Texas
San Antonio, Texas, 78257, United States
NCT Number: NCT00451152
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.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
San Antonio, Texas, 78257, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Administered by anterior juxtascleral depot (AJD) in study eye, either 0.25 mL or 0.5 mL. One injection, 24 months.
Administered by anterior juxtascleral depot (AJD) in study eye, 0.5 mL. One injection, 24 months.
Time frame: 3 months
Time frame: 3 months
Alcon Research
Industry
A Study of the Safety and IOP-Lowering Efficacy of Anecortave Acetate in Patients With Open-Angle Glaucoma
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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