drugset / Trial / NCT00192504

Safety Study of a Monoclonal Antibody to Respiratory Syncytial Virus (RSV) in Children Hospitalized With RSV Infection

NCT00192504

Phase 1 Completed 31 enrolled MedImmune LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the safety of motavizumab (MEDI-524) following a single intravenous dose in children hospitalized with respiratory syncytial virus (RSV).

Timeline

Start
2004-03
Primary completion
2005-01
Completion
2005-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Motavizumab Monoclonal antibody 3 mg/kg Intravenous
Subject Motavizumab Monoclonal antibody 15 mg/kg Intravenous
Subject Motavizumab Monoclonal antibody 30 mg/kg Intravenous