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
Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria:
1. Subjects voluntarily participate in this study and have signed the Informed Consent Form (ICF).
2. Male or female subjects aged ≥ 18 years and ≤ 70 years
3. A history of plaque psoriasis for ≥6 months at baseline
4. Meet the following three criteria:
1. Psoriasis Area and Severity Index (PASI) score ≥12
2. Static Physician's Global Assessment (sPGA) score ≥3
3. Psoriasis affected Body Surface Area (BSA) ≥10%
5. The subject requires systemic treatment and/or phototherapy.
Exclusion Criteria:
1. Diagnosed with non-plaque psoriasis.
2. Subject had laboratory values meeting any of the protocol-specified criteria at Screening.
3. Presence of clinically serious, progressive, or uncontrolled disease.
4. Previous history of alcoholism or drug abuse (except for those who have been completely abstinent for more than 6 months before randomization).
5. Pregnant or lactating women.
6. The investigator accepts ICP-332 for any reason that the subject is not suitable for this study.
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
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.
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