FDA grants Priority Review to Roche’s Lunsumio for people with relapsed or refractory follicular lymphoma

FDA grants Priority Review to Roche’s Lunsumio for people with relapsed or refractory follicular lymphoma
Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that the U.S. Food and Drug Administration (FDA) has accepted the company’s Biologics License Application (BLA) and granted Priority Review for Lunsumio® (mosunetuzumab), a potential first-in-class CD20xCD3 T-cell engaging bispecific antibody, for the treatment of adults with relapsed or refractory (R/R) follicular lymphoma (FL) who have received at least two prior systemic therapies.