Study of NGM707 as Monotherapy and in Combination with Pembrolizumab in Advanced or Metastatic Solid Tumor Malignancies
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Number of Patients with Dose-limiting Toxicities
Timeframe: Baseline up to 28 Days
Incidence of Adverse Events
Timeframe: Baseline up to Approximately 24 Months
Number of Patients with Clinically Significant Laboratory Abnormalities
Timeframe: Baseline up to Approximately 24 Months
Number of Patients in Expansion Cohorts with Objective Responses
Timeframe: Baseline up to approximately 24 months
Duration of Response for Patients in Expansion Cohorts
Timeframe: Baseline up to approximately 24 months
Progression-free Survival for Patients in Expansion Cohorts
Timeframe: Baseline up to approximately 24 months
Overall Survival for Patients in Combination Dose Expansion Cohorts
Timeframe: Up to approximately 48 months