RecruitingPhase 1NCT06303713

LuCarbo - a Study of 177Lu-PSMA-617 Plus Carboplatin in Metastatic Castrate-resistant Prostate Cancer

LuCarbo - a Phase 1a/1b Study of 177Lu-PSMA-617 Plus Carboplatin in Metastatic Castrate-resistant Prostate Cancer


Sponsor

Dana-Farber Cancer Institute

Enrollment

37 participants

Start Date

May 22, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to see whether the combination of a chemotherapy drug, carboplatin, along with the radioligand treatment, 177Lu-PSMA-617, is safe in treating prostate cancer and whether the combination is effective in shrinking or preventing growth of prostate cancer. The names of the study drugs used in this research study are: * Carboplatin (A type of chemotherapy) * 177Lu-PSMA-617 (A type of radioligand therapy)


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study (LuCarbo) tests whether combining lutetium-177 PSMA-617 (a radioactive treatment that targets prostate cancer cells) with carboplatin (a chemotherapy drug) can help men with metastatic castrate-resistant prostate cancer (mCRPC) — cancer that has spread and no longer responds to hormone therapy. This is an early-phase study evaluating safety and early signs of effectiveness. **You may be eligible if...** - You are 18 years or older - You have confirmed prostate adenocarcinoma that has spread and no longer responds to hormone therapy - Your cancer is progressing despite treatment (rising PSA, new lesions on imaging) - You have received certain prior treatments (such as an androgen receptor pathway inhibitor) - You are in reasonably good health with adequate organ function **You may NOT be eligible if...** - You have not had prior standard therapies for mCRPC - You have severe kidney, liver, or bone marrow problems - You have received prior lutetium-177 PSMA therapy or carboplatin - You are taking medications that significantly interact with carboplatin 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.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGCarboplatin

Platinum coordination compound, premixed aqueous solution of 10mg/ML, via intravenous (into the vein) infusion per protocol.

DRUG177Lu-PSMA-617

Radioligand therapy, single-dose vial, via intravenous (into the vein) infusion per protocol.


Locations(3)

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

Brigham and Women's Hospital

Boston, Massachusetts, United States

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

View Full Details on ClinicalTrials.gov

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

Visit

NCT06303713


Related Trials