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Study ID Status Title Patient Level Data
107531 Completed Assess the immunogenicity of 3 doses of Pediarix®, Prevnar® & ActHIB® given to healthy infants when administered with GSK Biologicals’ 2 dose oral live attenuated human rotavirus vaccine given during the same vaccination visit or separately Study Listed on ClinicalStudyDataRequest.com
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
107622 Completed Remifentanil effect in continuous infusion compared to bolus administration of fentanyl in thoracic surgery for pulmonary resection
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
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
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
107915 Completed ArchiMed Hospital : Prevention of venous thromboembolic events with ARIXTRA® 2,5 mg for medical ill patients.
107917 Completed Prevention of venous thromboembolic events with Arixtra 2.5mg for medical ill patients in general practice
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.
107973_1 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
108034 Completed A post marketing survailance to monitor the safety of Arixtra administered in Korean subjects according to the prescription information
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
108127 Completed An Open-Label, Non-Randomized, Single-Dose Study To Evaluate Serum Zanamivir Pharmacokinetics Following Intravenous Administration to Human Subjects With Renal Impairment Compared to Subjects Without Renal Impairment 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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