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Bayer AG Gebäude W 11 51368 Leverkusen, Germany http://www.bayer.de
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Bayer beantragt Zulassung von Vericiguat in der EU und Japan zur Behandlung chronischer Herzinsuffizienz

Die Zulassungsanträge basieren auf den kürzlich veröffentlichten positiven Ergebnissen der Phase-III-Studie VICTORIA im New England Journal of Medicine(1)

(PresseBox) (Berlin, )
Bayer hat zwei Zulassungsanträge für Vericiguat in der EU und in Japan eingereicht. Vericiguat ist ein einmal täglich oral einzunehmender Wirkstoff, der in Kombination mit verfügbaren Herzinsuffizienz-Therapien zur Behandlung von Patienten mit symptomatischer chronischer Herzinsuffizienz und verminderter Auswurfleistung von weniger als 45 % nach einem Verschlechterungsereignis (definiert als herzinsuffizienzbedingte Hospitalisierung oder intravenöse Verabreichung eines Diuretikums wegen Herzinsuffizienz ohne Hospitalisierung) entwickelt wurde. Vericiguat ist ein Stimulator der löslichen Guanylatcyclase (sGC) und der erste Vertreter dieser Substanzklasse, der bei Herzinsuffizienz geprüft wurde. Vericiguat wird gemeinsam mit MSD (ein Handelsname von Merck & Co., Inc., Kenilworth, NJ, USA) entwickelt.

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The publisher indicated in each case (see company info by clicking on image/title or company info in the right-hand column) is solely responsible for the stories above, the event or job offer shown and for the image and audio material displayed. As a rule, the publisher is also the author of the texts and the attached image, audio and information material. The use of information published here is generally free of charge for personal information and editorial processing. Please clarify any copyright issues with the stated publisher before further use. In case of publication, please send a specimen copy to service@pressebox.de.