drugset / Trial / NCT01017146

A Study to Evaluate the Safety and Efficacy of Tazarotene Foam, 0.1%, in Subjects With Common Facial Acne - W0260-301

NCT01017146

Phase 3 Completed 744 enrolled Stiefel, a GSK Company GlaxoSmithKline · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess safety and efficacy of a new foam formulation of tazarotene in subjects with acne vulgaris.

Timeline

Start
2009-10
Primary completion
2010-11
Completion
2010-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Tazarotene Small molecule 0.1 % Topical

Indications