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Study of UshStat in Patients With Retinitis Pigmentosa Associated With Usher Syndrome Type 1B

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Clinical Trial

NCT01505062 Completed
Study of UshStat in Patients With Retinitis Pigmentosa Associated With Usher Syndrome Type 1B

Study of UshStat in Patients With Retinitis Pigmentosa Associated With Usher Syndrome Type 1B.

Interventional
Interventional

Disease

Disease type

Hereditary retinal disease

Retinitis Pigmentosa

Usher Syndrome

Orphan drug recognition

NA

Patient type

Adult

Children

Inclusion / Exclusion

Opening date

25/04/2014

Closing date

25/04/2018

Inclusion criteria :

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Exclusion criteria :

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Funding

industry

Members involved

Main investigators

Pr José-Alain Sahel

France

Genetic Diagnostics (TWG6), Low Vision Daily Life and Patients Groups (TWG5), Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), Research (TWG8), Retinal Rare Eye Diseases (WG1)
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Others investigators

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