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QIAGEN Announces Partnership With Clovis Oncology to Co-develop Companion Diagnostic Targeting Drug-Resistant EGFR Mutations
Date:10/21/2013

n diagnostic for our lead compound CO-1686," said Patrick J. Mahaffy, President and CEO of Clovis Oncology. "QIAGEN's therascreen is a validated test and already FDA approved to detect both activating EGFR mutations and the resistance mutation T790M.  Working with QIAGEN will help support our accelerated clinical development plan for CO-1686."

The Rotor-Gene Q MDx platform, which has been adopted by most major U.S. laboratories and many labs around the world, runs a growing menu of molecular tests. Rotor-Gene Q MDx is approved in the U.S. for use with QIAGEN's therascreen® KRAS RGQ PCR Kit for colorectal cancer patients and therascreen EGFR test for metastatic NSCLC patients - important Personalized Healthcare products.

QIAGEN continues to expand its pipeline of Personalized Healthcare technologies and intends to submit more tests around the world for regulatory approvals to run on the Rotor-Gene Q MDx. The company already markets Personalized Healthcare tests covering over 30 biomarkers in Europe, Asia/Pacific and Japan. In addition, QIAGEN has more than 15 projects to co-develop and market companion diagnostics with leading pharmaceutical and biotech companies such as Amgen, AstraZeneca, Bayer, Bristol-Myers Squibb, Eli Lilly and Company, and Pfizer. QIAGEN is developing numerous companion diagnostics, plus a range of other molecular tests, as part of a broad menu of reliable, cost-effective molecular diagnostics.

About QIAGEN

QIAGEN N.V., a Netherlands holding company, is the leading global provider of Sample & Assay Technologies that are used to transform biological materials into valuable molecular information. Sample technologies are used to isolate and process DNA, RNA and proteins from biological samples such as blood or tissue. Assay techn
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SOURCE Qiagen N.V.
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