NIH-funded research Sbir 2 grant

Teal Wand at-home HPV self-collection kit for cervical screening

Official title: Evaluation of the Teal self-collect device for cervical cancer screening

Funded at Teal Health INC · NIH-11196220 · Data updated 2026-11-12

This project checks whether the Teal Wand lets people collect a reliable at-home vaginal sample for HPV testing to help detect cervical cancer early.

More Cervical Cancer research and trials

Quick facts

Grant typeSbir 2 grant
Study typeNIH-funded research
Funding institutionTeal Health INC
NIH-funded
Lab location1 site (San Francisco, United States)
Project startSeptember 23, 2024
Project endAugust 31, 2026
Funding year2025
Award (this year)$513,576
NIH project number5R44CA291336-02
Project IDNIH-11196220 on NIH RePORTER

Who could benefit from this research

Could help

People with a cervix who are eligible for HPV-based cervical cancer screening and who prefer or need an at-home option would be ideal candidates.

Less likely to help

People without a cervix, those already up-to-date with clinic-based screening, or those who need clinician-collected samples for specific follow-up may not benefit from this device.

What this research studies

From your home, you would use the Teal Wand’s textured sponge to collect a vaginal sample that can be tested for high-risk HPV on FDA-approved assays. The device is designed to store samples dry and then be eluted into approved preservatives so labs can process them using existing workflows. The team plans clinical and analytical testing informed by prior FDA feedback to support an at-home use approval. If approved, the device would be offered through Teal telehealth visits to reach people who face barriers to clinic-based screening.

Why it matters

Potential benefit: If successful, this could expand access to cervical cancer screening by making reliable at-home HPV testing available to people who cannot or do not attend clinic visits.

How similar studies have gone: Previous research shows HPV self-collection can increase screening uptake and often performs similarly to clinician samples on validated HPV tests, but at-home self-collection devices have not yet received FDA approval in the U.S.

Where this research is happening

  • Teal Health INC
    San Francisco, United States
    Active

Researchers

  • Principal investigator: Depel, Trena — Teal Health INC
  • Study coordinator: Depel, Trena

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.