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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
172
ICP-332 will be administered as tablet for 12 weeks
ICP-332 will be administered as tablet for 12 weeks
ICP-332 will be administered as tablet for 12 weeks
Shanghai Dermatology Hospital
Shanghai, Shanghai Municipality, China
RECRUITINGThe 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
Time frame: Day 1 to Day 85
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Placebo will be administered as tablet for 12 weeks