Clinical trial

A Study to Compare rhuFab V2 With Verteporfin Photodynamic in Treating Subfoveal…

NCT00061594 · Genentech, Inc., Industry · Completed

Key facts

NCT number NCT00061594
Title A Study to Compare rhuFab V2 With Verteporfin Photodynamic in Treating Subfoveal Neovascular Macular Degeneration
Official title A Phase III, Multicenter, Randomized, Double Masked, Active Treatment-Controlled Study of the Efficacy and Safety of rhuFab V2 (Ranibizumab) Compared With Verteporfin (Visudyne) Photodynamic Therapy in Subjects With Predominantly Classic Subfoveal Neovascular Age-Related Macular Degeneration
Lead sponsor Genentech, Inc., Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Macular Degeneration
Intervention type Drug
Interventions rhuFab V2 (ranibizumab)
Enrollment 426
Start date May 1, 2003
Completion Sep 1, 2006
First posted May 30, 2003
Last update posted Mar 19, 2014
Countries Australia, Czechia, France, Germany, Hungary, United States

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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