NewVac LLC reported meeting all primary endpoints in the phase II Clinical Trial of Quisinostat, novel selective oral histone deacetylase inhibitor, which NewVac licensed from Janssen Pharmaceutica NV.
EC granted marketing authorization for Elahere (mirvetuximab soravtansine) for the treatment of adult patients with folate receptor-alpha positive, platinum-resistant high grade serous epithelial ovarian, fallopian tube or primary peritoneal cancer who have received one to three prior systemic treatment regimens. Elahere is the first and only folate receptor alpha-directed antibody drug conjugate medicine approved in the EU, as well as Iceland, Liechtenstein, Norway, and Northern Ireland.
