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Clinical Trial Summary

A Randomized, Double-Blind, Vehicle-Controlled Study to Evaluate the Efficacy and Safety of Topical Administration of FMX101 for 12 Weeks in the Treatment of Moderate-to-Severe Acne Vulgaris (Study FX2017-22)


Clinical Trial Description

This is a randomized, multicenter, double-blind, vehicle-controlled, 2 arm study to evaluate the safety and efficacy over 12 weeks of FMX101 topical foam containing 4% minocycline compared to vehicle in the treatment of subjects with moderate-to-severe facial acne vulgaris. Qualified subjects will be randomized to receive 1 of the following 2 treatments: - FMX101 4% minocycline foam - Vehicle foam ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03271021
Study type Interventional
Source Vyne Therapeutics Inc.
Contact
Status Completed
Phase Phase 3
Start date July 17, 2017
Completion date September 4, 2018

See also
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