The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of nemtabrutinib in Japanese participants with mature B-cell neoplasms.
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Number of Participants who Experience Dose Limiting Toxicities (DLTs) per National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0
Timeframe: Up to approximately 4 weeks
Number of Participants who Experience Adverse Events (AEs)
Timeframe: Up to approximately 38 months
Number of Participants Discontinuing Study Treatment due to AEs
Timeframe: Up to approximately 38 months