drugset / Trial / NCT02269475

A Phase3 Study to Evaluate the Efficacy and Safety of MEDI3250 in Healthy Japanese Children Age 7 Years Through 18 Years

NCT02269475 ↗

Phase 3 Completed 1369 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindPrevention

Summary

The study is designed to gather the efficacy, safety and tolerability data in Japanese children 7 to 18 years of age that would support approval of MEDI3250 in Japan.

Timeline

Start
2014-10
Primary completion
2015-04
Completion
2015-04

Outcome

Missed primary endpoint

registry Vaccine efficacy (%) 100.0 (95% CI -1875.3 to 100.0) NCT02269475 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject MEDI3250 Vaccine 0.2 ml Intranasal

Indications

No indication recorded.