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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US FDA Probes Takeda’s Adzynma after Reported Pediatric Death
The US FDA has issued a safety communication saying it is investigating a pediatric death in a patient treated with Takeda Pharmaceutical’s congenital thrombotic thrombocytopenic purpura (cTTP) therapy Adzynma (apadamtase alfa + cinaxadamtase alfa), in whom neutralizing antibodies to ADAMTS13…
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