Phase 2 study is designed to assess the efficacy of ADX-038 compared with placebo in participants with GA secondary to AMD. Safety, pharmacokinetics (PK), and pharmacodynamics (PD) will also be assessed.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
240
ADARx Clinical Site
Gilbert, Arizona, United States
Evaluate the effect of ADX-038 on the preservation of the EZ layer
Rate of change in the area of total EZ loss in the study eye from baseline to Month 12
Time frame: 12 months
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