.
- Einreichung basiert auf den positiven Ergebnissen der ATLAS ACS 2-TIMI 51-Studie
- Xarelto ist der einzige neue Gerinnungshemmer, der in dieser Indikation in Kombination mit Standard-Plättchenaggregationshemmung signifikante klinische Vorteile zeigen konnte
Bayer HealthCare hat bei der europäischen Arzneimittel-zulassungsbehörde EMA (European Medicines Agency) die Zulassung des oralen Gerinnungshemmers Xarelto® (Rivaroxaban) in Kombination mit Standard-Plättchen-aggregationshemmung zur Sekundärprävention nach einem akuten Koronarsyndrom (ACS) beantragt.
Rivaroxaban ist ein oral wirksamer, direkter Hemmer des Blutgerinnungsfaktors Xa. Die Substanz wird gemeinsam von Bayer HealthCare und Janssen Research & Development, L.L.C. entwickelt. Rivaroxaban ist der einzige neue Gerinnungshemmer, der in dieser Indikation zur Zulassung eingereicht ist.
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- Einreichung basiert auf den positiven Ergebnissen der ATLAS ACS 2-TIMI 51-Studie
- Xarelto ist der einzige neue Gerinnungshemmer, der in dieser Indikation in Kombination mit Standard-Plättchenaggregationshemmung signifikante klinische Vorteile zeigen konnte
Bayer HealthCare hat bei der europäischen Arzneimittel-zulassungsbehörde EMA (European Medicines Agency) die Zulassung des oralen Gerinnungshemmers Xarelto® (Rivaroxaban) in Kombination mit Standard-Plättchen-aggregationshemmung zur Sekundärprävention nach einem akuten Koronarsyndrom (ACS) beantragt.
Rivaroxaban ist ein oral wirksamer, direkter Hemmer des Blutgerinnungsfaktors Xa. Die Substanz wird gemeinsam von Bayer HealthCare und Janssen Research & Development, L.L.C. entwickelt. Rivaroxaban ist der einzige neue Gerinnungshemmer, der in dieser Indikation zur Zulassung eingereicht ist.
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