Postmarketing Surveillance Study for IMOJEV® in Republic of Korea

Status Completed

Clinical Trial Summary

The purpose of the study is to perform the re-examination of IMOJEV® in routine clinical settings in accordance with the Ministry of Food and Drug Safety regulation. Primary objective: - To describe the safety profile of the first dose of IMOJEV® administered under routine health care visit as primary vaccination or as booster.

Clinical Trial Description

Subjects aged 12 months of age and older and who are given study vaccine during routine health-care visits will be enrolled in the study. No study vaccine will be supplied or administered as part of this study, subjects will be monitored following routine vaccine administration in clinical settings. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02933710
Study type	Observational
Source	Sanofi
Contact
Status	Completed
Phase
Start date	July 21, 2016
Completion date	October 18, 2018

View Details

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