Die U.S. Food and Drug Administration (FDA) hat Bayers Prüfpräparat Asundexian (BAY2433334) den Fast-Track-Status als potenzielle Behandlung zur Prävention von Schlaganfällen und systemischen Embolien bei Patienten mit Vorhofflimmern erteilt. Im Jahr 2022 hatte die FDA Asundexian bereits den Fast-Track-Status für die Sekundärprävention bei Patienten mit nicht-kardioembolischem ischämischem Wpvfpnmhishf vumhidd.
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