Last reviewed · How we verify

NCT04508426

Single-dose AME Study With [14C]AR882 in Healthy Male Subjects

Completed Phase 1 Last updated 16 November 2020
What this trial tests

Phase 1 trial testing [14C]AR882 in Healthy Volunteers in 6 participants. Completed in 12 August 2020.

Timeline
16 July 2020
Primary endpoint
12 August 2020
12 August 2020

Quick facts

Lead sponsorArthrosi Therapeutics
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment6
Start date16 July 2020
Primary completion12 August 2020
Estimated completion12 August 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

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):

  1. 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:

Other recruiting trials for Healthy Volunteers

Currently open trials in the same condition.

Other Arthrosi Therapeutics trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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