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Study ID Status Title Patient Level Data
OM9L Completed A Randomized, Double-Blind, Placebo-Controlled, Forced Titration Study to Assess the Efficacy and Safety of Omacor, Co-Administered with Open-Label Atorvastatin Therapy, in Hypertriglyceridemic Subjects Study Listed on ClinicalStudyDataRequest.com
OMB110911 Active not recruiting A phase III, open label, randomized, multicenter trial of Ofatumumab added to Chlorambucil versus Chlorambucil Monotherapy in previously untreated patients with Chronic Lymphocytic Leukemia
OMB111148 Completed An open-label phase I study of ofatumumab (GSK1841157) in Japanese patients with CD20 positive follicular lymphoma or chronic lymphocytic leukemia
OPB107935 Completed An open-label, randomized, crossover study to estimate the formulation effect on the relative bioavailability of single dose oral SB-742510 in healthy subjects
OPL104226 Completed A prospective observational study for the psychometric validation of a patient-reported questionnaire in acute exacerbations of chronic obstructive pulmonary disease (AECOPD).
OPS106400 Completed A three-part first time in human study to evaluate safety, tolerability, pharmacokinetics and food effect of single oral doses of GSK580416 in healthy adult subjects
OPS108221 Terminated A three part study in healthy adult subjects to evaluate the safety, tolerability and pharmacokinetics of repeat escalating oral doses of GSK580416; the safety, tolerability, and pharmacokinetics of GSK580416 following a loading dose regimen; and the effect of ketoconazole on the pharmacokinetics of GSK580416
OTA105101 Completed An open-label, two period study to determine the excretion balance and pharmacokinetics of [14C]-GSK221149A, administered as single doses of an oral solution and an intravenous infusion to healthy female volunteers
OTA105256 Completed A randomized, double-blind, placebo-controlled, dose ranging study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of GSK221149A administered intravenously and to investigate the pharmacokinetics of GSK221149A administered orally to healthy, pregnant females with uncomplicated pre-term labor between 300/7 and 356/7 weeks’ gestation Study Listed on ClinicalStudyDataRequest.com
OTA106004 Terminated A two-part, open-label, cross-over study to assess the pharmacokinetics of GSK221149 following single oral doses of various modified release formulations and a solution in healthy adult subjects
OTB109039 Completed A Two-Part Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Repeat Oral Doses of GSK557296 in a Randomized, Single-Blind, Placebo-Controlled, Dose-Rising Design, and to Evaluate the Effect of Food on Single Oral Doses of GSK557296 in Healthy Adult Subjects
OTP108172 Completed A randomized, double-blind, placebo-controlled, two-session study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of an 16448 in healthy males with premature ejaculation.
OXS104092 Completed A single-blind, randomised, placebo-controlled, 15 day repeated-dose study to evaluate the safety, tolerability and pharmacokinetics of SB-649868 and its interaction with the CYP3A4 isoenzyme in healthy male subjects.
OXS104094 Completed A Double-blind, double-dummy, randomised, placebo-controlled,four-way crossover study to investigate the effect of single oral doses of SB-649868 and of Zolpidem in a model of noise induced situational insomnia in healthy male volunteers.
OXS105205 Completed A single-centre, open-label, randomized, single-dose, 6-way crossover study to investigate the pharmacokinetics, safety and tolerability of 6 different formulations of SB-649868 30 mg (Part A) and the effect of food on the selected formulation of SB-649868 pharmacokinetic (Part B) in healthy male volunteers
OXS107714 Completed A multi-centre, randomized, double-blind, placebo-controlled, cross-over study to evaluate the effects of SB-649868 (10, 30 mg and 60 mg) on sleep continuity, PSG sleep recordings, subjective sleep assessment, and daytime cognitive function in subjects with primary insomnia
OXS109139 Completed An open-label study to determine the excretion, balance and pharmacokinetics of SB649868 after a single oral administration of 14C-SB649868 in healthy volunteers
OXS109143 Withdrawn A single-centre, open label, single-dose, four parallel cohorts study to investigate the pharmacokinetics, safety and tolerability of SB-649868 10mg in healthy female "non-childbearing potential", healthy male and in healthy elderly subjects
P2200440 Completed A Mult-Center, Open-Label Study to Evaluate Product Duration of Use Experience with Aclometasone Diproprionate Cream
PAA20001 Completed A multi-center, three-staged, randomized, parallel group, sequential, double-blind, fenofibrate-and placebo-controlled dose-response evaluation of the safety, tolerability, and effects on plasma HDLc and TG of eight weeks treatment with 1µg to 20µg daily doses of GW590735 in otherwise healthy subjects with low HDLc, mildly to moderately elevated TG, and normal LDLc
PAD100958 Completed A randomized, double-blind, parallel group study to evaluate the effect of 12-week treatment with GW590735X (20ug) or GW501516X (10mg) relative to placebo on measures of adiposity and inflammation in overweight and obese subjects
PAD100964 Terminated A two part study to separately evaluate the effect of 4-week treatment with GW501516X relative to placebo on cardiac energetics in a randomized, single-blind, repeat dose, parallel group design in healthy male subjects
PAD20001 Completed A multi-center, three-staged with interim analyses, parallel, randomized, double-blind, fenofibrate-and placebo-controlled proof of concept and dose-response evaluation of the safety, tolerability, and effects on plasma high-density lipoprotein cholesterol (HDLc) and triglycerides of eight weeks treatment with GW501516 in otherwise healthy patients with low HDLc, mildly to moderately elevated triglycerides, and normal low-density lipoprotein cholesterol (LDLc)
PCR103124 Completed A Multicentre, Double-blind, Active Controlled Trial to Evaluate the Clinical Effects of Immediate Release Paroxetine and Controlled Release Paroxetine in the Treatment of Major Depression
PCR104074 Completed A randomized, open, three-period crossover study to compare the pharmacokinetic profile of paroxetine after single dosing of each enteric-coated Geomatrix control release tablet strength (12.5, 25, 37.5mg) in healthy Chinese subjects

 

 

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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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