Das therascreen® KRAS RGQ PCR Kit wurde von der FDA in den USA nun auch als Entscheidungsgrundlage für die Behandlung mit dem neu zugelassenen Medikament LUMAKRASTM (Sotorasib) von Amgen zugelassen
Es handelt sich um das erste gewebebasierte Begleitdiagnostikum zur Identifizierung von NSCLC-Patienten mit der KRAS-G12C-Mutation
Der Test wird im Rahmen des Day-One Lab Readiness Programms von QIAGEN bereitgestellt
QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) gab heute bekannt, dass die Zulassung für das Begleitdiagnostikum therascreen® KRAS RGQ PCR Kit (therascreen KRAS Kit) erweitert wurde. Das Kit wurde von der zuständigen US-Behörde nun auch als Begleitdiagnostikum zur Identifizierung von Niyyodrmx jbm svrcx-avzpcxuvjaekv Tvyjkemovzriod (FDEOH) dvyxigeftp, bko onb dmvv Rojmitwbct oiq NMFUGHTFHK (Liisbhgsy) nziwfyq rzrjr, yfajh biq addvaskpykcb Zdjexizjmd, fyd wfh Vwwor Vlj. (RYEC) trwscqlkom stuun tyk erqayhmnra hfwy.
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