Viewing Study NCT00162071



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Last Modification Date: 2024-10-26 @ 9:15 AM
Study NCT ID: NCT00162071
Status: TERMINATED
Last Update Posted: 2017-02-01
First Post: 2005-09-09

Brief Title: A Phase II Optimization Study of BMS068645 and Sestamibi Planar Imaging
Sponsor: Forest Laboratories
Organization: Forest Laboratories

Study Overview

Official Title: A Phase II Open-Label Non-Randomized Single-Center Trial to Determine the Optimal Myocardial Perfusion Image Acquisition Time Following BMS068645 Administration
Status: TERMINATED
Status Verified Date: 2017-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Sponsor decided not to continue with the development program
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None