PO65 | Utilization of emicizumab in acquired hemophilia A: a case report

Background: Acquired hemophilia A (AHA) is a severe bleeding disorder caused by autoantibodies against coagulation Factor VIII (FVIII). Treatment consists of bleeding control with bypassing agents and immunosuppressive therapy (IST). Emicizumab, a bispecific antibody that mimics the function of act...

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Bibliographic Details
Format: Article
Language:English
Published: PAGEPress Publications 2025-08-01
Series:Bleeding, Thrombosis and Vascular Biology
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Online Access:https://www.btvb.org/btvb/article/view/334
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