drugset / Trial / NCT05253833

Phase 2 to Assess Efficacy and Safety in AR882 Alone or in Combination With Allopurinol in Patients With Tophaceous Gout

NCT05253833

Phase 2 Completed 42 enrolled Arthrosi Therapeutics
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will assess the serum urate lowering effect, tophi reduction, and safety of AR882 alone and in combination with allopurinol in patients with tophaceous gout at two doses compared to allopurinol over 24 weeks.

Timeline

Start
2022-08-12
Primary completion
2024-08-13
Completion
2024-10-28

Drugs

EvaluationDrugModalityDoseRoute
Subject AR882 Unknown Oral
Subject Allopurinol Small molecule

Indications