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Completed Phase 3 Interventional

Phase 3 Evaluation of Efficacy and Safety of AR882 in Gout Patients (AR882-302)

ClinicalTrials.gov ID: NCT06439602

Public ClinicalTrials.gov record NCT06439602. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 3:55 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3 Randomized, Double-blind, Multi-center, Placebo-controlled Study to Evaluate the Efficacy and Safety of AR882 in Participants With Gout

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will assess the serum uric acid lowering effect and safety of AR882 in gout patients at two doses compared to placebo over 12 months

Study identification

NCT ID
NCT06439602
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Arthrosi Therapeutics
Industry
Enrollment
818 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 85 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 26, 2024 (Actual)
Primary completion
Mar 20, 2026 (Actual)
Completion
Apr 10, 2026 (Actual)
Last update posted
Oct 14, 2026

2024 – 2026

United States locations

U.S. sites
52
U.S. states
24
U.S. cities
50
Facility City State ZIP Site status
Arthrosi Investigative Site (106) Foley Alabama 36535 —
Arthrosi Investigative Site (139) Anchorage Alaska 99508 —
Arthrosi Investigative Site (160) Peoria Arizona 85381 —
Arthrosi Investigative Site (112) Phoenix Arizona 85037 —
Arthrosi Investigative Site (114) Tempe Arizona 85281 —
Arthrosi Investigative Site (131) El Cajon California 92108 —
Arthrosi Investigative Site (117) Encinitas California 92024 —
Arthrosi Investigative Site (138) Rancho Cucamonga California 91730 —
Arthrosi Investigative Site (161) Valencia California 28277 —
Arthrosi Investigative Site (101) Aurora Colorado 80014 —
Arthrosi Investigative Site (149) Clearwater Florida 33756 —
Arthrosi Investigative Site (115) Coral Gables Florida 33134 —
Arthrosi Investigative Site (128) DeLand Florida 32720 —
Arthrosi Investigative Site (102) Hollywood Florida 33024 —
Arthrosi Investigative Site (156) Maitland Florida 32751 —
Arthrosi Investigative Site (103) Miami Florida 33176 —
Arthrosi Investigative Site (157) Palmetto Bay Florida 91355 —
Arthrosi Investigative Site (151) Winter Haven Florida 33880 —
Arthrosi Investigative Site (164) Atlanta Georgia 30329 —
Arthrosi Investigative Site (162) Lilburn Georgia 30047 —
Arthrosi Investigative Site (133) Boise Idaho 83713 —
Arthrosi Investigative Site (122) River Forest Illinois 48109 —
Arthrosi Investigative Site (154) Wichita Kansas 67207 —
Arthrosi Investigative Site (144) New Orleans Louisiana 70115 —
Arthrosi Investigative Site (150) Hagerstown Maryland 21740 —
Arthrosi Investigative Site (121) Ann Arbor Michigan 48109 —
Arthrosi Investigative Site (105) Detroit Michigan 48076 —
Arthrosi Investigative Site (153) Olive Branch Mississippi 38654-3514 —
Arthrosi Investigative Site (119) Kansas City Missouri 64151 —
Arthrosi Investigative Site (158) Brooklyn New York 11215 —
Arthrosi Investigative Site (137) Greensboro North Carolina 27410 —
Arthrosi Investigative Site (140) Shelby North Carolina 28150 —
Arthrosi Investigative Site (130) Wilmington North Carolina 28403 —
Arthrosi Investigative Site (148) Cleveland Ohio 44195 —
Arthrosi Investigative Site (146) Dayton Ohio 45429 —
Arthrosi Investigative Site (120) Hatboro Pennsylvania 19040 —
Arthrosi Investigative Site (147) Myrtle Beach South Carolina 29572 —
Arthrosi Investigative Site (132) Rapid City South Dakota 57702 —
Arthrosi Investigative Site (110) Amarillo Texas 79106 —
Arthrosi Investigative Site (104) Dallas Texas 75251 —
Arthrosi Investigative Site (116) Graham Texas 76450 —
Arthrosi Investigative Site (126) Lake Jackson Texas 77566 —
Arthrosi Investigative Site (136) Missouri City Texas 77459 —
Arthrosi Investigative Site (129) Plano Texas 75024 —
Arthrosi Investigative Site (127) Round Rock Texas 78681 —
Arthrosi Investigative Site (107) Tomball Texas 77375 —
Arthrosi Investigative Site (124) Tomball Texas 77377 —
Arthrosi Investigative Site (142) Bountiful Utah 98021 —
Arthrosi Investigative Site (145) Ogden Utah 84405 —
Arthrosi Investigative Site (111) Hampton Virginia 23666 —
Arthrosi Investigative Site (118) Hampton Virginia 23666 —
Arthrosi Investigative Site (134) Winchester Virginia 22601 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06439602, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 14, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06439602 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →