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NCT01508702 · ClinicalTrials.gov registry record · Phase 3
Lesinurad Monotherapy in Gout Subjects Intolerant to Xanthine Oxidase Inhibitors
A Phase 3 study, sponsored by Ardea Biosciences.
- Completed
- Registry status
- Phase 3
- Development phase
- 214
- Enrollment target
NCT01508702: Completed Phase 3 study, sponsored by Ardea Biosciences.
NCT01508702 is a Phase 3 study that has completed, run by Ardea Biosciences. The registered enrollment target is 214 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01508702, a Phase 3 study, has completed, sponsored by Ardea Biosciences.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 214 participants
- Enrollment target
Study 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.
Interventions
- DRUG Placebo
- DRUG lesinurad
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 214 participants |
| Start Date | 2012-01 |
| Est. Completion | 2013-11 |
| Phase | Phase 3 |
What the finished NCT01508702 record still lists
NCT01508702 is an interventional study that assigns participants to a tested intervention. The registered 214 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (72% lower).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT01508702 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01508702 about?
NCT01508702 is a clinical study titled "Lesinurad Monotherapy in Gout Subjects Intolerant to Xanthine Oxidase Inhibitors". 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.
What is the current status of trial NCT01508702?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 214 participants. The study started on 2012-01. Estimated completion is 2013-11.
What interventions are being tested in trial NCT01508702?
The interventions under investigation include: Placebo (DRUG), lesinurad (DRUG).
Who is sponsoring clinical trial NCT01508702?
This trial is sponsored by Ardea Biosciences, which has 32 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01508702's enrollment target sits among peer trials
214 1335th of 2000 higher than 666 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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