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QIAGEN N V : QIAGEN Forms Strategic Alliance With Sysmex Corporation for Global Cancer Companion Diagnostics Development and Commercialization Using NGS and Plasma-Safe-SeqS Technology

QIAGEN N V : QIAGEN Forms Strategic Alliance With Sysmex Corporation for Global Cancer Companion Diagnostics Development and Commercialization Using NGS and Plasma-Safe-SeqS Technology
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United statesJohn gilardiRobert reitzeAsia pacificJean pascal violaThomas theuringerPhoebe lohHiroshi kandaExchange commissionJapan sysmex corporation tokyo stock exchangeHead of corporate business development at sysmexSysmex corporationTokyo stock exchangeCorporate business developmentUs securities exchangeFrankfurt prime standard

QIAGEN launches first FDA-approved tissue companion diagnostic to identify the KRAS G12C mutation in NSCLC tumours and expand precision medicine options in lung cancer

QIAGEN has announced the launch of an expanded scope of companion diagnostic (CDx) claims for the therascreen® KRAS RGQ PCR Kit (therascreen KRAS Kit) after it received U.S. regulatory approval as a companion diagnostic to aid in the identification of non-small cell lung cancer (NSCLC) patients that may be eligible for treatment with LUMAKRASTM (sotorasib), a newly approved therapy developed and marketed by Amgen Inc. (AMGN).

Jean pascal violaLab readinessDrug administrationProduct newsSenior vice presidentDiagnostics businessDarryl sleepGlobal medicalOne lab readinessPrecision medicineQiagen launches first fda approved tissue companion diagnostic to identify the kras g12c mutation in nsclc tumours and expand precision medicine options lung cancerKras g12c mutationNon small cell lung cancerஜீன் பாஸ்கல் வயலஆய்வகம் ரெடிநெஸ்ப்ராடக்ட் செய்தி

QIAGEN Launches First FDA-approved Tissue Companion Diagnostic to Identify the KRAS G12C Mutation in NSCLC Tumours and Expand Precision Medicine Options in Lung Cancer

QIAGEN Launches First FDA-approved Tissue Companion Diagnostic to Identify the KRAS G12C Mutation in NSCLC Tumours and Expand Precision Medicine Options in Lung Cancer
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John gilardiRobert reitzeJean pascal violaThomas theuringerPhoebe lohExchange commissionAmgen incLab readinessDrug administrationDay one lab readinessUs securities exchangeOne lab readinessFrankfurt prime standardSenior vice presidentDiagnostics businessDarryl sleep

Qiagen (QGEN) Launches First FDA-approved Tissue Companion Diagnostic to Identify the KRAS G12C Mutation

Qiagen (QGEN) Launches First FDA-approved Tissue Companion Diagnostic to Identify the KRAS G12C Mutation
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Jean pascal violaAmgen incLab readinessDrug administrationWall streetSenior vice presidentDiagnostics businessDarryl sleepGlobal medicalOne lab readinessஜீன் பாஸ்கல் வயலமகேன் இன்க்ஆய்வகம் ரெடிநெஸ்சுவர் தெருமூத்தவர் துணை ப்ரெஸிடெஂட்பரிசோதனை வணிக

QIAGEN N V : QIAGEN Launches First FDA-approved Tissue Companion Diagnostic to Identify the KRAS G12C Mutation in NSCLC Tumours and Expand Precision Medicine Options in Lung Cancer

(0) The therascreen KRAS RGQ PCR Kit receives U.S. regulatory approval from FDA for expanded scope to include use in guiding treatment with the newly approved therapy LUMAKRAS TM (sotorasib) from Amgen KRAS G12C mutation in NSCLC Test will be available under QIAGEN s Day One Lab Readiness program QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) today announced the launch of an expanded scope of companion diagnostic (CDx) claims for the therascreen KRAS RGQ PCR Kit ( therascreen KRAS Kit) after it received U.S. regulatory approval as a companion diagnostic to aid in the identification of non-small cell lung cancer (NSCLC) patients that may be eligible for treatment with LUMAKRAS

John gilardiRobert reitzeJean pascal violaThomas theuringerPhoebe lohExchange commissionAmgen incLab readinessDrug administrationDay one lab readinessUs securities exchangeOne lab readinessFrankfurt prime standardSenior vice presidentDiagnostics businessDarryl sleep