Clinical Trial
NCT06591806 Recruiting, Active
An Observational Study in Children and Adults With Stargardt Disease
A Multicenter, Prospective, Longitudinal, Observational Study in Children and Adults With Stargardt Disease Related Atrophy Secondary to Biallelic Mutations in the ABCA4 Gene
Disease
Disease type
Stargardt Disease
Patient type
Adult
Children
Inclusion / Exclusion
Funding
Industry
Members involved
Others investigators
Pr Francesca Simonelli
Representative
Italy
Genetic Diagnostics (TWG6), National Integration (TWG9), Registries & Epidemiology (TWG7), Retinal Rare Eye Diseases (WG1)
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
Dr Ingeborgh VAN DEN BORN
Representative
Netherlands
Registries & Epidemiology (TWG7), Research (TWG8), Retinal Rare Eye Diseases (WG1)
ERN EYE member investigating site
HCP : Principal investigators
AOU Università degli Studi della Campania Luigi Vanvitelli, Napoli, Italy
Adress
Via Santa Maria di Costantinopoli
104, 80138 Napoli NA
Italy
Fondazione Policlinico Universitario A. Gemelli – Roma, Italy
Adress
Via della Pineta Sacchetti, 217
168 Roma RM
Italy
Ghent University Hospital, Ghent, Belgium
Adress
Corneel Heymanslaan 10
9000 Ghent
Belgium
The Rotterdam Eye Hospital, Rotterdam, Netherlands
Adress
Schiedamse Vest 180
3011 BH Rotterdam
Netherlands