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Study ID Status Title Patient Level Data
115489 Completed Special Drug Use Investigation for Arixtra® (fondaparinux) Venous Thromboembolism Treatment
115490 Completed Special Drug Use Investigation (retrospective) for Arixtra® (fondaparinux) Venous Thromboembolism Treatment (over 100kg)
115493 Terminated TRX4 Therapeutic Evaluation of Different Multi-Dose Regimens in Type 1 Diabetes Mellitus (TTEDD) Study Listed on
115494 Completed Durable-Response Therapy Evaluation For Early- or New-Onset Type 1 Diabetes Study Listed on
115495 Completed Durable-Response Therapy Evaluation For Early or New-Onset Type 1 Diabetes - DEFEND Study Listed on
115496 Completed DEFEND-1 Long Term Follow Up: Durable-Response Therapy Evaluation for Early or New Onset Type 1 Diabetes Extension Study Study Listed on
115515 Completed An open-label single and repeat dose study to investigate the pharmacokinetic profiles of tenofovir disoproxil fumarate 300 mg in healthy Chinese subjects
115517 Completed A single/repeat dose study with three oral formulations of Firategrast (immediate release tablet, modified release tablet, and naso-gastric infusion) in healthy male volunteers
115519 Completed Double-Blind, Randomized, Placebo-Controlled Study to Assess Safety, Efficacy, and Pharmacokinetics (PK) of GSK2336805 in Combination With Peginterferon and Ribavirin in Treatment-naive Chronic Hepatitis C Subjects With Hepatitis C Virus Genotypes 1 or 4
115523 Completed Observer-blind study to evaluate efficacy, safety, and immunogenicity of GSK Biologicals’ Herpes Zoster vaccine GSK1437173A
115524 Relinquished Immunogenicity and safety study of GSK Biologicals’ meningococcal vaccine GSK 134612 administered to at risk subjects from 1 to less than 18 years
115535 Completed A Randomized, Double Blind, Single Dose, Cross-Over Study to Assess the Cardiovascular Effects of GSK2336805 in Healthy Adult Volunteers
115550 Completed A Single Centre, 5-Period, Randomized Study To Evaluate The Relative Bioavailability Of An Immediate Release Tablet Formulation And Prototype Bioenhanced Formulations Of GSK1325756 In Healthy Elderly Subjects During Suppression Of Gastric Acid Secretion Study Listed on
115553 Completed PROACTYVE pilot:Pilot study of Patient’s adherence to TYKERB™/TYVERB™+capecitabine in metastatic breast cancer–observation of patient adherence and evaluation of predictive factors for patient adherence after providing educational programme
115555 Completed Immunogenicity and safety study of GlaxoSmithKline Biological's live attenuated measles mumps rubella varicella vaccine (PriorixTetra™) when co-administered with conjugated Meningococcal C vaccine (Meningitec®, Nuron Biotechs’ Vaccine) in healthy children
115563 Completed PGx418 Exploratory Pharmacogenetic Research on Efficacy of BENLYSTA (belimumab) in BEL110752 (BLISS-52) and BEL110751 (BLISS-76)
115570 Completed A Single Dose First in Human Study of GSK2398852 Co-Administered with GSK2315698 in Patients with Systemic Amyloidosis
115573 Terminated A repeat-dose, open-label, parallel-group study to assess the pharmacokinetics of GSK1278863 and metabolites in normal subjects and subjects with impaired renal function
115575 Completed MEA115575: A Randomised, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study of Mepolizumab Adjunctive Therapy to Reduce Steroid Use in Subjects with Severe Refractory Asthma Study Listed on
115576 Completed An Open-Label, 12-Week Study to Evaluate the Efficacy and Safety of the Acne System (Benzoyl Peroxide 2.5%, Salicylic Acid 0.5%) in Subjects with Acne Study Listed on
115578 Relinquished Post Marketing Surveillance (PMS) of safety and efficacy of Votrient in Korean patients
115579 Completed An open label, multi-centre, non-interventional post-marketing surveillance (PMS) to monitor the safety and efficacy of ALTARGO(retapamulin) administered in Korean patients according to the prescribing information
115588 Completed MEA115588 A randomised, double-blind, double-dummy, placebo-controlled, parallel-group, multi-centre study of the efficacy and safety of mepolizumab adjunctive therapy in subjects with severe uncontrolled refractory asthma Study Listed on
115596 Completed RES115596: Estimation of Skeletal Muscle Mass with D3 Creatine Pharmacokinetic Study in Healthy Volunteers
115597 Completed Study to determine protective efficacy against otitis media and assess safety of an investigational pneumococcal vaccine 2189242A in healthy infants



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GSK-sponsored clinical studies are those for which GSK is ultimately responsible for all aspects of the study even if some or all of these activities are transferred to another party.
GSK-sponsored clinical trials are those for which GSK is ultimately responsible for all aspects of the study even if some or all of these activities are transferred to another party. is a database that provides summary protocol information for ongoing clinical trials. is a search portal provided by the International Federation of Pharamceutical Manufacturers & Associations (IFPMA).

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EU Clinical Trials Register is a database of all clinical trials commencing in the European Community from 1 May 2004 onwards. It has been established in accordance with Directive 2001/20/EC.