This is a Phase 1, open-label, dose-escalation and expansion study, evaluating the safety, tolerability, pharmacokinetics (PK), preliminary antitumor activity, and effect on biomarkers of XL092 administered alone, in combination with atezolizumab, and in combination with avelumab to subjects with advanced solid tumors.
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Dose-Escalation Stage: MTD/recommended dose for XL092
Timeframe: Up to 24 months
Cohort-Expansion Stage: Objective Response Rate (ORR)
Timeframe: Up to 24 months
Cohort-Expansion Stage (except Cohort H): Progression-Free Survival (PFS)
Timeframe: Up to 24 months
Cohort-Expansion Stage (Cohort H only): Overall Survival (OS)
Timeframe: Up to 24 months