A Study of Lebrikizumab (LY3650150) With/Without Topical Corticosteroid Treatment in Participants With Moderate-to-Severe Atopic Dermatitis
- Disease/Condition
- Atopic Dermatitis
- Drug/Device/Intervention
- Placebo
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Eli Lilly and Company
- Location
- Wuhu,Beijing,Beijing,Beijing,Beijing,Beijing,Beijing,Beijing,Beijing,Chongqing,Xiamen,Guangzhou,Guangzhou,Shenzhen,Shenzhen,Shenzhen,Shenzhen,Haikou,Wuhan,Wuhan,Wuhan,Changsha,Changsha,Changsha,Suzhou, China,South Korea
- Phase
- Phase 3
- Start date
- May 06, 2024
- End date
- Nov 04, 2026
- Enrollment
- 430 participants
Percentage of Participants Achieving Eczema Area and Severity Index (EASI-75) (≥75% Reduction in EASI Score) at Week 16 for Mono Cohort,Percentage of Participants Achieving EASI-75 at Week 16 for Combo Cohort
The main purpose of this study is to evaluate the efficacy and safety of lebrikizumab
 with/without Topical Corticosteroid Treatment in Participants with Moderate-to-Severe Atopic
 Dermatitis. The study will last approximately 62 weeks.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06280716
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06280716 through Pure Global AI's free database. This Phase 3 trial is sponsored by Eli Lilly and Company and is currently Not yet recruiting. The study focuses on Atopic Dermatitis. Target enrollment is 430 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.