NIH-funded research R01 grant

Ferrochelatase: a new target to block abnormal eye blood vessel growth

Official title: Ferrochelatase as a mediator of ocular angiogenesis

Funded at University of Toronto · NIH-11307570 · Data updated 2026-11-12

A scientist is studying a gene called FECH to understand how to stop unwanted blood vessel growth in diseases like age-related macular degeneration and diabetic retinopathy.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Toronto
NIH-funded
Lab location1 site (Toronto, Canada)
Project startMarch 1, 2016
Project endMarch 31, 2028
Funding year2026
Award (this year)$305,695
NIH project number5R01EY025641-09
Project IDNIH-11307570 on NIH RePORTER

Who could benefit from this research

Could help

Patients with neovascular eye diseases such as AMD, diabetic retinopathy, or retinopathy of prematurity could benefit from future treatments stemming from this research.

Less likely to help

Patients without neovascular eye diseases may not directly benefit from this research.

What this research studies

This project looks at ferrochelatase (FECH), a key enzyme in making heme, and how it affects the growth of abnormal blood vessels in the eye. The team investigates how FECH activity influences energy production and metabolism in retinal cells, with the goal of slowing or stopping dangerous neovascularization. Building on prior findings, they will delve into the mechanisms by which FECH links heme synthesis to glycolysis and endothelial cell behavior, and they will test a drug-like FECH inhibitor in lab and animal models. The ultimate aim is to identify a new, targeted approach to treat or prevent vision loss from neovascular eye diseases.

Why it matters

Potential benefit: If successful, this work could lead to new therapies that more effectively prevent or reduce vision loss from retinal diseases by stopping abnormal blood vessel growth.

How similar studies have gone: Previous studies showed FECH involvement in ocular neovascularization and antiangiogenic effects of FECH inhibition in models, suggesting potential for translation.

Where this research is happening

  • University of Toronto
    Toronto, Canada
    Active

Researchers

  • Principal investigator: Corson, Timothy W — University of Toronto
  • Study coordinator: Corson, Timothy W

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.