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NYRVANA

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Clinical Trial

2025-520665-47-00 Recruiting, Active
NYRVANA

An Open-Label Dose Escalation Study to Assess the Safety and Tolerability of a Single Intravitreal Injection of SPVN20 Gene Therapy in Subjects with No Light Perception Due to End Stage Rod Cone Dystrophy, and Who Retain Dormant Foveal Cone Photoreceptors

Phase 1
Interventional

Disease

Disease type

Retinitis Pigmentosa

Patient type

Adult

Children

Funding

Industry

Members involved

Main investigators

Pr Bart LEROY

Representative

Belgium

Genetic Diagnostics (TWG6), Low Vision Daily Life and Patients Groups (TWG5), National Integration (TWG9), Research (TWG8), Retinal Rare Eye Diseases (WG1)
Working Group Leader
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Pr Isabelle Audo

Representative

France

Genetic Diagnostics (TWG6), Low Vision Daily Life and Patients Groups (TWG5), National Integration (TWG9), Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), Research (TWG8), Retinal Rare Eye Diseases (WG1)
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ERN EYE member investigating site

HCP : Principal investigators