The purpose of this study is to evaluate the efficacy, safety, and tolerability of IBI112 in the treatment of participants with moderate to severe psoriasis
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
566
Participants receive Dose 1 IBI112 through week 8 \& Dose 2 IBI112 on week 20 \& Dose 1 IBI112 through week 44
Participants receive Dose 1 IBI112 through week 8 \& Dose 2 IBI112 on week 20 \& placebo through week 44 by subcutaneous injection
Participants receive Dose 1 IBI112 through week 8 \& Dose 3 IBI112 on week 20 \& placebo through week 44
Shanghai Skin Disease Hospital
Shanghai, Shanghai Municipality, China
Percentage of participants with a Psoriasis Area and Severity Index (PASI) 90 Response
Time frame: Week 56
Percentage of participants with a PASI75 Response
Time frame: Week 56
Percentage of participants with a PASI100 Response
Time frame: Week 56
Percentage of participants with a static Investigator's Global Assessment (sIGA) score of 0 or 1
Time frame: Week 56
Percentage of participants with Dermatology Life Quality Index (DLQI) Score
Time frame: Week 56
Percentage of participants with a sIGA score of 0
Time frame: Week 56
Cumulative Maintenance Rate of PASI 90 Response Through Week 56 to Evaluate Loss of a PASI 90 Response
Time frame: Week 56
Changes of PASI Scores participants who relapse and retreatment
Time frame: Week 56
Changes of sIGA score in participants who relapse and retreatment
Time frame: Week 56
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Participants receive Dose 1 IBI112 through week 8 \& Dose 3 IBI112 on week 20 \& Dose 1 IBI112 through week 44
Participants receive Dose 1 IBI112 through week 8 \& Dose 3 IBI112 through week 44
Participants receive Dose 1 IBI112 through week 8 \& Dose 2 IBI112 through week 44 by subcutaneous injection