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Study ID Status Title Patient Level Data
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
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
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
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
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
114444 Completed Study to assess the replication of Porcine circovirus type 1 (PCV-1) GSK Biologicals’ oral live attenuated human rotavirus vaccine (444563) recipients aged 6 to 12 weeks who participated in 444563/022 (Rota-022), 444563/033 (Rota-033), 103477 (Rota-039) and 104480 (Rota-048)
114451 Completed Immunogenicity and Safety Study of GSK Biologicals' Seasonal (2010-2011) Influenza Vaccine Fluarix™ in Children Previously Vaccinated With GSK Biologicals' H1N1 Vaccine Pandemrix™ Study Listed on ClinicalStudyDataRequest.com
114452 Completed Immunogenicity and Safety Study of GSK Biologicals' Seasonal (2010-2011) Influenza Vaccine FluarixTM in Adolescents Previously Vaccinated With GSK Biologicals' H1N1 Vaccine PandemrixTM Study Listed on ClinicalStudyDataRequest.com
114454 Terminated Immunogenicity and safety of Fluarix™/ Influsplit SSW® 2010/2011 or Pandemrix™ Study Listed on ClinicalStudyDataRequest.com
114458 Completed A phase 2a study to evaluate the effect of rilapladib (SB-659032) on biomarkers related to the pathogenesis and progression of Alzheimer’s disease Study Listed on ClinicalStudyDataRequest.com
114460 Completed Safety, immunogenicity and efficacy against malaria in the sporozoite challenge model of one dose of Ad35.CS.01 malaria vaccine followed by two doses of malaria 257049 vaccine in healthy malaria-naïve adults Study Listed on ClinicalStudyDataRequest.com
114464 Completed Safety and immunogenicity of monovalent H5N1 vaccine GSK1557484A in children 6 months to < 18 years of age Study Listed on ClinicalStudyDataRequest.com
114471 Completed PGx320 Tykerb TEACH EGF105485 liver safety pharmacogenetics
114495 Completed An observer-blind safety and immunogenicity study of GSK Biologicals’ A/California/7/2009 (H1N1)v-like vaccines GSK2340274A and GSK2340272A in children 3 to less than 10 years old Study Listed on ClinicalStudyDataRequest.com
114496 Completed A randomised, double-blind, multi-centre study to evaluate the efficacy and safety of inhaled fluticasone furoate in the treatment of persistent asthma in adults and adolescents currently receiving mid to high strength inhaled corticosteroids. Study Listed on ClinicalStudyDataRequest.com
114522 Completed A nested case-control study of the association between Coreg IR and Coreg CR and hypersensitivity reactions: anaphylactic reaction/angioedema-Updated Analysis
114522_1 Completed A nested case-control study of the association between Coreg IR and Coreg CR and hypersensitivity reactions: anaphylactic reaction/angioedema-Updated Analysis
114535 Completed Blinded retrospective laboratory evaluations to assess the serologic response to Porcine circovirus type 1 (PCV-1) in the serum of infants aged 2 and 6 months and toddlers aged 4-6 years following administration of GlaxoSmithKline (GSK) Biologicals’ IPV-containing vaccines
114541 Completed Efficacy study of GSK Biologicals’ quadrivalent influenza vaccine, GSK2282512A, (FLU Q-QIV) when administered in children Study Listed on ClinicalStudyDataRequest.com
114544 Completed A single-blind, randomized, comparative pilot study evaluating the tolerability of two topical combination therapies in the treatment of acne vulgaris Study Listed on ClinicalStudyDataRequest.com
114546 Completed Two-week Study to Determine and Compare the Tolerance and Irritation Potential of Duac® Topical Gel (clindamycin 1% and benzoyl peroxide 5%) to ACANYA™ Gel (clindamycin phosphate 1.2% and benzoyl peroxide 2.5%) Topical Acne Medications Study Listed on ClinicalStudyDataRequest.com
114547 Completed A single-blind, randomized, comparative split-face study evaluating the tolerability of clindamycin and benzoyl peroxide gel to benzoyl peroxide/adapalene gel in the treatment of acne vulgaris. Study Listed on ClinicalStudyDataRequest.com

 

 

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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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