A Phase 3 Study of LNK01001 Capsule in Subjects With Moderate to Severe Atopic Dermatitis.
- Disease/Condition
- Atopic Dermatitis
- Drug/Device/Intervention
- LNK01001
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Lynk Pharmaceuticals Co., Ltd
- Location
- Guangzhou, China
- Phase
- Phase 3
- Start date
- Feb 06, 2024
- End date
- Nov 30, 2025
- Enrollment
- 354 participants
Eczema Area and Severity Index (EASI-75) at Week 16,Investigator's Global Assessment (IGA) score of 0/1 at Week 16
This is a randomized, double-blind study comparing LNK01001 to placebo in participants with
 moderately to severely atopic dermatitis who were candidates for systemic therapy (ie,
 patients with a history of inadequate response to topical treatments, those who were using a
 systemic treatment, or those for whom topical treatments are otherwise medically
 inadvisable).
 
 The objective of this study is to evaluate the efficacy and safety of LNK01001 in adult
 patients with moderate to severe AD who are candidates for systemic therapy.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06277245
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06277245 through Pure Global AI's free database. This Phase 3 trial is sponsored by Lynk Pharmaceuticals Co., Ltd and is currently Recruiting. The study focuses on Atopic Dermatitis. Target enrollment is 354 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.