Takeda Pharmaceutical has obtained the backing of a key European regulatory panel for the approval, under exceptional circumstances, of its recombinant ADAMTS13, known as Adzynma.The European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) issued a positive…
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We had just gotten off a call with a client in Europe, and we’d received a bit of an earful. “Philip,” the client pressed, “what can this candidate bring to us? We know what he does, but what has he…





