orvepitant
Sponsors
GlaxoSmithKline, Nerre Therapeutics Ltd.
Conditions
Atopic DermatitisDepressive DisorderDepressive Disorder, MajorPharmacokinetic Study in Healthy Male VolunteersPost-Traumatic Stress DisorderPruritus
Phase 1
Phase 2
A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Fixed Dose Study Evaluating the Efficacy and Safety of Orvepitant in Subjects With Major Depressive Disorder
TerminatedNCT00880399
Start: 2009-03-01End: 2010-06-16Updated: 2017-09-12
A Randomised, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy and Safety of Orvepitant in Subjects With Major Depressive Disorder
TerminatedNCT00880048
Start: 2009-03-11End: 2010-06-21Updated: 2017-10-13
Orvepitant (GW823296) in Adult Post Traumatic Stress Disorder
CompletedNCT01000493
Start: 2009-11-02End: 2010-06-28Updated: 2017-09-01
A Study of the Efficacy and Safety of Orvepitant in Subjects With Pruritus Associated With Atopic Dermatitis
WithdrawnNCT03464526
Start: 2018-05-31End: 2019-10-31Updated: 2018-05-15