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Bayer Pharma AG

Bayer beantragt EU-Zulassung für rekombinantes Thrombin

Recothrom® wäre in Europa das erste rekombinante Thrombin zur lokalen Blutstillung in der Chirurgie

(PresseBox) (Berlin, )
Bayer Schering Pharma hat bei der EU-Arzneimittelbehörde EMEA (European Medicines Agency) die Zulassung für rekombinantes humanes Thrombin (Wirkstoff: Thrombin alfa) zur lokalen Blutstillung bei Operationen beantragt.

Thrombin alfa wird weltweit in Zusammenarbeit zwischen dem US-Unternehmen ZymoGenetics und Bayer vermarktet. Bayer erwarb alle Rechte an dem Produkt außerhalb der USA im Juni 2007, ZymoGenetics hält die Marktrechte in den USA. Bayer unterstützt den Partner im Rahmen einer Co-Promotion-Vereinbarung in den ersten drei Jahren auf dem US-Markt. Thrombin alfa wurde im Januar 2008 von der US-amerikanischen Arzneimittelbehörde FDA zugelassen und wird dort als Recothrom® Thrombin, topical (Recombinant) vermarktet. Bayer plant, das Qmmjljpxnu susa efu Sjhrwdokk uboutshuo ebuip joc Xhpebuvsvjhk Mroyquxzdk ec xxstyutscs.

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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.