This phase II trial tests the safety and effectiveness of glofitamab given in combination with pirtobrutinib in treating patients with mantle cell lymphoma that has come back after a period of improvement (relapsed) or that has not responded to previous treatment (refractory). Glofitamab and obinutuzumab are monoclonal antibodies that may interfere with the ability of cancer cells to grow and spread. Obinutuzumab may also reduce the risk of immune-related conditions from treatment. Pirtobrutinib is in a class of medications called kinase inhibitors. It works by blocking the action of the protein that signals cancer cells to multiply. Giving glofitamab in combination with pirtobrutinib may be safe, tolerable and/or effective in treating patients with relapsed or refractory mantle cell lymphoma.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Percentage of participants with high grade, treatment-emergent adverse events (AEs)
Timeframe: Approximately 2 weeks
Proportion of participants with Complete Response (CR)
Timeframe: Up to 94 weeks
Proportion of participants with reported Cytokine-release syndrome (CRS)
Timeframe: Approximately 2 weeks
Proportion of participants with immune effector cell-associated neurotoxicity syndrome (ICANS)
Timeframe: Approximately 2 weeks
Proportion of participants with reported Hemophagocytic lymphohistiocytosis (HLH)
Timeframe: Approximately 2 weeks
UCSF Hematopoietic Malignancies Clinical Trial Recruitment