New hope for tough gout: drug combo targets uric acid after other treatments fail
NCT ID NCT07116746
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a new drug called AR882, taken with a standard gout medication (XOI), in 15 people with severe, uncontrolled gout who have already failed uricase therapy. The goal is to see if the combination can lower uric acid levels and shrink painful uric acid crystal deposits called tophi. Researchers will also monitor for side effects over 6 months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- AR882 (a drug that lowers uric acid) combined with a xanthine oxidase inhibitor (XOI)
- What this could lead to
- If it works, this could offer a new treatment option for people with severe gout who have not responded to or cannot tolerate uricase therapy.
- What could go wrong
- This is a small, early-phase trial with only 15 participants, so results may not apply to everyone. The drug combination may cause side effects or fail to control gout long-term.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
About 15 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Dec 2025
- Expected to finish
-
Feb 2027
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 85 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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 Criteria: * Malignancy within 5 years, except for successfully treated basal or squamous cell carcinoma 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 3 months
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Arthrosi Investigative Site (102)
Miami, Florida, 33155, United States
-
Arthrosi Investigative Site (103)
Duncansville, Pennsylvania, 16635, United States
-
Arthrosi Investigative Site (104)
West Lake Hills, Texas, 78746, United States
-
Arthrosi Investigative Site (105)
Margate, Florida, 33063, United States
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Arthrosi Investigative Site (106)
Jackson, Mississippi, 39202, United States
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Arthrosi Investigative Site (107)
Bellevue, Washington, 98004, United States
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Arthrosi Investigative Site (108)
Charlotte, North Carolina, 28202, United States
-
Arthrosi Investigative Site (109)
Tampa, Florida, 33609, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Gout's crystal clues: could urate deposits flag hidden heart risk?
- Can a new injection tame Gout's uric acid?
- One infusion, two targets: a uric-acid-lowering drug takes aim at heart and kidney disease in youth-onset diabetes
- Can an ancient herbal formula tame gout?
- New drug combo aims to tame stubborn gout flares
- Timing matters: study tests if starting gout drug during a flare is safe