drugset / Trial / NCT01508702

Lesinurad Monotherapy in Gout Subjects Intolerant to Xanthine Oxidase Inhibitors

NCT01508702

Phase 3 Completed 214 enrolled Ardea Biosciences, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

This study will assess the serum uric acid lowering effects and safety of lesinurad compared to placebo in patients who are intolerant or have a contraindication to allopurinol or febuxostat.

Timeline

Start
2012-01
Primary completion
2013-10
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Lesinurad Small molecule 400 mg Oral

Indications