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Study ID Status Title Patient Level Data
205875 Not yet recruiting A Post-Marketing Observational Study to Evaluate the Safety of Tykerb® in Chinese Patients
205905 Recruiting A Phase 1, open label, non-randomized, single center study to evaluate the safety and immunogenicity of 1 booster vaccination with (GVGH Shigella sonnei 1790GAHB) vaccine administered intramuscularly in healthy adults previously primed with three doses of the same vaccine in study H03_01TP compared to 1 vaccination with (1790GAHB) administered intramuscularly either to subjects who received placebo in the H03_01TP study or naïve subjects who were not part of H03_01TP study
205907 Not yet recruiting Phenotypes of Severe Asthma among Adults in Brazil: a descriptive report of characteristics of subjects followed up in the ProAR Cohort
205911 Completed A single centre, double-blind, randomised, placebo-controlled, and single dose-ascending study to investigate the safety, tolerability, pharmacokinetics, and pharmacodynamics, of single intravenous doses of GSK2315698 in healthy Japanese subjects
205913 Active not recruiting Subject Understanding of the Risks Associated with ZYBAN®, WELLBUTRIN®, WELLBUTRIN SR®, and WELLBUTRIN XL®
205915 Completed A Clinical Study to Evaluate the Ability of an Experimental Denture Adhesive to Prevent Food Particle Ingress Under Dentures
205920 Recruiting A randomized, open-label study to characterize the pharmacokinetics of inhaled oxytocin (GR121619) compared with IM oxytocin in women in the third stage of labour, and with IV oxytocin in non-pregnant, non-lactating women of childbearing potential
205930 Not yet recruiting Short term outcomes of Donation after Circulatory Death (DCD) renal transplantation in the United Kingdom
205932 Not yet recruiting New Study on the Prevalence of COPD in Spain EPI-Scan-II Study
206209 Active not recruiting An Interview Study in Adult Patients with Type 2 Diabetes Mellitus Using the Albiglutide Pen Injector
206215 Recruiting A randomized, open-label, cross-over, placebo-device study investigating critical and over all errors, training/teaching time, and preference attributes of the ELLIPTA dry powder Inhaler (DPI) as compared to HANDIHALER DPI used in combination with either DISKUS DPI or TURBUHALER DPI, in adult patients with Chronic Obstructive Pulmonary Disease (COPD)
206233 Not yet recruiting A Proof of Principle Bite Force Study Using Two New Test Adhesives and a Currently Marketed Denture Adhesive.
206239 Not yet recruiting A randomized, evaluator-blind, single-center, parallel-group clinical study designed to evaluate the local tolerance of two facial cleansers containing Benzoyl Peroxide (BPO) in comparison to a commercial control in healthy adults with mild to moderate acne vulgaris.
206251 Completed A Human Subject 24 Hour Patch Test to Assess the Irritation Potential of Four Skin Balm Products
206272 Active not recruiting Protocol for evidence synthesis to assess comparative efficacy of triple therapies versus other combination treatments for COPD in adult patients
206345 Not yet recruiting HO-16-16593 - Treatment Patterns, Discontinuation and pre-post analysis of Belimumab in the real-world setting
206347 Not yet recruiting HO-16-16611 - SLICC/SDI Indirect Cohort Comparison
206350 Completed Description of QoL data (SF-36 and FACIT) from the BLISS long-term extension study
206455 Not yet recruiting FF/UMEC/VI: Qualitative Interviews and Discrete Choice Experiment(s) Evaluating the Perceived Benefits of the Features of FF/UMEC/VI (single inhaler triple therapy) Treatment in the UK, US and Germany
206482 Active not recruiting HO-16-17302 - Assessment of adherence and costs in asthma patients using ICS/LABA in the US
206702 Not yet recruiting Assessment of FF/VI and other ICS/LABA’s on overall healthcare costs and outcomes in patients with COPD in the US
206707 Completed Indirect treatment comparison of ropinirole and pramipexole for management of symptoms in patients with advanced Parkinson’s disease
206774 Recruiting A randomized, evaluator-blind, single-center and two arm clinical study designed to evaluate the local tolerance and cosmetic efficacy of a topical skin care formulation in healthy female subjects with mild to advanced photo-damaged facial skin who have undergone a 70% Glycolic Acid facial peel procedure.
206784 Not yet recruiting Meta-analysis of Rotarix vaccine effectiveness
206822 Completed PGx7659: Exploratory Pharmacogenetic Investigation of Efficacy Response to Relvar/Breo in Asthma studies 106827, 106829, 106837, 113091 and 116863

 

 

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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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