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See today's BioWorld
Home » Pop quizartinib grades low as FDA panel puts red mark on OS in Daiichi AML effort
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Pop quizartinib grades low as FDA panel puts red mark on OS in Daiichi AML effort

May 15, 2019
By Randy Osborne
As expected, Tokyo-based Daiichi Sankyo Co. Ltd. faced rough sledding in its review by the FDA's Oncologic Drugs Advisory Committee (ODAC) of quizartinib tablets for adults with relapsed or refractory acute myeloid leukemia (AML) that is FMS-like tyrosine kinase (FLT) 3-internal tandem duplication (ITD) positive, as detected by an FDA-approved test.
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