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Clinical Trial Summary

This research study wants to develop advanced imaging methods to more accurately characterize prostate cancer or solid tumor aggressiveness. This observational study involves [18F]DCFPyL positron emission tomography and magnetic resonance imaging (PET/MRI)


Clinical Trial Description

This is an observational imaging study to evaluate the value of multimodal [18F]DCFPyL positron emission tomography and magnetic resonance imaging (PET/MRI) for solid tumor characterization and disease staging. This research study involves: - Screening visit, and 1-3 study Multimodal [18F]DCFPyL PET/MRI visits - Two cohorts of participants will be enrolled in this study: primary prostate cancer patients and patients with known or suspected solid tumors (hepatocellular carcinoma, glioma, clear cell renal carcinoma) - It is expected that about 135 people will take part in this research study - The PET dye used in this study is called [18F]DCFPyL. [18F]DCFPyL is approved by the U.S. Food and Drug administration (FDA). - The PET/MRI scanner was approved by the U.S. FDA. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04687969
Study type Observational
Source Massachusetts General Hospital
Contact Ciprian Catana, MD, Ph.D
Phone 617-643-4885
Email ccatana@mgh.harvard.edu
Status Recruiting
Phase
Start date October 23, 2022
Completion date August 31, 2024

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