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

GERMANTOWN, Maryland, and HILDEN, Germany, October 21, 2013 /PRNewswire/ --


  • Collaboration to expand label of QIAGEN's FDA-approved therascreen® EGFR RGQ PCR Kit and creates framework for long term development and commercialization partnership

  • Companion diagnostic will run on QIAGEN's efficient Rotor-Gene Q MDx platform

  • QIAGEN adds to growing portfolio of companion diagnostics in co-development with world's leading pharmaceutical and biotechnology companies

QIAGEN N.V. (NASDAQ: QGEN; Frankfurt Prime Standard: QIA) today announced a partnership with Clovis Oncology (NASDAQ: CLVS) to co-develop and co-commercialize a companion diagnostic test to guide the use of CO-1686, a novel Clovis Oncology product candidate currently in clinical development. The Clovis drug candidate will initially target an unmet clinical need in patients with epidermal growth factor receptor (EGFR) driven non-small cell lung cancer (NSCLC) for whom current EGFR-inhibiting drugs no longer control disease.

The diagnostic will build on QIAGEN's therascreen® EGFR RGQ PCR Kit, which was approved by the U.S. Food and Drug Administration (FDA) in July 2013 as a companion diagnostic for use in the treatment of metastatic NSCLC in patients whose tumors have certain EGFR mutations. Analytical performance of the therascreen EGFR test has been established for 21

SOURCE Qiagen N.V.
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