RecruitingPhase 2NCT05783609

Epcoritamab and Rituximab for First-line Follicular Lymphoma

A Phase 2 Study of Epcoritamab and Rituximab for First-line Treatment of Follicular Lymphoma


Sponsor

Reid Merryman, MD

Enrollment

100 participants

Start Date

Jun 21, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to determine how effective and safe the combination of rituximab and epcoritamab is in treating patients with Follicular Lymphoma (FL) and who have not received other treatments for their lymphoma. The names of the study drugs involved in this study are: * Rituximab (a type of monoclonal antibody therapy) * Epcoritamab (a T-cell bispecific antibody)


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of epcoritamab (a bispecific antibody that engages immune cells) and rituximab (a standard lymphoma drug) as a first-line treatment for follicular lymphoma — a slow-growing type of non-Hodgkin lymphoma. The goal is to see if this chemotherapy-free combination can effectively treat newly diagnosed follicular lymphoma. **You may be eligible if:** - You have been newly diagnosed with follicular lymphoma (grade 1–3A) confirmed by biopsy, with no prior transformation to aggressive lymphoma - You have not received any prior systemic (drug) treatment for follicular lymphoma - Your disease meets at least one criterion for starting treatment (such as symptomatic lymph nodes, organ impairment, or low blood counts caused by disease) **You may NOT be eligible if:** - You have previously received systemic therapy for follicular lymphoma - Your lymphoma has transformed to a more aggressive subtype - You do not meet the treatment threshold criteria 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

T-cell bispecific antibody, via subcutaneous injection

DRUGRituximab

Chimeric anti-CD20 monoclonal antibody, via IV infusion


Locations(5)

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

University of Rochester Medical Center

Rochester, New York, United States

The Ohio State University Wexner Medical Center

Columbus, Ohio, United States

Medical College of Wisconsin

Milwaukee, Wisconsin, United States

View Full Details on ClinicalTrials.gov

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NCT05783609


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