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 — DRUG
    IBI112 by subcutaneous injection
  • placebo — DRUG
    placebo 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: placebo
    Participants receive placebo through week 16,placebo participants will cross over to receive IBI112 through week 44
  • Experimental: IBI112
    Participants 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

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