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NCT00111657 · ClinicalTrials.gov registry record · Phase 2

Pegylated Recombinant Mammalian Uricase (PEG-uricase) as Treatment for Refractory Gout

A Phase 2 study, sponsored by John Sundy.

Completed
Registry status
Phase 2
Development phase
30
Enrollment target

NCT00111657: Completed Phase 2 study, sponsored by John Sundy.

NCT00111657 is a Phase 2 study that has completed, run by John Sundy. The registered enrollment target is 30 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00111657, a Phase 2 study, has completed, sponsored by John Sundy.

COMPLETED
Registry status
Phase 2
Development phase
30 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether PEG-uricase (a chemically modified recombinant mammalian enzyme that degrades uric acid) is effective in controlling hyperuricemia in patients with chronic gout, who cannot tolerate, or have not responded adequately, to conventional therapy for gout. Funding Source - FDA OOPD

Interventions

  • BIOLOGICAL Pegloticase

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2004-12
Est. Completion 2009-07
Phase Phase 2
John Sundy

6 total trials

What the finished NCT00111657 record still lists

NCT00111657 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 1 intervention - of which Pegloticase is the first listed.

NCT00111657 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00111657 about?

NCT00111657 is a clinical study titled "Pegylated Recombinant Mammalian Uricase (PEG-uricase) as Treatment for Refractory Gout". The purpose of this study is to determine whether PEG-uricase (a chemically modified recombinant mammalian enzyme that degrades uric acid) is effective in controlling hyperuricemia in patients with chronic gout, who cannot tolerate, or have not responded adequately, to conventional therapy for gout....

What is the current status of trial NCT00111657?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2004-12. Estimated completion is 2009-07.

What interventions are being tested in trial NCT00111657?

The interventions under investigation include: Pegloticase (BIOLOGICAL).

Who is sponsoring clinical trial NCT00111657?

This trial is sponsored by John Sundy, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00111657's enrollment target sits among peer trials

30 1582nd of 2000 higher than 332 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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Source: ClinicalTrials.gov NCT00111657, the US trial registry maintained by the National Library of Medicine. NCT00111657 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.