American Society of Hirudotherapy

Targeting factor XI as a compromise between thrombosis and bleeding

Research article published in Cardiology journal (2025)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Narrative reviewSafety & Infection ControlŻuk-Łapan et al. · Cardiology journal, 2025

Abstract

Thromboembolic diseases have long been a leading cause of morbidity and mortality, necessitating advances in anticoagulant drugs. Heparins, vitamin K inhibitors, and direct oral anticoagulants (DOACs) are well-established drug classes that help prevent thromboembolic complications. While effective, they pose significant risks during long-term therapy, including bleeding, osteoporosis, heparin-induced thrombocytopenia, and the need for frequent monitoring and dose adjustments. Factor XI (FXI) inhibitors represent an innovative approach in anticoagulation therapy, aiming to balance thromboembolic events with the risk of bleeding complications. They include: a) orally administered small molecule inhibitors such as milvexian and asundexian; b) monoclonal antibodies such as abelacimab, osocimab, and xisomab, which specifically bind and inactivate FXI; c) FXI-antisense oligonucleotide (FXI-ASO), which downregulate FXI synthesis at the mRNA level and reduce plasma FXI concentrations. Available data indicate that FXI inhibitors decrease the risk of thromboembolic events and are associated with a lower incidence of major bleeding than current gold standard methods. Hence, FXI inhibitors may become the preferred anticoagulant class, especially for patients with elevated bleeding risk. Their development is an important step in the history of anticoagulant therapy, striving to find a balance between preventing thromboembolism and reducing bleeding risk, ultimately improving patient outcomes. In this context, a discussion on the characteristics of FXI inhibitors, a summary on data regarding the efficacy and safety of FXI inhibitors based on preclinical and clinical studies, and an outline of future perspectives regarding therapeutic strategies of FXI inhibition in venous thrombosis are presented in this study.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal ArticleReview
Indexed MeSH termsHumansHemorrhageFactor XIAnticoagulantsThrombosisBlood CoagulationRisk Factors

Summary

Peer-reviewed research on safety and infection-control considerations relevant to leech therapy and anticoagulation. Indexed in PubMed and verified against the NCBI record.

Why This Matters for Hirudotherapy

This review surveys Factor XI (FXI) inhibitors — small molecules (milvexian, asundexian), monoclonal antibodies (abelacimab, osocimab, xisomab), and antisense oligonucleotides — as an anticoagulant class designed to decouple thrombosis prevention from bleeding risk, noting that available data suggest reduced thromboembolic events with less major bleeding than current standards. This matters to the leech-secretome story because it reflects the central pharmacologic goal that medicinal-leech salivary anticoagulants embody at the local level: interrupting coagulation while limiting systemic bleeding; the leech secretome contains FXa- and thrombin-directed inhibitors that historically informed anticoagulant drug discovery. The caveat is that this is a narrative review of investigational and emerging drugs, not original data and not about leech-derived compounds, so it provides background and rationale rather than any hirudotherapy-specific evidence.

Citation

Targeting factor XI as a compromise between thrombosis and bleeding.

Żuk-Łapan et al. · Cardiology journal, 2025

Added to ASH library: May 28, 2026 · Site last updated: June 18, 2026

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