REGULATORY

US FDA Probes Takeda’s Adzynma after Reported Pediatric Death

November 26, 2025
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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REGULATORY

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