drugset / Trial / NCT00211497
Safety and Efficacy of MBI 226 1.25% and 2.5% Topical Acne Solutions in the Treatment of Acne
RandomizedParallel-groupDouble-blindTreatment
Summary
This is a Phase II, randomized, vehicle-controlled, double-blind, multi center study to evaluate the efficacy and safety of topically applied MBI 226 1.25% and 2.5% Acne Solutions as anti-acne preparations in human subjects with facial acne vulgaris.
Timeline
- Start
- 2003-01
- Primary completion
- —
- Completion
- 2003-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MBI 226 | Unknown | 1.25 % | Topical |
| Subject | MBI 226 | Unknown | 2.5 % | Topical |