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Clinical Trial Summary

The purpose of the current study is to evaluate the ability of Eylea to induce a regression of PED height on patients previously extensively treated by Lucentis. The regimen proposed for this study is the 3 monthly injection followed by a 6 weeks interval injection until week 26.


Clinical Trial Description

The regimen proposed for this study is the 3 monthly injection followed by a 6 weeks interval injection until week 26. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02157077
Study type Interventional
Source Centre Hospitalier Intercommunal Creteil
Contact
Status Completed
Phase Phase 3
Start date December 2013
Completion date December 2015

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