Emicizumab: A Review in Haemophilia A
online resource
posted on 2019-09-22, 18:52 authored by Hannah A. Blair<p><b>Compliance with Ethical Standards</b></p>
<p><b>Funding</b> The preparation of this review was not supported by
any external funding.</p>
<p><b>Conflicts of interest<i> </i></b>Hannah Blair is a salaried employee
of Adis International Ltd/Springer Nature, is responsible for the article
content and declares no relevant conflicts of interest.</p>
<p> </p>
<p>Additional information about this Adis
Drug Review can be found <b><a href="http://www.springer.com/gp/adis/products-services/adis-journals-newsletters/adis-drug-reviews">here</a></b></p>
<p> </p>
<p><b>Abstract</b></p>
<p>Emicizumab (Hemlibra<sup>®</sup>), a recombinant, humanized, bispecific monoclonal
antibody, restores the function of missing activated factor VIII (FVIII) by
bridging FIXa and FX to facilitate effective haemostasis in patients with
haemophilia A. Subcutaneous emicizumab is approved in several countries,
including in the USA and Japan, for the routine prophylaxis of bleeding
episodes in patients with haemophilia A with or without FVIII inhibitors. It is
also approved in the EU for the routine prophylaxis of bleeding episodes in
patients with haemophilia A with inhibitors or severe haemophilia A without
inhibitors. In phase III clinical trials, emicizumab prophylaxis significantly
reduced annualized bleeding rates compared with no prophylaxis in adolescents
and adults with haemophilia A with or without inhibitors, and prevented or substantially reduced bleeding in
children with haemophilia A with or without inhibitors. Emicizumab was also associated with beneficial effects
on health-related quality of life and health status, and was generally well
tolerated. In view of its convenient
route of administration and versatile dosage regimens (maintenance dose of once
every 1, 2 or 4 weeks), emicizumab provides an effective and generally
well-tolerated alternative to conventional FVIII replacement products for the
prophylaxis of bleeding episodes in patients with haemophilia A, regardless of the presence or absence of
inhibitors.</p>
<p> </p>
<p>© Springer Nature
Switzerland AG 2019</p>
<p> </p>
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