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Completed Phase 2 Interventional Results available

Safety and Efficacy Iodofiltic Acid I 123 in the Treatment of Acute Coronary Syndrome

ClinicalTrials.gov ID: NCT00514501

Public ClinicalTrials.gov record NCT00514501. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:16 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Open-label, Phase 2 Study of the Safety and Efficacy of B-methyl-P-(123I)- Iodophenyl-pentadecanoic Acid (Iodofiltic Acid I 123) For Identification of Ischemic Myocardium Using Single Photon Emission Computed Tomography (Spect) in Adults With Symptoms Consistent With Acute Coronary Syndrome (ACS).

Study identification

NCT ID
NCT00514501
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Molecular Insight Pharmaceuticals, Inc.
Industry
Enrollment
510 participants

Conditions and interventions

Interventions

  • Iodofiltic acid I 123 Drug

Drug

Eligibility (public fields only)

Age range
40 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2007
Primary completion
May 31, 2008
Completion
Nov 30, 2008
Last update posted
Mar 30, 2016

2007 – 2008

United States locations

U.S. sites
36
U.S. states
20
U.S. cities
36
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Huntsville Alabama
Not listed Mesa Arizona
Not listed Los Angeles California
Not listed Mission Viejo California
Not listed Newport Beach California
Not listed Roseville California 95661
Not listed Hartford Connecticut
Not listed New Haven Connecticut
Not listed Newark Delaware
Not listed Jacksonville Florida
Not listed Aurora Illinois
Not listed Maywood Illinois
Not listed Louisville Kentucky 40207
Not listed Auburn Maine
Not listed Bethesda Maryland
Not listed Detroit Michigan
Not listed Royal Oak Michigan
Not listed Troy Michigan 48085
Not listed Minneapolis Minnesota
Not listed Kansas City Missouri 64111
Not listed Lebanon New Hampshire
Not listed Manchester New Hampshire
Not listed Albany New York
Not listed Brooklyn New York
Not listed Kingston New York
Not listed New York New York
Not listed Rochester New York
Not listed Syracuse New York 13210
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Providence Rhode Island
Not listed Houston Texas
Not listed Richmond Virginia
Not listed Madison Wisconsin

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00514501, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 30, 2016 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00514501 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →