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NCT00137332 · ClinicalTrials.gov registry record · Phase 2

Study Evaluating GAP-486 on Heart Rhythm in Patients With Coronary Artery Disease

A Phase 2 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

Terminated
Registry status
Phase 2
Development phase
90
Enrollment target

NCT00137332: Clinical Trial Phase 2 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

NCT00137332 is a Phase 2 study that was terminated before completion, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 90 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (32% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00137332, a Phase 2 study, was terminated before completion, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

TERMINATED
Registry status
Phase 2
Development phase
90 participants
Enrollment target

Study Summary

The purpose of this study is to learn the effects of a test drug on heart rhythms, which may become life-threatening if left untreated, and to provide data to see if the drug is well tolerated and safe.

Interventions

  • DRUG GAP-486 (ZP-123)
  • DRUG 0.9% Sodium Chloride, USP

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2005-11
Est. Completion 2006-10
Phase Phase 2

Why NCT00137332 stopped before completion

NCT00137332 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (32% lower).

The record links to 0 conditions, and to 2 interventions - of which GAP-486 (ZP-123) is the first listed.

NCT00137332 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00137332 about?

NCT00137332 is a clinical study titled "Study Evaluating GAP-486 on Heart Rhythm in Patients With Coronary Artery Disease". The purpose of this study is to learn the effects of a test drug on heart rhythms, which may become life-threatening if left untreated, and to provide data to see if the drug is well tolerated and safe.

What is the current status of trial NCT00137332?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 90 participants. The study started on 2005-11. Estimated completion is 2006-10.

What interventions are being tested in trial NCT00137332?

The interventions under investigation include: GAP-486 (ZP-123) (DRUG), 0.9% Sodium Chloride, USP (DRUG).

Who is sponsoring clinical trial NCT00137332?

This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00137332's enrollment target sits among peer trials

90 772nd of 2000 higher than 1,199 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 NCT00137332, the US trial registry maintained by the National Library of Medicine. NCT00137332 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.