|106827|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108360|NCT01165138|106827|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108361|NCT01165125|105548|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108362|NCT01165125|105548|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108363|NCT01165125|105548|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108364|NCT01165125|105548|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108365|NCT01165125|105548|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108366|NCT01165125|105548|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108367|NCT01165125|105548|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108368|NCT01164878||Individual Participant Data Set|https://dfzljdn9uc3pi.cloudfront.net/2016/2483/1/SPSS_repa_et_al.sav|SPSS Data Set for Analysis
108369|NCT01162590|113545|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108370|NCT01162590|113545|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108371|NCT01162590|113545|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108372|NCT01162590|113545|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108373|NCT01162590|113545|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108374|NCT01162590|113545|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108375|NCT01161160|114495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108376|NCT01161160|114495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108377|NCT01161160|114495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108378|NCT01161160|114495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108379|NCT01161160|114495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108380|NCT01161160|114495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108381|NCT01161160|114495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108382|NCT01160237|114454|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108383|NCT01160237|114454|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108384|NCT01160237|114454|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108385|NCT01160237|114454|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108386|NCT01160237|114454|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108387|NCT01160237|114454|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108388|NCT01160237|114454|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108389|NCT01160224|114312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108390|NCT01160224|114312|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108391|NCT01160224|114312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108392|NCT01160224|114312|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108393|NCT01160224|114312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108394|NCT01160224|114312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108395|NCT01160224|114312|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108396|NCT01160003|113209|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108397|NCT01160003|113209|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108398|NCT01160003|113209|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108399|NCT01160003|113209|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108400|NCT01160003|113209|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108401|NCT01160003|113209|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108402|NCT01160003|113209|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108403|NCT01159912|112059|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108404|NCT01159912|112059|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108405|NCT01159912|112059|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108406|NCT01159912|112059|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108407|NCT01159912|112059|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108408|NCT01159912|112059|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108409|NCT01159912|112059|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108410|NCT01158742|SDY291|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY291|ImmPort study identifier is SDY291
108411|NCT01158742|SDY291|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY291|ImmPort study identifier is SDY291. The study protocol is available through the Design tab on the site.
108412|NCT01158742|SDY291|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY291|ImmPort study identifier is SDY291
108413|NCT01156792|114255|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108414|NCT01156792|114255|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108415|NCT01156792|114255|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108416|NCT01156792|114255|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108417|NCT01156792|114255|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108418|NCT01156792|114255|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108419|NCT01156792|114255|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108420|NCT01155479||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05664&kw=P05664&tab=access|
108421|NCT01155466||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04938&kw=P04938&tab=access|
108422|NCT01154114|480848/028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108423|NCT01154114|480848/028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108424|NCT01154114|480848/028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108425|NCT01154114|480848/028|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108426|NCT01154114|480848/028|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108427|NCT01154114|480848/028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108428|NCT01154114|480848/028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108429|NCT01154101|114296|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108430|NCT01154101|114296|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108431|NCT01154101|114296|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108432|NCT01154101|114296|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108433|NCT01154101|114296|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108434|NCT01154101|114296|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108435|NCT01154088|114248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108436|NCT01154088|114248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108437|NCT01154088|114248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108438|NCT01154088|114248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108439|NCT01154088|114248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108440|NCT01154088|114248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108441|NCT01153893|113199|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108442|NCT01153893|113199|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108443|NCT01153893|113199|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108444|NCT01153893|113199|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108445|NCT01153893|113199|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108446|NCT01153893|113199|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108447|NCT01153841|113151|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108448|NCT01153841|113151|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108449|NCT01153841|113151|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108450|NCT01153841|113151|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108451|NCT01153841|113151|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108452|NCT01153841|113151|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108453|NCT01153802|112773|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108454|NCT01153802|112773|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108455|NCT01153802|112773|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108456|NCT01153802|112773|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108457|NCT01153802|112773|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108458|NCT01153802|112773|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108459|NCT01153802|112773|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108460|NCT01153685|110628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108461|NCT01153685|110628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108462|NCT01153685|110628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108463|NCT01153685|110628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108464|NCT01153685|110628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108465|NCT01153685|110628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108467|NCT01148459|112745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108468|NCT01148459|112745|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108469|NCT01148459|112745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108470|NCT01148459|112745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108471|NCT01148459|112745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108472|NCT01148459|112745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108473|NCT01147900|113055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108474|NCT01147900|113055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108475|NCT01147900|113055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108476|NCT01147900|113055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108477|NCT01147900|113055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108478|NCT01147900|113055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108479|NCT01147861|114187|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108480|NCT01147861|114187|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108481|NCT01147861|114187|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108482|NCT01147861|114187|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108483|NCT01147861|114187|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108484|NCT01147861|114187|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108485|NCT01147861|114187|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108486|NCT01147848|113091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108487|NCT01147848|113091|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108488|NCT01147848|113091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108489|NCT01147848|113091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108490|NCT01147848|113091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108491|NCT01147848|113091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108492|NCT01147848|113091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108493|NCT01147744|112186|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108494|NCT01147744|112186|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108495|NCT01147744|112186|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108496|NCT01147744|112186|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108497|NCT01147744|112186|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108498|NCT01147744|112186|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108499|NCT01147744|112186|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108500|NCT01147731|111681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108501|NCT01147731|111681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108502|NCT01147731|111681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108503|NCT01147731|111681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108504|NCT01147731|111681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108505|NCT01147731|111681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108506|NCT01147731|111681|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108507|NCT01147718|111680|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108508|NCT01147718|111680|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108509|NCT01147718|111680|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108510|NCT01147718|111680|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108511|NCT01147718|111680|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108512|NCT01147718|111680|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108513|NCT01147718|111680|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108514|NCT01147692|108366|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108515|NCT01147692|108366|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108516|NCT01147692|108366|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108517|NCT01147692|108366|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108518|NCT01147692|108366|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108519|NCT01147692|108366|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108520|NCT01147692|108366|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108521|NCT01146418||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06031&kw=P06031&tab=access|
108522|NCT01144741||Participant Information Sheet|https://drive.google.com/file/d/0B2gy05hAu1ILMVh0cE5xSHFlUmc/view?usp=sharing|This form is essentially the same as the informed consent document, except that it lacks signature blocks.
108523|NCT01144741||Letters to Doctors and Patients/Families|https://drive.google.com/file/d/0B2gy05hAu1ILVkVnWlltdXJHTlU/view?usp=sharing|These letters provide background and other information for those who may be interested.
108524|NCT01144299|114292|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108525|NCT01144299|114292|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108526|NCT01144299|114292|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108527|NCT01144299|114292|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108528|NCT01144299|114292|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108529|NCT01144299|114292|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108530|NCT01144299|114292|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108531|NCT01143688|DOI: 10.1056/NEJMoa1103319|Publication|http://www.nejm.org/doi/full/10.1056/NEJMoa1103319#t=article|Active Albuterol or Placebo, Sham Acupuncture, or No Intervention in Asthma Michael E. Wechsler, M.D., John M. Kelley, Ph.D., Ingrid O.E. Boyd, M.P.H., Stefanie Dutile, B.S., Gautham Marigowda, M.B., Irving Kirsch, Ph.D., Elliot Israel, M.D., and Ted J. Kaptchuk N Engl J Med 2011; 365:119-126 July 14, 2011 DOI: 10.1056/NEJMoa1103319
108532|NCT01140061||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-020&kw=0873-020&tab=access|
108533|NCT01139580|114743|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108534|NCT01139580|114743|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108535|NCT01139580|114743|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108536|NCT01139580|114743|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108537|NCT01139580|114743|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108538|NCT01139580|114743|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108539|NCT01139580|114743|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108540|NCT01138098|113954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108541|NCT01138098|113954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108542|NCT01138098|113954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108543|NCT01138098|113954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108544|NCT01138098|113954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108545|NCT01138098|113954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108546|NCT01138007|113351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108547|NCT01138007|113351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108548|NCT01138007|113351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108549|NCT01138007|113351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108550|NCT01138007|113351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108551|NCT01134042|106829|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108552|NCT01134042|106829|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108553|NCT01134042|106829|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108554|NCT01134042|106829|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108555|NCT01134042|106829|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108556|NCT01134042|106829|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108557|NCT01134042|106829|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108558|NCT01132443|115902|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108559|NCT01132443|115902|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108560|NCT01132443|115902|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108561|NCT01132443|115902|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108562|NCT01132443|115902|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108563|NCT01132443|115902|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108564|NCT01132443|115902|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108565|NCT01128894|114179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108566|NCT01128894|114179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108567|NCT01128894|114179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108568|NCT01128894|114179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108569|NCT01128894|114179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108570|NCT01128894|114179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108571|NCT01128894|114179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108572|NCT01128634|113950|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108573|NCT01128634|113950|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108574|NCT01128634|113950|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108575|NCT01128634|113950|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108576|NCT01128634|113950|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108577|NCT01128634|113950|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108578|NCT01128634|113950|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108579|NCT01128621|113132|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108580|NCT01128621|113132|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108581|NCT01128621|113132|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108582|NCT01128621|113132|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108583|NCT01128621|113132|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108584|NCT01128621|113132|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108585|NCT01128621|113132|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108586|NCT01128595|113126|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108587|NCT01128595|113126|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108588|NCT01128595|113126|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108589|NCT01128595|113126|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108590|NCT01128595|113126|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108591|NCT01128595|113126|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108592|NCT01128595|113126|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108593|NCT01128569|113090|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108594|NCT01128569|113090|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108595|NCT01128569|113090|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108596|NCT01128569|113090|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108597|NCT01128569|113090|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108598|NCT01128569|113090|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108599|NCT01128569|113090|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108600|NCT01125774||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-065&kw=0974-065&tab=access|
108601|NCT01124422|113877|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108602|NCT01124422|113877|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108603|NCT01124422|113877|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108604|NCT01124422|113877|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108605|NCT01124422|113877|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108606|NCT01124422|113877|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108607|NCT01124422|113877|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108608|NCT01123083|115494|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108609|NCT01123083|115494|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108610|NCT01123083|115494|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108611|NCT01123083|115494|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108612|NCT01123083|115494|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108613|NCT01123083|115494|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108614|NCT01123083|115494|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108615|NCT01119846|111598|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108616|NCT01119846|111598|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108617|NCT01119846|111598|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108618|NCT01119846|111598|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108619|NCT01119846|111598|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108620|NCT01119846|111598|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108621|NCT01119846|111598|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108622|NCT01119664||Journal Article - AACR Journal|http://clincancerres.aacrjournals.org/|www.aacrjournals.org Article Title: Pilot and Feasibility Trial Evaluating Immuno-Gene Therapy of Malignant Mesothelioma Using Intrapleural Delivery of Adenovirus-IFNa Combined with Chemotherapy
108623|NCT01119651|114574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108624|NCT01119651|114574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108625|NCT01119651|114574|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108626|NCT01119651|114574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108627|NCT01119651|114574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108628|NCT01119651|114574|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108629|NCT01119651|114574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108630|NCT01119625|113266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108631|NCT01119625|113266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108632|NCT01119625|113266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108633|NCT01119625|113266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108634|NCT01119625|113266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108635|NCT01119625|113266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108636|NCT01119625|113266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108637|NCT01116427|ACCLAIM ITN035AI|Study protocol synopsis, -navigator, -schedule of assessments, study schema, and manuscript(s) with overviews, data and reports, participant level data|https://www.itntrialshare.org/project/Studies/ITN035AIPRI/Study%20Data/begin.view?|ACCLAIM ITN035AI is the Study Identifier in the Immune Tolerance Network (ITN) TrialShare Clinical Trials Research Portal
108638|NCT01115322|114573|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108639|NCT01115322|114573|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108640|NCT01115322|114573|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108641|NCT01115322|114573|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108642|NCT01115322|114573|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108643|NCT01115322|114573|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108644|NCT01115322|114573|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108645|NCT01114841|114572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108646|NCT01114841|114572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108647|NCT01114841|114572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108648|NCT01114841|114572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108649|NCT01114841|114572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108650|NCT01114841|114572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108651|NCT01114841|114572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108652|NCT01114620|114270|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108653|NCT01114620|114270|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108654|NCT01114620|114270|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108655|NCT01114620|114270|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108656|NCT01114620|114270|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108657|NCT01114620|114270|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108658|NCT01114620|114270|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108659|NCT01114503|112480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108660|NCT01114503|112480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108661|NCT01114503|112480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108662|NCT01114503|112480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108663|NCT01114503|112480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108664|NCT01114503|112480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108665|NCT01114503|112480|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108666|NCT01112787|114571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108667|NCT01112787|114571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108668|NCT01112787|114571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108669|NCT01112787|114571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108670|NCT01112787|114571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108671|NCT01112787|114571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108672|NCT01112787|114571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108673|NCT01110200|113874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108674|NCT01110200|113874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108675|NCT01110200|113874|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108676|NCT01110200|113874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108677|NCT01110200|113874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108678|NCT01110200|113874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108679|NCT01110200|113874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108680|NCT01110057|113049|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108681|NCT01110057|113049|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108682|NCT01110057|113049|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108683|NCT01110057|113049|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108684|NCT01110057|113049|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108685|NCT01110057|113049|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108686|NCT01110057|113049|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108687|NCT01110018|112008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108688|NCT01110018|112008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108689|NCT01110018|112008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108690|NCT01110018|112008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108691|NCT01110018|112008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108692|NCT01110018|112008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108693|NCT01110018|112008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108694|NCT01107587|113518|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108695|NCT01107587|113518|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108696|NCT01107587|113518|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108697|NCT01107587|113518|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108698|NCT01107587|113518|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108699|NCT01107587|113518|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108700|NCT01106092|113264|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108701|NCT01106092|113264|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108702|NCT01106092|113264|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108703|NCT01106092|113264|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108704|NCT01106092|113264|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108705|NCT01106092|113264|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108706|NCT01106092|113264|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108707|NCT01101568|113506|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108708|NCT01101568|113506|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108709|NCT01101568|113506|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108710|NCT01101568|113506|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108711|NCT01101568|113506|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108712|NCT01101568|113506|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108713|NCT01101568|113506|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108714|NCT01101555|113299|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108715|NCT01101555|113299|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108716|NCT01101555|113299|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108717|NCT01101555|113299|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108718|NCT01101555|113299|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108719|NCT01101555|113299|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108720|NCT01101555|113299|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108721|NCT01098539|114130|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108722|NCT01098539|114130|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108723|NCT01098539|114130|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108724|NCT01098539|114130|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108725|NCT01098539|114130|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108726|NCT01098539|114130|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108727|NCT01098539|114130|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108728|NCT01098461|110932|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108729|NCT01098461|110932|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108730|NCT01098461|110932|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108731|NCT01098461|110932|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108732|NCT01098461|110932|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108733|NCT01098461|110932|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108734|NCT01098461|110932|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108735|NCT01098110||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06124&kw=P06124&tab=access|
108736|NCT01097629||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-029&kw=4305-029&tab=access|
108737|NCT01097616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-028&kw=4305-028&tab=access|
108738|NCT01096056|114182|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108739|NCT01096056|114182|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108740|NCT01096056|114182|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108741|NCT01096056|114182|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108742|NCT01096056|114182|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108743|NCT01096056|114182|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108744|NCT01090453|113615|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108745|NCT01090453|113615|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108746|NCT01090453|113615|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108747|NCT01090453|113615|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108748|NCT01090453|113615|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108749|NCT01090453|113615|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108750|NCT01088711||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3102-004&kw=3102-004&tab=access|
108751|NCT01086462|114041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108752|NCT01086462|114041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108753|NCT01086462|114041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108754|NCT01086462|114041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108755|NCT01086462|114041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108756|NCT01086462|114041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108757|NCT01086462|114041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108758|NCT01086449|113819|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108759|NCT01086449|113819|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108760|NCT01086449|113819|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108761|NCT01086449|113819|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108762|NCT01086449|113819|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108763|NCT01086449|113819|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108764|NCT01086449|113819|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108765|NCT01086436|113552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108766|NCT01086436|113552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108767|NCT01086436|113552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108768|NCT01086436|113552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108769|NCT01086436|113552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108770|NCT01086436|113552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108771|NCT01086410|106851|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108772|NCT01086410|106851|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108773|NCT01086410|106851|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108774|NCT01086410|106851|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108775|NCT01086410|106851|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108776|NCT01086410|106851|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108777|NCT01086410|106851|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108778|NCT01086384|106837|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108779|NCT01086384|106837|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108780|NCT01086384|106837|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108781|NCT01086384|106837|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108782|NCT01086384|106837|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108783|NCT01086384|106837|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108784|NCT01086384|106837|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108785|NCT01078233||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0518-058&kw=0518-058&tab=access|
108786|NCT01077856||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-033&kw=V501-033&tab=access|
108787|NCT01077531|111601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108788|NCT01077531|111601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108789|NCT01077531|111601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108790|NCT01077531|111601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108791|NCT01077531|111601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108792|NCT01077531|111601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108793|NCT01077531|111601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108794|NCT01077505|107032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108795|NCT01077505|107032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108796|NCT01077505|107032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108797|NCT01077505|107032|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108798|NCT01077505|107032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108799|NCT01077505|107032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108800|NCT01077505|107032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108801|NCT01075698||Study Protocol|https://prsinfo.clinicaltrials.gov/definitions.html|
108802|NCT01074242||CSR Synopsis|http://www.merck.com/clinical-trials/search.html?kw=V260-037|
108803|NCT01073293||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-007&kw=V503-007&tab=access|
108804|NCT01072149|110946|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108805|NCT01072149|110946|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108806|NCT01072149|110946|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108807|NCT01072149|110946|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108808|NCT01072149|110946|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108809|NCT01072149|110946|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108810|NCT01072149|110946|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108811|NCT01071369||Clinical Study Report|http://painphysicianjournal.com/current/pdf?article=MTk3Nw%3D%3D&journal=77|A Randomized, Double-Blind, Active Control Trial of Fluoroscopic Cervical Interlaminar Epidural Injections in Chronic Pain of Cervical Disc Herniation: Results of a 2-Year Follow-Up
108812|NCT01067443||Study Protocol|http://journals.plos.org/plosntds/article/file?type=supplementary&id=info:doi/10.1371/journal.pntd.0004880.s002|Final Study Protocol
108813|NCT01066923||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25939657|Report of vascular function testing
108814|NCT01066923||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/24548114|Report of platelet function and physiology
108815|NCT01064284|NEJM2016;374:2054-206|Article|http://www.nejm.org/doi/full/10.1056/NEJMoa1516437?af=R&rss=currentIssue&|
108816|NCT01062074||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V501-059&kw=V501-059&tab=access|
108817|NCT01061541|208108/091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108818|NCT01061541|208108/091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 208108/091 are summarised with study 208108/092 on the GSK Clinical Study Register.
108819|NCT01061541|208108/091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108820|NCT01061541|208108/091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108821|NCT01061541|208108/091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108822|NCT01061541|208108/091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108823|NCT01059851||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-023&kw=4305-023&tab=access|
108824|NCT01059617|113483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108825|NCT01059617|113483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108826|NCT01059617|113483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108827|NCT01059617|113483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108828|NCT01059617|113483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108829|NCT01059617|113483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108830|NCT01055379|2009-011144-19|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2009-011144-19/results|
108831|NCT01054885|112207|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108832|NCT01054885|112207|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108833|NCT01054885|112207|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108834|NCT01054885|112207|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108835|NCT01054885|112207|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108836|NCT01054885|112207|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108837|NCT01054885|112207|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108838|NCT01053988|112206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108839|NCT01053988|112206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108840|NCT01053988|112206|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108841|NCT01053988|112206|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108842|NCT01053988|112206|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108843|NCT01053988|112206|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108844|NCT01053988|112206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108845|NCT01051661|114000|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108846|NCT01051661|114000|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108847|NCT01051661|114000|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108848|NCT01051661|114000|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108849|NCT01051661|114000|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108850|NCT01051661|114000|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108851|NCT01049009|26285691|Publication|https://www.ncbi.nlm.nih.gov/pubmed/26285691|
108852|NCT01047345||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-006&kw=V503-006&tab=access|
108853|NCT01046331|H1N1|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/h1n1/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
108854|NCT01046331||Study Forms|http://biolincc.nhlbi.nih.gov/studies/h1n1/|
108855|NCT01043926||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-017&kw=4305-017&tab=access|
108856|NCT01039974|112648|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108857|NCT01039974|112648|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108858|NCT01039974|112648|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108859|NCT01039974|112648|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108860|NCT01039974|112648|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108861|NCT01039974|112648|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108862|NCT01039974|112648|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108863|NCT01039961|113022|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108864|NCT01039961|113022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108865|NCT01039961|113022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108866|NCT01039961|113022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108867|NCT01039961|113022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108868|NCT01039961|113022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108869|NCT01039961|113022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108870|NCT01039805|112571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108871|NCT01039805|112571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108872|NCT01039805|112571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108873|NCT01039805|112571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108874|NCT01039805|112571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108875|NCT01039805|112571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108876|NCT01039805|112571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108877|NCT01039675|113120|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108878|NCT01039675|113120|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108879|NCT01039675|113120|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108880|NCT01039675|113120|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108881|NCT01039675|113120|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108882|NCT01039675|113120|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108883|NCT01039675|113120|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108884|NCT01039454|109710|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108885|NCT01039454|109710|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108886|NCT01039454|109710|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108887|NCT01039454|109710|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108888|NCT01039454|109710|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108889|NCT01039454|109710|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108890|NCT01037114|112266|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108891|NCT01037114|112266|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108892|NCT01037114|112266|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108893|NCT01037114|112266|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108894|NCT01037114|112266|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108895|NCT01037114|112266|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108896|NCT01037114|112266|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108897|NCT01036061|108414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108898|NCT01036061|108414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108899|NCT01036061|108414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108900|NCT01036061|108414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108901|NCT01036061|108414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108902|NCT01036061|108414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108903|NCT01036022|111407|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108904|NCT01036022|111407|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108905|NCT01036022|111407|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108906|NCT01036022|111407|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108907|NCT01036022|111407|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108908|NCT01036022|111407|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108909|NCT01036022|111407|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108910|NCT01035749|113883|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108911|NCT01035749|113883|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108912|NCT01035749|113883|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108913|NCT01035749|113883|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108914|NCT01035749|113883|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108915|NCT01035749|113883|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108916|NCT01035645|110040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108917|NCT01035645|110040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108918|NCT01035645|110040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108919|NCT01035645|110040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108920|NCT01035645|110040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108921|NCT01035645|110040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108922|NCT01031186|113324|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108923|NCT01031186|113324|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108924|NCT01031186|113324|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108925|NCT01031186|113324|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108926|NCT01031186|113324|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108927|NCT01031186|113324|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108928|NCT01031186|113324|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108929|NCT01031108|114089|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108930|NCT01031108|114089|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108931|NCT01031108|114089|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108932|NCT01031108|114089|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108933|NCT01031108|114089|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108934|NCT01031108|114089|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108935|NCT01031108|114089|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108936|NCT01030965|113589|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108937|NCT01030965|113589|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108938|NCT01030965|113589|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108939|NCT01030965|113589|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108940|NCT01030965|113589|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108941|NCT01030965|113589|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108942|NCT01030965|113589|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108943|NCT01030939|112861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108944|NCT01030939|112861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108945|NCT01030939|112861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108946|NCT01030939|112861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108947|NCT01030939|112861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108948|NCT01030939|112861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108949|NCT01030939|112861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108950|NCT01030822|112909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108951|NCT01030822|112909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108952|NCT01030822|112909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108953|NCT01030822|112909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108954|NCT01030822|112909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108955|NCT01030822|112909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108956|NCT01030822|112909|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108957|NCT01027845|112640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108958|NCT01027845|112640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108959|NCT01027845|112640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108960|NCT01027845|112640|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108961|NCT01027845|112640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108962|NCT01027845|112640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109000|NCT01018186|106839|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108963|NCT01025973|Article|Clinical Study Report|https://doi.org/10.2337/dc14-0549|"Glycation of Fetal Hemoglobin Reflects Hyperglycemia Exposure In Utero Felix O. Dupont1, Marie-France Hivert1,2,3, Catherine Allard1, Julie Ménard1, Patrice Perron1,2, Luigi Bouchard1,4,5, Julie Robitaille6, Jean-Charles Pasquier1,7, Christiane Auray-Blais1,8 and Jean-Luc Ardilouze1,2⇑~+ Author Affiliations~Corresponding author: Jean-Luc Ardilouze, jean-luc.ardilouze@usherbrooke.ca. F.O.D. and M.-F.H. contributed equally to this study.~Diabetes Care 2014 Oct; 37(10): 2830-2833. https://doi.org/10.2337/dc14-0549"
108964|NCT01025843||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5478-001&kw=5478-001&tab=access|
108965|NCT01021852||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=6096-011&kw=6096-011&tab=access|
108966|NCT01021813||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-009&kw=4305-009&tab=access|
108967|NCT01021553|109059|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108968|NCT01021553|109059|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108969|NCT01021553|109059|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108970|NCT01021553|109059|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108971|NCT01021553|109059|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108972|NCT01021553|109059|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108973|NCT01021553|109059|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108974|NCT01021293|112679|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108975|NCT01021293|112679|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108976|NCT01021293|112679|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108977|NCT01021293|112679|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108978|NCT01021293|112679|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108979|NCT01021293|112679|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108980|NCT01019603|114565|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108981|NCT01019603|114565|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108982|NCT01019603|114565|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108983|NCT01019603|114565|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108984|NCT01019603|114565|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108985|NCT01019603|114565|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108986|NCT01019603|114565|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108987|NCT01018628|114011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108988|NCT01018628|114011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108989|NCT01018628|114011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108990|NCT01018628|114011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108991|NCT01018628|114011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108992|NCT01018628|114011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108993|NCT01018628|114011|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108994|NCT01018186|106839|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108995|NCT01018186|106839|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108996|NCT01018186|106839|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108997|NCT01018186|106839|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108998|NCT01018186|106839|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
108999|NCT01018186|106839|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109001|NCT01018017|114010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109002|NCT01018017|114010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109003|NCT01018017|114010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109004|NCT01018017|114010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109005|NCT01018017|114010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109006|NCT01018017|114010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109007|NCT01018017|114010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109008|NCT01017952|102970|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109009|NCT01017952|102970|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109010|NCT01017952|102970|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109011|NCT01017952|102970|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109012|NCT01017952|102970|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109013|NCT01017952|102970|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109014|NCT01017952|102970|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109015|NCT01017146|114575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109016|NCT01017146|114575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109017|NCT01017146|114575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109018|NCT01017146|114575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109019|NCT01017146|114575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109020|NCT01017146|114575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109021|NCT01017146|114575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109022|NCT01017120|114576|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109023|NCT01017120|114576|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109024|NCT01017120|114576|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109025|NCT01017120|114576|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109026|NCT01017120|114576|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109027|NCT01017120|114576|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109028|NCT01017120|114576|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109029|NCT01016977|114566|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109030|NCT01016977|114566|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109031|NCT01016977|114566|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109032|NCT01016977|114566|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109033|NCT01016977|114566|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109034|NCT01016977|114566|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109035|NCT01016977|114566|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109036|NCT01016366|2008-003662-25|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-003662-25/results|
109037|NCT01015677||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=6913-004&kw=6913-004&tab=access|
109038|NCT01015638|114546|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109039|NCT01015638|114546|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109040|NCT01015638|114546|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109041|NCT01015638|114546|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109042|NCT01015638|114546|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109043|NCT01014988|113678|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109044|NCT01014988|113678|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109045|NCT01014988|113678|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109046|NCT01014988|113678|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109047|NCT01014988|113678|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109048|NCT01014988|113678|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109049|NCT01014988|113678|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109050|NCT01014117|114009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109051|NCT01014117|114009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109052|NCT01014117|114009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109053|NCT01014117|114009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109054|NCT01014117|114009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109055|NCT01014117|114009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109056|NCT01014091|113810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109057|NCT01014091|113810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109058|NCT01014091|113810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109059|NCT01014091|113810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109060|NCT01014091|113810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109061|NCT01014091|113810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109062|NCT01014091|113810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109063|NCT01013974|113377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109064|NCT01013974|113377|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109065|NCT01013974|113377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109066|NCT01013974|113377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109067|NCT01013974|113377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109068|NCT01013974|113377|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109069|NCT01013974|113377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109070|NCT01013766|111823|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109071|NCT01013766|111823|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109072|NCT01013766|111823|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109073|NCT01013766|111823|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109074|NCT01013766|111823|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109075|NCT01013766|111823|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109076|NCT01013766|111823|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109077|NCT01010906||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-005&kw=7009-005&tab=access|
110658|NCT00702195||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
109078|NCT01009463|102871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109079|NCT01009463|102871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109080|NCT01009463|102871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109081|NCT01009463|102871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109082|NCT01009463|102871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109083|NCT01009463|102871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109084|NCT01009463|102871|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109085|NCT01009255|110651|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109086|NCT01009255|110651|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109087|NCT01009255|110651|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109088|NCT01009255|110651|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109089|NCT01009255|110651|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109090|NCT01009255|110651|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109091|NCT01009255|110651|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109092|NCT01009060|113147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109093|NCT01009060|113147|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109094|NCT01009060|113147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109095|NCT01009060|113147|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109096|NCT01009060|113147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109097|NCT01009060|113147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109098|NCT01009060|113147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109099|NCT01006616||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05575&kw=7123-019&tab=access|
109100|NCT01003418|113629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109101|NCT01003418|113629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109102|NCT01003418|113629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109103|NCT01003418|113629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109104|NCT01003418|113629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109105|NCT01003418|113629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109106|NCT01001169|113847|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109107|NCT01001169|113847|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109108|NCT01001169|113847|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109109|NCT01001169|113847|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109110|NCT01001169|113847|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109111|NCT01001169|113847|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109112|NCT01001169|113847|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109113|NCT01000857|112812|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109114|NCT01000857|112812|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109115|NCT01000857|112812|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110659|NCT00701389||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-026&kw=0974-026&tab=access|
109116|NCT01000857|112812|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109117|NCT01000727|480848/033|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109118|NCT01000727|480848/033|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109119|NCT01000727|480848/033|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109120|NCT01000727|480848/033|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109121|NCT01000727|480848/033|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109122|NCT01000727|480848/033|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109123|NCT01000597|113477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109124|NCT01000597|113477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109125|NCT01000597|113477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109126|NCT01000597|113477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109127|NCT01000597|113477|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109128|NCT01000597|113477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109129|NCT01000597|113477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109130|NCT01000506|112997|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109131|NCT01000506|112997|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109132|NCT01000506|112997|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109133|NCT01000506|112997|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109134|NCT01000506|112997|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109135|NCT01000506|112997|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109136|NCT01000506|112997|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109137|NCT01000324|112267|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109138|NCT01000324|112267|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109139|NCT01000324|112267|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109140|NCT01000324|112267|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109141|NCT01000324|112267|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109142|NCT01000324|112267|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109143|NCT01000324|112267|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109144|NCT00998985||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=5172-004&kw=5172-004&tab=access|
109145|NCT00996996|104517|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109146|NCT00996996|104517|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109147|NCT00996996|104517|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109148|NCT00996996|104517|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109149|NCT00996996|104517|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109150|NCT00996996|104517|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109151|NCT00996996|104517|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109152|NCT00996944|113079|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109153|NCT00996944|113079|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110660|NCT00700661||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
109154|NCT00996944|113079|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109155|NCT00996944|113079|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109156|NCT00996840|111592|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109157|NCT00996840|111592|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109158|NCT00996840|111592|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109159|NCT00996840|111592|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109160|NCT00996840|111592|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109161|NCT00996840|111592|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109162|NCT00996840|111592|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109163|NCT00996671|113581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109164|NCT00996671|113581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109165|NCT00996671|113581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109166|NCT00996671|113581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109167|NCT00996671|113581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109168|NCT00996671|113581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109169|NCT00996671|113581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109170|NCT00996593|104507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109171|NCT00996593|104507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109172|NCT00996593|104507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109173|NCT00996593|104507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109174|NCT00996593|104507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109175|NCT00996593|104507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109176|NCT00996593|104507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109177|NCT00996268|113412|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109178|NCT00996268|113412|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109179|NCT00996268|113412|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109180|NCT00996268|113412|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109181|NCT00996268|113412|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109182|NCT00996268|113412|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109183|NCT00996268|113412|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109184|NCT00996125|112022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109185|NCT00996125|112022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109186|NCT00996125|112022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109187|NCT00996125|112022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109188|NCT00996125|112022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109189|NCT00996125|112022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109190|NCT00993187||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0431A-202&kw=NCT00993187&tab=access|
109191|NCT00992784|113094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110777|NCT00687011||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
109192|NCT00992784|113094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109193|NCT00992784|113094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109194|NCT00992784|113094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109195|NCT00992784|113094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109196|NCT00992784|113094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109197|NCT00992784|113094|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109198|NCT00992758|104512|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109199|NCT00992758|104512|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109200|NCT00992758|104512|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109201|NCT00992758|104512|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109202|NCT00992758|104512|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109203|NCT00992758|104512|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109204|NCT00992758|104512|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109205|NCT00992511|113809|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109206|NCT00992511|113809|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109207|NCT00992511|113809|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109208|NCT00992511|113809|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109209|NCT00992511|113809|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109210|NCT00992511|113809|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109211|NCT00992511|113809|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109212|NCT00992160|111364|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109213|NCT00992160|111364|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109214|NCT00992160|111364|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109215|NCT00992160|111364|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109216|NCT00992160|111364|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109217|NCT00992160|111364|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109218|NCT00992160|111364|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109219|NCT00989664|104504|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109220|NCT00989664|104504|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109221|NCT00989664|104504|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109222|NCT00989664|104504|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109223|NCT00989664|104504|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109224|NCT00989664|104504|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109225|NCT00989664|104504|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109226|NCT00989625|108504|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109227|NCT00989625|108504|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109228|NCT00989625|108504|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109229|NCT00989625|108504|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109230|NCT00989625|108504|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109231|NCT00989625|108504|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109232|NCT00989625|108504|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109233|NCT00989612|113519|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109234|NCT00989612|113519|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109235|NCT00989612|113519|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109236|NCT00989612|113519|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109237|NCT00989612|113519|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109238|NCT00989612|113519|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109239|NCT00989612|113519|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109240|NCT00989404|113625|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109241|NCT00989404|113625|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109242|NCT00989404|113625|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109243|NCT00989404|113625|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109244|NCT00989404|113625|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109245|NCT00989404|113625|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109246|NCT00989404|113625|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109247|NCT00989287|113866|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109248|NCT00989287|113866|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109249|NCT00989287|113866|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109250|NCT00989287|113866|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109251|NCT00989287|113866|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109252|NCT00989287|113866|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109253|NCT00989287|113866|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109254|NCT00988884||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-005&kw=V503-005&tab=access|
109255|NCT00988260||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
109256|NCT00985790|113237|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109257|NCT00985790|113237|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109258|NCT00985790|113237|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109259|NCT00985790|113237|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109260|NCT00985790|113237|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109261|NCT00985790|113237|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109262|NCT00985751|113171|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109263|NCT00985751|113171|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109264|NCT00985751|113171|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109265|NCT00985751|113171|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109266|NCT00985751|113171|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109267|NCT00985673|113536|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109268|NCT00985673|113536|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109269|NCT00985673|113536|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109270|NCT00985673|113536|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109271|NCT00985673|113536|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109272|NCT00985673|113536|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109273|NCT00985673|113536|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109274|NCT00985465|113166|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109275|NCT00985465|113166|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109276|NCT00985465|113166|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109277|NCT00985465|113166|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109278|NCT00985465|113166|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109279|NCT00985465|113166|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109280|NCT00985465|113166|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109281|NCT00985140||Peer reviewed article with pooled results.|https://www.ncbi.nlm.nih.gov/pubmed/25476993|This publication contains data from this study as well as two other clinical trials. Analysis was done on data pooled from the three trials.
109282|NCT00985088|113440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109283|NCT00985088|113440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109284|NCT00985088|113440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109285|NCT00985088|113440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109286|NCT00985088|113440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109287|NCT00985088|113440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109288|NCT00985088|113440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109289|NCT00984659|112989|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109290|NCT00984659|112989|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109291|NCT00984659|112989|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109292|NCT00984659|112989|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109293|NCT00984659|112989|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109294|NCT00984659|112989|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109295|NCT00984659|112989|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109296|NCT00984139|112682|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109297|NCT00984139|112682|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109298|NCT00984139|112682|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109299|NCT00984139|112682|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109300|NCT00984139|112682|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109301|NCT00984139|112682|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109302|NCT00984139|112682|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109303|NCT00982904||Publication of results|http://www.dndi.org/wp-content/uploads/2009/06/ClinicalPK_Tarral_FexinidazoleHAT_2014.pdf|Publication of results
109304|NCT00981409|106206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109305|NCT00981409|106206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109306|NCT00981409|106206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109307|NCT00980200|113310|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109308|NCT00980200|113310|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109309|NCT00980200|113310|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109310|NCT00980200|113310|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109311|NCT00980200|113310|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109312|NCT00980200|113310|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109313|NCT00980200|113310|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109314|NCT00980005|112999|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109315|NCT00980005|112999|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109316|NCT00980005|112999|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109317|NCT00980005|112999|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109318|NCT00980005|112999|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109319|NCT00980005|112999|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109320|NCT00980005|112999|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109321|NCT00979641||Clinical Study Report|http://www.anticancerresearch.com|
109322|NCT00979602|113480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109323|NCT00979602|113480|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109324|NCT00979602|113480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109325|NCT00979602|113480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109326|NCT00979602|113480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109327|NCT00979602|113480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109328|NCT00979602|113480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109329|NCT00979407|113535|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109330|NCT00979407|113535|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109331|NCT00979407|113535|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109332|NCT00979407|113535|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109333|NCT00979407|113535|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109334|NCT00979407|113535|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109335|NCT00979303||Archived consent, protocol and analytic plan.|http://www.childrenshospital.org/|Study completed prior to change in common rule. Requests should be directed to the investigation team at Boston Children's Hospital through mark.alexander@cardio.chboston.org
109336|NCT00979121|ARDSNet-SAILS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/sails/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
109337|NCT00979121||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/sails/|
109338|NCT00979121||Study Forms|http://biolincc.nhlbi.nih.gov/studies/sails/|
109339|NCT00976820|113482|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109340|NCT00976820|113482|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109341|NCT00976820|113482|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109342|NCT00976820|113482|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109343|NCT00976820|113482|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109344|NCT00976820|113482|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110778|NCT00686699||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04628&kw=P04628&tab=access|
109345|NCT00976560|113009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109346|NCT00976560|113009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109347|NCT00976560|113009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109348|NCT00976560|113009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109349|NCT00976560|113009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109350|NCT00976560|113009|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109351|NCT00976560|113009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109352|NCT00976391|108486|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109353|NCT00976391|108486|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109354|NCT00976391|108486|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109355|NCT00976391|108486|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109356|NCT00976391|108486|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109357|NCT00976391|108486|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109358|NCT00976391|108486|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109359|NCT00976144|113208|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109360|NCT00976144|113208|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109361|NCT00976144|113208|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109362|NCT00976144|113208|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109363|NCT00976144|113208|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109364|NCT00976144|113208|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109365|NCT00976144|113208|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109366|NCT00976105|111849|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109367|NCT00976105|111849|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109368|NCT00976105|111849|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109369|NCT00976105|111849|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109370|NCT00976105|111849|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109371|NCT00976105|111849|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109372|NCT00976066|111848|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109373|NCT00976066|111848|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109374|NCT00976066|111848|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109375|NCT00976066|111848|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109376|NCT00976066|111848|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109377|NCT00976066|111848|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109378|NCT00976066|111848|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109379|NCT00975884|113630|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109380|NCT00975884|113630|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109381|NCT00975884|113630|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109382|NCT00975884|113630|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109383|NCT00975884|113630|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109384|NCT00975884|113630|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109385|NCT00972686|112826|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109386|NCT00972686|112826|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109387|NCT00972686|112826|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109388|NCT00972686|112826|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109389|NCT00972686|112826|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109390|NCT00972686|112826|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109391|NCT00972686|112826|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109392|NCT00972673|112018|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109393|NCT00972673|112018|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109394|NCT00972673|112018|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109395|NCT00972673|112018|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109396|NCT00972517|113638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109397|NCT00972517|113638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109398|NCT00972517|113638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109399|NCT00972517|113638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109400|NCT00972517|113638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109401|NCT00972517|113638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109402|NCT00972517|113638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109403|NCT00972504|112864|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109404|NCT00972504|112864|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109405|NCT00972504|112864|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109406|NCT00972504|112864|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109407|NCT00972504|112864|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109408|NCT00972504|112864|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109409|NCT00972504|112864|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109410|NCT00972322||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=8245-012&kw=8245-012&tab=access|
109411|NCT00971425|113572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109412|NCT00971425|113572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109413|NCT00971425|113572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109414|NCT00971425|113572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109415|NCT00971425|113572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109416|NCT00971425|113572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109417|NCT00971425|113572|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109418|NCT00971321|113462|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109419|NCT00971321|113462|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109420|NCT00971321|113462|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109421|NCT00971321|113462|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109422|NCT00971321|113462|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109423|NCT00971321|113462|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109424|NCT00971321|113462|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109425|NCT00970710||Study Protocol|http://bmcpediatr.biomedcentral.com/articles/10.1186/1471-2431-12-93|
109426|NCT00970710||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/?term=mustila+taina+vacopp|
109427|NCT00970307|112157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109428|NCT00970307|112157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109429|NCT00970307|112157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109430|NCT00970307|112157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109431|NCT00970307|112157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109432|NCT00970307|112157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109433|NCT00970307|112157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109434|NCT00969436|109995|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109435|NCT00969436|109995|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109436|NCT00969436|109995|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109437|NCT00969436|109995|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109438|NCT00969436|109995|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109439|NCT00969436|109995|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109440|NCT00969436|109995|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109441|NCT00969228|112269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109442|NCT00969228|112269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109443|NCT00969228|112269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109444|NCT00969228|112269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109445|NCT00969228|112269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109446|NCT00969228|112269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109447|NCT00969228|112269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109448|NCT00969059|112967|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109449|NCT00969059|112967|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109450|NCT00969059|112967|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109451|NCT00969059|112967|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109452|NCT00969059|112967|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109453|NCT00969059|112967|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109454|NCT00969059|112967|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109455|NCT00968890|113525|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109456|NCT00968890|113525|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109457|NCT00968890|113525|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109458|NCT00968890|113525|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109459|NCT00968890|113525|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109460|NCT00968890|113525|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109461|NCT00968890|113525|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109462|NCT00968539|113456|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109463|NCT00968539|113456|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109464|NCT00968539|113456|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109465|NCT00968539|113456|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109466|NCT00968539|113456|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109467|NCT00968539|113456|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109468|NCT00968539|113456|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109469|NCT00968526|113459|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109470|NCT00968526|113459|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109471|NCT00968526|113459|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109472|NCT00968526|113459|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109473|NCT00968526|113459|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109474|NCT00968526|113459|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109475|NCT00968526|113459|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109476|NCT00965458|SDY797|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY797|ImmPort study identifier is SDY797.
109477|NCT00965458|SDY797|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY797|ImmPort study identifier is SDY797. The study protocol is located under the design tab.
109478|NCT00965458|SDY797|Study summary, -design, -adverse event(s), -demographics, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY797|ImmPort study identifier is SDY797.ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. This archive is in support of the NIH mission to share data with the public. Data shared through ImmPort has been provided by NIH-funded programs, other research organizations and individual scientists ensuring these discoveries will be the foundation of future research.
109479|NCT00965458|T1DAL ITN045AI|Individual Participant Data Set|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare study ID is T1DAL ITN045AI.
109480|NCT00965458|T1DAL ITN045AI|Study Protocol|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare study ID is T1DAL ITN045AI.
109481|NCT00965458|T1DAL ITN045AI|Study overview, -data and reports, -schedule of assessments, -study design, -original article & abstracts et al.|https://www.itntrialshare.org/project/Studies/ITN045AIJCI/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.Creating an account for ITN TrialShare is free and allows for searching studies of interest.
109482|NCT00964340|113312|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109483|NCT00964340|113312|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109484|NCT00964340|113312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109485|NCT00964340|113312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109486|NCT00964340|113312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109487|NCT00964340|113312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109488|NCT00964249|112017|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109489|NCT00964249|112017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109490|NCT00964249|112017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109491|NCT00964249|112017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109492|NCT00964249|112017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109493|NCT00964223|114547|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109494|NCT00964223|114547|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109495|NCT00964223|114547|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109496|NCT00964223|114547|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109497|NCT00964223|114547|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109498|NCT00964223|114547|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109499|NCT00964223|114547|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109500|NCT00964158|113528|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109501|NCT00964158|113528|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109502|NCT00964158|113528|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109503|NCT00964158|113528|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109504|NCT00964158|113528|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109505|NCT00964158|113528|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109506|NCT00964158|113528|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109507|NCT00964106|112684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109508|NCT00964106|112684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109509|NCT00964106|112684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109510|NCT00964106|112684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109511|NCT00964106|112684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109512|NCT00964106|112684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109513|NCT00964106|112684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109514|NCT00963937|111035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109515|NCT00963937|111035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109516|NCT00963937|111035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109517|NCT00963937|111035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109518|NCT00960063||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05883&kw=P05883&tab=access|
109519|NCT00955682|112036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109520|NCT00955682|112036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109521|NCT00955682|112036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109522|NCT00955682|112036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109523|NCT00955682|112036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109524|NCT00955682|112036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109525|NCT00955383|112359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109526|NCT00955383|112359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109527|NCT00955383|112359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109528|NCT00955383|112359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109529|NCT00955383|112359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109530|NCT00955383|112359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109531|NCT00955383|112359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109532|NCT00954993||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-029&kw=7009-029&tab=access|
109533|NCT00954512||CSR Synospsi Links|http://www.merck.com/clinical-trials/study.html?id=P04722&kw=P04722&tab=access|
109534|NCT00951977|SDY290|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
109535|NCT00951977|SDY290|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
109536|NCT00951977|SDY290|Study summary, -design, -demographics, -files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY290|ImmPort study identifier is SDY290
109537|NCT00951353|SDY951|Study Protocol|http://www.immport.org/immport-open/public/home/studySearch|ImmPort study identifier is SDY951.
109538|NCT00951353|SDY951|Complete set of descriptive data and results|http://www.immport.org/immport-open/public/home/studySearch|"ImmPort study identifier is SDY951.~ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. This archive is in support of the NIH mission to share data with the public."
109539|NCT00951041|113574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109540|NCT00951041|113574|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109541|NCT00951041|113574|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109542|NCT00951041|113574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109543|NCT00951041|113574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109544|NCT00951041|113574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109545|NCT00951041|113574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109546|NCT00950833|112801|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109547|NCT00950833|112801|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109548|NCT00950833|112801|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109549|NCT00950833|112801|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109550|NCT00950833|112801|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109551|NCT00950833|112801|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109552|NCT00950833|112801|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109553|NCT00950807|113073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109554|NCT00950807|113073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109555|NCT00950807|113073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109556|NCT00950807|113073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109557|NCT00950807|113073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109558|NCT00950807|113073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109559|NCT00950807|113073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109560|NCT00950755|104505|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109561|NCT00950755|104505|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109562|NCT00950755|104505|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109563|NCT00950755|104505|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109564|NCT00950755|104505|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109565|NCT00950755|104505|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109566|NCT00950755|104505|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109567|NCT00950586|110792|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109568|NCT00950586|110792|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109569|NCT00950586|110792|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109570|NCT00950586|110792|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109571|NCT00950586|110792|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109572|NCT00950586|110792|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109573|NCT00950586|110792|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109574|NCT00947115|112772|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109575|NCT00947115|112772|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109576|NCT00947115|112772|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109577|NCT00947115|112772|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109578|NCT00947115|112772|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109579|NCT00946257|112438|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109580|NCT00946257|112438|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109581|NCT00946257|112438|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109582|NCT00946257|112438|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109583|NCT00946257|112438|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109584|NCT00946257|112438|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109585|NCT00946257|112438|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109586|NCT00945932|112851|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109587|NCT00945932|112851|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109588|NCT00945932|112851|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109589|NCT00945932|112851|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109590|NCT00945932|112851|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109591|NCT00945932|112851|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109592|NCT00945932|112851|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109593|NCT00945750||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0208-144&kw=0208-144&tab=access|
109594|NCT00945503|109731|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109595|NCT00945503|109731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109596|NCT00945503|109731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109597|NCT00945503|109731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109598|NCT00945503|109731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109599|NCT00945503|109731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109600|NCT00945503|109731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109601|NCT00943761||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-028&kw=7009-028&tab=access|
109602|NCT00943722||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-002&kw=V503-002&tab=access|
109603|NCT00942162|111476|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109604|NCT00942162|111476|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109605|NCT00942162|111476|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109606|NCT00942162|111476|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109607|NCT00942162|111476|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109608|NCT00942162|111476|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109609|NCT00942162|111476|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109610|NCT00941603||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05675&kw=P05675&tab=access|
109611|NCT00938392|112662|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109612|NCT00938392|112662|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109613|NCT00938392|112662|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109614|NCT00938392|112662|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109615|NCT00938392|112662|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109616|NCT00938392|112662|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109617|NCT00938392|112662|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109618|NCT00938275|113261|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109619|NCT00938275|113261|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109620|NCT00938275|113261|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109621|NCT00938275|113261|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109622|NCT00938275|113261|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109623|NCT00938275|113261|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109624|NCT00938275|113261|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109625|NCT00938184|112811|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109626|NCT00938184|112811|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109627|NCT00938184|112811|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109628|NCT00938184|112811|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109629|NCT00938158|108370|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109630|NCT00938158|108370|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109631|NCT00938158|108370|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109632|NCT00938158|108370|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109633|NCT00938158|108370|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109634|NCT00938158|108370|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109635|NCT00938158|108370|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109636|NCT00938041|393229/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109637|NCT00938041|393229/010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109638|NCT00938041|393229/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109639|NCT00938041|393229/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109640|NCT00938041|393229/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109641|NCT00938041|393229/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109642|NCT00938041|393229/010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109643|NCT00937846|110771|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109644|NCT00937846|110771|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109645|NCT00937846|110771|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109646|NCT00937846|110771|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109647|NCT00937846|110771|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109648|NCT00937846|110771|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109649|NCT00937846|110771|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109650|NCT00937404|112581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109651|NCT00937404|112581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109652|NCT00937404|112581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109653|NCT00937404|112581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109654|NCT00937404|112581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109655|NCT00937404|112581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109656|NCT00937326|113160|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109657|NCT00937326|113160|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109658|NCT00937326|113160|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109659|NCT00937326|113160|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109660|NCT00937326|113160|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109661|NCT00937326|113160|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109662|NCT00937326|113160|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109663|NCT00933595|LUNG-HIV|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
109664|NCT00933595||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
109665|NCT00933595||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
109666|NCT00933595||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/lung_hiv/|
109667|NCT00933335|393229/023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109668|NCT00933335|393229/023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109669|NCT00933335|393229/023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109670|NCT00933335|393229/023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109671|NCT00933335|393229/023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109672|NCT00933335|393229/023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109673|NCT00933335|393229/023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109674|NCT00933062|113140|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109675|NCT00933062|113140|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109676|NCT00933062|113140|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109677|NCT00933062|113140|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109678|NCT00933062|113140|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109679|NCT00933062|113140|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109680|NCT00933062|113140|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109681|NCT00929526|112949|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109682|NCT00929526|112949|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109683|NCT00929526|112949|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109684|NCT00929526|112949|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109685|NCT00929526|112949|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109686|NCT00929526|112949|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109687|NCT00929331|110586|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109688|NCT00929331|110586|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109689|NCT00929331|110586|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109690|NCT00929331|110586|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109691|NCT00929331|110586|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109692|NCT00929331|110586|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109693|NCT00929331|110586|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109694|NCT00924911|112034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109695|NCT00924911|112034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109696|NCT00924911|112034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109697|NCT00924911|112034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109698|NCT00924911|112034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109699|NCT00924911|112034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109700|NCT00924911|112034|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109701|NCT00920959|SAS30021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109702|NCT00920959|SAS30021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109703|NCT00920959|SAS30021|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109704|NCT00920959|SAS30021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109705|NCT00920959|SAS30021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109706|NCT00920959|SAS30021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109707|NCT00920959|SAS30021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109708|NCT00920803|113221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109709|NCT00920803|113221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109710|NCT00920803|113221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109711|NCT00920803|113221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109712|NCT00920803|113221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109713|NCT00920803|113221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109714|NCT00920660|113161|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109715|NCT00920660|113161|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109716|NCT00920660|113161|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109717|NCT00920660|113161|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109718|NCT00920660|113161|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109719|NCT00920660|113161|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109720|NCT00920660|113161|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109721|NCT00920556|113222|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109722|NCT00920556|113222|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109723|NCT00920556|113222|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109724|NCT00920556|113222|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109725|NCT00920556|113222|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109726|NCT00920556|113222|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109727|NCT00920543|SAM40086|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109728|NCT00920543|SAM40086|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109729|NCT00920543|SAM40086|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109730|NCT00920543|SAM40086|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109731|NCT00920543|SAM40086|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109732|NCT00920543|SAM40086|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109733|NCT00920543|SAM40086|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109734|NCT00920439|112683|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109735|NCT00920439|112683|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109736|NCT00920439|112683|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109737|NCT00920439|112683|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109738|NCT00920439|112683|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109739|NCT00920439|112683|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109740|NCT00920374|113018|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109741|NCT00920374|113018|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109742|NCT00920374|113018|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109743|NCT00920374|113018|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109744|NCT00920374|113018|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109745|NCT00920374|113018|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109746|NCT00920374|113018|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109747|NCT00920192|111645|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109748|NCT00920192|111645|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109749|NCT00920192|111645|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109750|NCT00920192|111645|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109751|NCT00920192|111645|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109752|NCT00920192|111645|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109753|NCT00911157|111436|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109754|NCT00911157|111436|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109755|NCT00911157|111436|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109756|NCT00911144|112933|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109757|NCT00911144|112933|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109758|NCT00911144|112933|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109759|NCT00911144|112933|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109760|NCT00911144|112933|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109761|NCT00911144|112933|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109762|NCT00911144|112933|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109763|NCT00910962|111810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109764|NCT00910962|111810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109765|NCT00910962|111810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109766|NCT00910962|111810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109767|NCT00910962|111810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109768|NCT00910962|111810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109769|NCT00910962|111810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109770|NCT00908115|208355/128|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109771|NCT00908115|208355/128|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109772|NCT00908115|208355/128|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109773|NCT00908115|208355/128|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109774|NCT00908115|208355/128|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109775|NCT00908115|208355/128|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109776|NCT00907985|112676|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109777|NCT00907985|112676|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109778|NCT00907985|112676|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109779|NCT00907985|112676|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109780|NCT00907985|112676|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109781|NCT00907985|112676|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109782|NCT00907985|112676|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109783|NCT00907933|111610|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109784|NCT00907933|111610|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109785|NCT00907933|111610|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109786|NCT00907933|111610|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109787|NCT00907933|111610|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109788|NCT00907933|111610|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109789|NCT00907933|111610|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109790|NCT00907777|112807|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109791|NCT00907777|112807|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109792|NCT00907777|112807|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109793|NCT00907777|112807|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109794|NCT00907777|112807|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109795|NCT00907777|112807|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109796|NCT00906178||Intervention website|http://www.cybersenga.com|
109797|NCT00906178||Informed Consent Form|http://innovativepublichealth.org/projects/cybersenga/|All study documents (consent form, surveys, etc) are available for free download at the study site
109798|NCT00903409|111818|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109799|NCT00903409|111818|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109800|NCT00903409|111818|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109801|NCT00903409|111818|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109802|NCT00903409|111818|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109803|NCT00903409|111818|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109804|NCT00903201|110399|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109805|NCT00903201|110399|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109806|NCT00903201|110399|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109807|NCT00903201|110399|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109808|NCT00903201|110399|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109809|NCT00903201|110399|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109810|NCT00903201|110399|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109811|NCT00896558|112668|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109812|NCT00896558|112668|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109813|NCT00896558|112668|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109814|NCT00896558|112668|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109815|NCT00896558|112668|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109816|NCT00896558|112668|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109817|NCT00896558|112668|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109818|NCT00896363|109035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109819|NCT00896363|109035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109820|NCT00896363|109035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109821|NCT00896363|109035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109822|NCT00896363|109035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109823|NCT00896363|109035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109824|NCT00896363|109035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109825|NCT00896064|112993|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109826|NCT00896064|112993|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109827|NCT00896064|112993|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109828|NCT00896064|112993|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109829|NCT00896064|112993|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109830|NCT00892775|108760|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109831|NCT00892775|108760|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109832|NCT00892775|108760|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109833|NCT00892775|108760|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109834|NCT00892775|108760|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109835|NCT00892775|108760|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109836|NCT00891176|112830|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109837|NCT00891176|112830|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109838|NCT00891176|112830|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109839|NCT00891176|112830|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109840|NCT00891176|112830|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109841|NCT00891176|112830|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109842|NCT00887484|114544|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109843|NCT00887484|114544|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109844|NCT00887484|114544|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109845|NCT00887484|114544|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109846|NCT00887484|114544|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109847|NCT00887406|104865|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109848|NCT00887406|104865|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109849|NCT00887406|104865|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109850|NCT00887406|104865|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109851|NCT00887406|104865|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109852|NCT00887406|104865|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109853|NCT00883948|ARDSNet-EDEN|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/eden/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
109854|NCT00883948||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/eden/|
109855|NCT00883948||Study Forms|http://biolincc.nhlbi.nih.gov/studies/eden/|
109856|NCT00883909|103094|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109857|NCT00883909|103094|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109858|NCT00883909|103094|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109859|NCT00883909|103094|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109860|NCT00883909|103094|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109861|NCT00883909|103094|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109862|NCT00883909|103094|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109863|NCT00880763||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-016&kw=7009-016&tab=access|
109864|NCT00880477|217744/069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109865|NCT00880477|217744/069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109866|NCT00880477|217744/069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109867|NCT00880477|217744/069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109868|NCT00880477|217744/069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109869|NCT00879970|111960|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109870|NCT00879970|111960|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109871|NCT00879970|111960|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109872|NCT00879970|111960|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109873|NCT00879970|111960|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109874|NCT00879970|111960|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109875|NCT00879970|111960|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109876|NCT00879827|217744/049|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109877|NCT00879827|217744/049|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109878|NCT00879827|217744/049|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109879|NCT00879827|217744/049|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109880|NCT00879827|217744/049|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109881|NCT00878462||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
109882|NCT00877877|111375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109883|NCT00877877|111375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109884|NCT00877877|111375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109885|NCT00877877|111375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109886|NCT00877877|111375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109887|NCT00877877|111375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109888|NCT00877877|111375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109889|NCT00875784|103629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109890|NCT00875784|103629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109891|NCT00875784|103629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109892|NCT00875784|103629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109893|NCT00875784|103629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109894|NCT00875784|103629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109895|NCT00875784|103629|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109896|NCT00875485|110699|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109897|NCT00875485|110699|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109898|NCT00875485|110699|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109899|NCT00875485|110699|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109900|NCT00875485|110699|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109901|NCT00873509||Individual Participant Data Set|https://ndar.nih.gov|
109902|NCT00871741|111761|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109903|NCT00871741|111761|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109904|NCT00871741|111761|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109905|NCT00871741|111761|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109906|NCT00871741|111761|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109907|NCT00871741|111761|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109908|NCT00871741|111761|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109909|NCT00871338|111709|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109910|NCT00871338|111709|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109911|NCT00871338|111709|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109912|NCT00871338|111709|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109913|NCT00871338|111709|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109914|NCT00871338|111709|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109915|NCT00871338|111709|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109916|NCT00871117|111852|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109917|NCT00871117|111852|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109918|NCT00871117|111852|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109919|NCT00871117|111852|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109920|NCT00871117|111852|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109921|NCT00871117|111852|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109922|NCT00871117|111852|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109923|NCT00871000|111815|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109924|NCT00871000|111815|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109925|NCT00871000|111815|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109926|NCT00871000|111815|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109927|NCT00871000|111815|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109928|NCT00871000|111815|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109929|NCT00871000|111815|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109930|NCT00868790||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=3577-009&kw=3577-009&tab=access|
109931|NCT00867191||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
109932|NCT00866619|110021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109933|NCT00866619|110021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109934|NCT00866619|110021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109935|NCT00866619|110021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109936|NCT00866619|110021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109937|NCT00866619|110021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109938|NCT00866515|112205|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109939|NCT00866515|112205|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109940|NCT00866515|112205|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109941|NCT00866515|112205|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109942|NCT00866515|112205|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109943|NCT00866515|112205|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109944|NCT00866515|112205|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109945|NCT00866294|112810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109946|NCT00866294|112810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109947|NCT00866294|112810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109948|NCT00866294|112810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109949|NCT00866294|112810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109950|NCT00863109||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05278&kw=P05278&tab=access|
109951|NCT00861809|111809|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109952|NCT00861809|111809|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109953|NCT00861809|111809|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109954|NCT00861809|111809|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109955|NCT00861809|111809|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109956|NCT00861809|111809|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109957|NCT00861809|111809|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109958|NCT00861744|111870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109959|NCT00861744|111870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109960|NCT00861744|111870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109961|NCT00861744|111870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109962|NCT00861744|111870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109963|NCT00861744|111870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109964|NCT00861744|111870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109965|NCT00861484|111155|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109966|NCT00861484|111155|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109967|NCT00861484|111155|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109968|NCT00861484|111155|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109969|NCT00861484|111155|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109970|NCT00861484|111155|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109971|NCT00861484|111155|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109972|NCT00861380|111442|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109973|NCT00861380|111442|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109974|NCT00861380|111442|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109975|NCT00861380|111442|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109976|NCT00861380|111442|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109977|NCT00861380|111442|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109978|NCT00861380|111442|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109979|NCT00861250||Clinical Study Report|http://www.ncbi.nlm.nih.gov/pubmed/25303369|First study article: http://www.ncbi.nlm.nih.gov/pubmed/23206270
109980|NCT00857883|111314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109981|NCT00857883|111314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109982|NCT00857883|111314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109983|NCT00857883|111314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109984|NCT00857883|111314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109985|NCT00857883|111314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109986|NCT00857883|111314|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109987|NCT00857857|110762|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109988|NCT00857857|110762|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109989|NCT00857857|110762|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109990|NCT00857857|110762|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109991|NCT00857857|110762|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109992|NCT00857857|110762|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109993|NCT00857857|110762|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109994|NCT00857766|112355|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109995|NCT00857766|112355|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109996|NCT00857766|112355|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109997|NCT00857766|112355|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109998|NCT00857766|112355|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
109999|NCT00857766|112355|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110000|NCT00857766|112355|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110001|NCT00852540|110978|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110002|NCT00852540|110978|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110003|NCT00852540|110978|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110004|NCT00852540|110978|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110005|NCT00852540|110978|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110006|NCT00852540|110978|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110007|NCT00852540|110978|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110008|NCT00851344|110163|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110009|NCT00851344|110163|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110010|NCT00851344|110163|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110011|NCT00851344|110163|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110012|NCT00851344|110163|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110013|NCT00851344|110163|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110014|NCT00851344|110163|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110015|NCT00851071||Publication|http://link.springer.com/article/10.1007%2Fs10840-015-9990-7|A prospective study of anxiety in ICD patients with a pilot randomized controlled trial of cognitive behavioral therapy for patients with moderate to severe anxiety Mohammed Qintar & Jason J. George & Melanie Panko & Scott Bea & Karen A. Broer & Julie St. John & Kecia-Ann Blissett & Elizabeth Ching & Samuel F. Sears & Susanne S. Pedersen & Leopoldo Pozuelo & Mina K. Chung
110016|NCT00850642|112046|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110017|NCT00850642|112046|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110018|NCT00850642|112046|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110019|NCT00850642|112046|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110020|NCT00850642|112046|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110021|NCT00850642|112046|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110022|NCT00850642|112046|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110023|NCT00849134|111383|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110024|NCT00849134|111383|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110025|NCT00849134|111383|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110026|NCT00849134|111383|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110027|NCT00849134|111383|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110028|NCT00849134|111383|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110029|NCT00849134|111383|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110030|NCT00849056|112755|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110031|NCT00849056|112755|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110032|NCT00849056|112755|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110033|NCT00849056|112755|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110034|NCT00849056|112755|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110035|NCT00849056|112755|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110036|NCT00849056|112755|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110037|NCT00849017|112756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110038|NCT00849017|112756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110039|NCT00849017|112756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110040|NCT00849017|112756|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110041|NCT00849017|112756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110042|NCT00849017|112756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110043|NCT00849017|112756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110044|NCT00843193|106870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110045|NCT00843193|106870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110046|NCT00843193|106870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110047|NCT00843193|106870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110048|NCT00843193|106870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110049|NCT00843193|106870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110050|NCT00843193|106870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110051|NCT00843024|107979|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110052|NCT00843024|107979|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110053|NCT00843024|107979|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110054|NCT00843024|107979|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110055|NCT00843024|107979|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110056|NCT00843024|107979|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110057|NCT00843024|107979|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110058|NCT00839657|COAG|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/coag/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
110059|NCT00839657||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/coag/|
110060|NCT00839657||Study Forms|http://biolincc.nhlbi.nih.gov/studies/coag/|
110061|NCT00839657||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/coag/|
110062|NCT00839527|112757|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110063|NCT00839527|112757|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110064|NCT00839527|112757|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110065|NCT00839527|112757|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110066|NCT00839527|112757|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110067|NCT00839527|112757|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110068|NCT00839527|112757|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110069|NCT00838916|112754|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110070|NCT00838916|112754|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110071|NCT00838916|112754|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110072|NCT00838916|112754|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110073|NCT00838916|112754|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110074|NCT00838916|112754|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110075|NCT00838916|112754|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110076|NCT00838903|112753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110077|NCT00838903|112753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110078|NCT00838903|112753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110079|NCT00838903|112753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110080|NCT00838903|112753|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110081|NCT00838903|112753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110082|NCT00838903|112753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110083|NCT00837434|SDY824|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY824|The Immunology Database and Analysis Portal (ImmPort) is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. The portal includes available analysis tools for researchers.
110084|NCT00837434|SDY824|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY824|ImmPort study identifier is SDY824.
110085|NCT00837434|SDY824|Study summary, -design, -adverse event(s), -summary of participant assessments, -medications, -demographics, -lab tests, -mechanistic assays, -study files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY824|ImmPort study identifier is SDY824.
110086|NCT00835237|111413|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110087|NCT00835237|111413|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110088|NCT00835237|111413|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110089|NCT00835237|111413|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110090|NCT00835237|111413|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110091|NCT00835237|111413|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110092|NCT00835237|111413|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110093|NCT00835094||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110094|NCT00834119||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110095|NCT00833989|111539|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110096|NCT00833989|111539|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110097|NCT00833989|111539|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110098|NCT00833989|111539|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110099|NCT00833989|111539|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110100|NCT00833989|111539|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110101|NCT00833989|111539|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110102|NCT00831545||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
110103|NCT00829985|SDY223|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY223|ImmPort study identifier is SDY223.
110104|NCT00829985|SDY223|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY223|ImmPort study identifier is SDY223.
110105|NCT00829985|SDY223|Study summary, -design, -adverse event(s), -interventions, -medications, -demographics, -study files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY223|ImmPort study identifier is SDY223.
110106|NCT00829010|111634|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110107|NCT00829010|111634|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110108|NCT00829010|111634|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110109|NCT00829010|111634|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110110|NCT00829010|111634|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110111|NCT00829010|111634|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110112|NCT00829010|111634|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110113|NCT00828867|111341|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110114|NCT00828867|111341|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110115|NCT00828867|111341|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110116|NCT00828867|111341|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110117|NCT00828867|111341|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110118|NCT00828867|111341|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110119|NCT00828867|111341|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110120|NCT00823940|111497|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110121|NCT00823940|111497|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110122|NCT00823940|111497|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110123|NCT00823940|111497|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110124|NCT00823940|111497|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110125|NCT00823940|111497|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110126|NCT00823940|111497|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110127|NCT00823836|106066|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110128|NCT00823836|106066|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110129|NCT00823836|106066|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110130|NCT00823836|106066|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110131|NCT00823836|106066|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110132|NCT00818259||CSR Snyopsis|http://www.merck.com/clinical-trials/study.html?id=0869-134&kw=0869-134&tab=access|
110133|NCT00817817||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110134|NCT00817050||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110135|NCT00814957|110269|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110136|NCT00814957|110269|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110137|NCT00814957|110269|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110138|NCT00814957|110269|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110139|NCT00814957|110269|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110140|NCT00814957|110269|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110141|NCT00814957|110269|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110142|NCT00814710|111188|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110143|NCT00814710|111188|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110144|NCT00814710|111188|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110145|NCT00814710|111188|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110146|NCT00814710|111188|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110147|NCT00814710|111188|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110148|NCT00814710|111188|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110149|NCT00812981|111954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110150|NCT00812981|111954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110151|NCT00812981|111954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110152|NCT00812981|111954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110153|NCT00812981|111954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110154|NCT00812981|111954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110155|NCT00812981|111954|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110156|NCT00812929|112025|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110157|NCT00812929|112025|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110158|NCT00812929|112025|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110159|NCT00812929|112025|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110160|NCT00812929|112025|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110161|NCT00812929|112025|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110162|NCT00812929|112025|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110163|NCT00812812|112487|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110164|NCT00812812|112487|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110165|NCT00812812|112487|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110166|NCT00812812|112487|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110167|NCT00812773|112356|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110168|NCT00812773|112356|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110169|NCT00812773|112356|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110170|NCT00812773|112356|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110171|NCT00812773|112356|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110172|NCT00812773|112356|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110173|NCT00812773|112356|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110174|NCT00811967||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110175|NCT00811798|111712|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110176|NCT00811798|111712|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110177|NCT00811798|111712|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110178|NCT00811798|111712|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110179|NCT00811798|111712|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110180|NCT00811798|111712|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110181|NCT00811798|111712|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110182|NCT00811356|111319|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110183|NCT00811356|111319|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110184|NCT00811356|111319|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110185|NCT00811356|111319|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110186|NCT00811356|111319|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110187|NCT00811356|111319|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110188|NCT00811356|111319|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110189|NCT00810667|2008-001441-26|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-001441-26/results|
110190|NCT00808444|111654|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110191|NCT00808444|111654|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110192|NCT00808444|111654|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110193|NCT00808444|111654|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110194|NCT00808444|111654|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110195|NCT00808444|111654|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110196|NCT00808444|111654|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110197|NCT00806572|ITN007AI-NDB01|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN007AIPUBLIC/Study%20Data/begin.view?|TrialShare is a portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.Creating an account for ITN TrialShare is free and allows for searching studies of interest.
110198|NCT00806572|ITN007AI-NDB01|Study protocol synopsis, -navigator, -schedule of events,-data &reports, -specimens et al.|http://www.itntrialshare.org/project/Studies/ITN007AIPUBLIC/Study%20Data/begin.view?|TrialShare is a portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.Creating an account for ITN TrialShare is free and allows for searching studies of interest.
110199|NCT00806572|SDY569|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY569|ImmPort study identifier is SDY569. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
110200|NCT00806572|SDY569|Study summary, -design, -medications, -demographics, -lab tests, and -files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY569|ImmPort study identifier is SDY569. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
110201|NCT00803673|110106|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110202|NCT00803673|110106|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110203|NCT00803673|110106|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110204|NCT00803673|110106|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110205|NCT00803673|110106|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110206|NCT00803673|110106|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110207|NCT00803673|110106|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110208|NCT00802464|112077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110209|NCT00802464|112077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110210|NCT00802464|112077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110211|NCT00802464|112077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110212|NCT00802464|112077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110213|NCT00802464|112077|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110214|NCT00802464|112077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110215|NCT00799903|100601|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110216|NCT00799903|100601|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110217|NCT00799903|100601|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110218|NCT00799903|100601|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110219|NCT00799903|100601|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110220|NCT00799903|100601|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110221|NCT00799903|100601|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110222|NCT00797667||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-049&kw=0974-049&tab=access|
110223|NCT00796250||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110224|NCT00794898||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110225|NCT00792909|111736|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110226|NCT00792909|111736|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110227|NCT00792909|111736|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110228|NCT00792909|111736|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110229|NCT00792909|111736|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110230|NCT00792909|111736|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110231|NCT00792636|110948|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110232|NCT00792636|110948|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110233|NCT00792636|110948|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110234|NCT00792636|110948|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110235|NCT00792636|110948|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110236|NCT00792636|110948|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110237|NCT00792636|110948|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110238|NCT00792623|208133/178|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110239|NCT00792623|208133/178|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110240|NCT00792623|208133/178|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110241|NCT00792623|208133/178|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110242|NCT00792623|208133/178|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110243|NCT00792623|208133/178|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110244|NCT00792298||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=4305-006&kw=4305-006&tab=access|
110245|NCT00790907|108888|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110246|NCT00790907|108888|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110247|NCT00790907|108888|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110248|NCT00790907|108888|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110249|NCT00790907|108888|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110250|NCT00790907|108888|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110251|NCT00790907|108888|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110252|NCT00789880|SDY14|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY14|ImmPort study identifier is SDY14.
110253|NCT00789880|SDY14|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY14|ImmPort study identifier is SDY14.
110254|NCT00789880|SDY14|Study summary, -design, -assessments, -adverse events, -intervention(s), -study files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY14|ImmPort study identifier is SDY14.
110255|NCT00789152||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110256|NCT00787371||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110257|NCT00784550|111114|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110258|NCT00784550|111114|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110259|NCT00784550|111114|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110260|NCT00784550|111114|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110261|NCT00784550|111114|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110262|NCT00784550|111114|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110263|NCT00784550|111114|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110264|NCT00784134|Data repository-VISTA|Data repository-VISTA|http://vista.gla.ac.uk|when available
110265|NCT00784134||Study Protocol|http://vista.gla.ac.uk|when available
110266|NCT00784134||Statistical Analysis Plan|http://vista.gla.ac.uk|when available
110267|NCT00783549|111596|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110268|NCT00783549|111596|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110269|NCT00783549|111596|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110270|NCT00783549|111596|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110271|NCT00783549|111596|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110272|NCT00783549|111596|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110273|NCT00783549|111596|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110274|NCT00783458||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110275|NCT00783393||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110276|NCT00783354||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110277|NCT00783237||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110278|NCT00783211||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110279|NCT00783146||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110280|NCT00783133||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110281|NCT00783003|112146|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110282|NCT00783003|112146|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110283|NCT00783003|112146|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110284|NCT00783003|112146|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110285|NCT00783003|112146|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110286|NCT00783003|112146|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110287|NCT00783003|112146|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110288|NCT00779935||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110289|NCT00779766|107638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110290|NCT00779766|107638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110291|NCT00779766|107638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110292|NCT00779766|107638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110293|NCT00779766|107638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110294|NCT00779766|107638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110295|NCT00779766|107638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110296|NCT00779740||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110297|NCT00779636||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110298|NCT00779545||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110299|NCT00779012||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110300|NCT00778895|111635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110301|NCT00778895|111635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110302|NCT00778895|111635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110303|NCT00778895|111635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110304|NCT00778895|111635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110305|NCT00778895|111635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110306|NCT00776919|114677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110307|NCT00776919|114677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110308|NCT00776919|114677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110309|NCT00776919|114677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110310|NCT00776919|114677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110311|NCT00776919|114677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110312|NCT00776919|114677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110313|NCT00774995|110073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110314|NCT00774995|110073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110315|NCT00774995|110073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110316|NCT00774995|110073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110317|NCT00774995|110073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110318|NCT00774995|110073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110319|NCT00772889|111738|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110320|NCT00772889|111738|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110321|NCT00772889|111738|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110322|NCT00772889|111738|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110323|NCT00772889|111738|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110324|NCT00772889|111738|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110325|NCT00772889|111738|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110326|NCT00771615|111729|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110327|NCT00771615|111729|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110328|NCT00771615|111729|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110329|NCT00771615|111729|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110330|NCT00771615|111729|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110331|NCT00771615|111729|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110332|NCT00771615|111729|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110333|NCT00771160||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110334|NCT00770744|2008-000479-11|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2008-000479-11/results|
110335|NCT00768326|2006-003739-57|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2006-003739-57/results|
110336|NCT00766090|112202|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110337|NCT00766090|112202|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110338|NCT00766090|112202|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110339|NCT00766090|112202|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110340|NCT00766090|112202|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110341|NCT00766090|112202|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110342|NCT00766090|112202|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110343|NCT00765076|112147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110344|NCT00765076|112147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110345|NCT00765076|112147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110346|NCT00765076|112147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110347|NCT00765076|112147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110348|NCT00765076|112147|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110349|NCT00764790|111751|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110350|NCT00764790|111751|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110351|NCT00764790|111751|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110352|NCT00764790|111751|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110353|NCT00764790|111751|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110354|NCT00764790|111751|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110355|NCT00764790|111751|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110356|NCT00764478||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05691&kw=P05691&tab=access|
110357|NCT00763529||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110358|NCT00763438|2007-002160-10|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-002160-10/results|
110359|NCT00760617|111737|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110360|NCT00760617|111737|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110361|NCT00760617|111737|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110362|NCT00760617|111737|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110363|NCT00760617|111737|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110364|NCT00760617|111737|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110365|NCT00760617|111737|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110366|NCT00758836||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-046&kw=0974-046&tab=access|
110367|NCT00758264|111393|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110368|NCT00758264|111393|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110369|NCT00758264|111393|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110370|NCT00758264|111393|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110371|NCT00758264|111393|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110372|NCT00758264|111393|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110373|NCT00758264|111393|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110374|NCT00758069||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110375|NCT00757770|444563/033|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110376|NCT00757770|444563/033|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110377|NCT00757770|444563/033|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110378|NCT00757770|444563/033|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110379|NCT00757770|444563/033|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110380|NCT00757770|444563/033|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110381|NCT00757562||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110382|NCT00756938||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0954-337&kw=0954-337&tab=access|
110383|NCT00756418||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110384|NCT00756067|111652|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110385|NCT00756067|111652|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110386|NCT00756067|111652|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110387|NCT00756067|111652|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110388|NCT00756067|111652|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110389|NCT00755794||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110390|NCT00753272|106372|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110391|NCT00753272|106372|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110392|NCT00753272|106372|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110393|NCT00753272|106372|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110394|NCT00753272|106372|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110395|NCT00753272|106372|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110396|NCT00753272|106372|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110397|NCT00751348|110876|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110398|NCT00751348|110876|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110399|NCT00751348|110876|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110400|NCT00751348|110876|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110401|NCT00751348|110876|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110402|NCT00751348|110876|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110403|NCT00751218||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110404|NCT00751166||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110405|NCT00751075||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110406|NCT00750750||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110407|NCT00750360|218352/054|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110408|NCT00750360|218352/054|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110409|NCT00750360|218352/054|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110410|NCT00750360|218352/054|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110411|NCT00750360|218352/054|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110412|NCT00750360|218352/054|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110413|NCT00750178||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
110414|NCT00749411|DB1111581|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110415|NCT00749411|DB1111581|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110416|NCT00749411|DB1111581|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110417|NCT00749411|DB1111581|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110418|NCT00749411|DB1111581|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110419|NCT00749411|DB1111581|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110420|NCT00749411|DB1111581|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110421|NCT00749359|PCR111656|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110422|NCT00749359|PCR111656|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110423|NCT00749359|PCR111656|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110424|NCT00749359|PCR111656|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110425|NCT00749359|PCR111656|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110426|NCT00749359|PCR111656|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110427|NCT00749359|PCR111656|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110428|NCT00748410|CUC111342|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110429|NCT00748410|CUC111342|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110430|NCT00748410|CUC111342|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110431|NCT00748410|CUC111342|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110432|NCT00748410|CUC111342|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110433|NCT00748410|CUC111342|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110434|NCT00748306|111834|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110435|NCT00748306|111834|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110436|NCT00748306|111834|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110437|NCT00748306|111834|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110438|NCT00748306|111834|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110439|NCT00748306|111834|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110440|NCT00748306|111834|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110441|NCT00746122||Study Protocol|http://www.imperial.ac.uk/department-surgery-cancer/research/surgery/clinical-trials/improve/documents/|Final protocol version 6.0 dated 28th August 2013
110442|NCT00743860|LPL112498|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110443|NCT00743860|LPL112498|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110444|NCT00743860|LPL112498|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110445|NCT00743860|LPL112498|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110446|NCT00743860|LPL112498|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110447|NCT00743860|LPL112498|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110448|NCT00743860|LPL112498|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110449|NCT00743067|MET111648|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110450|NCT00743067|MET111648|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110451|NCT00743067|MET111648|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110452|NCT00743067|MET111648|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110453|NCT00743067|MET111648|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110454|NCT00743067|MET111648|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110455|NCT00743067|MET111648|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110456|NCT00742885|111756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110457|NCT00742885|111756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110458|NCT00742885|111756|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110459|NCT00742885|111756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110460|NCT00742885|111756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110461|NCT00742885|111756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110462|NCT00742885|111756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110463|NCT00742508|CRV110734|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110464|NCT00742508|CRV110734|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110465|NCT00742508|CRV110734|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110466|NCT00742508|CRV110734|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110467|NCT00742508|CRV110734|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110468|NCT00742261|MET111516|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110469|NCT00742261|MET111516|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110470|NCT00742261|MET111516|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110471|NCT00742261|MET111516|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110472|NCT00742261|MET111516|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110473|NCT00742261|MET111516|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110474|NCT00742261|MET111516|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110475|NCT00742131|MET111647|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110476|NCT00742131|MET111647|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110477|NCT00742131|MET111647|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110478|NCT00742131|MET111647|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110479|NCT00742131|MET111647|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110480|NCT00742131|MET111647|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110481|NCT00742131|MET111647|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110482|NCT00734032|LPL110118|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110483|NCT00734032|LPL110118|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110484|NCT00734032|LPL110118|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110485|NCT00734032|LPL110118|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110486|NCT00734032|LPL110118|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110487|NCT00734032|LPL110118|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110488|NCT00733577|111829|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110489|NCT00733577|111829|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110490|NCT00733577|111829|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110491|NCT00733577|111829|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110492|NCT00733577|111829|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110493|NCT00733577|111829|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110494|NCT00733577|111829|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110495|NCT00733551|MOT109681|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110496|NCT00733551|MOT109681|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110497|NCT00733551|MOT109681|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110498|NCT00733551|MOT109681|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110499|NCT00733551|MOT109681|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110500|NCT00733551|MOT109681|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110501|NCT00732472|105211|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110502|NCT00732472|105211|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110503|NCT00732472|105211|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110504|NCT00732472|105211|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110505|NCT00732472|105211|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110506|NCT00732472|105211|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110507|NCT00732472|105211|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110508|NCT00732368||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110509|NCT00731822|HZC111348|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110510|NCT00731822|HZC111348|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110511|NCT00731822|HZC111348|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110512|NCT00731822|HZC111348|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110513|NCT00731822|HZC111348|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110514|NCT00731822|HZC111348|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110515|NCT00731822|HZC111348|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110516|NCT00731393|100351|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110517|NCT00731393|100351|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110518|NCT00731393|100351|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110519|NCT00731393|100351|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110520|NCT00731393|100351|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110521|NCT00731393|100351|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110522|NCT00731393|100351|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110523|NCT00731250|111611|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110524|NCT00731250|111611|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110525|NCT00731250|111611|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110526|NCT00731250|111611|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110527|NCT00731250|111611|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110528|NCT00731250|111611|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110529|NCT00731250|111611|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110530|NCT00731185||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110531|NCT00730756|FFR111158|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110532|NCT00730756|FFR111158|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110533|NCT00730756|FFR111158|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110534|NCT00730756|FFR111158|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110535|NCT00730756|FFR111158|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110536|NCT00730756|FFR111158|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110537|NCT00730756|FFR111158|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110538|NCT00729001|444563/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110539|NCT00729001|444563/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110540|NCT00729001|444563/005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110541|NCT00729001|444563/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110542|NCT00729001|444563/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110543|NCT00729001|444563/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110544|NCT00726323|MET111644|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110545|NCT00726323|MET111644|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110546|NCT00726323|MET111644|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110547|NCT00726323|MET111644|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110548|NCT00726323|MET111644|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110549|NCT00726323|MET111644|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110550|NCT00725764|MET111646|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110551|NCT00725764|MET111646|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110552|NCT00725764|MET111646|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110553|NCT00725764|MET111646|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110554|NCT00725764|MET111646|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110555|NCT00725764|MET111646|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110556|NCT00725764|MET111646|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110557|NCT00725712|MET111643|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110558|NCT00725712|MET111643|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110559|NCT00725712|MET111643|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110560|NCT00725712|MET111643|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110561|NCT00725712|MET111643|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110562|NCT00725712|MET111643|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110563|NCT00725712|MET111643|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110564|NCT00725374||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110565|NCT00723450|SCA102833|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110566|NCT00723450|SCA102833|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110567|NCT00723450|SCA102833|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110568|NCT00723450|SCA102833|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110569|NCT00723450|SCA102833|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110570|NCT00723450|SCA102833|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110571|NCT00723450|SCA102833|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110572|NCT00721812|111406|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110573|NCT00721812|111406|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110574|NCT00721812|111406|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110575|NCT00721812|111406|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110576|NCT00721812|111406|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110577|NCT00721812|111406|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110578|NCT00721812|111406|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110579|NCT00719043|110624|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110580|NCT00719043|110624|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110581|NCT00719043|110624|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110582|NCT00719043|110624|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110583|NCT00719043|110624|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110584|NCT00719043|110624|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110585|NCT00718666|112021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110586|NCT00718666|112021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110587|NCT00718666|112021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110588|NCT00718666|112021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110589|NCT00718666|112021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110590|NCT00718666|112021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110591|NCT00718120|110584|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110592|NCT00718120|110584|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110593|NCT00718120|110584|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110594|NCT00718120|110584|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110595|NCT00718120|110584|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110596|NCT00718120|110584|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110597|NCT00718120|110584|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110598|NCT00714285|111295|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110599|NCT00714285|111295|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110600|NCT00714285|111295|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110601|NCT00714285|111295|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110602|NCT00714285|111295|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110603|NCT00714285|111295|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110604|NCT00714285|111295|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110605|NCT00711126|B2C106180|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110606|NCT00711126|B2C106180|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110607|NCT00711126|B2C106180|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110608|NCT00711126|B2C106180|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110609|NCT00711126|B2C106180|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110610|NCT00711126|B2C106180|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110611|NCT00711126|B2C106180|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110612|NCT00710021|SDY474|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY474|ImmPort study identifier is SDY474.
110613|NCT00710021|SDY474|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY474|ImmPort study identifier is SDY474. The study protocol is located in the Design tab content.
110614|NCT00710021|SDY474|Study summary, -design, -adverse event(s), -meds,-demographics, -lab tests, -mechanistic assays, - files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY474|ImmPort study identifier is SDY474.
110615|NCT00707798|111651|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110616|NCT00707798|111651|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110617|NCT00707798|111651|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110618|NCT00707798|111651|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110619|NCT00707798|111651|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110620|NCT00706563|111631|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110621|NCT00706563|111631|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110622|NCT00706563|111631|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110623|NCT00706563|111631|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110624|NCT00706563|111631|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110625|NCT00706563|111631|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110626|NCT00706563|111631|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110627|NCT00705965||treatment manual and supplemental content|http://links.lww.com/PSYMED/A275|
110628|NCT00704431|LPL111814|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110629|NCT00704431|LPL111814|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110630|NCT00704431|LPL111814|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110631|NCT00704431|LPL111814|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110632|NCT00704431|LPL111814|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110633|NCT00704431|LPL111814|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110634|NCT00704405||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-009&kw=7009-009&tab=access|
110635|NCT00704184||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=7009-007&kw=7009-007&tab=access|
110636|NCT00703846|114568|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110637|NCT00703846|114568|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110638|NCT00703846|114568|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110639|NCT00703846|114568|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110640|NCT00703846|114568|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110641|NCT00703846|114568|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110642|NCT00703846|114568|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110643|NCT00703014||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05712&kw=P05712&tab=access|
110644|NCT00702910|B2C111401|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110645|NCT00702910|B2C111401|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110646|NCT00702910|B2C111401|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110647|NCT00702910|B2C111401|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110648|NCT00702910|B2C111401|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110649|NCT00702910|B2C111401|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110650|NCT00702910|B2C111401|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110651|NCT00702845||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05690&kw=P05690&tab=access|
110652|NCT00702806||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110653|NCT00702585||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110654|NCT00702520||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05783&kw=P05783&tab=access|
110655|NCT00702338||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05713&kw=P05713&tab=access|
110656|NCT00702273||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05716&kw=P05716&tab=access|
110657|NCT00702234||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05715&kw=P05715&tab=access|
110661|NCT00699764|208141/017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110662|NCT00699764|208141/017|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110663|NCT00699764|208141/017|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110664|NCT00699764|208141/017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110665|NCT00699764|208141/017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110666|NCT00699764|208141/017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110667|NCT00697866|208129/037|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110668|NCT00697866|208129/037|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110669|NCT00697866|208129/037|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110670|NCT00697866|208129/037|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110671|NCT00697866|208129/037|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110672|NCT00697866|208129/037|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110673|NCT00697749|208129/034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110674|NCT00697749|208129/034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110675|NCT00697749|208129/034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110676|NCT00697749|208129/034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110677|NCT00697749|208129/034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110678|NCT00697749|208129/034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110679|NCT00697554|208129/036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110680|NCT00697554|208129/036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110681|NCT00697554|208129/036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110682|NCT00697554|208129/036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110683|NCT00697554|208129/036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110684|NCT00697255||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05693&kw=P05693&tab=access|
110685|NCT00696878||Add data sharing links|http://www.merck.com/clinical-trials/study.html?id=P05714&kw=P05714&tab=access|
110686|NCT00696800||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05787&kw=P05787&tab=access|
110687|NCT00696423|111535|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110688|NCT00696423|111535|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110689|NCT00696423|111535|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110690|NCT00696423|111535|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110691|NCT00696423|111535|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110692|NCT00696423|111535|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110693|NCT00696423|111535|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110694|NCT00695669|111626|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110695|NCT00695669|111626|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110696|NCT00695669|111626|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110697|NCT00695669|111626|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110698|NCT00695669|111626|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110699|NCT00695669|111626|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110700|NCT00695669|111626|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110701|NCT00695448|PIK111051|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110702|NCT00695448|PIK111051|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110703|NCT00695448|PIK111051|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110704|NCT00695448|PIK111051|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110705|NCT00695448|PIK111051|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110706|NCT00695448|PIK111051|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110707|NCT00695448|PIK111051|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110708|NCT00695305|LP2105521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110709|NCT00695305|LP2105521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110710|NCT00695305|LP2105521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110711|NCT00695305|LP2105521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110712|NCT00695305|LP2105521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110713|NCT00695305|LP2105521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110714|NCT00695305|LP2105521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110715|NCT00694993|HHI110157|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110716|NCT00694993|HHI110157|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110717|NCT00694993|HHI110157|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110718|NCT00694993|HHI110157|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110719|NCT00694993|HHI110157|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110720|NCT00694993|HHI110157|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110721|NCT00694993|HHI110157|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110722|NCT00693966|580299/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110723|NCT00693966|580299/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110724|NCT00693966|580299/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110725|NCT00693966|580299/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110726|NCT00693966|580299/005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110727|NCT00693966|580299/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110728|NCT00693706|110127|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110729|NCT00693706|110127|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110730|NCT00693706|110127|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110731|NCT00693706|110127|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110732|NCT00693706|110127|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110733|NCT00693706|110127|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110734|NCT00693706|110127|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110735|NCT00693615|580299/004|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110736|NCT00693615|580299/004|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110737|NCT00693615|580299/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110738|NCT00693615|580299/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110739|NCT00693615|580299/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110740|NCT00693615|580299/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110741|NCT00693615|580299/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110742|NCT00689741|580299/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110743|NCT00689741|580299/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110744|NCT00689741|580299/001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110745|NCT00689741|580299/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110746|NCT00689741|580299/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110747|NCT00689741|580299/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110748|NCT00689481|114742|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110749|NCT00689481|114742|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110750|NCT00689481|114742|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110751|NCT00689481|114742|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110752|NCT00689481|114742|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110753|NCT00689481|114742|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110754|NCT00689390||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05063&kw=P05063&tab=access|
110755|NCT00688519|114741|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110756|NCT00688519|114741|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110757|NCT00688519|114741|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110758|NCT00688519|114741|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110759|NCT00688519|114741|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110760|NCT00688519|114741|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110761|NCT00688519|114741|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110762|NCT00688467||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05363&kw=P05363&tab=access|
110763|NCT00688207|AVA109941|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110764|NCT00688207|AVA109941|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110765|NCT00688207|AVA109941|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110766|NCT00688207|AVA109941|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110767|NCT00688207|AVA109941|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110768|NCT00688207|AVA109941|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110769|NCT00688207|AVA109941|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110770|NCT00687700|MAB110553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110771|NCT00687700|MAB110553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110772|NCT00687700|MAB110553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110773|NCT00687700|MAB110553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110774|NCT00687700|MAB110553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110775|NCT00687700|MAB110553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110776|NCT00687700|MAB110553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110779|NCT00684671|111572|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110780|NCT00684671|111572|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110781|NCT00684671|111572|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110782|NCT00684671|111572|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110783|NCT00684671|111572|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110784|NCT00684671|111572|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110785|NCT00684593||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04481&kw=7123-009&tab=access|
110786|NCT00684515||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05005&kw=P05005&tab=access|
110787|NCT00684463||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110788|NCT00684203||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04772&kw=P04772&tab=access|
110789|NCT00684177|TOC110977|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110790|NCT00684177|TOC110977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110791|NCT00684177|TOC110977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110792|NCT00684177|TOC110977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110793|NCT00684177|TOC110977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110794|NCT00684177|TOC110977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110795|NCT00684177|TOC110977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110796|NCT00682643|FFR110537|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110797|NCT00682643|FFR110537|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110798|NCT00682643|FFR110537|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110799|NCT00682643|FFR110537|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110800|NCT00682643|FFR110537|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110801|NCT00682643|FFR110537|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110802|NCT00682643|FFR110537|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110803|NCT00680914|110808|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110804|NCT00680914|110808|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110805|NCT00680914|110808|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110806|NCT00680914|110808|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110807|NCT00680914|110808|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110808|NCT00680914|110808|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110809|NCT00680914|110808|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110810|NCT00679939|AVD111179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110811|NCT00679939|AVD111179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110812|NCT00679939|AVD111179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110813|NCT00679939|AVD111179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110814|NCT00679939|AVD111179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110815|NCT00679939|AVD111179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110816|NCT00679939|AVD111179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110817|NCT00679055||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0736-006&kw=0736-006&tab=access|
110818|NCT00678886|115495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110819|NCT00678886|115495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110820|NCT00678886|115495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110821|NCT00678886|115495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110822|NCT00678886|115495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110823|NCT00678886|115495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110824|NCT00678886|115495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110825|NCT00678301|110521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110826|NCT00678301|110521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110827|NCT00678301|110521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110828|NCT00678301|110521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110829|NCT00678301|110521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110830|NCT00678301|110521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110831|NCT00678301|110521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110832|NCT00676052|AC2110664|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110833|NCT00676052|AC2110664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110834|NCT00676052|AC2110664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110835|NCT00676052|AC2110664|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110836|NCT00676052|AC2110664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110837|NCT00676052|AC2110664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110838|NCT00676052|AC2110664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110839|NCT00675090|H3B109689|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110840|NCT00675090|H3B109689|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110841|NCT00675090|H3B109689|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110842|NCT00675090|H3B109689|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110843|NCT00675090|H3B109689|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110844|NCT00675090|H3B109689|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110845|NCT00675090|H3B109689|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110846|NCT00674817|MAB110123|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110847|NCT00674817|MAB110123|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110848|NCT00674817|MAB110123|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110849|NCT00674817|MAB110123|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110850|NCT00674817|MAB110123|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110851|NCT00674817|MAB110123|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110852|NCT00674817|MAB110123|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110853|NCT00674635|104972|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110854|NCT00674635|104972|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110855|NCT00674635|104972|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110856|NCT00674635|104972|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110857|NCT00674635|104972|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110858|NCT00674635|104972|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110859|NCT00674635|104972|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110860|NCT00674583|111414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110861|NCT00674583|111414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110862|NCT00674583|111414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110863|NCT00674583|111414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110864|NCT00674583|111414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110865|NCT00674583|111414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110866|NCT00674583|111414|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110867|NCT00671216|DB1111509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110868|NCT00671216|DB1111509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110869|NCT00671216|DB1111509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110870|NCT00671216|DB1111509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110871|NCT00671216|DB1111509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110872|NCT00671216|DB1111509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110873|NCT00671216|DB1111509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110874|NCT00662818||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-034&kw=0974-034&tab=access|
110875|NCT00661674|PMID: 27712113|Published Manuscript|http://www.tandfonline.com/doi/full/10.1080/00952990.2016.1210614|Link to the manuscript which was published in The American Journal of Drug and Alcohol Abuse
110876|NCT00661557|107408|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110877|NCT00661557|107408|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110878|NCT00661557|107408|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110879|NCT00661557|107408|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110880|NCT00661557|107408|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110881|NCT00661557|107408|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110882|NCT00661557|107408|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110883|NCT00659178|ILI108621|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110884|NCT00659178|ILI108621|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110885|NCT00659178|ILI108621|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110886|NCT00659178|ILI108621|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110887|NCT00659178|ILI108621|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110888|NCT00659178|ILI108621|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110889|NCT00659178|ILI108621|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110890|NCT00657657|110071|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110891|NCT00657657|110071|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110892|NCT00657657|110071|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110893|NCT00657657|110071|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110894|NCT00657657|110071|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110895|NCT00657657|110071|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110896|NCT00654420||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0646-007&kw=0646-007&tab=access|
110897|NCT00653835||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110898|NCT00653796||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110899|NCT00653276||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
110900|NCT00652951|110142|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 110142 are summarised with study 111053 on GSK Clinical Study Register
110901|NCT00652951|110142|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110902|NCT00652951|110142|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110903|NCT00652951|110142|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110904|NCT00652951|110142|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110905|NCT00652951|110142|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110906|NCT00652951|110142|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110907|NCT00652938|111507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110908|NCT00652938|111507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110909|NCT00652938|111507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110910|NCT00652938|111507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110911|NCT00652938|111507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110912|NCT00652938|111507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110913|NCT00652938|111507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110914|NCT00652847||CSR Synopsi Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
110915|NCT00652743|111443|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110916|NCT00652743|111443|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 111470 are summarised with studies 111443, 111471, and 111472 on the GSK Clinical Study Register.
110917|NCT00652743|111443|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110918|NCT00652743|111443|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110919|NCT00652743|111443|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110920|NCT00652743|111443|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110921|NCT00652717||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110922|NCT00652301||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110923|NCT00651963||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
110924|NCT00651560||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
110925|NCT00651391||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110926|NCT00651378||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110927|NCT00651274||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110928|NCT00650819||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110929|NCT00650663||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
110930|NCT00642148|MKI102428|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110931|NCT00642148|MKI102428|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110932|NCT00642148|MKI102428|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110933|NCT00642148|MKI102428|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110934|NCT00642148|MKI102428|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110935|NCT00642148|MKI102428|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110936|NCT00642148|MKI102428|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110937|NCT00640081||Clinical Study Report|http://www.thelancet.com/journals/lanonc/article/PIIS1470-2045(14)70106-8/abstract|
110938|NCT00637195|111567|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110939|NCT00637195|111567|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110940|NCT00637195|111567|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110941|NCT00637195|111567|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110942|NCT00637195|111567|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110943|NCT00637195|111567|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110944|NCT00637195|111567|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110945|NCT00635804||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=3281-002&kw=3281-002&tab=access|
110946|NCT00635128|110947|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110947|NCT00635128|110947|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110948|NCT00635128|110947|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110949|NCT00635128|110947|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110950|NCT00635128|110947|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110951|NCT00635128|110947|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110952|NCT00635128|110947|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110953|NCT00633217|111117|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110954|NCT00633217|111117|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110955|NCT00633217|111117|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110956|NCT00633217|111117|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110957|NCT00633217|111117|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110958|NCT00633217|111117|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110959|NCT00633217|111117|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110960|NCT00633074|111454|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110961|NCT00633074|111454|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110962|NCT00633074|111454|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110963|NCT00633074|111454|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110964|NCT00633074|111454|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110965|NCT00633074|111454|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110966|NCT00633074|111454|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110967|NCT00633022|PM1111138|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110968|NCT00633022|PM1111138|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110969|NCT00633022|PM1111138|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110970|NCT00633022|PM1111138|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110971|NCT00633022|PM1111138|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110972|NCT00633022|PM1111138|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110973|NCT00633022|PM1111138|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110974|NCT00632736|101468/248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110975|NCT00632736|101468/248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110976|NCT00632736|101468/248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110977|NCT00632736|101468/248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110978|NCT00632736|101468/248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110979|NCT00632736|101468/248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110980|NCT00632736|101468/248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110981|NCT00632502||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05365&kw=7123-017&tab=access|
110982|NCT00627575|LEP108937|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110983|NCT00627575|LEP108937|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110984|NCT00627575|LEP108937|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110985|NCT00627575|LEP108937|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110986|NCT00627575|LEP108937|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110987|NCT00627575|LEP108937|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110988|NCT00627575|LEP108937|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110989|NCT00627458|111344|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110990|NCT00627458|111344|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110991|NCT00627458|111344|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110992|NCT00627458|111344|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110993|NCT00627458|111344|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110994|NCT00627458|111344|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110995|NCT00627458|111344|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110996|NCT00625196|HZA102940|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110997|NCT00625196|HZA102940|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110998|NCT00625196|HZA102940|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
110999|NCT00625196|HZA102940|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111000|NCT00625196|HZA102940|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111001|NCT00625196|HZA102940|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111002|NCT00625196|HZA102940|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111003|NCT00624819|111345 (Mth 12)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111004|NCT00624819|111345 (Mth 12)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111005|NCT00624819|111345 (Mth 12)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111006|NCT00624819|111345 (Mth 12)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111007|NCT00624819|111345 (Mth 12)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111008|NCT00624819|111345 (Mth 12)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111009|NCT00624065|COR111096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111010|NCT00624065|COR111096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111011|NCT00624065|COR111096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111012|NCT00624065|COR111096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111013|NCT00624065|COR111096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111014|NCT00624065|COR111096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111015|NCT00624065|COR111096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111016|NCT00622830|LPL110736|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111017|NCT00622830|LPL110736|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111018|NCT00622830|LPL110736|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111019|NCT00622830|LPL110736|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111020|NCT00622830|LPL110736|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111021|NCT00622830|LPL110736|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111022|NCT00622830|LPL110736|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111023|NCT00622609|MAG103114|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111024|NCT00622609|MAG103114|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111025|NCT00622609|MAG103114|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111026|NCT00622609|MAG103114|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111027|NCT00622609|MAG103114|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111028|NCT00622609|MAG103114|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111029|NCT00617890||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04720&kw=P04720&tab=access|
111030|NCT00617123||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P05183&kw=P05183&tab=access|
111031|NCT00616928|110464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111032|NCT00616928|110464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111033|NCT00616928|110464|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111034|NCT00616928|110464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111035|NCT00616928|110464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111036|NCT00616928|110464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111037|NCT00616928|110464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111038|NCT00614731|SDY3|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY3|ImmPort study identifier is SDY3.
111039|NCT00614731|SDY3|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY3|ImmPort study identifier is SDY3.
111040|NCT00614731|SDY3|Study design, -schedule of events, -demographics, -adverse events, -interventions, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY3|ImmPort study identifier is SDY3.
111041|NCT00614614|110870|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111042|NCT00614614|110870|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111043|NCT00614614|110870|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111044|NCT00614614|110870|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111045|NCT00614614|110870|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111046|NCT00614614|110870|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111047|NCT00614614|110870|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111048|NCT00612820|IPR110723|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111049|NCT00612820|IPR110723|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111050|NCT00612820|IPR110723|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111051|NCT00612820|IPR110723|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111052|NCT00612820|IPR110723|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111053|NCT00612820|IPR110723|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111054|NCT00612820|IPR110723|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111055|NCT00611559|110478|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111056|NCT00611559|110478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111057|NCT00611559|110478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111058|NCT00611559|110478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111059|NCT00611559|110478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111060|NCT00611559|110478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111061|NCT00611559|110478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111062|NCT00610168|110806|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111063|NCT00610168|110806|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111064|NCT00610168|110806|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111065|NCT00610168|110806|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111066|NCT00610168|110806|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111067|NCT00610168|110806|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111068|NCT00610168|110806|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111069|NCT00609674|FFU111439|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111070|NCT00609674|FFU111439|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111071|NCT00609674|FFU111439|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111072|NCT00609674|FFU111439|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111073|NCT00609674|FFU111439|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111074|NCT00609674|FFU111439|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111075|NCT00609674|FFU111439|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111076|NCT00609596|ARI111402|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111077|NCT00609596|ARI111402|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111078|NCT00609596|ARI111402|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111079|NCT00609596|ARI111402|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111080|NCT00609596|ARI111402|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111081|NCT00609596|ARI111402|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111082|NCT00609596|ARI111402|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111083|NCT00609492|109621|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111084|NCT00609492|109621|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111085|NCT00609492|109621|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111086|NCT00609492|109621|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111087|NCT00609492|109621|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111088|NCT00609492|109621|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111089|NCT00609492|109621|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111128|NCT00605371|LEP111102|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111090|NCT00609180|ARDSNet-Omega|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/omega/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
111091|NCT00609180||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/omega/|
111092|NCT00609180||Study Forms|http://biolincc.nhlbi.nih.gov/studies/omega/|
111093|NCT00608283|SDY289|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
111094|NCT00608283|SDY289|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
111095|NCT00608283|SDY289|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY289|ImmPort study identifier is SDY289
111096|NCT00607906|AXO110461|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111097|NCT00607906|AXO110461|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111098|NCT00607906|AXO110461|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111099|NCT00607906|AXO110461|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111100|NCT00607906|AXO110461|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111101|NCT00607906|AXO110461|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111102|NCT00607906|AXO110461|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111103|NCT00606697|NKI110334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111104|NCT00606697|NKI110334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111105|NCT00606697|NKI110334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111106|NCT00606697|NKI110334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111107|NCT00606697|NKI110334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111108|NCT00606697|NKI110334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111109|NCT00606697|NKI110334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111110|NCT00606684|B2C111045|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111111|NCT00606684|B2C111045|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111112|NCT00606684|B2C111045|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111113|NCT00606684|B2C111045|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111114|NCT00606684|B2C111045|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111115|NCT00606684|B2C111045|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111116|NCT00606684|B2C111045|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111117|NCT00605852|HH3110161|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111118|NCT00605852|HH3110161|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111119|NCT00605852|HH3110161|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111120|NCT00605852|HH3110161|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111121|NCT00605852|HH3110161|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111122|NCT00605852|HH3110161|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111123|NCT00605852|HH3110161|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111124|NCT00605371|LEP111102|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111125|NCT00605371|LEP111102|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111126|NCT00605371|LEP111102|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111127|NCT00605371|LEP111102|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114447|NCT00090272||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111129|NCT00605371|LEP111102|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111130|NCT00605371|LEP111102|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111131|NCT00605241|DAN106593|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111132|NCT00605241|DAN106593|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111133|NCT00605241|DAN106593|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111134|NCT00605241|DAN106593|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111135|NCT00605241|DAN106593|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111136|NCT00605241|DAN106593|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111137|NCT00605241|DAN106593|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111138|NCT00603746|FFA109684|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111139|NCT00603746|FFA109684|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111140|NCT00603746|FFA109684|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111141|NCT00603746|FFA109684|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111142|NCT00603746|FFA109684|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111143|NCT00603746|FFA109684|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111144|NCT00603746|FFA109684|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111145|NCT00603382|FFA109687|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111146|NCT00603382|FFA109687|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111147|NCT00603382|FFA109687|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111148|NCT00603382|FFA109687|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111149|NCT00603382|FFA109687|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111150|NCT00603382|FFA109687|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111151|NCT00603382|FFA109687|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111152|NCT00603278|FFA109685|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111153|NCT00603278|FFA109685|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111154|NCT00603278|FFA109685|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111155|NCT00603278|FFA109685|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111156|NCT00603278|FFA109685|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111157|NCT00603278|FFA109685|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111158|NCT00603278|FFA109685|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111159|NCT00603252|111149|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111160|NCT00603252|111149|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111161|NCT00603252|111149|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111162|NCT00603252|111149|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111163|NCT00603252|111149|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111164|NCT00600171|B2C109575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111165|NCT00600171|B2C109575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111166|NCT00600171|B2C109575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111167|NCT00600171|B2C109575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111168|NCT00600171|B2C109575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111169|NCT00600171|B2C109575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111170|NCT00600171|B2C109575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111171|NCT00599911|2007-001071-11|EMA EudraCT Results|https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-001071-11/results|
111172|NCT00598208||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111173|NCT00591786||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111174|NCT00591409||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111175|NCT00590668||Publication|http://www.sciencedirect.com/science/article/pii/S0894731711003932|
111176|NCT00586612|110215|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study are summarised with 110217 on the GSK Clinical Study Register.
111177|NCT00586612|110215|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111178|NCT00586612|110215|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111179|NCT00586612|110215|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111180|NCT00586612|110215|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111181|NCT00586612|110215|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111182|NCT00586612|110215|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111183|NCT00586469|111258|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111184|NCT00586469|111258|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111185|NCT00586469|111258|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111186|NCT00586469|111258|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111187|NCT00586469|111258|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111188|NCT00586469|111258|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111189|NCT00586469|111258|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111190|NCT00586339|107863|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111191|NCT00586339|107863|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111192|NCT00586339|107863|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111193|NCT00586339|107863|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111194|NCT00586339|107863|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111195|NCT00586339|107863|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111196|NCT00579982|LBI108884|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111197|NCT00579982|LBI108884|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111198|NCT00579982|LBI108884|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111199|NCT00579982|LBI108884|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111200|NCT00579982|LBI108884|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111201|NCT00579982|LBI108884|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111202|NCT00579982|LBI108884|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111203|NCT00578227|110886|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111204|NCT00578227|110886|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111205|NCT00578227|110886|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114448|NCT00090246||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111206|NCT00578227|110886|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111207|NCT00578227|110886|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111208|NCT00578227|110886|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111209|NCT00578227|110886|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111210|NCT00578175|110058|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111211|NCT00578175|110058|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111212|NCT00578175|110058|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111213|NCT00578175|110058|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111214|NCT00578175|110058|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111215|NCT00578175|110058|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111216|NCT00578175|110058|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111217|NCT00570492|FFR101782|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111218|NCT00570492|FFR101782|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111219|NCT00570492|FFR101782|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111220|NCT00570492|FFR101782|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111221|NCT00570492|FFR101782|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111222|NCT00570492|FFR101782|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111223|NCT00570492|FFR101782|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111224|NCT00569062|PKI108574|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111225|NCT00569062|PKI108574|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111226|NCT00569062|PKI108574|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111227|NCT00569062|PKI108574|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111228|NCT00569062|PKI108574|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111229|NCT00568334|109705|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111230|NCT00568334|109705|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111231|NCT00568334|109705|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111232|NCT00568334|109705|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111233|NCT00568334|109705|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111234|NCT00568334|109705|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111235|NCT00566020|SCA106052|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111236|NCT00566020|SCA106052|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111237|NCT00566020|SCA106052|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111238|NCT00566020|SCA106052|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111239|NCT00562848|MOT107043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111240|NCT00562848|MOT107043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111241|NCT00562848|MOT107043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111242|NCT00562848|MOT107043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111243|NCT00562848|MOT107043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111244|NCT00562848|MOT107043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111245|NCT00562848|MOT107043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111246|NCT00560833||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06459&kw=P06459&tab=access|
111247|NCT00559468||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111248|NCT00557622|PIR109164|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111249|NCT00557622|PIR109164|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111250|NCT00557622|PIR109164|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111251|NCT00557622|PIR109164|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111252|NCT00555061|TOC106489|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111253|NCT00555061|TOC106489|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111254|NCT00555061|TOC106489|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111255|NCT00555061|TOC106489|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111256|NCT00555061|TOC106489|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111257|NCT00555061|TOC106489|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111258|NCT00555061|TOC106489|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111259|NCT00553397|SDY293|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY293|ImmPort study identifier is SDY293
111260|NCT00553397|SDY293|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY293|ImmPort study identifier is SDY293. The study protocol is available in the Design tab section.
111261|NCT00553397|SDY293|Study summary, -design, -demographics, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY293|ImmPort study identifier is SDY293
111262|NCT00552929||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111263|NCT00552617||CSr Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111264|NCT00552279|109179|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111265|NCT00552279|109179|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111266|NCT00552279|109179|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111267|NCT00552279|109179|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111268|NCT00552279|109179|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111269|NCT00552279|109179|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111270|NCT00552279|109179|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111271|NCT00552097||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111272|NCT00551876||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
111273|NCT00551564|DIX110434|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111274|NCT00551564|DIX110434|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111275|NCT00551564|DIX110434|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111276|NCT00551564|DIX110434|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111277|NCT00551564|DIX110434|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111278|NCT00551564|DIX110434|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111279|NCT00551564|DIX110434|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111280|NCT00551447||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111281|NCT00551317|LPL110077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111282|NCT00551317|LPL110077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111283|NCT00551317|LPL110077|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114449|NCT00090207||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111284|NCT00551317|LPL110077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111285|NCT00551317|LPL110077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111286|NCT00551317|LPL110077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111287|NCT00551317|LPL110077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111288|NCT00551213||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04721&kw=P04721&tab=access|
111289|NCT00550420|AVA102677|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111290|NCT00550420|AVA102677|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111291|NCT00550420|AVA102677|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111292|NCT00550420|AVA102677|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111293|NCT00550420|AVA102677|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111294|NCT00550420|AVA102677|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111295|NCT00550420|AVA102677|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111296|NCT00550407|SCA104779|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111297|NCT00550407|SCA104779|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111298|NCT00550407|SCA104779|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111299|NCT00550407|SCA104779|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111300|NCT00550225|MAB108115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111301|NCT00550225|MAB108115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111302|NCT00550225|MAB108115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111303|NCT00550225|MAB108115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111304|NCT00550225|MAB108115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111305|NCT00550225|MAB108115|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111306|NCT00550225|MAB108115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111307|NCT00549900|107336|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111308|NCT00549900|107336|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111309|NCT00549900|107336|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111310|NCT00549900|107336|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111311|NCT00549900|107336|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111312|NCT00549900|107336|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111313|NCT00549120|MAB104954|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111314|NCT00549120|MAB104954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111315|NCT00549120|MAB104954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111316|NCT00549120|MAB104954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111317|NCT00549120|MAB104954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111318|NCT00549120|MAB104954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111319|NCT00549120|MAB104954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111320|NCT00548496|CR9108914|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111321|NCT00548496|CR9108914|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111322|NCT00548496|CR9108914|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111323|NCT00548496|CR9108914|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111324|NCT00548496|CR9108914|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111325|NCT00548496|CR9108914|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111326|NCT00548496|CR9108914|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111327|NCT00548171|110804|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111328|NCT00548171|110804|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111329|NCT00548171|110804|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111330|NCT00548171|110804|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111331|NCT00548171|110804|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111332|NCT00548171|110804|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111333|NCT00548171|110804|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111334|NCT00547248|109509|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111335|NCT00547248|109509|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111336|NCT00547248|109509|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111337|NCT00547248|109509|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111338|NCT00547248|109509|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111339|NCT00547248|109509|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111340|NCT00547248|109509|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111341|NCT00546286||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111342|NCT00546078|109628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111343|NCT00546078|109628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111344|NCT00546078|109628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111345|NCT00546078|109628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111346|NCT00546078|109628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111347|NCT00546078|109628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111348|NCT00546078|109628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111349|NCT00545324||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111350|NCT00545025|110674|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111351|NCT00545025|110674|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111352|NCT00545025|110674|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111353|NCT00545025|110674|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111354|NCT00545025|110674|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111355|NCT00545025|110674|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111356|NCT00544271|263855/035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111357|NCT00544271|263855/035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111358|NCT00544271|263855/035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111359|NCT00544271|263855/035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111360|NCT00544271|263855/035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111361|NCT00544271|263855/035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111362|NCT00543543||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=V503-001&kw=V503-001&tab=access|
111363|NCT00542087||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111364|NCT00541970|110659|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111365|NCT00541970|110659|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111366|NCT00541970|110659|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111367|NCT00541970|110659|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111368|NCT00541970|110659|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111369|NCT00541970|110659|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111370|NCT00541970|110659|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111371|NCT00541697||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111372|NCT00541684||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111373|NCT00541463||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111374|NCT00540592|110847|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111375|NCT00540592|110847|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111376|NCT00540592|110847|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111377|NCT00540592|110847|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111378|NCT00540592|110847|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111379|NCT00540592|110847|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111380|NCT00540592|110847|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111381|NCT00540228|110794|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111382|NCT00540228|110794|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111383|NCT00540228|110794|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111384|NCT00540228|110794|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111385|NCT00540228|110794|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111386|NCT00540228|110794|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111387|NCT00539994|ALB110247|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111388|NCT00539994|ALB110247|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111389|NCT00539994|ALB110247|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111390|NCT00539994|ALB110247|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111391|NCT00539994|ALB110247|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111392|NCT00539994|ALB110247|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111393|NCT00539994|ALB110247|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111394|NCT00539825|AC6108697|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111395|NCT00539825|AC6108697|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111396|NCT00539825|AC6108697|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111397|NCT00539825|AC6108697|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111398|NCT00539825|AC6108697|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111399|NCT00539825|AC6108697|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111400|NCT00539825|AC6108697|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111401|NCT00539006|FFU105924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111402|NCT00539006|FFU105924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111403|NCT00539006|FFU105924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111404|NCT00539006|FFU105924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111405|NCT00539006|FFU105924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111406|NCT00539006|FFU105924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111407|NCT00539006|FFU105924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111408|NCT00538473|110223|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111409|NCT00538473|110223|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111410|NCT00538473|110223|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111411|NCT00538473|110223|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111412|NCT00538473|110223|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111413|NCT00538473|110223|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111414|NCT00538213|110263|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111415|NCT00538213|110263|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111416|NCT00538213|110263|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111417|NCT00538213|110263|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111418|NCT00538213|110263|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111419|NCT00538213|110263|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111420|NCT00538213|110263|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111421|NCT00538057|HZA105871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111422|NCT00538057|HZA105871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111423|NCT00538057|HZA105871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111424|NCT00538057|HZA105871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111425|NCT00538057|HZA105871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111426|NCT00538057|HZA105871|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111427|NCT00538057|HZA105871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111428|NCT00537719|GLP107030|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111429|NCT00537719|GLP107030|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111430|NCT00537719|GLP107030|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111431|NCT00537719|GLP107030|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111432|NCT00537719|GLP107030|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111433|NCT00537719|GLP107030|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111434|NCT00537719|GLP107030|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111435|NCT00537654|ARI109882|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111436|NCT00537654|ARI109882|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111437|NCT00537654|ARI109882|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111438|NCT00537654|ARI109882|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111439|NCT00537654|ARI109882|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111440|NCT00537654|ARI109882|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111441|NCT00537654|ARI109882|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111442|NCT00536835|PLK107427|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111443|NCT00536835|PLK107427|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111444|NCT00536835|PLK107427|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111445|NCT00536835|PLK107427|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111446|NCT00536835|PLK107427|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111447|NCT00536835|PLK107427|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111448|NCT00536835|PLK107427|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111449|NCT00535743||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111450|NCT00535288||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P06472&kw=P06472&tab=access|
111451|NCT00534638|106636|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111452|NCT00534638|106636|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111453|NCT00534638|106636|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111454|NCT00534638|106636|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111455|NCT00534638|106636|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111456|NCT00534638|106636|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111457|NCT00534638|106636|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111458|NCT00533676||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111459|NCT00533611||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111460|NCT00533507|109861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111461|NCT00533507|109861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111462|NCT00533507|109861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111463|NCT00533507|109861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111464|NCT00533507|109861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111465|NCT00533507|109861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111466|NCT00533507|109861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111467|NCT00533312||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111468|NCT00532298|110620|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111469|NCT00532298|110620|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111470|NCT00532298|110620|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111471|NCT00532298|110620|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111472|NCT00532298|110620|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111473|NCT00532298|110620|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111474|NCT00532298|110620|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111475|NCT00530790|107846|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111476|NCT00530790|107846|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111477|NCT00530790|107846|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111478|NCT00530790|107846|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111479|NCT00530309|GLP107865|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111480|NCT00530309|GLP107865|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111481|NCT00530309|GLP107865|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111482|NCT00530309|GLP107865|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111483|NCT00530309|GLP107865|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111484|NCT00530309|GLP107865|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111485|NCT00530309|GLP107865|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111486|NCT00529516|109821|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111487|NCT00529516|109821|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111488|NCT00529516|109821|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111489|NCT00529516|109821|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111490|NCT00529516|109821|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111491|NCT00529516|109821|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111492|NCT00529516|109821|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111493|NCT00527943||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04736&kw=P04736&tab=access|
111494|NCT00527566|PubMed ID: 20513524|Publication|http://www.ncbi.nlm.nih.gov/pubmed/20513524|"Mepolizumab as a steroid-sparing treatment option in patients with Churg-Strauss syndrome.~Kim S, Marigowda G, Oren E, Israel E, Wechsler ME. J Allergy Clin Immunol. 2010 Jun;125(6):1336-43. doi:10.1016/j.jaci.2010.03.028."
111495|NCT00526474||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04737&kw=P04737&tab=access|
111496|NCT00525889|SDY565|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY565|ImmPort study identifier is SDY565. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts available to the Public.
111497|NCT00525889|SDY565|Study protocol summary and -schematic, -design, -demographics, -lab tests, -mechanistic assays, and -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY565|ImmPort study identifier is SDY565. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts available to the Public.
111498|NCT00524576|108988|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111499|NCT00524576|108988|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111500|NCT00524576|108988|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111501|NCT00524576|108988|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111502|NCT00524576|108988|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111503|NCT00523913|AVD105720|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111504|NCT00523913|AVD105720|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111505|NCT00523913|AVD105720|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111506|NCT00523913|AVD105720|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111507|NCT00523913|AVD105720|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111508|NCT00523913|AVD105720|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111509|NCT00523913|AVD105720|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111510|NCT00522678|HZA102928|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111511|NCT00522678|HZA102928|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111512|NCT00522678|HZA102928|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111513|NCT00522678|HZA102928|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111514|NCT00522678|HZA102928|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114450|NCT00090168||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111515|NCT00522678|HZA102928|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111516|NCT00522678|HZA102928|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111517|NCT00520039||Study Protocol|http://www.jaoa.org/content/110/5/278.full.pdf+html|Steele KM, Viola J, Burns E, Carreiro JE. Brief report of a clinical trial on the duration of middle ear effusion in young children using a standardized osteopathic manipulative medicine protocol. J Am Osteopath Assoc. May 2010, Vol. 110, 278-284.
111518|NCT00520039||Clinical Study Report|http://www.jaoa.org/content/114/6/436.full.pdf+html|"Steele KM, Carreiro JE, Viola, JH, Conte, JA, Ridpath, LC. The effect of osteopathic manipulative medicine on middle ear effusion following acute otitis media in young children: a pilot study. J Am Osteopath Assoc June 2014, Vol. 114, 436-447"
111519|NCT00519649|110474|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111520|NCT00519649|110474|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111521|NCT00519649|110474|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111522|NCT00519649|110474|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111523|NCT00519649|110474|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111524|NCT00519649|110474|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111525|NCT00519649|110474|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111526|NCT00519636|FFU105927|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111527|NCT00519636|FFU105927|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111528|NCT00519636|FFU105927|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111529|NCT00519636|FFU105927|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111530|NCT00519636|FFU105927|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111531|NCT00519636|FFU105927|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111532|NCT00519636|FFU105927|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111533|NCT00519467|714703/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111534|NCT00519467|714703/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111535|NCT00519467|714703/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111536|NCT00519467|714703/003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111537|NCT00519467|714703/003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111538|NCT00519467|714703/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111539|NCT00519467|714703/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111540|NCT00519376|B2C110165|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111541|NCT00519376|B2C110165|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111542|NCT00519376|B2C110165|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111543|NCT00519376|B2C110165|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111544|NCT00519376|B2C110165|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111545|NCT00519376|B2C110165|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111546|NCT00519376|B2C110165|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111547|NCT00518336|109616 (Y7)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111548|NCT00518336|109616 (Y7)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111549|NCT00518336|109616 (Y7)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 109624 are summarised with studies 109616 and 109625 on the GSK Clinical Study Register.
111550|NCT00518336|109616 (Y7)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111551|NCT00518336|109616 (Y7)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111552|NCT00518336|109616 (Y7)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111553|NCT00518115|GLP110125|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111554|NCT00518115|GLP110125|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111555|NCT00518115|GLP110125|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111556|NCT00518115|GLP110125|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111557|NCT00518115|GLP110125|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111558|NCT00518115|GLP110125|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111559|NCT00518115|GLP110125|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111560|NCT00517634|HZA109912|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111561|NCT00517634|HZA109912|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111562|NCT00517634|HZA109912|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111563|NCT00517634|HZA109912|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111564|NCT00517634|HZA109912|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111565|NCT00517634|HZA109912|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111566|NCT00517634|HZA109912|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111567|NCT00517309||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111568|NCT00517010||Clinical Study Report|http://ovidsp.tx.ovid.com/sp-3.20.0b/ovidweb.cgi?QS2=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|Published data
111569|NCT00516139|LEP105972|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111570|NCT00516139|LEP105972|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111571|NCT00516139|LEP105972|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111572|NCT00516139|LEP105972|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111573|NCT00516139|LEP105972|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111574|NCT00516139|LEP105972|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111575|NCT00516139|LEP105972|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111576|NCT00515502|AC4108123|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111577|NCT00515502|AC4108123|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111578|NCT00515502|AC4108123|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111579|NCT00515502|AC4108123|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111580|NCT00515502|AC4108123|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111581|NCT00515502|AC4108123|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111582|NCT00515502|AC4108123|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111583|NCT00515099|START ITN028AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN028AIPUBLIC/Study%20Data/begin.view?|START ITN028AI is the Study Identifier in the Immune Tolerance Network (ITN) TrialShare Clinical Trials Research Portal
111584|NCT00515099|START ITN028AI|Study Protocol|https://www.itntrialshare.org/project/Studies/ITN028AIPUBLIC/Study%20Data/begin.view?pageId=study.PARTICIPANTS|START ITN028AI is the Study Identifier in the Immune Tolerance Network (ITN) TrialShare Clinical Trials Research Portal
111585|NCT00515099|START ITN028AI|Study overview, -data and reports, -manuscripts and abstracts, -availability of biospecimens, et al|https://www.itntrialshare.org/project/Studies/ITN028AIPUBLIC/Study%20Data/begin.view?|START ITN028AI is the Study Identifier in the Immune Tolerance Network (ITN) TrialShare Clinical Trials Research Portal
111586|NCT00514904|109495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111587|NCT00514904|109495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111588|NCT00514904|109495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111589|NCT00514904|109495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111590|NCT00514904|109495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111591|NCT00514904|109495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111592|NCT00514904|109495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111593|NCT00513409|110031|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111594|NCT00513409|110031|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111595|NCT00513409|110031|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111596|NCT00513409|110031|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111597|NCT00513409|110031|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111598|NCT00513409|110031|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111599|NCT00511823|NKV110483|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111600|NCT00511823|NKV110483|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111601|NCT00511823|NKV110483|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111602|NCT00511823|NKV110483|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111603|NCT00511823|NKV110483|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111604|NCT00511823|NKV110483|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111605|NCT00511823|NKV110483|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111606|NCT00510874|110028|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111607|NCT00510874|110028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111608|NCT00510874|110028|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111609|NCT00510874|110028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111610|NCT00510874|110028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111611|NCT00510874|110028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111612|NCT00510874|110028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111613|NCT00508365|CFD109701|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111614|NCT00508365|CFD109701|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111615|NCT00508365|CFD109701|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111616|NCT00508365|CFD109701|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111617|NCT00508365|CFD109701|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111618|NCT00508365|CFD109701|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111619|NCT00508365|CFD109701|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111620|NCT00508261|109835|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111621|NCT00508261|109835|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114451|NCT00090155||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111622|NCT00508261|109835|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111623|NCT00508261|109835|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111624|NCT00508261|109835|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111625|NCT00508261|109835|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111626|NCT00508261|109835|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111627|NCT00506350|109817|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111628|NCT00506350|109817|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111629|NCT00506350|109817|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111630|NCT00506350|109817|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111631|NCT00506350|109817|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111632|NCT00506350|109817|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111633|NCT00506350|109817|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111634|NCT00505453|110502|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111635|NCT00505453|110502|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111636|NCT00505453|110502|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111637|NCT00505453|110502|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111638|NCT00505453|110502|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111639|NCT00505453|110502|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111640|NCT00505453|110502|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111641|NCT00503009|HZA109895|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111642|NCT00503009|HZA109895|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111643|NCT00503009|HZA109895|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111644|NCT00503009|HZA109895|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111645|NCT00503009|HZA109895|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111646|NCT00503009|HZA109895|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111647|NCT00502775|FFU109047|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111648|NCT00502775|FFU109047|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111649|NCT00502775|FFU109047|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111650|NCT00502775|FFU109047|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111651|NCT00502775|FFU109047|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111652|NCT00502775|FFU109047|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111653|NCT00502775|FFU109047|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111654|NCT00502593|107066|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111655|NCT00502593|107066|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study are summarised with studies 108498 (second cohort study) and 108500 (third cohort study) on the GSK Clinical Study Register.
111656|NCT00502593|107066|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111657|NCT00502593|107066|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111658|NCT00502593|107066|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111659|NCT00502593|107066|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111660|NCT00502593|107066|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111661|NCT00501020|49653/284|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111662|NCT00501020|49653/284|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111663|NCT00501020|49653/284|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111664|NCT00501020|49653/284|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111665|NCT00501020|49653/284|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111666|NCT00501020|49653/284|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111667|NCT00501020|49653/284|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111668|NCT00500955|BRL-49653/137|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111669|NCT00500955|BRL-49653/137|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111670|NCT00500955|BRL-49653/137|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111671|NCT00500955|BRL-49653/137|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111672|NCT00500955|BRL-49653/137|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111673|NCT00500955|BRL-49653/137|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111674|NCT00500461|AC2106213|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111675|NCT00500461|AC2106213|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111676|NCT00500461|AC2106213|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111677|NCT00500461|AC2106213|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111678|NCT00500461|AC2106213|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111679|NCT00500461|AC2106213|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111680|NCT00500461|AC2106213|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111681|NCT00500058|ILI105618|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111682|NCT00500058|ILI105618|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111683|NCT00500058|ILI105618|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111684|NCT00500058|ILI105618|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111685|NCT00500058|ILI105618|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111686|NCT00500058|ILI105618|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111687|NCT00500058|ILI105618|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111688|NCT00499707|712753/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111689|NCT00499707|712753/007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111690|NCT00499707|712753/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111691|NCT00499707|712753/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111692|NCT00499707|712753/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111693|NCT00499707|712753/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111694|NCT00499707|712753/007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111695|NCT00496327||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111696|NCT00496093||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111697|NCT00496015|107137|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111698|NCT00496015|107137|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111699|NCT00496015|107137|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111700|NCT00496015|107137|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111701|NCT00496015|107137|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111702|NCT00496015|107137|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111703|NCT00496015|107137|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111704|NCT00493818|AKT106757|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111705|NCT00493818|AKT106757|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111706|NCT00493818|AKT106757|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111707|NCT00493818|AKT106757|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111708|NCT00493818|AKT106757|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111709|NCT00493818|AKT106757|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111710|NCT00493818|AKT106757|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111711|NCT00492544|110168|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111712|NCT00492544|110168|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111713|NCT00492544|110168|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111714|NCT00492544|110168|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111715|NCT00492544|110168|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111716|NCT00492544|110168|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111717|NCT00492544|110168|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111718|NCT00490568|AVA102675|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111719|NCT00490568|AVA102675|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111720|NCT00490568|AVA102675|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111721|NCT00490568|AVA102675|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111722|NCT00490568|AVA102675|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111723|NCT00490568|AVA102675|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111724|NCT00490568|AVA102675|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111725|NCT00489554|109661|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111726|NCT00489554|109661|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111727|NCT00489554|109661|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111728|NCT00489554|109661|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111729|NCT00489554|109661|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111730|NCT00489554|109661|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111731|NCT00489346||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111732|NCT00489099||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111733|NCT00488514|TXA107977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111734|NCT00488514|TXA107977|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111735|NCT00488514|TXA107977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111736|NCT00488514|TXA107977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111737|NCT00488514|TXA107977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111738|NCT00488514|TXA107977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111739|NCT00488514|TXA107977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111740|NCT00485732|107291|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111741|NCT00485732|107291|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111742|NCT00485732|107291|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111743|NCT00485732|107291|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111744|NCT00485732|107291|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111745|NCT00485732|107291|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111746|NCT00485732|107291|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111747|NCT00483704||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-031&kw=0974-031&tab=access|
111748|NCT00482599||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111749|NCT00482079||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111750|NCT00481767|106069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111751|NCT00481767|106069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111752|NCT00481767|106069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111753|NCT00481767|106069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111754|NCT00481767|106069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111755|NCT00481767|106069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111756|NCT00481767|106069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111757|NCT00481702||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111758|NCT00481663||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111759|NCT00480805||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111760|NCT00480766||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
111761|NCT00480662||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111762|NCT00480324|107625|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111763|NCT00480324|107625|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111764|NCT00480324|107625|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111765|NCT00480324|107625|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111766|NCT00480324|107625|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111767|NCT00480324|107625|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111768|NCT00480324|107625|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111769|NCT00480025|109493|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111770|NCT00480025|109493|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111771|NCT00480025|109493|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111772|NCT00480025|109493|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111773|NCT00480025|109493|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111774|NCT00480025|109493|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111775|NCT00480025|109493|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111776|NCT00479882||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-063&kw=0524B-063&tab=access|
111777|NCT00479739|SAM40056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111778|NCT00479739|SAM40056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111779|NCT00479739|SAM40056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111780|NCT00479739|SAM40056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111781|NCT00479739|SAM40056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111782|NCT00479739|SAM40056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111783|NCT00479739|SAM40056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111784|NCT00478738|MAB104958|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111785|NCT00478738|MAB104958|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111786|NCT00478738|MAB104958|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111787|NCT00478738|MAB104958|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111788|NCT00478738|MAB104958|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111789|NCT00478738|MAB104958|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111790|NCT00478738|MAB104958|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111791|NCT00478621|109836|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111792|NCT00478621|109836|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111793|NCT00478621|109836|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111794|NCT00478621|109836|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111795|NCT00478621|109836|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111796|NCT00478621|109836|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111797|NCT00476307|110221|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111798|NCT00476307|110221|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111799|NCT00476307|110221|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111800|NCT00476307|110221|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111801|NCT00476307|110221|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111802|NCT00476307|110221|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111803|NCT00476307|110221|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111804|NCT00475436|AC4106889|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111805|NCT00475436|AC4106889|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111806|NCT00475436|AC4106889|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111807|NCT00475436|AC4106889|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111808|NCT00475436|AC4106889|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111809|NCT00475436|AC4106889|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111810|NCT00475436|AC4106889|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111811|NCT00475215||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111812|NCT00474617||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111813|NCT00474266|109670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111814|NCT00474266|109670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111815|NCT00474266|109670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111816|NCT00474266|109670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111817|NCT00474266|109670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111818|NCT00474266|109670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111819|NCT00474266|109670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111820|NCT00474253||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111821|NCT00473694||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111822|NCT00473668|104977|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111823|NCT00473668|104977|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111824|NCT00473668|104977|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111825|NCT00473668|104977|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111826|NCT00473668|104977|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111827|NCT00473668|104977|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111828|NCT00471237|CR9108963|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111829|NCT00471237|CR9108963|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111830|NCT00471237|CR9108963|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111831|NCT00471237|CR9108963|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111832|NCT00471237|CR9108963|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111833|NCT00471237|CR9108963|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111834|NCT00471237|CR9108963|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111835|NCT00471081|109375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111836|NCT00471081|109375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111837|NCT00471081|109375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111838|NCT00471081|109375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111839|NCT00471081|109375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111840|NCT00471081|109375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111841|NCT00471081|109375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111842|NCT00470834|AVO108943|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111843|NCT00470834|AVO108943|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111844|NCT00470834|AVO108943|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111845|NCT00470834|AVO108943|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111846|NCT00470834|AVO108943|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111847|NCT00470834|AVO108943|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111848|NCT00470834|AVO108943|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111849|NCT00470483|TMT106386|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111850|NCT00470483|TMT106386|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111851|NCT00470483|TMT106386|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111852|NCT00470483|TMT106386|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111853|NCT00470483|TMT106386|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111854|NCT00470483|TMT106386|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111855|NCT00469040|B2C108784|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111856|NCT00469040|B2C108784|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111857|NCT00469040|B2C108784|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111858|NCT00469040|B2C108784|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111859|NCT00469040|B2C108784|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111860|NCT00469040|B2C108784|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111861|NCT00469040|B2C108784|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111862|NCT00466947|109563|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111863|NCT00466947|109563|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111864|NCT00466947|109563|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111865|NCT00466947|109563|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111866|NCT00466947|109563|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111867|NCT00466947|109563|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111868|NCT00465816|109063|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111869|NCT00465816|109063|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111870|NCT00465816|109063|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111871|NCT00465816|109063|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111872|NCT00465816|109063|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111873|NCT00465816|109063|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111874|NCT00465816|109063|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111875|NCT00465595||Final Manuscript|http://journals.sagepub.com/doi/abs/10.1177/0269881116675513|Griffiths, R. R., Johnson, M. W., Carducci, M. A., Umbricht, A., Richards, W. A., Richards, B. D., Cosimano, M. P., & Klinedinst, M. A. (2016). Psilocybin produces substantial and sustained decreases in depression and anxiety in patients with life-threatening cancer: A randomized double-blind trial. Journal of Psychopharmacology, 30(12), 1181-1197.
111876|NCT00464815|109069|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111877|NCT00464815|109069|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111878|NCT00464815|109069|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111879|NCT00464815|109069|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111880|NCT00464815|109069|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111881|NCT00464815|109069|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111882|NCT00464815|109069|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111883|NCT00463697|B2C106996|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111884|NCT00463697|B2C106996|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111885|NCT00463697|B2C106996|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111886|NCT00463697|B2C106996|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111887|NCT00463697|B2C106996|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111888|NCT00463697|B2C106996|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111889|NCT00463697|B2C106996|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111890|NCT00463437|109507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111891|NCT00463437|109507|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111892|NCT00463437|109507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111893|NCT00463437|109507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111894|NCT00463437|109507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111895|NCT00463437|109507|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111896|NCT00463437|109507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111897|NCT00461097|SDY218|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY218|ImmPort study identifier is SDY218
111898|NCT00461097|SDY218|Study summary, -design, -adverse events, -demographics,-lab tests,-mechanistic assays, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY218|ImmPort study identifier is SDY218
111899|NCT00460707|NKV109990|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111900|NCT00460707|NKV109990|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111901|NCT00460707|NKV109990|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111902|NCT00460707|NKV109990|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111903|NCT00460707|NKV109990|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111904|NCT00460707|NKV109990|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111905|NCT00460707|NKV109990|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111906|NCT00460148|ROP109087|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111907|NCT00460148|ROP109087|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111908|NCT00460148|ROP109087|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111909|NCT00460148|ROP109087|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111910|NCT00460148|ROP109087|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111911|NCT00460148|ROP109087|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111912|NCT00460148|ROP109087|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111913|NCT00459550|106006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111914|NCT00459550|106006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111915|NCT00459550|106006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111916|NCT00459550|106006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111917|NCT00459550|106006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111918|NCT00459550|106006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111919|NCT00457275||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
111920|NCT00456807|109801|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111921|NCT00456807|109801|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111922|NCT00456807|109801|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111923|NCT00456807|109801|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111924|NCT00456807|109801|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111925|NCT00456807|109801|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111926|NCT00456625|108984|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111927|NCT00456625|108984|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111928|NCT00456625|108984|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111929|NCT00456625|108984|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111930|NCT00456625|108984|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111931|NCT00456625|108984|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111932|NCT00456625|108984|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111933|NCT00455572|107240|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111934|NCT00455572|107240|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111935|NCT00455572|107240|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111936|NCT00455572|107240|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111937|NCT00455572|107240|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111938|NCT00455572|107240|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111939|NCT00455572|107240|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111940|NCT00454987|109664|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111941|NCT00454987|109664|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111942|NCT00454987|109664|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111943|NCT00454987|109664|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111944|NCT00454987|109664|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111945|NCT00454909|109377|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111946|NCT00454909|109377|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111947|NCT00454909|109377|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111948|NCT00454909|109377|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111949|NCT00454909|109377|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111950|NCT00454909|109377|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111951|NCT00454909|109377|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111952|NCT00453986|109067|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111953|NCT00453986|109067|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111954|NCT00453986|109067|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111955|NCT00453986|109067|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111956|NCT00453986|109067|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111957|NCT00453986|109067|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111958|NCT00453986|109067|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111959|NCT00453687|AC2108380|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111960|NCT00453687|AC2108380|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111961|NCT00453687|AC2108380|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111962|NCT00453687|AC2108380|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111963|NCT00453687|AC2108380|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111964|NCT00453687|AC2108380|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111965|NCT00453687|AC2108380|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111966|NCT00453479|AC2108378|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111967|NCT00453479|AC2108378|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111968|NCT00453479|AC2108378|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111969|NCT00453479|AC2108378|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111970|NCT00453479|AC2108378|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111971|NCT00453479|AC2108378|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111972|NCT00453479|AC2108378|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111973|NCT00452699|ADA109055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111974|NCT00452699|ADA109055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111975|NCT00452699|ADA109055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111976|NCT00452699|ADA109055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111977|NCT00452699|ADA109055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111978|NCT00452699|ADA109055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111979|NCT00452699|ADA109055|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111980|NCT00452686|108638|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111981|NCT00452686|108638|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111982|NCT00452686|108638|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111983|NCT00452686|108638|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111984|NCT00452686|108638|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111985|NCT00452686|108638|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111986|NCT00452686|108638|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111987|NCT00452348|ADA109057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111988|NCT00452348|ADA109057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111989|NCT00452348|ADA109057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111990|NCT00452348|ADA109057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111991|NCT00452348|ADA109057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111992|NCT00452348|ADA109057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111993|NCT00452348|ADA109057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111994|NCT00451386||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
111995|NCT00451321|115493|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111996|NCT00451321|115493|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111997|NCT00451321|115493|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111998|NCT00451321|115493|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
111999|NCT00451321|115493|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112000|NCT00451321|115493|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112001|NCT00451321|115493|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112002|NCT00451217||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112003|NCT00451100||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112004|NCT00449774|LBI108617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112005|NCT00449774|LBI108617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112006|NCT00449774|LBI108617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112007|NCT00449774|LBI108617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112008|NCT00449774|LBI108617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112009|NCT00449774|LBI108617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112010|NCT00449774|LBI108617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112011|NCT00449670|109630|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112012|NCT00449670|109630|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112013|NCT00449670|109630|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112014|NCT00449670|109630|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112015|NCT00449670|109630|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112016|NCT00449670|109630|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112017|NCT00449670|109630|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112018|NCT00449111||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112019|NCT00447603||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0954A-327&kw=0954A-327&tab=access|
112020|NCT00447603||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112021|NCT00446186||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112022|NCT00446056||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112023|NCT00445107||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112024|NCT00445094||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112025|NCT00444899||Clinical Study Report|http://www.nrcresearchpress.com/doi/pdf/10.1139/h2012-025|
112026|NCT00444509|HZA108799|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112027|NCT00444509|HZA108799|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112028|NCT00444509|HZA108799|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112029|NCT00444509|HZA108799|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112030|NCT00444509|HZA108799|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112031|NCT00444509|HZA108799|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112032|NCT00444509|HZA108799|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112033|NCT00443209||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-012&kw=0974-012&tab=access|
112034|NCT00443131|107731|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112035|NCT00443131|107731|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112036|NCT00443131|107731|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112037|NCT00443131|107731|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112038|NCT00443131|107731|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112039|NCT00443131|107731|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112040|NCT00442936||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0974-011&kw=0974-011&tab=access|
112041|NCT00441701||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04592&kw=7123-012&tab=access|
112042|NCT00441441|SFA106484|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112043|NCT00441441|SFA106484|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112044|NCT00441441|SFA106484|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112045|NCT00441441|SFA106484|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112046|NCT00441441|SFA106484|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112047|NCT00441441|SFA106484|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112048|NCT00441441|SFA106484|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112049|NCT00440128|NKV100781|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112050|NCT00440128|NKV100781|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112051|NCT00440128|NKV100781|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112052|NCT00440128|NKV100781|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112053|NCT00440128|NKV100781|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112054|NCT00440128|NKV100781|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112055|NCT00440128|NKV100781|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112056|NCT00438022|Study ID is SDY4|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
112057|NCT00438022|Study ID is SDY4|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
112058|NCT00438022|Study ID is SDY4|Study details, -download packages, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY4|
112059|NCT00436007|106369|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112060|NCT00436007|106369|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112061|NCT00436007|106369|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112062|NCT00436007|106369|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112063|NCT00436007|106369|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112064|NCT00436007|106369|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112065|NCT00435461|FFU109045|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112066|NCT00435461|FFU109045|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112067|NCT00435461|FFU109045|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112068|NCT00435461|FFU109045|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112069|NCT00435461|FFU109045|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112070|NCT00435461|FFU109045|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112071|NCT00435045|OM9L|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112072|NCT00435045|OM9L|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112073|NCT00435045|OM9L|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112074|NCT00435045|OM9L|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112075|NCT00435045|OM9L|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112076|NCT00435045|OM9L|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112077|NCT00435045|OM9L|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112078|NCT00434993|ARDSNet-ALTA|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/alta/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
112079|NCT00434993||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/alta/|
112080|NCT00434993||Study Forms|http://biolincc.nhlbi.nih.gov/studies/alta/|
112081|NCT00434811|SDY1178|Study Protocol|http://www.immport.org/immport-open/public/home/studySearch|ImmPort study ID is SDY1178.
112082|NCT00434811|SDY1178|Complete set of descriptive data and results|http://www.immport.org/immport-open/public/home/studySearch|ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. This archive is in support of the NIH mission to share data with the public.
112083|NCT00434577|108494|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112084|NCT00434577|108494|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112085|NCT00434577|108494|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112086|NCT00434577|108494|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112087|NCT00434577|108494|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112088|NCT00434577|108494|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112089|NCT00434577|108494|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112090|NCT00432679|AVD105248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112091|NCT00432679|AVD105248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112092|NCT00432679|AVD105248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112093|NCT00432679|AVD105248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112094|NCT00432679|AVD105248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112095|NCT00432679|AVD105248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112096|NCT00432679|AVD105248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112097|NCT00432380|109216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112098|NCT00432380|109216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112099|NCT00432380|109216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112100|NCT00432380|109216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112101|NCT00432380|109216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112102|NCT00432380|109216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112103|NCT00432380|109216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112104|NCT00431431||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112105|NCT00430521|107495|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112106|NCT00430521|107495|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112107|NCT00430521|107495|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112108|NCT00430521|107495|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112109|NCT00430521|107495|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112110|NCT00430521|107495|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112111|NCT00430521|107495|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112112|NCT00429481|444563/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112113|NCT00429481|444563/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112114|NCT00429481|444563/007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112115|NCT00429481|444563/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112116|NCT00429481|444563/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112117|NCT00429481|444563/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112118|NCT00428090|105640|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112119|NCT00428090|105640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112120|NCT00428090|105640|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112121|NCT00428090|105640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112122|NCT00428090|105640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112123|NCT00428090|105640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112124|NCT00428090|105640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112125|NCT00427908|108658|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112126|NCT00427908|108658|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112127|NCT00427908|108658|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112128|NCT00427908|108658|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112129|NCT00427908|108658|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112130|NCT00427908|108658|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112131|NCT00427908|108658|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study is summarised with long term immunogenicity studies 108660 (year 1), 108661 (year 2), 108663 (year 3) and 108665 (year 4) on the GSK Cli
112132|NCT00426361|108464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112133|NCT00426361|108464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112134|NCT00426361|108464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112135|NCT00426361|108464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112136|NCT00426361|108464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112137|NCT00426361|108464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112138|NCT00426361|108464|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112139|NCT00425737|444563/004|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112140|NCT00425737|444563/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112141|NCT00425737|444563/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112142|NCT00425737|444563/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112143|NCT00425737|444563/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112144|NCT00425737|444563/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112145|NCT00424476|HGS1006-C1057|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112146|NCT00424476|HGS1006-C1057|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112147|NCT00424476|HGS1006-C1057|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112148|NCT00424476|HGS1006-C1057|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112149|NCT00424476|HGS1006-C1057|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112150|NCT00424476|HGS1006-C1057|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112151|NCT00424476|HGS1006-C1057|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112152|NCT00423995||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112153|NCT00423046|108933|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112154|NCT00423046|108933|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112155|NCT00423046|108933|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112156|NCT00423046|108933|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112157|NCT00423046|108933|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112158|NCT00423046|108933|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112159|NCT00423046|108933|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112160|NCT00422994|RRL103628|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112161|NCT00422994|RRL103628|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112162|NCT00422994|RRL103628|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112163|NCT00422994|RRL103628|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112164|NCT00422994|RRL103628|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112165|NCT00422994|RRL103628|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112166|NCT00422994|RRL103628|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112167|NCT00422955|49653/376|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112168|NCT00422955|49653/376|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112169|NCT00422955|49653/376|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112170|NCT00422955|49653/376|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112171|NCT00422955|49653/376|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112172|NCT00422955|49653/376|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112173|NCT00422955|49653/376|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112174|NCT00422604|AC2106956|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112175|NCT00422604|AC2106956|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112176|NCT00422604|AC2106956|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112177|NCT00422604|AC2106956|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112178|NCT00422604|AC2106956|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112179|NCT00422604|AC2106956|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112180|NCT00422604|AC2106956|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112181|NCT00421148||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112182|NCT00420745|106481|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112183|NCT00420745|106481|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112184|NCT00420745|106481|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112185|NCT00420745|106481|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112186|NCT00420745|106481|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112187|NCT00420745|106481|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112188|NCT00420745|106481|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112189|NCT00420680||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112190|NCT00420316|109810|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112191|NCT00420316|109810|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112192|NCT00420316|109810|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112193|NCT00420316|109810|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112194|NCT00420316|109810|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112195|NCT00420316|109810|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112196|NCT00420316|109810|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112197|NCT00419237|FFA10013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112198|NCT00419237|FFA10013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112199|NCT00419237|FFA10013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112200|NCT00419237|FFA10013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112201|NCT00419237|FFA10013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112202|NCT00419237|FFA10013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112203|NCT00419237|FFA10013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112204|NCT00413023|NKF100096|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112205|NCT00413023|NKF100096|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112206|NCT00413023|NKF100096|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112207|NCT00413023|NKF100096|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112208|NCT00413023|NKF100096|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112209|NCT00413023|NKF100096|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112210|NCT00413023|NKF100096|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112211|NCT00412854|104567|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112212|NCT00412854|104567|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112213|NCT00412854|104567|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112214|NCT00412854|104567|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112215|NCT00412854|104567|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112216|NCT00412854|104567|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112217|NCT00412854|104567|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112218|NCT00412191|LAM105379|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112219|NCT00412191|LAM105379|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112220|NCT00412191|LAM105379|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112221|NCT00412191|LAM105379|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112222|NCT00412191|LAM105379|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112223|NCT00412191|LAM105379|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112224|NCT00412191|LAM105379|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112225|NCT00411697|106789|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112226|NCT00411697|106789|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112227|NCT00411697|106789|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112228|NCT00411697|106789|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112229|NCT00411697|106789|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112230|NCT00411697|106789|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112231|NCT00411073|SB 480848/035|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112232|NCT00411073|SB 480848/035|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112233|NCT00411073|SB 480848/035|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112234|NCT00411073|SB 480848/035|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112235|NCT00411073|SB 480848/035|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112236|NCT00411073|SB 480848/035|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112237|NCT00411073|SB 480848/035|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112238|NCT00410384|HGS1006-C1056|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112239|NCT00410384|HGS1006-C1056|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112240|NCT00410384|HGS1006-C1056|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112241|NCT00410384|HGS1006-C1056|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112242|NCT00410384|HGS1006-C1056|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112243|NCT00410384|HGS1006-C1056|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112244|NCT00410384|HGS1006-C1056|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112245|NCT00410371|LBI108614|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112246|NCT00410371|LBI108614|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112247|NCT00410371|LBI108614|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112248|NCT00410371|LBI108614|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112249|NCT00410371|LBI108614|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112250|NCT00410371|LBI108614|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112251|NCT00410371|LBI108614|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112252|NCT00407979|SDY5|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY5|ImmPort study identifier is SDY5
112253|NCT00407979|SDY5|Study design, -schedule of events, -demographics, -adverse events, -interventions, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY5|ImmPort study identifier is SDY5
112254|NCT00407069|SDY10|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY10|ImmPort study identifier is SDY10.
112255|NCT00407069|SDY10|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY10|ImmPort study identifier is SDY10.
112256|NCT00407069|SDY10|Study design, -summary, -files; participant demographics, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY10|ImmPort study identifier is SDY10.
112257|NCT00406562|107924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112258|NCT00406562|107924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112259|NCT00406562|107924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112260|NCT00406562|107924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112261|NCT00406562|107924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112262|NCT00406562|107924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112263|NCT00406562|107924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112264|NCT00406211|208136/039|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112265|NCT00406211|208136/039|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112266|NCT00406211|208136/039|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112267|NCT00406211|208136/039|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112268|NCT00406211|208136/039|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112269|NCT00406211|208136/039|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112270|NCT00406081|SDY2|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY2|ImmPort study identifier is SDY2.
112271|NCT00406081|SDY2|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY2|ImmPort study identifier is SDY2.
112272|NCT00406081|SDY2|Study design, -schedule of events, -demographics, -adverse events, -interventions, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY2|ImmPort study identifier is SDY2.
112273|NCT00405080|NKV105091|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112274|NCT00405080|NKV105091|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112275|NCT00405080|NKV105091|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112276|NCT00405080|NKV105091|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112277|NCT00405080|NKV105091|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112278|NCT00405080|NKV105091|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112279|NCT00404768||Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112280|NCT00404768||Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112281|NCT00404768||Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112282|NCT00404768||Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112283|NCT00404768||Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112284|NCT00404768||Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112285|NCT00404768||Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112286|NCT00404378|NKV105093|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112287|NCT00404378|NKV105093|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112288|NCT00404378|NKV105093|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112289|NCT00404378|NKV105093|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112290|NCT00404378|NKV105093|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112291|NCT00404378|NKV105093|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112292|NCT00404378|NKV105093|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112293|NCT00404274|NKV105097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112294|NCT00404274|NKV105097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112295|NCT00404274|NKV105097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112296|NCT00404274|NKV105097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112297|NCT00404274|NKV105097|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112298|NCT00404274|NKV105097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112299|NCT00404274|NKV105097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112300|NCT00403962|NKP103401|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112301|NCT00403962|NKP103401|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112302|NCT00403962|NKP103401|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112303|NCT00403962|NKP103401|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112304|NCT00403962|NKP103401|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112305|NCT00403962|NKP103401|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112306|NCT00403962|NKP103401|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112307|NCT00402363|OM8 Afib|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112308|NCT00402363|OM8 Afib|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112309|NCT00402363|OM8 Afib|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112310|NCT00402363|OM8 Afib|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112311|NCT00402363|OM8 Afib|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112312|NCT00402363|OM8 Afib|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112313|NCT00402363|OM8 Afib|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112314|NCT00400855|SIG103337|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112315|NCT00400855|SIG103337|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112316|NCT00400855|SIG103337|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112317|NCT00400855|SIG103337|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112318|NCT00400855|SIG103337|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112319|NCT00400855|SIG103337|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112320|NCT00400855|SIG103337|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112321|NCT00400608|SAS105519|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112322|NCT00400608|SAS105519|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112323|NCT00400608|SAS105519|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112324|NCT00400608|SAS105519|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112325|NCT00400608|SAS105519|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112326|NCT00400608|SAS105519|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112327|NCT00400608|SAS105519|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112328|NCT00400478||Clinical Study Report|https://www.clinicaltrialsregister.eu/ctr-search/search;jsessionid=cJHnlkSBP30JjfQV2K-KXCK3mdjOE64o0FAsUcmzHmslzlaX5yhQ!675812678|
112329|NCT00400218||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112330|NCT00398645|FFA106783|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112331|NCT00398645|FFA106783|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112332|NCT00398645|FFA106783|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112333|NCT00398645|FFA106783|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112334|NCT00398645|FFA106783|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112335|NCT00398645|FFA106783|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112336|NCT00398645|FFA106783|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112337|NCT00398541||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112338|NCT00398294||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112339|NCT00398151||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112340|NCT00398099||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112341|NCT00397215|108251|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112342|NCT00397215|108251|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112343|NCT00397215|108251|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112344|NCT00397215|108251|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112345|NCT00397215|108251|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112346|NCT00397215|108251|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 108251 are summarised with studies 108252, 111275, and 111276 on the GSK Clinical Study Register.
112347|NCT00396630|106260|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112348|NCT00396630|106260|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112349|NCT00396630|106260|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112350|NCT00396630|106260|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112351|NCT00396630|106260|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112352|NCT00396630|106260|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112353|NCT00396630|106260|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112354|NCT00395603||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
112355|NCT00395408||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112356|NCT00394160||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112357|NCT00394069||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112358|NCT00394056|NKP106254|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112359|NCT00394056|NKP106254|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112360|NCT00394056|NKP106254|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112361|NCT00394056|NKP106254|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112362|NCT00394056|NKP106254|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112363|NCT00394056|NKP106254|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112364|NCT00394030|GLP107724|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112365|NCT00394030|GLP107724|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112366|NCT00394030|GLP107724|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112367|NCT00394030|GLP107724|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112368|NCT00394030|GLP107724|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112369|NCT00394030|GLP107724|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112370|NCT00394030|GLP107724|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112371|NCT00390910|107737|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112372|NCT00390910|107737|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112373|NCT00390910|107737|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112374|NCT00390910|107737|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112375|NCT00390910|107737|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112376|NCT00390910|107737|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112377|NCT00390910|107737|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112378|NCT00390260||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112379|NCT00390143|108595 Mth18|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112380|NCT00390143|108595 Mth18|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112381|NCT00390143|108595 Mth18|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112382|NCT00390143|108595 Mth18|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112383|NCT00390143|108595 Mth18|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112384|NCT00390143|108595 Mth18|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112385|NCT00390104||Kunkel lab newsletters|http://www.childrenshospital.org/research-and-innovation/research/labs/kunkel-laboratory|
112386|NCT00389987||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112387|NCT00389896||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112388|NCT00389740||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112389|NCT00388440|209762/147|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112390|NCT00388440|209762/147|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112391|NCT00388440|209762/147|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112392|NCT00388440|209762/147|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112393|NCT00388440|209762/147|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112394|NCT00387881|TXA107563|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112395|NCT00387881|TXA107563|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112396|NCT00387881|TXA107563|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112397|NCT00387881|TXA107563|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112398|NCT00387881|TXA107563|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112399|NCT00387881|TXA107563|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112400|NCT00387881|TXA107563|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112401|NCT00386698|104887|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112402|NCT00386698|104887|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112403|NCT00386698|104887|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112404|NCT00386698|104887|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112405|NCT00386698|104887|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112406|NCT00386698|104887|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112407|NCT00386100|AVT105913|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112408|NCT00386100|AVT105913|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112409|NCT00386100|AVT105913|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112410|NCT00386100|AVT105913|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112411|NCT00386100|AVT105913|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112412|NCT00386100|AVT105913|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112413|NCT00386100|AVT105913|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112414|NCT00385840|108708|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112415|NCT00385840|108708|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112416|NCT00385840|108708|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112417|NCT00385840|108708|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112418|NCT00385840|108708|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112419|NCT00385840|108708|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112420|NCT00385320|444563/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112421|NCT00385320|444563/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112422|NCT00385320|444563/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112423|NCT00385320|444563/006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112424|NCT00385320|444563/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112425|NCT00385320|444563/006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112426|NCT00385255|106323|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112427|NCT00385255|106323|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112428|NCT00385255|106323|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112429|NCT00385255|106323|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112430|NCT00385255|106323|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112431|NCT00385255|106323|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112432|NCT00385008|TRX105848|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112433|NCT00385008|TRX105848|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112434|NCT00385008|TRX105848|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112435|NCT00385008|TRX105848|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112436|NCT00385008|TRX105848|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112437|NCT00385008|TRX105848|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112438|NCT00385008|TRX105848|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112439|NCT00383903|444563/013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112440|NCT00383903|444563/013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112441|NCT00383903|444563/013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112442|NCT00383903|444563/013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112443|NCT00383903|444563/013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112444|NCT00383903|444563/013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112445|NCT00383227|208129/032|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112446|NCT00383227|208129/032|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112447|NCT00383227|208129/032|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112448|NCT00383227|208129/032|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112449|NCT00383227|208129/032|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112450|NCT00383227|208129/032|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112451|NCT00383162|TRX106571|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112452|NCT00383162|TRX106571|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112453|NCT00383162|TRX106571|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112454|NCT00383162|TRX106571|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112455|NCT00383162|TRX106571|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112456|NCT00383162|TRX106571|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112457|NCT00383162|TRX106571|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112458|NCT00383123|104858|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112459|NCT00383123|104858|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112460|NCT00383123|104858|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112461|NCT00383123|104858|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112462|NCT00383123|104858|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112463|NCT00383123|104858|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112464|NCT00383123|104858|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112465|NCT00382993|TRX106573|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112466|NCT00382993|TRX106573|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112467|NCT00382993|TRX106573|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112468|NCT00382993|TRX106573|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112469|NCT00382993|TRX106573|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112470|NCT00382993|TRX106573|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112471|NCT00382993|TRX106573|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112472|NCT00382772|107876|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112473|NCT00382772|107876|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112474|NCT00382772|107876|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112475|NCT00382772|107876|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112476|NCT00382772|107876|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112477|NCT00382772|107876|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112478|NCT00381667|B2C104604|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112479|NCT00381667|B2C104604|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112480|NCT00381667|B2C104604|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112481|NCT00381667|B2C104604|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112482|NCT00381667|B2C104604|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112483|NCT00381667|B2C104604|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112484|NCT00381667|B2C104604|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112485|NCT00381472|101468/169|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112486|NCT00381472|101468/169|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112487|NCT00381472|101468/169|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112488|NCT00381472|101468/169|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112489|NCT00381472|101468/169|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112490|NCT00381472|101468/169|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112491|NCT00381472|101468/169|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112492|NCT00381238|AVA104617|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112493|NCT00381238|AVA104617|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112494|NCT00381238|AVA104617|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112495|NCT00381238|AVA104617|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112496|NCT00381238|AVA104617|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112497|NCT00381238|AVA104617|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112498|NCT00381238|AVA104617|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112499|NCT00380705||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112500|NCT00380627||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112501|NCT00380393|106464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112502|NCT00380393|106464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112503|NCT00380393|106464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112504|NCT00380393|106464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112505|NCT00380393|106464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112506|NCT00380393|106464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112507|NCT00380211|IDB-200-001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112508|NCT00380211|IDB-200-001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112509|NCT00380211|IDB-200-001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112510|NCT00380211|IDB-200-001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112511|NCT00380211|IDB-200-001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112512|NCT00379977|106345|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112513|NCT00379977|106345|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112514|NCT00379977|106345|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112515|NCT00379977|106345|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112516|NCT00379977|106345|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112517|NCT00379977|106345|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112518|NCT00379964||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112519|NCT00379951||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112520|NCT00379769|BRL-049653/231|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112521|NCT00379769|BRL-049653/231|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112522|NCT00379769|BRL-049653/231|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112523|NCT00379769|BRL-049653/231|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112524|NCT00379769|BRL-049653/231|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112525|NCT00379769|BRL-049653/231|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112526|NCT00379769|BRL-049653/231|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112527|NCT00379613||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112528|NCT00379600|ARA102198|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112529|NCT00379600|ARA102198|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112530|NCT00379600|ARA102198|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112531|NCT00379600|ARA102198|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112532|NCT00379600|ARA102198|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112533|NCT00379600|ARA102198|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112534|NCT00379600|ARA102198|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112535|NCT00378833||CSR synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112536|NCT00377611|107564|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112537|NCT00377611|107564|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112538|NCT00377611|107564|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112539|NCT00377611|107564|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112540|NCT00377611|107564|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112541|NCT00377611|107564|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112542|NCT00377585|104888|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study104888 are summarised with study 107509 on the GSK Clinical Study Register.
112543|NCT00377585|104888|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112544|NCT00377585|104888|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112545|NCT00377585|104888|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112546|NCT00377585|104888|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112547|NCT00377585|104888|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112548|NCT00377572|SDY211|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY211|ImmPort study identifier is SDY211.
112549|NCT00377572|SDY211|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY211|ImmPort study identifier is SDY211.
112550|NCT00377572|SDY211|Study summary, -design, -adverse event(s), -interventions, -medications, -demographics, -study files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY211|ImmPort study identifier is SDY211.
112551|NCT00376779|106786|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112552|NCT00376779|106786|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112553|NCT00376779|106786|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112554|NCT00376779|106786|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112555|NCT00376779|106786|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112556|NCT00376779|106786|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112557|NCT00376714|AC2105333|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112558|NCT00376714|AC2105333|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112559|NCT00376714|AC2105333|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112560|NCT00376714|AC2105333|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112561|NCT00376714|AC2105333|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112562|NCT00376714|AC2105333|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112563|NCT00376714|AC2105333|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112564|NCT00376584||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112565|NCT00374842|108656|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112566|NCT00374842|108656|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112567|NCT00374842|108656|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112568|NCT00374842|108656|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112569|NCT00374842|108656|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112570|NCT00373542|RRL103660|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112571|NCT00373542|RRL103660|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112572|NCT00373542|RRL103660|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112573|NCT00373542|RRL103660|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112574|NCT00373542|RRL103660|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112575|NCT00373542|RRL103660|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112576|NCT00373542|RRL103660|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112577|NCT00372255|106252|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112578|NCT00372255|106252|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112579|NCT00372255|106252|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112580|NCT00372255|106252|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112581|NCT00372255|106252|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112582|NCT00372255|106252|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112583|NCT00372112|B2C108562|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112584|NCT00372112|B2C108562|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112585|NCT00372112|B2C108562|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112586|NCT00372112|B2C108562|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112587|NCT00372112|B2C108562|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112588|NCT00372112|B2C108562|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112589|NCT00372112|B2C108562|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112590|NCT00371735|CDA 714703/006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112591|NCT00371735|CDA 714703/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112592|NCT00371735|CDA 714703/006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112593|NCT00371735|CDA 714703/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112594|NCT00371735|CDA 714703/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112595|NCT00371735|CDA 714703/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112596|NCT00371735|CDA 714703/006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112597|NCT00371007||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112598|NCT00370591|SAM40104|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112599|NCT00370591|SAM40104|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112600|NCT00370591|SAM40104|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112601|NCT00370591|SAM40104|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112602|NCT00370591|SAM40104|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112603|NCT00370591|SAM40104|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112604|NCT00370591|SAM40104|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112605|NCT00370396|107046|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112606|NCT00370396|107046|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112607|NCT00370396|107046|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112608|NCT00370396|107046|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112609|NCT00370396|107046|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112610|NCT00370396|107046|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112611|NCT00370318|107017|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112612|NCT00370318|107017|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112613|NCT00370318|107017|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112614|NCT00370318|107017|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112615|NCT00370318|107017|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112616|NCT00370318|107017|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112617|NCT00370227|107706|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112618|NCT00370227|107706|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112619|NCT00370227|107706|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112620|NCT00370227|107706|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112621|NCT00370227|107706|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112622|NCT00370227|107706|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112623|NCT00370097|FAS106533|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112624|NCT00370097|FAS106533|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112625|NCT00370097|FAS106533|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112626|NCT00370097|FAS106533|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112627|NCT00370097|FAS106533|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112628|NCT00370097|FAS106533|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112629|NCT00370097|FAS106533|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112630|NCT00369993|SAS104449|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112631|NCT00369993|SAS104449|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112632|NCT00369993|SAS104449|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112633|NCT00369993|SAS104449|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112634|NCT00369993|SAS104449|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112635|NCT00369993|SAS104449|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112636|NCT00369993|SAS104449|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112637|NCT00369824|107682|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112638|NCT00369824|107682|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112639|NCT00369824|107682|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112640|NCT00369824|107682|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112641|NCT00369824|107682|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112642|NCT00369824|107682|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112643|NCT00368576|LPL107629|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112644|NCT00368576|LPL107629|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112645|NCT00368576|LPL107629|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112646|NCT00368576|LPL107629|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112647|NCT00368576|LPL107629|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112648|NCT00368576|LPL107629|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112649|NCT00368576|LPL107629|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112650|NCT00368199||Individual Participant Data Set|https://peerj.com/articles/2037/|
112651|NCT00366366|217744/075|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112652|NCT00366366|217744/075|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112653|NCT00366366|217744/075|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112654|NCT00366366|217744/075|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112655|NCT00366366|217744/075|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112656|NCT00366366|217744/075|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112657|NCT00364442|SAS10019|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112658|NCT00364442|SAS10019|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112659|NCT00364442|SAS10019|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112660|NCT00364442|SAS10019|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112661|NCT00364442|SAS10019|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112662|NCT00364442|SAS10019|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112663|NCT00364442|SAS10019|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112664|NCT00364273|B2F104300|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112665|NCT00364273|B2F104300|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112666|NCT00364273|B2F104300|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112667|NCT00364273|B2F104300|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112668|NCT00364273|B2F104300|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112669|NCT00364273|B2F104300|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112670|NCT00364273|B2F104300|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112671|NCT00363870|108134|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112672|NCT00363870|108134|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112673|NCT00363870|108134|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112674|NCT00363870|108134|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112675|NCT00363870|108134|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112676|NCT00363870|108134|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112677|NCT00363870|108134|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112678|NCT00363857|101468/249|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112679|NCT00363857|101468/249|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112680|NCT00363857|101468/249|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112681|NCT00363857|101468/249|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112682|NCT00363857|101468/249|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112683|NCT00363857|101468/249|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112684|NCT00363857|101468/249|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112685|NCT00363727|101468/228|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112686|NCT00363727|101468/228|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112687|NCT00363727|101468/228|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112688|NCT00363727|101468/228|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112689|NCT00363727|101468/228|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112690|NCT00363727|101468/228|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112691|NCT00363727|101468/228|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112692|NCT00363545|107077|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112693|NCT00363545|107077|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112694|NCT00363545|107077|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112695|NCT00363545|107077|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112696|NCT00363545|107077|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112697|NCT00363545|107077|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112698|NCT00363311|AVO105948|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112699|NCT00363311|AVO105948|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112700|NCT00363311|AVO105948|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112701|NCT00363311|AVO105948|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112702|NCT00363311|AVO105948|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112703|NCT00363311|AVO105948|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112704|NCT00363311|AVO105948|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112705|NCT00363077|107975|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112706|NCT00363077|107975|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112707|NCT00363077|107975|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112708|NCT00363077|107975|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112709|NCT00363077|107975|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112710|NCT00361959|SCO40036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112711|NCT00361959|SCO40036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112712|NCT00361959|SCO40036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112713|NCT00361959|SCO40036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112714|NCT00361959|SCO40036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112715|NCT00361959|SCO40036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112716|NCT00361959|SCO40036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112717|NCT00360230|106367|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112718|NCT00360230|106367|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112719|NCT00360230|106367|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112720|NCT00360230|106367|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112721|NCT00360230|106367|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112722|NCT00360230|106367|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112723|NCT00359983|107824|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112724|NCT00359983|107824|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112725|NCT00359983|107824|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112726|NCT00359983|107824|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112727|NCT00359983|107824|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112728|NCT00359983|107824|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112729|NCT00359619|108052 (FU month 18)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112730|NCT00359619|108052 (FU month 18)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112731|NCT00359619|108052 (FU month 18)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112732|NCT00359619|108052 (FU month 18)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112733|NCT00359619|108052 (FU month 18)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112734|NCT00359177|NKT102785|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112735|NCT00359177|NKT102785|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112736|NCT00359177|NKT102785|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112737|NCT00359177|NKT102785|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112738|NCT00359177|NKT102785|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112739|NCT00359177|NKT102785|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112740|NCT00359177|NKT102785|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112741|NCT00358813|NKT102783|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112742|NCT00358813|NKT102783|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112743|NCT00358813|NKT102783|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112744|NCT00358813|NKT102783|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112745|NCT00358813|NKT102783|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112746|NCT00358813|NKT102783|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112747|NCT00358813|NKT102783|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112748|NCT00358488|B2E106359|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112749|NCT00358488|B2E106359|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112750|NCT00358488|B2E106359|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112751|NCT00358488|B2E106359|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112752|NCT00358488|B2E106359|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112753|NCT00358488|B2E106359|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112754|NCT00358488|B2E106359|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112755|NCT00358449|MEE103219|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112756|NCT00358449|MEE103219|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112757|NCT00358449|MEE103219|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112758|NCT00358449|MEE103219|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112759|NCT00358449|MEE103219|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112760|NCT00358449|MEE103219|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112761|NCT00358449|MEE103219|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112762|NCT00358358|SCO104925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112763|NCT00358358|SCO104925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112764|NCT00358358|SCO104925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112765|NCT00358358|SCO104925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112766|NCT00358358|SCO104925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112767|NCT00358358|SCO104925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112768|NCT00358358|SCO104925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112769|NCT00356564|106744|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112770|NCT00356564|106744|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112771|NCT00356564|106744|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112772|NCT00356564|106744|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112773|NCT00356564|106744|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112774|NCT00356564|106744|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112775|NCT00356369|107386|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112776|NCT00356369|107386|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112777|NCT00356369|107386|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112778|NCT00356369|107386|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112779|NCT00356369|107386|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112780|NCT00356369|107386|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112781|NCT00355641|101468/206|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112782|NCT00355641|101468/206|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112783|NCT00355641|101468/206|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112784|NCT00355641|101468/206|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112785|NCT00355641|101468/206|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112786|NCT00355641|101468/206|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112787|NCT00355641|101468/206|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112788|NCT00355342|SCO40041|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112789|NCT00355342|SCO40041|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112790|NCT00355342|SCO40041|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112791|NCT00355342|SCO40041|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112792|NCT00355342|SCO40041|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112793|NCT00355342|SCO40041|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112794|NCT00355342|SCO40041|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112795|NCT00355082|LAM30055|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112796|NCT00355082|LAM30055|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112797|NCT00355082|LAM30055|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112798|NCT00355082|LAM30055|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112799|NCT00355082|LAM30055|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112800|NCT00355082|LAM30055|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112801|NCT00355082|LAM30055|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112802|NCT00354991||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112803|NCT00354965|AUG102821|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112804|NCT00354965|AUG102821|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112805|NCT00354965|AUG102821|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112806|NCT00354965|AUG102821|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112807|NCT00354965|AUG102821|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112808|NCT00354965|AUG102821|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112809|NCT00354874|B2C101762|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112810|NCT00354874|B2C101762|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112811|NCT00354874|B2C101762|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112812|NCT00354874|B2C101762|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112813|NCT00354874|B2C101762|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112814|NCT00354874|B2C101762|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112815|NCT00354874|B2C101762|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112816|NCT00354666|B2E101312|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112817|NCT00354666|B2E101312|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112818|NCT00354666|B2E101312|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112819|NCT00354666|B2E101312|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112820|NCT00354666|B2E101312|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112821|NCT00354536|GLP106073|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112822|NCT00354536|GLP106073|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112823|NCT00354536|GLP106073|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112824|NCT00354536|GLP106073|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112825|NCT00354536|GLP106073|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112826|NCT00354536|GLP106073|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112827|NCT00354536|GLP106073|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112828|NCT00353873|SAM104926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112829|NCT00353873|SAM104926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112830|NCT00353873|SAM104926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112831|NCT00353873|SAM104926|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112832|NCT00353873|SAM104926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112833|NCT00353873|SAM104926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112834|NCT00353873|SAM104926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112835|NCT00353288|105908|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112836|NCT00353288|105908|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112837|NCT00353288|105908|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112838|NCT00353288|105908|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112839|NCT00353288|105908|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112840|NCT00353288|105908|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112841|NCT00352963|217744/097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112842|NCT00352963|217744/097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112843|NCT00352963|217744/097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112844|NCT00352963|217744/097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112845|NCT00352963|217744/097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112846|NCT00352963|217744/097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112847|NCT00352898|105909|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112848|NCT00352898|105909|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112849|NCT00352898|105909|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112850|NCT00352898|105909|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112851|NCT00352898|105909|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112852|NCT00352898|105909|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112853|NCT00351702||published manuscript|http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0047400|the study has been published and has been provided in the citation. the paper conatins the required information regarding study results and conclusion
112854|NCT00348309|AVA102672|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112855|NCT00348309|AVA102672|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112856|NCT00348309|AVA102672|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112857|NCT00348309|AVA102672|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112858|NCT00348309|AVA102672|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112859|NCT00348309|AVA102672|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112860|NCT00348309|AVA102672|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112861|NCT00348140|AVA102670|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112862|NCT00348140|AVA102670|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112863|NCT00348140|AVA102670|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112864|NCT00348140|AVA102670|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112865|NCT00348140|AVA102670|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112866|NCT00348140|AVA102670|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112867|NCT00348140|AVA102670|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112868|NCT00347360|CFD105453|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112869|NCT00347360|CFD105453|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112870|NCT00347360|CFD105453|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112871|NCT00347360|CFD105453|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112872|NCT00347360|CFD105453|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112873|NCT00347360|CFD105453|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112874|NCT00347360|CFD105453|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112875|NCT00347139|B2C106093|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112876|NCT00347139|B2C106093|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112877|NCT00347139|B2C106093|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112878|NCT00347139|B2C106093|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112879|NCT00347139|B2C106093|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112880|NCT00347139|B2C106093|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112881|NCT00347139|B2C106093|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112882|NCT00346892|444563/014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112883|NCT00346892|444563/014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112884|NCT00346892|444563/014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112885|NCT00346892|444563/014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112886|NCT00346892|444563/014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112887|NCT00346892|444563/014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112888|NCT00346775|FFR105693|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112889|NCT00346775|FFR105693|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112890|NCT00346775|FFR105693|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112891|NCT00346775|FFR105693|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112892|NCT00346775|FFR105693|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112893|NCT00346775|FFR105693|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112894|NCT00346775|FFR105693|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112895|NCT00346749|ADC105931|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112896|NCT00346749|ADC105931|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112897|NCT00346749|ADC105931|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112898|NCT00346749|ADC105931|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112899|NCT00346749|ADC105931|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112900|NCT00346749|ADC105931|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112901|NCT00346398|SDY545|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY545|ImmPort study identifier is SDY545.
112902|NCT00346398|SDY545|Study summary, -design with synopsis, -adverse events, -assessment, -medications, -demographics, -lab tests, -files, et al.|http://www.itntrialshare.org/project/Studies/ITN025ADPUBLIC/Study%20Data/begin.view?|ImmPort study identifier is SDY545.
112903|NCT00346398|ITN025AD|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN025ADPUBLIC/Study%20Data/begin.view?|TrialShare is the ITN clinical trials research portal available to the public.
112904|NCT00346398|ITN025AD|Study overview with synopsis, -navigator, -schedule of events, -data and reports, biospecimens and availability.|http://www.itntrialshare.org/project/Studies/ITN025ADPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is ITN025AD.
112905|NCT00346151|SDY674|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY674|ImmPort study identifier is SDY674
112906|NCT00346151|SDY674|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY674|ImmPort study identifier is SDY674. The study protocol is available in the Design tab section.
112907|NCT00346151|SDY674|Study summary, -design, -synopsis,- medications, -demographics, -lab tests, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY674|ImmPort study identifier is SDY674
112908|NCT00346151|ITN023ST|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN023STPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available.
112909|NCT00346151|ITN023ST|Protocol synopsis, -data and reports, -specimens availability|http://www.itntrialshare.org/project/Studies/ITN023STPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available.
112910|NCT00346073|106316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112911|NCT00346073|106316|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112912|NCT00346073|106316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112913|NCT00346073|106316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112914|NCT00346073|106316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112915|NCT00346073|106316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112916|NCT00345956|105722|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112917|NCT00345956|105722|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112918|NCT00345956|105722|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112919|NCT00345956|105722|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112920|NCT00345956|105722|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112921|NCT00345956|105722|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112922|NCT00345904|107507|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112923|NCT00345904|107507|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112924|NCT00345904|107507|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112925|NCT00345904|107507|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112926|NCT00345904|107507|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112927|NCT00345878|105926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112928|NCT00345878|105926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112929|NCT00345878|105926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112930|NCT00345878|105926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112931|NCT00345878|105926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112932|NCT00345878|105926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112933|NCT00345683|105988|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112934|NCT00345683|105988|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112935|NCT00345683|105988|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112936|NCT00345683|105988|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112937|NCT00345683|105988|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112938|NCT00345683|105988|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112939|NCT00345683|105988|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112940|NCT00345579|105987|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112941|NCT00345579|105987|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112942|NCT00345579|105987|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112943|NCT00345579|105987|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112944|NCT00345579|105987|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112945|NCT00345579|105987|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112946|NCT00345358|107058|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112947|NCT00345358|107058|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112948|NCT00345358|107058|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112949|NCT00345358|107058|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112950|NCT00345358|107058|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112951|NCT00345358|107058|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112952|NCT00344513|105517/358|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112953|NCT00344513|105517/358|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112954|NCT00344513|105517/358|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112955|NCT00344513|105517/358|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112956|NCT00344318|107007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112957|NCT00344318|107007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112958|NCT00344318|107007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112959|NCT00344318|107007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112960|NCT00344318|107007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112961|NCT00344318|107007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112962|NCT00344032|104479|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112963|NCT00344032|104479|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112964|NCT00344032|104479|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112965|NCT00344032|104479|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112966|NCT00344032|104479|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112967|NCT00344032|104479|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112968|NCT00344006|CDA 714703/005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112969|NCT00344006|CDA 714703/005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112970|NCT00344006|CDA 714703/005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112971|NCT00344006|CDA 714703/005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112972|NCT00344006|CDA 714703/005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112973|NCT00344006|CDA 714703/005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112974|NCT00344006|CDA 714703/005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112975|NCT00343915|101695 Ext. Mth30|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112976|NCT00343915|101695 Ext. Mth30|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112977|NCT00343915|101695 Ext. Mth30|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112978|NCT00343915|101695 Ext. Mth30|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 101695 (Ext HBV-280 M30) are summarised with studies 103860/280 (HBV-280), 101696 (Ext HBV-280 M42), 101697 (Ext HBV-280 M54) and 101698
112979|NCT00343915|101695 Ext. Mth30|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112980|NCT00343707|NKP102280|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112981|NCT00343707|NKP102280|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112982|NCT00343707|NKP102280|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112983|NCT00343707|NKP102280|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112984|NCT00343707|NKP102280|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112985|NCT00343707|NKP102280|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112986|NCT00338351|106208|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112987|NCT00338351|106208|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112988|NCT00338351|106208|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112989|NCT00338351|106208|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112990|NCT00338351|106208|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112991|NCT00338351|106208|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112992|NCT00335881|106745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112993|NCT00335881|106745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112994|NCT00335881|106745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112995|NCT00335881|106745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112996|NCT00335881|106745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112997|NCT00335881|106745|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
112998|NCT00335075||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
112999|NCT00334607|107531|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113000|NCT00334607|107531|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113001|NCT00334607|107531|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113002|NCT00334607|107531|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113003|NCT00334607|107531|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113004|NCT00334607|107531|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113005|NCT00334334|107005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113006|NCT00334334|107005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113007|NCT00334334|107005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113008|NCT00334334|107005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113009|NCT00334334|107005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113010|NCT00334334|107005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113011|NCT00334152|NKT102552|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113012|NCT00334152|NKT102552|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113013|NCT00334152|NKT102552|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113014|NCT00334152|NKT102552|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113015|NCT00334152|NKT102552|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113016|NCT00334152|NKT102552|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113017|NCT00334152|NKT102552|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113018|NCT00333723|49653/143|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113019|NCT00333723|49653/143|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113020|NCT00333723|49653/143|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113021|NCT00333723|49653/143|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113022|NCT00333723|49653/143|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113023|NCT00333723|49653/143|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113024|NCT00333723|49653/143|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113025|NCT00333450|106623|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113026|NCT00333450|106623|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113027|NCT00333450|106623|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113028|NCT00333450|106623|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113029|NCT00333450|106623|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113030|NCT00333450|106623|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113031|NCT00332566|106602|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113032|NCT00332566|106602|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113033|NCT00332566|106602|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113034|NCT00332566|106602|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113035|NCT00332566|106602|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113036|NCT00332566|106602|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113037|NCT00330395||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113038|NCT00329784|SDY660|Individual Participant Data Set|https://immport.niaid.nih.gov/home|ImmPort study identifier is SDY660
113039|NCT00329784|SDY660|Study summary, -design, -adverse event(s), -demographics, -study files|https://immport.niaid.nih.gov/home|ImmPort study identifier is SDY660
113040|NCT00329784|LEAP (ITN032AD)|Individual Participant Data Set|https://www.itntrialshare.org/project/Studies/ITN032ADNEJM/Study%20Data/begin.view?pageId=study.PARTICIPANTS|TrialShare study identifier is LEAP (ITN032AD)
113041|NCT00329784|LEAP (ITN032AD)|Overview, Date & Reports, Manuscripts et al.|https://www.itntrialshare.org/project/Studies/ITN032ADNEJM/Study%20Data/begin.view?|TrialShare study identifier is LEAP (ITN032AD)
113042|NCT00329745|107070|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113043|NCT00329745|107070|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113044|NCT00329745|107070|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113045|NCT00329745|107070|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 107070 are summarised with studies 444563/028, 444563/029, 444563/030, 107072, and 107076 on the GSK Clinical Study Register.
113046|NCT00329745|107070|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113047|NCT00329745|107070|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113048|NCT00329602|ROR104836|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113049|NCT00329602|ROR104836|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113050|NCT00329602|ROR104836|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113051|NCT00329602|ROR104836|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113052|NCT00329602|ROR104836|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113053|NCT00329602|ROR104836|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113054|NCT00329602|ROR104836|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113055|NCT00329576|106640|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113056|NCT00329576|106640|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113057|NCT00329576|106640|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113058|NCT00329576|106640|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113059|NCT00329576|106640|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113060|NCT00329459|TRX105850|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113061|NCT00329459|TRX105850|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113062|NCT00329459|TRX105850|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113063|NCT00329459|TRX105850|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113064|NCT00329459|TRX105850|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113065|NCT00329459|TRX105850|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113066|NCT00329459|TRX105850|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113067|NCT00329355|TRX105852|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113068|NCT00329355|TRX105852|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113069|NCT00329355|TRX105852|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113070|NCT00329355|TRX105852|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113071|NCT00329355|TRX105852|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113072|NCT00329355|TRX105852|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113073|NCT00329355|TRX105852|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113074|NCT00329225|49653/347|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113075|NCT00329225|49653/347|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113076|NCT00329225|49653/347|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113077|NCT00329225|49653/347|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113078|NCT00329225|49653/347|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113079|NCT00329225|49653/347|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113080|NCT00328523||CSRSynopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113081|NCT00327665|106068|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113082|NCT00327665|106068|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113083|NCT00327665|106068|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113084|NCT00327665|106068|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113085|NCT00327665|106068|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113086|NCT00327665|106068|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113087|NCT00327184|106388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113088|NCT00327184|106388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113089|NCT00327184|106388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113090|NCT00327184|106388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113091|NCT00327184|106388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113092|NCT00327184|106388|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 106388 are summarised with study 106390 on the GSK Clinical Study Register.
113093|NCT00326248|NKT102553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113094|NCT00326248|NKT102553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113095|NCT00326248|NKT102553|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113096|NCT00326248|NKT102553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113097|NCT00326248|NKT102553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113098|NCT00326248|NKT102553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113099|NCT00326248|NKT102553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113100|NCT00326118|106445|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113101|NCT00326118|106445|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113102|NCT00326118|106445|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113103|NCT00326118|106445|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113104|NCT00326118|106445|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113105|NCT00326118|106445|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113106|NCT00325169|104962|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113107|NCT00325169|104962|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113108|NCT00325169|104962|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113109|NCT00325169|104962|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113110|NCT00325169|104962|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113111|NCT00325169|104962|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113112|NCT00325169|104962|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113113|NCT00325156|100917|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113114|NCT00325156|100917|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113115|NCT00325156|100917|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113116|NCT00325156|100917|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113117|NCT00325156|100917|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113118|NCT00325156|100917|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113119|NCT00325143|217744/100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113120|NCT00325143|217744/100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113121|NCT00325143|217744/100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113122|NCT00325143|217744/100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113123|NCT00325143|217744/100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113124|NCT00325143|217744/100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113125|NCT00323622|104297|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113126|NCT00323622|104297|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113127|NCT00323622|104297|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113128|NCT00323622|104297|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113129|NCT00323622|104297|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113130|NCT00323622|104297|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113131|NCT00323050|102547|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113132|NCT00323050|102547|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113133|NCT00323050|102547|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113134|NCT00323050|102547|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113135|NCT00323050|102547|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113136|NCT00323050|102547|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113137|NCT00322361||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113138|NCT00322335|106672|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113139|NCT00322335|106672|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113140|NCT00322335|106672|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 106672 are summarised with studies 106673, 106675, 106679, and 106680 on the GSK Clinical Study Register.
113141|NCT00322335|106672|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113142|NCT00322335|106672|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113143|NCT00322335|106672|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113144|NCT00321763|107192|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113145|NCT00321763|107192|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113146|NCT00321763|107192|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113147|NCT00321763|107192|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113148|NCT00321763|107192|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113149|NCT00321373|107022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113150|NCT00321373|107022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113151|NCT00321373|107022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113152|NCT00321373|107022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113153|NCT00321373|107022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113154|NCT00320606|SDY662:WISP-R ITN029ST|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY662|ImmPort study identifier is Study ID is SDY662:WISP-R ITN029ST
113155|NCT00320606|SDY662:WISP-R ITN029ST|Study summary, -schematic, -detailed description, -download packages et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY662|ImmPort study identifier is Study ID is SDY662:WISP-R ITN029ST
113156|NCT00320606|WISP-R ITN029ST|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN029STJAMA/Study%20Data/begin.view|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge. Creating an account for ITN TrialShare is free and allows for searching studies of interest.
113157|NCT00320606|WISP-R ITN029ST|Study protocol synopsis, -navigator, abstracts and manuscripts, datasets et al.|https://www.itntrialshare.org/project/Studies/ITN029STJAMA/Study%20Data/begin.view|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge. Creating an account for ITN TrialShare is free and allows for searching studies of interest.
113158|NCT00320463|105910|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113159|NCT00320463|105910|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113160|NCT00320463|105910|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113161|NCT00320463|105910|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113162|NCT00320463|105910|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113163|NCT00320463|105910|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113164|NCT00319995||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113165|NCT00319098|107064|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113166|NCT00319098|107064|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113167|NCT00319098|107064|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113168|NCT00319098|107064|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113169|NCT00319098|107064|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 107064 are summarised with study 107217 on the GSK Clinical Study Register.
113170|NCT00319098|107064|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113171|NCT00318630|104385|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113172|NCT00318630|104385|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113173|NCT00318630|104385|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113174|NCT00318630|104385|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113175|NCT00318630|104385|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113176|NCT00318630|104385|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113177|NCT00318630|104385|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113178|NCT00318149|104886|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113179|NCT00318149|104886|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113180|NCT00318149|104886|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113181|NCT00318149|104886|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113182|NCT00318149|104886|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113183|NCT00318149|104886|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113184|NCT00318058|104540|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113185|NCT00318058|104540|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113186|NCT00318058|104540|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113187|NCT00318058|104540|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113188|NCT00318058|104540|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113189|NCT00318058|104540|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113190|NCT00317174|759346/002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113191|NCT00317174|759346/002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113192|NCT00317174|759346/002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113193|NCT00317174|759346/002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113194|NCT00317174|759346/002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113195|NCT00317174|759346/002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113196|NCT00317161|100480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113197|NCT00317161|100480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113198|NCT00317161|100480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113199|NCT00317161|100480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113200|NCT00317161|100480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113201|NCT00317161|100480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113202|NCT00317122|759346/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113203|NCT00317122|759346/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113204|NCT00317122|759346/007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113205|NCT00317122|759346/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113206|NCT00317122|759346/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113207|NCT00317122|759346/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113208|NCT00317109|104756|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113209|NCT00317109|104756|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113210|NCT00317109|104756|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113211|NCT00317109|104756|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113212|NCT00317109|104756|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113213|NCT00317109|104756|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113214|NCT00316693|104798|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113215|NCT00316693|104798|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113216|NCT00316693|104798|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113217|NCT00316693|104798|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113218|NCT00316693|104798|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113219|NCT00316693|104798|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113220|NCT00316680|104489|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113221|NCT00316680|104489|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113222|NCT00316680|104489|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113223|NCT00316680|104489|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113224|NCT00316680|104489|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113225|NCT00316680|104489|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113226|NCT00316147|104005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113227|NCT00316147|104005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113228|NCT00316147|104005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113229|NCT00316147|104005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113230|NCT00316147|104005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113231|NCT00316147|104005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113232|NCT00315744|102318|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113233|NCT00315744|102318|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113234|NCT00315744|102318|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113235|NCT00315744|102318|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113236|NCT00315744|102318|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113237|NCT00315744|102318|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113238|NCT00315731|393229/027|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113239|NCT00315731|393229/027|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113240|NCT00315731|393229/027|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113241|NCT00315731|393229/027|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113242|NCT00315731|393229/027|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113243|NCT00315731|393229/027|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113244|NCT00315731|393229/027|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113245|NCT00314860|101468/204|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113246|NCT00314860|101468/204|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113247|NCT00314860|101468/204|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113248|NCT00314860|101468/204|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113249|NCT00314860|101468/204|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113250|NCT00314860|101468/204|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113251|NCT00314860|101468/204|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113252|NCT00312013|FRX106365|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113253|NCT00312013|FRX106365|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113254|NCT00312013|FRX106365|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113255|NCT00312013|FRX106365|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113256|NCT00312013|FRX106365|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113257|NCT00312013|FRX106365|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113258|NCT00312013|FRX106365|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113259|NCT00311844||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113260|NCT00310388|VRX-RET-E22-304|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113261|NCT00310388|VRX-RET-E22-304|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113262|NCT00310388|VRX-RET-E22-304|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113263|NCT00310388|VRX-RET-E22-304|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113264|NCT00310388|VRX-RET-E22-304|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113265|NCT00310388|VRX-RET-E22-304|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113266|NCT00310388|VRX-RET-E22-304|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113267|NCT00309634|106750|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113268|NCT00309634|106750|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113269|NCT00309634|106750|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113270|NCT00309634|106750|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113271|NCT00309634|106750|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113272|NCT00309634|106750|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113273|NCT00309166|580299/011|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113274|NCT00309166|580299/011|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113275|NCT00309166|580299/011|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113276|NCT00309166|580299/011|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113277|NCT00309166|580299/011|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113278|NCT00309166|580299/011|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113279|NCT00307567|105555|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113280|NCT00307567|105555|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113281|NCT00307567|105555|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113282|NCT00307567|105555|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113283|NCT00307567|105555|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113284|NCT00307567|105555|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113285|NCT00307554|105553|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113286|NCT00307554|105553|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113287|NCT00307554|105553|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113288|NCT00307554|105553|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113289|NCT00307554|105553|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113290|NCT00307554|105553|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113291|NCT00307541|105554|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113292|NCT00307541|105554|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113293|NCT00307541|105554|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113294|NCT00307541|105554|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113295|NCT00307541|105554|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113296|NCT00307541|105554|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113297|NCT00307060||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113298|NCT00307034|105539|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113299|NCT00307034|105539|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113300|NCT00307034|105539|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113301|NCT00307034|105539|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113302|NCT00307034|105539|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113303|NCT00307034|105539|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113304|NCT00307021|105874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113305|NCT00307021|105874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113306|NCT00307021|105874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113307|NCT00307021|105874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113308|NCT00307021|105874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113309|NCT00307021|105874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113310|NCT00306995|102499|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113311|NCT00306995|102499|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113312|NCT00306995|102499|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113313|NCT00306995|102499|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113314|NCT00306995|102499|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113315|NCT00306982|106622|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113316|NCT00306982|106622|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113317|NCT00306982|106622|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113318|NCT00306982|106622|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113319|NCT00306982|106622|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113320|NCT00306982|106622|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113321|NCT00306943|104745|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113322|NCT00306943|104745|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113323|NCT00306943|104745|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113324|NCT00306943|104745|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113325|NCT00306943|104745|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113326|NCT00306696|49653/342|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113327|NCT00306696|49653/342|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113328|NCT00306696|49653/342|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113329|NCT00306696|49653/342|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113330|NCT00306696|49653/342|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113331|NCT00306696|49653/342|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113332|NCT00306696|49653/342|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113333|NCT00306644|49653/334|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113334|NCT00306644|49653/334|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113335|NCT00306644|49653/334|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113336|NCT00306644|49653/334|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113337|NCT00306644|49653/334|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113338|NCT00306644|49653/334|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113339|NCT00306644|49653/334|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113340|NCT00306293|VLX105832|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113341|NCT00306293|VLX105832|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113342|NCT00306293|VLX105832|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113343|NCT00306293|VLX105832|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113344|NCT00306293|VLX105832|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113345|NCT00306293|VLX105832|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113346|NCT00306293|VLX105832|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113347|NCT00306241|106001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113348|NCT00306241|106001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113349|NCT00306241|106001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113350|NCT00306241|106001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113351|NCT00306241|106001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113352|NCT00306241|106001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113353|NCT00302952|SDY473|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY473|ImmPort study identifier: SDY473. Participant level data is available.
113354|NCT00302952|SDY473|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY473|ImmPort study identifier: SDY473
113355|NCT00302952|SDY473|Study summary, -design, -adverse events, -medications, -demographics, -lab tests, -mechanistic assays, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY473|ImmPort study identifier: SDY473
113356|NCT00298831||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113357|NCT00298155||Paper with attached protocol and outcomes|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887479/|
113358|NCT00297206|HS210914|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113359|NCT00297206|HS210914|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113360|NCT00297206|HS210914|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113361|NCT00297206|HS210914|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113362|NCT00297206|HS210914|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113363|NCT00297206|HS210914|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113364|NCT00297206|HS210914|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113365|NCT00297063|AVD104742|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113366|NCT00297063|AVD104742|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113367|NCT00297063|AVD104742|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113368|NCT00297063|AVD104742|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113369|NCT00297063|AVD104742|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113370|NCT00297063|AVD104742|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113371|NCT00297063|AVD104742|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113372|NCT00296530|ADA103578|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113373|NCT00296530|ADA103578|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113374|NCT00296530|ADA103578|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113375|NCT00296530|ADA103578|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113376|NCT00296530|ADA103578|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113377|NCT00296530|ADA103578|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113378|NCT00296530|ADA103578|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113379|NCT00296491|ADA103575|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113380|NCT00296491|ADA103575|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113381|NCT00296491|ADA103575|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113382|NCT00296491|ADA103575|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113383|NCT00296491|ADA103575|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113384|NCT00296491|ADA103575|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113385|NCT00296491|ADA103575|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113386|NCT00296140||Clinical Study Report|https://link.springer.com/article/10.1007/s13142-011-0070-y|Publication: Damush TM, Ofner S, Yu Z, Nicholas G, Williams LS. Implementation of a stroke self-management program. Translational Behavioral Medicine 2011;1:561-572
113387|NCT00294047|104820|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113388|NCT00294047|104820|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113389|NCT00294047|104820|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113390|NCT00294047|104820|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113391|NCT00294047|104820|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113392|NCT00294047|104820|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113393|NCT00292071||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113394|NCT00291876|100571 (M138)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100571 are summarised with studies 100572, 100573, 100574, 100575, 110677, 110678, 110679, 110680, and 110681 on the GSK Clinical Study
113395|NCT00291876|100571 (M138)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113396|NCT00291876|100571 (M138)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113397|NCT00291876|100571 (M138)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113398|NCT00291876|100571 (M138)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113399|NCT00291876|100571 (M138)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113400|NCT00291343|105239 (mth24-30)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113401|NCT00291343|105239 (mth24-30)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113402|NCT00291343|105239 (mth24-30)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113403|NCT00291343|105239 (mth24-30)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113404|NCT00291343|105239 (mth24-30)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 105239 are summarised with study 105245 on the GSK Clinical Study Register.
113405|NCT00291343|105239 (mth24-30)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113406|NCT00290355|249553/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113407|NCT00290355|249553/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113408|NCT00290355|249553/004|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113409|NCT00290355|249553/004|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113410|NCT00290355|249553/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113411|NCT00290355|249553/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113412|NCT00290355|249553/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113413|NCT00290342|104871|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113414|NCT00290342|104871|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113415|NCT00290342|104871|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113416|NCT00290342|104871|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113417|NCT00290342|104871|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113418|NCT00290342|104871|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113419|NCT00290303|100478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113420|NCT00290303|100478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113421|NCT00290303|100478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113422|NCT00290303|100478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113423|NCT00290303|100478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113424|NCT00290303|100478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113425|NCT00290277|104951|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113426|NCT00290277|104951|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113427|NCT00290277|104951|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113428|NCT00290277|104951|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113429|NCT00290277|104951|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113430|NCT00290277|104951|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113431|NCT00290277|104951|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113432|NCT00289900||CSR Synopsis Link|http://www.merck.com/clinical-trials/study.html?id=0524B-024&kw=0524B-024&tab=access|
113433|NCT00289796|210602-002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113434|NCT00289796|210602-002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113435|NCT00289796|210602-002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113436|NCT00289796|210602-002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113437|NCT00289796|210602-002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113438|NCT00289796|210602-002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113439|NCT00289783|103813|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113440|NCT00289783|103813|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113441|NCT00289783|103813|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113442|NCT00289783|103813|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113443|NCT00289783|103813|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 103813 are summarised with study 105067 on the GSK Clinical Study Register.
113444|NCT00289770|100551 (EXT Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113445|NCT00289770|100551 (EXT Y11)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100551 are summarised with studies 100552, 100553, 100554, and 100555 on the GSK Clinical Study Register.
113446|NCT00289770|100551 (EXT Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113447|NCT00289770|100551 (EXT Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113448|NCT00289770|100551 (EXT Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113449|NCT00289757|100576 (Y11)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113450|NCT00289757|100576 (Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113451|NCT00289757|100576 (Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113452|NCT00289757|100576 (Y11)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100576 are summarised with studies 100577, 100578, 100579, 100580, 111028, 111029, 111030, 111031, and 111032 on the GSK Clinical Study
113453|NCT00289757|100576 (Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113454|NCT00289757|100576 (Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113455|NCT00289731|100382|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113456|NCT00289731|100382|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113457|NCT00289731|100382|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100382 are summarised with studies 100383, 100384, and 100385 on the GSK Clinical Study Register.
113458|NCT00289731|100382|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113459|NCT00289731|100382|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113460|NCT00289731|100382|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113461|NCT00289718|100556 (Y11)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113462|NCT00289718|100556 (Y11)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113463|NCT00289718|100556 (Y11)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113464|NCT00289718|100556 (Y11)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100556 are summarised with studies 100557, 100558, 100559, and 100560 on the GSK Clinical Study Register.
113465|NCT00289718|100556 (Y11)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113466|NCT00289198|FFR106080|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113467|NCT00289198|FFR106080|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113468|NCT00289198|FFR106080|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113469|NCT00289198|FFR106080|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113470|NCT00289198|FFR106080|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113471|NCT00289198|FFR106080|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113472|NCT00289198|FFR106080|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113473|NCT00289185|104298|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113474|NCT00289185|104298|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113475|NCT00289185|104298|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113476|NCT00289185|104298|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113477|NCT00289185|104298|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113478|NCT00289185|104298|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113479|NCT00289172|103792|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113480|NCT00289172|103792|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113481|NCT00289172|103792|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113482|NCT00289172|103792|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113483|NCT00289172|103792|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113484|NCT00289172|103792|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113485|NCT00288626|SDY549|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY549|Deidentified participant ID mapping to manuscript ID. ImmPort study identifier is SDY549.
113486|NCT00288626||Study summary, -design, -demographics, and -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY549|ImmPort study identifier is SDY549
113487|NCT00283712|SDY655|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY655|Participant level data and additional relevant materials are available to the public in the Immunology Database and Analysis Portal (ImmPort), a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. Data analysis tools are also available to researchers.
113488|NCT00283712|SDY655|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY655|ImmPort study identifier is SDY655
113489|NCT00283712|SDY655|Study summary, -design, -adverse event(s), -summary of participant assessments, -interventions, -medications, -demographics, -lab tests, -mechanistic Assays, -study files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY655|ImmPort study identifier is SDY655
113490|NCT00282386||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113491|NCT00282295|105753|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113492|NCT00282295|105753|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113493|NCT00282295|105753|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113494|NCT00282295|105753|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113495|NCT00282295|105753|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113496|NCT00282295|105753|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113497|NCT00279045|49653/048|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113498|NCT00279045|49653/048|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113499|NCT00279045|49653/048|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113500|NCT00279045|49653/048|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113501|NCT00279045|49653/048|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113502|NCT00279045|49653/048|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113503|NCT00279045|49653/048|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113504|NCT00279019|AC2103473|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113505|NCT00279019|AC2103473|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113506|NCT00279019|AC2103473|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113507|NCT00279019|AC2103473|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113508|NCT00279019|AC2103473|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113509|NCT00279019|AC2103473|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113510|NCT00279019|AC2103473|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113511|NCT00274703|MEE103226|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113512|NCT00274703|MEE103226|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113513|NCT00274703|MEE103226|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113514|NCT00274703|MEE103226|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113515|NCT00274703|MEE103226|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113516|NCT00274677|SCA100223|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113517|NCT00274677|SCA100223|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113518|NCT00274677|SCA100223|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113519|NCT00274677|SCA100223|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113520|NCT00274677|SCA100223|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113521|NCT00274677|SCA100223|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113522|NCT00274677|SCA100223|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113523|NCT00273052|COR103561|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113524|NCT00273052|COR103561|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113525|NCT00273052|COR103561|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113526|NCT00273052|COR103561|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113527|NCT00273052|COR103561|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113528|NCT00273052|COR103561|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113529|NCT00273052|COR103561|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113530|NCT00273039|NKF100110|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113531|NCT00273039|NKF100110|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113532|NCT00273039|NKF100110|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113533|NCT00273039|NKF100110|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113534|NCT00273039|NKF100110|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113535|NCT00273039|NKF100110|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113536|NCT00273039|NKF100110|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113537|NCT00269217||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
113538|NCT00269191||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113539|NCT00269048|LPL104884|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113540|NCT00269048|LPL104884|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113541|NCT00269048|LPL104884|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113542|NCT00269048|LPL104884|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113543|NCT00269048|LPL104884|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113544|NCT00269048|LPL104884|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113545|NCT00269048|LPL104884|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113546|NCT00268996|SB-480848/026|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113547|NCT00268996|SB-480848/026|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113548|NCT00268996|SB-480848/026|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113549|NCT00268996|SB-480848/026|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113550|NCT00268996|SB-480848/026|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113551|NCT00268996|SB-480848/026|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113552|NCT00268996|SB-480848/026|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113553|NCT00268983|393229/028|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113554|NCT00268983|393229/028|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113555|NCT00268983|393229/028|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113556|NCT00268983|393229/028|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113557|NCT00268983|393229/028|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113558|NCT00268983|393229/028|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113559|NCT00268983|393229/028|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113560|NCT00268216|SCO30003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113561|NCT00268216|SCO30003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113562|NCT00268216|SCO30003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113563|NCT00268216|SCO30003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113564|NCT00268216|SCO30003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113565|NCT00268216|SCO30003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113566|NCT00268216|SCO30003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113567|NCT00268203|BEX104545|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113568|NCT00268203|BEX104545|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113569|NCT00268203|BEX104545|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113570|NCT00268203|BEX104545|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113571|NCT00268177|SCO30005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113572|NCT00268177|SCO30005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113573|NCT00268177|SCO30005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113574|NCT00268177|SCO30005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113575|NCT00268177|SCO30005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113576|NCT00268177|SCO30005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113577|NCT00268177|SCO30005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113578|NCT00265941|NCT00265941|Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
113579|NCT00265148|BRL-49653/461|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113580|NCT00265148|BRL-49653/461|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113581|NCT00265148|BRL-49653/461|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113582|NCT00265148|BRL-49653/461|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113583|NCT00265148|BRL-49653/461|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113584|NCT00265148|BRL-49653/461|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113585|NCT00265148|BRL-49653/461|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113586|NCT00264667|ADG103440|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113587|NCT00264667|ADG103440|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113588|NCT00264667|ADG103440|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113589|NCT00264667|ADG103440|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113590|NCT00264667|ADG103440|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113591|NCT00264667|ADG103440|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113592|NCT00264667|ADG103440|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113593|NCT00264615|LEP103944|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113594|NCT00264615|LEP103944|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113595|NCT00264615|LEP103944|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113596|NCT00264615|LEP103944|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113597|NCT00264615|LEP103944|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113598|NCT00264615|LEP103944|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113599|NCT00264615|LEP103944|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113600|NCT00263692|213503/047|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113601|NCT00263692|213503/047|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113602|NCT00263692|213503/047|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113603|NCT00263692|213503/047|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113604|NCT00263692|213503/047|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113605|NCT00263692|213503/047|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113606|NCT00263679|100406/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113607|NCT00263679|100406/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113608|NCT00263679|100406/004|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113609|NCT00263679|100406/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113610|NCT00263679|100406/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113611|NCT00263679|100406/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113612|NCT00263666|444563/022|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113613|NCT00263666|444563/022|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113614|NCT00263666|444563/022|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113615|NCT00263666|444563/022|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113616|NCT00263666|444563/022|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113617|NCT00263666|444563/022|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113618|NCT00263653|103954|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113619|NCT00263653|103954|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113620|NCT00263653|103954|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113621|NCT00263653|103954|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113622|NCT00263653|103954|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113623|NCT00263653|103954|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113624|NCT00258700|103974 (primary study)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113625|NCT00258700|103974 (primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113626|NCT00258700|103974 (primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113627|NCT00258700|103974 (primary study)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113628|NCT00258700|103974 (primary study)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113629|NCT00258700|103974 (primary study)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113630|NCT00256893|ROF102100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113631|NCT00256893|ROF102100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113632|NCT00256893|ROF102100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113633|NCT00256893|ROF102100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113634|NCT00256893|ROF102100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113635|NCT00256893|ROF102100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113636|NCT00256893|ROF102100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113637|NCT00256867|AVS101946|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113638|NCT00256867|AVS101946|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113639|NCT00256867|AVS101946|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113640|NCT00256867|AVS101946|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113641|NCT00256867|AVS101946|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113642|NCT00256867|AVS101946|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113643|NCT00256867|AVS101946|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113644|NCT00256854|ROX104805|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113645|NCT00256854|ROX104805|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113646|NCT00256854|ROX104805|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113647|NCT00256854|ROX104805|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113648|NCT00256854|ROX104805|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113649|NCT00256854|ROX104805|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113650|NCT00256854|ROX104805|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113651|NCT00251576||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113652|NCT00250276|104772|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113653|NCT00250276|104772|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113654|NCT00250276|104772|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113655|NCT00250276|104772|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113656|NCT00250276|104772|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113657|NCT00250276|104772|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113658|NCT00250276|104772|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113659|NCT00241644|102248|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 102248 are summarised with study 111274 on the GSK Clinical Study Register.
113660|NCT00241644|102248|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113661|NCT00241644|102248|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113662|NCT00241644|102248|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113663|NCT00241644|102248|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113664|NCT00241644|102248|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113665|NCT00241644|102248|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113666|NCT00240994|SDY134|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY134|ImmPort study identifier is SDY134
113667|NCT00240994|SDY134|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY134|ImmPort study identifier is SDY134
113668|NCT00240994|SDY134|Study summary, - schedule of events, -download packages et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY134|ImmPort study identifier is SDY134
113669|NCT00240617|TRX103635|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113670|NCT00240617|TRX103635|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113671|NCT00240617|TRX103635|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113672|NCT00240617|TRX103635|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113673|NCT00240617|TRX103635|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113674|NCT00240617|TRX103635|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113675|NCT00240617|TRX103635|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113676|NCT00240539|100449|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113677|NCT00240539|100449|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113678|NCT00240539|100449|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113679|NCT00240539|100449|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113680|NCT00240539|100449|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113681|NCT00240526|100450|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113682|NCT00240526|100450|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113683|NCT00240526|100450|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113684|NCT00240526|100450|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113685|NCT00240526|100450|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113686|NCT00240526|100450|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113687|NCT00240500|100448|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113688|NCT00240500|100448|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113689|NCT00240500|100448|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113690|NCT00240500|100448|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113691|NCT00240500|100448|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113692|NCT00239720|ITN011AI/NPA01 is Study ID|Study overview, - synopsis, -navigator, -schedule of events, -available biospecimen(s) et al.|https://www.itntrialshare.org/project/Studies/ITN011AIPUBLIC/Study%20Data/begin.view?|TrialShare is the ITN clinical research portal that provides public access to study data.
113693|NCT00237484||CSR Synopsis|https://www.merck.com/clinical-trials/study.html?id=P04257&kw=NCT00237484&tab=access|
113694|NCT00235755|VRX-RET-E22-302|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113695|NCT00235755|VRX-RET-E22-302|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113696|NCT00235755|VRX-RET-E22-302|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113697|NCT00235755|VRX-RET-E22-302|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113698|NCT00235755|VRX-RET-E22-302|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113699|NCT00235755|VRX-RET-E22-302|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113700|NCT00235755|VRX-RET-E22-302|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113701|NCT00232596|VRX-RET-E22-301|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113702|NCT00232596|VRX-RET-E22-301|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113703|NCT00232596|VRX-RET-E22-301|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113704|NCT00232596|VRX-RET-E22-301|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113705|NCT00232596|VRX-RET-E22-301|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113706|NCT00232596|VRX-RET-E22-301|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113707|NCT00232596|VRX-RET-E22-301|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113708|NCT00231413|102115|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113709|NCT00231413|102115|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113710|NCT00231413|102115|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113711|NCT00231413|102115|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 102115 are summarised with studies 107919 and 108052 on the GSK Clinical Study Register.
113712|NCT00231413|102115|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113713|NCT00231413|102115|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113714|NCT00230243||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113715|NCT00229112||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113716|NCT00228917|103812|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113717|NCT00228917|103812|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 103812 are summarised with study 104727 on the GSK Clinical Study Register.
113718|NCT00228917|103812|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113719|NCT00228917|103812|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113720|NCT00228917|103812|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113721|NCT00228917|103812|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113722|NCT00227422|102394|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113723|NCT00227422|102394|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113724|NCT00227422|102394|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113725|NCT00227422|102394|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113726|NCT00227422|102394|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113727|NCT00227422|102394|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113728|NCT00226499|100388|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113729|NCT00226499|100388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113730|NCT00226499|100388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113731|NCT00226499|100388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113732|NCT00226499|100388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113733|NCT00226499|100388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113734|NCT00225862|100310|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113735|NCT00225862|100310|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113736|NCT00225862|100310|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113737|NCT00225862|100310|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113738|NCT00225862|100310|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113739|NCT00225862|100310|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113740|NCT00225862|100310|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113741|NCT00225823|FFR103184|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113742|NCT00225823|FFR103184|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113743|NCT00225823|FFR103184|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113744|NCT00225823|FFR103184|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113745|NCT00225823|FFR103184|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113746|NCT00225823|FFR103184|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113747|NCT00225823|FFR103184|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113748|NCT00224523|FFR104503|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113749|NCT00224523|FFR104503|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113750|NCT00224523|FFR104503|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113751|NCT00224523|FFR104503|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113752|NCT00224523|FFR104503|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113753|NCT00224523|FFR104503|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113754|NCT00224523|FFR104503|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113755|NCT00224484|208141/040|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113756|NCT00224484|208141/040|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113757|NCT00224484|208141/040|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113758|NCT00224484|208141/040|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113759|NCT00224484|208141/040|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113760|NCT00224484|208141/040|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113761|NCT00224471|208141/042|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113762|NCT00224471|208141/042|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113763|NCT00224471|208141/042|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113764|NCT00224471|208141/042|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113765|NCT00224471|208141/042|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113766|NCT00224471|208141/042|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113767|NCT00212836||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113768|NCT00212784||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113769|NCT00202878||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=P04103&kw=P04103&tab=access|
113770|NCT00202865||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113771|NCT00202852||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113772|NCT00197288|104437|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113773|NCT00197288|104437|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113774|NCT00197288|104437|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113775|NCT00197288|104437|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113776|NCT00197288|104437|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113777|NCT00197288|104437|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113778|NCT00197288|104437|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113779|NCT00197275|104733|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113780|NCT00197275|104733|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113781|NCT00197275|104733|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113782|NCT00197275|104733|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113783|NCT00197275|104733|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113784|NCT00197275|104733|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113785|NCT00197262|FFR104861|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113786|NCT00197262|FFR104861|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113787|NCT00197262|FFR104861|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113788|NCT00197262|FFR104861|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113789|NCT00197262|FFR104861|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113790|NCT00197262|FFR104861|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113791|NCT00197262|FFR104861|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113792|NCT00197249|270362/006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113793|NCT00197249|270362/006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113794|NCT00197249|270362/006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113795|NCT00197249|270362/006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113796|NCT00197249|270362/006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113797|NCT00197236|208109/232|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113798|NCT00197236|208109/232|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113799|NCT00197236|208109/232|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113800|NCT00197236|208109/232|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113801|NCT00197236|208109/232|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113802|NCT00197236|208109/232|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113803|NCT00197223|104438|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113804|NCT00197223|104438|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113805|NCT00197223|104438|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113806|NCT00197223|104438|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113807|NCT00197223|104438|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113808|NCT00197223|104438|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113809|NCT00197223|104438|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113810|NCT00197210|444563/028/029/030|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113811|NCT00197210|444563/028/029/030|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113812|NCT00197210|444563/028/029/030|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113813|NCT00197210|444563/028/029/030|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 444563/028 are summarised with studies 444563/029, 444563/030, 107070, 107072, and 107076 on the GSK Clinical Study Register.
113814|NCT00197210|444563/028/029/030|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113815|NCT00197210|444563/028/029/030|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113816|NCT00197184|208127/132 (EXT Y2)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113817|NCT00197184|208127/132 (EXT Y2)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113818|NCT00197184|208127/132 (EXT Y2)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113819|NCT00197184|208127/132 (EXT Y2)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113820|NCT00197184|208127/132 (EXT Y2)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113821|NCT00197184|208127/132 (EXT Y2)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 208127/132 are summarised with studies 208122/133, 208127/134 and 208127/137 on the GSK Clinical Study Register.
113822|NCT00197171|100386 (EXT Y5)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113823|NCT00197171|100386 (EXT Y5)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113824|NCT00197171|100386 (EXT Y5)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100386 are summarised with study 100387 on the GSK Clinical Study Register.
113825|NCT00197171|100386 (EXT Y5)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113826|NCT00197171|100386 (EXT Y5)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113827|NCT00197158|104387|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113828|NCT00197158|104387|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113829|NCT00197158|104387|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113830|NCT00197158|104387|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113831|NCT00197158|104387|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113832|NCT00197158|104387|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113833|NCT00197132|49653/375|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113834|NCT00197132|49653/375|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113835|NCT00197132|49653/375|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113836|NCT00197132|49653/375|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113837|NCT00197132|49653/375|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113838|NCT00197132|49653/375|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113839|NCT00197132|49653/375|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113840|NCT00197119|100566|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 100566 are summarised with studies 100567, 100568, 100569, and 100570 on the GSK Clinical Study Register.
113841|NCT00197119|100566|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113842|NCT00197119|100566|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113843|NCT00197119|100566|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113844|NCT00197119|100566|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113845|NCT00197119|100566|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113846|NCT00197080|101468/205|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113847|NCT00197080|101468/205|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113848|NCT00197080|101468/205|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113849|NCT00197080|101468/205|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113850|NCT00197080|101468/205|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113851|NCT00197080|101468/205|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113852|NCT00197080|101468/205|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113853|NCT00197041|257049/026|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113854|NCT00197041|257049/026|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113855|NCT00197041|257049/026|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113856|NCT00197041|257049/026|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113857|NCT00197041|257049/026|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113858|NCT00197041|257049/026|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113859|NCT00197041|257049/026|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113860|NCT00197028|103967|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113861|NCT00197028|103967|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113862|NCT00197028|103967|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113863|NCT00197028|103967|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113864|NCT00197028|103967|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113865|NCT00197028|103967|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113866|NCT00197015|208109/231|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113867|NCT00197015|208109/231|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113868|NCT00197015|208109/231|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113869|NCT00197015|208109/231|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113870|NCT00197015|208109/231|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113871|NCT00197015|208109/231|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113872|NCT00197002|208109/220|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113873|NCT00197002|208109/220|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113874|NCT00197002|208109/220|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113875|NCT00197002|208109/220|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113876|NCT00197002|208109/220|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113877|NCT00197002|208109/220|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113878|NCT00196989|ADG20001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113879|NCT00196989|ADG20001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113880|NCT00196989|ADG20001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113881|NCT00196989|ADG20001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113882|NCT00196989|ADG20001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113883|NCT00196989|ADG20001|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113884|NCT00196989|ADG20001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113885|NCT00196976|103533|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113886|NCT00196976|103533|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113887|NCT00196976|103533|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113888|NCT00196976|103533|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 103533 are summarised with study 103534 on the GSK Clinical Study Register.
113889|NCT00196976|103533|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113890|NCT00196976|103533|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113891|NCT00196963|103532|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113892|NCT00196963|103532|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113893|NCT00196963|103532|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113894|NCT00196963|103532|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113895|NCT00196963|103532|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113896|NCT00196950|134612/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113897|NCT00196950|134612/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113898|NCT00196950|134612/003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 134612/003 are summarised with studies 102252, 102253, and 102254 on the GSK Clinical Study Register.
113899|NCT00196950|134612/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113900|NCT00196950|134612/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113901|NCT00196950|134612/003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113902|NCT00196937|103514|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113903|NCT00196937|103514|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 103514 are summarised with studies 105880 and 105881 on the GSK Clinical Study Register.
113904|NCT00196937|103514|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113905|NCT00196937|103514|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113906|NCT00196937|103514|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113907|NCT00196937|103514|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113908|NCT00196937|103514|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113909|NCT00196924|580299/013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113910|NCT00196924|580299/013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113911|NCT00196924|580299/013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113912|NCT00196924|580299/013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 580299/013 are summarised with studies 104896 (M18), 104902 (M24), 104904 (M36) and 104918 (M48) on the GSK Clinical Study Register.
113913|NCT00196924|580299/013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113914|NCT00196924|580299/013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113915|NCT00196924|580299/013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113916|NCT00180700||Clinical Study Report|https://doi.org/10.1002/ch.297|Published the results in 2004 Hypnotizability and immunological response to psychological intervention in HIV
113917|NCT00169546|SAM40100|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113918|NCT00169546|SAM40100|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113919|NCT00169546|SAM40100|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113920|NCT00169546|SAM40100|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113921|NCT00169546|SAM40100|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113922|NCT00169546|SAM40100|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113923|NCT00169546|SAM40100|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113924|NCT00169494|580299/012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113925|NCT00169494|580299/012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113926|NCT00169494|580299/012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113927|NCT00169494|580299/012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113928|NCT00169494|580299/012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113929|NCT00169494|580299/012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113930|NCT00169494|580299/012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 580299/012 are summarised with studies 107476 (M18), 107477 (M24), and 107479 (M36) on the GSK Clinical Study Register.
113931|NCT00169481|103488|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113932|NCT00169481|103488|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113933|NCT00169481|103488|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113934|NCT00169481|103488|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113935|NCT00169481|103488|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113936|NCT00169455|103477|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113937|NCT00169455|103477|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113938|NCT00169455|103477|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113939|NCT00169455|103477|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113940|NCT00169455|103477|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113941|NCT00169455|103477|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113942|NCT00169442|104065|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113943|NCT00169442|104065|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113944|NCT00169442|104065|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113945|NCT00169442|104065|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113946|NCT00169442|104065|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113947|NCT00169442|104065|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113948|NCT00166530||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
113949|NCT00159796||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113950|NCT00159744||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113951|NCT00158860|HS2100275|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113952|NCT00158860|HS2100275|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113953|NCT00158860|HS2100275|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113954|NCT00158860|HS2100275|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113955|NCT00158860|HS2100275|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113956|NCT00158860|HS2100275|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113957|NCT00158860|HS2100275|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113958|NCT00158756|104021|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113959|NCT00158756|104021|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113960|NCT00158756|104021|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113961|NCT00158756|104021|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113962|NCT00158756|104021|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113963|NCT00158756|104021|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113964|NCT00157963||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113965|NCT00157937||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113966|NCT00157924||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113967|NCT00157911||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113968|NCT00157898||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113969|NCT00157872||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113970|NCT00156117||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113971|NCT00156104||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113972|NCT00151424||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
113973|NCT00148941|213503/048|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113974|NCT00148941|213503/048|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113975|NCT00148941|213503/048|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113976|NCT00148941|213503/048|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113977|NCT00148941|213503/048|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113978|NCT00148941|213503/048|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113979|NCT00144911|SCO40043|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113980|NCT00144911|SCO40043|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113981|NCT00144911|SCO40043|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113982|NCT00144911|SCO40043|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113983|NCT00144911|SCO40043|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113984|NCT00144911|SCO40043|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113985|NCT00144911|SCO40043|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113986|NCT00144872|LAM100118|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113987|NCT00144872|LAM100118|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113988|NCT00144872|LAM100118|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113989|NCT00144872|LAM100118|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113990|NCT00144872|LAM100118|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113991|NCT00144872|LAM100118|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113992|NCT00144872|LAM100118|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113993|NCT00144846|SB030002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113994|NCT00144846|SB030002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113995|NCT00144846|SB030002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113996|NCT00144846|SB030002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113997|NCT00144846|SB030002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113998|NCT00144846|SB030002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
113999|NCT00144846|SB030002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114000|NCT00143182||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114001|NCT00142558||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114002|NCT00141037|SDY132|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY132|ImmPort study identifier is SDY132
114003|NCT00141037|SDY132|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY132|ImmPort study identifier is SDY132
114004|NCT00141037|SDY132|Study summary, -design,-demographics, -mechanistic assays, -files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY132|ImmPort study identifier is SDY132
114005|NCT00140972||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114006|NCT00140959||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114007|NCT00140920||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114008|NCT00140907||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114009|NCT00140881||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114010|NCT00140738|100633|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114011|NCT00140738|100633|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114012|NCT00140738|100633|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114013|NCT00140738|100633|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114014|NCT00140738|100633|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114015|NCT00140738|100633|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114016|NCT00140712|101468/253|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114017|NCT00140712|101468/253|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114018|NCT00140712|101468/253|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114019|NCT00140712|101468/253|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114020|NCT00140712|101468/253|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114021|NCT00140712|101468/253|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114022|NCT00140712|101468/253|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114023|NCT00140686|102247/036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114024|NCT00140686|102247/036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114025|NCT00140686|102247/036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114026|NCT00140686|102247/036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114027|NCT00140686|102247/036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114028|NCT00140686|102247/036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114029|NCT00140686|102247/036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114030|NCT00140673|444563/023|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114031|NCT00140673|444563/023|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114032|NCT00140673|444563/023|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114033|NCT00140673|444563/023|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114034|NCT00140673|444563/023|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114035|NCT00140673|444563/023|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114036|NCT00140673|444563/023|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114037|NCT00139932||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114038|NCT00139815|103420|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114039|NCT00139815|103420|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114040|NCT00139815|103420|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114041|NCT00139815|103420|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114042|NCT00139815|103420|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114043|NCT00139815|103420|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114044|NCT00139815|103420|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114045|NCT00139347|444563/024|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114046|NCT00139347|444563/024|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114047|NCT00139347|444563/024|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114048|NCT00139347|444563/024|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114049|NCT00139347|444563/024|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114050|NCT00139347|444563/024|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114051|NCT00139347|444563/024|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114052|NCT00139334|103992|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114053|NCT00139334|103992|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114054|NCT00139334|103992|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114055|NCT00139334|103992|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114056|NCT00139334|103992|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114057|NCT00139334|103992|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114058|NCT00137930|104480|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114059|NCT00137930|104480|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114060|NCT00137930|104480|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114061|NCT00137930|104480|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114062|NCT00137930|104480|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114063|NCT00137930|104480|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114064|NCT00137917|710158/002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114065|NCT00137917|710158/002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114066|NCT00137917|710158/002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114067|NCT00137917|710158/002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114068|NCT00137917|710158/002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114069|NCT00136604|104727 (Booster - 15-24 mths)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114070|NCT00136604|104727 (Booster - 15-24 mths)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114071|NCT00136604|104727 (Booster - 15-24 mths)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114072|NCT00136604|104727 (Booster - 15-24 mths)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114073|NCT00136604|104727 (Booster - 15-24 mths)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114074|NCT00136604|104727 (Booster - 15-24 mths)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114075|NCT00135564|711202/008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114076|NCT00135564|711202/008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114077|NCT00135564|711202/008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114078|NCT00135564|711202/008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114079|NCT00135564|711202/008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114080|NCT00135564|711202/008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114081|NCT00135486|711202/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114082|NCT00135486|711202/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114083|NCT00135486|711202/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114084|NCT00135486|711202/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114085|NCT00135486|711202/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114086|NCT00135486|711202/001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114087|NCT00134732|103478|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114088|NCT00134732|103478|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114089|NCT00134732|103478|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114090|NCT00134732|103478|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114091|NCT00134732|103478|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114092|NCT00134732|103478|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114093|NCT00134719|102370 (primary study)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114094|NCT00134719|102370 (primary study)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114095|NCT00134719|102370 (primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114096|NCT00134719|102370 (primary study)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 102370 are summarised with study 102371 on the GSK Clinical Study Register.
114097|NCT00134719|102370 (primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114098|NCT00133874|TOC100224|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114099|NCT00133874|TOC100224|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114100|NCT00133874|TOC100224|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114101|NCT00133874|TOC100224|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114102|NCT00133874|TOC100224|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114103|NCT00133874|TOC100224|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114104|NCT00133874|TOC100224|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114105|NCT00133848|TOC103469|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114106|NCT00133848|TOC103469|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114107|NCT00133848|TOC103469|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114108|NCT00133848|TOC103469|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114109|NCT00133848|TOC103469|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114110|NCT00133848|TOC103469|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114111|NCT00133848|TOC103469|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114112|NCT00132912||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114113|NCT00132730||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0873-005&kw=0873-005&tab=access|
114114|NCT00132717||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114115|NCT00129259|SDY524|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY524|ImmPort study identifier is SDY524.
114116|NCT00129259|SDY524|Study summary, -design (and protocol synopsis), adverse events, medications, demographics, lab tests, study files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY524|ImmPort study identifier is SDY524.
114117|NCT00129259|AbaTE - ITN027AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN027AIDB/Study%20Data/begin.view|TrialShare is the Immune Tolerance Network (ITN) clinical trials research portal that makes data from their clinical trials publicly available without charge.
114118|NCT00129259|AbaTE-ITN027AI|Study overview and synopsis, -data and reports, -schedule of assessments, -participant flow diagram, -abstracts and manuscripts|http://www.itntrialshare.org/project/Studies/ITN027AIDB/Study%20Data/begin.view|TrialShare is the Immune Tolerance Network (ITN) clinical trials research portal that makes data from their clinical trials publicly available without charge.
114119|NCT00129129|101858|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114120|NCT00129129|101858|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114121|NCT00129129|101858|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114122|NCT00129129|101858|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 101858 are summarised with study 102015 on the GSK Clinical Study Register.
114123|NCT00129129|101858|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114124|NCT00129116|792014/003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114125|NCT00129116|792014/003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114126|NCT00129116|792014/003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114127|NCT00129116|792014/003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114128|NCT00129116|792014/003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114129|NCT00127855|792014/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114130|NCT00127855|792014/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114131|NCT00127855|792014/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114132|NCT00127855|792014/001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114133|NCT00127855|792014/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114134|NCT00127647||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114135|NCT00127179||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114136|NCT00127023|104389|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114137|NCT00127023|104389|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114138|NCT00127023|104389|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114139|NCT00127023|104389|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114140|NCT00127023|104389|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114141|NCT00127023|104389|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114142|NCT00127010|103388|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114143|NCT00127010|103388|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114144|NCT00127010|103388|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114145|NCT00127010|103388|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 103388 are summarised with followup study 104690 on the GSK Clinical Study Register.
114146|NCT00127010|103388|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114147|NCT00127010|103388|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114148|NCT00126997|104020|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114149|NCT00126997|104020|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114150|NCT00126997|104020|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114151|NCT00126997|104020|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114152|NCT00126997|104020|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114153|NCT00126997|104020|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114154|NCT00126984|104703 (Primary study)|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114155|NCT00126984|104703 (Primary study)|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114156|NCT00126984|104703 (Primary study)|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114157|NCT00126984|104703 (Primary study)|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114158|NCT00126984|104703 (Primary study)|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register. The results of this study 104703 are summarised with study 104704 on the GSK Clinical Study Register.
114159|NCT00126984|104703 (Primary study)|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114160|NCT00126945|104702|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114161|NCT00126945|104702|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114162|NCT00126945|104702|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114163|NCT00126945|104702|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114164|NCT00126945|104702|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114165|NCT00126945|104702|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114166|NCT00126451||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114167|NCT00123903|COR103560|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114168|NCT00123903|COR103560|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114169|NCT00123903|COR103560|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114170|NCT00123903|COR103560|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114171|NCT00123903|COR103560|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114172|NCT00123903|COR103560|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114173|NCT00123903|COR103560|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114174|NCT00122681|580299/008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114175|NCT00122681|580299/008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114176|NCT00122681|580299/008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114177|NCT00122681|580299/008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114178|NCT00122681|580299/008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114179|NCT00122681|580299/008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114180|NCT00122681|580299/008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114181|NCT00120848|580299/007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114182|NCT00120848|580299/007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114183|NCT00120848|580299/007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114184|NCT00120848|580299/007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114185|NCT00120848|580299/007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114186|NCT00120848|580299/007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114187|NCT00120848|580299/007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114188|NCT00120289|AIM-HIGH|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114189|NCT00120289|AIM-HIGH|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|
114190|NCT00120289|AIM-HIGH|Study forms|http://biolincc.nhlbi.nih.gov/studies/aimhigh/|
114191|NCT00119743|347414/010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114192|NCT00119743|347414/010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114193|NCT00119743|347414/010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114194|NCT00119743|347414/010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114195|NCT00119743|347414/010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114196|NCT00119743|347414/010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114197|NCT00118729|FFR101816|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114198|NCT00118729|FFR101816|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114199|NCT00118729|FFR101816|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114200|NCT00118729|FFR101816|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114201|NCT00118729|FFR101816|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114202|NCT00118729|FFR101816|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114203|NCT00118729|FFR101816|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114204|NCT00118716|SFA100314|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114205|NCT00118716|SFA100314|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114206|NCT00118716|SFA100314|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114207|NCT00118716|SFA100314|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114208|NCT00118716|SFA100314|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114209|NCT00118716|SFA100314|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114210|NCT00118703|FFR30007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114211|NCT00118703|FFR30007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114212|NCT00118703|FFR30007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114213|NCT00118703|FFR30007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114214|NCT00118703|FFR30007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114215|NCT00118703|FFR30007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114216|NCT00118703|FFR30007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114217|NCT00118690|SFA100316|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114218|NCT00118690|SFA100316|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114219|NCT00118690|SFA100316|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114220|NCT00118690|SFA100316|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114221|NCT00118690|SFA100316|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114222|NCT00117325|FFR30006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114223|NCT00117325|FFR30006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114224|NCT00117325|FFR30006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114225|NCT00117325|FFR30006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114226|NCT00117325|FFR30006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114227|NCT00117325|FFR30006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114228|NCT00117325|FFR30006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114229|NCT00116883|FFR100012|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114230|NCT00116883|FFR100012|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114231|NCT00116883|FFR100012|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114232|NCT00116883|FFR100012|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114233|NCT00116883|FFR100012|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114234|NCT00116883|FFR100012|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114235|NCT00116883|FFR100012|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114236|NCT00116844|VLX103596|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114237|NCT00116844|VLX103596|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114238|NCT00116844|VLX103596|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114239|NCT00116844|VLX103596|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114240|NCT00116844|VLX103596|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114241|NCT00116844|VLX103596|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114242|NCT00116844|VLX103596|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114243|NCT00116831|AVD100521|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114244|NCT00116831|AVD100521|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114245|NCT00116831|AVD100521|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114246|NCT00116831|AVD100521|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114247|NCT00116831|AVD100521|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114248|NCT00116831|AVD100521|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114249|NCT00116831|AVD100521|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114250|NCT00116818|FFR20002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114251|NCT00116818|FFR20002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114252|NCT00116818|FFR20002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114253|NCT00116818|FFR20002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114254|NCT00116818|FFR20002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114255|NCT00116818|FFR20002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114256|NCT00116818|FFR20002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114257|NCT00115622|FFR30003|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114258|NCT00115622|FFR30003|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114259|NCT00115622|FFR30003|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114260|NCT00115622|FFR30003|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114261|NCT00115622|FFR30003|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114262|NCT00115622|FFR30003|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114263|NCT00115622|FFR30003|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114264|NCT00115492|SCO100250|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114265|NCT00115492|SCO100250|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114266|NCT00115492|SCO100250|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114267|NCT00115492|SCO100250|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114268|NCT00115492|SCO100250|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114269|NCT00115492|SCO100250|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114270|NCT00115492|SCO100250|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114271|NCT00114413|SDY210|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY210|ImmPort study identifier is SDY210. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
114272|NCT00114413|SDY210|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY210|ImmPort study identifier is SDY210. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
114273|NCT00114413|SDY210|Study summary and schematic, -design, adverse event(s), -interventions,-medications, -demographics, and -files.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY210|ImmPort study identifier is SDY210. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
114274|NCT00113165|LAM100034|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114275|NCT00113165|LAM100034|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114276|NCT00113165|LAM100034|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114277|NCT00113165|LAM100034|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114278|NCT00113165|LAM100034|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114279|NCT00113165|LAM100034|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114280|NCT00113165|LAM100034|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114281|NCT00111891||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114282|NCT00111800|100925|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114283|NCT00111800|100925|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114284|NCT00111800|100925|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114285|NCT00111800|100925|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114286|NCT00111800|100925|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114287|NCT00111800|100925|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114288|NCT00111800|100925|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114289|NCT00111722||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114290|NCT00111709||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114291|NCT00110435||CSR Snyopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114292|NCT00109486|FFR101747|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114293|NCT00109486|FFR101747|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114294|NCT00109486|FFR101747|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114295|NCT00109486|FFR101747|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114296|NCT00109486|FFR101747|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114297|NCT00109486|FFR101747|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114298|NCT00109486|FFR101747|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114299|NCT00109330|776423/001|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114300|NCT00109330|776423/001|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114301|NCT00109330|776423/001|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114302|NCT00109330|776423/001|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114303|NCT00109330|776423/001|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114304|NCT00109330|776423/001|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114305|NCT00109278||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114306|NCT00109122||CSR Synopsiis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114307|NCT00109109||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114308|NCT00108914|FFR30008|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114309|NCT00108914|FFR30008|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114310|NCT00108914|FFR30008|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114311|NCT00108914|FFR30008|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114312|NCT00108914|FFR30008|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114313|NCT00108914|FFR30008|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114314|NCT00108914|FFR30008|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114315|NCT00108082|COR100216|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114316|NCT00108082|COR100216|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114317|NCT00108082|COR100216|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114318|NCT00108082|COR100216|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114319|NCT00108082|COR100216|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114320|NCT00108082|COR100216|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114321|NCT00108082|COR100216|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114322|NCT00107757|FFR100010|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114323|NCT00107757|FFR100010|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114324|NCT00107757|FFR100010|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114325|NCT00107757|FFR100010|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114326|NCT00107757|FFR100010|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114327|NCT00107757|FFR100010|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114328|NCT00107757|FFR100010|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114329|NCT00104416|LAM100036|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114330|NCT00104416|LAM100036|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114331|NCT00104416|LAM100036|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114332|NCT00104416|LAM100036|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114333|NCT00104416|LAM100036|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114334|NCT00104416|LAM100036|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114335|NCT00104416|LAM100036|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114336|NCT00104299|SDY91|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY91|ImmPort study identifier is SDY91.
114337|NCT00104299|SDY91|Study summary, -design, -adverse event(s), -summary of participant assessments, -interventions, -medications, -demographics, -lab tests, -mechanistic assays, -files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY91|ImmPort study identifier is SDY91.
114338|NCT00104299|ITN021AI|Individual Participant Data Set|https://www.itntrialshare.org/project/home/begin.view?|TrialShare study ID is ITN021AI.
114339|NCT00104299|ITN021AI|Study overview, -data and reports, -participant list, -manuscripts and abstracts, -availability of biospecimens.|https://www.itntrialshare.org/project/home/begin.view?|TrialShare study ID is ITN021AI.
114340|NCT00103922|CIL103657|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114341|NCT00103922|CIL103657|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114342|NCT00103922|CIL103657|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114343|NCT00103922|CIL103657|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114344|NCT00103922|CIL103657|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114345|NCT00103922|CIL103657|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114346|NCT00103857||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114347|NCT00103454|FFR30002|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114348|NCT00103454|FFR30002|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114349|NCT00103454|FFR30002|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114350|NCT00103454|FFR30002|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114351|NCT00103454|FFR30002|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114352|NCT00103454|FFR30002|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114353|NCT00103454|FFR30002|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114354|NCT00102882|SFA100062|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114355|NCT00102882|SFA100062|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114356|NCT00102882|SFA100062|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114357|NCT00102882|SFA100062|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114358|NCT00102882|SFA100062|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114359|NCT00102882|SFA100062|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114360|NCT00102882|SFA100062|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114361|NCT00102765|SFA103153|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114362|NCT00102765|SFA103153|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114363|NCT00102765|SFA103153|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114364|NCT00102765|SFA103153|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114365|NCT00102765|SFA103153|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114366|NCT00102765|SFA103153|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114367|NCT00102765|SFA103153|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114368|NCT00101829|SDY961|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY961|ImmPort study identifier is SDY961
114369|NCT00101829|SDY961|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY961|ImmPort study identifier is SDY961
114370|NCT00101829|SDY961|Study summary, -design, -adverse event(s), - assessments, -medications, -demographics, -files , -laboratory tests, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY961|ImmPort study identifier is SDY961
114371|NCT00101439||CSR Synopsis|http://www.merck.com/clinical-trials/study.html?id=0653-072&kw=0653-072&tab=access|
114372|NCT00097929||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
114373|NCT00097370|100901|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114374|NCT00097370|100901|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114375|NCT00097370|100901|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114376|NCT00097370|100901|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114377|NCT00097370|100901|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114378|NCT00097370|100901|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114379|NCT00097370|100901|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114380|NCT00097006|REDS II-CORE|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/core/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114381|NCT00097006|REDS II-CORE|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/core/|
114382|NCT00097006|REDS II-LAPS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/laps/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114383|NCT00097006|REDS II-LAPS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/laps/|
114384|NCT00097006|REDS II-LAPS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/laps/|
114385|NCT00097006|REDS II-LAPS|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/laps/|
114386|NCT00097006|REDS II-MS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/redsms/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114387|NCT00097006|REDS II-MS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/redsms/|
114388|NCT00097006|REDS II-MS|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/redsms/|
114389|NCT00097006|REDS II-RISE|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/rise/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114390|NCT00097006|REDS II-RISE|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/rise/|
114391|NCT00097006|REDS II-RISE|Study Forms|http://biolincc.nhlbi.nih.gov/studies/rise/|
114392|NCT00097006|REDS II-RISE|Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/rise/|
114393|NCT00095004||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114394|NCT00094380|SDY798|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY798|ImmPort study identifier is SDY798.
114395|NCT00094380|SDY798|Study protocol synopsis; -Study summary; -design; -adverse event; -Assessment; -Medications, -demographics; -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY798|ImmPort study identifier is SDY798.
114396|NCT00094380|ITN002AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN002AIPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.
114397|NCT00094380|ITN002AI|Informed Consent Form|http://www.itntrialshare.org/project/Studies/ITN002AIPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.
114398|NCT00094380|ITN002AI|Study synopsis, -schedule of events, -adverse events, et al.|http://www.itntrialshare.org/project/Studies/ITN002AIPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.
114399|NCT00094172|SDY547|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY547|ImmPort study identifier is SDY547. ImmPort is the long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts.
114400|NCT00094172|SDY547|Study summary, -design with synopsis, -adverse events, -medications, -demographics, -lab tests, -files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY547|ImmPort study identifier is SDY547
114401|NCT00094172|ITN020AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN020AIPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is ITN020AI
114402|NCT00094172|ITN020AI|Study overview with synopsis, -navigator, -schedule of assessments, data and reports, -manuscripts and abstracts et al.|http://www.itntrialshare.org/project/Studies/ITN020AIPUBLIC/Study%20Data/begin.view?|TrialShare is the research portal of the Immune Tolerance Network (ITN) that makes data from the consortium's studies publicly available.
114403|NCT00093899||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114404|NCT00092989||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114405|NCT00092963||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114406|NCT00092898||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114407|NCT00092885||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114408|NCT00092846||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114409|NCT00092833||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114410|NCT00092820||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114411|NCT00092807||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114412|NCT00092781||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114413|NCT00092768||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114414|NCT00092755||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114415|NCT00092729||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114416|NCT00092716||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114417|NCT00092703||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114418|NCT00092664||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114419|NCT00092651||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114420|NCT00092586||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114421|NCT00092573||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114422|NCT00092560||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114423|NCT00092638||CSR Synopsis link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114424|NCT00092625||CSR Snyopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114425|NCT00092612||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114426|NCT00092599||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114427|NCT00092482||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114428|NCT00092430||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114429|NCT00092404||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114430|NCT00092378||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114431|NCT00092365||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114432|NCT00092352||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114433|NCT00092339||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114434|NCT00092196||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114435|NCT00092183||CSR Snyopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114436|NCT00092170||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114437|NCT00092157||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114438|NCT00092144||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114439|NCT00092105||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114440|NCT00092092||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114441|NCT00092066||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114442|NCT00092040||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114443|NCT00092027||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114444|NCT00092014||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114445|NCT00091559||CSR Snyopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
114446|NCT00090298||CSR Snyopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114452|NCT00090194|SDY356|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY356|ImmPort study identifier is SDY356
114453|NCT00090194|SDY356|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY356|ImmPort study identifier is SDY356
114454|NCT00090194|SDY356|Study summary, -design, -demographics, -lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY356|ImmPort study identifier is SDY356
114455|NCT00090103|ARI40005|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114456|NCT00090103|ARI40005|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114457|NCT00090103|ARI40005|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114458|NCT00090103|ARI40005|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114459|NCT00090103|ARI40005|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114460|NCT00090103|ARI40005|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114461|NCT00090103|ARI40005|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114462|NCT00086593|101464|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114463|NCT00086593|101464|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114464|NCT00086593|101464|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114465|NCT00086593|101464|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114466|NCT00086593|101464|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114467|NCT00086593|101464|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114468|NCT00086515||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114469|NCT00083343||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114470|NCT00082537||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114471|NCT00082524||CSRSynopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114472|NCT00079911|100181|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114473|NCT00078195|SDY1|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1|ImmPort study identifier is SDY1
114474|NCT00078195|SDY1|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY1|ImmPort study identifier is SDY1
114475|NCT00078195|SDY1|Study design, -summary, -files, -interventions, participant schedule of events, -demographics, et al.|http://www.itntrialshare.org/project/Studies/ITN019ADPUBLIC/Study%20Data/begin.view?|ImmPort study identifier is SDY1
114476|NCT00078195|CASALE ITN019AD|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN019ADPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is CASALE ITN019AD
114477|NCT00078195|CASALE ITN019AD|Study protocol synopsis; -schedule of assessments; -data and reports; -specimens availability et al.|http://www.itntrialshare.org/project/Studies/ITN019ADPUBLIC/Study%20Data/begin.view?|TrialShare study identifier is CASALE ITN019AD
114478|NCT00076973||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114479|NCT00076934|SDY661|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY661|ImmPort study identifier is SDY661
114480|NCT00076934|SDY661|Study protocol synopsis, -summary, -design, -adverse events, -medications,-demographics, - lab tests, -files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY661|ImmPort study identifier is SDY661
114481|NCT00076934|ITN006AI/NMS02|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN006AIPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available.
114482|NCT00076934|ITN006AI/NMS02|Study protocol synopsis; -schedule of assessments; data and reports; adverse event(s); -specimens availability; -manuscripts and abstracts|http://www.itntrialshare.org/project/Studies/ITN006AIPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available.
114483|NCT00076856||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
114484|NCT00075829|BMT CTN-0102|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local Institutional Review Board (IRB) approval or certification of exemption from IRB review, and completion of a data use agreement.
114485|NCT00075829|BMT CTN-0102|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|
114486|NCT00075829|BMT CTN-0102|Study Forms|http://biolincc.nhlbi.nih.gov/studies/bmtctn0102/|
114487|NCT00071747|SCA30926|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114488|NCT00071747|SCA30926|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114489|NCT00071747|SCA30926|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114490|NCT00071747|SCA30926|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114491|NCT00071747|SCA30926|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114492|NCT00071747|SCA30926|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114493|NCT00064428|103413|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114494|NCT00064428|103413|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114495|NCT00064428|103413|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114496|NCT00064428|103413|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114497|NCT00064428|103413|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114498|NCT00064428|103413|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114499|NCT00064428|103413|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114500|NCT00070707||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114501|NCT00069836|712753/009|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114502|NCT00069836|712753/009|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114503|NCT00069836|712753/009|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114504|NCT00069836|712753/009|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114505|NCT00069836|712753/009|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114506|NCT00069836|712753/009|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114507|NCT00069836|712753/009|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114508|NCT00067951|712753/004|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114509|NCT00067951|712753/004|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114510|NCT00067951|712753/004|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114511|NCT00067951|712753/004|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114512|NCT00067951|712753/004|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114513|NCT00067951|712753/004|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114514|NCT00067951|712753/004|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114515|NCT00067938|SCA40917|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114516|NCT00067938|SCA40917|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114517|NCT00067938|SCA40917|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114518|NCT00067938|SCA40917|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114519|NCT00067938|SCA40917|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114520|NCT00067938|SCA40917|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114521|NCT00067444|29060/874|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114522|NCT00067444|29060/874|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114523|NCT00067444|29060/874|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114524|NCT00067444|29060/874|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114525|NCT00067444|29060/874|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114526|NCT00067444|29060/874|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114527|NCT00062790|ARI40014|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114528|NCT00062790|ARI40014|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114529|NCT00062790|ARI40014|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114530|NCT00062790|ARI40014|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114531|NCT00062790|ARI40014|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114532|NCT00062790|ARI40014|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114533|NCT00062790|ARI40014|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114534|NCT00060476||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114535|NCT00057499|SDY568|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY568|ImmPort study identifier is SDY568.
114536|NCT00057499|SDY568|Study summary, -schematic, -design, medications,-demographics, - lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY568|ImmPort study identifier is SDY568.
114537|NCT00057499|ITN012AI|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN012AIPUBLIC/Study%20Data/begin.view?|TrialShare is the Immune Tolerance Network (ITN) portal that makes data from the consortium's clinical trials publicly available without charge. Creating an account for ITN TrialShare is free and allows for searching studies of interest.
114538|NCT00057499|ITN012AI|Study protocol synopsis, -navigator, -schedule of events,-data &reports, -specimens et al.|http://www.itntrialshare.org/project/Studies/ITN012AIPUBLIC/Study%20Data/begin.view?|TrialShare is the Immune Tolerance Network (ITN) portal that makes data from the consortium's clinical trials publicly available without charge. Creating an account for ITN TrialShare is free and allows for searching studies of interest.
114539|NCT00056407|ARI40006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114540|NCT00056407|ARI40006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114541|NCT00056407|ARI40006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114542|NCT00056407|ARI40006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114543|NCT00056407|ARI40006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114544|NCT00056407|ARI40006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114545|NCT00056407|ARI40006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114546|NCT00056277|SCA30924|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114547|NCT00056277|SCA30924|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114548|NCT00056277|SCA30924|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114549|NCT00056277|SCA30924|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114550|NCT00056277|SCA30924|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114551|NCT00056277|SCA30924|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114552|NCT00056277|SCA30924|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114553|NCT00056134||Publication|https://www.ncbi.nlm.nih.gov/pubmed/23958949|"Denileukin diftitox (ONTAK) induces a tolerogenic phenotype in dendritic cells and stimulates survival of resting Treg.~Baur AS1, Lutz MB, Schierer S, Beltrame L, Theiner G, Zinser E, Ostalecki C, Heidkamp G, Haendle I, Erdmann M, Wiesinger M, Leisgang W, Gross S, Pommer AJ, Kämpgen E, Dudziak D, Steinkasserer A, Cavalieri D, Schuler-Thurner B, Schuler G."
114554|NCT00056134|DOI:10.1182/blood-2012-09-4569|Clinical Study Report|https://www.ncbi.nlm.nih.gov/pubmed/23958949|Denileukin diftitox (ONTAK) induces... Baur AS et al
114555|NCT00004124||Individual Participant Data Set|https://nctn-data-archive.nci.nih.gov/|Data Available: Select individual patient-level data from this trial can be requested from the NCTN/NCORP Data Archive.
114556|NCT00048607||CSR Synospis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114557|NCT00048594||CSR Synopsis Link|http://www.merck.com/clinical-trials/policies-perspectives.html|
114558|NCT00048204|NKD20006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114559|NCT00048204|NKD20006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114560|NCT00048204|NKD20006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114561|NCT00048204|NKD20006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114562|NCT00048204|NKD20006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114563|NCT00048204|NKD20006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114564|NCT00048204|NKD20006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114565|NCT00047983|SDY352|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY352|ImmPort study identifier is SDY352.
114566|NCT00047983|SDY352|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY352|ImmPort study identifier is SDY352.
114567|NCT00047983|SDY352|Study summary, -design, -demographics, -lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY352|ImmPort study identifier is SDY352.
114568|NCT00044486||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114569|NCT00044460|49653/326|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114570|NCT00044460|49653/326|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114571|NCT00044460|49653/326|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114572|NCT00044460|49653/326|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114573|NCT00044460|49653/326|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114574|NCT00044460|49653/326|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114575|NCT00044460|49653/326|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114576|NCT00044278|LAM20007|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114577|NCT00044278|LAM20007|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114578|NCT00044278|LAM20007|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114579|NCT00044278|LAM20007|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114580|NCT00044278|LAM20007|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114581|NCT00044278|LAM20007|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114582|NCT00044278|LAM20007|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114583|NCT00043914|LAM40013|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114584|NCT00043914|LAM40013|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114585|NCT00043914|LAM40013|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114586|NCT00043914|LAM40013|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114587|NCT00043914|LAM40013|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114588|NCT00043914|LAM40013|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114589|NCT00043914|LAM40013|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114590|NCT00043901|LAM40097|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114591|NCT00043901|LAM40097|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114592|NCT00043901|LAM40097|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114593|NCT00043901|LAM40097|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114594|NCT00043901|LAM40097|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114595|NCT00043901|LAM40097|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114596|NCT00043901|LAM40097|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114597|NCT00043875|LAM20006|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114598|NCT00043875|LAM20006|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114599|NCT00043875|LAM20006|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114600|NCT00043875|LAM20006|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114601|NCT00043875|LAM20006|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114602|NCT00043875|LAM20006|Annotated Case Report Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114603|NCT00043875|LAM20006|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114604|NCT00042029||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114605|NCT00039988|Study identifier is SDY471|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY471|
114606|NCT00039988|Study identifier is SDY471|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY471|
114607|NCT00039988|Study identifier is SDY471|Study summary, -design, -adverse events, -medications, -demographics, -lab tests, -mechanistic assays, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY471|
114608|NCT00038961|103414|Statistical Analysis Plan|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114609|NCT00038961|103414|Study Protocol|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114610|NCT00038961|103414|Individual Participant Data Set|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114611|NCT00038961|103414|Dataset Specification|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114612|NCT00038961|103414|Informed Consent Form|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114613|NCT00038961|103414|Clinical Study Report|https://www.clinicalstudydatarequest.com|For additional information about this study please refer to the GSK Clinical Study Register
114614|NCT00036491|SDY625|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY625|Participant level data and additional relevant materials are available to the public in the Immunology Database and Analysis Portal (ImmPort), a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts.
114615|NCT00036491|SDY625|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY625|ImmPort study identifier is SDY625.
114616|NCT00036491|SDY625|Study summary, -design, -adverse event(s), -summary of participant assessments, -interventions, -medications, -demographics, -lab tests, -study files, et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY625|ImmPort study identifier is SDY625.
114617|NCT00035360||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114618|NCT00035295||CSR Snyopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
114619|NCT00035048||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
114620|NCT00035009||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
114621|NCT00034944||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114622|NCT00034697||CSR Synopsis Links|http://www.merck.com/clinical-trials/policies-perspectives.html|
114623|NCT00034658||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114624|NCT00034645||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114625|NCT00034632||CSR Synopsis|http://www.merck.com/clinical-trials/policies-perspectives.html|
114626|NCT00023244|SDY133|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY133|ImmPort study identifier is SDY133
114627|NCT00023244|SDY133|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY133|ImmPort study identifier is SDY133
114628|NCT00023244|SDY133|Study summary, -design,-demographics, -files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY133|ImmPort study identifier is SDY133
114629|NCT00023231|SDY131|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY131|ImmPort study identifier is SDY131
114630|NCT00023231|SDY131|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY131|ImmPort study identifier is SDY131
114631|NCT00023231|SDY131|Study summary, -design,-demographics, -mechanistic assays, -files et al.|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY131|ImmPort study identifier is SDY131
114632|NCT00014911|SDY567|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY567|ImmPort study identifier is SDY567. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
114633|NCT00014911|SDY567|Study summary, -schematic, -design, -adverse event(s),-medications,-demographics, - lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY567|ImmPort study identifier is SDY567. ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts and is available to the Public.
114634|NCT00014911|ITN005CT|Individual Participant Data Set|http://www.itntrialshare.org/project/Studies/ITN005CTPUBLIC/Study%20Data/begin.view?|TrialShare is the Immune Tolerance Network (ITN) portal that makes data from the consortium's clinical trials publicly available without charge. Creating an account for ITN TrialShare is free and allows for searching studies of interest.
114635|NCT00014911|ITN005CT|Study overview & protocol synopsis, -navigator, -schedule of assessments, -data&reports, -specimens, etc.|http://www.itntrialshare.org/project/Studies/ITN005CTPUBLIC/Study%20Data/begin.view?|TrialShare is a clinical trials research portal developed by the Immune Tolerance Network (ITN) that makes data from the consortium's clinical trials publicly available without charge.
114636|NCT00005009|SDY357|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY357|ImmPort study identifier is SDY357.
114637|NCT00005009|SDY357|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY357|ImmPort study identifier is SDY357
114638|NCT00005009|SDY357|Study summary, -design, -demographics, -lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY357|ImmPort study identifier is SDY357
114639|NCT00000936|SDY354|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY354|ImmPort study identifier is SDY354.
114640|NCT00000936|SDY354|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY354|ImmPort study identifier is SDY354.
114641|NCT00000936|SDY354|Study summary, -design, -demographics, -lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY354|ImmPort study identifier is SDY354.
114642|NCT00000935|SDY355|Individual Participant Data Set|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY355|ImmPort study identifier is SDY355.
114643|NCT00000935|SDY355|Study Protocol|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY355|ImmPort study identifier is SDY355.
114644|NCT00000935|SDY355|Study summary, -design, -demographics, -lab tests, -study files|http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY355|ImmPort study identifier is SDY355.
114645|NCT00005739||Abstract|http://ajph.aphapublications.org/doi/pdf/10.2105/AJPH.86.8_Pt_1.1146|
114646|NCT00005541|HEIRS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/heirs/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114647|NCT00005541||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/heirs/|
114648|NCT00005541||Study Forms|http://biolincc.nhlbi.nih.gov/studies/heirs/|
114649|NCT00005541||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/heirs/|
114650|NCT00005479||NCBI website|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724776/|
114651|NCT00005306|NANB-TAH|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/NANB-TAH/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114652|NCT00005306||Study Forms|http://biolincc.nhlbi.nih.gov/studies/NANB-TAH/|
114653|NCT00005301|TSS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/tss/|Samples and characterization data. NHLBI provides controlled access to samples through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a materials use agreement.
114654|NCT00005300|CSSCD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/csscd/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114655|NCT00005300||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/csscd/|
114656|NCT00005300||Study Forms|http://biolincc.nhlbi.nih.gov/studies/csscd/|
114657|NCT00005292|AADR|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/aadr|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114658|NCT00005292||Study Forms|https://biolincc.nhlbi.nih.gov/studies/aadr/Forms/|
114659|NCT00005278|REDS-GSR/GLPR|Operations Manual|http://biolincc.nhlbi.nih.gov/studies/gsrglpr/|Samples and characterization data. NHLBI provides controlled access to samples through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a materials use agreement.
114660|NCT00005278|REDS-HTLV|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/reds/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114661|NCT00005278|REDS-HTLV|Study Forms|http://biolincc.nhlbi.nih.gov/studies/reds/|
114662|NCT00005278|REDS-RADAR|Operations Manual|http://biolincc.nhlbi.nih.gov/studies/radar/|Samples and characterization data. NHLBI provides controlled access to samples through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a materials use agreement.
114663|NCT00005276|ACCESS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/access|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114664|NCT00005276||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/access|
114665|NCT00005276||Study Forms|http://biolincc.nhlbi.nih.gov/studies/access|
114666|NCT00005276||Procedures Manual|http://biolincc.nhlbi.nih.gov/studies/access|
114667|NCT00005274|P2C2|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/p2c2/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114668|NCT00005274||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
114669|NCT00005274||Study Forms|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
114670|NCT00005274||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/p2c2/|
114671|NCT00005235||NCBI website|http://www.ncbi.nlm.nih.gov/pubmed/8353919|
114672|NCT00005159|NLMS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/nlms/|Public-use IPD through BioLINCC. Registration is required for access.
114673|NCT00005133|CHS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/chs/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114674|NCT00005132|NGHS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/nghs/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114675|NCT00005132||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/nghs/|
114676|NCT00005132||Study Forms|http://biolincc.nhlbi.nih.gov/studies/nghs/|
114677|NCT00005131|ARIC|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/aric/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114678|NCT00005131||Study Forms|http://www2.cscc.unc.edu/aric/cohort-forms|
114679|NCT00005131||Study Manuals|http://www2.cscc.unc.edu/aric/cohort-forms|
114680|NCT00005130|CARDIA|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/cardia/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114681|NCT00005130||Study Protocol|http://www.cardia.dopm.uab.edu/exam-materials2|
114682|NCT00005130||Informed Consent Form|http://www.cardia.dopm.uab.edu/exam-materials2|
114683|NCT00005130||Study Forms|http://www.cardia.dopm.uab.edu/exam-materials2|
114684|NCT00005130||Study Manuals|http://www.cardia.dopm.uab.edu/exam-materials2|
114685|NCT00005128|LRC-PS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/lrcps/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114686|NCT00005128||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lrcps/|
114687|NCT00005123|HHP|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/hhp/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114688|NCT00005123||Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/hhp/|
114689|NCT00005121|FHS-Cohort|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/framcohort/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval, and completion of a data use agreement.
114690|NCT00005121|FHS-Cohort|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
114691|NCT00005121|FHS-Cohort|Study Forms|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
114692|NCT00005121|FHS-Cohort|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/framcohort/|
114693|NCT00005121|FHS-OS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval, and completion of a data use agreement.
114694|NCT00005121|FHS-OS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
114695|NCT00005121|FHS-OS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
114696|NCT00005121|FHS-OS|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/framoffspring/|
114697|NCT00005121|FHS-Gen III|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/gen3/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval, and completion of a data use agreement.
114698|NCT00005121|FHS-Gen III|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/gen3/|
114699|NCT00005121|FHS-Gen III|Study Forms|http://biolincc.nhlbi.nih.gov/studies/gen3/|
114700|NCT00005121|FHS-Gen III|Data Coding Manuals|http://biolincc.nhlbi.nih.gov/studies/gen3/|
114701|NCT00004560|PAD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/pad/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114702|NCT00004560||Study Forms|http://biolincc.nhlbi.nih.gov/studies/pad/|
114703|NCT00000620|ACCORD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/accord|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114704|NCT00000620||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/accord|
114705|NCT00000620||Study Forms|http://biolincc.nhlbi.nih.gov/studies/accord|
114706|NCT00000620||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/accord|
114707|NCT00000619|ESCAPE|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/escape/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114708|NCT00000619||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/escape/|
114709|NCT00000619||Study Forms|http://biolincc.nhlbi.nih.gov/studies/escape/|
114710|NCT00000610|MAGIC|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/magic/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114711|NCT00000610||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/magic/|
114712|NCT00000610||Study Forms|http://biolincc.nhlbi.nih.gov/studies/magic/|
114713|NCT00000607||NHLBI website|http://www.nhlbi.nih.gov/news/press-releases/2001/nhlbi-funded-study-finds-heart-assist-device-extends-and-improves-lives-of-patients-with-end-stage-heart-failure|
114714|NCT00000606|NETT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/nett/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114715|NCT00000606||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/nett/|
114716|NCT00000606||Study Forms|http://biolincc.nhlbi.nih.gov/studies/nett/|
114717|NCT00000603|COBLT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/coblt/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114718|NCT00000603||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/coblt/|
114719|NCT00000603||Study Forms|http://biolincc.nhlbi.nih.gov/studies/coblt/|
114720|NCT00000603||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/coblt/|
114721|NCT00000593|VATS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/vats/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114722|NCT00000593||Study Forms|http://biolincc.nhlbi.nih.gov/studies/vats/|
114723|NCT00000591|TCD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/tcd/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114724|NCT00000591||Study Forms|http://biolincc.nhlbi.nih.gov/studies/tcd/|
114725|NCT00000590|PACTG|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/pactg/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114726|NCT00000590||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/pactg/|
114727|NCT00000590||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/pactg/|
114728|NCT00000589|TRAP|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/trap/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114729|NCT00000589||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/trap/|
114730|NCT00000589||Study Forms|http://biolincc.nhlbi.nih.gov/studies/trap/|
114731|NCT00000586|MSH|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/MSH/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114732|NCT00000586||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/MSH/|
114733|NCT00000586||Study Forms|http://biolincc.nhlbi.nih.gov/studies/MSH/|
114734|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114735|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|
114736|NCT00000579|ARDSNet-ARMA/KARMA/LARMA|Study Forms|http://biolincc.nhlbi.nih.gov/studies/ardsnet/|
114737|NCT00000579|ARDSNet-LASRS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/lasrs/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114738|NCT00000579|ARDSNet-LASRS|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/lasrs/|
114739|NCT00000579|ARDSNet-LASRS|Study Forms|http://biolincc.nhlbi.nih.gov/studies/lasrs/|
114740|NCT00000579|ARDSNet-ALVEOLI|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/alveoli/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114741|NCT00000579|ARDSNet-ALVEOLI|Study Forms|http://biolincc.nhlbi.nih.gov/studies/alveoli/|
114742|NCT00000579|ARDSNet-FACTT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/factt/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114743|NCT00000579|ARDSNet-FACTT|Study Protocol|http://biolincc.nhlbi.nih.gov/studies/factt/|
114744|NCT00000579|ARDSNet-FACTT|Study Forms|http://biolincc.nhlbi.nih.gov/studies/factt/|
114745|NCT00000568|LHS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/LHS/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114746|NCT00000567|HIFI|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/hifi/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114747|NCT00000567||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/hifi/|
114748|NCT00000567||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hifi/|
114749|NCT00000567||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/hifi/|
114750|NCT00000566|PIOPED|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/pioped/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114751|NCT00000566||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/pioped/|
114752|NCT00000566||Study Forms|http://biolincc.nhlbi.nih.gov/studies/pioped/|
114753|NCT00000565|IPPB|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/ippb/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114754|NCT00000565||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/ippb/|
114755|NCT00000565||Study Forms|http://biolincc.nhlbi.nih.gov/studies/ippb/|
114756|NCT00000565||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/ippb/|
114757|NCT00000560|BEST|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/best/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114758|NCT00000560||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/best/|
114759|NCT00000560||Study Forms|http://biolincc.nhlbi.nih.gov/studies/best/|
114760|NCT00000558|PEACE|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/peace/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114761|NCT00000558||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/peace/|
114762|NCT00000558||Study Forms|http://biolincc.nhlbi.nih.gov/studies/peace/|
114763|NCT00000557|ENRICHD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/enrichd/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114764|NCT00000557||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/enrichd/|
114765|NCT00000557||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/enrichd/|
114766|NCT00000556|AFFIRM|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/affirm/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114767|NCT00000556||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/affirm/|
114768|NCT00000556||Study Forms|http://biolincc.nhlbi.nih.gov/studies/affirm/|
114769|NCT00000555|WAVE|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/wave/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114770|NCT00000555||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/wave/|
114771|NCT00000555||Study Forms|http://biolincc.nhlbi.nih.gov/studies/wave/|
114772|NCT00000555||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/wave/|
114773|NCT00000551|ACT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/act/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114774|NCT00000551||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/act/|
114775|NCT00000551||Study Forms|http://biolincc.nhlbi.nih.gov/studies/act/|
114776|NCT00000551||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/act/|
114777|NCT00000544|DASH|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/dash/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114778|NCT00000544||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/dash/|
114779|NCT00000544||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/dash/|
114780|NCT00000531|AVID|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/avid/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114781|NCT00000531||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/avid/|
114782|NCT00000531||Study Forms|http://biolincc.nhlbi.nih.gov/studies/avid/|
114783|NCT00000531||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/avid/|
114784|NCT00000530|RTS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/rts/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114785|NCT00000530||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/rts/|
114786|NCT00000530||Study Forms|http://biolincc.nhlbi.nih.gov/studies/rts/|
114787|NCT00000526|CAST|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/cast/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114788|NCT00000526||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/cast/|
114789|NCT00000526||Study Forms|http://biolincc.nhlbi.nih.gov/studies/cast/|
114790|NCT00000516|SOLVD|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/solvd/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114791|NCT00000516||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/solvd/|
114792|NCT00000516||Study Forms|http://biolincc.nhlbi.nih.gov/studies/solvd/|
114793|NCT00000516||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/solvd/|
114794|NCT00000514|SHEP|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/shep/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114795|NCT00000514||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/shep/|
114796|NCT00000514||Study Forms|http://biolincc.nhlbi.nih.gov/studies/shep/|
114797|NCT00000514||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/shep/|
114798|NCT00000492|BHAT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/bhat/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114799|NCT00000492||Study Forms|http://biolincc.nhlbi.nih.gov/studies/bhat/|
114800|NCT00000491|AMIS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/amis/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114801|NCT00000488|LRC-CPPT|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/lrccppt/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114802|NCT00000488||Study Forms|http://biolincc.nhlbi.nih.gov/studies/lrccppt/|
114803|NCT00000485|HDFP|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/hdfp/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114804|NCT00000485||Study Forms|http://biolincc.nhlbi.nih.gov/studies/hdfp/|
114805|NCT00000478|ACIP|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/acip|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114806|NCT00000476|DIG|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/dig/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114807|NCT00000476||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/dig/|
114808|NCT00000476||Study Forms|http://biolincc.nhlbi.nih.gov/studies/dig/|
114809|NCT00000474|PATHS|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/paths/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
114810|NCT00000474||Study Protocol|http://biolincc.nhlbi.nih.gov/studies/paths/|
114811|NCT00000474||Manual of Procedures|http://biolincc.nhlbi.nih.gov/studies/paths/|
114812|NCT00000463|CABG|Individual Participant Data Set|http://biolincc.nhlbi.nih.gov/studies/cabg/|NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
