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SYL040012. Tolerance and Effect on Intraocular Pressure in Subjects With Intraocular Pressure (IOP) >= 21 mm Hg

Glaucoma Clinical Trial

Official title:
Study With SYL040012. Tolerance and Effect on Intraocular Pressure in Subjects With IOP >= 21 mm Hg.

Clinical Trial Summary

The aim of this study is to evaluate the tolerance and effect on unmedicated subjects with elevated IOP.

Clinical Trial Description

The aim of this study is to evaluate the tolerance and effect on unmedicated subjects with elevated IOP. An unmedicated subject is considered a person without any IOP/glaucoma treatment at least one month before recruitment. ;

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01227291
Study type Interventional
Source Sylentis, S.A.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date October 2010
Completion date September 2012
View Details
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