Broader label to support greater US growth for Libtayo
The checkpoint blocker Libtayo (cemiplimab-rwlc) has secured US approval for the first-line treatment of certain adults with advanced non-small cell lung cancer (NSCLC).
The therapy is approved for use, in combination with platinum-based chemotherapy, in the treatment of cancer with no EGFR, ALK or ROS1 aberrations.
The product has been developed by French pharma major Sanofi (Euronext: SAN), together with its US partner Regeneron Pharmaceutical (Nasdaq: REGN).
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