Clinical Trial
Disease
Disease type
Hereditary retinal disease
Retinitis Pigmentosa
Usher Syndrome
Orphan drug recognition
NA
Patient type
Adult
Children
Inclusion / Exclusion
Funding
patient organisation
Members involved
Main investigators
Dr Ingeborgh VAN DEN BORN
Representative
Netherlands
Registries & Epidemiology (TWG7), Research (TWG8), Retinal Rare Eye Diseases (WG1)
Others investigators
Pr Francesca Simonelli
Representative
Italy
Genetic Diagnostics (TWG6), National Integration (TWG9), Registries & Epidemiology (TWG7), Retinal Rare Eye Diseases (WG1)
ERN EYE member investigating site
HCP : Principal investigators
The Rotterdam Eye Hospital, Rotterdam, Netherlands
Adress
Schiedamse Vest 180
3011 BH Rotterdam
Netherlands
HCP : Others investigators
AOU Università degli Studi della Campania Luigi Vanvitelli, Napoli, Italy
Adress
Via Santa Maria di Costantinopoli
104, 80138 Napoli NA
Italy