Phase 2 to Assess Efficacy and Safety in AR882 Alone or in Combination With Allopurinol in Patients With Tophaceous Gout

PHASE2CompletedINTERVENTIONAL
Enrollment

42

Participants

Timeline

Start Date

August 12, 2022

Primary Completion Date

August 13, 2024

Study Completion Date

October 28, 2024

Conditions
GoutArthritis, GoutyHyperuricemiaGout Chronic
Interventions
DRUG

AR882 Dose 1

Solid Oral Capsule

DRUG

AR882 Dose 2

Solid Oral Capsule

DRUG

Allopurinol Tablet

Solid tablet

Trial Locations (12)

402

Arthrosi Investigative Site (303), Taichung

1023

Arthrosi Investigative Site (201), Auckland

27410

Arthrosi Investigative Site (406), Greensboro

29577

Arthrosi Investigative Site (408), Myrtle Beach

33606

Arthrosi Investigative Site (402), Tampa

35233

Arthrosi Investigative Site (410), Birmingham

48109

Arthrosi Investigative Site (409), Ann Arbor

75231

Arthrosi Investigative Site (401), Dallas

83713

Arthrosi Investigative Site (404), Boise

85032

Arthrosi Investigative Site (403), Phoenix

85351

Arthrosi Investigative Site (416), Sun City

85704

Arthrosi Investigative Site (417), Tucson

Sponsors
All Listed Sponsors
lead

Arthrosi Therapeutics

INDUSTRY