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FDA approves Ventana CDx to ID patients eligible for Elahere

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Nov. 17, 2022—Roche announced FDA approval of the Ventana FOLR1 (FOLR1-2.1) RxDx assay, the first immunohistochemistry companion diagnostic test to aid in identifying epithelial ovarian cancer patients who are eligible for targeted treatment with Elahere (mirvetuximab soravtansine-gynx). Elahere is a first-in-class antibody-drug conjugate therapy developed by ImmunoGen and approved under the FDA’s accelerated approval program for the treatment of folate receptor alpha–positive platinum-resistant ovarian cancer.

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