A Study to Evaluate Efficacy and Safety of IBI112 in Adolescent Participants With Moderate to Severe Plaque Psoriasis
- Sponsor
- Innovent Biopharmaceutical Technology (Hangzhou) Co., LTD.
- Study ID
- NCT07265284
- Phase
- PHASE3
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 12 Years - 18 Years
- Healthy Volunteers
- Not accepted
Interventions
- IBI112 — DRUGIBI112 by subcutaneous injection
- placebo — DRUGplacebo by subcutaneous injection
Study Details
The purpose of this study is to evaluate the efficacy and safety of IBI112 in the treatment of adolescent participants with moderate to severe plaque-type psoriasis.
Key Dates
- First listed
- Dec 4, 2025
- Start date
- Dec 3, 2025
- Status verified
- Dec 2025
- Primary completion
- Sep 30, 2026
- Completion
- Jan 31, 2029
Study Design
- Enrollment
- 104 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Placebo Comparator: placeboParticipants receive placebo through week 16,placebo participants will cross over to receive IBI112 through week 44
- Experimental: IBI112Participants receive IBI112 through week 44
Primary Outcome Measure
Percentage of patients achieving Psoriasis Area and severity index(PASI) 75 at week 16 [ Time Frame: week 16 ]
Central Contacts
- Bingjing Feng+86 18361923769
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