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RecruitingProstate CancerProstatic Neoplasms

Positron Emission Tomography Using 64Cu-SAR-bisPSMA in Participants With High-risk Prostate Cancer Prior to Radical Prostatectomy

Eligible age

18+ yrs

Accepts

Men

Locations

20 states

Healthy volunteers

No

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About this study

The aim for this study is to assess the diagnostic performance of 64Cu-SAR-bisPSMA PET to detect regional nodal metastases.

Sponsor: Clarity Pharmaceuticals Ltd

You may qualify if…

  • ✓ At least 18 years of age.
  • ✓ Signed informed consent.
  • ✓ Untreated, histologically confirmed adenocarcinoma of the prostate.
  • ✓ High-risk or greater PC defined by National Comprehensive Cancer Network Guidelines Version 1.202327 (clinical stage ≥T3a, or Grade Group ≥4, or PSA \>20 ng/mL).
  • ✓ Patients electing to undergo RP with PLND.

You may not qualify if…

  • ✕ Administration of any high energy (\>300 KeV) gamma-emitting radioisotope within 5 physical half-lives prior to Day 1.
  • ✕ Known or expected hypersensitivity to 64Cu-SAR-bisPSMA or any of its components.
  • ✕ Patients with known predominant small cell or neuroendocrine PC.

Where it's recruiting

Alabama

Birmingham

Arizona

Phoenix

Arkansas

Little Rock

California

Los Angeles · Orange · Stanford

Florida

Jacksonville · Miami

Illinois

Glenview

Indiana

Indianapolis

Kansas

Wichita

Michigan

Grand Rapids

Minnesota

Rochester

New York

Albany · New York

Source: ClinicalTrials.gov · NCT06056830 · last updated 2026-09-11

Positron Emission Tomography Using 64Cu-SAR-bisPSMA in Participants Wi · TrialPath