Dako, an Agilent Technologies Company, Announces Expanded Use of PD-L1 Diagnostic Test in Europe
Previously approved in the U.S. for non-squamous non-small-cell lung cancer (ns-NSCLC) and melanoma and later launched in Europe for ns-NSCLC, the PD-L1 IHC 28-8 pharmDx test has now been expanded to include melanoma in Europe. This allows physicians to determine PD-L1 expression for melanoma patients using a clinically validated test. The PD-L1 IHC 28-8 PharmDx test was used to assess PD-L1 expression in the CheckMate -067 trial and is now approved to be used as an aid in the assessment of patients for whom OPDIVO® (nivolumab) and YERVOY® (ipilimumab) combination treatment is being considered.
"This important launch enables standardized testing for PD-L1 expression," said Jacob Thaysen, president of Agilent's Diagnostics and Genomics Group. "Pathology laboratories in the EU now have access to CE-marked clinically-validated PD-L1 tests for ns-NSCLC correlated with outcomes from treatment with OPDIVO, and melanoma correlated with outcomes from combination treatment with OPDIVO® (nivolumab) and YERVOY® (ipilimumab)."
About Agilent Technologies and Dako
Agilent Technologies Inc. (NYSE: A), a global leader in life sciences, diagnostics and applied chemical markets, is the premier laboratory partner for a better world. Agilent works with customers in more than 100 countries, providing instruments, software, services and consumables for the entire laboratory workflow. The company generated revenues of \\$4.04 billion in fiscal 2015 and employs about 12,000 people worldwide.
In 2012, Agilent acquired Dako, a well-known provider of reagents, instruments, software and expertise. Agilent's Dako pathology solutions help pathologists make accurate diagnoses and determine the most effective treatment for cancer patients.
Information about Agilent is available at www.agilent.com, and information about Agilent's Dako pathology solutions is available here.
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