RecruitingPhase 2NCT06866938

Study of Re-treatment With [177Lu]Lu-PSMA in Men With Metastatic Castration Resistance Prostate Cancer

An Open Label, Single Arm Phase IIb Study of Re-treatment With [177Lu]Lu-PSMA in Men With Metastatic Castration Resistance Prostate Cancer


Sponsor

Hospices Civils de Lyon

Enrollment

58 participants

Start Date

Apr 11, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Prostate cancer is the third leading cause of cancer-related death in men in the United States and Europe. The treatment of metastatic castration-resistant prostate cancer (mCRPC) has evolved with the arrival of the radioligand \[177Lu\]Lu-PSMA-617, which specifically targets PSMA-expressing cancer cells. The randomized phase III VISION study showed that \[177Lu\]Lu-PSMA-617 significantly improved progression-free survival and overall survival with an acceptable toxicity profile. The ReaLuP study will evaluate the efficacy of a re-treatment of \[177Lu\]Lu-PSMA-617 in patients with progressive PSMA-positive mCRPC and who have been previously treated with \[177Lu\]Lu-PSMA without evidence of progression during this first course of treatment. Patients will be treated until disease progression, unacceptable toxicity or death, or alternatively up to 9 months after the last dose of treatment. At the end of this follow up period, patients will enter the " long term follow up ", at least for 2 years after the end of the last active follow-up.


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests re-treatment with a radioactive drug called lutetium-177 PSMA (which targets prostate cancer cells) in men with metastatic castration-resistant prostate cancer (mCRPC) who have already received this therapy before and initially responded to it. **You may be eligible if...** - You are male, 18 or older - You have prostate cancer that has spread and is no longer responding to hormone therapy - You have already completed at least 4 doses of lutetium-177 PSMA therapy and your cancer responded initially - Your cancer has progressed again after that treatment - You are in adequate general health **You may NOT be eligible if...** - Your cancer progressed during or immediately after your first lutetium-177 PSMA course - You have brain metastases - You have serious kidney, liver, or bone marrow problems - You are currently on other cancer treatments 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

DRUG[177Lu]Lu-PSMA-617 (Pluvicto, Novartis)

Patients will be treated with intravenous \[177Lu\]Lu-PSMA-617 (Pluvicto, Novartis). One injection every 6 weeks at the dose of 7.4 GBq (±10%)


Locations(16)

Médecine Nucléaire, Institut Bergonié

Bordeaux, France

Oncologie Médicale, CHU Brest-Hôpital Morvan

Brest, France

Hôpital Louis Pradel, Hospices Civils de Lyon

Bron, France

Oncologie Médicale, Centre François Baclesse

Caen, France

Oncologie Médicale, Centre Jean Perrin

Clermont-Ferrand, France

Médecine Nucléaire, Centre Hospitalier de Grenoble Alpes

Grenoble, France

Médecine Nucléaire, Centre Léon Berard

Lyon, France

Médecine Nucléaire, CHU de Nantes Hôtel-Dieu

Nantes, France

Oncologie Médicale, Centre Antoine Lacassagne

Nice, France

Institut de cancérologie du Gard

Nîmes, France

Oncologie Médicale, Centre Hospitalier Lyon Sud, HCL

Pierre-Bénite, France

Oncologie Médicale, Centre Henri Becqueret

Rouen, France

Oncologie Médicale, CHU Saint Etienne

Saint-Priest-en-Jarez, France

Médecine Nucléaire, Institut de Cancérologie de Strasbourg

Strasbourg, France

CHU de Nancy

Vandœuvre-lès-Nancy, France

Médecine Nucléaire, Institut Gustave Roussy

Villejuif, France

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NCT06866938


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