Efficacy and Safety of ICP-332 Versus Placebo in Participants With Moderate to Severe Plaque Psoriasis
Condition(s) studied
Investigational drug(s) / intervention(s)
ICP-332 Tablets: ICP-332 will be administered as tablet for 12 weeks
ICP-332 Tablets: ICP-332 will be administered as tablet for 12 weeks
ICP-332 Tablets: ICP-332 will be administered as tablet for 12 weeks
ICP-332 Placebo Tablets: Placebo will be administered as tablet for 12 weeks
Study summary
The purpose of this study is to compare the efficacy and safety of ICP-332 to placebo in participants with moderate-to-severe plaque psoriasis.
Eligibility
Primary outcome measure(s)
- The Percentage of Participants With Moderate to Severe Psoriasis Experiencing a 75% Improvement (Reduction From Baseline) in PASI Score (PASI-75 Response Rate) at Week 12 — Day 1 to Day 85
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Shanghai Dermatology Hospital | Shanghai | Shanghai Municipality | Recruiting |
More Beijing InnoCare Pharma Tech 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 NCT07251998 on ClinicalTrials.gov ↗ ← All trials in China