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QIAGEN N.V. Hulsterweg 82 5912 Venlo, Netherlands http://www.qiagen.com
Contact Mr John Gilardi +49 2103 2911711
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QIAGEN N.V.

QIAGEN erreicht mit US-Zulassung seines Begleitdiagnostikums für Darmkrebs einen Meilenstein in der personalisierten Medizin

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- US-Markteinführung des therascreen® KRAS RGQ PCR-Kits ermöglicht eine verbesserte Entscheidungsgrundlage für die Therapie von jährlich etwa 110.000 Darmkrebspatienten in den USA
- Erste FDA-Zulassung eines therapiebegleitenden Diagnostikums von QIAGEN stellt Meilenstein für den globalen Ausbau des Unternehmens im schnell wachsenden Markt der personalisierten Medizin dar
- Wichtiger Krebstest liefert zusätzlich wertvollen Inhalt für die weitere Verbreitung von QIAGENs Automationsplattformen

QIAGEN N.V. (NASDAQ: QGEN; Frankfurt Prime Standard: QIA) hat heute bekanntgegeben, dass die US-Gesundheitsbehörde FDA (Food and Drug Administration) die Zulassung für das therascreen® KRAS RGQ PCR-Kit (therascreen KRAS-Test) erteilt hat. Damit kann das Produkt nun als therapiebegleitender Test für die
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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.