NIH-funded research R37 grant

New ways to prevent and reverse chemotherapy-related nerve damage

Official title: Developing mechanism-based strategies to treat chemotherapy-induced peripheral neuropathy

Funded at Washington University · NIH-11284066 · Data updated 2026-11-12

Researchers are trying approaches that block a nerve‑destroying protein to prevent or reverse painful nerve damage in people treated with chemotherapy.

More Chemotherapy research and trials

Quick facts

Grant typeR37 grant
Study typeNIH-funded research
Funding institutionWashington University
NIH-funded
Lab location1 site (Saint Louis, United States)
Project startJanuary 13, 2022
Project endDecember 31, 2026
Funding year2026
Award (this year)$377,467
NIH project number5R37CA267905-05
Project IDNIH-11284066 on NIH RePORTER

Who could benefit from this research

Could help

People receiving or about to receive neurotoxic chemotherapy (for example vincristine or bortezomib) who are at risk for or already have signs of peripheral neuropathy would be the primary candidates.

Less likely to help

Patients with neuropathy from non‑chemotherapy causes or those with longstanding, complete nerve loss unlikely to be reversible may not benefit from these approaches.

What this research studies

Chemotherapy often injures the long nerve fibers that carry feeling from hands and feet, causing lasting pain and disability. This project targets a protein called SARM1 that triggers axon (nerve fiber) self‑destruction and tests strategies to stop that final step. The team is developing a blocking version of SARM1 delivered by adeno‑associated virus and other mechanism‑based approaches to keep nerves alive during or after treatment with drugs like vincristine and bortezomib. Work includes laboratory and preclinical testing aimed at methods that could be translated into treatments for patients receiving neurotoxic chemotherapy.

Why it matters

Potential benefit: If successful, these approaches could prevent or reverse chemotherapy‑induced peripheral neuropathy, improve quality of life, and allow patients to complete effective cancer treatment.

How similar studies have gone: Related SARM1‑targeting strategies have shown promising results in animal and laboratory models but are still novel and unproven in human patients.

Where this research is happening

  • Washington University
    Saint Louis, United States
    Active

Researchers

  • Principal investigator: Geisler, Stefanie — Washington University
  • Study coordinator: Geisler, Stefanie

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.