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Study ID Status Title Patient Level Data
201594 Completed An open-label study of the ease of use and correct use of placebo ELLIPTA dry powder inhaler in subjects with asthma
201595 Completed Post-hoc Analyses of Eosinophil Subgroups using Pooled Data from HZC102871 and HZC102970
201598 Recruiting An exploratory, retrospective laboratory evaluation of the humoral immune response in adults and children to the H1 HA stalk domain and other influenza A virus protein epitopes, after administration of GSK Biologicals’ pandemic influenza vaccines
201600 Not yet recruiting BOTOX Drug Use Investigation (Strabismus)
201604 Completed Patient Satisfaction and Symptom Management Goal: Survey of Japanese adult patients with bronchial asthma receiving inhaled corticosteroid-containing medications
201608 Completed PGx7592: Evaluation of the Effect of BIM Germline Variants on Pazopanib Efficacy in Patients with Cancer
201614 Completed An Open Label, Single-arm Study Evaluating a New Thermostable Formulation of FLOLAN™ in Japanese Subjects with Pulmonary Arterial Hypertension (PAH)
201624 Completed PGx7571: Pharmacogenetic Evaluation of FCGR Variation in patients treated with ofatumumab in study OMB115991
201625 Completed PGx7602: Pharmacogenetic Evaluation of FCGR Variation in patients treated with ofatumumab in study OMB110927
201627 Completed PGx7604: Pharmacogenetic Evaluation of FCGR Variation in patients treated with ofatumumab in study OMB114242
201630 Recruiting Long term hepatitis A virus (HAV) antibody persistence in children vaccinated with 1 dose and those vaccinated with 2 doses of Havrix® in Panama
201634 Completed PGx7575: Pharmacogenetic Evaluation of FCGR Variation in patients treated with ofatumumab in study OMB110928
201636 Active, not recruiting A Phase III, Randomized, Multicenter, Parallel-group, Non-inferiority Study Evaluating the Efficacy, Safety, and Tolerability of Switching to Dolutegravir Plus Rilpivirine From Current INI-, NNRTI-, or PI-based Antiretroviral Regimen in HIV-1-Infected Adults who are Virologically Suppressed (SWORD-1)
201637 Active, not recruiting A Phase III, Randomized, Multicenter, Parallel-group, Non-inferiority Study Evaluating the Efficacy, Safety, and Tolerability of Switching to Dolutegravir Plus Rilpivirine From Current INI-, NNRTI-, or PI-based Antiretroviral Regimen in HIV-1-Infected Adults who are Virologically Suppressed (SWORD-2)
201641 Active, Not Recruiting HO-14-14607 - OBSERVATIONAL STUDY TO EXPLORE THE SAFETY, COSTS AND HEALTH CARE RESOURCE UTILIZATION, ASSOCIATED WITH FIRST LINE ARZERRA (OFATUMUMAB) OR GAZYVA (OBINUTUZUMAB) THERAPIES IN PATIENTS WITH UNTREATED CHRONIC LYMPHOCYTIC LEUKEMIA (CLL) IN REAL WORLD SETTING
201657 Completed Meta-analysis of clinical efficacy studies of licensed Rheumatoid Arthritis (RA) treatments
201659 Terminated An Adaptive Design Open Label Pilot Study in Rheumatoid Arthritis Patients to Assess Inflammation Using Molecular Imaging Techniques
201661 Completed Skin Residency Study of Topically Applied GSK2894512 Cream in Healthy Volunteers
201663 Not yet recruiting Immunogenicity, reactogenicity and safety study of Pediarix®, Hiberix® and Prevenar 13® co-administered with two different formulations of GSK Biologicals’ HRV vaccine (444563) in healthy infants 6-12 weeks of age
201664 Recruiting A three-part open-label, non-randomised, dose-escalation study to investigate the safety and tolerability of GSK3039294 administered as a single dose to healthy volunteers, and as repeat dose to healthy volunteers and patients with systemic amyloidosis
201670 Completed Indirect Comparison of Albiglutide and Exenatide QW using the Bucher method
201672 Withdrawn A Phase I, Open-Label, Dose-Finding Study of Afuresertib Administered in Combination with either Enzalutamide (Xtandi) or Abiraterone (Zytiga) in Male Subjects with Metastatic Castration-Resistant Prostate Cancer (mCRPC)
201673 Not yet recruiting Impact of early versus late co-administration of Advair in patients treated with tiotropium for the management of COPD in Quebec
201674 Completed A Phase I, 2-part relative oral bioavailability study of different fixed dose combinations of dolutegravir and rilpivirine in fasted and fed healthy subjects
201677 Recruiting A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Sirukumab in the Treatment of Patients with Giant Cell Arteritis

 

 

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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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