Making anticoagulation safer
- PMID: 35385696
- PMCID: PMC9540354
- DOI: 10.1016/S0140-6736(22)00563-3
Making anticoagulation safer
Conflict of interest statement
I receive funding from the US National Institutes of Health for research into the roles of FXI and other plasma proteins in thrombosis and inflammation. I receive or have received consulting fees from companies with interests in targeting FXI or FXIa for therapeutic purposes (Anthos Therapeutics, Aronora, Bayer, Bristol-Myers Squibb, Ionis, Janssen, and Novartis), including Bayer, the sponsor of the PACIFIC-AF trial, but unrelated to asundexian. I serve, or have served, on boards of clinical trials of FXIa inhibitors run by Bristol-Myers Squibb and Janssen and have received travel honoraria to attend meetings at the invitation of Anthos Therapeutics.
Comment on
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Safety of the oral factor XIa inhibitor asundexian compared with apixaban in patients with atrial fibrillation (PACIFIC-AF): a multicentre, randomised, double-blind, double-dummy, dose-finding phase 2 study.Lancet. 2022 Apr 9;399(10333):1383-1390. doi: 10.1016/S0140-6736(22)00456-1. Epub 2022 Apr 3. Lancet. 2022. PMID: 35385695 Clinical Trial.
References
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- Wysowski DK, Nourjah P, Swartz L. Bleeding complications with warfarin use: a prevalent adverse effect resulting in regulatory action. Arch Intern Med 2007; 167: 1414–19. - PubMed
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