The U.S. Food and Drug Administration (FDA) has approved Genentech‘s Tecentriq (atezolizumab) as an initial treatment of people with metastatic non-small cell lung cancer (NSCLC) whose tumors produce high levels of the PD-L1 protein but have no alterations in the EGFR or ALK genes. Approval was based on findings from the IMpower110 Phase 3 trial (NCT02409342), which showed that Tecentriq significantly extended patients’ survival compared with chemotherapy, without impacting quality of life. This is the second immunotherapy regimen…

May 21, 2020May 21, 2020