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Study ID Status Title Patient Level Data
999920/040 Completed A study of the Pharmacodynamic Effects of Prednisolone on Whole Blood Protein and Gene Expression in Rheumatoid Arthritis Patients
A1900832 Completed A Pharmacokinetic Study to Evaluate the Rate and Extent of Absorption of Paracetamol from Two Formulations in an Indian Population.
A1901106 Completed A Study to Investigate the Gastrointestinal Safety of OTC Analgesics in Healthy Volunteers by Endoscopic Examination
A1A20004 Completed A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Tolerability of a 14 Day Treatment Course of GW493838 50mg Compared to Placebo in Subjects with Peripheral Neuropathic Pain
A2260597 Terminated A study to assess the efficacy of paracetamol taken in combination with caffeine for the treatment of episodic tension type headache
A2260665 Completed A pivotal pharmacokinetic study investigating the extent of absorptions of paracetamol and caffeine for two different paracetomol formulations containing caffeine
A2750596 Completed A study investigating the pharmacokinetic profiles of four extended release paracetamol formulations
A2750605 Completed A single dose PK study investigating the extent of paracetamol absorption from two different sustained released paracetamol formulations
A2750606 Completed A single dose PK study investigating the extent of paracetamol absorption from two sustained release paracetamol formulations
A2750607 Completed A repeat dose PK study investigating the extent of paracetamol absorption from two sustained release paracetamol formulations
A2750894 Completed A Proof of Principal Study to Investigate the Pharmacokinetic Profiles of Sustained Release and Standard Paracetamol Formulations
A3360529 Completed A randomised, double-blind, evaluation of the effects of paracetamol on the BOLD fMRI response to painful stimuli in subjects with osteoarthritis
A3940666 Completed A Proof of Principle Study to Explore the Utility of Guaifenesin in Upper Back Pain
A3950669 Completed A pharmacokinetic study investigating the rate and extent of paracetamol absorption of three experimental sustained release pediatric suspensions
A4000684 Completed A study to compare the analgesic efficacy of two different paracetamol doses as measured by post-operative dental pain relief
A4000685 Completed A study to compare the analgesic efficacy of two different paracetamol doses as measured by post-operative pain relief
A4040689 Withdrawn A single dose pharmacoscintigraphic study investigating the differences in gastrointestinal behavior and paracetamol absorption between sustained release formula and standard release formula
A4M105038 Completed Randomised, Double-blind, Placebo-controlled, Parallel-group, Dose-ranging Study to Investigate the MRI Efficacy and the Safety of Six Months Administration of SB-683699 in Subjects with Relapsing-Remitting Multiple Sclerosis
A4M108119 Completed An open-label study of leukocyte counts in the cerebrospinal fluid and blood of subjects with relapsing forms of multiple sclerosis following treatment with firategrast
A4M109079 Completed An open-label, randomised, four period crossover study to investigate the relative pharmacokinetic profiles of tablets from three batches of firategrast with different surface areas and two different tablet formulations containing the same batch of firategrast, given as single 900mg doses to male and female subjects with a diagnosis of Multiple Sclerosis
A6480791 Completed A pharmacokinetic study investigating the rate and extent of absorption of paracetamol and an adjuvant from two different paracetamol formulations.
A6480804 Completed A single dose pharmacoscintigraphic study investigating the differences in gastrointestinal behaviour and paracetamol absorption between two paracetamol formulations
ABC107442 Completed A retrospective case-control study to estimate the sensitivity and specificity of a pharmacogenetic marker (HLA-B*5701) in subjects with and without hypersensitivity to abacavir.
AC2103473 Completed A randomised, double blind, placebo-controlled, double dummy, 4-way cross-over, dose ascending study to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of single inhaled doses of GSK233705 and tiotropium bromide (18µg) via DPI in COPD patients Study Listed on ClinicalStudyDataRequest.com
AC2105333 Completed A Randomised, Double-Blind, Placebo-Controlled, Dose Ascending, 3 Period Crossover Study To Examine The Safety, Tolerability, Pharmacodynamics And Pharmacokinetics Of Repeat Inhaled Doses Of GSK233705B In COPD Subjects. 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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