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Trials / Completed

CompletedNCT00716144

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

A Randomized, Evaluator-Blind, Placebo-Controlled, Parallel-Group Dose-Ranging Study of the Safety and Efficacy of Oral R115866 and R115866 Placebo in the Treatment of Plaque Psoriasis

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
176 (actual)
Sponsor
Stiefel, a GSK Company · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGTalarozoleOral Capsule Once Daily

Timeline

Start date
2006-06-01
Primary completion
2007-05-01
Completion
2007-05-01
First posted
2008-07-16
Last updated
2018-01-29
Results posted
2018-01-29

Locations

22 sites across 5 countries: Germany, Ireland, Netherlands, Russia, United Kingdom

Source: ClinicalTrials.gov record NCT00716144. Inclusion in this directory is not an endorsement.

Dose Ranging Study of the Safety and Efficacy of R115966 in Plaque Psoriasis (NCT00716144) · Clinical Trials Directory