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Half‐life extended factor VIII for the treatment of hemophilia A

Authors :
Andreas Tiede
Source :
Journal of Thrombosis and Haemostasis. 13:S176-S179
Publication Year :
2015
Publisher :
Elsevier BV, 2015.

Abstract

Prophylactic infusion of factor VIII (FVIII) prevents joint bleeding and other hemorrhages in patients with hemophilia A. Conventional FVIII concentrates have a short half-life, with an average of about 12 h in adults, ranging in individual patients between 6 and 24 h, and even shorter in younger children. Therefore, effective prophylaxis requires frequent intravenous injection, usually three times per week or every other day. Several technologies are currently under investigation to extend the half-life of FVIII, including Fc fusion (Eloctate, Elocta, efmoroctocog alfa), addition of polyethylene glycol (turoctocog alfa pegol [N8-GP], BAY 94-9027, BAX 855), and a single-chain construct (CSL627). This review summarizes characteristics of products in clinical development and discusses their potential benefits.

Details

ISSN :
15387836
Volume :
13
Database :
OpenAIRE
Journal :
Journal of Thrombosis and Haemostasis
Accession number :
edsair.doi.dedup.....61a581323e93394c6bab487817385cd3
Full Text :
https://doi.org/10.1111/jth.12929