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Live News REGULATION ARTICLE M impact

FDA grants Priority Review for Genentech’s Enspryng sBLA for MOGAD

Genentech said the U.S. Food and Drug Administration granted Priority Review to a supplemental Biologics License Application for Enspryng (satralizumab) for treatment of myelin oligodendrocyte glycoprotin-associated disease (MOGAD).

ROP

S. Food and Drug Administration (FDA) has granted Priority Review to a supplemental Biologics License Application (sBLA) for Enspryng® (satralizumab) in myelin oligodendrocyte glycoprot… treatment.