NIH-funded research U01 cooperative agreement

Fast, low-cost cervical cancer screening using CRISPR and light-based detection

Official title: Composing CODAs to cervical cancer screening through an integrated CRISPR and fluorescent nucleic acid approach

Funded at Massachusetts General Hospital · NIH-11399240 · Data updated 2026-11-12

A rapid, affordable CRISPR-based test is being brought to clinics in Uganda and Ghana to help find precancerous cervical changes in women who lack easy access to screening.

Quick facts

Grant typeU01 cooperative agreement
Study typeNIH-funded research
Funding institutionMassachusetts General Hospital
NIH-funded
Lab location1 site (Boston, United States)
Project startJuly 1, 2023
Project endJune 30, 2028
Funding year2025
Award (this year)$126,580
NIH project number3U01CA279858-03S2
Project IDNIH-11399240 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates are women eligible for cervical cancer screening who visit participating clinics in the project’s partner sites in Uganda and Ghana.

Less likely to help

People without a cervix, men, and women who do not attend participating clinics or whose conditions are not detected by HPV/DNA screening would not directly benefit from this project.

What this research studies

From a patient perspective, this project adapts a handheld lab test that uses CRISPR and a light-based fluorescence method to spot HPV and other DNA markers linked to cervical precancer. The test produces automated results in under 30 minutes and was already checked on human samples in the lab. Researchers will work with clinicians and lab staff at partner clinics in Uganda and Ghana to make the test easy to use in low-resource settings. The goal is to set up practical workflows so women can be screened more widely and quickly at point-of-care locations.

Why it matters

Potential benefit: If successful, the test could make cervical screening faster, cheaper, and more widely available in low-resource settings, helping detect precancer earlier.

How similar studies have gone: The team has already validated the CODA CRISPR-fluorescence method on human samples, and other CRISPR-based diagnostics have shown promising rapid detection, though routine point-of-care use in low-resource settings is still relatively new.

Where this research is happening

  • Massachusetts General Hospital
    Boston, United States
    Active

Researchers

  • Principal investigator: Castro, Cesar M — Massachusetts General Hospital
  • Study coordinator: Castro, Cesar M

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.