Status:
TERMINATED
Anecortave Acetate Risk Reduction Trial (AART)
Lead Sponsor:
Alcon Research
Conditions:
AMD
Eligibility:
All Genders
50+ years
Phase:
PHASE3
Brief Summary
The purpose of this study is to demonstrate that Anecortave Acetate for Depot Suspension (15 mg or 30 mg) is safe and effective in arresting the progression of dry age-related macular degeneration (AM...
Eligibility Criteria
Inclusion
- Dry AMD in study eye, Wet AMD non-study eye.
- Other protocol-defined inclusion criteria may apply.
Exclusion
- Under 50.
- Other protocol-defined exclusion criteria may apply.
Key Trial Info
Start Date :
September 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2008
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT00332657
Start Date
September 1 2006
End Date
December 1 2008
Last Update
November 28 2012
Active Locations (1)
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1
India
Bangalore, India, 76134