Pharmaceutical Japanese drug major Astellas Pharma’s New Drug Application (NDA) for the oral once-daily therapy Xospata (gilteritinib), for the treatment of adult patients who have relapsed (disease that has returned) or refractory (resistant to treatment) acute myeloid leukemia (AML) with a FLT3 mutation (FLT3mut+), has been accepted by the National Medical Products Administration (NMPA) for regulatory review in China. 10 April 2020