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Agilent Technologies receives US FDA approval for MAGE-A4 IHC 1F9 pharmDx
Precision Medicine
Aug 2, 2024
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Precision Medicine

Precision Medicine

Aug 2, 2024

Agilent Technologies receives US FDA approval for MAGE-A4 IHC 1F9 pharmDx

FDA approval

  • Agilent Technologies has received US FDA approval for its MAGE-A4 IHC 1F9 pharmDx, a diagnostic tool used to detect MAGE-A4 (melanoma-associated antigen A4), a cancer antigen found in various cancers, including synovial sarcoma, within formalin-fixed paraffin-embedded synovial sarcoma tissue.

  • MAGE-A4 IHC 1F9 pharmDx is claimed to be the first of its kind in the market and aids in marking eligible patients for TECELRA treatment, a prescription medication approved for treating advanced MAGE-A4 positive synovial sarcoma in adults with specific HLA types who have previously undergone chemotherapy.

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