RecruitingPhase 2NCT06563596

Epco, Zanu, Ritux for R/R FL or MZL

A Phase 2 Study of Epcoritamab, Zanubrutinib, and Rituximab (EZR) for Treatment of Relapsed or Refractory Follicular Lymphoma or Marginal Zone Lymphoma


Sponsor

Reid Merryman, MD

Enrollment

45 participants

Start Date

Jan 21, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to determine how effective and safe the combination of epcoritamab, zanubrutinib, and rituximab is in treating participants with relapse or refractory Follicular Lymphoma (FL) or marginal zone lymphoma (MZL). * The names of the study drugs involved in this research study are: * Epcoritamab (a type of antibody) * Zanubrutinib (a type of Bruton tyrosine kinase inhibitor) * Rituximab (a type of monoclonal antibody)


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a three-drug combination — epcoritamab, zanubrutinib, and rituximab — for patients with follicular lymphoma (FL) or marginal zone lymphoma (MZL) that has come back or is no longer responding to prior treatment. These drugs work together to target cancer cells using different mechanisms. **You may be eligible if...** - You are 18 or older with confirmed follicular lymphoma (grade 1–3A) or marginal zone lymphoma (any subtype) - You have received at least one prior treatment that included a CD20-targeting drug (like rituximab) - You have measurable disease visible on imaging - Your disease meets certain criteria indicating treatment is needed (symptoms, organ problems, large tumors, or certain blood count changes) **You may NOT be eligible if...** - Your lymphoma has transformed into a more aggressive (higher-grade) type - You have active hepatitis B or C, or HIV not well controlled - You have had a prior stem cell transplant within 6 months - You are pregnant or breastfeeding - You have poor overall health status 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

DRUGZanubrutinib

Bruton tyrosine kinase inhibitor, 80 mg immediate-release capsule, taken orally per protocol.

DRUGRituximab

Chimeric anti-CD20 monoclonal antibody, 10 or 50 mL single-use vials, via intravenous infusion per institutional standard.

DRUGEpcoritamab

Bispecific antibody, 5 or 60 mg/mL vials, via subcutaneous (under the skin) injection per protocol.


Locations(3)

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

Memorial Sloan Kettering Cancer Center

New York, New York, United States

The Ohio State University Wexner Medical Center

Columbus, Ohio, United States

View Full Details on ClinicalTrials.gov

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NCT06563596


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