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Study ID Status Title Patient Level Data
2003-Pediatric-Review Completed Paediatric-only clinical trials results of investigation of suicide attempts and “possibly suicide-related” events (2003 Paediatric Review).
200401 Completed A Phase 1, Single Dose, Crossover, Relative Bioavailability Study of a Dolutegravir Dispersible Tablet as Compared to a Dolutegravir Pediatric Granule Formulation and Effect of Different Types of Water on the Dispersible Tablet in Healthy Volunteers(200401)
200405 Completed An observational retrospective database analysis to estimate the risk of multiple sclerosis following vaccination with Arepanrix™ in Manitoba, Canada
200559 Recruiting Special drug use investigation of XYZAL® Syrup 0.05%
200561 Completed An open-label, randomized, single dose, three-way crossover, six sequence pilot study to evaluate the relative bioavailability of one amlodipine 10mg tablet and rosuvastatin 20mg tablet to two fixed dose combination tablet formulations of amlodipine (10mg) and rosuvastatin (20mg) in healthy adult male and female subjects under fasting conditions Study Listed on ClinicalStudyDataRequest.com
200585 Recruiting Special Drug Use Investigation of ALLERMIST Nasal Spray in Pediatric Patients
200587 Completed An Open Label, Randomised, Four-Period Crossover, Single Dose Study in Healthy Volunteers to Evaluate the Pharmacokinetics of FF/UMEC/VI Combination Administered at Dose Levels 100/62.5/25 mcg and 100/125/25 mcg and in Comparison with FF/VI (100/25 mcg) and UMEC/VI (62.5/25 mcg). Study Listed on ClinicalStudyDataRequest.com
200591 Completed A Single-Center In Vitro Study to Evaluate GSK1325756 Inhibition of CD11b Cell Surface Expression in Healthy Adults and Respiratory Syncytial Virus-Infected Children <2 Years (200591)
200592 Terminated Single-blind, randomised, placebo-controlled study to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of repeat doses of GSK2647544 and its potential pharmacokinetic interaction with simvastatin in healthy volunteers
200600 Completed Evaluation of clinical and economic benefits of fluticasone furoate compared with mometasone furoate and budesonide in the treatment of allergic rhinitis
200606 Active not recruiting Risk of Adverse Events and Costs Associated with Chronic Systemic Corticosteroid Use in UK Patients with Severe Asthma
200612 Completed A protocol to collect human serum samples from healthy adults
200613 Completed An observer-blind study to evaluate the safety and immunogenicity of GSK Biologicals’ influenza vaccine(s) GSK2789869A administered in adults 65 years of age and older
200619 Active not recruiting A Meta-analysis Evaluation of Baseline Factors Which Correlate with High Baseline BLyS Levels (>2ng/mL) (BLISS-52 & BLISS 76)
200632 Completed PGX6847: Exploratory PGx investigation of dabrafenib efficacy in melanoma monotherapy studies BRF113710, BRF113929, and BRF113683
200633 Completed PGX6848: Exploratory PGx investigation of trametinib efficacy in a melanoma monotherapy study MEK114267
200638 Completed Contac Bien Z Adverse Effect Survey
200638 Completed Contac Bien Z Adverse Effect Survey
200697 Completed A Single-Dose, Open-Label, Randomized, Parallel-Group Study to Demonstrate the Bioequivalence of Lamotrigine Dispersible/Chewable Tablet (100mg) and Lamotrigine Compressed Tablet (100mg) in Healthy Chinese Male Subjects Study Listed on ClinicalStudyDataRequest.com
200699 Completed 200699: A Clinical Study to Evaluate Four Doses of Umeclidinium Bromide in Combination with Fluticasone Furoate in COPD Subjects with an Asthmatic Component
2006-Analysis Completed Paroxetine Adult Suicidality Analysis (2006 Dataset)
200713 Not yet recruiting Characteristics of out-patients with epilepsy and patterns of antiepileptic drug utilisation in neurology department at tertiary hospitals: A Cross-Sectional Study in China
200725 Not yet recruiting TENOZET® Drug Use Investigation
200726 Active not recruiting TENOZET® Special Drug Use Investigation
200773 Completed Pazopanib Sarcoma Named Patient Programme Chart Review

 

 

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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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