drugset / Trial / NCT05110261

Evaluate the Safety and Efficacy of Nirsevimab in Healthy Preterm and Term Infants in China

NCT05110261

Phase 3 Completed 800 enrolled AstraZeneca IQVIA RDS Inc. · collab
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to evaluate the Safety and Efficacy of Nirsevimab, in Healthy Preterm and Term Infants in China

Timeline

Start
2021-11-24
Primary completion
2025-11-24
Completion
2025-11-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Nirsevimab Monoclonal antibody 50 mg Intramuscular
Subject Nirsevimab Monoclonal antibody 100 mg Intramuscular