Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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Takeda Scores 1st US Nod for Ultra-Rare Blood Clotting Disorder
Takeda Pharmaceutical said on November 9 that it has bagged US regulatory clearance for Adzynma as the first FDA-approved therapy for an ultra-rare blood clotting disorder called congenital thrombotic thrombocytopenic purpura (cTTP). Adzynma, a recombinant form of the ADAMTS13 protein,…
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