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Study ID Status Title Patient Level Data
A2410337 Completed Assessment of in vivo penetration of topical diclofenac using a novel iontophoretic delivery system
A2500522 Completed A Pilot Study to Evaluate the Relative Bioavailability of Diclofenac as Measured by Microdialysis after Repeated Doses of Two Topical Diclofenac Formulations
A2530352 Completed A Proof of Principle Pharmacokinetic (PK) Study to Evaluate the Absorption of Paracetamol from the Oral Cavity
A2620383 Completed A Proof of Principle Study to Investigate the Efficacy of a Medical Device and Topical Analgesic Combination for the Treatment of Pain and Performance Related Function in Osteoarthritis
A2720382 Completed A Proof-of-Principle Analgesic Adjuvant Pilot Study in Post-Operative Dental Pain
A2750380 Completed A proof of principle pharmacokinetic study investigating the rate of absorption of paracetamol from modified release tablet formulations
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
A4010001 Completed A two centre, randomised, partially double-blind, double dummy, placebo-controlled, crossover study to investigate the effects of pre-treatment with a new chemical entity (NCE) and a single inhaled dose of fluticasone propionate (0.5 mg) on the allergen induced late asthmatic response in mild as ...
A4A10003 Completed A randomised, double-blind, placebo-controlled, 3-way cross-over study to investigate the effects of pre-treatment with single inhaled doses of an NCE and fluticasone propionate on the allergen induced late phase asthmatic response in mild asthmatic subjects. Study Listed on ClinicalStudyDataRequest.com
A4A10008 Completed An 8-day, randomised, placebo-controlled, three-way crossover trial of repeat doses of a new chemical entity (NCE), fluticasone propionate and placebo administered intranasally, blinded for fluticasone propionate versus placebo, in an environmental exposition unit, the Vienna Challenge Chamber (VCC) in subjects with seasonal allergic rhinitis (SAR) Study Listed on ClinicalStudyDataRequest.com
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
AA210005 Completed A randomised, double-blind, placebo-controlled, cross-over study to investigate the effects of pre-treatment with repeat inhaled doses of a new chemical entity on the allergen-induced late phase asthmatic response in mild asthmatic 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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