SEATTLE, Aug. 26 /PRNewswire/ -- The New York State Department of Health has licensed
"This is an important advance for personalized medicine in New York, especially for the 100,000 or more patients who live there and are failing their Plavix treatment," said Howard Coleman, CEO, Genelex. "The Plavitest™ DNA test identifies these at-risk patients, allowing doctors to personalize treatments and reduce the risks of recurrent heart attack, stroke or other cardiovascular risks." Coleman added that these assertions are based on a series of large clinical studies that led the US Food and Drug Administration to add a boxed warning to the Plavix label. A boxed warning requires physicians to take described risks into account when planning treatments. Similar genetic risks apply to many other important drugs used to treat cardiovascular disease, cancer, pain and mental conditions. These risks are exacerbated disproportionately in the elderly because of the many drugs they take and their already diminished drug processing capacity.
Earning the New York State Permit required Genelex to successfully complete a comprehensive evaluation considered the most rigorous in the United States. The evaluation program included on-site inspections, proficiency testing, and assessment of personnel qualifications to ensure the accuracy and reliability of laboratory test results. According to Dr. Tia Aulinskas, Genelex laboratory director, the company now has all required state clinical laboratory licenses in the U.S. and can receive and test specimens from every state--a critical milestone for Genelex.
Genelex (jen-uh-LEX) Corporation, with headquarters in Seattle, sells a combination of DNA Drug Sensitivity Testing and the GeneMedRx (jeen-med-r-x) software to doctors to help them choose the safest, most effective medicines for their patients. Wide adoption of these technologies is aimed at dramatically reducing deaths and injuries from adverse drug reactions, interactions and treatment failure.
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SOURCE Genelex Corporation
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