drugset / Trial / NCT04250350

Study to Assess the Safety and Efficacy of Lebrikizumab (LY3650150) in Adolescent Participants With Moderate-to-Severe Atopic Dermatitis

NCT04250350

Phase 3 Completed 206 enrolled Eli Lilly and Company Dermira, Inc. · collab
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, single arm study of 52 weeks duration. The study will assess the safety and efficacy of lebrikizumab in adolescent participants (≥12 to \<18 years weighing ≥40 kilograms) with moderate-to-severe atopic dermatitis (AD) who are candidates for systemic therapy.

Timeline

Start
2020-02-11
Primary completion
2022-04-20
Completion
2022-06-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Lebrikizumab Monoclonal antibody 250 mg Subcutaneous

Indications