Clinical Trials Directory

Trials / Completed

CompletedNCT01493531

Combining Lesinurad With Allopurinol in Inadequate Responders

A Phase 3 Randomized, Double-Blind, Multicenter, Placebo- Controlled, Combination Study to Evaluate the Efficacy and Safety of Lesinurad and Allopurinol Compared to Allopurinol Alone in Subjects With Gout Who Have Had an Inadequate Hypouricemic Response to Standard of Care Allopurinol

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
610 (actual)
Sponsor
Ardea Biosciences, Inc. · Industry
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

This study will compare the serum uric acid lowering effects, clinical benefits, and safety of lesinurad in combination with allopurinol to allopurinol alone in subjects with gout who have had an inadequate response to allopurinol.

Detailed description

Allopurinol is the standard of care for the treatment of gout. Nevertheless, most patients treated with allopurinol do not achieve the recommended sUA target of \< 6.0 mg/dL and need additional therapy to achieve the target. Probenecid and benzbromarone are URAT1 inhibitors, generally recommended as second-line agents for patients who are either resistant to or intolerant of allopurinol. However, benzbromarone is not available in the US and probenecid is rarely used. Consequently, there is a clear unmet medical need for a new safe and effective therapy for gout, such as lesinurad, a potent URAT1 inhibitor, that can be used in combination with allopurinol in patients not responding adequately to allopurinol monotherapy so that very high rates of response can be achieved by nearly all gout patients, rather than a minority.The subjects selected for this study will have moderate to severe gout with an inadequate response to allopurinol

Conditions

Interventions

TypeNameDescription
DRUGLesinuradTablets, 200 mg QD
DRUGLesinuradTablets, 400 mg QD
DRUGPlaceboTablets, Placebo QD
DRUGAllopurinolTablets

Timeline

Start date
2011-12-01
Primary completion
2014-05-01
Completion
2014-07-01
First posted
2011-12-16
Last updated
2016-05-26
Results posted
2016-05-26

Locations

175 sites across 11 countries: United States, Australia, Belgium, Canada, Germany, New Zealand, Poland, South Africa, Spain, Switzerland, Ukraine

Source: ClinicalTrials.gov record NCT01493531. Inclusion in this directory is not an endorsement.