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Study ID Status Title Patient Level Data
393229/028 Completed A Multi-Center, Randomized, Phase 3 Study of Rituximab versus Iodine I 131 Tositumomab Therapeutic Regimen For Patients With Relapsed Follicular Non-Hodgkins Lymphoma Study Listed on ClinicalStudyDataRequest.com
393229/032 Completed A single arm, open-label, multicentre, phase II study of Tositumomab and Iodine 131-Tositumomab in subjects with indolent non-Hodgkin's Lymphoma who have previously received Rituximab. Study Listed on ClinicalStudyDataRequest.com
402764/004 Completed A phase III, open, randomized study to evaluate the immunogenicity and reactogenicity of investigational vaccination regimens Study Listed on ClinicalStudyDataRequest.com
402764-003 Completed A phase II, open, randomized study to assess the immune memory induced by a primary vaccination course of an investigational vaccination regimen and the immunogenicity and reactogenicity of a fourth dose of an investigational vaccination regimen given to healthy toddlers primed in study 402764-001
404 Completed Effect of chronic Wellbutrin SR administration on craving, withdrawal, and impairment of cognitive performance associated with nicotine abstinence.
404286/006 Completed A phase II, open, randomized, controlled study to assess the immune memory induced by an investigational vaccination regimen and the safety, reactogenicity and immunogenicity of a booster dose of an investigational vaccination regimen in toddlers primed in study 404286/001. Study Listed on ClinicalStudyDataRequest.com
407 Completed Pharmacokinetics and metabolism of Wellbutrin (bupropion hydrochloride) sustained-release in healthy smokers versus non-smokers.
408DP-02 Completed A Multi-Centre Randomized, Double-Blind, Parallel-Group, Comparison of Salmeterol Xinafoate Inhalation Rotadisk Versus Tulobuterol Tape in Subjects with Persistent Adult Asthma Treated with Inhaled Corticosteroid.
408DP-03 Completed A Multi-Centre, Randomized, Double-Blind, Parallel-Group, Comparison of Salmeterol Xinafoate Inhalation Rotadisk Versus Placebo in Subjects with Chronic Obstructive Pulmonary Disease Treated with Current Medications.
40UK Completed Effect of multiple doses of bupropion on antipyrine disposition in healthy volunteers.
40UKA Completed The disposition of bupropion and its basic metabolites in young and elderly healthy volunteers.
424323/007 Completed A study to assess the effect of repeat dosing of a New Chemical Entity (NCE) on the steady-state pharmacokinetics and pharmacodynamics of digoxin in healthy volunteers.
430C/83/6 Completed The single dose kinetics in man of 120mg of BW430C, a potential anticonvulsant.
444563/001 Completed A phase I, double-blind, randomized, placebo-controlled study of the safety and reactogenicity of a single oral dose of the SmithKline Beecham Biologicals’ live attenuated human rotavirus (HRV) vaccine in healthy adults aged 18 to 45 years
444563/002 Completed A phase I, double-blind, randomized, placebo-controlled study of the safety and reactogenicity of GSK Biologicals’ live attenuated human rotavirus vaccine at 2 different virus concentrations in healthy seropositive children between 1 and 3 years of age, when given as a single oral administration Study Listed on ClinicalStudyDataRequest.com
444563/003 Completed A phase II, double-blind, randomized, placebo-controlled, dose-escalating, stepwise study to assess safety, reactogenicity and immunogenicity of GlaxoSmithKline Biologicals’ live attenuated human rotavirus (HRV) vaccine in healthy infants previously uninfected with human rotavirus. Study Listed on ClinicalStudyDataRequest.com
444563/004 Completed A study to assess the efficacy, immunogenicity and safety of two doses of oral live attenuated human rotavirus (HRV) vaccine (Rotarix) in healthy infants. Study Listed on ClinicalStudyDataRequest.com
444563/004 Annex Completed A phase IIb, double-blind, randomized, placebo-controlled study to assess the efficacy, immunogenicity, reactogenicity and safety of two doses of GSK Biologicals oral live attenuated human rotavirus (HRV) vaccine in healthy infants approximately 2 months of age and previously uninfected with HRV
444563/005 Completed Phase II, double-blind, randomized, placebo-controlled study of 2 doses of GSK Biologicals’ live attenuated human rotavirus vaccine at different virus concentrations (10 5.2 and 10 6.4 ffu) in healthy infants following a 0, 2 month schedule and previously uninfected with human rotavirus. Study Listed on ClinicalStudyDataRequest.com
444563/006 Completed To assess the efficacy, immuno & safety of 2 doses of GSK HRV vaccine at different virus concentrations in healthy infants aged 2 months & previously uninfected with HRV, concurrently given with DTPw-HBV, Hib. Study Listed on ClinicalStudyDataRequest.com
444563/006 Annex Completed A study to assess efficacy, immunogenicity, reactogenicity and safety of two doses of GSK Biological’s live attenuated human rotavirus vaccine at different virus concentrations in healthy infants and previously uninfected with HRV, when administered concurrently with DTPw-HBV and Hib vaccines
444563/007 Completed Study to assess efficacy, immunogenicity, reactogenicity and safety of two doses of GSK Biologicals' oral live attenuated human rotavirus vaccine at different viral concentrations in healthy infants previously uninfected with human rotavirus and approximately 3 months of age. Study Listed on ClinicalStudyDataRequest.com
444563/013 Completed A phase II, randomized, double-blind, placebo-controlled study of safety, reactogenicity and immunogenicity of 2 or 3 doses of GSK Biologicals’ oral live attenuated human rotavirus vaccine at 10E6.5 CCID50 viral concentration in healthy infants (approximately 5-10 weeks old) in the Republic of South Africa Study Listed on ClinicalStudyDataRequest.com
444563/014 Completed Reactogenicity & immunogenicity study of two doses of GSK Biologicals’ oral live attenuated HRV vaccine co-administered with either OPV or IPV in healthy infants (approximately 5-10 weeks old) in South Africa Study Listed on ClinicalStudyDataRequest.com
444563/020 Completed Phase II, double-blind randomised, placebo controlled clinical dose-range study to assess immunogenicity and reactogenicity of an investigational vaccination regimen, and to assess immunogenicity of OPV orally co-administered to healthy infants at 2, 4 and 6 months of age 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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