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Bridging the Missing Link with Emicizumab: A Bispecific Antibody for Treatment of Hemophilia A.

Abstract
Hemophilia A, characterized by absent or ineffective coagulation factor VIII (FVIII), is a serious bleeding disorder that entails severe and potentially life-threatening bleeding events. Current standard therapy still involves replacement of FVIII, but is often complicated by the occurrence of neutralizing alloantibodies (inhibitors). Management of patients with inhibitors is challenging and necessitates immune tolerance induction for inhibitor eradication and the use of bypassing agents (activated prothrombin complex concentrates or recombinant activated factor VII), which are expensive and not always effective. Emicizumab is the first humanized bispecific monoclonal therapeutic antibody designed to replace the hemostatic function of activated FVIII by bridging activated factor IX and factor X (FX) to activate FX and allow the coagulation cascade to continue. In the majority of hemophilic patients with and without inhibitors, emicizumab reduced the annualized bleeding rate to almost zero in several clinical trials and demonstrated a good safety profile. However, the concurrent use of emicizumab and activated prothrombin complex concentrate imposes a high risk of thrombotic microangiopathy and thromboembolic events on patients and should be avoided. Yet, the management of breakthrough bleeds and surgery remains challenging with only limited evidence-based recommendations being available. This review summarizes published clinical trials and preliminary reports of emicizumab and discusses the clinical implications of emicizumab in treatment of hemophilia A.
AuthorsGeorg Gelbenegger, Christian Schoergenhofer, Paul Knoebl, Bernd Jilma
JournalThrombosis and haemostasis (Thromb Haemost) Vol. 120 Issue 10 Pg. 1357-1370 (Oct 2020) ISSN: 2567-689X [Electronic] Germany
PMID32717759 (Publication Type: Journal Article, Review)
CopyrightThieme. All rights reserved.
Chemical References
  • Antibodies, Bispecific
  • Antibodies, Monoclonal, Humanized
  • Isoantibodies
  • emicizumab
  • F8 protein, human
  • Factor VIII
Topics
  • Animals
  • Antibodies, Bispecific (immunology, pharmacokinetics, therapeutic use)
  • Antibodies, Monoclonal, Humanized (immunology, pharmacokinetics, therapeutic use)
  • Blood Coagulation (drug effects)
  • Factor VIII (analysis, immunology, therapeutic use)
  • Hemophilia A (blood, drug therapy, immunology)
  • Humans
  • Isoantibodies (blood, immunology)

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