FDA approves Regeneron’s Libtayo and chemotherapy combination for NSCLC
Pharmaceutical Technology
NOVEMBER 9, 2022
The US Food and Drug Administration (FDA) has approved Regeneron Pharmaceuticals ’ PD-1 inhibitor Libtayo (cemiplimab-rwlc) and chemotherapy combination as the first-line treatment for advanced non-small cell lung cancer (NSCLC). The regulatory approval is based on results obtained from the international Phase III EMPOWER-Lung 3 trial.
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