The purpose of this study is to determine the safety and tolerability of monotherapy CR-001 and identify the maximum tolerated dose (MTD), and/or optimal biologic dose and Recommended Phase 2 Dose(s) (RP2D) in participants with locally advanced or metastatic solid tumors.
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Dose Escalation - Incidence and nature of dose-limiting toxicities
Timeframe: From the first dose of study drug up until approximately 1 month
Dose Escalation - Characterization of the maximum tolerated dose, if applicable
Timeframe: From the first dose of study drug up until approximately 1 month
All parts - Incidence, nature, and severity of treatment emergent adverse events (TEAEs) and treatment - emergent serious adverse events
Timeframe: From the first dose of study drug until 90 days after the last dose of study drug
All parts - Incidence and severity of TEAEs leading to dose modifications
Timeframe: From the first dose of study drug until 90 days after the last dose of study drug
All parts - Incidence and severity of TEAEs leading to treatment discontinuation
Timeframe: From the first dose of study drug until 90 days after the last dose of study drug