Clinical Trials Directory

Trials / Terminated

TerminatedNCT01514721

Efficacy of Changing to DuoTrav® (Travoprost 0.004%/Timolol 0.5% BAK-Free Fixed Combination) From Prior Therapy

Assessing the Efficacy and Tolerability of Changing to DuoTrav® (Travoprost 0.004%/Timolol 0.5% BAK-Free Fixed Combination), as Replacement Therapy in Patients Previously on Prior Prostaglandin Fixed Combination

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
37 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess efficacy and tolerability of changing to DuoTrav® (Travoprost 0.004%/Timolol 0.5% BAK-free) from prior Xalacom® or Ganfort® fixed combination pharmacotherapy in patients with open-angle glaucoma or ocular hypertension with uncontrolled intraocular pressure (IOP).

Conditions

Interventions

TypeNameDescription
DRUGTravoprost/Timolol Maleate BAK-Free Fixed CombinationCommercially marketed Travoprost/Timolol BAK-free ophthalmic solution indicated for the treatment of patients with open angle glaucoma (OAG) or ocular hypertension (OH).

Timeline

Start date
2012-06-01
Primary completion
2013-11-01
Completion
2013-11-01
First posted
2012-01-23
Last updated
2014-12-03

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT01514721. Inclusion in this directory is not an endorsement.

Efficacy of Changing to DuoTrav® (Travoprost 0.004%/Timolol 0.5% BAK-Free Fixed Combination) From Prior Therapy (NCT01514721) · Clinical Trials Directory