Apixaban, an oral, direct inhibitor of activated Factor Xa
Research article published in Current opinion in investigational drugs (London, England : 2000) (2008)
Abstract
Apixaban is an oral, direct Factor Xa inhibitor that is being developed by Bristol-Myers Squibb Co and Pfizer Inc. Apixaban is currently undergoing phase III clinical trials for cerebrovascular ischemia, deep vein thrombosis and lung embolism, and phase II clinical trials for coronary artery disease.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Summary
Peer-reviewed research on anticoagulant and antithrombotic drug development relevant to thrombin and factor inhibition. Indexed in PubMed and verified against the NCBI record.
Why This Matters for Hirudotherapy
This short drug-profile review summarizes apixaban, an oral direct inhibitor of activated Factor Xa, noting that at the time of writing it was in phase III trials for cerebrovascular ischemia, deep vein thrombosis, and pulmonary embolism and in phase II for coronary artery disease. Its relevance to ASH is mainly as background on the modern anticoagulant landscape: apixaban represents the Factor Xa branch of targeted oral anticoagulants that developed alongside the thrombin-directed agents (including the hirudin-derived drugs) tied to the medicinal-leech secretome, helping situate where leech-inspired anticoagulants fit among contemporary options. The caveat is twofold: this is a brief review describing a development pipeline rather than reporting trial results, and as a 2008 snapshot its statements about trial phases are dated, so it should be treated as historical context, not current evidence, and it does not concern leech therapy.
Citation
Added to ASH library: May 28, 2026 · Site last updated: June 18, 2026