Clinical study of ivonescimab for first-line treatment of metastatic NSCLC patients with high PD-L1. Evaluating overall survival and progression free survival.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
780
Subject will receive ivonescimab as an IV injection
Subject will receive Pembrolizumab as an IV injection
Overall Survival (OS)
Time frame: Up to approximately 36 months
Progression free survival (PFS)
Time frame: Up to approximately 36 months
Objective response rate (ORR)
Time frame: Up to approximately 36 months
Disease control rate ( DCR)
Time frame: Up to approximately 36 months
Duration of response (DoR)
Time frame: Up to approximately 36 months
Adverse Events (AE): incidence and severity of adverse events (AEs) and clinically significant abnormal laboratory test results
Time frame: [Time Frame: From the subject signs the ICF to 30 days (AE) and 90 days (SAE related to ivonescimab/pembrolizumab ) after the last dose of study treatment or initiation of other anticancer therapy, whichever occurs first, Up to approximately 24 months.
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Clinical Study Site
Chandler, Arizona, United States
RECRUITINGClinical Study Site
Phoenix, Arizona, United States
RECRUITINGClinical Study Site
Hot Springs, Arkansas, United States
RECRUITINGClinical Study Site
Cerritos, California, United States
RECRUITINGClinical Study Site
Glendale, California, United States
RECRUITINGClinical Study Site
Irvine, California, United States
RECRUITINGClinical Study Site
Los Angeles, California, United States
RECRUITINGClinical Study Site
Mountain View, California, United States
RECRUITINGClinical Study Site
Murrieta, California, United States
RECRUITINGClinical Study Site
Newport Beach, California, United States
RECRUITING...and 192 more locations