drugset / Trial / NCT02390531

Phase 1 Trial of Bevacizumab Treatment for Severe Retinopathy of Prematurity

NCT02390531 ↗

RandomizedSequentialQuadruple-blindTreatment

Summary

The purpose of this study is to find a dose of intravitreal bevacizumab that is lower than currently used for severe retinopathy of prematurity (ROP), is effective in this study, and can be tested in future larger studies.

Timeline

Start
2015-04-28
Primary completion
2019-06-04
Completion
2021-05-11

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 0.002 mg Intravitreal
Subject Bevacizumab Monoclonal antibody 0.004 mg Intravitreal
Subject Bevacizumab Monoclonal antibody 0.008 mg Intravitreal
Subject Bevacizumab Monoclonal antibody 0.016 mg Intravitreal
Subject Bevacizumab Monoclonal antibody 0.031 mg Intravitreal
Subject Bevacizumab Monoclonal antibody 0.063 mg Intravitreal
Subject Bevacizumab Monoclonal antibody 0.125 mg Intravitreal
Subject Bevacizumab Monoclonal antibody 0.25 mg Intravitreal