RecruitingPhase 2NCT06510309

Rituximab Plus Venetoclax in Front Line Marginal Zone Lymphoma

A Phase II Study Using Rituximab Plus Venetoclax in the Front Line Treatment of Marginal Zone Lymphoma


Sponsor

Gottfried von Keudell, MD PhD

Enrollment

33 participants

Start Date

Feb 11, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to see if the combination of rituximab and venetoclax is effective in treating participants with untreated Marginal Zone Lymphoma (MZL). The names of the study drugs involved in this study are: * Venetoclax (a type of inhibitor) * Rituximab (a type of antibody)


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of two drugs — rituximab (a targeted antibody) and venetoclax (a targeted oral drug) — as a new front-line treatment for patients with marginal zone lymphoma (MZL), a slow-growing type of blood cancer, who have not previously received treatment for their lymphoma. **You may be eligible if...** - You have been diagnosed with marginal zone lymphoma (confirmed by biopsy) - You have measurable disease (at least one lymph node ≥1.5 cm or enlarged spleen) - If you have gastric MALT lymphoma, you are either H. pylori-negative or have already failed H. pylori eradication therapy - You have not received prior systemic treatment for MZL (some exceptions allowed) **You may NOT be eligible if...** - You have received prior rituximab or venetoclax treatment - Your MZL has transformed into a more aggressive lymphoma - You have significant heart, liver, or kidney problems - You have active, uncontrolled infections 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.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGVenetoclax

B-cell lymphoma inhibitor, tablets taken orally per protocol.

DRUGRituximab

Anti-CD20 monoclonal antibody, 10mL or 50 mL single-use vials, via intravenous (into the vein) infusion per protocol.


Locations(1)

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06510309


Related Trials