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Anecortave Acetate in Patients With Open-angle Glaucoma

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

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00320203
Enrollment
86
Registered
2006-05-03
Start date
2006-03-31
Completion date
2008-01-31
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

Keywords

open-angle, glaucoma

Brief summary

The purpose of this study is to evaluate the safety, efficacy, and duration of effect of a single administration of Anecortave Acetate Depot for treatment of elevated intraocular pressure (IOP) in patients with open-angle glaucoma.

Interventions

Single injection, anterior juxtascleral depot (AJD)

Single injection, anterior juxtascleral depot (AJD)

Single injection, anterior juxtascleral depot (AJD)

Single injection, anterior juxtascleral depot (AJD)

Sponsors

Alcon Research
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, 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. * Other protocol-defined inclusion criteria may apply.

Exclusion criteria

* Patients with open-angle glaucoma with a pseudoexfoliation or pigment dispersion component. * Other protocol-defined

Design outcomes

Primary

MeasureTime frame
Mean change in intraocular pressure at 9 am from baselineWeeks 2 and 6, Months 2, 3, 4, 5, 6, 7.5, 9, 10.5, and 12

Secondary

MeasureTime frame
Time to treatment failureAt time point

Outcome results

None listed

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