FDA approves Astellas’ Xospata for FLT3-mutated acute myeloid leukemia


FDA approves Astellas’ Xospata for FLT3-mutated acute myeloid leukemia

Text FDA Approved appearing behind ripped brown paper.

The drug is the second FLT3 inhibitor to win approval, after Novartis’ Rydapt in first-line disease. Daiichi Sankyo’s quizartinib could present competition if it wins approval, but it would target a somewhat narrower population of FLT3-mutated patients.



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