FDA approves Opdivo for lung cancer before and after surgery

4 October 2024

Bristol Myers Squibb (NYSE: BMY) has received a new approval from the US Food and Drug Administration for its blockbuster checkpoint blocker, Opdivo (nivolumab).

The nod covers use of the therapy, in combination with chemotherapy, as a perioperative treatment for adult patients with resectable non-small cell lung cancer (NSCLC).

The approval marks a key development for those without specific mutations like EGFR or ALK rearrangements.

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