Overview

Dose Ranging Study of the Safety and Efficacy of R115966 in Plaque Psoriasis

Status:
Completed
Trial end date:
2007-05-01
Target enrollment:
Participant gender:
Summary
Eligible subjects will be randomly assigned to one of three dose regimens of oral R115866 or placebo for the treatment of severe plaque psoriasis for 12 twelve weeks. The safety and efficacy of R115866 will be evaluated during the treatment period and the 8-week post treatment follow-up period.
Phase:
Phase 2
Details
Lead Sponsor:
Stiefel, a GSK Company
Collaborator:
GlaxoSmithKline
Treatments:
R 115866