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Study ID Status Title Patient Level Data
114910 Completed A study on the impact of rotavirus vaccination on hospitalisations for rotavirus gastroenteritis in children aged <5 years in Australia
114915 Completed A Phase IIIb, randomized, open-label study of the safety and efficacy of GSK1349572 (dolutegravir, DTG) 50 mg once daily compared to darunavir/ritonavir (DRV/r) 800 mg/100 mg once daily each administered with fixed-dose dual nucleoside reverse transcriptase inhibitor therapy over 96 weeks in HIV-1 infected antiretroviral naïve adult subjects
114917 Completed Assessment of safety of GlaxoSmithKline (GSK) Biologicals’ combined diphtheria-tetanus-acellular pertussis-inactivated poliovirus vaccine, Infanrix-IPV when administered according to the approved Prescribing Information in Korea
114919 Completed An open-label, randomised, crossover study to assess the relative bioavailability of different 2mg formulations of GSK2018682(S1P1 agonist) in healthy volunteers Study Listed on ClinicalStudyDataRequest.com
114922 Completed A randomized cross-over study to evaluate the pharmacokinetics and pharmacodynamics of twice daily oral administration of GSK1325756, compared to placebo, in healthy subjects; and the pharmacokinetic profile of twice daily oral administration of GSK1325756 in healthy fed and fasted elderly subjects Study Listed on ClinicalStudyDataRequest.com
114926 Completed An Open-label, Randomized, Single Period, Parallel-Cohort Study To Evaluate Serum and Pulmonary Pharmacokinetics following Single and Multiple Dose Administration of Intravenous GSK2251052 in Healthy Adult Subjects
114930 Completed DB2114930: A randomized, multi-center, double-blind, double-dummy, parallel group study to evaluate the efficacy and safety of umeclidinium/vilanterol compared with fluticasone propionate/salmeterol over 12 weeks in subjects with COPD Study Listed on ClinicalStudyDataRequest.com
114937 Completed Burden of Frequent and Infrequent Exacerbating Patients with Chronic Obstructive Pulmonary Disease (COPD)
114940 Active, Not Recruiting USHO-11-3281: Predictors of stepping down asthma therapy: observational study and Fluticasone propionate-Salmeterol Combination Therapy outcomes study
114941 Active, Not Recruiting Assessment of asthma-related resources after initiation of an inhaled corticosteroid switch: Observational study
114951 Completed DB2114951: A randomized, multi-center, double-blind, double-dummy, parallel group study to evaluate the efficacy umeclidinium/vilanterol compared with fluticasone propionate/salmeterol over 12 weeks in subjects with COPD Study Listed on ClinicalStudyDataRequest.com
114955 Completed Retrospective Administrative Claims Database Evaluation of Utilization of Belimumab in United States Managed Care Settings
114956 Completed A 4-Week Randomized Cross-Over Study to Evaluate Daily Lung Function Following the Administration of Albuterol/Salbutamol and Ipratropium in Subjects with Chronic Obstructive Pulmonary Disease Study Listed on ClinicalStudyDataRequest.com
114957 Completed A Randomized, Open-label, Single-dose, Two-period, Crossover Study to Demonstrate the Bioequivalence of the Fixed Dose Combination (FDC) of lamivudine and adefovir dipivoxil (100mg/10mg) to Heptodin® (100mg ) and Hepsera® (10mg) Study Listed on ClinicalStudyDataRequest.com
114974 Completed A randomised, double blind placebo controlled, 2 way cross over study in adults with non-allergic rhinits to evaluate the effect of once daily administration of intranasal SB-705498 12mg for two weeks and the response to a chamber challenge of cold dry air Study Listed on ClinicalStudyDataRequest.com
114985 Completed A first time in human, single blind, randomized, placebo-controlled,dose escalating crossover study to evaluate the safety,tolerability, pharmacokinetic and pharmacodynamic parameters of single doses of GSK2330672 in healthy volunteers Study Listed on ClinicalStudyDataRequest.com
114987 Terminated An open-label, phase 2a study to evaluate pazopanib eye drops administered for 12 weeks to patients with neovascular age-related macular degeneration
114989 Completed Neisseria meningitidis burden of disease
114991 Completed Neisseria meningitidis carriage study Study Listed on ClinicalStudyDataRequest.com
114993 Completed SUrvey of Guideline Adherence for treatment of systolic heart failure in Real WorldMulticenter, retrospective observation study in Korea
114995 Completed A Phase I, Randomized, Placebo-Controlled, Parallel-Group, Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of a Single Intravenous Dose of the Captisol™ Formulation of Vestipitant (GW597599) in Healthy Adult Subjects
115002 Active, Not Recruiting PGx308, PGx309, PGx310 and PGx382 evaluation of efficacy and safety endpoints in pazopanib-treated renal cell carcinoma (RCC) patients in studies VEG102616, VEG105192, and VEG107769
115003 Completed PGx367 evaluation of ALT elevation in patients receiving pazopanib and statins in 11 pazopanib clinical studies (VEG102616, VEG105192, VEG107769, VEG10003, VEG10004, VEG10005, VEG10007, VEG20002, VEG20006, VEG104450, VEG105281)
115-003 Completed A Multicentre Pilot Study in the United Kingdom to Determine Whether 566C80 Exhibits Antimalarial Activity in Patients with P. Falciparum Malaria.
115005 Completed PGx368 Genetics asthma exacerbation in ADA109055, ADA109057, SFA103153, I13106870

 

 

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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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