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FDA Issues Complete Response Letter for Quizartinib in AML

Jason M. Broderick @jasoncology
Published: Friday, Jun 21, 2019

Antoine Yver, MD

Antoine Yver, MD
The FDA has issued a complete response letter to Daiichi Sankyo informing the company that its new drug application (NDA) would not be approved for quizartinib for the treatment of adult patients with relapsed/refractory FLT3-ITD–positive acute myeloid leukemia (AML).
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