Agilent receives EU approval for PD-L1 test in ovarian cancer
The approval enables pathologists to identify patients who may be eligible for treatment with pembrolizumab, expanding companion diagnostic indications in the EU.
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Manufacturer of analytical instruments and laboratory solutions
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In short: Agilent reported strong Q2 2026 financial growth, completed its acquisition of Biocare Medical, and secured several key FDA and EU approvals.
The approval enables pathologists to identify patients who may be eligible for treatment with pembrolizumab, expanding companion diagnostic indications in the EU.
The assay identifies PD-L1 expression in tumors, enabling treatment with nivolumab.
The module simplifies label-free imaging analysis by reducing manual cell segmentation and parameter tuning.
The deal expands Agilent's pathology portfolio and is expected to be accretive in the first year.
On July 23, 2026, Agilent Technologies Inc (A) announced the attainment of European Union...
Agilent Technologies Inc. (NYSE: A) today announced it has received European Union (EU) certification for PD-L1 IHC 22C3 pharmDx, Code SK006, as a companion diagnostic...
In July 2026, Agilent Technologies received U.S. Food and Drug Administration approval for its PD-L1 IHC 28-8 pharmDx assay as a companion diagnostic to identify...
Detailed price information for Agilent Technologies (A-N) from The Globe and Mail including charting and trades.
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