NIH-funded research R37 grant

Targeted immune-boosting therapy for head and neck cancer

Official title: Tumor-Targeted STING Agonism in Head and Neck Squamous Cell Carcinoma

Funded at Yale University · NIH-11252352 · Data updated 2026-11-12

This work uses a tumor-targeted drug that turns on a cancer-cell immune alarm called STING to help radiation and chemotherapy work better for people with head and neck cancer.

Quick facts

Grant typeR37 grant
Study typeNIH-funded research
Funding institutionYale University
NIH-funded
Lab location1 site (New Haven, United States)
Project startJanuary 1, 2025
Project endDecember 31, 2029
Funding year2026
Award (this year)$482,918
NIH project number5R37CA295952-02
Project IDNIH-11252352 on NIH RePORTER

Who could benefit from this research

Could help

People with head and neck squamous cell carcinoma, especially those with tumors that are resistant to radiation or chemotherapy, would be the most likely candidates.

Less likely to help

Patients with cancer types outside head and neck squamous cell carcinoma, tumors that lack the STING pathway, or those who cannot tolerate experimental treatments may not benefit.

What this research studies

Researchers found that the STING pathway inside tumor cells changes how head and neck cancers respond to DNA-damaging treatments like radiation and chemotherapy. They used a whole-genome CRISPR screen to identify STING as a key driver of treatment sensitivity and studied how STING affects reactive oxygen and DNA damage in cancer cells. To deliver STING activation specifically to tumors, they are developing a pH-sensitive carrier (pHLIP) that releases a STING-activating compound in the acidic tumor environment. Work includes laboratory and preclinical tests combining the targeted STING activator with standard therapies to overcome treatment resistance.

Why it matters

Potential benefit: If successful, this approach could make radiation and chemotherapy work better against resistant head and neck tumors, potentially shrinking cancers and improving survival.

How similar studies have gone: STING activation has shown promise in lab and some early clinical work, but using a tumor-targeted pHLIP delivery of a STING agonist is a novel and largely untested approach in patients.

Where this research is happening

  • Yale University
    New Haven, United States
    Active

Researchers

  • Principal investigator: Hayman, Thomas — Yale University
  • Study coordinator: Hayman, Thomas

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.