Aug 2026· Journal of Thrombosis and Haemostasis· 0 citations
Medicine
TL;DR
The fundamental pharmacological background of anticoagulants promotes better understanding of their current clinical applications, and progress in the development of FXI and FXII inhibitors may lead to innovative, effective anticoagulants with favorable safety profiles.
Abstract
Anticoagulants are the drugs of choice for the management of various thromboembolic disorders affecting both arteries and veins. This review delineates the pharmacological characteristics of currently available anticoagulants. The potential roles of novel investigational anticoagulants are also briefly discussed. Although heparins and warfarin are conventional anticoagulants with a number of limitations, a thorough understanding of their pharmacological properties can help prevent undesirable outcomes. Due to strong clinical evidence and more favorable pharmacological characteristics, direct oral anticoagulants are currently utilized in place of heparins and warfarin to treat a range of thromboembolic conditions, including prevention of cardioembolic stroke and systemic embolism secondary to atrial fibrillation and the management of venous thromboembolism. However, novel potent anticoagulants with low bleeding risk are needed. Emerging targets for the development of anticoagulants are clotting factor XI (FXI) and clotting factor XII (FXII). Currently, many FXI inhibitors are undergoing phase II or III clinical studies, whereas FXII inhibitors are mainly in the preclinical stage. Targeting FXI and FXII appears to promote low bleeding propensity. Overall, the fundamental pharmacological background of anticoagulants promotes better understanding of their current clinical applications. Progress in the development of FXI and FXII inhibitors may lead to innovative, effective anticoagulants with favorable safety profiles.
Thromboembolic diseases impose a significant burden on global health. However, the currently approved anticoagulant drugs, including heparin, vitamin K antagonists, and direct oral anticoagulants (DOACs), all carry certain bleeding risks. The proteases inhibited by these drugs play crucial roles in both pathological th...
Hui Yuan, Yuan-Yuan He, Mao Zhang et al.· Frontiers in Immunology· 0 citations
Cardiovascular diseases remain the leading global cause of morbidity and mortality, and thrombotic events contribute substantially to their clinical burden. Established anticoagulants, including vitamin K antagonists and direct oral anticoagulants, reduce thromboembolic events but remain limited by bleeding risk in sel...
Zhao-Wei Zhu, W. Gong, Xin-Qun Hu et al.· Vessel Plus· 0 citations
Anticoagulant therapy has undergone substantial evolution over the past century, progressing from early parenteral agents such as heparin to vitamin K antagonists (VKAs) and, more recently, to direct oral anticoagulants (DOACs). This review provides an overview of the major classes of anticoagulants, including unfracti...
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Following completion of the primary phase of anticoagulant therapy (ACT) in patients with venous thromboembolic complications (VTEs), discontinuation of anticoagulant agents significantly increases the risk of recurrent venous thrombosis and pulmonary embolism. This consideration provides a compelling rationale for con...
D. V. Rylnikov, E. V. Loginovskaya, E. S. An et al.· Journal of Venous Disorders· 0 citations
A pattern emerges, where FXI/FXIa inhibition offers a favorable safety profile across multiple settings and high-risk subgroups, yet clear efficacy has so far been established only in secondary prevention of noncardioembolic ischemic stroke over existing antiplatelet strategies.
Ermioni Oikonomou, Mark Goldin, A. Spyropoulos· Journal of Clinical Medicine· 0 citations
A unified theoretical framework is established, grounded in mechanistic rationale and supported by experimentation, to better define the pharmacodynamics of anticoagulation therapy using thrombin generation as a common language to compare anticoagulant effects across drug classes.
Joseph R. Shaw, Dylan Burger, J. Vassart et al.· Pharmacology and Therapeutic...· 0 citations
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