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Halfâlife extended factor VIII for the treatment of hemophilia A
- 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.
- Subjects :
- medicine.medical_specialty
Every other day
Pediatrics
Hemorrhage
Hemophilia A
Hemostatics
hemic and lymphatic diseases
Efmoroctocog alfa
Drug Discovery
medicine
Animals
Humans
In patient
Joint bleeding
Hemostasis
Factor VIII
business.industry
Half-life
Drugs, Investigational
Hematology
Turoctocog alfa
Recombinant Proteins
Surgery
Fc fusion
Treatment Outcome
business
Half-Life
Subjects
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