Safety and Efficacy Iodofiltic Acid I 123 in the Treatment of Acute Coronary Syndrome
Summary
The lay summary the sponsor registered on ClinicalTrials.gov.
Investigators
The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.
- Norman LaFrance, MD
Molecular Insight Pharmaceuticals, Inc.
Study Director
A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.
Sites
38 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.
- Facility name not stated
North Vancouver, British Columbia, Canada
- Facility name not stated
Scarborough Village, Ontario, Canada
- Facility name not stated
Birmingham, Alabama, United States
- Facility name not stated
Huntsville, Alabama, United States
- Facility name not stated
Mesa, Arizona, United States
- Facility name not stated
Los Angeles, California, United States
- Facility name not stated
Mission Viejo, California, United States
- Facility name not stated
Newport Beach, California, United States
- Facility name not stated
Roseville, California, United States
- Facility name not stated
Hartford, Connecticut, United States
- Facility name not stated
New Haven, Connecticut, United States
- Facility name not stated
Newark, Delaware, United States
- Facility name not stated
Jacksonville, Florida, United States
- Facility name not stated
Aurora, Illinois, United States
- Facility name not stated
Maywood, Illinois, United States
- Facility name not stated
Louisville, Kentucky, United States
- Facility name not stated
Auburn, Maine, United States
- Facility name not stated
Bethesda, Maryland, United States
- Facility name not stated
Detroit, Michigan, United States
- Facility name not stated
Royal Oak, Michigan, United States
- Facility name not stated
Troy, Michigan, United States
- Facility name not stated
Minneapolis, Minnesota, United States
- Facility name not stated
Kansas City, Missouri, United States
- Facility name not stated
Lebanon, New Hampshire, United States
- Facility name not stated
Manchester, New Hampshire, United States
- Facility name not stated
Albany, New York, United States
- Facility name not stated
Brooklyn, New York, United States
- Facility name not stated
Kingston, New York, United States
- Facility name not stated
New York, New York, United States
- Facility name not stated
Rochester, New York, United States
- Facility name not stated
Syracuse, New York, United States
- Facility name not stated
Cincinnati, Ohio, United States
- Facility name not stated
Cleveland, Ohio, United States
- Facility name not stated
Columbus, Ohio, United States
- Facility name not stated
Providence, Rhode Island, United States
- Facility name not stated
Houston, Texas, United States
- Facility name not stated
Richmond, Virginia, United States
- Facility name not stated
Madison, Wisconsin, United States
Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.
Drugs studied
The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.
Registration & key dates
Registry attributes as recorded on the ClinicalTrials.gov study record.
- Start
- 31 May 2007
- Primary completion
- 30 Jun 2008
- Completion
- 31 Dec 2008
- Last update posted
- 31 Mar 2016
- Registered enrollment
- 510
- Registry id
- NCT00514501
Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 11 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.