Innovent Announces First Patient Dosed in a Phase 2 Clinical Trial of IBI112 (IL-23 Monoclonal Antibody) in Patients with Moderate-to-severe Plaque Psoriasis

SAN FRANCISCO and SUZHOU, China, Sept. 23, 2021 /PRNewswire/ — Innovent Biologics, Group. (“Innovent”) (HKEX: 01801), a world-class biopharmaceutical company that develops, manufactures and commercializes high quality medicines for the treatment of cancer, metabolic, autoimmune and other major diseases, today announced that the first patient with moderate-to-severe plaque psoriasis has been successfully dosed in a Phase 2 clinical trial (clinicaltrials.gov, NCT05003531) of recombinant anti-interleukin 23p19 subunit antibody injection (R & D code: IBI112) in China.

Study CIBI112A201 is a multicenter, randomized, double-blind, parallel, placebo-controlled Phase 2 clinical trial, evaluating the efficacy and safety of IBI112 at different doses administered subcutaneously in the treatment of moderate-to-severe plaque psoriasis. The primary objective of the study is to evaluate the efficacy of subcutaneous injection of IBI112 at different doses in Chinese subjects with moderate-to-severe plaque psoriasis. The safety of drugs and the difference of administration interval between different therapeutic regimens will also be investigated, so as to provide dose information for Phase 3 clinical studies. This is also the first Phase 2 clinical study of domestic innovative drugs targeting IL-23p19, which is a significant milestone.

Click the button below to read the entire Press Release:

Continue Reading The Press Release