Last updated on June 2019

A Study to Assess the Efficacy and Safety of MSTT1041A in Participants With Moderate to Severe Atopic Dermatitis

Brief description of study

This study will assess the efficacy and safety of MSTT1041A in participants with moderate to severe atopic dermatitis (AD). The study consists of a screening period, a 16-week treatment period, and an 8-week follow-up period.

Clinical Study Identifier: NCT03747575

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Alabama Allergy & Asthma

Birmingham, AL United States
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Jonathan Corren MD, Inc.

Los Angeles, CA United States
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Clinical Science Institute

Santa Monica, CA United States
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Asthma & Allergy; Associates, P.C.

Colorado Springs, CO United States
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Harmony Clinical Research, Inc

North Miami Beach, FL United States
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GCP Global Clinical Professionals

Saint Petersburg, FL United States
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Forward Clinical Trials

Tampa, FL United States
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DS Research

New Albany, IN United States
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Clinical Research of Charlotte

Charlotte, NC United States
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Center for Clinical Studies

Houston, TX United States
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Grey Canyon Family Medicine PA

San Antonio, TX United States
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Laser Clinic

Szczecin, Poland
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Recruitment Status: Open

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