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Study ID Status Title Patient Level Data
115444 Completed A Randomized, Placebo-Controlled, Single-Blind, Dose-Escalation, First-Time-in-Human Study to Assess the Safety and Pharmacokinetics of Single and Repeat Doses of SRT3025 in Normal Healthy Volunteers
115450 Completed A two part, double-blind, randomized, placebo-controlled and open-label study to investigate the efficacy, safety and tolerability of eltrombopag, a thrombopoietin receptor agonist, in pediatric patients with previously treated chronic immune (idiopathic) thrombocytopenic purpura (ITP). PETIT2: Eltrombopag in PEdiatric patients with Thrombocytopenia from ITP
115458 Completed A Randomized, Double-blind, Four-period Crossover Study to Investigate the Effect of Intravenous Ondansetron, a 5-HT3 Antagonist, on Cardiac Conduction as Compared to Placebo and Moxifloxacin in Healthy Adult Subjects.
115470 Completed A Phase 4, Multi-Center, Randomized, Open-Label Study to Evaluate the Effect of BENLYSTA™ (belimumab; HGS1006) on Vaccine Responses in Subjects with Systemic Lupus Erythematosus (SLE)
115476 Completed Meta-Analysis of VRX-RET-E22-303 and VRX-RET-E22-304: Two Multicenter, Open-Label, Long-Term, Safety, Tolerability and Efficacy Studies of Retigabine in Adult Epilepsy Patients with Partial-onset Seizures (Extensions of Studies VRX-RET-E22-301 and VRX-RET-E22-302)
115478 Completed PGx 377: Pharmacogenetic evaluation of the association of functional variation in ADRB1 and ADRB2 genes with tolerability to carvedilol in the Phase I/II study CRV110734
115484 Completed A randomized, double blind, placebo controlled study to investigate the effect of donepezil and gabapentin combination on an experimental pain model in healthy subjects
115486 Completed Tolerability and safety of multiple dose regimens of TRX4 anti-CD3 monoclonal antibody in Type 1 Diabetes Mellitus
115487 Completed Randomized, double-blind, 5 period cross over study assessing lung function in healthy volunteers following single inhalations of GSK573719 Inhalation Powder from two configurations of the Novel Dry Powder Inhaler Study Listed on ClinicalStudyDataRequest.com
115489 Completed Special Drug Use Investigation for Arixtra® (fondaparinux) Venous Thromboembolism Treatment
115490 Completed Special Drug Use Investigation (retrospective) for Arixtra® (fondaparinux) Venous Thromboembolism Treatment (over 100kg)
115493 Completed TRX4 Therapeutic Evaluation of Different Multi-Dose Regimens in Type 1 Diabetes Mellitus (TTEDD)
115494 Completed DEFEND 2: Durable-Response Therapy Evaluation ForEarly- or New-Onset Type 1 Diabetes Study Listed on ClinicalStudyDataRequest.com
115495 Completed Durable-Response Therapy Evaluation For Early or New-Onset Type 1 Diabetes - DEFEND Study Listed on ClinicalStudyDataRequest.com
115496 Completed DEFEND-1 Long Term Follow Up: Durable-Response Therapy Evaluation for Early or New Onset Type 1 Diabetes Extension Study Study Listed on ClinicalStudyDataRequest.com
115515 Completed An open-label single and repeat dose study to investigate the pharmacokinetic profiles of tenofovir disoproxil fumarate 300 mg in healthy Chinese subjects
115517 Completed A single/repeat dose study with three oral formulations of Firategrast (immediate release tablet, modified release tablet, and naso-gastric infusion) in healthy male volunteers
115519 Completed Double-Blind, Randomized, Placebo-Controlled Study to Assess Safety, Efficacy, and Pharmacokinetics (PK) of GSK2336805 in Combination With Peginterferon and Ribavirin in Treatment-naive Chronic Hepatitis C Subjects With Hepatitis C Virus Genotypes 1 or 4
115524 Completed Immunogenicity and safety study of GSK Biologicals’ meningococcal vaccine GSK 134612 administered to at risk subjects from 1 to less than 18 years
115535 Completed A Randomized, Double Blind, Single Dose, Cross-Over Study to Assess the Cardiovascular Effects of GSK2336805 in Healthy Adult Volunteers
115550 Completed A Single Centre, 5-Period, Randomized Study To Evaluate The Relative Bioavailability Of An Immediate Release Tablet Formulation And Prototype Bioenhanced Formulations Of GSK1325756 In Healthy Elderly Subjects During Suppression Of Gastric Acid Secretion Study Listed on ClinicalStudyDataRequest.com
115553 Completed PROACTYVE pilot:Pilot study of Patient’s adherence to TYKERB™/TYVERB™+capecitabine in metastatic breast cancer–observation of patient adherence and evaluation of predictive factors for patient adherence after providing educational programme
115555 Completed Immunogenicity and safety study of GlaxoSmithKline Biological's live attenuated measles mumps rubella varicella vaccine (PriorixTetra™) when co-administered with conjugated Meningococcal C vaccine (Meningitec®, Nuron Biotechs’ Vaccine) in healthy children
115563 Completed PGx418 Exploratory Pharmacogenetic Research on Efficacy of BENLYSTA (belimumab) in BEL110752 (BLISS-52) and BEL110751 (BLISS-76)
115570 Completed A Single Dose First in Human Study of GSK2398852 Co-Administered with GSK2315698 in Patients with Systemic Amyloidosis

 

 

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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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