Mosunetuzumab and Zanubrutinib for Relapsed/Refractory Marginal Zone Lymphoma
This study is testing two drugs, mosunetuzumab and zanubrutinib, given by IV, for people with marginal zone lymphoma (a type of slow-growing B-cell lymphoma) that has come back or not responded to previous treatments. You may be able to join if you are 18 or older, have been diagnosed with marginal zone lymphoma, and have received at least one prior treatment, including a CD20 monoclonal antibody. The main goal is to see how safe and effective this combination treatment is, specifically looking at how many people have a complete response. The study plans to enroll 36 participants. The current recruitment status is unclear.
- Study design
- This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 36 participants.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Safety and side effects will be measured throughout the study, for an average of 1 year.
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NCT06563505
A Phase 2 Trial of Mosunetuzumab and Zanubrutinib for Patients With Relapsed/Refractory Marginal Zone Lymphoma
Recruiting
PHASE2Ages 18+InterventionalTreatmentM.D. Anderson Cancer CenterInvestigator-initiated
~36 participants
Updated 2026-07-24 on ClinicalTrials.gov
What's tested:MosunetuzumabZanubrutinib
At a glance
Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety and Adverse Events (AEs)
Measured over Through study completion; an average of 1 year.
Conditions
Where it's being run
1 sites across 1 statesTexas1
Study leadership
- Dai Chihara, MD,PHD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center
Who to contact
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Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Eligibility criteria
Inclusion
A nodal or extranodal (except spleen) mass \> 7 cm in its greater diameter
At least 3 nodal or extranodal sites ≥ 3 cm in diameter
Presence of at least one B symptom
Fever (\>38 C), night sweats, weight loss \> 10% in the past 6 months
Symptomatic splenomegaly (or size \>13cm)
Impending organ compression or involvement (ureteral, orbital, gastrointestinal)
Any of the following cytopenias due to bone marrow involvement of lymphoma
Hemoglobin ≤ 10 g/dL
Platelets ≤ 100 x 109/L
Absolute neutrophil count (ANC) \< 1.5x109/L
Pleural effusion or ascites
LDH \> ULN or β2 microglobulin \> ULN 8. Bi-dimensionally measurable disease, with at least one nodal lesion ≥ 1.5 cm or one extra-nodal lesion \> 1 cm in longest diameter by CT, PET/CT, and/or MRI
Subjects with splenic MZL who do not meet the radiographically measurable disease criteria are eligible for participation if spleen is enlarged over 16 cm and MZL is histologically confirmed by bone marrow biopsy or peripheral blood flow cytometry
Subjects with EMZL such as skin of conjunctival EMZL who do not meet the radiographically measurable disease criteria are eligible for participation if at least one of the skin lesions is histologically confirmed as MZL and measures ≥1.5 cm in diameter 9. Patients must have adequate organ and marrow function as defined below:
Total bilirubin ≤ 1.5 institutional ULN, unless consistent with Gilbert's (ratio between total and direct bilirubin \> 5)
AST (SGOT) and ALT (SGPT) ≤ 3 x institutional ULN
Alkaline phosphatase \< 2.5 ULN
Creatinine clearance ≥ 40 ml/min calculated by modified Cockcroft-Gault formula
Blood counts below if without lymphoma cause for cytopenia
Hemoglobin ≥ 8 g/dL
Platelets ≥ 75 x 109/L
Absolute neutrophil count (ANC) ≥ 1.0x109/L
Blood counts below if cytopenia are due to lymphoma (such as bone marrow involvement or splenomegaly)
Hemoglobin ≥ 6 g/dL (no transfusion within 7 days prior to treatment)
Platelets ≥ 50 x 109/L
Absolute neutrophil count (ANC) ≥ 0.5x109/L
Exclusion
Adequately treated localized skin cancer without evidence of disease.
Adequately treated or monitored low risk localized prostate cancer.
Adequately treated localized breast cancer without evidence of disease.
Adequately treated cervical carcinoma in situ without evidence of disease. 4. Any life-threatening illness, medical condition, or organ system dysfunction which, in the investigator's opinion, could compromise the subject's safety, interfere with the absorption or metabolism of lenalidomide capsules, or put the study outcomes at undue risk. 5. Uncontrolled human immunodeficiency virus (HIV), or active Hepatitis C Virus, or active Hepatitis B Virus infection, or any uncontrolled active significant infection, including suspected or confirmed JC virus infection and SARS-CoV2. 6. Patients with inactive hepatitis B infection must adhere to hepatitis B reactivation prophylaxis unless contraindicated. Hepatitis B or C serologic status: subjects who are hepatitis B core antibody (anti-HBc) positive and who are surface antigen negative will need to have a negative polymerase chain reaction (PCR). Those who are hepatitis B surface antigen (HBsAg) positive or hepatitis B PCR positive will be excluded. Subjects who are hepatitis C antibody positive will need to have a negative PCR result. Those who are hepatitis C PCR positive will be excluded. Subjects with a history of Hepatitis C who received antiviral treatment are eligible as long as PCR is negative. 7. History of immunodeficiency (with the exception of hypogammaglobulinemia) or concurrent systemic immunosuppressant therapy (e.g., cyclosporine, tacrolimus, etc., or chronic administration glucocorticoid equivalent of \>10mg/day of prednisone) within 28 days of the first dose of study drug with exception of steroid used for IV contrast allergy. In addition, use of inhaled, topical, intranasal corticosteroids or local steroid injection (eg, intra- articular injection) is permitted. 8. Use of strong/moderate inhibitors within 7 days or 5 half-lives prior to the first dose of zanubrutinib; usage of strong/moderate CYP3A inducers within 14 days prior to the first dose of zanubrutinib. 9. Requiring ongoing therapy with strong or moderate CYP3A inducers. 10. Clinically significant cardiovascular disease such as uncontrolled or symptomatic arrhythmias, congestive heart failure, or myocardial infarction within 6 months of Screening, or any Class 3 (moderate) or Class 4 (severe) cardiac disease as defined by the New York Heart Association Functional Classification. Subjects with controlled, asymptomatic atrial fibrillation during screening can enroll on study. 11. Significant screening electrocardiogram (ECG) abnormalities including 2nd degree atrioventricular (AV) block, type II AV block, or 3rd degree block. 12. Active bleeding or known bleeding diathesis (e.g., von Willebrand's disease) or hemophilia. 13. History of stroke or intracranial hemorrhage within 6 months prior to study entry. 14. Lactating or pregnant subjects. 15. Administration of any investigational agent within 28 days of first dose of study drug. 16. Patients who have undergone major surgery within 28 days or minor surgery within 3 days of first dose of study drug. 17. Patients taking corticosteroids during the last 4 weeks, unless administered at a dose equivalent to \< 10 mg/day prednisone (over these 4 weeks) with the exception of pre-study steroid treatment with prednisone up to 100mg x 5 days which is allowed to improve symptoms and treatment tolerance. 18. Known or suspected chronic active Epstein-Barr virus (CAEBV) infection 19. Administration of a live, attenuated vaccine within 4 weeks before first mosunetuzumab administration or anticipation that such a live, attenuated vaccine will be required during the study. 20. Prior solid organ transplantation 21. Prior allogeneic stem cell transplant (autologous stem cell transplants are allowed if conducted at least 100 days prior to C1D1.) 22. Contraindication to tocilizumab 23. Patients who have difficulty with or are unable to swallow oral medication, or have disease significantly affecting gastrointestinal function that would limit absorption of oral medication. 24. Patients who have an active autoimmune disease that has required systemic treatment in past 2 years (i.e., with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is not considered a form of systemic treatment and is allowed. 25. Patients who have a history of (non-infectious) autoimmune pneumonitis that required steroids or has current autoimmune pneumonitis.
What this trial measures
- Safety and Adverse Events (AEs)Through study completion; an average of 1 year.
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0