Clinical trial
A Post-Authorization, Multicenter, Longitudinal, Observational Safety Registry Study for Patients Treated With Voretigene Neparvovec in US
NCT03597399 is registered in ClinicalTrials.gov with Spark Therapeutics, Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Post-Authorization, Multicenter, Longitudinal, Observational Safety Registry Study for Patients Treated With Voretigene Neparvovec in US
- Lead sponsor
- Spark Therapeutics, Inc.
- Phase
- Observational
- Overall status
- Completed
- Start date
- January 10, 2019
- Completion date
- June 30, 2025
- Enrollment
- 87 (actual)
- Sites
- 10
Conditions
As the registry lists them; a condition with its own page is linked.
confirmed biallelic rpe65 mutation-associated retinal dystrophy