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Emicizumab for acquired hemophilia A: Report of two cases and dosing strategies

Abstract Acquired hemophilia A (AHA) is a rare autoimmune bleeding disorder caused by autoantibodies against FVIII. Severe AHA is life‐threatening. Currently, licensed hemostatic agents for the treatment of severe AHA have short half‐lives and require intravenous administration, leading to a need fo...

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Huvudupphov: Faiza Ahmed, Mariia Kasianchyk, Alejandro Moreno, Simone Chang, Satish Maharaj
Materialtyp: Artigo
Språk:Inglês
Utgiven: Wiley 2024-04-01
Serie:eJHaem
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Länkar:https://doi.org/10.1002/jha2.878
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