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Clinical Trials/NCT00451152
NCT00451152
Completed
Phase 2

A Study of the Safety and IOP-Lowering Efficacy of Anecortave Acetate in Patients With Open-Angle Glaucoma

Alcon Research1 site in 1 country89 target enrollmentMarch 2007

Overview

Phase
Phase 2
Intervention
Anecortave Acetate Sterile Suspension, 30 mg/mL
Conditions
Open-angle Glaucoma
Sponsor
Alcon Research
Enrollment
89
Locations
1
Primary Endpoint
Mean Intraocular Pressure (IOP)
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The purpose of this study was to evaluate the safety and intraocular pressure (IOP)-lowering efficacy of anecortave acetate for treatment of elevated IOP in patients with open-angle glaucoma.

Registry
clinicaltrials.gov
Start Date
March 2007
End Date
July 2009
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of open-angle glaucoma;
  • Other protocol-defined inclusion criteria may apply.

Exclusion Criteria

  • Pseudoexfoliation;
  • Pigment dispersion component;
  • Other protocol-defined exclusion criteria may apply.

Arms & Interventions

Anecortave Acetate Depot

Intervention: Anecortave Acetate Sterile Suspension, 30 mg/mL

Anecortave Acetate Vehicle

Intervention: Anecortave Acetate Vehicle

Outcomes

Primary Outcomes

Mean Intraocular Pressure (IOP)

Time Frame: 3 months

Secondary Outcomes

  • Percent Treatment Failures(3 months)

Study Sites (1)

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