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NCT01265264 · ClinicalTrials.gov registry record · Phase 2
Study to Evaluate sUA Lowering Activity, Safety and Efficacy of Oral Ulodesine Added to Allopurinol
A Phase 2 study, sponsored by BioCryst Pharmaceuticals.
- Completed
- Registry status
- Phase 2
- Development phase
- 279
- Enrollment target
NCT01265264: Completed Phase 2 study, sponsored by BioCryst Pharmaceuticals.
NCT01265264 is a Phase 2 study that has completed, run by BioCryst Pharmaceuticals. The registered enrollment target is 279 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (110% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01265264, a Phase 2 study, has completed, sponsored by BioCryst Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 279 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether ulodesine and allopurinol combined for 12 weeks are effective in treating gout in patients who are not adequately responding to allopurinol alone.
Primary Outcome
Level of serum uric acid levels be measured at Day 85 to evaluate in subjects with Gout.
Interventions
- DRUG Placebo
- DRUG ulodesine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 279 participants |
| Start Date | 2010-12 |
| Est. Completion | 2013-02 |
| Phase | Phase 2 |
What the finished NCT01265264 record still lists
NCT01265264 is an interventional study that assigns participants to a tested intervention. The registered 279 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (110% higher).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT01265264 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01265264 about?
NCT01265264 is a clinical study titled "Study to Evaluate sUA Lowering Activity, Safety and Efficacy of Oral Ulodesine Added to Allopurinol". The purpose of this study is to determine whether ulodesine and allopurinol combined for 12 weeks are effective in treating gout in patients who are not adequately responding to allopurinol alone.
What is the current status of trial NCT01265264?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 279 participants. The study started on 2010-12. Estimated completion is 2013-02.
What interventions are being tested in trial NCT01265264?
The interventions under investigation include: Placebo (DRUG), ulodesine (DRUG).
Who is sponsoring clinical trial NCT01265264?
This trial is sponsored by BioCryst Pharmaceuticals, which has 29 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01265264's enrollment target sits among peer trials
279 201st of 2000 higher than 1,799 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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