drugset / Trial / NCT03959488

A Study to Evaluate the Safety of MEDI8897 for the Prevention of Medically Attended Respiratory Syncytial Virus(RSV) Lower Respiratory Track Infection (LRTI) in High-risk Children

NCT03959488

Phase 2/3 Completed 925 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to evaluate the safety and tolerability of MEDI8897 compared to palivizumab when administered to preterm infants entering their first RSV season and children with chronic lung disease (CLD) and congenital heart disease (CHD) entering their first and second RSV season.

Timeline

Start
2019-07-30
Primary completion
2021-05-03
Completion
2023-01-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Nirsevimab Monoclonal antibody
Comparator Palivizumab Monoclonal antibody