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Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of FID 112903 given as an immediate treatment replacement in dry eye subjects that discontinue at least 6 months use of RESTASIS.


Clinical Trial Description

n/a


Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01198782
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase Phase 4
Start date September 2010
Completion date May 2011

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