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Clinical Trial Summary

The purpose of this study is to evaluate the immunogenicity and safety of Recombinant Human Papillomavirus Bivalent (Types 16,18) Vaccine (Escherichia coli) (HPV)and Measles Mumps and Rubella Combined Vaccine, Live(MMR)


Clinical Trial Description

Main subjects: To evaluate the immunogenicity of HPV vaccine and MMR vaccine at the same time but at different sites as not inferior to vaccination of HPV vaccine or MMR vaccine alone. Secondary subjects: To evaluate the safety of simultaneous administration of HPV vaccine and MMR vaccine. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05279248
Study type Interventional
Source Zhejiang Provincial Center for Disease Control and Prevention
Contact
Status Active, not recruiting
Phase Phase 4
Start date August 25, 2021
Completion date June 20, 2023

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