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Clinical Trial Summary

The research objective is to evaluate lot-to-lot consistency and immune persistence of three commercial batches of 23 valent pneumococcal polysaccharide vaccine.


Clinical Trial Description

This study adopted a randomized, double-blind, equivalency design with different batches of experimental vaccine. 990 individuals aged 18-59 were included and divided into three groups at a ratio of 1:1:1, with 330 individuals in each group receiving three batches of experimental vaccines, respectively. All subjects were vaccinated with 1 dose of 0.5ml, intramuscularly injected into the lateral deltoid muscle of the upper arm. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06314867
Study type Interventional
Source Beijing Zhifei Lvzhu Biopharmaceutical Co., Ltd
Contact
Status Active, not recruiting
Phase Phase 3
Start date January 30, 2023
Completion date June 30, 2028

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