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Eftrenonacog Alfa: A Review in Haemophilia B
Eftrenonacog alfa (Alprolix(®)) is an extended half-life recombinant factor IX (rFIX)-Fc fusion protein (hereafter referred to as rFIXFc). Administered as an intravenous bolus, it is approved for prophylactic use and the treatment of bleeding in patients with haemophilia B in various countries world...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247827/ https://www.ncbi.nlm.nih.gov/pubmed/37081241 http://dx.doi.org/10.1007/s40265-023-01868-7 |
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author | Lamb, Yvette N. Hoy, Sheridan M. |
author_facet | Lamb, Yvette N. Hoy, Sheridan M. |
author_sort | Lamb, Yvette N. |
collection | PubMed |
description | Eftrenonacog alfa (Alprolix(®)) is an extended half-life recombinant factor IX (rFIX)-Fc fusion protein (hereafter referred to as rFIXFc). Administered as an intravenous bolus, it is approved for prophylactic use and the treatment of bleeding in patients with haemophilia B in various countries worldwide, including those of the EU, as well as the USA. In multinational, phase III trials, rFIXFc was effective for the prophylaxis, perioperative management or on-demand treatment of bleeding in male patients with severe haemophilia B regardless of age and irrespective of whether or not they had been previously treated with FIX replacement products. Prophylactic efficacy was maintained over the longer term (up to 5 years) in previously treated patients. rFIXFc effectiveness in the real-world setting is supported by results of prospective studies, as well as the outcomes of several retrospective trials. rFIXFc was well tolerated in clinical trials in previously treated and untreated children, adolescents and/or adults with severe haemophilia B. Thus, rFIXFc continues to represent a useful treatment option among the haemophilia B patient population. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40265-023-01868-7. |
format | Online Article Text |
id | pubmed-10247827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-102478272023-06-09 Eftrenonacog Alfa: A Review in Haemophilia B Lamb, Yvette N. Hoy, Sheridan M. Drugs Adis Drug Evaluation Eftrenonacog alfa (Alprolix(®)) is an extended half-life recombinant factor IX (rFIX)-Fc fusion protein (hereafter referred to as rFIXFc). Administered as an intravenous bolus, it is approved for prophylactic use and the treatment of bleeding in patients with haemophilia B in various countries worldwide, including those of the EU, as well as the USA. In multinational, phase III trials, rFIXFc was effective for the prophylaxis, perioperative management or on-demand treatment of bleeding in male patients with severe haemophilia B regardless of age and irrespective of whether or not they had been previously treated with FIX replacement products. Prophylactic efficacy was maintained over the longer term (up to 5 years) in previously treated patients. rFIXFc effectiveness in the real-world setting is supported by results of prospective studies, as well as the outcomes of several retrospective trials. rFIXFc was well tolerated in clinical trials in previously treated and untreated children, adolescents and/or adults with severe haemophilia B. Thus, rFIXFc continues to represent a useful treatment option among the haemophilia B patient population. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40265-023-01868-7. Springer International Publishing 2023-04-21 2023 /pmc/articles/PMC10247827/ /pubmed/37081241 http://dx.doi.org/10.1007/s40265-023-01868-7 Text en © Springer Nature 2023, corrected publication 2023 https://creativecommons.org/licenses/by-nc/4.0/ Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Adis Drug Evaluation Lamb, Yvette N. Hoy, Sheridan M. Eftrenonacog Alfa: A Review in Haemophilia B |
title | Eftrenonacog Alfa: A Review in Haemophilia B |
title_full | Eftrenonacog Alfa: A Review in Haemophilia B |
title_fullStr | Eftrenonacog Alfa: A Review in Haemophilia B |
title_full_unstemmed | Eftrenonacog Alfa: A Review in Haemophilia B |
title_short | Eftrenonacog Alfa: A Review in Haemophilia B |
title_sort | eftrenonacog alfa: a review in haemophilia b |
topic | Adis Drug Evaluation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247827/ https://www.ncbi.nlm.nih.gov/pubmed/37081241 http://dx.doi.org/10.1007/s40265-023-01868-7 |
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