RecruitingPhase 2NCT07128641

Odronextamab in Low Tumor Volume Advanced FL

A Phase II Study of Odronextamab in Treatment Naïve Patients With Low Tumor Volume Advanced Stage Follicular Lymphoma


Sponsor

Gottfried von Keudell, MD PhD

Enrollment

35 participants

Start Date

Sep 8, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate the safety and effectiveness of treating previously untreated Follicular Lymphoma (FL) with odronextamab. The name of the study drug in this research study is: -Odronextamab (a type of monoclonal antibody)


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a drug called odronextamab — a bispecific antibody that helps the immune system attack lymphoma cells — in people with follicular lymphoma (a slow-growing blood cancer) that has not yet grown large or caused symptoms. **You may be eligible if...** - You are 18 or older - You have been diagnosed with follicular lymphoma grade 1, 2, or 3A confirmed by biopsy - Your cancer is CD20-positive - You had a lymph node biopsy in the past 6 months - You have at least one enlarged lymph node (1.5 cm or larger) - Your organ function (blood counts, heart, etc.) is adequate **You may NOT be eligible if...** - Your lymphoma has transformed to a more aggressive type - You have cancer spread to the brain or spinal fluid - You have active autoimmune disease requiring treatment - You have serious heart, liver, kidney, or lung problems - You are pregnant or breastfeeding 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

BIOLOGICALOdronextamab

A CD20xCD3 bispecific monoclonal antibody, glass vials, via intravenous (into the vein) infusion per protocol.


Locations(1)

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

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NCT07128641


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