EC grants approval for AbbVie’s Elahere in ovarian cancer
The European Commission (EC) on Monday granted marketing authorization for Elahere (mirvetuximab soravtansine) from US pharma major AbbVie (NYSE: ABBV).
The drug is approved for the treatment of adult patients with folate receptor-alpha (FRα) positive, platinum-resistant high grade serous epithelial ovarian, fallopian tube or primary peritoneal cancer who have received one to three prior systemic treatment regimens.
AbbVie says that Elahere is the first and only folate receptor alpha (FRɑ)-directed antibody drug conjugate (ADC) medicine approved in the European Union (EU), as well as Iceland, Liechtenstein, Norway, and Northern Ireland.
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