A Twelve Week Safety and Efficacy Study in Rosacea

Completed · Phase 2 · Has a placebo group

Conditions studied: Papulopustular Rosacea

In brief

The purpose of this study is to evaluate th safety and efficacy of one-daily topical application of CLS001 low, mid and high dose compared to vehicle gel in subjects with papulopustular rosacea.

Key facts

Study ID

NCT01784133

Run by

Maruho Co., Ltd.

People needed

240

Starts

2013-03-01

Last updated by the study team

2015-05-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• diagnosis of papulopustular rosacea (at least 15 lesions)

You may not qualify if…

• nodular rosacea or subtype 3
• clinically significant abnormal findings that would interfere with study objectives

Where it is running

• Radiant Research Inc. — Birmingham, Alabama, United States
• ATS Clinical Research — Santa Monica, California, United States
• The Savin Center, PC — New Haven, Connecticut, United States
• Skin Care Research, Inc — Boca Raton, Florida, United States
• Dunedin Research Specialists — Dunedin, Florida, United States
• North Florida Dermatology Associates — Jacksonville, Florida, United States
• Dawes Fretzin Clinical Research Group — Indianapolis, Indiana, United States
• Grekin Skin Institute — Warren, Michigan, United States
• Rochester General Medical Group Center for Dermatology at Linden Oaks — Rochester, New York, United States
• Derm Research Center of NY Inc. — Stoney Brook, New York, United States
• Wake Resarch — Raleigh, North Carolina, United States
• Oregon Dermatology and Research Center — Portland, Oregon, United States
• TriCities Skin and Cancer — Johnson City, Tennessee, United States
• Tennessee Clinical Research Center — Nashville, Tennessee, United States
• Progressive Clinical Research, PA — San Antonio, Texas, United States
• Dermatology Research Center — Salt Lake City, Utah, United States
• Virginia Clinical Research Inc. — Norfolk, Virginia, United States

Full record on ClinicalTrials.gov

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