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Study ID Status Title Patient Level Data
111821 Completed A Second Open-Label Extension of a Double-Blind, Parallel, Phase IV Study to Assess the Efficacy and Safety of Adjunctive Lovaza® (formerly known as Omacor®) Therapy in Hypertriglyceridemic Subjects Treated with Antara™
111823 Completed A Randomized, Open-Label Study to Evaluate the Safety,Tolerability, Pharmacokinetics, and Pharmacodynamics ofGSK1362885 in Subjects with Type 2 Diabetes Mellitus Study Listed on ClinicalStudyDataRequest.com
111827 Completed A single-arm, international, multi-center trial investigating the efficacy and safety of ofatumumab retreatment and maintenance in CLL patients who progressed following response or stable disease after ofatumumab treatment in Hx-CD20-406
111829 Completed A single-blinded randomized, placebo-controlled, staggered-parallel, escalating-dose study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of oral SB756050 administered for 6 days to Subjects with Type 2 Diabetes Mellitus Study Listed on ClinicalStudyDataRequest.com
111834 Completed A randomised, double-blind, placebo-controlled, 2-period cross-over study to evaluate the effect of treatment with GSK2190915 on the allergen-induced asthmatic response in subjects with mild asthma Study Listed on ClinicalStudyDataRequest.com
111839 Completed A Phase I, open label crossover study to evaluate the effect of etravirine on GSK1265744 pharmacokinetics in healthy adult subjects
111848 Completed An open-label, non-randomized [11C]carfentanil PET study in healthy male subjects to investigate brain mu-opioid receptor occupancy, pharmacokinetics, and pharmacodynamics of single oral doses of GSK1521498 and naltrexone. Study Listed on ClinicalStudyDataRequest.com
111849 Completed A randomised, double-blind, placebo-controlled study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamic effects of 10 days of repeat dosing of GSK1521498 in overweight or obese but otherwise healthy subjects. Study Listed on ClinicalStudyDataRequest.com
111850 Completed A 35-Day, Multi-Centre, Randomised, Parallel-Group, Double-Blind, Placebo-Controlled Proof of Concept Study to Investigate the Effects of GSK1521498 on Body Weight and Composition, Eating Behaviour and Related Brain Function, in Obese Subjects with Over-Eating Behaviours. Study Listed on ClinicalStudyDataRequest.com
111852 Completed Immunogenicity and safety study of Kinrix® co-administered with Varivax® Study Listed on ClinicalStudyDataRequest.com
111853 Completed An Open Label, Non-Randomized, Single dose, Mass Balance Study to Investigate the Recovery, Excretion, and Pharmacokinetics of 14C-GSK1349572 20 mg, Administered as a Single Oral Suspension Dose to Healthy Adult Subjects (ING111853)
111854 Completed Phase I, Open Label, Randomized, Drug-Drug Interaction Study in Healthy Subjects to Investigate the Effects of Co-administered Atazanavir/Ritonavir (300mg/100mg) or Atazanavir 400mg Administered Once Daily on the Steady-State Plasma Pharmacokinetics of GSK1349572 30mg Administered Once Daily
111855 Completed A Double-Blind study to Evaluate the Pharmacokinetics of an Oral Contraceptive Containing Norgestimate and Ethinyl Estradiol when Co-administered with Dolutegravir in Healthy Adult Female Subjects
111856 Completed A Study to Evaluate the Effect of a Single 250 mg Oral Dose of GSK1349572 on Cardiac Conduction as Assessed by 12-lead Electrocardiogram Compared to Placebo and a Single Oral Dose of Moxifloxacin (ING111856).
111861 Completed A Pharmacokinetic Interaction Study Evaluating the Effect of Reliant Pharmaceuticals Inc. (Lovaza®) Omega-3-Acid Ethyl Esters Capsules on the Plasma Pharmacokinetics of Reliant Pharmaceuticals Inc. (Antara™) Fenofibrate Capsules in Healthy Adult Volunteers Under Fasting Conditions
111862 Completed A Pharmacokinetic Interaction Study Evaluating the Effect of Lovaza® on Plasma Pharmacokinetics of Zocor® in Healthy Adult Volunteers Under Fasting Conditions Study Listed on ClinicalStudyDataRequest.com
111863 Completed A Pharmacokinetic Interaction Study Evaluating the Effect of Reliant Pharmaceuticals Inc. (Lovaza®) Omega-3-Acid Ethyl Esters Capsules on the Plasma Pharmacokinetics of Parke Davis (Lipitor®) Atorvastatin Tablets in Healthy Adult Volunteers Under Fasting Conditions Study Listed on ClinicalStudyDataRequest.com
111864 Completed A Pharmacokinetic Interaction Study Evaluating the Effect of Omega-3-Acid Ethyl Esters Capsules (Omacor®; Reliant Pharmaceuticals Inc.) on the Plasma Pharmacokinetics of Rosuvastatin Tablets (Crestor®; AstraZeneca) in Healthy Adult Volunteers under Fasting Conditions. Study Listed on ClinicalStudyDataRequest.com
111867 Completed A pilot single-dose, 6-treatment, 4-period crossover relative bioavailability study of a fixed-dose combination of omega3+fenofibrate vs. Omacor+AntaraTM vs Antara alone n healthy adults under fed and fasted conditions
111870 Completed A phase II, randomized, observer blind, controlled, multicenter study to assess immunogenicity and antibody persistence following vaccination with GSK's candidate combined measles, mumps, and rubella vaccine (MMR) versus M-M-R® II as a first dose, both administered subcutaneously at 12-15 months of age, concomitantly with hepatitis A vaccine (HAV), varicella vaccine (VV) and pneumococcal conjugate vaccine (PCV) but at separate sites. Study Listed on ClinicalStudyDataRequest.com
111891 Completed An Evaluation of Lung Function and Symptoms in Patients with Chronic Obstructive Pulmonary Disease (COPD) on Long-Acting Bronchodilator Monotherapy
111905 Completed Observational survey on diagnosis and treatment of M. Parkinson
111913 Completed TPL111913, a Multi-centre, Open Label, Dose Ranging Phase II Study to Assess Efficacy, Safety and Pharmacokinetics of Eltrombopag in Japanese Thrombocytopenic Subjects with Chronic Liver Disease
111914 Completed A Single-Blind, Randomised, Placebo-Controlled Study to Evaluate Safety, Tolerability and Pharmacokinetics of Single Oral Escalating Doses of GSK1360707 Study Listed on ClinicalStudyDataRequest.com
111924 Completed A randomized, double-blind, placebo controlled, incomplete block, 3 way cross over study in subjects with allergic rhinitis to assess the effect of intranasal repeat doses of SB-705498 when administered alone or in conjunction with intranasal fluticasone propionate on the symptoms of rhinitis in the Vienna allergen challenge chamber Study Listed on ClinicalStudyDataRequest.com

 

 

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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.

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