Clinical Trial · NCT02687139

Study of PSMA-targeted 18F-DCFPyL PET/CT in the Evaluation of Patients With Renal Cell Carcinoma

Overview

In this study the investigators aim to evaluate diagnostic utility of prostate-specific membrane antigen (PSMA)-targeted 18F-DCFPyL PET/CT in patients with renal cell carcinoma (RCC).

Sponsor

Johns Hopkins University

Phase

N/A

Contacts

Mohamad Allaf, MD (PRINCIPAL_INVESTIGATOR)

ClinicalTrials.gov

NCT02687139

Drug / Compound

DCFPyL

Isotope(s):
Target(s):
  • PSMA
Ligand Class: Small Molecules

Eligibility

Inclusion

  • Completed staging evaluation with computed tomography (CT) or magnetic resonance imaging (MRI) of the chest, abdomen and pelvis ≤90 days prior to study enrollment
  • Clinically diagnosed or histologically proven stage II-IV renal cell carcinoma

Exclusion

  • Pregnancy ((as determined in accordance with the policies of the positron emission tomography (PET) center))
  • Intention to enroll in a blinded therapeutic clinical trial following Positron emission tomography-computed tomography (PET/CT)
  • Administered a radioisotope within 5 physical half-lives prior to study enrollment