18F-AmBF3-TATE PET/CT for Imaging NET Patients

CompletedOBSERVATIONAL
Enrollment

10

Participants

Timeline

Start Date

June 9, 2020

Primary Completion Date

September 21, 2020

Study Completion Date

January 15, 2021

Conditions
Neuroendocrine Tumors
Interventions
DIAGNOSTIC_TEST

18F-AmBF3-TATE PET/CT

Blood pressure, heart rate, and oxygen saturation levels and EKG monitoring (vital signs) will be recorded prior to the injection and at three other stages of the scan visit. Each study subject will have an intravenous catheter inserted. Prior to the radiotracer injection an ultra low dose CT will be taken. Subjects are positioned supine, arms down. The subject will receive a bolus intravenous dose of the radiotracer from an approved study supplier site. A Dynamic PET scan will be taken of the heart. Then a serial whole body PET scan will be done. Vital signs will be taken again and the subject will have a bathroom break. The patient will return to the scanner bed for a standard low dose CT and whole body PET scan. Vital signs will be taken again, and subject will be allowed to use the washroom again. The subject will return to the scanner bed for the final time for an ultra low dose CT and whole body PET scan. A final set of vitals will be taken and the subject will be discharged.

DIAGNOSTIC_TEST

Routine blood draw

Complete blood counts and routine clinical chemistry performed before and repeated within 18-72 hours after \[18F\]AmBF3-TATE administration.

Trial Locations (1)

V5Z 4E6

BC Cancer, Vancouver

All Listed Sponsors
lead

British Columbia Cancer Agency

OTHER

NCT04207762 - 18F-AmBF3-TATE PET/CT for Imaging NET Patients | Biotech Hunter | Biotech Hunter