drugset / Trial / NCT04804111

Study of of URC102 to Assess the Efficacy and Safety in Gout Patients

NCT04804111

Phase 2 Completed 171 enrolled JW Pharmaceutical
RandomizedParallel-groupDouble-blindTreatment

Summary

To confirm the safety and efficacy (dose response and optimal dose according to the serum uric acid response rate) of URC102 when orally-administered to patients with gout and gout-related hyperuricemia in comparison with placebo. Therapeutic dose-finding study, Placebo-controlled, randomized, double-blind, multicenter, phase 2 clinical trial.

Timeline

Start
2019-01-21
Primary completion
2020-09-04
Completion
2020-11-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Febuxostat Small molecule 80 mg
Subject URC102 Unknown 3 mg Oral
Subject URC102 Unknown 6 mg Oral
Subject URC102 Unknown 9 mg Oral

Indications