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Study ID Status Title Patient Level Data
B2C108562 Completed A 2-wk study to evaluate the safety, tolerability,pharmacodynamics and pharmacokinetics of GW642444H(100 administered once daily in the morning via DISKUS™ dry-powder inhaler)compared with SEREVENT(salmeterol)(50mcg administered twice daily via DISKUS dry-powder inhaler)and placebo in subject w/COPD Study Listed on
B2C108784 Completed A randomised, double-blind, placebo-controlled, parallel-group, 14 day repeat dose study to investigate the safety, tolerability, pharmacokinetics and extra-pulmonary pharmacodynamics of inhaled doses of GW642444M formulated with magnesium stearate in healthy subjects Study Listed on
B2C109575 Completed A randomised, double-blind, placebo controlled, parallel group, dose ranging study evaluating the efficacy and safety of GW642444M administered once daily compared with placebo for 28 days in adolescent and adult subjects with persistent asthma Study Listed on
B2C110165 Completed A randomised, single-dose, dose ascending, double-blind, placebo controlled, four-way, incomplete block crossover study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of inhaled doses of GW642444M with magnesium stearate in COPD patients. Study Listed on
B2C111045 Completed Study B2C111045, A Dose-Finding Study of GW642444 versus Placebo in Patients with COPD Study Listed on
B2C111401 Completed A randomised, single-dose, double-blind, placebo-controlled, 5-way crossover study to investigate the efficacy, safety, tolerability, pharmacokinetics and pharmacodynamics of inhaled doses of GW642444M with and without magnesium stearate in asthmatic patients Study Listed on
B2E106359 Completed A multi-enter, randomized, double-blind, placebo-controlled, four-way incomplete block crossover study to examine efficacy, safety, tolerability, pharmacodynamics and pharmacokinetics of single and repeat administration of three inhaled doses (10, 15, and 20 mcg) of GSK159797 Study Listed on
B2F104300 Completed A randomised, double blind, placebo controlled study to examine the safety, tolerability, pharmacodynamics and pharmacokinetic profile of single inhaled dry powder doses of GSK159802 in healthy male subjects Study Listed on
B3I105940 Completed A Randomized, Double-Blind, Placebo-Controlled, Crossover, Phase IIa Study to Evaluate Efficacy and Safety of the beta-3-Adrenergic Receptor Agonist Solabegron in Subjects with Irritable Bowel Syndrome
B3P104833 Completed An Eight- Week Randomized, Double-Blind, Placebo-Controlled, Parallel Group Proof of Concept Study to Assess the Efficacy, Safety and Tolerability as well as the Pharmacokinetic Profile of oral Solabegron (GW427353) 125mg and 50mg Administered Twice Daily vs Placebo in Women with Overactive Bladder
BCM30002 Completed A Single-Centre, Randomised, Double-Blind, Three Way Crossover Study to Investigate Longitudinal Growth, Using Knemometry, in Children with Mild Asthma During Treatment with Beclomethasone Dipropionate 400?g bd (800?g/Day), Beclomethasone Dipropionate 200?g bd (400?g/Day) and Fluticasone Propion ...
BCR10001 Completed A Phase I, Randomized, Open-Label, Parallel-Cohort, Dose-Finding Study of Elacridar (GF120918) in Combination with 2.0 mg Oral Topotecan in Cancer Patients
BDPA/88/001 (UK20) Completed The Disposition, Metabolism and Pharmacokinetics of 14C-Lamotrigine After Single Oral Administration of 240mg (15?Ci) to Six Healthy Male Subjects
BDR3780 Completed A single dose bioequivalence study comparing a new formulation of Org31540/SR90107A and the reference formulation in healthy male subjects
BDR4979 Completed A single dose bioequivalence study comparing a new formulation of fondaparinux sodium at 12.5 mg/mL and the reference formulation at 10 mg/mL, in healthy male subjects. Open, randomized, crossover and single center study Study Listed on
BEX104545 Completed Expanded Access Study of Iodine I 131 Tositumomab for Relapsed/Refractory Low-Grade and Transformed Low-Grade Non-Hodgkin's Lymphoma Study Listed on
BGS105049 Completed A randomised, placebo-controlled, 4-period, incomplete block, crossover study of 7 days dosing of intranasal GW784568X (100mcg, 200mcg and 400mcg od), fluticasone propionate (200mcg od) and placebo (blinded for GW784568X vs placebo) to evaluate the efficacy and safety using an environmental chamber in male subjects with allergic rhinitis Study Listed on
BON103593 Completed A one year, parallel, placebo-controlled, double-blind, randomized study to assess the effect of monthly 150mg oral ibandronate dosing versus placebo on bone quality and strength at the proximal femur in women with osteoporosis Study Listed on
BRL 49653/392 Completed A 52 weeks open label, randomised, parallel group, multicetre study to investigate the effects of rosiglitazone or metformin on blood pressure when administered to subjects with Impaired Glucose Tolerance
BRL-025000/672 Completed An open-label, three period crossover, incomplete block study to determine the pharmacokinetics of five novel mixed component formulations of amoxicillin once-daily in healthy volunteers.
BRL-049653/231 Completed A long term, open label, randomised study in patients with type 2 diabetes, comparing the combination of rosiglitazone and either metformin or sulfonylurea with metformin plus sulfonylurea on cardiovascular endpoints and glycaemia Study Listed on
BRL29060A/856 Completed Clinical Evaluation of BRL29060 A in Generalized Anxiety Disorder
BRL-49653/137 Completed A Study to Evaluate the Efficacy of Rosiglitazone (BRL-049653) on Reduction of Microalbuminuria in Subjects with Type 2 Diabetes Mellitus Study Listed on
BRL-49653/461 Completed Effects of Avandia on cognition and cerebral glucose utilisation in subjects with mild to moderate Alzheimer's Disease (AD). Study Listed on
BT0300-302-INT Completed A Phase III Randomized, Evaluator-Blind, Parallel Group Study of the Safety and Efficacy of Itraconazole Tablets, Itraconazole Capsules and Placebo in the Treatment of Onychomycosis of the Toenail.



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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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