TECVAYLI™ Approval Brings New Options For Multiple Myeloma Treatment

In October 2022, the U.S. Food and Drug Administration (FDA) granted accelerated TECVAYLI™ (teclistamab-cqyv) FDA approval, a bispecific B-cell maturation antigen (BCMA)-directed CD3 T-cell engager. For the treatment of adult patients with relapsed or refractory…











