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NCT00124891 · ClinicalTrials.gov registry record · Phase 2

Study Evaluating GAP-486 in Non-sustained Ventricular Tachycardia

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

Terminated
Registry status
Phase 2
Development phase
500
Enrollment target

NCT00124891: Clinical Trial Phase 2 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

NCT00124891 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 500 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (276% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00124891, 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
500 participants
Enrollment target

Study Summary

To determine whether the administration of test article will decrease the occurrence of ventricular arrhythmias in patients who have acute coronary syndrome (unstable angina, ST segment elevated myocardial infarction or myocardial infarction without ST elevation).

Interventions

  • DRUG Double-blind investigational anti-arrhythmic
  • DRUG GAP-486

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2005-06-01
Est. Completion 2006-11-01
Phase Phase 2

Why NCT00124891 stopped before completion

NCT00124891 is an interventional study that assigns participants to a tested intervention. The registered 500 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 (276% higher).

The record links to 0 conditions, and to 2 interventions - of which Double-blind investigational anti-arrhythmic is the first listed.

NCT00124891 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00124891 about?

NCT00124891 is a clinical study titled "Study Evaluating GAP-486 in Non-sustained Ventricular Tachycardia". To determine whether the administration of test article will decrease the occurrence of ventricular arrhythmias in patients who have acute coronary syndrome (unstable angina, ST segment elevated myocardial infarction or myocardial infarction without ST elevation).

What is the current status of trial NCT00124891?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 500 participants. The study started on 2005-06-01. Estimated completion is 2006-11-01.

What interventions are being tested in trial NCT00124891?

The interventions under investigation include: Double-blind investigational anti-arrhythmic (DRUG), GAP-486 (DRUG).

Who is sponsoring clinical trial NCT00124891?

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 NCT00124891's enrollment target sits among peer trials

500 70th of 2000 higher than 1,927 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 NCT00124891, the US trial registry maintained by the National Library of Medicine. NCT00124891 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.