AbbVie (ABBV) announced that the EMA’s Committee for Medicinal Products for Human Use (CHMP) recommended approving the regulatory filing seeking approval for its ovarian cancer drug Elahere (mirvetuximab soravtansine) in the EU.AbbVie’s filing seeks marketing authorization for Elahere to treat adult patients with FRα-positive, platinum-resistant and high-grade serious epithelial ovarian, fallopian tube or primary peritoneal cancer who have received one to three prior treatments.This recommendation is based ...