Tralokinumab for Dupilumab Failures
NCT06773455 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 7
Last updated 2026-05-22
Summary
24-week study of 20 atopic dermatitis patients who have been treated with dupilumab will receive Tralokinumab 600mg at week 0 followed by 300mg Q2W for 24 weeks.
Conditions
Interventions
- DRUG
-
tralokinumab
600mg at week 0 followed by 300mg Q2W for 24 weeks
Sponsors & Collaborators
-
LEO Pharma
collaborator INDUSTRY -
Psoriasis Treatment Center of Central New Jersey
lead OTHER
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-09-11
- Primary Completion
- 2026-01-13
- Completion
- 2026-01-13
- FDA Drug
- Yes
Countries
- United States
Study Locations
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