Studien mit schwer kranken Patienten bestätigen und untermauern das Sicherheitsprofil von Rivaroxaban / Ergebnisse zeigen keine statistischen Unterschiede in den primären Endpunkten / Die Phase-III-Studie COMMANDER HF untersuchte Rivaroxaban bei Patienten nach akuter Dekompensation einer Herzinsuffizienz bei gleichzeitiger koronarer Herzkrankheit / Die Phase-III-Studie MARINER untersuchte Rivaroxaban bei akut erkrankten internistischen Hochrisikopatienten
Die Bayer AG und ihr Entwicklungspartner Janssen Research & Development, LLC haben heute neue Daten aus klinischen Studien zu dem oralen Faktor-Xa-Inhibitor Rivaroxaban (Xarelto®) bekanntgegeben. Sie wurden auf dem Kongress der europäischen Gesellschaft für Kardiologie (ESC) 2018 vorgestellt, der vom 25. bis zum 29. August in München stattfindet.
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Die Bayer AG und ihr Entwicklungspartner Janssen Research & Development, LLC haben heute neue Daten aus klinischen Studien zu dem oralen Faktor-Xa-Inhibitor Rivaroxaban (Xarelto®) bekanntgegeben. Sie wurden auf dem Kongress der europäischen Gesellschaft für Kardiologie (ESC) 2018 vorgestellt, der vom 25. bis zum 29. August in München stattfindet.
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