CLINICAL TRIAL / NCT05144841

Inclusion Criteria: - Has relapsed or refractory (rr) DLBCL; has progressed after at least 2 lines of prior therapy; and has progressed after auto- stem cell transplant (SCT) or are auto-SCT ineligible. Must have received prior multiagent regimen that includes an alkylating agent. anthracycline, and anti-CD20 (cluster of differentiation 20) monoclonal antibody. - Has histologically confirmed diagnosis of DLBCL. - Has radiographically measurable DLBCL per the Lugano Response Criteria. - Should either be post- chimeric antigen receptor T cell therapy (CAR-T) failure or ineligible for CAR-T (for any reason). - Life expectancy of at least 3 months. - Has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2 assessed within 7 days before time of enrollment. - Has adequate organ function. Exclusion Criteria: - Has received a diagnosis of Primary mediastinal B-cell lymphoma (PMBCL). - Has undergone solid organ transplant at any time. - Has a history of any clinically significant cardiovascular conditions within 6 months of screening or serious cardiac arrhythmia requiring medication. - Has known history of liver cirrhosis. - Has pericardial effusion or clinically significant pleural effusion. - Has ongoing Grade >1 peripheral neuropathy. - Has a history of a second malignancy, unless potentially curative treatment has been completed with no evidence of malignancy for 2 years. - Transformed DLBCL from indolent lymphoma. - In participants with prior allo-SCT, acute graft versus host disease (GVHD) or ongoing evidence of chronic GVHD. - Has received prior systemic anticancer therapy, including investigational agents within 4 weeks prior to the first dose of study intervention. - Has received prior radiotherapy within 28 days of start of study intervention. Participants. must have recovered from all radiation-related toxicities. - Has ongoing corticosteroid therapy (exceeding 30 mg daily of prednisone equivalent). - Has received a live or live-attenuated vaccine within 30 days before the first dose of study intervention. - Is currently participating in or has participated in a study of an investigational agent or has used an investigational device within 4 weeks before the first dose of study intervention. - Has known active central nervous system (CNS) lymphoma involvement or active CNS involvement by lymphoma. - Has an active infection requiring systemic therapy. - Has a known history of human immunodeficiency virus (HIV) infection. - Has a known history of hepatitis B or known active hepatitis C virus (HCV).