This is a phase 1b study to assess the safety and tolerability of tarlatamab in combination with programmed death ligand (PD-L1) inhibition with and without chemotherapy.
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Number of Participants with a Dose Limiting Toxicity (DLT)
Timeframe: 24 months
Number of Participants with Treatment-emergent Adverse Events (TEAE)
Timeframe: 24 months
Number of Participants with Treatment-related Adverse Events
Timeframe: 24 months
Number of Participants with Clinically Significant Changes in Vital Signs
Timeframe: 24 months
Number of Participants with Clinically Significant Changes in Electrocardiogram (ECG) Measurements
Timeframe: 24 months
Number of Participants with Clinically Significant Changes in Clinical Laboratory Tests
Timeframe: 24 months