Opdivo keeps growing with new approval in lung cancer

7 March 2022

New York-based cancer specialist Bristol Myers Squibb (NYSE: BMY) has picked up a new US Food and Drug Administration approval for its checkpoint blocker Opdivo (nivolumab).

The label update covers use of the therapy, in combination with platinum-doublet chemotherapy, to treat non-small cell lung cancer (NSCLC) in the neoadjuvant setting.

The approval is based on the CheckMate -816 trial, which met primary endpoints of event-free survival (EFS) and pathologic complete response (pCR).

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