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Study ID Status Title Patient Level Data
114677 Completed A Phase 3 Multicenter, Randomized, Double-Blind, Active And Vehicle-Controlled Study Of The Safety And Efficacy Of A Clindamycin / Benzoyl Peroxide Gel Versus Clindamycin Gel Versus Benzoyl Peroxide Gel Versus Vehicle Gel In Subjects With Acne Vulgaris Study Listed on ClinicalStudyDataRequest.com
114678 Completed Prospective 2-Year Longitudinal Study to Assess for Miconazole Resistance in Candida spp. with Repeated Treatment Courses of 0.25% Miconazole Nitrate ointment in Neonates and Infants up to 1 Year of Age with Recurrent Moderate-Severe Diaper Dermatitis complicated by Cutaneous Candidiasis
114679 Completed A Phase 3B, Multicenter, Assessor-Blinded Study of the Tolerability of Clindamycin 1%-Tretinoin 0.025% Gel used in Conjunction with Benzoyl Peroxide 4% Wash in Subjects with Mild to Moderate Facial Acne Vulgaris
114681 Completed A Phase 3 Multicenter, Randomized, Double-Blind, Active And Vehicle-Controlled Study Of The Safety And Efficacy Of CT Gel in Subjects With Acne Vulgaris
114688 Terminated A randomised, double-blind, dose-finding, multicenter study of the safety, tolerability, and efficacy of GSK2251052 therapy compared to imipenem-cilastatin in the treatment of adult subjects with febrile complicated lower urinary tract infections and acute pyelonephritis
114689 Terminated A prospective, randomized, double-blind, multi-center, dose-ranging study of the safety, tolerability and efficacy of GSK2251052 in the treatment of complicated intra-abdominal infections in adults
114693 Completed Two part study to investigate pharmacokinetics (PK) & pharmacodynamics (PD) of SB-705498, TRPV1 antagonist, in cough. Part A: open label study in healthy subjects to determine exposure to SB-705498. Part B: double-blind, placebo controlled, cross over study to investigate effect of SB-705498 on capsaicin induced cough and 24 hour cough counts in cough patients Study Listed on ClinicalStudyDataRequest.com
114694 Completed An Open-label, Randomized, Single Dose, Two-Period Crossover study to Determine the Bioavailability of a Fixed Dose Combination Capsule Formulation of Dutasteride and Tamsulosin Hydrochloride (0.5mg/0.2mg) Relative to Co-administration of Dutasteride 0.5mg capsules and Tamsulosin Hydrochloride 0.2mg Study Listed on ClinicalStudyDataRequest.com
114695 Completed Immunogenicity and safety of GlaxoSmithKline Biologicals’ (pre-) pandemic influenza vaccine Prepandrix™ in Korean subjects aged 18 to 60 years old
114700 Completed Immunogenicity and safety study of GlaxoSmithKline Biologicals' HPV-16/18 L1 AS04 vaccine when administered according to alternative 2-dose schedules in 9 - 14 year old females Study Listed on ClinicalStudyDataRequest.com
114703 Completed A randomized, open-label, 3-period crossover study in healthy subjects to determine the effect of particle size on the pharmacokinetics of single oral 100mg doses of GSK1278863A Study Listed on ClinicalStudyDataRequest.com
114720 Active not recruiting Immunogenicity and safety of the diphtheria, tetanus, pertussis and inactivated poliovirus (DPT-IPV) vaccine Squarekids™ co-administered with GSK Biologicals’ human rotavirus (HRV) vaccine Rotarix™ (GSK444563) in healthy infants
114728 Completed A multicenter, two part, randomized, parallel group, placebo and sitagliptin controlled study to evaluate the safety and efficacy of GSK256073 administered once or twice daily for 12 weeks in subjects with type 2 diabetes mellitus who are being treated with metformin Study Listed on ClinicalStudyDataRequest.com
114729 Completed A Single-Center, Evaluator-Blinded, Randomized, Placebo Controlled, Phase 1 Clinical Trial Evaluating The Phototoxic Potential Of Topically Applied Clindamycin 1.0% - Tretinoin 0.025% Gel (Ct Gel) In Healthy Volunteers
114730 Completed A Single-Center, Evaluator-Blinded, Randomized, Placebo-Controlled, Phase 1 Clinical Trial Evaluating the Photoallergic Potential of Topically Applied Clindamycin phosphate 1.0% and Tretinoin 0.025% (CT Gel) in Healthy Volunteers
114741 Completed A Multicenter, Randomized, Double-Blind, Phase 3 Study of the Safety and Efficacy of Emulsion Formulation U0267, versus Vehicle in Subjects with Plaque-type Psoriasis Study Listed on ClinicalStudyDataRequest.com
114742 Completed A Multicenter, Randomized, Double-Blind, Phase 3 Study of the Safety and Efficacy of Emulsion Formulation U0267 , versus Vehicle Foam in Subjects with Plaque-type Psoriasis Study Listed on ClinicalStudyDataRequest.com
114743 Completed A Multicenter, Randomized, Double-Blind Study of the Safety and Efficacy of Calcipotriene Foam, 0.005%, Versus Vehicle Foam In The Treatment Of Moderate Plaque-Type Scalp And Body Psoriasis Study Listed on ClinicalStudyDataRequest.com
114746 Completed A Phase 1b, multi-center, open-label, dose escalation study of GSK2256098 (FAK inhibitor) in combination with Trametinib (MEK inhibitor) in subjects with advanced solid tumors
114747 Completed An evaluation of MRI measures of lung water increases with postural changes in healthy subjects and in patients with cardiac failure: A methods validation study for evaluation of novel treatments limiting pulmonary oedema in cardiac failure
114748 Completed A randomized, double blind, placebo-controlled three-way crossover study in mild asthmatics to evaluate the effect of smoking status on the attenuation by inhaled corticosteroids of the allergen-induced asthmatic response. Study Listed on ClinicalStudyDataRequest.com
114749 Completed A Phase II Randomised, Double-Blind, Placebo-Controlled, Parallel Group, Multicentre Study to determine the efficacy and dose response of repeat inhaled doses of GW870086X on FEV1 in adults with Persistent Asthma Study Listed on ClinicalStudyDataRequest.com
114769 Completed A Meta Analysis of malignancy serious adverse events in the ADOPT, 49653/048, and RECORD, 49653/231, studies, comparing metformin with rosiglitazone.
114777 Completed The prevalence of osteoporotic vertebral compression fractures (OVCF) in Korean post menopausal women
114778 Completed Immunogenicity and safety study of GSK Biologicals’ Boostrix™ vaccine using a new syringe presentation in healthy adolescents aged 10–15 years 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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