Regeneron announces FDA acceptance for sBLA review of Libtayo with chemotherapy for NSCLC

Regeneron Pharmaceuticals has announced the acceptance of U.S. Food and Drug Administration (FDA) for review of the supplemental Biologics License Application (sBLA) for PD-1 inhibitor Libtayo (cemiplimab-rwlc) along with chemotherapy as first-line treatment in advanced non-small cell lung cancer (NSCLC).