drugset / Trial / NCT00121407

Visudyne® in Occult (VIO)

NCT00121407 ↗

Phase 3 Completed 364 enrolled QLT Inc.
RandomizedParallel-groupDouble-blindTreatment

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).

Timeline

Start
2002-03
Primary completion
—
Completion
2005-08

Outcome

Missed primary endpoint

paper The differences between the two groups in the primary efficacy variables were not significant. PMID 19530976 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Verteporfin Other / unclassified — Intravenous

Indications