Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
Days after Japan OK, FDA Spurns Daiichi Sankyo’s Quizartinib
The US FDA has turned down Daiichi Sankyo’s FLT3 inhibitor quizartinib for the treatment of adult patients with relapsed/refractory FLT3-ITD acute myeloid leukemia (AML), the company said on June 21, just three days after the drug won approval on the…
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