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Safety and Efficacy Study of a Topical Minocycline Foam in Patients With Papulopustular Rosacea — EMIRA  

Rosacea Clinical Trial

Official title:
A Randomized, Multicenter, Double-blind, Vehicle-controlled Study to Evaluate the Safety and Efficacy of Two Different Doses of a Topical Minocycline Foam Compared to Vehicle in the Treatment of Papulopustular Rosacea - Study FX2015-10

Clinical Trial Summary

The purpose of this study is to see if the study drug, FMX-103, is safe to give and if it helps people with moderate-to-severe papulopustular rosacea.

The investigational product is FMX-103 minocycline foam. Two concentrations of the investigational product, 1.5% and 3%, will be studied along with vehicle. The foam will be applied once daily to the face for the 12-week treatment duration of the study.

Approximately 210 patients will participate in this study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02601963
Study type Interventional
Source Foamix Ltd.
Contact
Status Completed
Phase Phase 2
Start date September 2015
Completion date August 2016
View Details
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