Massachusetts Society of Clinical Oncologists - FDA Approves gilteritinib (XOSPata) for treatment of adult patients who have relapsed or refractory AML

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FDA Approves gilteritinib (XOSPata) for treatment of adult patients who have relapsed or refractory AML

FDA Approves gilteritinib (XOSPata) for treatment of adult patients who have relapsed or refractory AML

14 Jan 2019 3:27 PM | Nathan Strunk (Administrator)

The U.S. Food and Drug Administration approved gilteritinib (Xospata; Astellas) for treatment of adult patients who have relapsed or refractory acut myeloid leukemia (AML) with a FLT3 mutation as detected by an FDA approved test. Read full press release.

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