Stopped: Business objectives have changed
This study will evaluate the safety, MTD and/or RP2D, PK, and clinical activity of the combination of adagrasib with nab-sirolimus in patients with advanced solid tumors/NSCLC with a KRAS G12C mutation.
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Phase 1: Safety and tolerability in the study population.
Timeframe: 30 months
Phase 1: Maximum tolerated dose (MTD) and Recommended Phase 2 Dose (RP2D)
Timeframe: 30 months
Phase 2: Objective Response Rate (ORR) using Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) (Phase 2)
Timeframe: 30 months