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Study ID Status Title Patient Level Data
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
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
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
111925 Completed A randomized, double blind, placebo controlled study to assessthe effect of intranasal single dose SB-705498 on the response tointranasal capsaicin challenge in non-allergic rhinitis patients Study Listed on ClinicalStudyDataRequest.com
111951 Completed First trimester Paroxetine use and the occurrence of congenital malformations: Systematic review and meta-analysis of epidemiological data
111954 Completed Non-inferiority study of GSK Biologicals’ Pandemic influenza vaccine 1562902A. Study Listed on ClinicalStudyDataRequest.com
111960 Terminated Thiazolidinedione Intervention with vitamin D Evaluation (TIDE) A Multicenter Randomized Double-Blind Placebo Controlled Trial of a Thiazolidinedione or Placebo and of Vitamin D or Placebo In People With Type 2 Diabetes at Risk For Cardiovascular Disease Study Listed on ClinicalStudyDataRequest.com
111982 Completed Post-marketing carcinogenicity study of Bupropion
111983 Completed Fluticasone propionate nasal spray (Flixonase) safety in patients with allergic rhinitis registered in the UK General Practice Research Database
111985 Completed The long-term use of Advair/Seretide and risk of events (incident non-vertebral fracture, glaucoma, and cataracts) among COPD patients in the UK General Research Practice Database
111985_1 Completed The long-term use of Advair/Seretide and risk of events (incident non-vertebral fracture, glaucoma, and cataracts) among COPD patients in the UK General Research Practice Database
111985_2 Completed The long-term use of Advair/Seretide and risk of events (incident non-vertebral fracture, glaucoma, and cataracts) among COPD patients in the UK General Research Practice Database
111985_3 Completed The long-term use of Advair/Seretide and risk of events (incident non-vertebral fracture, glaucoma, and cataracts) among COPD patients in the UK General Research Practice Database
112008 Completed A single-centre, open-label, sequential, cross-over study to examine the safety, tolerability and pharmacokinetics of 3 ascending single intravenous doses, a single 1000μg oral dose and a single 1000μg inhaled dose of GSK573719 in healthy male volunteers. Study Listed on ClinicalStudyDataRequest.com
112014 Completed An open-label, two period study to determine the excretion balance and pharmacokinetics of 14C-GSK573719, administered as single dose of an oral solution and an intravenous infusion, to healthy male adults Study Listed on ClinicalStudyDataRequest.com
112022 Completed Immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals’ Human Papillomavirus (HPV) 580299 vaccine in healthy Chinese female subjects Study Listed on ClinicalStudyDataRequest.com
112025 Completed A multi-centre, randomized, double-blind, five-way crossover study evaluating the dose response and duration of action of GSK2190915 compared to placebo in subjects with mild asthma who experience exercise induced bronchoconstriction. Study Listed on ClinicalStudyDataRequest.com
112034 Completed A Two Part Single Dose, Randomized, Balanced, Crossover Study to Assess the Relative Bioavailability of Three Formulations, Drug Interaction and Food Effect on an GSK1322322 in Healthy Subjects Study Listed on ClinicalStudyDataRequest.com
112046 Terminated The efficacy of orally administered GSK2190915 as an add-on to current therapy in subjects with moderate to severe asthma who have elevated sputum neutrophils Study Listed on ClinicalStudyDataRequest.com
112059 Completed A randomised, double-blind, double-dummy, placebo controlled (with rescue medication), multicenter study to evaluate the efficacy and safety of Fluticasone Furoate inhalation powder in the treatment of persistent asthma in adults and adolescents. Study Listed on ClinicalStudyDataRequest.com
112060 Completed A randomized, double-blind, double-dummy, parallel-group, placebo controlled (on inhaled corticosteroid medication), multicenter study to evaluate the efficacy and safety of vilanterol inhalation powder (GW642444) and salmeterol, compared with placebo in the treatment of persistent asthma in adults and adolescents uncontrolled on inhaled corticosteroids 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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