RecruitingPhase 4NCT06099093

Pilot of 18F-DCFPyL-PSMA PET in mCRPC Patients Receiving 117Lu-Vipivotide Tetraxetan

A Pilot Study of 18F-DCFPyL-PSMA PET in Patients Receiving 177Lu-Vipivotide Tetraxetan Therapy for Metastatic Castrate-resistant Prostate Cancer


Sponsor

Brigham and Women's Hospital

Enrollment

30 participants

Start Date

Apr 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this research study is to see how well an imaging test, called 18FDCFPyL prostate specific membrane antigen (PSMA) positron emission tomography (PET), can show the extent of prostate cancer when comparing to 68Ga-PSMA-11 PET/CT (another type of diagnostic scan for prostate cancer).


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is using a new type of specialized PET scan (called 18F-DCFPyL PSMA PET) to better understand how prostate cancer responds to a radioactive treatment called Lutetium-177 (Lu-177 PSMA therapy). Researchers want to see if this improved scan gives more accurate information about where the cancer is compared to the standard scan. **You may be eligible if...** - You are a man aged 18 or older with confirmed prostate cancer - You are already scheduled to receive standard-of-care Lu-177 PSMA therapy (a targeted radioactive treatment) - A prior PSMA scan within the last 120 days showed at least one cancer lesion - You are willing and able to follow study procedures **You may NOT be eligible if...** - You have uncontrolled serious illness (infections, heart failure, or irregular heart rhythms) - You are severely claustrophobic and cannot tolerate a PET/CT scan - You have had allergic reactions to similar imaging agents 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

DRUG18F-DCFPyl

Fluorine-labeled small molecule, via intravenous infusion per protocol.


Locations(2)

Dana Farber Cancer Institute

Boston, Massachusetts, United States

Brigham and Womens Hospital

Boston, Massachusetts, United States

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NCT06099093


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