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
| Type | Name | Description |
|---|---|---|
| DRUG | Lesinurad | Tablets, 200 mg QD |
| DRUG | Lesinurad | Tablets, 400 mg QD |
| DRUG | Placebo | Tablets, Placebo QD |
| DRUG | Allopurinol | Tablets |
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.