RecruitingPhase 2NCT06919939

Epcoritamab in Combination With Loncastuximab Tesirine in Relapsed/Refractory Large B-cell Lymphoma

Phase 2 Study of Epcoritamab in Combination With Loncastuximab Tesirine in Relapsed/Refractory Large B-cell Lymphoma


Sponsor

University of Miami

Enrollment

26 participants

Start Date

Jan 7, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to determine whether combining Loncastuximab Tesirine with Epcoritamab is tolerable and effective for reducing and/or eliminating lymphoma cells in the body.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing the combination of two immunotherapy drugs — epcoritamab and loncastuximab tesirine — for people with large B-cell lymphoma (a type of blood cancer) that has come back or stopped responding to previous treatment. **You may be eligible if...** - You are 18 or older - You have large B-cell lymphoma (including DLBCL or related subtypes) that has relapsed or is no longer responding to treatment - You have measurable disease on imaging - Your heart, liver, kidney, and bone marrow function are adequate **You may NOT be eligible if...** - You have not had any prior treatment for lymphoma - You have active autoimmune disease requiring treatment - You have received prior CAR-T cell therapy within a certain timeframe - You are pregnant or breastfeeding - You have active infections or other serious medical conditions 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 will be administered via subcutaneous injection at the following dose levels and schedule over a total of twelve cycles: * Cycle 1 Day 1: Step-up dose of 0.16 mg * Cycle 1 Day 8: Step-up dose of 0.80 mg * Cycle 1 Day 15: First full dose of 48 mg. * Cycles 2 through 4 Days 1, 8 and 15: 48 mg * Cycles 5 through 12 Days 1 and 15: 48 mg

DRUGLoncastuximab Tesirine

Loncastuximab will be administered intravenously (IV) at the following dose level and schedule over a total of four cycles: * Cycles 1 and 2 Day 1: 120 mcg/kg * Cycles 3 and 4 Day 1: 75 mcg/kg * Cycle 4 Day 22: 75 mcg/kg


Locations(1)

University of Miami

Miami, Florida, United States

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NCT06919939


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