Find clinical trials for retinitis pigmentosa. Search for retinitis pigmentosa clinical trials in different cities and states across the United States.
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Active & Responsive
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
for
Rare Disorders, Undiagnosed Disorders,
Location: 1 recruiting location
Sponsor: Sanford Health
Sex: All
Age: 0+
Code: NCT01793168
Recruiting
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A Repeat-Dose, Open-Label, Two Arm Safety and Efficacy Study of Two Doses of VP-001 Administered Intravitreally in Participants With Confirmed PRPF31 Mutation-Associated Retinal Dystrophy, Including Participants Previously Treated With VP001