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Study ID Status Title Patient Level Data
114957 Completed A Randomized, Open-label, Single-dose, Two-period, Crossover Study to Demonstrate the Bioequivalence of the Fixed Dose Combination (FDC) of lamivudine and adefovir dipivoxil (100mg/10mg) to Heptodin® (100mg ) and Hepsera® (10mg) Study Listed on
114974 Completed A randomised, double blind placebo controlled, 2 way cross over study in adults with non-allergic rhinits to evaluate the effect of once daily administration of intranasal SB-705498 12mg for two weeks and the response to a chamber challenge of cold dry air Study Listed on
114985 Completed A first time in human, single blind, randomized, placebo-controlled,dose escalating crossover study to evaluate the safety,tolerability, pharmacokinetic and pharmacodynamic parameters of single doses of GSK2330672 in healthy volunteers Study Listed on
114987 Relinquished An open-label, phase 2a study to evaluate pazopanib eye drops administered for 12 weeks to patients with neovascular age-related macular degeneration
114989 Completed Neisseria meningitidis burden of disease
114991 Completed Neisseria meningitidis carriage study Study Listed on
114993 Completed SUrvey of Guideline Adherence for treatment of systolic heart failure in Real WorldMulticenter, retrospective observation study in Korea
114995 Completed A Phase I, Randomized, Placebo-Controlled, Parallel-Group, Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of a Single Intravenous Dose of the Captisol™ Formulation of Vestipitant (GW597599) in Healthy Adult Subjects
115002 Active, Not Recruiting PGx308, PGx309, PGx310 and PGx382 evaluation of efficacy and safety endpoints in pazopanib-treated renal cell carcinoma (RCC) patients in studies VEG102616, VEG105192, and VEG107769
115003 Completed PGx367 evaluation of ALT elevation in patients receiving pazopanib and statins in 11 pazopanib clinical studies (VEG102616, VEG105192, VEG107769, VEG10003, VEG10004, VEG10005, VEG10007, VEG20002, VEG20006, VEG104450, VEG105281)
115-003 Completed A Multicentre Pilot Study in the United Kingdom to Determine Whether 566C80 Exhibits Antimalarial Activity in Patients with P. Falciparum Malaria.
115005 Completed PGx368 Genetics asthma exacerbation in ADA109055, ADA109057, SFA103153, I13106870
115-005 Completed An Open Study to Determine Whether 566C80 (Atovaquone) Exhibits Antimalarial Activity in Thai Patients with P. falciparum Malaria
115008 Completed Medical Record Review and Data Abstraction for Pediatric, Adolescent and Pregnant Patients treated with IV zanamivir in the Relenza Compassionate Use Program Study Listed on
115-012 Completed An open study to determine whether 566C80 (atovaquone) exhibits antimalarial activity in Zambian patients with P. falciparum malaria
115014 Completed SLE in CEE setting( Hungary, Poland, Romania) an insight on medical, economic and social burden
115030 Completed Efficacy and Safety of Belimumab in a Subgroup of Systemic Lupus Erythematosus (SLE) Patients with Higher Disease Activity (anti-dsDNA positive and low complement): A Pooled Analysis of the HGS1006-C1056 (BLISS-52) and HGS1006-C1057 (BLISS-76) Studies
115032 Completed A 4-week Dose-Ranging, Dose-Interval, Efficacy, Safety and Tolerability Study of GSK961081 in Subjects with Chronic Obstructive Pulmonary Disease (COPD) Study Listed on
115040 Terminated A Randomized, Double Blind, Dose Escalation, Fusion, First Time in Human Study to Assess the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of Single and Repeat Doses of GSK2485852 in Chronically Infected Hepatitis C Subjects Study Listed on
115049 Completed Systematic Review: Retigabine for Adjunctive Therapy in Partial Epilepsy
115050 Completed PGx250: An Exploratory Pharmacogenetic Analysis of Asthma exacerbations in African-Americans treated with Advair
115051 Completed PGx363 Investigation of the impact of functional glucose 6-phosphate dehydrogenase (G6PD) variants on hemoglobin decline in two healthy subjects following repeat dosing with tafenoquine
115054 Completed Ethanol-Free Clobetasol Propionate Foam 0.05% (Olux-E Foam) vs Vehicle Foam in the Treatment of Chronic Hand Dermatitis. Study Listed on
115058 Completed Assessment of Comorbidities in Chronic Obstructive Pulmonary Disease (COPD) in European Symptomatic Subjects from primary care
115060 Completed A meta-analysis of three studies to evaluate key efficacy outcomes in subjects with moderate-to-severe Restless Legs Syndrome treated with Gabapentin Enacarbil at doses ranging from 600 mg/day to 2400 mg/day



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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.
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