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FDA Approves Takeda’s ADZYNMA for cTTP

Phase 3 trial data showed efficacy, pharmacokinetic, safety and tolerability.

Takeda received approval from the U.S. FDA for ADZYNMA (ADAMTS13, recombinant-krhn) for the prophylactic and on-demand treatment of congenital thrombotic thrombocytopenic purpura (cTTP). ADZYNMA is the first and only FDA-approved recombinant ADAMTS13 (rADAMTS13) protein designed to address an unmet medical need in people with cTTP by replacing the deficient ADAMTS13 enzyme. TTP is an ultra-rare, chronic blood clotting disorder caused by a deficiency in the ADAMTS13 enzyme. It is associated wi...

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