The purpose of this study is to evaluate the safety, tolerability, and efficacy of escalating doses of BMS-986463 in participants with select advanced malignant tumors.
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Number of participants with adverse events (AEs)
Timeframe: Up to 108 weeks
Number of participants with serious adverse events (SAEs)
Timeframe: Up to 108 weeks
Number of participants with AEs meeting protocol defined dose-limiting toxicity (DLT) criteria
Timeframe: Up to 108 weeks
Number of participants with AEs leading to discontinuation
Timeframe: Up to 108 weeks
Number of participants with AEs leading to death
Timeframe: Up to 108 weeks
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