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  • FDA accepts BMS’s application for non-small cell lung cancer treatment pharmaceutical-technology
    June 28, 2018
    The US Food and Drug Administration (FDA) has accepted Bristol-Myers Squibb Company’s (BMY) supplemental biologics licence application (sBLA) for Opdivo (nivolumab) plus low-dose Yervoy (ipilimumab) to treat first-line advanced non-small cell lung cancer

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