Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
FDA Fast-Tracks Astellas’s AML Med Gilteritinib
Astellas Pharma said on October 11 that its FLT3/AXL inhibitor gilteritinib has earned the US FDA’s fast-track designation for the treatment of adult patients with FLT3 mutation-positive (FLT3+) relapsed or refractory acute myeloid leukemia (AML). Gilteritinib, also known with the…
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Japan’s all-important reimbursement policy panel on December 20 approved an outline of drug pricing reforms for FY2024, which enshrines a…