Clinical trial

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

NCT00211497 · BioWest Therapeutics Inc, Industry · Completed

Key facts

NCT number NCT00211497
Title Safety and Efficacy of MBI 226 1.25% and 2.5% Topical Acne Solutions in the Treatment of Acne
Official title A Phase II, Randomized, Vehicle-Controlled, Double-Blind, Multi-Center Study to Evaluate Safety and Efficacy of MBI 226 1.25% and 2.5% Acne Solutions Applied Topically for 12 Weeks to Subjects With Acne Vulgaris
Lead sponsor BioWest Therapeutics Inc, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Acne Vulgaris, Acne, Propionibacterium Acnes
Intervention type Drug
Interventions MBI 226 Acne Solutions
Enrollment 255
Start date Jan 1, 2003
Completion Sep 1, 2003
First posted Sep 21, 2005
Last update posted Sep 21, 2005

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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