Abbott Launches a CE Marked KIF6 Test in Europe
Wiesbaden, Germany — Abbott announced today the availability of the CE-marked KIF6 diagnostic test for use on the m2000 instrument system. The KIF6 genotyping assay, detects a genetic marker that may be used in conjunction with clinical evaluation and patient assessment for the identification of individuals at risk for coronary heart disease (CHD) and in treatment of patients with elevated cholesterol, for whom statin treatment is being considered.
Previous research has shown that carriers of the KIF6 risk variant (60 percent of the population) have had significantly fewer fatal or nonfatal coronary events from statin therapy. According to Herbert Schuster, M.D. Ph.D., Geneticist and Preventive Cardiologist, Berlin, Germany, "The new pharmacogenetic KIF6 biomarker is very useful for my daily practice in cardiovascular risk factor management, particularly for patients with intermediate cardiovascular risk. I use this marker to reclassify patients to further support individualized indication of statin therapy. In addition, carriers of the variant will significantly benefit from statin therapy and are more likely to benefit from continuous therapy."On September 22, 2010, Celera Corporation and Abbott announced their non-exclusive distribution agreement to market a CE-marked KIF6 diagnostic test for use on Abbott’s m2000 instrument system. Under the 4-year agreement, Celera will manufacture the KIF6 test kit which Abbott Molecular will distribute in the European Union, other geographic areas that recognize the CE mark, and elsewhere worldwide, excluding the United States.
Abbott Launches a CE Marked KIF6 Test in Europe
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