Al18F-NOTA-octreotide PET Imaging in Neuroendocrine Tumors

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

85

Participants

Timeline

Start Date

October 7, 2020

Primary Completion Date

February 8, 2022

Study Completion Date

February 8, 2022

Conditions
Neuroendocrine Tumors
Interventions
DRUG

Al18F-NOTA-octreotide

One intravenous injection of 4 MBq/kg

DEVICE

PET/CT

Patients in part A of the trial will undergo a whole-body PET/CT scan 120 minutes (acceptable range: 105 - 240 minutes) after injection of the tracer. The CT-scan is a low-dose CT that will be acquired for both PET attenuation correction and anatomical information.

DEVICE

PET/MR

Patients in part B of the trial will undergo a whole-body PET/MR scan 120 minutes (acceptable range: 105 - 240 minutes) after injection of the tracer. The MR scan is a fully diagnostic MR requiring intravenous contrast (Dotarem®) injection and Buscopan® administration to minimize bowel movement.

Trial Locations (1)

3000

Universitaire Ziekenhuizen Leuven, Leuven

All Listed Sponsors
collaborator

University Hospital, Antwerp

OTHER

collaborator

University Hospital, Ghent

OTHER

collaborator

NETwerk, Belgium

UNKNOWN

lead

Universitaire Ziekenhuizen KU Leuven

OTHER

NCT04552847 - Al18F-NOTA-octreotide PET Imaging in Neuroendocrine Tumors | Biotech Hunter | Biotech Hunter