Clinical Trials for Retinal Dystrophy Due to Biallelic ABCA4 Mutations

Find clinical trials for retinal dystrophy due to biallelic abca4 mutations. Discover research opportunities and treatment options in your area.

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Safety and Preliminary Efficacy of VG801 in Patients With ABCA4 Mutation-associated Retinal Dystrophy (Stargardt Disease)

NCT ID: NCT07002398

This clinical trial is studying a new treatment called VG801 for patients with Stargardt disease, a type of inherited eye condition that affects vision. Stargardt disease is linked to specific chan...

Recruiting

Phase: PHASE1 Type: interventional Locations: Shanghai, Shanghai, China

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