caplacizumab treatment for acquired thrombotic thrombocytopenic purpura

Simona Sica, M. Scully, S. R. Cataland, F. Peyvandi, P. Coppo, P. Knöl, J. A. Kremer Hovinga, A. Metjian, J. De La Rubia, K. Pavenski, F. Callewaert, D. Biswas, H. De Winter, R. K. Zeldin

Risultato della ricerca: Contributo in rivistaArticolo in rivista

207 Citazioni (Scopus)


In acquired thrombotic thrombocytopenic purpura (TTP), an immune-mediated deficiency of the von Willebrand factor–cleaving protease ADAMTS13 allows unrestrained adhesion of von Willebrand factor multimers to platelets and microthrombosis, which result in thrombocytopenia, hemolytic anemia, and tissue ischemia. Caplacizumab, an anti–von Willebrand factor humanized, bivalent variable-domain-only immunoglobulin fragment, inhibits interaction between von Willebrand factor multimers and platelets. Methods In this double-blind, controlled trial, we randomly assigned 145 patients with TTP to receive caplacizumab (10-mg intravenous loading bolus, followed by 10 mg daily subcutaneously) or placebo during plasma exchange and for 30 days thereafter. The primary outcome was the time to normalization of the platelet count, with discontinuation of daily plasma exchange within 5 days thereafter. Key secondary outcomes included a composite of TTP-related death, recurrence of TTP, or a thromboembolic event during the trial treatment period; recurrence of TTP at any time during the trial; refractory TTP; and normalization of organ-damage markers.
Lingua originaleEnglish
pagine (da-a)335-346
Numero di pagine12
RivistaNew England Journal of Medicine
Stato di pubblicazionePubblicato - 2019


  • caplacizumab treatment for acquired


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