The purpose of this study is to evaluate the safety, tolerability, and effects of investigational drug AL-39324 for the treatment of wet AMD.
Following a single administration, patients will be followed for 6 months postinjection.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
35
Incidence of targeted adverse events occurring in the study eye
Time frame: Up to Day 7 after injection
Mean change from baseline in central foveal thickness (CFT) at Month 1
Time frame: Baseline (Day 0), Month 1
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