Tolerance and Efficacy Nicotinamide (Vitamin B3) in Dominant Optic Atrophy OPA1 (NICOPA1-TOL)
Nicotinamide Adverse Reaction
About this trial
This is an interventional treatment trial for Nicotinamide Adverse Reaction
Eligibility Criteria
Inclusion Criteria: Adult patients Patients with DOA or DOA+ due to a heterozygous pathogenic variant in the OPA1 gene Naïve patients (> 3 months) in terms of taking nicotinamide Patients able to take oral medication and comply with specific study procedures Patients affiliated or beneficiaries of a social security scheme Signature of voluntary, free and informed consent to participate in the study Exclusion Criteria: Asymptomatic patients (= healthy carriers of an OPA1 mutation but not having developed optic neuropathy) Patients with another associated severe ophthalmological pathology (advanced glaucoma, retinal pathology, etc.) Patients treated with Idebenone Patients with a level of transaminase(s) (ASAT and/or ALAT) twice higher than the high normal value. Pregnant, breastfeeding or parturient women Patients with a contraindication to nicotinamide Persons deprived of liberty by administrative or judicial decision Patients subject to a legal protection measure Persons undergoing psychiatric treatment under duress Persons unable to express their consent
Sites / Locations
Arms of the Study
Arm 1
Experimental
nicotinamide