Condition: Gout · Sponsor: Innovent Biologics Technology Limited (Shanghai R&D Center)
The primary purpose of this study is to compare the efficacy of Tigulixostat (IBI128) versus Febuxostat on the proportion of Chinese adults with gout achieving a serum uric acid (sUA) level \< 360 μmol/L at Week 24. The study also evaluates safety, gout attacks, kidney function, inflammation, and quality of life over 52 weeks of treatment. Approximately 600 eligible participants will be randomized to receive either Tigulixostat or Febuxostat.
This description comes directly from the study's public registry record.
Chunmiao Li · +8618321232774 · chunmiao.li@innoventbio.com
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| Shanghai Fudan University HuaShan Hospital | Shanghai, Shanghai Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07414394