RecruitingPhase 3NCT06970847

64Cu-SAR-bisPSMA Positron Emission Tomography: A Phase 3 Study of Participants With Biochemical Recurrence of Prostate Cancer


Sponsor

Clarity Pharmaceuticals Ltd

Enrollment

220 participants

Start Date

May 16, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The aim for this study is to investigate the ability of 64Cu-SAR-bisPSMA PET/CT to detect recurrence of prostate cancer


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is a Phase 3 trial testing a specialized PET scan using a radioactive tracer called 64Cu-SAR-bisPSMA to detect where prostate cancer has returned after initial treatment (called biochemical recurrence, when PSA levels rise again after surgery or radiation). **You may be eligible if...** - You are 18 or older with a confirmed history of prostate cancer (adenocarcinoma) - You have had definitive treatment (surgery or radiation) and now have rising PSA levels suggesting the cancer is returning - You are potentially eligible for additional local or regional treatments aimed at cure - Your life expectancy is at least 6 months **You may NOT be eligible if...** - You have already confirmed spread of cancer to distant organs beyond the local/regional area - You have a condition preventing you from receiving the radioactive tracer or undergoing a PET scan - You are pregnant or breastfeeding - You have had prior treatments that would affect PSA interpretation in ways that interfere with study goals Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUG64Cu-SAR-bisPSMA

All Patients will receive a single administration, a bolus injection of 200MBq 64Cu-SAR-bisPSMA


Locations(28)

East Valley Urology Center of Arizona

Mesa, Arizona, United States

Arkansas Urology Research Center

Little Rock, Arkansas, United States

UC Irvine

Irvine, California, United States

Comprehensive Urology Medical Group

Los Angeles, California, United States

Alarcon Urology Center

Montebello, California, United States

University of Florida Health- Jacksonville

Jacksonville, Florida, United States

Biogenix Molecular

Miami, Florida, United States

Endeavor Health- Glenbrook Hospital

Glenview, Illinois, United States

Indiana University Health-IU Simon Cancer Center

Indianapolis, Indiana, United States

Wichita Urology Group

Wichita, Kansas, United States

XCancer Research Network / LCMC Health EJGH

Metairie, Louisiana, United States

M. Health Fairview University of Minnesota Medical Center

Minneapolis, Minnesota, United States

St. Louis University

St Louis, Missouri, United States

XCancer

Omaha, Nebraska, United States

New Mexico Oncology Hematology Consultants

Albuquerque, New Mexico, United States

Albany Medical College

Albany, New York, United States

University of Pittsburgh Medical Center

Pittsburgh, Pennsylvania, United States

Carolina Urologic Research Center

Myrtle Beach, South Carolina, United States

Urology Associates, P.C.

Nashville, Tennessee, United States

Urology Clinics of North Texas

Dallas, Texas, United States

Houston Metro Urology-SW

Houston, Texas, United States

The Urology Place

San Antonio, Texas, United States

Summit Urology

Murray, Utah, United States

Intermountain Medical Center

Salt Lake City, Utah, United States

St. Vincent's Hospital, Sydney

Darlinghurst, New South Wales, Australia

Sydney Adventist Hospital

Wahroonga, New South Wales, Australia

Westmead Private Hosptial

Westmead, New South Wales, Australia

Royal Brisbane and Women's Hospital

Herston, Queensland, Australia

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

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NCT06970847


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