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Study ID Status Title Patient Level Data
104888 Completed A phase II/III, observer-blind, Multi-Country, Multi-Centre, randomized study to demonstrate the superiority in terms of immunogenicity of adjuvanted influenza vaccine administered in adults aged 50 years and older compared to Fluarix™ Study Listed on ClinicalStudyDataRequest.com
104896 (month 18 FU) Completed A long-term, open follow-up of the immunogenicity and safety of GSK Biologicals’ HPV vaccine (580299) in healthy female subjects vaccinated in study HPV-013
104912 Completed Evaluation of the Efficacy and Safety of Cetirizine Dry Syrup in Children -Suffering from Perennial Allergic Rhinitis-
104913 Completed Evaluation of the Efficacy and Safety of Cetirizine Dry Syrup in Children -Suffering from Atopic Dermatitis-
104914 Completed Long-term Study of Cetirizine Dry Syrup in Children. Suffering from Perennial Allergic Rhinitis.
104915 Completed Long-term Study of Cetirizine Dry Syrup in Children suffering from Various Type of Cutaneous Disease Accompanied with Pruritus.
104916 Completed An open-label, single dose study to investigate the safety, tolerability and pharmacokinetics of 90mg of GW274150 in adult and elderly RA subjects.
104951 Completed Evaluate the immunogenicity & safety of GSK Biologicals’ HPV-16/18 L1/AS04 vaccine administered intramuscularly according to a 0,1,6 mth schedule in healthy female subjects aged 10–14 yrs Study Listed on ClinicalStudyDataRequest.com
104972 Completed A randomised (with respect to placebo), double-blind, placebo-controlled, adaptive dose ascending study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of GSK315234A (a humanised monoclonal antibody to oncostatin M) in patients with active rheumatoid arthritis (RA) Study Listed on ClinicalStudyDataRequest.com
104977 Completed Non-inferiority of one formulation of GSK Biologicals' DTPw-HBV/Hib to 2 formulations of GSK Biologicals' DTPw-HBV/Hib with respect to the immune response to the PRP antigen, when administered to healthy infants at 6, 10, 14 weeks of age Study Listed on ClinicalStudyDataRequest.com
104988 Completed Comparison of the effects of rosiglitazone and glimepiride, both given in combination with metformin, on 24-hour glycemia in type 2 diabetes patients not controlled with metformin alone. A 3-month multicentre, randomized, parallel-group, open-label study.
105011 Completed A single blind, randomised, placebo controlled, single ascending dose study to evaluate the safety, tolerability and pharmacokinetics of GSK424887 in healthy male subjects and an open label Positron Emission Tomography study to evaluate the serotonin transporter and neurokinin- receceptor occupancy
105012 Completed Emotional processing in healthy male volunteers treated with GSK424887. A single centre, randomised, double-blind, placebo-controlled parallel group study Study Listed on ClinicalStudyDataRequest.com
105106 Completed A parallel-group, double-blind, randomized, placebo-controlled, active comparator, multicenter study to evaluate the efficacy, safety, tolerability and pharmacokinetics of two doses of GSK232802 administered orally as monotherapy for 12 weeks in healthy postmenopausal women with moderate to extremely severe vasomotor symptoms
105194 Completed An open label, multi-centre, non-interventional post-marketing surveillance to monitor the safety and/or efficacy of AVODART(dutasteride) administered in Korean BPH(Benign Prostatic Hyperplasia) patients according to the prescribing information
105211 Completed A randomised, double-blind, placebo-controlled, dose ascending, 2-cohort, parallel group study to examine the safety, tolerability and pharmacokinetics of once-daily inhaled doses of GSK573719 formulated with the excipient Magnesium Stearatein COPD subjects for 7 days Study Listed on ClinicalStudyDataRequest.com
105239 (mth24-30) Completed Booster Vaccination Study to Assess Immunogenicity & Safety of a Dose of GSK Biologicals' Mencevax™ ACWY & 1/5th of a Dose of Mencevax™ ACWY in Subjects Primed in the DTPW-HBV=HIB-MENAC-TT-011 Study Study Listed on ClinicalStudyDataRequest.com
105407 Completed A multi-center, epidemiologic survey to describe the current medical practice of general practitioners treating subjects with type 2 diabetes mellitus in Latin America
105467 Completed A placebo-controlled, single-blind, randomised, parallel group, 28-day repeat dose study to investigate the tolerability, safety and steady state pharmacokinetics of GSK372475 in healthy young and elderly, male and female subjects
105517/346 Completed A Randomized, Double-Blind, Multicenter Study Comparing the Glycemic Control Characteristics of Carvedilol and Metoprolol in Hypertensive Patients With Type II Diabetes Mellitus.
105517/347 Completed A Randomized, Double-Blind, Multicenter Study Comparing the Effects of Carvedilol and Metoprolol on Glycemic Control in Hypertensive Patients with Type II Diabetes Mellitus.
105517/358 Completed Organized Program to Initiate Lifesaving Treatment in Hospitalized Patients with Heart Failure (OPTIMIZE-HF): An Internet-based Registry and Process of Care Improvement Program for Heart Failure Patients Study Listed on ClinicalStudyDataRequest.com
105539 Completed An open, randomized, phase IIIa study to evaluate the safety and immunogenicity of GSK Biologicals' 10-valent pneumococcal conjugate vaccine, when administered intramuscularly according to a 2-4-11 months vaccination schedule Study Listed on ClinicalStudyDataRequest.com
105548 Completed A double-blind, randomized, placebo-controlled, repeat dose, 2-way crossover drug interaction study to investigate the pharmacokinetic and pharmacodynamic effects following administration of fluticasone furoate/GW642444M Inhalation Powder with ketoconazole Study Listed on ClinicalStudyDataRequest.com
105553 Completed Assess lot-to-lot consistency of 3 lots (double blind design) of GlaxoSmithKline Biologicals' 10-valent pneumococcal vaccine and evaluate non-inferiority to Prevenar™ (single blind design) when administered as 3-dose primary immunization course before 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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