Clinical Trials Directory

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

TypeNameDescription
DRUGAnecortave Acetate Sterile Suspension, 30 mg/mLSingle administration by anterior juxtascleral depot
DRUGAnecortave Acetate Sterile Suspension, 60 mg/mLSingle administration by anterior juxtascleral depot
DRUGAnecortave Acetate Sterile Suspension, 75 mg/mLSingle administration by anterior juxtascleral depot
OTHERAnecortave Acetate VehicleSingle 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.