Last updated on August 2017

A Study To Evaluate ASN002 In Subjects With Atopic Dermatitis

Brief description of study

This is a dose escalation study to test the safety, tolerability and preliminary efficacy of ASN002 in people with moderate to severe atopic dermatitis (AD).

Detailed Study Description

This study is a dose escalation study to determine a safe and tolerable dose of ASN002 for people with moderate to severe atopic dermatitis. This study will also characterize the pharmacokinetics and pharmacodynamics of ASN002 through blood sampling and skin biopsies. Subjects will also be assessed for improvement in their atopic dermatitis. There will be a screening period (up to 30 days) and a treatment period for 4 weeks with a 14 day follow up with an end-of-study visit.

Clinical Study Identifier: NCT03139981

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Sunil Dhawan, MD

Center for Dermatology Clinical Research, Inc.
Fremont, CA United States
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Howard Sofen, MD

Dermatology Research Associates
Los Angeles, CA United States
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Neal Bhatia, MD

TCR Medical Corporation
San Diego, CA United States
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Matthew Zook, MD

Olympian Clinical Research
Tampa, FL United States
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Seth Forman, MD

Forward Clinical Trials, Inc.
Tampa, FL United States
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Joseph Fowler, MD

Dermatology Specialists Research
Louisville, KY United States
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Stephen Tyring, MD

Center for Clinical Studies, Ltd., LLP
Houston, TX United States
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Mark Lee, MD

Progressive Clinical Research, P.A.
San Antonio, TX United States
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David Pariser, MD

Virginia Clinical Research, Inc.
Norfolk, VA United States
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Catherine Maari, MD

Innovaderm Research
Montréal, Canada
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Recruitment Status: Open

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