A Study to Evaluate JYP0061 Tablets in Patients With Moderate-to-severe Atopic Dermatitis
Condition(s) studied
Investigational drug(s) / intervention(s)
JYP0061 15 mg: Participants in the JYP0061 15 mg group will receive a 15 mg oral tablet of JYP0061 once daily for 12 weeks.
JYP0061 30 mg: articipants in the JYP0061 30 mg group will receive a 30 mg oral tablet of JYP0061 once daily for 12 weeks.
Placebo: Participants in the placebo group will receive a matching placebo tablet once daily for 12 weeks.
Study summary
The goal of this clinical trial is to evaluate the efficacy and safety of JYP0061 in adult patients with moderate-to-severe atopic dermatitis. The main questions it aims to answer are:
* The efficacy of JYP0061 in treating adult patients with moderate-to-severe atopic dermatitis.
* The safety profile of JYP0061 when administered to adult patients with moderate-to-severe atopic dermatitis.
Participants will:
* Be treated with either a low-dose or high-dose of JYP0061.
* Undergo efficacy and safety evaluations as stipulated in the trial protocol.
Eligibility
Primary outcome measure(s)
- Proportion of participants achieving at least a 75% reduction in Eczema Area and Severity Index (EASI 75) from baseline. — Evaluations will be conducted weekly for up to 12 weeks
The Eczema Area and Severity Index (EASI) is a measure of eczema severity, combining area coverage and symptom intensity (erythema, edema/papulation, excoriation, lichenification) for four body regions. EASI scores range from 0 (no eczema) to 72 (maximum severity), with higher scores indicating worse outcomes. This primary outcome assesses the proportion of participants who achieve at least a 75% reduction in EASI from baseline to Week 12.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Huashan Hospital, Fudan University | Shanghai | Shanghai Municipality |
More Guangzhou JOYO Pharma Co., Ltd trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06158490 on ClinicalTrials.gov ↗ ← All trials in China