This study is conducted to determine the safety and tolerability of INCB161734 as a single agent or in combination with other anticancer therapies.
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Number of participants with Dose Limiting Toxicities (DLTs)
Timeframe: Up to 28 days
Number of participants with Treatment-emergent Adverse Events (TEAEs)
Timeframe: Up to 2 years and 90 days
Number of participants with TEAEs leading to dose modification or discontinuation
Timeframe: Up to 2 years and 90 days