Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
EMA Accepts Quizartinib Application, with Accelerated Assessment Status: Daiichi Sankyo
Daiichi Sankyo said on November 6 that the European Medicines Agency (EMA) has accepted a marketing approval application (MAA) for quizartinib for the treatment of adults with relapsed or refractory FLT3-ITD positive acute myeloid leukemia (AML). The regulators also granted…
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