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Japanese Phase 3 Study of Aflibercept in Neovascular Glaucoma Patients — VEGA  

Glaucoma, Neovascular Clinical Trial

Official title:
A Randomized, Double-masked, and Controlled Phase 3 Study to Evaluate the Efficacy, Safety, and Tolerability of Intravitreal Administration of Aflibercept in Japanese Patients With Neovascular Glaucoma

Clinical Trial Summary

To assess the efficacy and safety of the administration of aflibercept by intravitreal injection in comparison to sham to control intraocular pressure in patients with neovascular glaucoma.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02396316
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 3
Start date April 2015
Completion date September 2016
View Details
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