The latest data and expert opinions on BCMA-directed bispecific antibodies for multiple myeloma – including Johnson & Johnson’s Tecvayli (teclistamab-cqyv) and Pfizer’s Elrexfio (elranatamab-bcmm), which have US Food and Drug Administration approval, and Regeneron Pharmaceuticals’ linvoseltamab, which is pending at the FDA – are sparking discussions about how they will fit into the market relative to each other and relative to CAR-T cell therapies.
All three bispecifics were the subject of presentations at the American Society of Hematology annual meeting, which took place in San Diego between 7-10 December, including data from the Phase III MajesTEC-4 and the Phase II MajesTEC-5 trials of Tecvayli, the Phase Ib MagnetisMM-20 study and
Key Takeaways
- Multiple BCMA-directed bispecific antibodies for multiple myeloma were the subject of oral and poster presentations at ASH, showing a rapidly evolving marketplace.
- The plethora of data sparked discussion on how to position bispecifics relative to CAR-Ts as well as to each other
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