drugset / Trial / NCT00344227

Prospective OCT Study With Lucentis for Neovascular AMD (PrONTO Study)

NCT00344227

Phase 2 Completed 40 enrolled University of Miami Genentech, Inc. · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The PrONTO Study was designed to evaluate the response of neovascular age-related macular degeneration (AMD) patients to intravitreal Lucentis using Optical Coherence Tomography (OCT) imaging. OCT was then used to determine the need for retreatment after 3 monthly injections of Lucentis. Patients would be followed for 2 years.

Timeline

Start
2004-08
Primary completion
Completion
2007-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Ranibizumab Monoclonal antibody 500 ug Intravitreal