The purpose of this study is to characterize the safety and tolerability of KFA115 and KFA115 in combination with pembrolizumab in patients with select advanced cancers, and to identify the maximum tolerated dose and/or recommended dose.
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Incidence and severity of dose limiting toxicities (DLTs) during the DLT evaluation period of single-agent KFA115 (dose escalation only)
Timeframe: 28 days
Incidence and severity of dose limiting toxicities (DLTs) during the DLT evaluation period of KFA115 in combination with pembrolizumab (dose escalation only)
Timeframe: 28 days
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs)
Timeframe: 35 months
Frequency of dose interruptions, reductions
Timeframe: 35 months
Dose intensity
Timeframe: 35 months