Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Adenocarcinoma of Prostate
  • Glioma
  • Hepatocellular Carcinoma (HCC)
  • Prostate Cancer
  • Radical Prostatectomy
  • Renal Cell Carcinoma (RCC)
Type
Observational
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

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/M...

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 not approved by the U.S. Food and Drug administration (FDA). This means [18F]DCFPyL can only be used in research studies. The PET/MRI scanner was approved by the U.S. FDA.

Tracking Information

NCT #
NCT04687969
Collaborators
National Cancer Institute (NCI)
Investigators
Principal Investigator: Ciprian Catana, MD, Ph.D Massachusetts General Hospital