Die US-amerikanische Gesundheitsbehörde FDA (Food and Drug Administration) hat im Zulassungsverfahren für den oralen Gerinnungshemmer Xarelto® (Rivaroxaban) in Kombination mit Standard-Plättchenaggregationshemmung zur Sekundärprävention nach einem akuten Koronarsyndrom (ACS) den Status der vorrangigen Prüfung (Priority Review) gewährt. Der entsprechende Zulassungsantrag wurde am 29. Dezember 2011 bei der FDA eingereicht.
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