Clinical Trials Directory

Trials / Completed

CompletedNCT00735449

Comparing Efficacy and Safety of Combigan With Timolol Adjunctive to Xalatan in Glaucoma or Ocular Hypertension Subjects

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
204 (actual)
Sponsor
Allergan · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Efficacy and safety evaluation of Combigan with timolol when each is used as adjunctive therapy to Xalatan in subjects with glaucoma or ocular hypertension.

Conditions

Interventions

TypeNameDescription
DRUGFixed combination of brimonidine tartrate 0.2% timolol maleate 0.5%1 drop of fixed combination of brimonidine tartrate 0.2% timolol maleate 0.5% taken approximately 12 hours apart, up to 2 times a day.
DRUGtimolol maleate 0.5%1 drop of timolol maleate 0.5% taken approximately 12 hours apart, up to 2 times a day.
DRUGlatanoprost 0.005%1 drop of latanoprost 0.005% once nightly.

Timeline

Start date
2008-07-01
Primary completion
2009-12-01
Completion
2009-12-01
First posted
2008-08-15
Last updated
2019-04-23
Results posted
2011-11-24

Locations

2 sites across 2 countries: United States, Canada

Source: ClinicalTrials.gov record NCT00735449. Inclusion in this directory is not an endorsement.

Comparing Efficacy and Safety of Combigan With Timolol Adjunctive to Xalatan in Glaucoma or Ocular Hypertension Subjects (NCT00735449) · Clinical Trials Directory