This is a Phase 1, open-label, multicenter, study of the safety, tolerability, PK, PD, and anti-tumor activity of MRTX1719 patients with advanced, unresectable or metastatic solid tumor malignancy with homozygous deletion of the MTAP gene.
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Number of Patients who Experience Dose-Limiting Toxicity
Timeframe: 21 days
Number of patients who experience a treatment-related adverse event
Timeframe: Up to 2 years
Objective response rate (ORR)
Timeframe: 2 years
Duration of response (DOR)
Timeframe: 2 years
Progression free survival (PFS)
Timeframe: 2 years
Overall survival (OS)
Timeframe: 2 years
Number of Patients With Clinically Significant Laboratory Assessments
Timeframe: Up to 4 years
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