RecruitingPhase 1Phase 2NCT07052695

Mosunetuzumab for CLL MRD Clearance

A Pilot Study Evaluating Mosunetuzumab for Clearance of Detectable Minimal Residual Disease in Chronic Lymphocytic Leukemia


Sponsor

Inhye Ahn

Enrollment

40 participants

Start Date

Nov 24, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this study is to test mosunetuzumab given alone or in combination with a Bruton tyrosine kinase inhibitor (BTKi, such as ibrutinib, acalabrutinib, zanubrutinib, or pirtobrutinib) in participants with CLL (chronic lymphocytic leukemia) or small lymphocytic lymphoma (SLL). The names of the study drugs in this research study are: * Mosunetuzumab * BTK inhibitor: Ibrutinib, acalabrutinib, zanubrutinib, or pirtobrutinib


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial tests mosunetuzumab — a drug that helps the immune system find and destroy cancer cells — in people with chronic lymphocytic leukemia (CLL) who still have detectable cancer cells in their blood after completing standard treatment. The goal is to eliminate these remaining cancer traces and potentially achieve a deeper remission. **You may be eligible if...** - You have been diagnosed with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) - You still have detectable cancer cells in your blood after finishing treatment (measurable residual disease) - You are in otherwise good general health - You meet blood count and organ function requirements **You may NOT be eligible if...** - You have active autoimmune disease requiring systemic treatment - You have a serious infection or uncontrolled illness - You have had prior treatment with certain immune therapies that may interfere - You have other significant health conditions that make participation unsafe 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

DRUGMosunetuzumab

Subcutaneous injection of a CD20xCD3 bispecific antibody

DRUGIbrutinib

For participants who have been ibrutinib PO prior to enrollment

DRUGAcalabrutinib

For participants who have been acalabrutinib PO prior to enrollment

DRUGZanubrutinib

For participants who have been zanubrutinib PO prior to enrollment

DRUGPirtobrutinib

For participants who have been pirtobrutinib PO prior to enrollment


Locations(2)

Brigham & Women's Hospital

Boston, Massachusetts, United States

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

View Full Details on ClinicalTrials.gov

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NCT07052695


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