Prodesse's ProFlu+ test was cleared by the FDA in January2008 for the detection and discrimination of influenza A virus, influenza Bvirus and respiratory syncytial virus. It is, reportedly, the only commerciallyavailable, FDA-cleared molecular test for these respiratory viruses that usesreal-time PCR technology. Test results are said to be obtainable in as littleas three hours using the assay, which Gen-Probe and Prodesse call "asignificant improvement over culture-based methods," adding that during apublic health emergency, "this speed to result and the high sensitivity ofmolecular tests can make important contributions to effective infection controlefforts."
Prodesse also sells FDA-approved, real-time PCR assays forthe clinical diagnosis of
Clostridium difficile, a bacteria that is the most serious cause of antibiotic-associateddiarrhea, and human metapneumovirus, a common cause of lower respiratoryinfection in children.
Gen-Probe expects to finance the transaction with cashcurrently on its balance sheet. Gen-Probe's initial expectation is that theacquisition will add approximately 5 cents to the company's 2010 earnings pershare, based on approximately $15 million in total revenues.