Overview

Open-Label Posterior Juxtascleral Injections of Anecortave Acetate 15mg Dose for Long Term Use in Patients With AMD

Status:
Terminated
Trial end date:
2008-10-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to investigate the long-term efficacy and safety of posterior juxtascleral injections of open label Anecortave Acetate 15mg administered every 6 months.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Alcon Research
Treatments:
Anecortave
Criteria
Inclusion Criteria:

- Patients with subfoveal exudative age-related macular degeneration (AMD) who were
previously enrolled in long-term studies with anecortave acetate.

- Other protocol-defined inclusion criteria may apply.

Exclusion Criteria:

- Other protocol-defined exclusion criteria may apply.