The primary purpose of this study is to determine whether the investigational drug XmAb541 is safe and well tolerated, and to determine an optimal and safe dose(s) for further study. The study will also evaluate the effect of XmAb541 on tumor outcomes.
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Incidence of adverse events
Timeframe: Day 1 to 2 years
Incidence of dose-limiting toxicities (DLTs)
Timeframe: Day 1 to Day 28
Incidence of cytokine release syndrome (CRS)
Timeframe: Day 1 to Day 28