24-hr Intraocular Pressure Control With SIMBRINZA ®

Status Completed

Clinical Trial Summary

The purpose of this study is to evaluate differences between treatments in mean change from baseline in 24-hr intraocular pressure (IOP) at Week 4.

Clinical Trial Description

Subjects will undergo washout of pre-study IOP-lowering medications for the appropriate duration, then undergo 2 eligibility visits. Eligible subjects will be randomized 1:1, to receive masked SIMBRINZA ® or Vehicle for 4 weeks. Two 24-hour visits will be conducted (Day 0 and Week 4) during which intraocular pressure will be collected every 2 hours. The expected duration of subject participation in the study is 10 weeks. ;

Study Design

Related Conditions & MeSH terms

Glaucoma

Clinical Trial Details

NCT number	NCT02770248
Study type	Interventional
Source	Alcon Research
Contact
Status	Completed
Phase	Phase 4
Start date	May 23, 2016
Completion date	January 14, 2017

View Details

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