This is a multicenter, open-label study aim to evaluate the efficacy and safety of IBI112 in Chinese participants with plaque psoriasis who were treated with biologics and switched to IBI112. The study will enroll 160 participants who were diagnosed with plaque psoriasis. The whole study consists of 4 weeks of screening, 32 or 36 weeks of treatment and a safety follow-up visit at Week 44.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
152
IBI112 200mg s.c. at week 0, 12, 24 and 36.
IBI112 200mg s.c. at week 0, 4, 8, 20 and 32.
Dermatology Hospital of Shandong First Medical University (Shandong Provincial Hospitial of Dermatology)
Jinan, Shandong, China
Percentage of participants who achieve sPGA clean (0) or nearly clean (1) ,and BSA < 3%
Time frame: Week 16
Percentage of participants who achieve sPGA clean (0) at Week 16.
Time frame: Week 16
Percentage of participants with a DLQI score of 0/1 at Week 16.
Time frame: Week 16
Percentage of participants with sPGA 0/1 or sPGA 0 or DLQI 0/1 at Week 44.
Time frame: Week 44
Percentage of participants who achieve sPGA 0 or 1 at week 16 and maintain that up to Week 44
Time frame: Week 16 up to Week 44
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