RECRUITING

A Study of Dotinurad Versus Allopurinol in Tophaceous Gout

Description

The primary objective of this study is to evaluate the efficacy of dotinurad in lowering serum uric acid (sUA) at Week 24 compared with allopurinol in adult participants with tophaceous gout.

Conditions

Study Overview

Study Details

Study overview

The primary objective of this study is to evaluate the efficacy of dotinurad in lowering serum uric acid (sUA) at Week 24 compared with allopurinol in adult participants with tophaceous gout.

A Phase 3, Randomized, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Dotinurad Compared With Allopurinol in Adult Participants With Tophaceous Gout

A Study of Dotinurad Versus Allopurinol in Tophaceous Gout

Condition
Tophaceous Gout
Intervention / Treatment

-

Contacts and Locations

Houston

Pioneeer Research Solutions, Houston, Texas, United States, 77099

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

    Ages Eligible for Study

    18 Years to 75 Years

    Sexes Eligible for Study

    ALL

    Accepts Healthy Volunteers

    No

    Collaborators and Investigators

    Crystalys Therapeutics,

    Study Record Dates

    2027-10