Astellas' XOSPATA® (gilteritinib) Receives Conditional Approval by China's National Medical Products Administration for Relapsed or Refractory Acute Myeloid Leukemia with a FLT3 Mutation - Accelerated approval follows priority review designation and inclusion in overseas new drugs urgently needed in clinical settings - XOSPATA® is the first and only FLT3 inhibitor approved by the NMPA for patients with relapsed or refractory AML News provided by Share this article Share this article TOKYO, Feb. 3, 2021 /PRNewswire/ -- Astellas Pharma Inc. (TSE: 4503, President and CEO: Kenji Yasukawa, Ph.D., "Astellas") today announced that the China National Medical Products Administration (NMPA) has granted conditional approval to XOSPATA