Member info
Pr Isabelle MEUNIER
Representative
France
Working Group(s): Retinal Rare Eye Diseases (WG1)
HCP Center
Labelized in 2004, MAOLYA is a national reference center for the diagnosis and management of multisensory inherited diseases with isolated or...
contact
Reference Center Rare Diseases ‘Genetic Sensory Diseases’, MAOLYA, Montpellier, France
Hôpital Gui de ChauliacService Ophtalmologie80, avenue Augustin Fliche 1er étage, bureau 1414
34 295 Montpellier Cedex 5
France
Clinical trials
NCT02994368 Recruiting Active
A Multicenter Prospective Observational « Natural History » Study in Patients With Choroideremia.
Observational
NCT01235624 Completed
Autosomal Dominant Retinitis Pigmentosa: Prevalence of Known Genes Identification of New Loci/Genes.
Interventional
NCT01461213 Completed
Gene therapy study on choroideremia : to assess the safety and tolerability of the AAV.REP1 vector, administered at two different doses to the retina in patients with a diagnosis of choroideremia.
Interventional
NCT03328130 Recruiting Active
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 PDE6B Expression
Interventional
NCT03314207 Recruiting Active
Natural history of the progression of X-linked retinitis pigmentosa.
Observational