NIH-funded research R01 grant

Understanding a protein called EMP2 in retinopathy of prematurity

Official title: Targeting epithelial membrane protein 2 (EMP2) in retinopathy of prematurity

Funded at University of California Los Angeles · NIH-11115608 · Data updated 2026-11-12

This work explores how a specific protein called EMP2 contributes to abnormal blood vessel growth in the eyes of premature infants with retinopathy of prematurity.

More Prematurity research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of California Los Angeles
NIH-funded
Lab location1 site (Los Angeles, United States)
Project startJune 1, 2021
Project endMay 31, 2027
Funding year2025
Award (this year)$391,647
NIH project number5R01EY032561-05
Project IDNIH-11115608 on NIH RePORTER

Who could benefit from this research

Could help

This foundational research focuses on understanding disease mechanisms in retinopathy of prematurity, which primarily affects extremely low birth weight premature infants.

Less likely to help

Patients who do not have retinopathy of prematurity or are not premature infants would not directly benefit from this specific research.

What this research studies

Retinopathy of prematurity (ROP) is a major cause of childhood blindness, affecting many premature babies. When premature infants are exposed to too much oxygen due to underdeveloped lungs, it can cause blood vessels in their eyes to shrink, leading to a lack of oxygen. This oxygen shortage then triggers the growth of abnormal, leaky blood vessels. We are looking into how a protein called EMP2 might be involved in this process, as it appears to regulate other factors that promote abnormal vessel growth. Our goal is to understand if targeting EMP2 could help prevent or treat the damaging eye changes seen in ROP.

Why it matters

Potential benefit: If successful, this work could lead to new ways to prevent or treat the abnormal blood vessel growth that causes blindness in premature infants with retinopathy of prematurity.

How similar studies have gone: Preliminary data in mouse models suggest that reducing EMP2 can lessen abnormal blood vessel growth, indicating a promising new direction for this approach.

Where this research is happening

  • University of California Los Angeles
    Los Angeles, United States
    Active

Researchers

  • Principal investigator: Chu, Alison — University of California Los Angeles
  • Study coordinator: Chu, Alison

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.