Anecortave Acetate 15 mg sterile suspension
Drug0.5 ml of 30 mg/ml administered as a posterior juxtascleral injection
NCT Number: NCT00051129
The purpose of this study was to evaluate anecortave acetate compared to placebo for maintenance of visual acuity after 24 months of treatment in patients with subfovial choroidal neovascularization (CNV) due to exudative age-related macular degeneration (AMD).
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Notify Me50 year and older
All sexes
Interventional
Phase 3
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
0.5 ml of 30 mg/ml administered as a posterior juxtascleral injection
Administered as a posterior juxtascleral injection
Time frame: Month 12
Alcon Research
Industry
An Evaluation of Safety and Efficacy of Anecortave Acetate Versus Placebo in Patients With Subfoveal Choroidal Neovascularization Due to Exudative Age-Related Macular Degeneration.
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