This study is to evaluate the safety and tolerability of JAB-21822 monotherapy and combination therapy in adult participants with advanced solid tumors harboring KRAS G12C mutation.
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Dose Escalation phase: Number of participants with dose limiting toxicities (DLTs)
Timeframe: At the end of Cycle 1 (each cycle is 21 days)
Dose Escalation and Dose Expansion phase: Number of participants with adverse events
Timeframe: Up to 4 years
Dose Expansion phase: Overall response rate (ORR)
Timeframe: Up to 4 years - from baseline to RECIST confirmed Progressive Disease
Dose Expansion phase: Duration of response ( DOR )
Timeframe: Up to 4 years