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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| ICP-332 Dose A | Experimental |
| |
| ICP-332 Dose B | Experimental |
| |
| ICP-332 Dose C | Experimental |
| |
| ICP-332 Placebo | Placebo Comparator |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ICP-332 Tablets | Drug | ICP-332 will be administered as tablet for 12 weeks |
| |
| Measure | Description | Time Frame |
|---|---|---|
| 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 |
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Inclusion Criteria:
Subjects voluntarily participate in this study and have signed the Informed Consent Form (ICF).
Male or female subjects aged ≥ 18 years and ≤ 70 years
A history of plaque psoriasis for ≥6 months at baseline
Meet the following three criteria:
The subject requires systemic treatment and/or phototherapy.
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Molly Lin | Contact | +86 15198230043 | molly.lin@innocarepharma.com |
| Name | Affiliation | Role |
|---|---|---|
| Yuling Shi | Shanghai Dermatology Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Shanghai Dermatology Hospital | Recruiting | Shanghai | Shanghai Municipality | 200443 | China |
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| ICP-332 Tablets |
| Drug |
ICP-332 will be administered as tablet for 12 weeks |
|
| ICP-332 Tablets | Drug | ICP-332 will be administered as tablet for 12 weeks |
|
| ICP-332 Placebo Tablets | Other | Placebo will be administered as tablet for 12 weeks |
|