RecruitingPhase 2NCT06931652

Study of Epcoritamab in R/R Primary Diffuse Large B-cell Lymphoma of the CNS Treated With Lenalidomide and Rituximab

A Phase 2 Study Evaluating Epcoritamab in Subjects With Relapsed and Refractory Primary Diffuse Large B-cell Lymphoma of the CNS Treated With Lenalidomide and Rituximab


Sponsor

The Lymphoma Academic Research Organisation

Enrollment

60 participants

Start Date

Sep 22, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this phase 2 study is to evaluate the efficacy and safety of epcoritamab in subjects with relapsed or refractory primary diffuse large B-cell lymphoma of the Central Nervous System treated with rituximab and lenalidomide.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a drug called epcoritamab combined with lenalidomide and rituximab for people with a rare type of brain lymphoma called primary CNS diffuse large B-cell lymphoma (PCNSL) or primary vitreoretinal lymphoma (PVRL) — lymphomas that occur in the brain/spinal cord or in the eye — that have come back after prior treatment. **You may be eligible if...** - You are 18 years or older - You have confirmed PCNSL or PVRL that has relapsed or is refractory (not responding to treatment) - You have previously received high-dose methotrexate (a standard first-line treatment) - You have measurable disease visible on brain MRI - You are in adequate health (ECOG performance status 0–2) - You can swallow capsules **You may NOT be eligible if...** - You have severe blood count problems - You have significant liver or kidney dysfunction - You are pregnant or breastfeeding - You have active infections such as HIV, hepatitis B, or hepatitis C 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

DRUGEpcoritamab

Epcoritamab Investigational Medicinal Product (IMP): Epcoritamab will be used during induction phase and Maintenance phase.


Locations(13)

INSTITUT BERGONIE - Service d'Oncologie Médicale

Bordeaux, France

INSTITUT D'HEMATOLOGIE DE BASSE NORMANDIE - Service Hématologie

Caen, France

CHU ESTAING - Service Thérapie Cellulaire et Hématologie Clinique

Clermont-Ferrand, France

CHU DE LILLE - HOPITAL CLAUDE HURIEZ - Service des Maladies du Sang

Lille, France

CHR DE MARSEILLE - CHU TIMONE - Service de Neuro-Oncologie

Marseille, France

CHRU DE NANCY - HOPITAL CENTRAL - Service de Neurologie

Nancy, France

GHU PITIE-SALPETRIERE - CHARLES FOIX - Service Neurologie

Paris, France

HOPITAL DE LA PITIE SALPETRIERE - Service Hématologie Clinique

Paris, France

CHU LYON-SUD - Hématologie Clinique

Pierre-Bénite, France

CHU PONTCHAILLOU - Hématologie Clinique

Rennes, France

INSTITUT CURIE - SITE SAINT-CLOUD - Service Hématologie

Saint-Cloud, France

IUCT ONCOPOLE - Service Hématologie

Toulouse, France

CHU BRETONNEAU - Service Cancérologie - Hématologie et Thérapie Cellulaire

Tours, France

View Full Details on ClinicalTrials.gov

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NCT06931652


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