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A Safety and Efficacy Study of DE-120 Injectable Solution for Age-related Macular Degeneration — VAPOR1  

Age-Related Macular Degeneration Clinical Trial

Official title:
A Multicenter, Randomized, Open Label, Phase IIa Study Assessing the Efficacy, Safety and Duration of Effect of Intravitreal Injections of DE-120 as Monotherapy and With a Single Eylea® Injection in Subjects With Treatment-Naive Exudative Age-Related Macular Degeneration

Clinical Trial Summary

The purpose of the study is to evaluate the safety and efficacy of intravitreal (IVT) administration of DE-120 in subjects with treatment-naive active subfoveal choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02401945
Study type Interventional
Source Santen Inc.
Contact
Status Completed
Phase Phase 2
Start date April 2015
Completion date October 31, 2016
View Details
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