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FDA Approves First At-Home Syphilis Test by NOWDiagnostics

Aug 16, 2024, 02:57 PM

The U.S. Food and Drug Administration (FDA) has granted marketing authorization to NOWDiagnostics for the First To Know Syphilis Test. This is the first at-home, over-the-counter test designed to detect Treponema pallidum (syphilis) antibodies in human blood. The approval marks a significant advancement in accessible testing options for syphilis, allowing individuals to conduct the test at home without the need for a healthcare provider. The test aims to enhance early detection and treatment of syphilis, a critical step in managing and controlling the spread of the infection.