18F-MFBG Imaging for Evaluation of Neuroendocrine Malignancies

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

January 31, 2015

Primary Completion Date

March 17, 2025

Study Completion Date

March 17, 2025

Conditions
Neuroendocrine Tumors
Interventions
RADIATION

18F-MFBG (meta-fluoro benzylguanidine)

About 8mCi of 18F-MFBG will be administered to adult patients. Pediatric dose will be based upon adjustment using BSA to the dose of 8 mCi for 1.7m2 BSA ± 10% with maximum activity of 8 mCi. The tracer will be given intravenously.

DEVICE

Positron emission tomography (PET) imaging

Dynamic imaging for the first 30 min over the chest and Whole body (WB) PET-CT scan. Imaging 2 (\~1.0 - 2 hours post dose): Whole body (vertex to feet) PET-CT scan. Imaging 3 (\~3-4 hours post dose): Whole body (vertex to feet) PET-CT scan.

OTHER

Blood draws

Blood samples to be collected: at baseline, 5, 15, 30, 60, 90, 120 and 180 mins post injection on the day of administration. (Phase I only)

Trial Locations (1)

10065

Memorial Sloan Kettering Cancer Center, New York

All Listed Sponsors
lead

Memorial Sloan Kettering Cancer Center

OTHER

NCT02348749 - 18F-MFBG Imaging for Evaluation of Neuroendocrine Malignancies | Biotech Hunter | Biotech Hunter