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Study ID Status Title Patient Level Data
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)
108223 Completed A retrospective, multi-centre observational study to evaluate disease management and adverse events in adult subjects with HIV-1 infection who were withdrawn from CNA106030 due to a positive HLA-B*5701 test result.
108251 Completed Evaluate immunogenicity & safety of a single or double-dose of the pandemic influenza candidate vaccine (GSK1562902A) given following a two-administration schedule (21 days apart) in adults over 60 yrs Study Listed on ClinicalStudyDataRequest.com
108257 Completed OCSIGEN study – Longitudinal follow-up of a cohort of patients with asthma treated with inhaled corticosteroids in primary care
108286 Completed An Italian Registry on the appropriate management of type 2 diabetes in a primary care setting
108314 Completed Seretide utilisation study in COPD
108344 Completed An open, multicentric, post-marketing surveillance study to monitor the safety and reactogenicity of GlaxoSmithKline Biologicals’ Poliomyelitis vaccine (inactivated) -Poliorix™, administered in Korean children as a primary vaccination in healthy subjects aged two to six months or as a booster vaccination in subjects aged four to six years
108366 Completed An Open-label, Sequential Study to Evaluate the Pharmacokinetics of Simvastatin When Coadministered With Albiglutide in Healthy Adult Subjects Study Listed on ClinicalStudyDataRequest.com
108370 Completed An adaptive design study for the assessment of the pharmacokinetics of albiglutide in subjects with normal renal function and subjects with moderate-to-severe renal impairment and hemodialysis. Study Listed on ClinicalStudyDataRequest.com
108372 Completed A single-site, randomized, double-blind, placebo-controlled, parallel-group, stepped glucose clamp study to assess the effects of albiglutide on counter-regulatory hormone responses and recovery from hypoglycemia in subjects with Type 2 diabetes mellitus. Study Listed on ClinicalStudyDataRequest.com
108392 Completed An open-label, multi-centre rollover study to assess the safety and efficacy of eltrombopag in thrombocytopenic subjects with hepatitis C virus (HCV) infection who are otherwise eligible to initiate antiviral therapy (peginterferon alfa-2a or peginterferon alfa-2b plus ribavirin)
108414 Completed A placebo-controlled, single blind, randomized two part study toinvestigate the tolerability, pharmacokinetics, and brainDopamine D3 receptor occupancy of increasing repeat doses ofGSK618334 for up to 21 days in healthy volunteers. Study Listed on ClinicalStudyDataRequest.com
108464 Completed A multicentre study to evaluate the immunogenicity and safety of GSK Biologicals’ HPV vaccine (580299) Co-administered with Boostrix Polio (dTpa-IPV) in healthy female subjects aged 10–18 years Study Listed on ClinicalStudyDataRequest.com
108486 Completed A Randomized, Open-Label, Active-Controlled, Parallel-Group, Multicenter Study to Determine the Safety and Efficacy of Albiglutide Administered in Combination With Insulin Glargine as Compared with the Combination of Insulin Glargine and Preprandial Lispro Insulin in Subjects With Type 2 Diabetes Mellitus Study Listed on ClinicalStudyDataRequest.com
108494 Completed A phase II, single-blind, randomized, controlled, multicentre vaccination study to evaluate the safety and immune response of the GSK Biologicals Zoster vaccine, gE/AS01B, and to compare 3 doses of gE with AS01B adjuvant in healthy elderly subjects, aged 60 to 69 years and 70 years and above.
108504 Completed An open label, single dose, randomised, parallel group pharmacokinetic study to evaluate a combination product containing naproxen sodium and sumatriptan in adolescent subjects with migraine and healthy adult subjects administered at three doses. Study Listed on ClinicalStudyDataRequest.com
108595 Mth18 Completed Assess long term persistence of a primary dose of GSK Biologicals' meningococcal vaccine 134612 versus one dose of Mencevax™ ACWY in healthy adolescents/young adults (15 to 19 years at vaccination) Study Listed on ClinicalStudyDataRequest.com
108638 Completed Immunogenicity and safety study of GlaxoSmithKline (GSK) Biologicals’ Boostrix (dTpa) vaccine and the Chinese DT vaccine, when administered as booster vaccination in healthy children aged 6-8 years Study Listed on ClinicalStudyDataRequest.com
108656 Completed A study to evaluate the immunogenicity, safety and reactogenicity of adjuvanted influenza vaccine candidates compared to Fluarix™ administered intramuscularly in subjects aged 18-59 years. Study Listed on ClinicalStudyDataRequest.com
108658 Completed Evaluate Non-Inferiority and Persistence of the Immune Response of GSK Biologicals' Meningococcal Vaccine 134612 Versus Meningitec™ or Mencevax™ ACWY in Healthy Subjects (1-10 Years of Age) Study Listed on ClinicalStudyDataRequest.com
108701 Terminated A randomized, open label, multicentre study to compare the pharmaco-economic implications of an analgesia based regimen with remifentanil and a conventional sedation based regimen using propofol in medical and post-surgical ICU subjects requiring mechanical ventilation for at least 2 days.
108706 Completed A dose-ranging study to compare the safety and immunogenicity of a candidate Human deficiency virus (HIV) vaccine 732461, adjuvanted or not, administered according to a 0, 1 month schedule to healthy adult HIV seronegative volunteers.
108708 Completed A study to evaluate the immunogenicity, safety and reactogenicity of a second vaccination with the adjuvanted influenza vaccine candidate compared to Fluarix™ administered intramuscularly in elderly aged 60 years and above. Study Listed on ClinicalStudyDataRequest.com
108712 Completed An open-label, 2-period, sequential treatment, drug interaction study to evaluate the effect of low-dose ritonavir on buproprion pharmacokinetics in healthy volunteers

 

 

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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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