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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.