Skip to content

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
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00691717
Enrollment
201
Registered
2008-06-05
Start date
2008-06-30
Completion date
2009-09-30
Last updated
2012-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Open-angle Glaucoma, Oular Hypertension

Keywords

Anecortave acetate, Open-angle glaucoma, IOP, OHT

Brief 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.

Interventions

Single administration by anterior juxtascleral depot

Single administration by anterior juxtascleral depot

DRUGAnecortave Acetate Sterile Suspension, 75 mg/mL

Single administration by anterior juxtascleral depot

Single administration by anterior juxtascleral depot

Sponsors

Alcon Research
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients 18 years of age or older with open-angle glaucoma (with or without pigment dispersion or pseudoexfoliation) or ocular hypertension. * Other protocol-defined inclusion criteria may apply.

Exclusion criteria

* Patients with any form of glaucoma other than open-angle. * Other protocol-defined

Design outcomes

Primary

MeasureTime frame
Mean Intraocular Pressure at 8 amUp to 6 months

Secondary

MeasureTime frame
Percent of Patients Who Remained Rescue Medication-Free at Month 3 (8 am)Month 3, 8 am

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026