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Efficacy Study of GS010 for Treatment of Vision Loss From 7 Months to 1 Year From Onset in LHON Due to the ND4 Mutation.
Status of the trial: Completed
Orphan Drug Recognition: No
- Opening Date: 2016-02-01
- Closing Date: 2017-08-01
Inclusion: Patients with Leber hereditary optic neuropathy (LHON) carrying the m.11778G>A mitochondrial DNA mutationcarrying the m.11778G>A mitochondrial DNA mutation
Exclusion: Disease duration of more than one year in one or both eyes
Funder Type: industry
HCP: Principal investigators
HCP: Other investigators
Within ERN-EYE members
- Neuro-Ophthalmology Rare Diseases (WG2)
This ERN is supported by:
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