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Dra. Catherine Vignal-Clermont

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Dr Catherine Vignal-Clermont

France

Líder do Grupo de Trabalho: Neuro-Oftalmologia Doenças Raras (GT2)
Outros grupos de trabalho: Neuro-Oftalmologia Doenças Raras (GT2)

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Dr Elise Boulanger-Scemana

France

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Centro de saúde

Criado em 1905, graças a um legado do Barão Adolphe de Rothschild, o Hospital da Fundação Rothschild é um hospital universitário reconhecido...

Contacto

Fondation Adolphe de Rothschild, Paris, France

25-29 Rue Manin
75019 Paris
France

Centro de saúde

O Centro de Referência REFERET é especializado em doenças genéticas da retina, mácula e nervo óptico. Reúne três sites com...

Contacto

RÉFÉRET National Hospital of Ophthalmology of Quinze-Vingts, Paris, France

28 Rue de Charenton
75012 Paris
France

Ensaios clínicos

NCT02064569). Efetuado

An open label dose escalation clinical trial to evaluate the safety and the tolerability of gs010 (rAAV2/2-ND4) in patients with leber hereditary optic neuropathy due to mutations in the mitochondrial nadh dehydrogenase 4 gene.

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NCT02771379). Efetuado

A Non-interventional Study of Clinical Experience in Patients Prescribed Raxone® for the Treatment of Leber’s Hereditary Optic Neuropathy (LHON).

Observacional
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NCT03295071). Efetuado

Observational Registry Study of Leber Hereditary Optic Neuropathy (LHON) Affected Patients.

Observacional
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NCT03293524). Efetuado

Efficacy & Safety Study of Bilateral Intravitreal Injection of GS010 in LHON Subjects Due to the ND4 Mutation for up to 1 Year (REFLECT).

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NCT02652767). Efetuado

Efficacy Study of GS010 for the Treatment of Vision Loss up to 6 Months From Onset in LHON Due to the ND4 Mutation.

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NCT03406104). Efetuado

Long-term Follow-up of ND4 LHON Subjects Treated With GS010 Ocular Gene Therapy in the RESCUE or REVERSE Phase III Clinical Trials (RESTORE)

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NCT02652780). Efetuado

Efficacy Study of GS010 for Treatment of Vision Loss From 7 Months to 1 Year From Onset in LHON Due to the ND4 Mutation.

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NCT07303296). Recrutamento, Ativo

Efficacy and Safety Study of Bilateral IVT Injection of GS010 at Two Dose Levels in LHON Patients (REVISE)

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Publicações científicas

Five-Year Outcomes of Lenadogene Nolparvovec Gene Therapy in Leber Hereditary Optic Neuropathy

ADhoc–An immersive serious game that raises awareness among healthcare professionals about announcing a diagnosis of rare diseases

Predictors of Final Visual Outcome in Patients With Leber Hereditary Optic Neuropathy Treated With Lenadogene Nolparvovec Gene Therapy

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Meta-analysis of treatment outcomes for patients with m.11778G>A MT-ND4 Leber hereditary optic neuropathy

Phenotypic variability related to dominant UCHL1 mutations: about three families with optic atrophy and ataxia