Clinical trial
Safety and Efficacy of a Unilateral Subretinal Administration of HORA-PDE6B in Patients With Retinitis Pigmentosa Harbouring Mutations in the PDE6B Gene Leading to a Defect in PDE6ß Expression
NCT03328130 is registered in ClinicalTrials.gov with eyeDNA Therapeutics as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Safety and Efficacy of a Unilateral Subretinal Administration of HORA-PDE6B in Patients With Retinitis Pigmentosa Harbouring Mutations in the PDE6B Gene Leading to a Defect in PDE6ß Expression
- Lead sponsor
- eyeDNA Therapeutics
- Phase
- Phase 1/2
- Overall status
- Terminated
- Start date
- November 6, 2017
- Completion date
- June 30, 2025
- Enrollment
- 19 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.