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FDA grants accelerated approval to tafasitamab-cxix (Monjuvi) for diffuse large B-cell lymphoma

05 Aug 2020 9:55 AM | Nathan Strunk (Administrator)

The U.S. Food and Drug Administration granted accelerated approval to tafasitamab-cxix (MONJUVI, MorphoSys US Inc.), a CD19-directed cytolytic antibody, indicated in combination with lenalidomide for adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) not otherwise specified, including DLBCL arising from low grade lymphoma, and who are not eligible for autologous stem cell transplant. Read full press release.

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