Trials / Completed
CompletedNCT00620256
Adjunctive Study of AL-37807 Ophthalmic Suspension
Comparison of Safety and Efficacy of Al-37807 Ophthalmic Suspension vs. Timolol Gel Forming Solution and Vehicle, All Dosed Concomitantly With Xalatan in Patients With Open-Angle Glaucoma or Ocular Hypertension
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 129 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the study is to compare the safety and intraocular pressure-lowering efficacy of AL-37807 ophthalmic suspension vs. Timolol gel forming solution vs. AL-37807 vehicle, all dosed concomitantly with Xalatan, in patients with open-angle glaucoma or ocular hypertension.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | AL-37807 ophthalmic suspension, 0.1% | |
| DRUG | Timolol gel forming solution, 0.5% | |
| OTHER | AL-37807 ophthalmic solution vehicle | |
| DRUG | Latanoprost ophthalmic solution |
Timeline
- Start date
- 2007-11-01
- Primary completion
- 2008-07-01
- Completion
- 2008-07-01
- First posted
- 2008-02-21
- Last updated
- 2012-12-05
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00620256. Inclusion in this directory is not an endorsement.