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Study ID Status Title Patient Level Data
114554 Completed A phase 2, randomized, double-blind, placebo-controlled, parallel-group, dose-ranging study to investigate the efficacy and safety of 4 dose regimens of oral albaconazole in subjects with distal subungual onychomycosis
114555 Completed A Randomized, Double-Blind, Multiple-Dose, Placebo-Controlled Tolerability And Pharmacokinetic Study Of Escalating Doses Of Albaconazole In Healthy Subjects
114556 Completed Relative bioavailability study of a tablet formulation vs. pediatric granule formulation of Dolutegravir 50 mg and Effect of Different Types of Water plus Infant Formula on the Pediatric Granule Formulation in healthy male and female volunteers
114563 Completed A Phase 1, Randomized, Open-Label, Crossover Safety and Pharmacokinetic Study of 400 mg Albaconazole as a Tablet Formulation Versus a Capsule Formulation in Healthy Subjects
114565 Completed A Single-Center, Randomized, Open-Label Study to Evaluate the Bioavailability of Tazarotene Foam, 0.1%, and Tazorac Gel, 0.1%, in Subjects with Acne Vulgaris Study Listed on ClinicalStudyDataRequest.com
114566 Completed A Phase 4, Single-Blind, Randomized, Study to Compare the Tolerability and Efficacy of Tazorac Cream when used in Combination with Either Duac Gel or Acanya Gel for the Treatment of Facial Acne Vulgaris Study Listed on ClinicalStudyDataRequest.com
114567 Completed Single-blind, multicenter, parallel, comparative, randomized, phase 4 clinical trial for the evaluation of the quality of life, efficacy and tolerance of Duac® gel against Differin® gel in the topical treatment of mild to moderate acne vulgaris.
114568 Completed A PHASE 4, OPEN-LABEL STUDY TO ASSESS THE LONG-TERM SAFETY OF EXTINA (KETOCONAZOLE) FOAM, 2% IN THE TREATMENT OF SEBORRHEIC DERMATITIS Study Listed on ClinicalStudyDataRequest.com
114569 Completed A Study to Evaluate Safety and Efficacy of Clobetasol Propionate for Treatment of Plaque-Type Psoriasis in Adult Subjects.
114570 Completed A Multi-center, Randomized, Double-blind, Vehicle-Controlled, Phase 2 Study of the Safety and Efficacy of Benzoyl peroxide/Clindamycin gel and Tazarotene cream when used in combination in the Treatment of Acne Vulgaris
114571 Completed A Phase 1, Evaluator-Blinded, Randomized, Vehicle Controlled, Study To Evaluate The Cumulative Irritation Potential Of Topically Applied Tazarotene Foam In Healthy Volunteers Study Listed on ClinicalStudyDataRequest.com
114572 Completed A Phase 1, Evaluator-Blinded, Randomized, Vehicle Controlled, Study To Evaluate The Contact Sensitization Potential Of Topically Applied Tazarotene Foam In Healthy Volunteers Study Listed on ClinicalStudyDataRequest.com
114573 Completed A Phase 1, Evaluator-Blinded, Randomized, Vehicle Controlled Study To Evaluate The Phototoxic Potential Of Topically Applied Tazarotene Foam In Healthy Volunteers Study Listed on ClinicalStudyDataRequest.com
114574 Completed A Phase 1, Evaluator-Blinded, Randomized, Vehicle Controlled, Study To Evaluate The Photoallergic Potential Of Topically Applied Tazarotene Foam In Healthy Volunteers Study Listed on ClinicalStudyDataRequest.com
114575 Completed A Multicenter, Randomized, Double-Blind, Vehicle-Controlled, Parallel-Group Study to Evaluate the Safety and Efficacy of Tazarotene Foam, 0.1%, in Subjects with Acne Vulgaris Study Listed on ClinicalStudyDataRequest.com
114576 Completed A Multicenter, Randomized, Double-Blind, Vehicle-Controlled, Parallel-Group Study to Evaluate the Safety and Efficacy of Tazarotene Foam, 0.1%, in Subjects with Acne Vulgaris Study Listed on ClinicalStudyDataRequest.com
114580 Completed An Evaluation of the Bioequivalence of a Combined Formulated Tablet (50mg/600mg/300mg dolutegravir/abacavir/lamivudine)Compared to One Dolutegravir 50mg Tablet and One EPZICOM† (600mg/300mg abacavir/lamivudine) Tablet Administered Concurrently and the Effect of Food on Bioavailability of the Combined Formulation in Healthy Adult Subjects
114581 Completed A Randomized, Open-Label, Single‑Dose, 3‑Period, Crossover Evaluation of the Relative Bioavailability of Two Experimental Fixed-Dose Combination Tablet Formulations of Dolutegravir 50 mg/Abacavir 600 mg/Lamivudine 300 mg Compared to Co‑administered Dolutegravir 50 mg and EPZICOM™ (Abacavir 600 mg/Lamivudine 300 mg) Tablets in Healthy Adult Subjects
114582 Completed A Randomized, Placebo-Controlled Study to Evaluate the Effect of Tafenoquine (SB252263) on the Electrocardiogram (ECG) with Focus on Cardiac Repolarization (QTc duration) in Healthy Subjects Study Listed on ClinicalStudyDataRequest.com
114588 Recruiting An open-label, long term extension study for treatment of pulmonary arterial hypertension in paediatric patients aged 8 years up to 18 years who have participated in AMB112529 and in whom continued treatment with ambrisentan is desired
114589 Completed A Multi-centre, Randomised, Double-blind, Parallel Active-controlled Study Evaluating the Efficacy, Safety and Tolerability of Bupropion Hydrochloride Extended-release (bupropion XL 300mg once daily), Escitalopram oxalate (escitalopram, 10mg-20mg once daily) in Subjects with Major Depressive Disorder
114590 Completed Immunogenicity and safety study of GSK Biologicals’ HPV vaccine (GSK 580299) in healthy adult Chinese female subjects Study Listed on ClinicalStudyDataRequest.com
114592 Completed Bupropion and specific cardiovascular malformations
114593 Completed WEUSRTP4850: Phase II: Asthma treatment in pregnancy and the frequency of adverse pregnancy outcomes
114594 Completed An exploratory First Time in Human (FTIH) study investigating the pharmacokinetics (PK), immunogenicity, safety and tolerability of GSK2434735 administered as a single low dose in healthy male subjects Study Listed on ClinicalStudyDataRequest.com

 

 

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