Actively Recruiting

Phase Not Applicable
Age: 18Years +
MALE
NCT07011342

Utility of 18F-rhPSMA-7.3 in the Diagnosis of Prostate Cancer After Focal Gland Treatment

Led by Hackensack Meridian Health · Updated on 2026-03-23

70

Participants Needed

1

Research Sites

161 weeks

Total Duration

On this page

Sponsors

H

Hackensack Meridian Health

Lead Sponsor

B

Blue Earth Diagnostics

Collaborating Sponsor

AI-Summary

What this Trial Is About

To evaluate the effectiveness of a PSMA-PET scan in identifying recurrent prostate cancer after focal therapy

CONDITIONS

Official Title

Utility of 18F-rhPSMA-7.3 in the Diagnosis of Prostate Cancer After Focal Gland Treatment

Who Can Participate

Age: 18Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult males 18 years or older
  • Patient must have a pre-treatment MRI
  • Patient underwent SOC focal therapy with either focal or hemiablation for intermediate risk prostate cancer in the past 9 months prior to enrollment
  • Intermediate risk disease as defined by American Urology Academy (AUA)/National Comprehensive Cancer Network (NCCN) guidelines
  • Life expectancy of 10 years or more
  • Underwent standard template biopsy before treatment with a minimum of 2 cores into the MRI visible lesion if lesion was present
  • Patient understands the purpose of the trial and can provide signed informed consent
  • Ability to adhere to the study visit schedule and all protocol requirements, including surveillance imaging and blood sample collection
Not Eligible

You will not qualify if you...

  • Patients under 18 years of age
  • Patients previously treated with whole gland ablation or partial gland ablation more than 9 months prior to enrollment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

John Theurer Cancer Center at Hackensack University Medical Center

Hackensack, New Jersey, United States, 07601

Actively Recruiting

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Research Team

O

Oncology Clinical Research Referral Office

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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