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Study ID Status Title Patient Level Data
201851 Completed A Pharmacokinetic Study for Systemic Exposure of Twice Daily Topically applied GSK2894512 Cream in Subjects with Atopic Dermatitis
201857 Completed Adjusting for treatment crossover in the METRIC trial comparing trametinib to dacarbazine using the ITT population (based on final data cut off)
201884 Completed Clinical Evaluation of Efficacy at 2 Weeks of Duac® Fixed Dose Combination Gel in Treatment of Facial Acne Vulgaris in Japanese Subjects
201897 Completed An Open-label, Randomized, Single Dose, Two-way Crossover study to Determine the Bioavailability of one Fixed Dose Combination Capsule Formulation of Dutasteride and Tamsulosin Hydrochloride (0.5 mg/0.2 mg) Relative to Coadministration of one Dutasteride 0.5 mg capsule and one Tamsulosin Hydrochloride 0.2 mg tablet in Healthy Male Subjects in the Fed and Fasted States
201908 Active not recruiting HO-14-15413 - Evidence Synthesis and Mixed Treatment Comparison of Efficacy of Treatments for the Maintenance of Asthma (annual updates)
201909 Completed An open-label study investigating critical and overall errors following 14 days of treatment with SERETIDE Metered Dose Inhaler (EVOHALER) in adult subjects with controlled asthma currently using the SERETIDE DISKUS Inhaler Study Listed on ClinicalStudyDataRequest.com
201929 Recruiting Efficacy of ropinirole controlled-release on the motor symptoms in advanced Parkinson’s disease patients: A post-hoc analysis of Japanese phase III clinical trial (Study ID: 201929)
201934 Recruiting An investigation of drug concentrations in hair and sweat of subjects with respiratory diseases following the exposure of inhaled chronic respiratory therapies as a future means of assessing treatment related compliance
201935 Recruiting Etude des conditions d'utilisation et du profil de securite de'allli OR Study of the conditions of use and safety profile of Alli
201955 Completed Incidence of Gall Bladder Related Events Among Type 2 Diabetes Patients
201958 Completed An open label, six-period cross-over, single and repeat dose study to determine the pharmacokinetics of fluticasone furoate and GSK961081 when administered alone, in combination, or concurrently via the ELLIPTA
201959 Completed A Phase III study for the evaluation of the immunogenicity and reactogenicity of GSK Biologicals' Quadrivalent Split Virion Influenza Vaccine Fluarix Tetra (2015 season Southern Hemisphere) in adults 18 years of age and above Study Listed on ClinicalStudyDataRequest.com
201986 Completed PGx7611: Genetic Investigation of ALT elevations in Eltrombopag studies in ITP subjects
202 Completed A Single-Dose Bioequivalence/Effect of Food Evaluation of WELLBUTRIN® Sustained-Release
202012 PRJ2429: Effect of inhaled corticosteroid (ICS) particle size on asthma efficacy and safety outcomes: A systematic literature review and meta-analysis
202026 Not yet recruiting LAMICTAL Special Drug Use Investigation(mono-therapy for Typical Absence Seizure)
202029 Recruiting ZAGALLO Capsules Drug Use Investigation
202050 Completed PGx7607: PGx evaluation of pyrexia by meta-analysis of melanoma subjects from BRF113710, BRF113929, BRF113683, MEK115306 and MEK116513
202051 Completed PGX7608: PGx evaluation of efficacy of dabrafenib and trametinib by meta-analysis of melanoma subjects from BRF113710, BRF113929, BRF113683, MEK114267, MEK115306 and MEK116513
202055 Completed European Medicines Agency (EMA) post-authorisation safety study of influenza vaccine
202063 Completed Additional subgroup analysis of onabotulinumtoxinA phase III trial in post-stroke patients with upper limb spasticity
202065 Completed Meta-Analysis Plan for an exploratory analysis of a composite endpoint for deterioration to compare the efficacy of Umeclidinium/Vilanterol Inhalation Powder 62.5/25 mcg with tiotropium 18mcg in subjects with Chronic Obstructive Pulmonary Disease (COPD)
202066 Completed Meta-Analysis Plan for an analysis to compare the efficacy of Umeclidinium/Vilanterol Inhalation Powder 62.5/25 mcg with tiotropium 18mcg in subjects with Chronic Obstructive Pulmonary Disease (COPD)
202067 Completed Meta-Analysis Plan for an analysis to compare the addition of Umeclidinium Inhalation Powder 62.5mcg to ICS/LABA with Placebo plus ICS/LABA in subjects with Chronic Obstructive Pulmonary Disease (COPD).
202089 Completed Predictive effect of eosinophil counts on bronchodilator response in COPD

 

 

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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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