drugset / Trial / NCT04804111
Study of of URC102 to Assess the Efficacy and Safety in Gout Patients
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Febuxostat | Small molecule | 80 mg | — |
| Subject | URC102 | Unknown | 3 mg | Oral |
| Subject | URC102 | Unknown | 6 mg | Oral |
| Subject | URC102 | Unknown | 9 mg | Oral |