Sanofi - Regeneron's Immunotherapy Scores European Approval For Skin And Lung Cancer Settings

  • The European Commission (EC) has approved Sanofi SA SNY and Regeneron Pharmaceuticals Inc's REGN Libtayo (cemiplimab) for two additional indications - basal cell carcinoma (BCC) and non-small cell lung cancer with over 50% PD-L1 expression.
  • BCC (skin cancer) approval covers adults with locally advanced or metastatic disease who have progressed on or are intolerant to a hedgehog pathway inhibitor.
  • Concurrently, the Commission approved Libtayo for the first-line treatment of adult patients with advanced non-small-cell lung cancer whose tumor cells have over 50% PD-L1 expression and no EGFR, ALK, or ROS1 aberrations. 
  • In 2019, Libtayo was approved by the EC as the first treatment for adults with metastatic or locally advanced cutaneous squamous cell carcinoma who are not candidates for curative surgery or curative radiation.
  • Libtayo is now approved by the European Commission for three advanced cancers.
  • Price Action: REGN shares closed at $544.4, and SNY closed at $52.32 on Friday.
Market News and Data brought to you by Benzinga APIs
Comments
Loading...
Posted In: BiotechNewsHealth CareFDAGeneralBriefslung cancerSkin Cancer
Benzinga simplifies the market for smarter investing

Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.

Join Now: Free!