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Home › Diagnostics › Molecular Diagnostics › FDA Approves Expanded Use of Agilent Assay as Keytruda CDx for Cervical Cancer

FDA Approves Expanded Use of Agilent Assay as Keytruda CDx for Cervical Cancer

Jun 12, 2018
|
staff reporter

NEW YORK (GenomeWeb) – Agilent Technologies said after the close of the market on Tuesday that the US Food and Drug Administration has approved the Dako PD-L1 IHC 22C3 pharmDx assay for expanded use as a companion diagnostic test for Keytruda (pembrolizumab) for cervical cancer.

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