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Study ID Status Title Patient Level Data
116727 Completed The vaccine response and long-term antibody persistence of GSK Biologicals’ MenACWY-TT vaccine (GSK134612) administered as one dose at 6 years post-MenC primary vaccination in healthy subjects aged 12-18 months at primary vaccination
116728 Completed AN OPEN LABEL, BALANCED, RANDOMIZED, TWO-TREATMENT, TWO-PERIOD, TWO-SEQUENCE, CROSSOVER, SINGLE ORAL DOSE, BIOEQUIVALENCE STUDY OF METFORMIN GSK 850 MG TABLETS MANUFACTURED BY SAVIPHARM J.S.C, VIETNAM AND GLUCOPHAGE® 850 MG TABLETS MANUFACTURED BY MERCK SANTE S.A.S.2, RUE DU PRESSOIR VERT-45400 SEMOY-FRANCE AND BE REGISTERED IN VIETNAM IN HEALTHY, ADULT, HUMAN MALE SUBJECTS UNDER FASTING CONDITION
116729 Completed AN OPEN LABEL, BALANCED, RANDOMIZED, TWO-TREATMENT, TWO-PERIOD, TWO-SEQUENCE, CROSSOVER, SINGLE ORAL DOSE, BIOEQUIVALENCE STUDY OF METFORMIN 1000 MG TABLETS MANUFACTURED BY SAVIPHARM J.S.C, VIETNAM AND GLUCOPHAGE® 1000 MG TABLETS MANUFACTURED BY MERCK SANTE S.A.S.2, RUE DU PRESSOIR VERT-45400 SEMOY-FRANCE AND BE REGISTERED IN VIETNAM IN HEALTHY, ADULT, HUMAN MALE SUBJECTS UNDER FASTING CONDITION
116730 Completed Burden of Influenza in the United States, July 1997 up to April 2009
116741 Completed A Phase I Non-Randomized Multi Cohort, Open Label, Bridging Study to Evaluate the Pharmacokinetics, Safety and Tolerability of GSK557296 in Healthy Women Volunteers after Single and Repeat Dosing Study Listed on ClinicalStudyDataRequest.com
116745 Completed Bioequivalence study between two medications for oral administration of minocycline in 100 mg oral solids in healthy volunteers
116747 Completed PGx6202: Genetic Evaluation of Efficacy and Safety Endpoints in Patients with Ovarian Cancer in VEG110655/VEG114012
116753 Completed A randomized, double-blind, placebo-controlled, crossover study to evaluate the influence of the A118G polymorphism in the mu opioid receptor gene (OPRM1) on effects of GSK1521498 and naltrexone on physiological and behavioural markers of brain function in healthy social drinkers Study Listed on ClinicalStudyDataRequest.com
116757 Active, Not Recruiting Chronic Obstructive REspiratory diseases in CIS countries (CORE Study). Cross-sectional, multinational, population-based study of the point prevalence of COPD, bronchial asthma and allergic rhinitis with risk factor assessments in adult population of major cities of four Commonwealth of Independent States (CIS) countries
116760 Completed Safety and immunogenicity study of GSK Biologicals’ Herpes Zoster subunit (HZ/su) vaccine GSK1437173A when administered subcutaneously versus intramuscularly in adults aged 50 years or older Study Listed on ClinicalStudyDataRequest.com
116764 Not yet recruiting Meta analysis of the efficacy and tolerability of dutasteride in BPH treatment
116768 Completed Investigation of airway inflammation in Japanese COPD patients, smoking controls and non-smoking controls
116771 Completed European Survey of Patient and Prescriber Understanding of Risks Associated with Trobalt™
116777 Completed Evaluation of the kinetics of mRNA expression after two doses of GSK Biologicals’ candidate tuberculosis (Tuberculosis) vaccine GSK 692342 in healthy adults
116778 Completed A Randomized, Single Blind, Placebo-Controlled Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Repeat Escalating Oral Doses of GSK2140944 in Healthy Adult Subjects (BTZ116778) Study Listed on ClinicalStudyDataRequest.com
116781 Completed AOA: Lamictal Generic Switching Feasibility Analysis
116787 Completed A Double-Blind, Randomized, Placebo-Controlled, Single Dose Escalation First Time in Human Study to Investigate the Safety, Tolerability and Pharmacokinetics of GSK2838232 and to Evaluate the Effect of Food and Ritonavir on GSK2838232 in Healthy Subjects
116789 Active, Not Recruiting Drug Use Investigation for ARZERRA® Chronic Lymphocytic Leukemia (CLL)
116796 Completed Immunogenicity and safety of GSK Biologicals’ Herpes Zoster vaccine GSK1437173A in adults with a prior episode of herpes zoster Study Listed on ClinicalStudyDataRequest.com
116797 Completed An open-label, randomized, single dose, three-way crossover study to determine the comparative bioavailability of two fixed dose combination tablet formulations of amlodipine (5mg) and losartan (100mg) in healthy adult male and female Subjects under fasting conditions Study Listed on ClinicalStudyDataRequest.com
116798 Completed An Open-Label, Randomized, Single Dose, Two-Way Crossover Pilot Study to Evaluate the Relative Bioavailability of One Amlodipine 5 mg Tablet and One Enalapril Maleate 20mg Tablet to a Fixed Dose Combination Tablet Formulation of Amlodipine (5 mg) and Enalapril Maleate (20 mg), in Healthy Adult Male and Female Subjects under Fasting Conditions Study Listed on ClinicalStudyDataRequest.com
116799 Completed An open-label, randomised, single dose, three-way crossover, parallel groups study to determine the bioequivalence of two fixed dose combination (FDC) tablet formulations of amlodipine and losartan FDC5/50 and FDC5/100 to respective reference dosages in healthy adult male and female subjects under fasting conditions Study Listed on ClinicalStudyDataRequest.com
116804 Completed Seroprevalence of Bordetella pertussis in adults in Hungary
116805 Completed Indirect comparison lapatinib+capecitabine vs trastuzumab+capecitabine in metastic breast cancer
116806 Terminated An Open-Label, Randomized, Single Dose, Four-way Crossover, Multi-stage Study to determine the Comparative Bioavailability of two fixed dose combination tablet formulations, 500 mg or 1000 mg extended release metformin and 1 mg or 2 mg extended release glimepiride, in healthy adult male and female subjects in the fed state 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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