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NCT00080210 · ClinicalTrials.gov registry record · Phase 2
A Study of Persons With Gout Who Do Not Respond to or Are Allergic to Conventional Therapy
A Phase 2 study, sponsored by Savient Pharmaceuticals.
- Completed
- Registry status
- Phase 2
- Development phase
- 40
- Enrollment target
NCT00080210: Completed Phase 2 study, sponsored by Savient Pharmaceuticals.
NCT00080210 is a Phase 2 study that has completed, run by Savient Pharmaceuticals. The registered enrollment target is 40 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00080210, a Phase 2 study, has completed, sponsored by Savient Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 40 participants
- Enrollment target
Study Summary
This is a randomized, open-label, multicenter, parallel-groups study of multiple intravenous doses of Puricase, administered intravenously, in 40 patients with symptomatic gout. Subjects must wash out of any uric acid-lowering agents for one week before being dosed, and must refrain from using such agents throughout the study.
Interventions
- DRUG Puricase
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2004-03 |
| Est. Completion | 2005-02 |
| Phase | Phase 2 |
What the finished NCT00080210 record still lists
NCT00080210 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower).
The record links to 0 conditions, and to 1 intervention - of which Puricase is the first listed.
NCT00080210 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00080210 about?
NCT00080210 is a clinical study titled "A Study of Persons With Gout Who Do Not Respond to or Are Allergic to Conventional Therapy". This is a randomized, open-label, multicenter, parallel-groups study of multiple intravenous doses of Puricase, administered intravenously, in 40 patients with symptomatic gout. Subjects must wash out of any uric acid-lowering agents for one week before being dosed, and must refrain from using such ...
What is the current status of trial NCT00080210?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2004-03. Estimated completion is 2005-02.
What interventions are being tested in trial NCT00080210?
The interventions under investigation include: Puricase (DRUG).
Who is sponsoring clinical trial NCT00080210?
This trial is sponsored by Savient Pharmaceuticals, which has 5 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00080210's enrollment target sits among peer trials
40 1362nd of 2000 higher than 542 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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