FDA approves Daiichi Sankyo's new first-line AML drug quizartinib with boxed warning for heart disorders
Patients with a rarer form of acute myeloid leukemia now have a frontline treatment option for the first time, thanks to the FDA’s approval of Vanflyta (quizartinib), Daiichi Sankyo announced late Thursday.
Vanflyta has been approved for FLT3-ITD-positive AML patients in combination with chemo and as a maintenance monotherapy after initial treatment. The agency also approved a companion diagnostic to detect the mutation.
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