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Clinical Trial Summary

The primary objectives of this study are to assess the safety, tolerability, and efficacy of ABP-671 in lowering serum uric acid (sUA) in participants with gout who roll over from Study ABP-671-301 after they complete the double-blind 28-week Treatment Period of Part 1 (Phase 2b) or Part 2 (Phase 3).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06276556
Study type Interventional
Source Jiangsu Atom Bioscience and Pharmaceutical Co., Ltd.
Contact
Status Enrolling by invitation
Phase Phase 2/Phase 3
Start date April 22, 2024
Completion date July 2, 2025

See also
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