Agilent Technologies Receives FDA Approval For MAGE-A4 IHC 1F9 pharmDx As Diagnostic Tool To Identify Synovial Sarcoma Patients Eligible For TECELRA TCR T-Cell Therapy
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Agilent Technologies has received FDA approval for its MAGE-A4 IHC 1F9 pharmDx diagnostic tool, which will help identify synovial sarcoma patients eligible for TECELRA TCR T-Cell Therapy.
August 02, 2024 | 12:03 pm
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Agilent Technologies has received FDA approval for its MAGE-A4 IHC 1F9 pharmDx diagnostic tool, which will help identify synovial sarcoma patients eligible for TECELRA TCR T-Cell Therapy.
FDA approval is a significant milestone for Agilent Technologies, as it validates the efficacy and safety of their diagnostic tool. This approval is likely to boost investor confidence and positively impact the stock price in the short term.
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