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Study ID Status Title Patient Level Data
204771 Completed Determination of UVA Protection Factor (UVAPF) for a cosmetic product
204773 Completed A Clinical Study Investigating the Efficacy of Two Experimental Oral Rinses in Providing Long Term Relief from Dentinal Hypersensitivity
204777 Completed Intra-oral kinetics of fluoride containing dentifrices in a modified saliva clearance study
204779 Completed Single blinded, two-period, two-treatment, crossover, randomized, single dose bioequivalence study of two oral formulations with 500 mg of paracetamol (mejoral® 500 tablets, glaxosmithkline méxico s.a. De c.v. Vs. Tylenol® caplets, janssen cilag de méxico, s. De r.l. De c.v.) in healthy subjects under fasting conditions
204782 Completed Determination of UVA Protection Factor (UVAPF) for a cosmetic product
204785 Terminated Determination of SPF, before and after (40 and 80 minutes) of immersion in water, for a cosmetic product
204786 Terminated Determination of SPF, before and after (40 and 80 minutes) of immersion in water, for a cosmetic product
204787 Terminated Determination of SPF, before and after (40 and 80 minutes) of immersion in water, for a cosmetic product
204788 Terminated Determination of SPF, before and after (40 and 80 minutes) of immersion in water, for a cosmetic product
204789 Terminated Determination of SPF, before and after (40 and 80 minutes) of immersion in water, for a cosmetic product
204790 Terminated Determination of SPF, before and after (40 and 80 minutes) of immersion in water, for a cosmetic product
204791 Completed Determination of UVA Protection Factor (UVAPF) for a cosmetic product
204792 Completed Determination of UVA Protection Factor (UVAPF) for a cosmetic product
204799 Terminated Determination of SPF, before and after (40 and 80 minutes) of immersion in water, for a cosmetic product
204800 Terminated Determination of SPF, before and after (40 and 80 minutes) of immersion in water, for a cosmetic product
204802 Withdrawn Clinical, Single-blind and Controlled Study of the Potential of Irritability and Cutaneous Sensitization (RIPT) of a Cosmetic product SB.
204803 Withdrawn Clinical, Single-blind and Controlled Study of the Potential of Irritability and Cutaneous Sensitization (RIPT) of a Cosmetic product SB.
204804 Withdrawn Clinical, Single-blind and Controlled Study of the Potential of Cutaneous Photosensitization and Phototoxicity of a cosmetic product SB
204805 Withdrawn Clinical, Single-blind and Controlled Study of the Potential of Cutaneous Photosensitization and Phototoxicity of a cosmetic product SB
204810 Withdrawn An observer-blind study to assess the safety, reactogenicity and immunogenicity of GSK Biologicals’ investigational RSV vaccine (GSK3003891A), in healthy pregnant women and infants born to vaccinated mothers
204812 Active, not recruiting An observer-blind study to rank different formulations of GSK Biologicals’ investigational RSV vaccine (GSK3003891A) administered to healthy women
204813 Completed An observer-blind safety and reactogenicity study to assess GlaxoSmithKline (GSK) Biologicals’ investigational respiratory syncytial virus (RSV) vaccine (GSK3003891A) in healthy women
204824 Recruiting A Phase 2 Pilot, Multicenter, Single Arm Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of GSK1070806 plus Standard of Care for the Prevention of Delayed Graft Function in Adult Subjects After Renal Transplantation
204836 Completed A 29-day, randomized, double-blinded, placebo-controlled, parallel-group, multi-center study to evaluate the efficacy, safety and pharmacokinetics of three-times weekly dosing of GSK1278863 in hemodialysis-dependent subjects with anemia associated with chronic kidney disease who are switched from a stable dose of an erythropoiesis-stimulating agent
204838 Recruiting A study to evaluate safety, reactogenicity and immunogenicity of GSK Biologicals’ RSV investigational vaccine based on viral proteins encoded by chimpanzee-derived adenovector (ChAd155-RSV) (GSK3389245A) in RSV-seropositive infants

 

 

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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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