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NCT00849108 · ClinicalTrials.gov registry record · Phase 2

Development of 1-Day Rest/Stress Cardiac PET Perfusion Imaging Protocol of BMS747158

A Phase 2 study, sponsored by Lantheus Medical Imaging.

Completed
Registry status
Phase 2
Development phase
176
Enrollment target

NCT00849108: Completed Phase 2 study, sponsored by Lantheus Medical Imaging.

NCT00849108 is a Phase 2 study that has completed, run by Lantheus Medical Imaging. The registered enrollment target is 176 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (32% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00849108, a Phase 2 study, has completed, sponsored by Lantheus Medical Imaging.

COMPLETED
Registry status
Phase 2
Development phase
176 participants
Enrollment target

Study Summary

The main purpose of this study is to get more information on using BMS747158 (the study drug),a drug with small amounts of radioactivity to allow for heart imaging, during a PET scan which can then be compared to other images such as SPECT. The safety and quality of images will be studied.

Primary Outcome

The rest flurpiridaz dose to be used for subsequent efficacy studies was determined by a modeling method that simulated a range of injected doses using a single fixed injected dose at rest in each subject and a range of acquisition durations. From this, a dose acquisition time product (DATP was determined for each subject that specified the minimal dose for a given acquisition duration that yielded an image in that subject that was negligibly affected by photon counting statistics. Descriptive s

Interventions

  • DRUG BMS747158

Trial Details

FieldValue
Enrollment Target 176 participants
Start Date 2009-01
Est. Completion 2010-06
Phase Phase 2
Lantheus Medical Imaging

22 total trials

What the finished NCT00849108 record still lists

NCT00849108 is an interventional study that assigns participants to a tested intervention. The registered 176 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 (32% higher).

The record links to 0 conditions, and to 1 intervention - of which BMS747158 is the first listed.

NCT00849108 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00849108 about?

NCT00849108 is a clinical study titled "Development of 1-Day Rest/Stress Cardiac PET Perfusion Imaging Protocol of BMS747158". The main purpose of this study is to get more information on using BMS747158 (the study drug),a drug with small amounts of radioactivity to allow for heart imaging, during a PET scan which can then be compared to other images such as SPECT. The safety and quality of images will be studied.

What is the current status of trial NCT00849108?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 176 participants. The study started on 2009-01. Estimated completion is 2010-06.

What interventions are being tested in trial NCT00849108?

The interventions under investigation include: BMS747158 (DRUG).

Who is sponsoring clinical trial NCT00849108?

This trial is sponsored by Lantheus Medical Imaging, which has 22 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00849108's enrollment target sits among peer trials

176 394th of 2000 higher than 1,605 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 NCT00849108, the US trial registry maintained by the National Library of Medicine. NCT00849108 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.