drugset / Trial / NCT01019603

A Study to Evaluate the Bioavailability of Tazarotene Foam, 0.1%, and Tazorac Gel, 0.1%, in Subjects With Acne Vulgaris

NCT01019603

Phase 1 Completed 30 enrolled Stiefel, a GSK Company GlaxoSmithKline · collab
RandomizedParallel-groupOpen-labelBasic science

Summary

The purpose of this study is to assess systemic exposure of a new foam formulation of tazarotene, 0.1% compared with Tazorac Gel, 0.1%. The study design and dosing regimen are based on previous clinical studies with Tazorac Gel and Tazorac Cream.

Timeline

Start
2009-10-12
Primary completion
2009-12-20
Completion
2009-12-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Tazarotene Small molecule 0.1 % Topical

Indications