CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 143 enrolled
Drug / intervention
lesinuraddrug
Likely dose
lesinurad 400 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01650246
NCT01650246Phase 3Completed

A Long-Term Open-Label Extension Study for Subjects Completing a Phase 3 Efficacy and Safety Study of Lesinurad Monotherapy in Subjects With Gout

Ardea Biosciences, Inc.·interventional·Posted Jul 26, 2012·Updated May 26, 2016

In Brief

A Phase 3 clinical trial evaluating lesinurad for Gout. Completed, enrolled 143 participants across 75 sites in 7 countries.

Detailed Summary

This study will assess the serum uric acid lowering effects and safety of lesinurad over a long-term timeframe.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsGout
CountriesAustralia, Belgium, Canada, Germany, New Zealand, South Africa, United States
Collaborators--

Timeline

Phase 3CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJul 26, 2012
Enrollment StartAug 1, 2012
Primary CompletionApr 1, 2014
Study CompletionAug 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1.7 yearsPosted 13.9 years ago

Interventions

lesinuraddrug

Tablets, 400 mg QD