Natural History of Autosomal Dominant Optic Atrophy (ADOA), Caused by OPA1 Mutation

Clinical trial NCT06140329 · TERMINATED

Trial details

NCT number: NCT06140329
Sponsor: PYC Therapeutics
Status: TERMINATED
Study type: OBSERVATIONAL

Autosomal Dominant Optic Atrophy Optic Atrophy, Autosomal Dominant Optic Atrophies, Hereditary Kjer Optic Atrophy

Start date: 2024-02-28
Primary completion: 2025-03-01
Enrollment: 1

View on ClinicalTrials.gov

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