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Study identifier: NCT07362355 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

The Efficacy and Safety of SHR4640 Tablet Combined With 40 mg Febuxostat Tablets in the Treatment of Primary Gout and Hyperuricemia

Condition: Primary Gout and Hyperuricemia  ·  Sponsor: Jiangsu HengRui Medicine Co., Ltd.

PhasePhase 2
Planned participants340
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

SHR4640 tablets is a highly selective and potent URAT1 inhibitors. The study is being conducted to evaluate the efficacy, and safety of SHR4640 tablet combined with 40 mg/d febuxostat tablet in reducing uric acid in subjects with primary gout and hyperuricemia The primary purpose of the study is to evaluate the efficacy and safety of the combination of SHR4640 and 40 mg/d febuxostat compared with 60 mg/d febuxostat in primary gout and hyperuricemia subjects with inadequate control on 40 mg/d febuxostat for 12 weeks.

This description comes directly from the study's public registry record.

Talk to the study team

Haoshu Cui  ·  0518-82342973  ·  haoshu.cui.hc11@hengrui.com

Always discuss trial participation with your own doctor first.

Locations (1)

Huashan Hospital, Fudan UniversityShanghai, Shanghai Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07362355