EMA validates MAA for tafasitamab + lenalidomide to treat relapsed or refractory diffuse large B-cell lymphoma . Incyte + Morphosys AG
Incyte and MorphoSys AG announced the validation of the European Marketing Authorization Application (MAA) for tafasitamab, an anti-CD19 antibody. The application seeks approval of tafasitamab in combination with… read more.