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A Safety and Efficacy Study of DRM02 in Subjects With Rosacea

Rosacea Clinical Trial

Official title:
A Randomized, Double-blind, Vehicle Controlled Study of the Safety and Efficacy of Topical DRM02 in Subjects With Rosacea

Clinical Trial Summary

The purpose of this study is to determine whether DRM02 is safe and effective in the treatment of rosacea when applied twice daily for 6 weeks.

Clinical Trial Description

This is a double-blind, randomized, vehicle controlled, study enrolling 30 subjects with rosacea and designed to assess the safety, tolerability, and preliminary efficacy of DRM02. Safety will be assessed during the study, through adverse events, local skin responses, urinalysis, serum chemistry and hematology laboratory testing, physical examination and vital signs. Preliminary efficacy will be assessed through inflammatory lesion counts, the Investigator's Global Evaluation (IGE) and the Rosacea Signs and Symptoms (RSS) scale. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01993446
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 2
Start date October 2013
Completion date March 2014
View Details
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