Key result
Asundexian fails to prevent stroke versus apixaban, prompting premature discontinuation of OCEANIC-AF.
Why the study?
Conventional anticoagulants carry risks of bleeding that preclude treatment in some patients, whereas factor XIa inhibitors may attenuate thrombosis with minimal interference with hemostasis.
Does asundexian provide safe and effective anticoagulation for patients with atrial fibrillation, stroke, or acute myocardial infarction compared to standard of care or placebo?
Does asundexian provide safe and effective anticoagulation for patients with atrial fibrillation, stroke, or acute myocardial infarction compared to standard of care or placebo?
While phase 2 trials of the factor XIa inhibitor asundexian showed promising safety profiles, the phase 3 OCEANIC-AF trial was halted due to inferior efficacy compared to apixaban for stroke prevention in atrial fibrillation.
Asundexian should not replace apixaban for AF stroke prevention; leaves open factor XIa inhibition in other thromboembolic settings.
PURPOSE: Factor XIa inhibitors are a promising novel class of anticoagulants that attenuate pathological thrombosis with minimal interference with hemostasis. These effects contrast with those of conventional anticoagulants, which may exhibit adverse events of untoward bleeding precluding treatment in some patients. A variety of investigational pharmacological modalities have been developed and studied to target factor XIa. SUMMARY: Asundexian is a small molecule inhibitor of factor XIa that has been evaluated in several clinical studies. It has been studied as an oral, once-daily medication and found to inhibit approximately 90% of factor XIa activity at doses of 20 to 50 mg. Phase 2 trials have demonstrated the potential for improved safety compared to standard of care in certain treatment settings, such as in atrial fibrillation. For other indications, such as noncardioembolic stroke and acute myocardial infarction, asundexian has been used in addition to background antiplatelet therapy. In these instances, asundexian did not show a difference in the incidence of bleeding events compared to placebo. CONCLUSION: Phase 3 trials have recently been launched; however, the OCEANIC-AF trial was prematurely discontinued due to inefficacy of asundexian vs apixaban for stroke prevention in atrial fibrillation. Another phase 3 trial, OCEANIC-AFINA, is planned to compare asundexian to placebo in patients with atrial fibrillation at high risk for stroke who are deemed ineligible for anticoagulation.
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Edwards et al. (2024) conducted a review in Atrial fibrillation, noncardioembolic stroke, acute myocardial infarction. Asundexian vs. Standard of care, placebo, apixaban was evaluated. Asundexian showed potential for improved safety in phase 2 trials, but the phase 3 OCEANIC-AF trial was prematurely discontinued due to inefficacy versus apixaban for stroke prevention.
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