The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) of escalating doses of RMC-6291 (KRAS G12C(ON) inhibitor) monotherapy in adult subjects with advanced solid tumors and to identify the maximum tolerated dose (MTD), and the recommended Phase 2 dose.
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Adverse events
Timeframe: up to 3 years
Dose Limiting Toxicities
Timeframe: The first 21 days (i.e. Cycle 1)