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

Last updated: May 13, 2026
Sponsor: Arthrosi Therapeutics
Overall Status: Active - Not Recruiting

Phase

2

Condition

Joint Injuries

Bone Diseases

Arthritis And Arthritic Pain

Treatment

XOI High Dose

AR882 75 mg

XOI Low Dose

Clinical Study ID

NCT07116746
AR882-204
  • Ages 18-85
  • All Genders

Study 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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • History of uncontrolled gout

  • Presence of ≥1 clinically visible tophus

  • Last uricase infusion occurred ≥3 months

  • Body weight no less than 50 kg

  • Serum creatinine must be < 3.0 mg/dL and estimated CLcr ≥ 40 mL/min

Exclusion

Exclusion Criteria:

  • Malignancy within 5 years, except for successfully treated basal or squamous cellcarcinoma of the skin

  • Pregnant or breastfeeding

  • History of symptomatic kidney stones within the past 6 months

  • Received pegloticase, rasburicase or other experimental uricases within the last 3months

Study Design

Total Participants: 15
Treatment Group(s): 3
Primary Treatment: XOI High Dose
Phase: 2
Study Start date:
December 03, 2025
Estimated Completion Date:
February 28, 2027

Connect with a study center

  • Arthrosi Investigative Site (105)

    Margate, Florida 33063
    United States

    Site Not Available

  • Arthrosi Investigative Site (102)

    Miami, Florida 33155
    United States

    Site Not Available

  • Arthrosi Investigative Site (109)

    Tampa, Florida 33609
    United States

    Site Not Available

  • Arthrosi Investigative Site (105)

    Margate 4163407, Florida 4155751 33063
    United States

    Site Not Available

  • Arthrosi Investigative Site (102)

    Miami 4164138, Florida 4155751 33155
    United States

    Site Not Available

  • Arthrosi Investigative Site (109)

    Tampa 4174757, Florida 4155751 33609
    United States

    Site Not Available

  • Arthrosi Investigative Site (106)

    Jackson, Mississippi 39202
    United States

    Site Not Available

  • Arthrosi Investigative Site (106)

    Jackson 4431410, Mississippi 4436296 39202
    United States

    Site Not Available

  • Arthrosi Investigative Site (108)

    Charlotte, North Carolina 28202
    United States

    Site Not Available

  • Arthrosi Investigative Site (108)

    Charlotte 4460243, North Carolina 4482348 28202
    United States

    Site Not Available

  • Arthrosi Investigative Site (103)

    Duncansville, Pennsylvania 16635
    United States

    Site Not Available

  • Arthrosi Investigative Site (103)

    Duncansville 5187508, Pennsylvania 6254927 16635
    United States

    Site Not Available

  • Arthrosi Investigative Site (104)

    West Lake Hills, Texas 78746
    United States

    Site Not Available

  • Arthrosi Investigative Site (104)

    West Lake Hills 4740928, Texas 4736286 78746
    United States

    Site Not Available

  • Arthrosi Investigative Site (107)

    Bellevue, Washington 98004
    United States

    Site Not Available

  • Arthrosi Investigative Site (107)

    Bellevue 5786882, Washington 5815135 98004
    United States

    Site Not Available

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