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NCT00691717 · ClinicalTrials.gov registry record · Phase 2
Anecortave Acetate Safety in Patients With Open-Angle Glaucoma or Ocular Hypertension
A Phase 2 study of Open Angle Glaucoma and Oular Hypertension, sponsored by Alcon Research.
- Completed
- Registry status
- Phase 2
- Development phase
- 201
- Enrollment target
- 1
- Study location
NCT00691717 is a Phase 2 study of Open Angle Glaucoma and Oular Hypertension that has completed, run by Alcon Research. The registered enrollment target is 201 participants, below the 327-participant average among 28 other Open Angle Glaucoma trials with a reported enrollment target (39% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00691717, a Phase 2 study of Open Angle Glaucoma and Oular Hypertension, has completed, sponsored by Alcon Research.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 201 participants
- Enrollment target
- 1
- Study location
Study 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 Studied
Interventions
- DRUG Anecortave Acetate Sterile Suspension, 30 mg/mL
- DRUG Anecortave Acetate Sterile Suspension, 60 mg/mL
- OTHER Anecortave Acetate Vehicle
- DRUG Anecortave Acetate Sterile Suspension, 75 mg/mL
Study Locations (1)
South Carolina
- Charleston - Charleston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 201 participants |
| Start Date | 2008-06 |
| Est. Completion | 2009-09 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00691717
The ClinicalTrials.gov registry entry for NCT00691717 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 201 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 327-participant average among 28 other Open Angle Glaucoma trials with a reported enrollment target (39% lower). The listed sponsor is Alcon Research, which has 275 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Open Angle Glaucoma appearing as the primary indexed condition, and to 4 interventions - of which Anecortave Acetate Sterile Suspension, 30 mg/mL is the first listed.
NCT00691717 reports 1 study location spanning 1 distinct geographic area - top geographies include South Carolina.
Frequently Asked Questions
What is clinical trial NCT00691717 about?
NCT00691717 is a clinical study titled "Anecortave Acetate Safety in Patients With Open-Angle Glaucoma or Ocular Hypertension". 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.
What is the current status of trial NCT00691717?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 201 participants. The study started on 2008-06. Estimated completion is 2009-09.
What conditions does trial NCT00691717 study?
This clinical trial studies the following conditions: Open Angle Glaucoma, Oular Hypertension.
What interventions are being tested in trial NCT00691717?
The interventions under investigation include: Anecortave Acetate Sterile Suspension, 30 mg/mL (DRUG), Anecortave Acetate Sterile Suspension, 60 mg/mL (DRUG), Anecortave Acetate Vehicle (OTHER), Anecortave Acetate Sterile Suspension, 75 mg/mL (DRUG).
Who is sponsoring clinical trial NCT00691717?
This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00691717 being conducted?
This trial has 1 study location across South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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