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NCT04508426
Single-dose AME Study With [14C]AR882 in Healthy Male Subjects
Phase 1 trial testing [14C]AR882 in Healthy Volunteers in 6 participants. Completed in 12 August 2020.
12 August 2020
Quick facts
| Lead sponsor | Arthrosi Therapeutics |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 6 |
| Start date | 16 July 2020 |
| Primary completion | 12 August 2020 |
| Estimated completion | 12 August 2020 |
| Sites | 1 location across United States |
Drugs / interventions tested
- [14C]AR882 — full drug profile →
Conditions studied
- Healthy Volunteers — all drugs for Healthy Volunteers →
Sponsor
Arthrosi Therapeutics — full company profile →
Who can join
Adults 18 to 55, male only, with Healthy Volunteers. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This is an open-label, single-dose, absorption, metabolism, excretion, and mass balance study following a single dose of \[14C\]AR882 in healthy adult male subjects. Whole blood, plasma, urine, and fecal samples will be analyzed for at least 144 hours following the single dose of AR882 to measure total radioactivity and plasma drug concentrations.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Review of Urate-Lowering Therapeutics: From the Past to the Future.
Jenkins C, Hwang JH, Kopp JB, Winkler CA, et al · · 2022 · cited 38× · PMID 36081938 · DOI 10.3389/fphar.2022.925219
Verify or expand the search:
- PubMed search for NCT04508426
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Arthrosi Therapeutics trials
Trials by the same sponsor.
- NCT05253833 — Phase 2 to Assess Efficacy and Safety in AR882 Alone or in Combination With Allopurinol in Patients With Tophaceous Gout · Phase 2 · completed
- NCT05119686 — Phase 2b Evaluation of Efficacy and Safety of AR882 in Gout Patients · Phase 2 · completed
- NCT04646889 — Pharmacokinetic Study of AR882 in Subjects With Various Degrees of Renal Impairment · Phase 1 · completed
- NCT04155918 — Phase 2a Study of AR882 Alone and in Combination With Febuxostat or Allopurinol in Gout Patients · Phase 2 · completed
- NCT04314986 — Multiple Ascending Dose Study of AR882 in Healthy Adult Male Volunteers · Phase 1 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04508426 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Arthrosi Therapeutics
- Last refreshed: 16 November 2020
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04508426.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing