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
| Type | Name | Description |
|---|---|---|
| DRUG | Travoprost/Timolol Maleate BAK-Free Fixed Combination | Commercially 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.