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Clinical Trial Summary

To evaluate the immunogenicity, lot-to-lot consistency and safety of three consecutive batches of Measles, Mumps and Rubella Combined Vaccine, Live.


Clinical Trial Description

To assess Measles Mumps and Rubella Combined Vaccine, Live, (MMR) lot-to-lot consistency in healthy Chinese Children at the age of 8-12 months, and the participants randomized to receive one injections of 0.5 mL Measles, Mumps and Rubella Combined Vaccine, Live at day 0. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05161845
Study type Interventional
Source Shanghai Institute Of Biological Products
Contact
Status Completed
Phase Phase 4
Start date December 23, 2021
Completion date October 1, 2022

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