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7.66636001228099E-05 0.000306654400490804 -0.000613308800981172 -0.000919963201471976 -0.00229990800367972 -0.000153327200245184 0.000459981600735988 0.00168659920269855
Stock impact report

Agilent Companion Diagnostic Gains Expanded FDA Approval in Urothelial Carcinoma

Agilent Technologies, Inc. (A) 
Last agilent technologies, inc. earnings: 2/18 04:05 pm Check Earnings Report
US:NYSE Investor Relations: investor.agilent.com
Company Research Source: Business Wire
PD-L1 IHC 22C3 pharmDx Now Approved to Identify Certain Urothelial Carcinoma Patients for Treatment With KEYTRUDA® (pembrolizumab) SANTA CLARA, Calif.--(BUSINESS WIRE)-- Agilent Technologies Inc. (NYSE: A) today announced that the U.S. Food and Drug Administration (FDA) has approved its Dako PD-L1 IHC 22C3 pharmDx assay for expanded use in urothelial carcinoma. The assay is now approved to identify patients with urothelial carcinoma who may benefit from KEYTRUDA, an anti-PD-1 therapy manufactured by Merck (known as MSD outside the United States and Canada), as a first-line treatment option. KEYTRUDA is approved for patients with locally advanced or metastatic urothelial carcinoma who are not eligible for cisplatin-containing chemotherapy and whose tumors express PD-L1 [Combined Positive Score (CPS) = 10] as determined by an FDA-approved test, or in patients who are not eligible for any pl Show less Read more
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