Cargando…
Factor Xa inhibitors: critical considerations for clinical development and testing
The selection of factor (F) X and its activated protease FXa for targeted inhibition to prevent and treat thrombotic conditions is based on an understanding of coagulation biochemistry, sequential steps that occur on tissue factor bearing cells and the interface of coagulation proteins, platelets, m...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122197/ https://www.ncbi.nlm.nih.gov/pubmed/33991266 http://dx.doi.org/10.1007/s11239-021-02455-x |
_version_ | 1783692537147424768 |
---|---|
author | Becker, Richard C. |
author_facet | Becker, Richard C. |
author_sort | Becker, Richard C. |
collection | PubMed |
description | The selection of factor (F) X and its activated protease FXa for targeted inhibition to prevent and treat thrombotic conditions is based on an understanding of coagulation biochemistry, sequential steps that occur on tissue factor bearing cells and the interface of coagulation proteins, platelets, mononuclear cells and the nuclear constituents of inflammatory cells. The goal for developing direct oral FXa inhibitors was to achieve rapid, selective, predictable, safe and effective anticoagulation across a broad group of patients expected to derive benefit. The history and development in patient care are exemplars of knowledge, translation and collaboration between the public and private sectors. |
format | Online Article Text |
id | pubmed-8122197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-81221972021-05-17 Factor Xa inhibitors: critical considerations for clinical development and testing Becker, Richard C. J Thromb Thrombolysis Article The selection of factor (F) X and its activated protease FXa for targeted inhibition to prevent and treat thrombotic conditions is based on an understanding of coagulation biochemistry, sequential steps that occur on tissue factor bearing cells and the interface of coagulation proteins, platelets, mononuclear cells and the nuclear constituents of inflammatory cells. The goal for developing direct oral FXa inhibitors was to achieve rapid, selective, predictable, safe and effective anticoagulation across a broad group of patients expected to derive benefit. The history and development in patient care are exemplars of knowledge, translation and collaboration between the public and private sectors. Springer US 2021-05-15 2021 /pmc/articles/PMC8122197/ /pubmed/33991266 http://dx.doi.org/10.1007/s11239-021-02455-x Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Becker, Richard C. Factor Xa inhibitors: critical considerations for clinical development and testing |
title | Factor Xa inhibitors: critical considerations for clinical development and testing |
title_full | Factor Xa inhibitors: critical considerations for clinical development and testing |
title_fullStr | Factor Xa inhibitors: critical considerations for clinical development and testing |
title_full_unstemmed | Factor Xa inhibitors: critical considerations for clinical development and testing |
title_short | Factor Xa inhibitors: critical considerations for clinical development and testing |
title_sort | factor xa inhibitors: critical considerations for clinical development and testing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122197/ https://www.ncbi.nlm.nih.gov/pubmed/33991266 http://dx.doi.org/10.1007/s11239-021-02455-x |
work_keys_str_mv | AT beckerrichardc factorxainhibitorscriticalconsiderationsforclinicaldevelopmentandtesting |