The purpose of this study is to evaluate the safety, tolerability, pharmacokinetic (PK), and pharmacodynamic (PD) profiles of escalating doses of RMC-5552 monotherapy in adult participants with relapsed/refractory solid tumors and to identify the recommended Phase 2 dose (RP2D).
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Number of participants with adverse events (AEs)
Timeframe: up to 3 years
Number of participants with dose limiting toxicities (DLTs)
Timeframe: 21 days