July 31st 2025
On July 2, linvoseltamab-gcpt (Lynozyfic; Regeneron) received an accelerated approval from the FDA in relapsed/refractory multiple myeloma (MM), and the most recent update to the National Comprehensive Cancer Network guidelines for MM has added the BCMA-targeted bispecific antibody as a preferred treatment option.
Experts explore the latest bispecific antibody approvals and clinical applications, discuss barriers in community oncology, address management of cytokine release syndrome, and consider how these therapies can expand patient access to care.
FDA Approves Brentuximab Vedotin, Lenalidomide, Rituximab Triplet for R/R LBCL
Treosulfan Regimen Approved for Allo-HSCT Conditioning in AML/MDS