BMS provides update on regulatory review of Opdivo + Yervoy in first-line lung cancer

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Bristol-Myers Squibb Co. announced updates regarding regulatory actions by health authorities in the U.S. and European Union for the ongoing review of its applications for an indication in metastatic first-line non-small cell lung cancer with Opdivo (nivolumab) plus low-dose Yervoy (ipilimumab) in patients with tumor mutational burden ≥10 mutations/megabase.

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