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Clinical Trial Summary

This study investigates the safety and efficacy of MBI 226 2.5% and 5.0% Acne Solutions, applied topically for six weeks, in the treatment of acne.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00211523
Study type Interventional
Source BioWest Therapeutics Inc
Contact
Status Completed
Phase Phase 2
Start date October 2000
Completion date September 2001

See also
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