Luminex Corporation and ViroNovative Announce License Agreement for Human Metapneumovirus Rights
"We are pleased to announce this license agreement in place with ViroNovative for human metapneumovirus," said Jeremy Bridge-Cook, vice president of Luminex Molecular Diagnostics. "This virus is of increasing concern to healthcare providers worldwide. Having this license as part of our xTAG RVP assay is important to us as it allows our customers to use this cutting-edge test without the need to individually secure rights to this intellectual property."
Luminex's xTAG RVP received 510(k) clearance from the U.S. Food and Drug Administration (FDA) on January 3, 2008. The test was cleared for the detection and identification of 12 viruses and viral subtypes that are together responsible for more than 85 percent of respiratory viral infections. xTAG RVP is the first multiplexed nucleic acid test for respiratory viruses cleared for in vitro diagnostic use by the FDA and is the first and only test cleared by FDA for the detection of hMPV.
Most read news
Other news from the department business & finance
Get the life science industry in your inbox
From now on, don't miss a thing: Our newsletter for biotechnology, pharma and life sciences brings you up to date every Tuesday and Thursday. The latest industry news, product highlights and innovations - compact and easy to understand in your inbox. Researched by us so you don't have to.