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Study ID Status Title Patient Level Data
114324 Completed BOTOX®(BOTOX is a registered trade mark of Allergan, Inc) Injection 50 and 100Treatment of Equinus Foot due to Lower Limb Spasticity in Juvenile Cerebral Palsy Patients Aged 2-year or Older:Investigation of Patient Background Characteristics
114332 Completed Drug Use Investigation for Cervarix®
114334 Completed A comparative bioavailability study to compare the pharmacokinetic (PK)and pharmacodynamic (PD) effects of Fluticasone propionate and Salmeterol delivered by Fluticasone propionate/ Salmeterol combination in a capsule-based inhaler and a multi-dose dry powder inhaler, in moderate asthma patients and moderate to severe COPD patients.
114341 Completed A phase 2, multi-centre, randomised, double-masked, placebo-controlled, parallel-group study to investigate the safety, tolerability, efficacy, pharmacokinetics and pharmacodynamics of GSK933776 in adult patients with geographic atrophy (GA) secondary to age-related macular degeneration (AMD)
114346 Completed A Phase I, Randomized, Placebo-Controlled, Four-Way Crossover Study to Evaluate the Effect of Intravenous (IV) Zanamivir on Cardiac Conduction as Assessed by 12-lead Electrocardiogram (ECG) with Moxifloxacin as a Positive Control in Healthy Volunteers Study Listed on ClinicalStudyDataRequest.com
114347 Completed A single-blind, placebo-controlled study to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of repeat ascending doses of GSK2018682 (S1P1 agonist) in healthy volunteers Study Listed on ClinicalStudyDataRequest.com
114350 Completed Study on the MAGE A3 polymorphism and MAGE A3 and PRAME expression levels in Chinese NSCLC patients (NOT FINAL TITLE)
114351 Completed Immunogenicity, reactogenicity and safety study of GlaxoSmithKline (GSK) Biologicals’ oral live attenuated human rotavirus (HRV) vaccine in healthy Taiwanese infants who received hepatitis B immunoglobulin after birth. Study Listed on ClinicalStudyDataRequest.com
114371 Completed Immunogenicity and safety study of GSK Biologicals’ cell culture derived pandemic influenza vaccines GSK2590066A and GSK2592984A administered to healthy adults 18 - 49 years old Study Listed on ClinicalStudyDataRequest.com
114373 Completed A Phase III international, randomized, double-blind, double-dummy study to evaluate the efficacy and safety of 300 mg or 600 mg of intravenous zanamivir twice daily compared to 75 mg of oral oseltamivir twice daily in the treatment of hospitalized adults and adolescents with influenza
114379 Completed Safety study of GSK Biologicals’ human papillomavirus vaccine (GSK-580299) in healthy female control subjects from the GSK HPV-023 study
114382 Completed An open label, multi-centre, non-interventional post-marketing surveillance (PMS) to monitor the safety and efficacy of ZIAGEN® administered in Korean patients according to the prescribing information
114386 Completed Immunogenicity and safety of a booster dose of GlaxoSmithKline Biologicals’ IPV (Poliorix™) and DTPa/Hib (Infanrix+Hib™) in healthy Chinese toddlers
114387 Completed A Randomized, Double-Blind, Double-Dummy, Placebo-Controlled, Three-Treatment, Three 6-Week Period Cross-Over, Multi-Center Study to Evaluate the Effect of Adding GSK2190915 300mg as Compared to Adding Montelukast 10mg or Placebo Tablets QD to Fluticasone Propionate/Salmeterol 250/50mcg Diskus BID Study Listed on ClinicalStudyDataRequest.com
114397 Completed Documentation of Factor V Leiden R506Q and prothrombin 20210G>A risk variants in chronic idiopathic thrombocytopaenic purpura (ITP) and chronic liver disease (CLD) patients experiencing thrombotic/thromboembolic events (TEE) during clinical studies with eltrombopag
114398 Completed Paroxetine Pharmacokinetics Gender Differences
114403 Completed A single-blinded, randomized, placebo-controlled, staggered-parallel, escalating dose study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of GSK2374697 in healthy volunteers Study Listed on ClinicalStudyDataRequest.com
114411 Completed A Phase I study of Pazopanib as a single agent for children with refractory solid tumors
114416 Completed A Randomised, Single Blind, Placebo-Controlled, Cross-over, Phase 1 Methodology Study to validate the Cantharidin Blister Model in Healthy Male Volunteers
114417 Completed An exercise endurance study to evaluate the effects of treatment of Chronic Obstructive Pulmonary Disease (COPD) patients with a dual bronchodilator: GSK573719/GW642444. Study A Study Listed on ClinicalStudyDataRequest.com
114418 Completed An exercise endurance study to evaluate the effects of treatment of Chronic Obstructive Pulmonary Disease (COPD) patients with a dual bronchodilator: GSK573719/GW642444. Study B Study Listed on ClinicalStudyDataRequest.com
114420 Completed Additional Health and Economic Impact of the bivalent versus the quadrivalent HPV vaccine in Taiwan: results of a prevalence-based model
114422 Completed A Randomized, Placebo Controlled Dose Escalation Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Single Oral Doses of GSK1322888 in Healthy Caucasian and Japanese Asian Adult Subjects Study Listed on ClinicalStudyDataRequest.com
114424 Completed BEL114424: A Phase 2 Pilot, Multicentered, Randomised, Double Blind, Placebo-Controlled Study to Evaluate the Potential for Efficacy and the Safety of Belimumab plus Standard of Care versus Placebo plus Standard of Care in the Prevention of Allograft Rejection in Adult Subjects After Renal Transplantation
114427 Completed Risk of pancreatic cancer and renal cancer in patients exposed to gabapentin in the United Kingdom General Practice Research Database

 

 

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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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