CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 363 enrolled
Drug / intervention
Calcipotriene Foam +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01139580
NCT01139580Phase 3Completed

A Multicenter, Randomized, Double-Blind Study of the Safety and Efficacy of Calcipotriene Foam, 0.005%, Versus Vehicle Foam In The Treatment Of Moderate Plaque-Type Scalp And Body Psoriasis

Stiefel, a GSK Company·interventional·Posted Jun 8, 2010·Updated Jan 18, 2017

In Brief

A Phase 3 clinical trial evaluating Calcipotriene Foam and Vehicle Foam for Psoriasis. Completed, enrolled 363 participants across 26 sites.

Detailed Summary

The purpose of this study is to determine the safety and effectiveness in the treatment of psoriasis on the scalp and on the body.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPsoriasis
CountriesUnited States
CollaboratorsGlaxoSmithKline

Timeline

Phase 3CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedJun 8, 2010
Enrollment StartMay 1, 2010
Primary CompletionDec 1, 2010
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 16.1 years ago

Interventions

Calcipotriene Foamdrug

Calcipotriene Foam 0.005%. All treatments will be administered to the skin twice daily (am-pm) for 8 weeks for subjects in this group

Vehicle Foamdrug

Vehicle Foam. All treatments will be administered to the skin twice daily (am-pm) for 8 weeks for subjects in this group