Overview

Visudyne® in Occult (VIO)

Status:
Completed
Trial end date:
2005-08-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to demonstrate that Visudyne therapy in patients who have occult with no classic subfoveal choroidal neovascularization (CNV) lesions will, with an acceptable safety profile, significantly reduce the risk of vision loss compared with placebo (sham treatment).
Phase:
Phase 3
Details
Lead Sponsor:
QLT Inc.
Treatments:
Verteporfin