MOR - MorphoSys FDA Approval And Other News: The Good Bad And Ugly Of Biopharma
MorphoSys receives FDA approval for Monjuvi
MorphoSys AG (MOR) announced that the FDA has approved the use of Monjuvi in conjunction with lenalidomide, for treating adult patients suffering from relapsed/refractory diffuse large B-cell lymphoma (DLBCL) not otherwise specified, including DLBCL concerning low grade lymphoma, and who do not qualify for autologous stem cell transplant. The company is collaborating with Incyte (INCY) for developing this drug candidate.
Monjuvi is the first FDA approval for a second-line treatment for adult patients with the condition. Jean-Paul Kress, M.D., Chief Executive Officer, MorphoSys said “This approval marks