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Trial + Data / Events	Status	Ph	N	Region	Interventions	Sponsor	Conditions	Primary compl	Study compl
Uwaydat, Sami
Uni-Rare, NCT05589714: Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants	Recruiting	N/A	1500	Europe, Canada, US, RoW		Jaeb Center for Health Research, Foundation Fighting Blindness	Inherited Retinal Degeneration, Retinitis Pigmentosa	12/28	12/28
Uwaytdat, Sami
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