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Study ID Status Title Patient Level Data
103413 Completed An International Randomized Study Evaluating the Efficacy and Safety of Fondaparinux Versus Control Therapy in a Broad Range of Patients With ST Segment Elevation Acute Myocardial Infarction. Study Listed on ClinicalStudyDataRequest.com
103414 Completed A multicenter, randomized, double-blind, parallel group trial to demonstrate the efficacy of fondaparinux sodium in association with Intermittent Pneumatic Compression (IPC) versus IPC used alone for the prevention of venous thromboembolic events in subjects at increased risk undergoing major abdomi Study Listed on ClinicalStudyDataRequest.com
103420 Completed An international, randomized, double-blind study evaluating the efficacy and safety of fondaparinux versus enoxaparin in the acute treatment of unstable angina/non ST-segment elevation MI acute coronary syndromes Study Listed on ClinicalStudyDataRequest.com
103441 Completed A Randomised, Open-Label Study to Evaluate the Efficacy and Safety of a treatment optimisation with Trizivir during 96 weeks after a first antiretroviral treatment in HIV-1 Infected Subjects
103447 Completed A study to evaluate the effect of casoptiant on cardiac conduction as assessed by 12-lead electrocardiogram as compared to placebo and moxifloxacin Study Listed on ClinicalStudyDataRequest.com
103471 Completed A randomised, double blind, placebo-controlled, double dummy, five-way cross over dose-escalation study to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of single inhaled doses of GSK233705 (20-500ug via DPI), and , tiotropium bromide (18ug via DPI) in healthy male subjects Study Listed on ClinicalStudyDataRequest.com
103477 Completed See Detailed Description Study Listed on ClinicalStudyDataRequest.com
103478 Completed Assess the immunogenicity, safety & reactogenicity of 2 doses of GSK Biologicals’ oral live attenuated human rotavirus (HRV) vaccine in healthy infants (6-12 weeks of age at first dose) previously uninfected with human rotavirus Study Listed on ClinicalStudyDataRequest.com
103488 Completed A randomized, controlled, phase II study to evaluate the safety and immunogenicity of different formulations of GlaxoSmithKline Biologicals’ 11-valent pneumococcal conjugate vaccine, when administered intramuscularly as a 3-dose primary immunization (2-3-4 month schedule) before 6 months of age Study Listed on ClinicalStudyDataRequest.com
103506 Completed Immunogenicity and safety study of GlaxoSmithKline Biologicals’ Infanrix hexa vaccine in healthy infants
103514 Completed Phase 3, open, age-stratified study to assess immunogenicity and safety of GSK Biologicals' HPV-16/18 vaccine administered intramuscularly according to 3-dose schedule (0,1,6 months) in healthy female subjects aged 15 - 55 years and long term follow-up Study Listed on ClinicalStudyDataRequest.com
103532 Completed Assess the immunogenicity, safety, reactogenicity of 1 dose of 4 different formulations of GSK Biologicals’ meningococcal conjugate vaccine (MenACWY) vs 1 dose of Mencevax™ ACWY in healthy subjects aged 15-19 yrs Study Listed on ClinicalStudyDataRequest.com
103533 Completed Evaluate the immunogenicity, reactogenicity, safety of 4 different formulations of GSK Biologicals' conjugate vaccine (MenACWY) vs 1 dose of MenC-CRM197 or Mencevax™ ACWY in children aged 12-14 months & 3-5 years Study Listed on ClinicalStudyDataRequest.com
103629 Completed An open-label, randomized, 3-period crossover study to evaluate sumatriptan pharmacokinetics for a TREXIMA™ (sumatriptan succinate / naproxen sodium) Tablet followed by IMITREX® (sumatriptan succinate) Injection 4mg administered using the IMITREX STATdose System® and a TREXIMA tablet followed by IMI Study Listed on ClinicalStudyDataRequest.com
103632 Completed A Randomized, Double-Blind, Multi-Center, Placebo-Controlled, Cross-Over Study to Determine the Consistency of Response for TREXIMA™ (sumatriptan 85mg/naproxen sodium 500mg)*, Administered During the Mild Pain Phase for the Acute Treatment of Multiple Migraine Attacks Study Listed on ClinicalStudyDataRequest.com
103792 Completed A multicenter study of the immunogenicity & safety of 2 doses of GSK Biologicals’ oral live attenuated human rotavirus vaccine (RIX4414) as primary dosing of healthy infants in India aged approximately 8 wks at the time of the first dose
103811 Completed See Detailed Description
103812 & 104727 Completed Study to assess safety and reactogenicity of booster dose of either an investigational vaccination regimen or DTPw-HBV/Hib when administered at 15 to 18 months of age and of a dose of Mencevax ACWY vaccine.
103813 Completed A phase III, randomized, multinational study, double-blinded for the immunogenicity and consistency evaluation of 3 Hib-MenCY-TT vaccine lots and single-blinded and controlled for the evaluation of safety and immunogenicity of GSK Biologicals' Haemophilus influenzae type b and Neisseria meningitidis serogroups C and Y-tetanus toxoid conjugate vaccine combined (Hib-MenCY-TT) compared to monovalent Hib vaccine in healthy infants at 2, 4, 6, and 12 to 15 months of age. Study Listed on ClinicalStudyDataRequest.com
103814 Completed An open label, multicenter phase IV study of adefovir dipivoxil in Korean patients with chronic hepatitis B (CHB)
103860/015 Completed A study of the reactogenicity, immunogenicity, and protective efficacy of three doses (20mcg or 40mcg) of the Smith Kline – RIT recombinant DNA yeast-derived hepatitis B vaccine in homosexual males
103860/064 Completed Immunogenicity and protective efficacy of SmithKline Beecham Biological’s recombinant-DNA hepatitis B vaccine (10µg) in newborns of HbeAg+ and HbsAg+ mothers in comparison with a historical control group
103860/115bis Completed Immunogenicity and protective efficacy of SmithKline Beecham Biologicals’ hepatitis B vaccine (10 µg) in newborns of HBeAg and HBsAg positive mothers compared with a historical control group.
103860/128 Completed A study to evaluate antibody responses to 10 and 20 µg of licensed recombinant hepatitis B vaccine among elderly patients
103860/215 Completed Assessment of the clinical acceptability and immunogenicity of SmithKline Biologicals’ recombinant DNA hepatitis B vaccine in HIV seropositive (HIV+) and HIV seronegative (HIV-) subjects

 

 

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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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