Innovent doses first patient in 600-participant Phase 3 IBI128 gout trial versus febuxostat

Reuters03-23

Innovent doses first patient in 600-participant Phase 3 IBI128 gout trial versus febuxostat

Innovent reported that the first participant has been dosed in a randomized, double-blind, multi-center Phase 3 study of tigulixostat (IBI128), a xanthine oxidase inhibitor, in Chinese patients with gout.
The trial plans to enroll 600 patients and will randomize them 1:1 to tigulixostat 100 mg or febuxostat 40 mg for 24 weeks.
The primary endpoint is the proportion of patients achieving serum uric acid below 360 μmol/L at week 24.
Phase 2 data were previously presented at the 2025 Asia-Pacific League of Associations for Rheumatology conference, and the Phase 3 study is intended to assess longer-term outcomes over a one-year treatment period.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Innovent Biologics Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: 202603222000PR_NEWS_USPR_____CN15344) on March 23, 2026, and is solely responsible for the information contained therein.

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