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European Medicines Agency Validates Bristol Myers Squibb’s Application for Opdivo

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Jan 05

FDA Grants Priority Review to Merck’s Supplemental Biologics License Application for KEYTRUDA

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Dec 18

Bristol Myers Squibb Receives European Commission Approval for Opdivo

Bristol Myers Squibb announced the approval of Opdivo for the treatment of adults with unresectable advanced, recurrent or metastatic esophageal squamous cell carcinoma ...
Nov 25
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