drugset / Trial / NCT05372419

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

NCT05372419

Phase 3 Completed 90 enrolled Eli Lilly and Company
NaSingle-groupOpen-labelTreatment

Summary

The main purpose of this study is to determine the safety and efficacy lebrikizumab in adolescent and adult participants with moderate-to-severe atopic dermatitis (AD) and skin of color.

Timeline

Start
2023-01-12
Primary completion
2024-05-03
Completion
2025-02-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Lebrikizumab Monoclonal antibody 250 mg Subcutaneous

Indications