๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-05-13

Evaluation of Efficacy and Safety of AR882 and XOI Co-administration in Uricase Treatment Failed Patients (NCT07116746)

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

๐Ÿ”ต Active, Not Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Arthrosi Therapeutics

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: Arthrosi Investigative Site (105) โ€” Margate, Florida

Age range: 18 Years to 85 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (8 Sites)

  • Arthrosi Investigative Site (105) โ€” Margate, Florida
  • Arthrosi Investigative Site (102) โ€” Miami, Florida
  • Arthrosi Investigative Site (109) โ€” Tampa, Florida
  • Arthrosi Investigative Site (106) โ€” Jackson, Mississippi
  • Arthrosi Investigative Site (108) โ€” Charlotte, North Carolina
  • Arthrosi Investigative Site (103) โ€” Duncansville, Pennsylvania
  • Arthrosi Investigative Site (104) โ€” West Lake Hills, Texas
  • Arthrosi Investigative Site (107) โ€” Bellevue, Washington

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Gout clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—