drugset / Trial / NCT00622726

Bevacizumab Eliminates the Angiogenic Threat for Retinopathy of Prematurity

NCT00622726 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study was to determine the efficacy and additional advantages of intravitreal bevacizumab in the treatment of ROP for both Zone I and Zone II Posterior.

Timeline

Start
2008-03
Primary completion
2010-08
Completion
2020-08

Outcome

Met primary endpoint

paper 4 infants in the bevacizumab group (6 of 140 eyes [4%]) and 19 infants in the laser-therapy group (32 of 146 eyes [22%], P=0.002). PMID 21323540 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 0.625 mg Intravitreal