David Pearce1, Charlotte Gaydos2
12:30 - 14:30 | Thu 21 Nov | Room E1&2 | B1P-A.5
The binx io Chlamydia trachomatis/Neisseria gonorrhoeae (CT/NG) Assay running on the binx io platform is designed to reduce the time taken between testing for CT and NG and treating appropriately from days and weeks to minutes – enabling a ‘test and treat’ approach for the first time. The io was recently cleared by the FDA for use in point-of-care or clinical laboratory settings for the detection of CT and NG in female vaginal swab samples following a validation study that demonstrated a 96.1% sensitivity and 99.1% specificity for CT and 100% sensitivity and 99.9% specificity for NG.