Phase 3 Evaluation of Efficacy and Safety of AR882 in Gout Patients
About the study
This study will assess the serum uric acid lowering effect and safety of AR882 in gout patients at two doses compared to placebo over 12 months

Study Locations
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How to Apply
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Study’s details
Age (in years)
18 - 85
Phase
PHASE3
Participants needed
750
Treatment type
INTERVENTIONAL
Sponsor
Arthrosi Therapeutics
ClinicalTrials.gov identifier
NCT06439602
Study number
AR882-302
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