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Study ID Status Title Patient Level Data
107564 Completed An observational study to investigate the incidence of influenza and influenza-related complications, in adults between 50-64 years and elderly adults 65 years and over vaccinated with Fluarix™ Study Listed on ClinicalStudyDataRequest.com
107625 Completed Efficacy, safety, reactogenicity and immunogenicity study of the lyophilised formulation of Rotarix vaccine in healthy Japanese infants Study Listed on ClinicalStudyDataRequest.com
107638 Completed Efficacy, immunogenicity and safety of GlaxoSmithKline Biologicals’ HPV GSK 580299 vaccine in healthy Chinese female subjects Study Listed on ClinicalStudyDataRequest.com
107671 Terminated Study EGF107671 – a Phase II Study of Lapatinib plus Topotecan or Lapatinib plus Capecitabine in the Treatment of Recurrent Brain Metastases from ErbB2-Positive Breast Cancer Following Cranial Radiotherapy
107682 Completed A randomized, open study to evaluate the safety and immunogenicity of GlaxoSmithKline Biologicals’ HPV vaccine Co-administered intramuscularly with Boostrix® and/or Menactra™ in healthy female subjects aged 11–18 years Study Listed on ClinicalStudyDataRequest.com
107706 Completed To assess safety, reactogenicity & immunogenicity of a booster dose of pneumococcal conjugate vaccine, co-admin with GSK Biologicals’ MMRV vaccine in children (2nd yr of life) primed with the pneumococcal conjugate vaccine in study 105553. Study Listed on ClinicalStudyDataRequest.com
107727 Completed Single-blind, randomised, placebo-controlled study to assess the safety, tolerability and pharmacokinetics of repeat doses of GSK1014802 and its interaction with food in healthy volunteers
107731 Completed Adjuvant justification study of candidate malaria vaccines (257049), administered according to a 0, 1, 2 months schedule . Study Listed on ClinicalStudyDataRequest.com
107737 Completed Study to assess the safety and immunogenicity of GSK Biologicals 10-valent pneumococcal conjugate vaccine when Co-administered with DTPa-HBV-IPV/Hib (Infanrix-Hexa) vaccine in preterm infants as a 3-dose primary immunization course during the first 6 months of life. Study Listed on ClinicalStudyDataRequest.com
107806 Completed An open label study to determine the safety, tolerability, excretion balance and pharmacokinetics of [14C]GW856553, administered as a single dose of an oral solution to healthy adult male subjects
107824 Completed A study to evaluate the long-term antibody persistence at 1, 3 & 5 years after the administration of a fourth dose of Hib-MenCY-TT Vaccine compared to ActHIB in subjects boosted in a previous study. Study Listed on ClinicalStudyDataRequest.com
107846 Completed Clinical Evaluation of Ropinirole CR-RLS Tablets in Restless Legs Syndrome-Open-Label, Uncontrolled Study. Classification: Clinical Pharmacology, Exploratory Study Listed on ClinicalStudyDataRequest.com
107863 Completed Evaluation of the safety and immunogenicity of GlaxoSmithKline Biologicals' HPV vaccine 580299 (Cervarix TM) in adult human immunodeficiency virus (HIV) infected female subjects Study Listed on ClinicalStudyDataRequest.com
107876 Completed Study to evaluate clinical consistency of the liquid formulation of GSK Biologicals' HRV vaccine and to evaluate liquid formulation compared to lyophilised formulation of the HRV vaccine administered as a two-dose primary vaccination. Study Listed on ClinicalStudyDataRequest.com
107895 Withdrawn A single center four part study in healthy adult subjects to evaluate: the safety, tolerability and pharmacokinetics of a single oral dose and repeat escalating oral doses of GSK945237; the effect of linezolid on hematology safety parameters; and the effects of GSK945237 and moxifloxacin on QTc.
107915 Completed ArchiMed Hospital : Prevention of venous thromboembolic events with ARIXTRA® 2,5 mg for medical ill patients.
107924 Completed Open, booster vaccination study to assess safety and reactogenicity of GSK Biologicals’ dTpa vaccine (Boostrix) when administered to healthy chinese children 6-8 years of age. Study Listed on ClinicalStudyDataRequest.com
107973 Completed A phase II, open, controlled study to evaluate the reactogenicity and the immunogenicity of GlaxoSmithKline Biologicals' adjuvanted influenza vaccine in elderly adults previously vaccinated with either Fluarix™ or the adjuvanted vaccine.
107975 Completed A study to evaluate the immunogenicity, safety and reactogenicity of adjuvanted influenza vaccine candidate compared to Fluarix™ (GlaxoSmithKline Biologicals) administered intramuscularly in elderly aged 60 years and older. Study Listed on ClinicalStudyDataRequest.com
107979 Completed TXA107979: A Randomized, Multicenter, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of a Combination Product Containing Sumatriptan and Naproxen Sodium for the Acute Treatment of Migraine in Adolescents Study Listed on ClinicalStudyDataRequest.com
108052 (FU month 18) Completed A long-term, follow-up of the immunogenicity and safety of GlaxoSmithKline Biologicals’ novel HPV vaccine in healthy female subjects vaccinated in the primary study Study Listed on ClinicalStudyDataRequest.com
108062 Completed A three part, staggered cohort, open-label and double blind, randomized, placebo controlled study to investigate the efficacy, safety, tolerability and pharmacokinetics of eltrombopag, a thrombopoietin receptor agonist, in previously treated pediatric patients with chronic ITP.
108109 Completed Clinical Evaluation of SB-497115-GR in Chronic Idiopathic Thrombocytopenic Purpura (ITP) -A Multicenter Study in Subjects with Chronic ITP Receiving a Double-Blind, Placebo-Controlled, Short-Term Treatment Followed by an Open-Label, Uncontrolled, Long-Term Treatment
108134 Completed A study to demonstrate the efficacy of GSK Biologicals’ influenza vaccine (Fluarix™) administered intramuscularly in adults Study Listed on ClinicalStudyDataRequest.com
108160 Terminated Post-marketing surveillance study to monitor safety of vaccination (according to Prescribing Information) with GlaxoSmithKline Biologicals' human papillomavirus vaccine (HPV-16/18 L1/AS04) in healthy filipino females (3,000; aged 10 years or older)

 

 

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