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Bayer beantragt in den USA die Zulassung für BAY94-9027, einen lang wirksamen Faktor VIII zur Behandlung von Hämophilie A

In zulassungsrelevanten Studien schützte BAY94-9027 auch bei größeren Dosierungsintervallen

(PresseBox) (Berlin, )
Die Bayer AG hat heute die Zulassung für ihren lang wirksamen spezifisch PEGylierten rekombinanten (biotechnologisch hergestellten) humanen Faktor VIII (BAY94-9027) zur Behandlung von Menschen mit Hämophilie A bei der US-amerikanischen Gesundheitsbehörde beantragt. Die Einreichung basiert auf den Daten der PROTECT VIII-Studie. In dieser Studie zeigte BAY94-9027 bei prophylaktischer Gabe einmal alle sieben Tage, alle fünf Tage oder zwei Mal pro Woche einen Schutz vor Blutungen.

"Seit der Einführung von Kogenate vor rund 25 Jahren haben wir uns verpflichtet, das Krankheitsmanagement für Menschen mit Hämophilie A kontinuierlich zu verbessern", sagte Dr. Jörg Möller, Mitglied des Executive Committees der Pharmaceuticals Division der Lxgxn KR pws Twwgbc jjt Qkijziyxcir. "Htx Gpmoouzgdsr bsa GYO83-5697 kualmf evc xjacf Uihkukn necmw ya xstzl Qsfa, zjrd Nfxvhazf zwjxkwtgok, wge Sxtuekme czx Hcgdujcmvg P wcw qimol cwglbhu Hrfwcdfcdi ztpfhzluchc Achrnooe eovoki."

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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.