Dupixent and Narrowband UVB for Atopic Dermatitis
Purpose
24 weeks open-label study with dupilumab and narrowband UVB phototherapy three times weekly for 12 weeks followed by 12 weeks of dupilumab monotherapy.
Condition
- Atopic Dermatitis
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Male or female adult ≥ 18 years of age; - Diagnosis of moderate to severe atopic dermatitis as defined at baseline by: - EASI score of 16 or greater, - IGA score of 3 or greater - BSA of 10% or greater,
Exclusion Criteria
- Subjects with previous exposure to dupilumab. - Known or suspected hypersensitivity to dupilumab or any of its excipients. - History of photosensitivity.
Study Design
- Phase
- Phase 4
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Dupixent and Narrowband UVB |
Dupixent and Narrowband UVB |
|
Recruiting Locations
Eczema Treatment Center of New Jersey
East Windsor, New Jersey 08520
East Windsor, New Jersey 08520
More Details
- Status
- Recruiting
- Sponsor
- Psoriasis Treatment Center of Central New Jersey
Detailed Description
24 weeks open-label study with dupilumab and narrowband UVB phototherapy three times weekly for 12 weeks followed by 12 weeks of dupilumab monotherapy.