Study Summary
This is a single-arm, open-label, non-randomized, single dose-escalation, first-in-human (FIH) clinical trial to evaluate the safety and preliminary efficacy of VG801 for treatment of patients with retinal dystrophy (Stargardt disease) due to biallelic ABCA4 mutations.
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VG801DRUG
Administered as specified in the single treatment arm. Study Cohort: Low dose, medium dose and high dose cohort
Study Locations
| Facility | City | State | Country |
|---|---|---|---|
| Shanghai General Hospital | Shanghai | Shanghai Municipality | China |