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Clinical Trial Summary

Patients with advanced dry AMD with GA meeting inclusion criteria will be randomized in one eye in a 1:1:1 ratio comparing intravitreal high or low dose AAVCAGsCD59 with a sham injection. All enrolled subjects will be followed for 24 months to evaluate reduction in GA growth and safety of intravitreal AAVCAGsCD59.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04358471
Study type Interventional
Source Hemera Biosciences
Contact
Status Withdrawn
Phase Phase 2
Start date July 31, 2021
Completion date September 1, 2023

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