Prostate Cancer Monitoring Using [18F]DCFPyL and Blood Based Biomarkers

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

11

Participants

Timeline

Start Date

December 11, 2018

Primary Completion Date

December 31, 2022

Study Completion Date

December 31, 2022

Conditions
Metastatic Prostate Cancer
Interventions
DRUG

[F-18] DCFPyL

\[18F\]DCFPyL will be used for study imaging. It will be administered intravenously on the day of imaging. Subjects will receive a bolus injection of 9mCi (331 MBq) of \[18F\]DCFPyL through a peripheral IV catheter. 60 to 120 minutes after injection, a whole body (toes to vertex) lowdose CT will be obtained (120 kVp, 80 mA maximum).

PROCEDURE

PET/CT imaging

As per standard of care, acquisition will be performed on PET/CT scanner (Siemens, Germany) operating in 3D emission mode with CT-derived attenuation correction.

Trial Locations (1)

10032

Columbia University Irving Medical Center, New York

All Listed Sponsors
lead

Columbia University

OTHER

NCT03585114 - Prostate Cancer Monitoring Using [18F]DCFPyL and Blood Based Biomarkers | Biotech Hunter | Biotech Hunter