NIH-funded research R21 grant

A direct, point-of-care test to detect infectious and congenital syphilis

Official title: Development of a Direct Diagnostic Test for Infectious and Congenital Syphilis

Funded at University of Victoria · NIH-11166664 · Data updated 2026-11-12

A new diagnostic test is being developed to directly detect active syphilis infections, including congenital cases, and to work at the point of care.

More Syphilis research and trials

Quick facts

Grant typeR21 grant
Study typeNIH-funded research
Funding institutionUniversity of Victoria
NIH-funded
Lab location1 site (Victoria, Canada)
Project startAugust 9, 2024
Project endJuly 31, 2027
Funding year2025
Award (this year)$75,363
NIH project number5R21AI186005-02
Project IDNIH-11166664 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates would be people with possible syphilis exposure or symptoms, pregnant people and their newborns at risk for congenital syphilis, or individuals needing confirmation of active versus past infection.

Less likely to help

People without suspected syphilis or those needing immediate clinical treatment rather than diagnostic development work may not gain direct benefit from this early-stage project.

What this research studies

From a patient perspective, researchers are building a simple test that looks for markers of the syphilis bacterium in blood so it can tell if an infection is current or from the past. The team aims for high sensitivity and specificity across early, late, and congenital disease and wants the test to tell syphilis apart from related infections like yaws. Development will use blood plasma/serum samples and laboratory methods to identify antigens or antibodies and refine algorithms for staging. The final goal is a version that can be used at clinics or in remote settings for rapid, easy-to-read results.

Why it matters

Potential benefit: If successful, this test could give faster, more accurate diagnoses, help guide timely treatment, and reduce transmission including congenital infections.

How similar studies have gone: Existing treponemal and non-treponemal tests and some molecular methods partially work but cannot reliably distinguish active versus past or congenital infections, so this project builds on prior approaches but aims for a more definitive, point-of-care solution.

Where this research is happening

  • University of Victoria
    Victoria, Canada
    Active

Researchers

  • Principal investigator: Cameron, Caroline E — University of Victoria
  • Study coordinator: Cameron, Caroline E

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.