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Agilent Receives FDA Approval for PD-L1 IHC 22C3 pharmDx in Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Carcinoma (EOC)
Agilent Technologies, Inc. (A)
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Source: Business Wire
Last agilent technologies, inc. earnings: 2/18 04:05 pm
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US:NYSE Investor Relations: investor.agilent.com
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Approval expands first-line PD-L1 testing to support treatment decisions with KEYTRUDA® (pembrolizumab)1, 2 SANTA CLARA, Calif.--(BUSINESS WIRE)--Agilent Technologies
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