240
Participants
Start Date
March 31, 2005
Primary Completion Date
April 30, 2008
Study Completion Date
April 30, 2008
Anecortave Acetate Sterile Suspension, 30 mg/mL
One 0.5 mL posterior juxtascleral depot injection at 3 or 6 month intervals
Anecortave Acetate Sterile Suspension, 60 mg/mL
One 0.5 mL posterior juxtascleral depot injection at 6 month intervals
Anecortave Acetate Vehicle
One 0.5 mL sham injection at 6 month intervals
Alcon Study Sites, Fort Worth
Lead Sponsor
Alcon Research
INDUSTRY