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While you may still be able to get your current supply until the cut-off date, March 19, 2025, its best to have a plan now so you have time to consider your options
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July 20: Four years after it was rejected by the FDA due to safety concerns, Daiichi Sankyos Vanflyta (quizartinib) won approval to treat patients with acute myeloid leukemia that has a FLT3-ITD gene mutation
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