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Innovent Announces First Participant Dosed of IBI128 (Tigulixostat, XOI) in Phase 3 Clinical Study

Innovent's Phase 3 trial enrolls 600 Chinese gout patients to compare tigulixostat and febuxostat, addressing safety and efficacy gaps in current treatments.

  • On yesterday, Innovent Biologics announced the first participant was dosed in a Phase 3 head-to-head study comparing tigulixostat versus febuxostat for Chinese gout patients.
  • Nearly 60% of gout patients in China are aged 18–35 years, and hyperuricemia prevalence reaches 17.7% nationwide, creating urgent demand for safer, more effective therapies.
  • Phase 2 data showed tigulixostat 100 mg achieved 81% serum uric acid compliance at 16 weeks, significantly outperforming febuxostat 40 mg with good renal and cardiovascular safety.
  • Innovent is building a broader gout portfolio including IBI3011 and mazdutide to address different disease stages; the company in-licensed exclusive China rights from LG Chem in December 2022.
  • The randomized, double-blind Phase 3 will enroll 600 Chinese patients receiving tigulixostat 100 mg or febuxostat 40 mg for 24 weeks within a one-year treatment period.
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Helena Independent RecordHelena Independent Record
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Innovent Announces First Participant Dosed of IBI128 (Tigulixostat, XOI) in Phase 3 Clinical Study

SAN FRANCISCO and SUZHOU, China, March 22, 2026 /PRNewswire/ -- Innovent Biologics, Inc. ("Innovent", HKEX: 01801), a world-class biopharmaceutical company that develops, manufactures and commercializes high quality medicines for the treatment of oncology, cardiovascular and metabolic, autoimmune, ophthalmology and other…

·Helena, United States
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Helena Independent Record broke the news in Helena, United States on Monday, March 23, 2026.
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