drugset / Trial / NCT03989349

Efficacy & Safety of Nemolizumab in Subjects With Moderate-to-Severe Atopic Dermatitis

NCT03989349

Phase 3 Completed 787 enrolled Galderma R&D
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The main purpose of the study was to assess the efficacy and safety of nemolizumab after a 16-week treatment period in adult and adolescent subjects with moderate-to-severe atopic dermatitis (AD) not adequately controlled with topical treatments.

Timeline

Start
2019-06-30
Primary completion
2022-02-23
Completion
2022-09-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Nemolizumab Monoclonal antibody 30 mg Subcutaneous

Indications