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Study ID Status Title Patient Level Data
205883 Recruiting A multi-centre, one-arm prospective study to evaluate efficacy and safety of switching from Entecavir (ETV) to Tenofovir Disoproxil Fumarate (TDF) in Japanese chronic hepatitis B HBeAg-positive and HBV-DNA undetectable subjects
205905 Completed 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 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
206213 Active, not recruiting An Ancillary Study Protocol to GlaxoSmithKline Phase IIb RTS,S/AS01E Malaria Vaccine Trial (Study Number 204889 [MALARIA-094]) entitled, “Efficacy, safety and immunogenicity study of GSK Biologicals’ candidate malaria vaccine (SB257049) evaluating schedules with or without fractional doses, early Dose 4 and yearly doses, in children 5-17 months of age"
206215 Completed 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 Completed A Proof of Principle Bite Force Study Using Two New Test Adhesives and a Currently Marketed Denture Adhesive.
206239 Completed 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.
206243 Not yet recruiting A Prospective, Longitudinal Study to Investigate the Effect of Thermal Injury on Intestinal Permeability and Systemic Inflammation (HESTIA)
206246 Not yet recruiting An Open-label, Dose-escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Doses of GSK2586881 in Participants with Pulmonary Arterial Hypertension
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
206325 Recruiting Qualitative research to characterize the patient experience of nasal polyps
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
206351 Not yet recruiting Pooled analysis of the real-world effectiveness of belimumab using multi-country data from the OBSErve studies
206408 Not yet recruiting Disease progression and economic evaluation of clinically important deterioration (CID): conceptual development, applications and validation
206409 Completed Comparative Effectiveness of Early versus Late Start with Umeclidinium/vilanterol

 

 

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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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