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Study of Dupilumab and Immune Responses in Adults With Atopic Dermatitis (AD)

CompletedPhase 2

Sponsor: Regeneron Pharmaceuticals

Conditions: Atopic Dermatitis

Interventions: Dupilumab, Placebo

Countries: United States

This was a 32-week, randomized, double-blind, placebo-controlled, parallel-group study assessing immunization responses to vaccination in adults with moderate to severe atopic dermatitis who are treated with subcutaneous dupilumab.

Eligibility overview

Sex: ALL

Age: 18 Years to 64 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Key Inclusion Criteria:

1. Male or female adults ages 18 to 64 years with Chronic AD (according to the American Academy of Dermatology Consensus Criteria, \[Eichenfeld 2004\])that has been present for at least 3 years before the screening visit
2. Participants with documented recent history (within 6 months before the screening visit) of inadequate response to a sufficient course of outpatient treatment with topical AD medication(s), or for whom topical AD therapies are otherwise inadvisable (e.g., because of side effects or safety risks).
3. Eczema Area and Severity Index (EASI) score ≥16 at the screening visit and the baseline visit
4. Investigator's Global Assessment (IGA) score ≥3 (on the 0-4 IGA scale) at the screening and baseline visits
5. ≥10% body surface area (BSA) of AD involvement at the screening and baseline visits

Key Exclusion Criteria:

1. Prior treatment with dupilumab (REGN668/ SAR231893)
2. Patients needing \>10 mg of daily prednisone (including equivalent doses of other steroids) or high dose systemic corticosteroids (≥2 mg/kg) for 14 days or longer during the 16 week treatment period of the study
3. History of Guillain-Barre syndrome
4. History of severe allergic reaction to either vaccine or to vaccine components including alum, thimerosal, phenol
5. Patients with a severe reaction to natural rubber latex products (some packaging components of the vaccines contain rubber latex and may cause a reaction in susceptible individuals)
6. Treatment with biologics within 4 months of baseline visit
7. Chronic or acute infection requiring treatment with antibiotics, antivirals, antiparasitics, antifungals within 4 weeks before screening visit or superficial skin infections within 1 week of screening visit

The information listed above is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial and not all inclusion/ exclusion criteria are listed.

Locations (42)

Birmingham, Alabama, United States
Fort Smith, Arkansas, United States
Long Beach, California, United States
Los Angeles, California, United States
Mission Viejo, California, United States
Rolling Hills Estates, California, United States
San Diego, California, United States
Santa Monica, California, United States
Denver, Colorado, United States
Jacksonville, Florida, United States
Miami, Florida, United States
Tampa, Florida, United States
Macon, Georgia, United States
Chicago, Illinois, United States
Maywood, Illinois, United States
West Dundee, Illinois, United States
Indianapolis, Indiana, United States
Plainfield, Indiana, United States
Overland Park, Kansas, United States
Boston, Massachusetts, United States
Ann Arbor, Michigan, United States
Troy, Michigan, United States
St Louis, Missouri, United States
Hackensack, New Jersey, United States
Albuquerque, New Mexico, United States
Buffalo, New York, United States
Forest Hills, New York, United States
New York, New York, United States
Cleveland, Ohio, United States
Norman, Oklahoma, United States
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