Grants and Contracts Details
Description
This natural history study of patients with EYS mutations will accelerate the development of outcome
measures for clinical trials. Sensitive, reliable outcome measures of retinal degeneration will greatly
facilitate development of treatments for retinitis pigmentosa due to EYS mutations. Together these
approaches are expected to have an impact on understanding EYS-related retinal degeneration,
developing experimental treatment protocols, and assessing their effectiveness.
The goals and expected impact of this natural history study are to:
1. Describe the natural history of retinal degeneration in patients with biallelic mutations in the
EYS gene
2. Identify sensitive structural and functional outcome measures to use for future multicenter
clinical trials in EYS-related retinal degeneration
3. Identify well-defined subpopulations for future clinical trials of investigative treatments for
EYS-related retinal degeneration
Status | Finished |
---|---|
Effective start/end date | 4/17/20 → 5/9/22 |
Fingerprint
Explore the research topics touched on by this project. These labels are generated based on the underlying awards/grants. Together they form a unique fingerprint.