drugset / Trial / NCT07116746

Evaluation of Efficacy and Safety of AR882 and XOI Co-administration in Uricase Treatment Failed Patients

NCT07116746

Phase 2 Active not recruiting 15 enrolled Arthrosi Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

This study will assess the effect of AR882 and XOI co-administration on sUA lowering as well as reducing tophus burden in the population that has failed uricase treatment (eg., pegloticase). Failed uricase treatment is defined as having an inherent intolerance, anaphylaxis, infusion reaction, antibody development, and/or at least one sUA level that rose to greater than 6 mg/dL while on therapy.

Timeline

Start
2025-12-03
Primary completion
2026-11
Completion
2027-02

Drugs

EvaluationDrugModalityDoseRoute
Subject AR882 Unknown 75 mg Oral

Indications