Pharmacokinetic and safety considerations when switching from standard to extended half-life clotting factor concentrates in hemophilia
Author:
Affiliation:
1. Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Italian Association of Haemophilia Centres (AICE), Milan, Italy
2. Faculty of Medicine, Dentistry & Health Sciences, University of Western Australia, Crawley, Australia
Publisher
Informa UK Limited
Subject
Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/17474086.2019.1645002
Reference67 articles.
1. Prospective study of the evaluation of hepatitis C virus infectivity in a high-purity, solvent/detergent-treated factor VIII concentrate: parallel evaluation of other markers for lipid-enveloped and non-lipid- enveloped viruses. The Ad Hoc Study Group of the Fondazione dell'Emofilia
2. Human immunodeficiency and hepatitis virus infections and their associated conditions and treatments among people with haemophilia
3. Pharmacokinetic-based prediction of real-life dosing of extended half-life clotting factor concentrates on hemophilia
4. The use of enhanced half-life coagulation factor concentrates in routine clinical practice: guidance from UKHCDO
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Efanesoctocog alfa elicits functional clot formation that is indistinguishable to that of recombinant factor VIII;Journal of Thrombosis and Haemostasis;2022-07
2. Prophylaxis for hemophilia A without inhibitors: treatment options and considerations;Expert Review of Hematology;2020-06-23
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