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Clinical Trial Summary

The purpose of this study is to compare the safety and efficacy of intravitreal Eylea injections at a set interval, versus a variable dosing schedule (likely longer than one month), based on a specific individual's disease progression. There will be approximately 50 men and women at least 18 years of age, diagnosed with type 1 or type 2 diabetes, taking part in this study at 5 locations in the United States.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02392364
Study type Interventional
Source California Retina Consultants
Contact
Status Completed
Phase Phase 4
Start date April 15, 2015
Completion date November 15, 2018

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