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The US Food and Drug Administration (FDA) has approved belantamab mafodotin-blmf (Blenrep) for adult patients with relapsed or refractory multiple myeloma who have received at least 4 prior therapies, including an anti-CD38 monoclonal antibody, a proteasome inhibitor, and an immunomodulatory agent...
The US Food and Drug Administration (FDA) granted accelerated approval to tafasitamab-cxix (Monjuvi), 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,...
The US Food and Drug Administration (FDA) approved brexucabtagene autoleucel (Tecartus) for the treatment of adult patients diagnosed with mantle cell lymphoma (MCL) who have not responded to or who have relapsed following other kinds of treatment. Tecartus, a chimeric antigen receptor (CAR) T-...
The US Food and Drug Administration (FDA) granted accelerated approval to selinexor (Xpovio) for adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), including DLBCL arising from follicular lymphoma, after at least 2 lines of systemic therapy. Approval was based on...
The US Food and Drug Administration (FDA) granted accelerated approval to tazemetostat (Tazverik.), an EZH2 inhibitor, for adult patients with relapsed or refractory follicular lymphoma whose tumours are positive for an EZH2 mutation as detected by an FDA-approved test and who have received at...

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