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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 erhält FDA-Zulassung für therascreen® KRAS RGQ PCR Kit als Begleitdiagnostikum für weiteres Darmkrebsmedikament

(PresseBox) (Hilden, Deutschland und Germantown, Maryland (USA), )
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- Klinisch validiertes Begleitdiagnostikum erhält US-Zulassung zur Steuerung von Therapien mit Amgens Vectibix® (Panitumumab) bei metastasierendem Darmkrebs
- ​FDA-Zulassung (PMA) des therascreen KRAS RGQ PCR Kits für Vectibix stärkt QIAGENs Marktführerschaft bei molekularen Tests für die personalisierte Medizin
- QIAGEN treibt die Verbreitung molekularer Begleitdiagnostika mit der Erweiterung des Testangebots für die QIAsymphony-Automationsplattform weiter voran

QIAGEN N.V. (NASDAQ: QGEN; Frankfurt Prime Standard: QIA) gab heute bekannt, dass die US-Gesundheitsbehörde FDA (Food and Drug Administration) das therascreen® KRAS RGQ PCR Kit (therascreen KRAS-Test) zur Steuerung von Therapien mit Amgens Medikament Vectibix® (Panitumumab) bei metastasierendem Darmkrebs zugelassen hat. Dies stellt die dritte FDA-Zulassung vmb mau wzuioqhmnvrlwqalgkoe Fhqvtxnyzdsf hxt NCWBCV pbh Dsgqxopnnm lua jhlco ofsjjkerbu Jbfmiihzjw hks.

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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.