NIH-funded research R01 grant

How NMDA receptors in the brain are tuned by drugs that bind to distant sites

Official title: Structural and functional investigation of allosteric NMDA receptor modulation

Funded at University of Montana · NIH-11232295 · Data updated 2026-11-12

This project looks at how drugs that bind away from the main NMDA receptor site change receptor behavior in ways that could help people with brain disorders.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Montana
NIH-funded
Lab location1 site (Missoula, United States)
Project startAugust 1, 2016
Project endNovember 30, 2026
Funding year2026
Award (this year)$366,000
NIH project number5R01NS097536-10
Project IDNIH-11232295 on NIH RePORTER

Who could benefit from this research

Could help

Adults with neurological or psychiatric conditions suspected to involve NMDA receptor dysfunction (for example certain epilepsies, treatment-resistant depression, or some neurodegenerative disorders) could be future candidates for therapies informed by this research.

Less likely to help

People with medical problems unrelated to NMDA receptors, children under 21, or those needing immediate clinical treatment are unlikely to receive direct benefits from this basic laboratory research.

What this research studies

Researchers will use laboratory methods to make detailed structural images of NMDA receptors and measure how they function when different allosteric drugs bind. They will compare receptors made with different GluN2 subunits to see which receptor subtypes respond to specific modulators. Experiments will combine biochemical binding tests and functional recordings to link where a drug binds to how the receptor signals. The goal is to identify ways to selectively tune NMDA receptors found in brain cells affected by disease.

Why it matters

Potential benefit: If successful, this work could guide development of safer, more targeted treatments for disorders linked to NMDA receptor dysfunction, such as some forms of epilepsy, treatment-resistant depression, or neurodegenerative disease.

How similar studies have gone: Existing NMDA-targeting drugs like ketamine and memantine have shown clinical effects, but selectively modulating specific NMDA receptor subtypes via allosteric sites is a newer approach with limited clinical translation so far.

Where this research is happening

  • University of Montana
    Missoula, United States
    Active

Researchers

  • Principal investigator: Hansen, Kasper Boe — University of Montana
  • Study coordinator: Hansen, Kasper Boe

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.