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NCT07116746 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study of Gout and Hyperuricemia, sponsored by Arthrosi Therapeutics.

Recruiting
Registry status
Phase 2
Development phase
25
Enrollment target
8
Study locations

NCT07116746 is a Phase 2 study of Gout and Hyperuricemia that is actively recruiting participants, run by Arthrosi Therapeutics. The registered enrollment target is 25 participants, below the 8,888-participant average among 34 other Gout trials with a reported enrollment target (100% lower). The trial reports 8 study locations across 6 states.

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The verdict

NCT07116746, a Phase 2 study of Gout and Hyperuricemia, is actively recruiting participants, sponsored by Arthrosi Therapeutics.

RECRUITING
Registry status
Phase 2
Development phase
25 participants
Enrollment target
8
Study locations

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.

Interventions

  • DRUG AR882 75 mg
  • DRUG XOI Low Dose
  • DRUG XOI High Dose

Study Locations (8)

Florida

  • Arthrosi Investigative Site (105) - Margate
  • Arthrosi Investigative Site (102) - Miami
  • Arthrosi Investigative Site (109) - Tampa

Mississippi

  • Arthrosi Investigative Site (106) - Jackson

North Carolina

  • Arthrosi Investigative Site (108) - Charlotte

Pennsylvania

  • Arthrosi Investigative Site (103) - Duncansville

Texas

  • Arthrosi Investigative Site (104) - West Lake Hills

Washington

  • Arthrosi Investigative Site (107) - Bellevue

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2025-12-03
Est. Completion 2027-01
Phase Phase 2

Sponsor

Arthrosi Therapeutics

7 total trials

What the Registry Record Tells You About NCT07116746

The ClinicalTrials.gov registry entry for NCT07116746 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 8,888-participant average among 34 other Gout trials with a reported enrollment target (100% lower). The listed sponsor is Arthrosi Therapeutics, which has 7 total studies on file at ClinicalTrials.gov.

The record links to 7 conditions, with Gout appearing as the primary indexed condition, and to 3 interventions - of which AR882 75 mg is the first listed.

NCT07116746 reports 8 study locations spanning 6 distinct geographic areas - top geographies include Florida, Mississippi, North Carolina.

Frequently Asked Questions

What is clinical trial NCT07116746 about?

NCT07116746 is a clinical study titled "Evaluation of Efficacy and Safety of AR882 and XOI Co-administration in Uricase Treatment Failed Patients". 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, antibo...

What is the current status of trial NCT07116746?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 25 participants. The study started on 2025-12-03. Estimated completion is 2027-01.

What conditions does trial NCT07116746 study?

This clinical trial studies the following conditions: Gout, Hyperuricemia, Gout Chronic, Uncontrolled Gout, Gouty Arthritis.

What interventions are being tested in trial NCT07116746?

The interventions under investigation include: AR882 75 mg (DRUG), XOI Low Dose (DRUG), XOI High Dose (DRUG).

Who is sponsoring clinical trial NCT07116746?

This trial is sponsored by Arthrosi Therapeutics, which has 7 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07116746 being conducted?

This trial has 8 study locations across Florida, Mississippi, North Carolina, Pennsylvania, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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