drugset / Trial / NCT04678882

Dupilumab in Japanese Patients With Atopic Dermatitis

NCT04678882

Phase 3 Completed 62 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

Primary Objective: To evaluate the efficacy of dupilumab administered concomitantly with topical corticosteroids (TCS) Secondary Objective: To evaluate the efficacy of dupilumab administered concomitantly with TCS. To assess the safety of dupilumab over 16 weeks of treatment when administered concomitantly with TCS in participants. To assess immunogenicity as determined by the incidence, titer, and clinical impact of treatment-emergent anti-drug antibodies (ADA) to dupilumab over time in pediatric patients with atopic dermatitis (AD) (aged ≥6 months to \<18 years old) To assess the concentration of dupilumab in serum following administration concomitantly with TCS.

Timeline

Start
2021-01-15
Primary completion
2021-12-14
Completion
2023-10-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Dupilumab Monoclonal antibody Subcutaneous

Indications