On November 28, 2018, the Food and Drug Administration (FDA) approved gilteritinib (XOSPATA, Astellas Pharma) for treatment of adult patients who have relapsed or refractory.......
The US Food and Drug Administration (FDA) has accepted Astellas Pharma’s new drug application (NDA) for gilteritinib and granted priority review for the product’s use in the treatment of acute myeloid leukaemia (AML).