The VENTANA FOLR1 RxDx Assay has received CE Mark approval, identifying ovarian cancer patients compatible with the ELAHERE treatment, marking a significant advancement in diagnostics.
This assay is the first widely available immunohistochemistry companion diagnostic in Europe focused on targeting epithelial ovarian cancer patients for ELAHERE therapy.
Regulators granted early exemption approval for the test in Germany and Austria, indicating its urgent need and potential to improve patient treatment decisions.
ELAHERE is a pioneering antibody-drug conjugate created by AbbVie, specifically aimed at treating FRɑ-positive, platinum-resistant ovarian cancer.
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