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Clinical Trial 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).


Clinical Trial Description

The study is a randomized, double-blind, controlled phase Ⅳ clinical trial. And 920 infants will be assigned to investigational group and controlled group in a 1:1 ratio. The investigational vaccine is manufactured by Sinovac (Dalian) Vaccine Technology Co., Ltd. The controlled vaccine is manufactured by Shanghai institute of biological products Co., Ltd. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04364399
Study type Interventional
Source Sinovac (Dalian) Vaccine Technology Co., Ltd.
Contact
Status Completed
Phase Phase 4
Start date November 18, 2020
Completion date April 7, 2021

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