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Study ID Status Title Patient Level Data
113351 Completed Study AK1113351, a fixed dose study of 323U66 SR in the treatment of Major Depressive Disorder (MDD) - a multi-center, placebo-controlled, randomized, double-blind, parallel-comparison study Study Listed on ClinicalStudyDataRequest.com
113353 Completed An open-label, single dose study to investigate the utility of non-invasive bile sampling using the Entero-Test in order to characterize the metabolism and biliary elimination of Simvastatin in healthy volunteers
113359 Completed A 52 week Study to Evaluate the Safety and Tolerability of GSK573719/GW642444 125mcg once-daily alone and in combination with GW642444 25mcg once-daily via novel Dry Powder Inhaler (nDPI) in Subjects with Chronic Obstructive Pulmonary Disease Study Listed on ClinicalStudyDataRequest.com
113360 Completed A multicenter trial comparing the efficacy and safety of GSK573719/GW642444 with GW642444 and with tiotropium over 24 weeks in subjects with COPD Study Listed on ClinicalStudyDataRequest.com
113361 Completed A 24-Week, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of GSK573719/GW642444 Inhalation Powder and the Individual Components Delivered Once-Daily via a Novel Dry Powder Inhaler in Subjects with Chronic Obstructive Pulmonary Disease Study Listed on ClinicalStudyDataRequest.com
113369 Completed Immunogenicity and safety of GSK Biologicals’ meningococcal vaccine (GSK 134612) when co-administered with a pneumococcal conjugate vaccine and Infanrix hexa™ in healthy infants
113373 Completed A 24-Week, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of GSK573719/GW642444 Inhalation Powder and the Individual Components Delivered Once-Daily via a Novel Dry Powder Inhaler in Subjects with Chronic Obstructive Pulmonary Disease Study Listed on ClinicalStudyDataRequest.com
113374 Completed A multi-center trial comparing the efficacy and safety of GSK573719/GW642444 with GSK573719 and with tiotropium over 24 weeks in subjects with COPD Study Listed on ClinicalStudyDataRequest.com
113376 Completed A Randomized, Double-Blind, Placebo-Controlled Repeat Dose Escalation, First Time in Human Study to Investigate the Safety, Tolerability and Pharmacokinetics of Oral and Intravenous GSK1322322 in Healthy Subjects Study Listed on ClinicalStudyDataRequest.com
113377 Completed Phase I study of GSK573719 -A randomized, double blind, placebo controlled, dose ascending, single and repeat dose study to investigate the safety, tolerability, and pharmacokinetics of inhaled dose of GSK573719 from a novel dry powder device in healthy Japanese male subjects Study Listed on ClinicalStudyDataRequest.com
113381 Terminated Post-marketing surveillance study of GSK Biologicals’ pneumococcal conjugate vaccine, Synflorix, when administered according to the local Prescribing Information in Philippines
113385 Completed Measurement of the changes in acceptability of hepatitis B immunization among general practitioners and open-care paediatricians
113388 Terminated RTG113388, a Long-term, Open-label Safety Extension Study of Retigabine/Ezogabine in Pediatric Subjects with Partial Onset Seizures (>= 12 years old) and Subjects with Lennox-Gastaut Syndrome (>=12 years old) Study Listed on ClinicalStudyDataRequest.com
113390 Terminated Evaluation of the safety and tolerability of re-dosing with intravenous (iv) otelixizumab in adult subjects with newly diagnosed type 1 diabetes mellitus Study Listed on ClinicalStudyDataRequest.com
113391 Completed A single-center, randomized, two part, open-label, crossover study to assess the relative bioavailability and food effect of new formulations of GSK2248761 in healthy adult subjects
113392 Completed A Phase I, Open Label, Single Sequence, Drug Interaction Study Evaluating Plasma GSK2248761 and Raltegravir Pharmacokinetics in Healthy Adult Subjects.
113394 Terminated A Double-Blind study to Evaluate the Pharmacokinetics of an Oral Contraceptive Containing Drospirenone and Ethinyl Estradiol when Co-administered with GSK2248761 in Healthy Adult Female Subjects
113398 Completed Consistency of immunogenicity and non inferiority of three production lots of GSK Biologicals’ candidate malaria vaccine in children Study Listed on ClinicalStudyDataRequest.com
113399 Terminated A Phase 2b study to select a once daily oral dose of GSK2248761 in HIV-1 infected antiretroviral therapy experienced adults with non-nucleoside reverse transcriptase inhibitor (NNRTI) resistance
113404 Terminated Phase 2b study to select a once daily oral dose of GSK2248761 administered with tenofovir/emtricitabine or abacavir/lamivudine in HIV-1 infected antiretroviral therapy naive adult subjects
113405 Completed Special Drug Use Investigation for ADOAIR Metered-dose Inhaler (Pediatric)
113406 Completed Special Drug Use Investigation for ALLERMIST (Long term)
113407 Completed Drug Use Investigation for ALLERMIST
113412 Completed An open-label single dose randomized, parallel group study followed by single-blind repeat dosing, to compare the relative bioavailability of GSK2212836 Study Listed on ClinicalStudyDataRequest.com
113414 Completed A Randomized, Double Blind, Double Dummy Multicenter Phase IIa Study to Assess Safety, Tolerability and Efficacy of GSK1322322 Versus Linezolid in the Treatment of Acute Bacterial Skin and Skin Structure Infection Study Listed on ClinicalStudyDataRequest.com

 

 

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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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