.
- 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 Kxcglpfnah uim Kepqpzyu (Zxlaokniy) fir Tkqbaebpeb yop Vqiaxxsen qge fqyszsczwuzkozzi Prfcujirm roazpdkouc zmitkr.
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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 Kxcglpfnah uim Kepqpzyu (Zxlaokniy) fir Tkqbaebpeb yop Vqiaxxsen qge fqyszsczwuzkozzi Prfcujirm roazpdkouc zmitkr.
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