Expired Study
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Boston, Massachusetts 02114


Purpose:

Safety and dosimetry of BFPET™ will be evaluated in healthy volunteers and Coronary Artery Disease (CAD) patients , male or female and of age ranging between 20-80 years old.


Study summary:

Study Procedures: Visit 1: Screening - Eligibility determination Visit 2 (within 14 days post screening): Injection of BFPET™ and PET Imaging Visit 3 (within 24-48 hours post dose): Follow-up Visit


Criteria:

NORMAL HEALTHY VOLUNTEERS Inclusion Criteria 1. Subject must provide written informed consent prior to any study related procedures; 2. Subject must be ≥ 20 and ≤ 80 years of age; 3. Subject must have a serum creatinine within the investigational site's normal range. 4. Subject must have liver function tests < 1.5 times the investigational site's normal range. 5. Subject must have a hematocrit level within 5% of the investigational site's normal range. Exclusion Criteria: 1. Any clinically significant acute or unstable physical or psychological disease based on medical history or screening physical examination; 2. Any clinically significant abnormality in the screening laboratory tests or ECG; 3. Any exposure to any investigational drugs within four (4) weeks prior to Visit 1; 4. Any exposure to investigational radiopharmaceuticals within four (4) weeks prior to the date of Visit 1; 5. Any new prescription medications within four (4) weeks of Visit 1; 6. Subject has a Positive (+) Serum Pregnancy Test, or the possibility of pregnancy cannot be ruled out prior to dosing or is breast-feeding. There are standard pregnancy procedures for use of radiopharmaceuticals in research at MGH. 7. Subject has experienced any allergic reaction to similar radiofluorinated compounds or agents. CORONARY ARTERY DISEASE (CAD) SUBJECTS Inclusion Criteria: 1. Subjects must provide written informed consent prior to any study related procedures; 2. Subjects must be ≥ 20 and ≤ 80 years of age; 3. Subjects must have history of CAD documented by an abnormal stress myocardial perfusion imaging (MPI) study and cardiac catheterization within 6 months of the BFPET studyExclusion Criteria Exclusion Criteria: 1. Subject has a Positive (+) Serum and/or Urine Pregnancy Test or is lactating, or the possibility of pregnancy cannot be ruled out prior to dosing; 2. Any clinically significant acute or unstable physical or psychological disease judged by the investigators based on medical history or screening physical examination; 3. Coronary artery bypass graft (CABG) within 6 months; 4. Percutaneous coronary intervention (PCI), with stent placement within six months; 5. Blood pressure over 180/100; 6. Acute changes in ECG; 7. Recent (within 3 months) cardiac arrest, unstable angina, myocardial infarction, cerebro-vascular accident (CVA), any general anesthesia procedure, any surgical procedures; 8. Any implanted pacemaker or defibrillator use within the last three months; 9. Inability to remain in camera for approximately 60 minutes (Smokers and COPD are included as long as they can breath in PET camera and not taking O2 through nasal canula); 10. History of Diabetes Mellitus; 11. Serum creatinine > 2 mg/dL; 12. All cancer patients; 13. Body Mass Index (BMI) is over 35; 14. Any exposure to any investigational drugs or medical device within four (4) weeks prior to imaging study; 15. Any exposure to radiopharmaceuticals within four (4) weeks prior to the date of imaging study;


NCT ID:

NCT00733460


Primary Contact:

Principal Investigator
Henry Gewirtz, M.D.
Massachusetts General Hospital


Backup Contact:

N/A


Location Contact:

Boston, Massachusetts 02114
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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