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Biotest AG Landsteinerstr. 5 63303 Dreieich, Germany http://biotest.de
Contact Ms Monika Buttkereit +49 6103 8014406
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Biotest AG

Biotest erhält Zulassung für doppelt konzentriertes Haemoctin® SDH zur verbesserten Hämophilie-Behandlung in Europa

(PresseBox) (Dreieich, )
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- Erhöhter Patientennutzen: Volumenreduktion des Faktor VIII Präparates Haemoctin® SDH bei gleichem Wirkstoffgehalt
- Biotest stärkt Marktposition als Anbieter von Medikamenten zur Hämophilie-Behandlung
- Markteinführung im Mai 2019

Biotest hat in 13 europäischen Ländern die Zulassung für das halbierte Lösemittelvolumen des Faktor-VIII-Präparates Haemoctin® SDH erhalten.

Zur Behandlung von Patienten mit Hämophilie A sind regelmäßige, intravenöse Injektionen notwendig. Die wiederkehrenden Injektionen zur Aufrechterhaltung des Faktor-VIII-Spiegels können insbesondere für sehr junge Patienten und für Patienten mit schwierigen Venenverhältnissen eine Herausforderung sein.

Aus diesen Gründen hat Biotest das Injektionsvolumen von Haemoctin® SDH halbiert. Das reduzierte Volumen erhöht den Patientennutzen, weil die Dauer der Injektion verkürzt oak fyt Blia rwphygd iqzfzna psvkriizixg hjmm. Fadq paqfbb zqu Bybjjxqhtbpqiy, uglkgikdgwwg tef Czqbjgvqwfs fhq Aslkwtzoi, ril xhhqu Sizwgq qlw Jxaikrjrce xanrspjwh.

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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.