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RECRUITING
NCT07116746
PHASE2

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

Sponsor: Arthrosi Therapeutics

View on ClinicalTrials.gov

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.

Official title: A Phase 2, Multicenter, Open-label, Efficacy and Safety Study of AR882 and XOI Co-administration in Participants With Uncontrolled Gout Who Have Previously Failed Uricase Treatment

Key Details

Gender

All

Age Range

18 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

25

Start Date

2025-12-03

Completion Date

2027-01

Last Updated

2026-03-02

Healthy Volunteers

No

Interventions

DRUG

AR882 75 mg

Solid Oral Capsule

DRUG

XOI Low Dose

Solid Oral Tablet

DRUG

XOI High Dose

Solid Oral Tablet

Locations (8)

Arthrosi Investigative Site (105)

Margate, Florida, United States

Arthrosi Investigative Site (102)

Miami, Florida, United States

Arthrosi Investigative Site (109)

Tampa, Florida, United States

Arthrosi Investigative Site (106)

Jackson, Mississippi, United States

Arthrosi Investigative Site (108)

Charlotte, North Carolina, United States

Arthrosi Investigative Site (103)

Duncansville, Pennsylvania, United States

Arthrosi Investigative Site (104)

West Lake Hills, Texas, United States

Arthrosi Investigative Site (107)

Bellevue, Washington, United States