This is a first-in-human, Phase 1/2, multicenter, open-label study designed to evaluate the safety and tolerability of vilastobart (XTX101) as monotherapy and vilastobart (XTX101) and atezolizumab combination therapy in patients with advanced solid tumors.
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Incidence of Dose Limiting Toxicities (DLTs) in Part 1A
Timeframe: Cycle 1 Day 1 up to just prior to the second dose of study drug at Cycle 2 day 1 (approximately 3 weeks)
Incidence of Dose Limiting Toxicities (DLTs) in Part 1C
Timeframe: Cycle 1 Day 1 up to Cycle 3 Day 1 (approximately 6 weeks)
Incidence of treatment-emergent adverse events in Part 1
Timeframe: Up to 24 months
Incidence of changes in clinical laboratory abnormalities in Part 1
Timeframe: Up to 24 months
Investigator-assessed objective response rate (ORR) per iRECIST in Phase 2
Timeframe: Up to 24 months