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Clinical Trial Summary

This Phase 3, multicenter, randomized, masked, controlled, parallel group study is designed to demonstrate that suprachoroidal (SC) CLS-TA administered with intravitreal (IVT) anti-VEGF agent in subjects with treatment naive RVO is superior to IVT anti-VEGF agent used alone.


Clinical Trial Description

A Randomized, Masked, Controlled Trial to Study the Safety and Efficacy of Suprachoroidal CLS-TA With Intravitreal Anti-VEGF Agent in Subjects With Retinal Vein Occlusion ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03203447
Study type Interventional
Source Clearside Biomedical, Inc.
Contact
Status Terminated
Phase Phase 3
Start date March 5, 2018
Completion date December 18, 2018

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