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NCT00162071 · ClinicalTrials.gov registry record · Phase 2

A Phase II Optimization Study of BMS068645 and Sestamibi Planar Imaging

A Phase 2 study, sponsored by Forest Laboratories.

Terminated
Registry status
Phase 2
Development phase
20
Enrollment target

NCT00162071: Clinical Trial Phase 2 study, sponsored by Forest Laboratories.

NCT00162071 is a Phase 2 study that was terminated before completion, run by Forest Laboratories. The registered enrollment target is 20 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00162071, a Phase 2 study, was terminated before completion, sponsored by Forest Laboratories.

TERMINATED
Registry status
Phase 2
Development phase
20 participants
Enrollment target

Study Summary

The primary purpose of this study is to determine the optimal time for myocardial perfusion imaging with Technetium Tc99m Sestamibi following the administration of BMS068645. The safety of BMS068645 will also be studied.

Interventions

  • DRUG apadenoson

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2005-07
Phase Phase 2
Forest Laboratories

145 total trials

Why NCT00162071 stopped before completion

NCT00162071 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower).

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

NCT00162071 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00162071 about?

NCT00162071 is a clinical study titled "A Phase II Optimization Study of BMS068645 and Sestamibi Planar Imaging". The primary purpose of this study is to determine the optimal time for myocardial perfusion imaging with Technetium Tc99m Sestamibi following the administration of BMS068645. The safety of BMS068645 will also be studied.

What is the current status of trial NCT00162071?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2005-07.

What interventions are being tested in trial NCT00162071?

The interventions under investigation include: apadenoson (DRUG).

Who is sponsoring clinical trial NCT00162071?

This trial is sponsored by Forest Laboratories, which has 145 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00162071's enrollment target sits among peer trials

20 1805th of 2000 higher than 107 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 NCT00162071, the US trial registry maintained by the National Library of Medicine. NCT00162071 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.