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Study ID Status Title Patient Level Data
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
206409 Completed Comparative Effectiveness of Early versus Late Start with Umeclidinium/vilanterol
206435 Recruiting Observational Vignette Study to Examine Patient, Healthcare Provider, and Informal Caregiver Perceived Burden of Asthma-Related Exacerbations
206455 Active, not 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
206477 Active, not recruiting Administration and Usage Patterns for Albuterol and Asthma Controllers in Patients Using Inhaler Monitoring Technology
206482 Active, Not Recruiting HO-16-17302 - Assessment of adherence and costs in asthma patients using ICS/LABA in the US
206577 Recruiting Patient Interviews to Better Understand Disease Experience and Unmet Treatment Needs in Rheumatoid Arthritis
206599 Not yet recruiting HO-16-16395 - Research to understand the key concepts and endpoints within OA from patient perspective
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 Completed 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
206807 Not yet recruiting Medical Chart Review Study to Assess the Effectiveness and Safety of Dutasteride versus Finasteride in a Real World Clinical Setting in Patients with Androgenic Alopecia in South Korea
206817 Completed A Single Centre, Double Blind (Sponsor Open), Placebo Controlled, 3-Period Crossover, Ascending Dose Study in Japanese Healthy Elderly Male Subjects to Evaluate the Safety, Tolerability and Pharmacokinetics of Danirixin in the Fed State (Part1) and an open label, 2-way crossover to evaluate food effect on the pharmacokinetics of Danirixin (Part2)
206822 Completed PGx7659: Exploratory Pharmacogenetic Investigation of Efficacy Response to Relvar/Breo in Asthma studies 106827, 106829, 106837, 113091 and 116863
206823 Completed PGx7660: Exploratory Pharmacogenetic Investigation of Efficacy Response to Relvar/Breo in Phase III COPD studies 112206, 112207, 113108, and 200820
206827 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.
206886 Completed Dose Response of Three Experimental Dentifrices in Plaque Removal in a Single Brushing Model
206901 Not yet recruiting A randomized, open-label, cross-over, placebo inhaler study to evaluate the correct use of ELLIPTA™ dry powder inhaler (DPI) compared to DISKUS™ DPI used in combination with HandiHaler DPI in participants with Chronic Obstructive Pulmonary Disease (COPD)
206938 Not yet recruiting Meta Analysis of Dual Bronchodilators Impact of Lung Function Benefit vs. Spiriva
207014 Not yet recruiting A Clinical Study Investigating the Gingivitis Efficacy of a Stannous Fluoride Dentifrice in a Chinese Population.
207136 Recruiting Patient Characteristics and Treatment Modalities in COPD Patients Assessed by GOLD2016 : a Cross-Sectional Study in China
207192 Recruiting Impact of a Nutritional supplement on Bone turnover markers in Indian healthy premenopausal women (25-45 yrs; inclusive) after 6 months of intervention: a randomised double blind controlled trial

 

 

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