The purpose of this study is to evaluate the safety and tolerability profile of ascending doses of GS010 in Leber Hereditary Optic Neuropathy (LHON) patients.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
19
CIC du CHNO DES QUINZE-VINGTS
Paris, France
Incidence of local and general adverse events and Serious Adverse Events
Time frame: Up to 48 weeks
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