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FDA Clears Gen-Probe Unit Prodesse's ProParaflu+ Assay For US Marketing - Quick Facts

By RTTNews Staff Writer   ✉  | Published:  | Google News Follow Us  | Join Us
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Gen-Probe Inc. (GPRO) said Tuesday that the US Food and Drug Administration has cleared for marketing Prodesse's ProParaflu+ assay, a molecular test that detects and differentiates parainfluenza 1, 2 and 3 viruses, which cause lower respiratory tract infections. Prodesse is a wholly-owned subsidiary of Gen-Probe.

The ProParaflu+ assay uses real-time RT- polymerase chain reaction to identify the parainfluenza 1, 2 and 3 viruses from nasal swabs. The assay uses the same internal control as Prodesse's other tests for respiratory infectious diseases, so a single nucleic acid extract can be tested with any combination of those products.

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Global Economics Weekly Update - Jun 01 - Jun 05, 2026

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