Brint Family Translational Research Award
Foundation for Fighting Blindness
This program funds research and development efforts that are creating novel, clinically relevant treatments and cures for inherited retinal disease and dry age-related macular degeneration.
Priority areas are, but not limited to:
(1) Novel Medical Therapies – approaches that use chemistry, biology, and bioengineering to formulate new therapies (e.g., small molecules, biologics) that mitigate inherited retinal degenerations and dry age-related macular degenerations.
(2) Genetic Technologies – the manipulation and modification of human gene expression to alter the biological properties of living cells/tissues with the goal of providing retinal therapeutic solutions.
(3) Regenerative Medicine – the development, regeneration, and employment of human cells, tissues, and cellular/tissue-based products for the restoration of retinal function and vision.
Funding up to $1M USD available over three years.
Deadlines
UM Internal Deadline | Sponsor Deadline | |
---|---|---|
Letter of Intent |
| 12-Jun-2025 |
Application (Upon Invitation Only) | 24-Sep-2025 4:30 pm CST | 16-Oct-2025 |
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