drugset / Trial / NCT00211497

Safety and Efficacy of MBI 226 1.25% and 2.5% Topical Acne Solutions in the Treatment of Acne

NCT00211497 ↗

Phase 2 Completed 255 enrolled BioWest Therapeutics Inc
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

EvaluationDrugModalityDoseRoute
Subject MBI 226 Unknown 1.25 % Topical
Subject MBI 226 Unknown 2.5 % Topical

Indications