A worldwide study led by McMaster University in Hamilton, Canada, has shown that milvexian can be used to prevent venous blood clots with minimal side-effects.
Milvexian is unique in that it works by targeting factor XIa, a clotting enzyme that causes thrombosis, but is not vital for stopping bleeding from injuries, a press release details.
Researchers compared milvexian with enoxaparin for prevention of blood clots in 1,242 patients from 18 countries undergoing knee replacement surgery who were enrolled between June 2019 and February 2021.
They found that at a total daily dose of 100mg or more, milvexian resulted in better clot protection but no increase in bleeding compared with enoxaparin, the control drug. Milvexian was evaluated in daily doses ranging from 25 to 400mg; there was no increase in bleeding over this wide range of doses.
“The major side effect of current oral anti-clotting drugs is bleeding, and the fear of bleeding leads to their underuse. This sets the need for safer oral anticoagulants and that is where milvexian comes in,” said senior author Jeffrey Weitz, professor of medicine and biochemistry and biomedical sciences at McMaster and executive director of the Thrombosis and Atherosclerosis Research Institute of McMaster and Hamilton Health Sciences.
The study was published this week in the New England Journal of Medicine and Weitz presented a summary of the findings in a late-breaking session at the 2021 American Heart Association (AHA) Scientific Sessions (13–15 November, Boston, USA).
He said the study focused on patients undergoing knee replacement surgery because they are at high risk for postoperative blood clots and such clots can be readily identified with venograms. Therefore, this patient population provides an ideal testing ground for new anticoagulants because effective and safe doses can be identified, he explained.
Weitz said his milvexian study is the first of several investigations of oral factor XIa inhibitors. The results of the other studies will likely be released next year.
Funding for the study was provided by the pharmaceutical firms Bristol Myers Squibb and Janssen Research and Development.
McMaster University is located in Hamilton, Ontario, Canada