AR882 clinical trials
How each study uses AR882 is sorted by a rule, right about nine times in ten. Readers can ask us to read every study one by one.Ask us to read each study
Approvals
The first approval found in each region, with its record
- United States
- Not in FDA's approval records
- European Union
- Not in EMA's list of EU-wide authorisations
From FDA's Drugs@FDA and Purple Book (through openFDA) and the European Medicines Agency, files of Sept 2026 and 27 Oct 2026. National approvals in Europe and other countries are not included. How this is worked out
How studies write it
Studies that test it under each name
Studies by the year they started
9 studies that test it; most in 2021 (2)
| Year | Studies |
|---|---|
| 2019 | 1 |
| 2020 | 1 |
| 2021 | 2 |
| 2022 | 1 |
| 2024 | 2 |
| 2025 | 2 |
By phase
A phase 1/2 study counts in both.
What it is tested for
Each study’s main condition, where its own words name it, so a study counts once.
Who runs them
Industry 9 · Other 0
Arthrosi Therapeutics (8) · Guangzhou Ruianbo Pharmaceutical Technology Co., Ltd (1)
Often tested with
Tested in the same studies.
Coming up
From the study records. Dates are the sponsors’ own estimates and often move.
Reaching primary completion within a year · 1
Studies that test AR882.
- Nov 2026Evaluation of Efficacy and Safety of AR882 and XOI Co-administration in Uricase Treatment Failed PatientsPhase 2 · Arthrosi Therapeutics
Studies
Open first, then newest update. How each study uses AR882 is read from its arms, and is right about nine times in ten. Ask us to read each study. These are the studies that list it as an intervention; a search of ClinicalTrials.gov also finds studies that mention it only in a description, such as earlier treatment.
Testing it · 9
- Phase 3 Evaluation of Efficacy and Safety of AR882 in Gout Patients (AR882-302)CompletedPhase 3Arthrosi TherapeuticsNCT06439602Written as AR882 50 mg
- Phase 3 Evaluation of Efficacy and Safety of AR882 in Gout Patients (AR882-301)CompletedPhase 3Arthrosi TherapeuticsNCT06846515Written as AR882 50 mg
- Evaluation of Efficacy and Safety of AR882 and XOI Co-administration in Uricase Treatment Failed PatientsActive, not recruitingPhase 2Arthrosi TherapeuticsNCT07116746Written as AR882 75 mg
- Phase 2 to Assess Efficacy and Safety in AR882 Alone or in Combination With Allopurinol in Patients With Tophaceous GoutCompletedPhase 2Arthrosi TherapeuticsNCT05253833Written as AR882 Dose 1
- Phase II/III Study of AR882 Capsules Compared to Febuxostat Tablets in Patients with Primary Gout and HyperuricemiaActive, not recruitingPhase 2/3Guangzhou Ruianbo Pharmaceutical Technology Co., LtdNCT06603142Written as AR882 25MG
- Phase 2b Evaluation of Efficacy and Safety of AR882 in Gout PatientsCompletedPhase 2Arthrosi TherapeuticsNCT05119686Written as AR882 Dose 1
- Pharmacokinetic Study of AR882 in Subjects With Various Degrees of Renal ImpairmentCompletedPhase 1Arthrosi TherapeuticsNCT04646889Written as AR882 Single Dose
- Single-dose AME Study With [14C]AR882 in Healthy Male SubjectsCompletedPhase 1Arthrosi TherapeuticsNCT04508426Written as [14C]AR882
- The Study is Designed to Evaluate Single Ascending Doses of AR882 in Healthy Adult MalesCompletedPhase 1Arthrosi TherapeuticsNCT04347005Written as Cohort 1: AR882