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Safety and Efficacy of an Injectable Fluocinolone Acetonide Intravitreal Insert — FAI  

Non-Infectious Uveitis Clinical Trial

Official title:
A Phase III, Multi-National, Multi-Center, Randomized, Masked, Controlled, Safety and Efficacy Study of a Fluocinolone Acetonide Intravitreal Insert in Subjects With Chronic Non-Infectious Uveitis Affecting the Posterior Segment of the Eye

Clinical Trial Summary

A study to evaluate the safety and efficacy of an FAI insert for the management of subjects with non-infectious uveitis affecting the posterior segment of the eye.

Clinical Trial Description

This is a phase 3, multi-national, multi-center, randomized, masked, controlled study to evaluate the safety and efficacy of an injectable fluocinolone acetonide intravitreal (FAI) insert for the management of subjects with non-infectious uveitis affecting the posterior segment of the eye. Patients will be randomized to receive either a sham injection or the FAI insert and will be observed for three years following treatment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01694186
Study type Interventional
Source EyePoint Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 3
Start date August 2, 2013
Completion date March 26, 2018
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