RecruitingPhase 2NCT06458439

Epcoritamab-CAR T Cells for Large B-cell Lymphomas

Phase IIa Trial to Evaluate Epcoritamab Administered Before and After CAR-T Cell Therapy in Patients With Relapsed or Refractory Large B-cell Lymphomas


Sponsor

Abramson Cancer Center at Penn Medicine

Enrollment

31 participants

Start Date

Sep 24, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This study investigates the feasibility and efficacy of epcoritamab treatment before CAR T cells. This study also investigates if, when patients have residual lymphoma after CAR T cells, epcoritamab can help to effectively treat that lymphoma.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination treatment using epcoritamab (an antibody-based immunotherapy) together with CAR T-cell therapy for people with large B-cell lymphoma — an aggressive blood cancer — that has come back or stopped responding to prior treatment. **You may be eligible if...** - You are over 18 years old - You have been diagnosed with large B-cell lymphoma confirmed by a pathology report - Your cancer has relapsed (come back) or is refractory (not responding) to prior treatment - You are in good enough health to participate (ECOG 0–2) - You or your legal representative can provide informed consent **You may NOT be eligible if...** - Your lymphoma diagnosis is not confirmed by pathology - Your performance status is too poor - You are unable or unwilling to follow the study protocol 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

* C1D1: fixed priming dose of 0.16 mg subcutaneous injection * C1D8: fixed intermediate dose of 0.8 mg subcutaneous injection * C1D15 onward: fixed full dose of 48 mg subcutaneous injection


Locations(1)

Abramson Cancer Center at the University of Pennsylvania

Philadelphia, Pennsylvania, United States

View Full Details on ClinicalTrials.gov

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NCT06458439


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