About this trial
This phase II trial tests the safety, side effects and effectiveness of mosunetuzumab in treating patients with slow growing (indolent) B-cell lymphoma. Mosunetuzumab is a monoclonal antibody that may interfere with the ability of tumor cells to grow and spread.
Eligibility criteria
Qualifiers
18 years or older at time of signing informed consent
Capable of understanding and providing written informed consent
Follicular lymphoma (grade 1-2 or 3A)
Marginal zone lymphoma
Disqualifiers
History of severe allergic reaction to monoclonal antibody therapy
History of a second primary malignancy that could affect compliance with the protocol or interpretation of results except with permission of the principal investigator. Malignancies treated curatively or at low-risk of progressing at the judgment of the principal investigator (PI) may be included
Known active and uncontrolled bacterial, viral, fungal, mycobacterial, or other infection at study enrollment
Infection with human immunodeficiency virus (unless viral load is undetectable and CD4 count ≥ 200)
Trial design
Treatments tested in this trial
- Biospecimen Collection
- Computed Tomography
- Magnetic Resonance Imaging
- Mosunetuzumab
- Positron Emission Tomography
- Questionnaire Administration