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Takeda launches Adzynma

Adzynma is the first recombinant ADAMTS13 enzyme replacement therapy for treating Congenital Thrombotic Thrombocytopenic Purpura.

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Takeda's FDA approval for life-threatening blood disorder

The first and only enzyme replacement therapy for the treatment of a very rare and complex blood disorder has been approved by the US Food and Drug Administration.

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Adzynma Approved for Congenital Thrombotic Thrombocytopenic Purpura

The FDA has approved Adzynma for prophylactic or on demand enzyme replacement therapy in patients with congenital thrombotic thrombocytopenic purpura.

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FDA Approves Adzynma for Treatment of Congenital Thrombotic Thrombocytopenic Purpura

Adzynma is the first product to be approved for the treatment of the rare blood disorder that has 90% mortality when left untreated.

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Takeda Pharmaceutical (TAK) Announces FDA Approval of ADZYNMA

Takeda Pharmaceutical (TAK) Announces FDA Approval of ADZYNMA
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