Atlas Trials

Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants

Clinical trial NCT05589714 · RECRUITING

Trial details

NCT number
NCT05589714
Sponsor
Jaeb Center for Health Research
Status
RECRUITING
Study type
OBSERVATIONAL
Inherited Retinal DegenerationRetinitis Pigmentosa
Start date
2023-05-11
Primary completion
2029-12-15
Enrollment
1500

View on ClinicalTrials.gov

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