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FDA
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On December 22, 2022, the Food and Drug Administration (FDA) granted accelerated approval to mosunetuzumab-axgb (Lunsumio, Genentech, Inc.), a bispecific CD20-directed CD3 T-cell engager for adult patients with relapsed or refractory follicular lymphoma (FL).
Baca selengkapnya di : http://www.fda.gov...
Baca selengkapnya di : http://www.fda.gov...