The purpose of this study is to evaluate the safety, biological activity and pharmacodynamic effect of repeated intravitreal doses of hI-con1 0.3 mg administered as monotherapy and in combination with ranibizumab 0.5 mg compared to ranibizumab 0.5 mg monotherapy in treating patients with choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD).
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Change From Baseline in Best Corrected Visual Acuity (BCVA) in the Study Eye at Month 3
Timeframe: Baseline and Month 3
Change From Baseline in Central Retinal Subfield Thickness (CST) in the Study Eye at Month 3
Timeframe: Baseline and Month 3