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Bayer's Asundexian reduced recurrent stroke risk in trial, meeting key goals.
Bayer reported positive results from a Phase 3 trial of its drug Asundexian, showing it significantly reduced recurrent ischemic stroke risk when used with antiplatelet therapy, meeting both primary efficacy and safety goals.
The drug, tested in patients with prior non-cardioembolic ischemic strokes, received Fast Track designation from the U.S. FDA, potentially speeding its review.
Bayer plans to discuss regulatory submissions with global health authorities and will present full data at a scientific conference.
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Asundexian de Bayer redujo el riesgo de accidente cerebrovascular recurrente en el ensayo, cumpliendo objetivos clave.