A short review of ciraparantag in perspective of the currently available anticoagulant reversal agents.
Autor: | Leentjens J; Department of Internal Medicine & Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, the Netherlands. Electronic address: Jenneke.leentjens@radboudumc.nl., Middeldorp S; Department of Internal Medicine & Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, the Netherlands., Jung C; Heinrich-Heine-University Duesseldorf, Medical Faculty, Department of Cardiology, Pulmonology and Vascular Medicine, Duesseldorf, Germany. |
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Jazyk: | angličtina |
Zdroj: | Drug discovery today [Drug Discov Today] 2022 Oct; Vol. 27 (10), pp. 103332. Date of Electronic Publication: 2022 Aug 03. |
DOI: | 10.1016/j.drudis.2022.07.017 |
Abstrakt: | Despite the improved safety-profile of direct oral anticoagulants (DOACs), bleeding complications remain an important side effect of anticoagulant treatment. Although anticoagulant-specific antidotes are available, an universal anticoagulant reversal agent in case of life-threatening bleeding or emergency surgery is not yet available. Ciraparantag, a synthetic small molecule that inactivates heparins and DOAC, is a promising new reversal agent that has been investigated in phase 2 trials. In this short review we provide an overview of the preclinical and clinical evidence of ciraparantag, and compare strengths and weaknesses of ciraparantag and the currently available anticoagulant reversal strategies. (Copyright © 2022 The Author(s). Published by Elsevier Ltd.. All rights reserved.) |
Databáze: | MEDLINE |
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