Status:
UNKNOWN
BFPET for Regional Myocardial Perfusion Imaging
Lead Sponsor:
Fluoropharma, Inc.
Conditions:
Coronary Artery Disease
Eligibility:
All Genders
21-85 years
Phase:
PHASE2
Brief Summary
BFPET will be evaluated as a diagnostic PET agent for assessing myocardial perfusion in subjects with known or suspected coronary artery disease (CAD) as compared to standard nuclear myocardial perfus...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- Subjects must provide written informed consent prior to any study related procedures;
- Subjects must be ≥ 21 and ≤ 85 years of age;
- Subjects must have known or suspected CAD documented by ≥2 segments of reversible perfusion abnormalities on a SPECT (MPI)study
- Exclusion Criteria
- Any clinically significant acute or unstable physical or psychological disease judged by the investigators based on medical history or screening physical examination;
- Blood pressure over 180/100mmHg
- Acute changes in comparison to most recent ECG;
- Recent (within 3 months) cardiac arrest, unstable angina, cerebro-vascular accident (CVA), CABG or PCI
- Any pacemaker or defibrillator implanted within the last three months;
- Inability to remain in camera for approximately 60 minutes
- Bronchospasm
- Serum creatinine \> 2 mg/dL;
- Cancer patients who have received chemotherapy or radiation therapy within the past 60 days.
- Any exposure to any investigational drug(s) or medical device(s) within four (4) weeks prior to imaging study;
- Any physical or psychological disease judged by the investigators to be incompatible with the study, based on medical history or screening physical examination.
- NYHA Class III or IV Congestive heart failure;
- Subject has symptomatic hypotension
- Allergic or intolerant to aminophylline, nitroglycerin or metoprolol
- Allergic or intolerant to regadenoson or any of its excipients
- Prior participants in the study.
- Female subjects only: Positive serum and/or urine pregnancy test or is lactating or the possibility of pregnancy cannot be ruled out prior to dosing.
- Females not of child-bearing potential require confirmatory documentation in their medical records or must have a negative pregnancy test within 4 hours prior to receiving the test drug and agree to use an acceptable form of birth control for at least 30 days following BFPET administration.
Exclusion
Key Trial Info
Start Date :
October 1 2018
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 30 2019
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT02252783
Start Date
October 1 2018
End Date
September 30 2019
Last Update
August 1 2018
Active Locations (1)
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1
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114