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Clinical Trial Summary

A randomized and blind clinical consistency study for three commercial batches of Inactivated Poliomyelitis Vaccine Made From Sabin Strain (sIPV) for immunogenicity and safety evaluation.


Clinical Trial Description

This randomized and blind clinical study includes three test groups with 400 infants for each group. Sample estimation for this study has been conducted using statistical methods. A total of 1,200 2-month old healthy subjects were enrolled for inoculation of vaccine from 3 different lots with 1 month interval. All subjects received blood collection for immunogenicity test before and after primary immunization for evaluation of immunogenicity consistency, while safety observation was conducted within 30 days after each vaccination (30min via close safety monitoring, 0-7 days via participant diary card and 8-30 days via contact card for collection of adverse events) for safety evaluation of sIPV of 3 commercial lots. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04224519
Study type Interventional
Source Institute of Medical Biology, Chinese Academy of Medical Sciences
Contact
Status Completed
Phase Phase 4
Start date April 15, 2018
Completion date October 12, 2019

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