Genentech says Phase III IMpower132 study met co-primary endpoint
Genentech, a member of the Roche Group, announced that the Phase III IMpower132 study met its co-primary endpoint of progression-free survival, or PFS, and demonstrated that the combination of TECENTRIQ plus chemotherapy reduced the risk of disease worsening or death, or PFS, compared to chemotherapy alone in the initial treatment of advanced non-squamous non-small cell lung cancer, or NSCLC. While a numerical improvement for the co-primary endpoint of overall survival, or OS, was observed, statistical significance was not met at this interim analysis, and the study will continue as planned with final OS results expected next year. Safety for the TECENTRIQ and chemotherapy combination appeared consistent with the known safety profile of the individual medicines, and no new safety signals were identified with the combination. These data will be presented at an upcoming medical meeting.