drugset / Trial / NCT04364399

Clinical Trial to Evaluate the Safety and Immunogenicity of Mumps Vaccine

NCT04364399 ↗

Phase 4 Completed 920 enrolled Sinovac (Dalian) Vaccine Technology Co., Ltd.
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to evaluate the safety and immunogenicity of mumps vaccine in healthy infants aged 8-12months, compared with measles, mumps and rubella combined vaccine, live (MMRV).

Timeline

Start
2020-11-18
Primary completion
2020-11-18
Completion
2021-04-07

Drugs

EvaluationDrugModalityDoseRoute
Subject MUMPS VIRUS VACCINE LIVE Vaccine 0.5 ml —
Comparator measles, mumps and rubella combined vaccine, live Vaccine 0.5 ml —