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With FDA filing, Lexington firm targets a scourge of hospitals: sepsis

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Lexington-based T2 Biosystems made waves in the diagnostics industry in 2014 when the FDA approved its test for sepsis, a complication of infections that is one of the leading causes of death in the U.S. The product, called the T2Candida Panel, can diagnose sepsis in a matter of hours, compared to traditional blood cultures that can take up to six days. T2 (Nasdaq: TTOO) took another major step forward on Monday when it announced that it had formally asked the FDA to approve a similar product, called…

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