Study to Assess the Efficacy and Long-term Safety of Dupilumab (REGN668/SAR231893) in Adult Participants With Moderate-to-Severe Atopic Dermatitis



Status:Completed
Conditions:Psoriasis, Dermatology, Dermatology
Therapuetic Areas:Dermatology / Plastic Surgery
Healthy:No
Age Range:18 - Any
Updated:10/19/2017
Start Date:September 2014
End Date:October 2016

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A Randomized, Double-Blind, Placebo-Controlled Study to Demonstrate the Efficacy and Long-Term Safety of Dupilumab in Adult Patients With Moderate-to-Severe Atopic Dermatitis

The primary objective of the study was to demonstrate the efficacy of Dupilumab administered
concomitantly with topical corticosteroid (TCS) through Week 16 in adult participants with
moderate-to-severe atopic dermatitis (AD) compared to placebo administered concomitantly with
TCS.


Key Inclusion Criteria:

1. Chronic AD that had been present for at least 3 years before the screening visit;

2. Documented recent history (within 6 months before the screening visit) of inadequate
response to a sufficient course of out-patient treatment with topical AD
medication(s).

Key Exclusion Criteria:

1. Participation in a prior Dupilumab clinical trial;

2. Important side effects of topical medication (e.g. intolerance to treatment,
hypersensitivity reactions, significant skin atrophy, systemic effects), as assessed
by the investigator or treating physician;

3. Having used any of the following treatments within 4 weeks before the baseline visit,
or any condition that, in the opinion of the investigator, was likely to require such
treatment(s) during the first 2 weeks of study treatment:

1. Immunosuppressive/immunomodulating drugs (e.g, systemic steroids, cyclosporine,
mycophenolate-mofetil, Janus kinase inhibitors, interferon-gamma [IFN-γ],
azathioprine, methotrexate, etc.);

2. Phototherapy for AD;

4. Treatment with a live (attenuated) vaccine within 12 weeks before the baseline visit;

5. History of human immunodeficiency virus (HIV) infection or positive HIV serology at
screening;

6. Positive hepatitis B surface antigen (HBsAg), hepatitis B core antibody (HBcAb), or
hepatitis C antibody at the screening visit;

7. Active or acute infection requiring systemic treatment within 2 weeks before baseline
visit;

8. Known or suspected history of immunosuppression;

9. Pregnant or breastfeeding women, or planning to become pregnant or breastfeed during
the participant's participation in this study.

Note: The eligibility criteria listed above is not intended to contain all considerations
relevant to a participant's potential participation in a clinical trial therefore not all
inclusion/ exclusion criteria are listed.
We found this trial at
50
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Edgewater, FL
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Albuquerque, NM
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Alpharetta, GA
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Ann Arbor, MI
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Austin, TX
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Cincinnati, OH
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Columbus, GA
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Corning, NY
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Dallas, TX
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Edina, MN
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Fridley, MN
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Hazleton, PA
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Henderson, NV
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Henrico, VA
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Hot Springs, AR
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Lake Oswego, OR
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Little Rock, AR
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Miami Lakes, FL
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New Albany, IN
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New York, NY
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Norfolk, VA
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1169
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Norman, OK
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73
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Oceanside, CA
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Oklahoma City, OK
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1300
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Omaha, NE
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2182
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Orlando, FL
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Palmdale, CA
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Philadelphia, PA
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Phoenix, AZ
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Portland, OR
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Rockville, MD
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105
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Smithtown, NY
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South Burlington, Vermont 05403
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South Burlington, VT
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939
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Spokane, WA
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Stony Brook, NY
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Tampa, FL
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Verona, NJ
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West Dundee, IL
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561
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West Jordan, UT
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