Trials / Completed
CompletedNCT00691717
Anecortave Acetate Safety in Patients With Open-Angle Glaucoma or Ocular Hypertension
A Study of the Safety and IOP-Lowering Efficacy of Anecortave Acetate in Patients With Open-Angle Glaucoma or Ocular Hypertension
- Status
- Completed
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 201 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study was to evaluate the safety and intraocular-lowering efficacy of anecortave acetate depot when administered by anterior juxtascleral depot (AJD) for the treatment of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Anecortave Acetate Sterile Suspension, 30 mg/mL | Single administration by anterior juxtascleral depot |
| DRUG | Anecortave Acetate Sterile Suspension, 60 mg/mL | Single administration by anterior juxtascleral depot |
| DRUG | Anecortave Acetate Sterile Suspension, 75 mg/mL | Single administration by anterior juxtascleral depot |
| OTHER | Anecortave Acetate Vehicle | Single administration by anterior juxtascleral depot |
Timeline
- Start date
- 2008-06-01
- Primary completion
- 2009-09-01
- Completion
- 2009-09-01
- First posted
- 2008-06-05
- Last updated
- 2012-11-28
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00691717. Inclusion in this directory is not an endorsement.