NIH-funded research NIH-funded research

Creating a resource of non-human primate models for human genetic diseases

Official title: A National NHP Embryo Resource of Human Genetic Disease Models

Funded at Oregon Health & Science University · NIH-11003343 · Data updated 2026-11-12

This study is working to create a special resource of non-human primates that can help scientists test new treatments for genetic diseases that affect humans, with the hope of finding better options for patients facing tough health challenges.

More Genetic Disease research and trials

Quick facts

Grant typeNIH-funded research
Study typeNIH-funded research
Funding institutionOregon Health & Science University
NIH-funded
Lab location1 site (Portland, United States)
Project startMarch 1, 2023
Project endDecember 31, 2026
Funding year2025
Award (this year)$494,142
NIH project number5R24OD034055-03
Project IDNIH-11003343 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for participation or benefit from this research are individuals with genetic diseases that have been modeled in non-human primates.

Less likely to help

Patients with common conditions that do not have a genetic basis may not receive any benefit from this research.

What this research studies

This research aims to establish a national resource for preserving and utilizing non-human primate (NHP) models that mimic human genetic diseases. By developing these models, the project seeks to facilitate the testing of new therapies and precision medicine approaches that could lead to breakthroughs in treating currently uncurable conditions. The research will focus on overcoming challenges related to breeding and availability of these models, ensuring that they can be effectively used in pre-clinical testing. Patients may benefit from advancements in treatment options that arise from this innovative approach.

Why it matters

Potential benefit: If successful, this research could lead to the development of new therapies for genetic diseases that currently have no cure.

How similar studies have gone: Other research has shown success in using animal models for studying human diseases, making this approach promising and not entirely novel.

Where this research is happening

  • Oregon Health & Science University
    Portland, United States
    Active

Researchers

  • Principal investigator: Sherman, Larry S. — Oregon Health & Science University
  • Study coordinator: Sherman, Larry S.

Related research

Other NIH-funded projects on the same topics.

  • Evidence-based diagnostic criteria for pediatric genetic diseases

    A clinician-scientist is testing clearer, data-driven criteria to diagnose rare genetic diseases in children, starting with Basal Cell Nevus Syndrome, to help families get faster, more accurate genetic testing.

    NIH research Children's Hosp of Philadelphia · Philadelphia, United States · NIH-11327359

  • Mapping protein changes that cause cystic fibrosis

    This project uses a new computer method to map how genetic changes in the CFTR protein affect its folding and trafficking, with the goal of guiding treatments for people with cystic fibrosis.

    NIH research Scripps Research Institute, the · La Jolla, United States · NIH-11318888

  • National primate embryo resource for human genetic disease models

    They are building a national collection of primate embryos that carry human-like genetic mutations to help speed development of new treatments for inherited diseases.

    NIH research Oregon Health & Science University · Portland, United States · NIH-11253307

  • Creating better animal models for Alpha-1 antitrypsin deficiency

    This work aims to develop improved animal models to help us understand and find new treatments for Alpha-1 antitrypsin deficiency.

    NIH research Univ of Massachusetts Med Sch Worcester · Worcester, United States · NIH-11146477

  • Improving diagnosis of rare genetic diseases in children

    This study is working to improve how doctors diagnose over 7,000 rare genetic diseases in children by creating better guidelines that combine medical history, physical exams, and lab results, so kids can get the right treatment more easily.

    NIH research Children's Hosp of Philadelphia · Philadelphia, United States · NIH-11094052

  • Investigating how RNA structure changes contribute to genetic diseases

    This study is looking at how the shape of RNA affects how genes work after they are copied, which could help us understand more about certain diseases and genetic disorders.

    NIH research Univ of North Carolina Chapel Hill · Chapel Hill, United States · NIH-11088257

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.