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

See also
Status	Clinical Trial	Phase
Completed	`NCT03282370` - Evaluate Safety and Immunogenicity of a Vero Cell-Derived JE Vaccine in 9-24 Months of Age Children in Vietnam	Phase 3
Recruiting	`NCT05568953` - An Experimental Medicine Decipher of a Minimum Correlate of Cellular Immunity	Phase 2
Completed	`NCT00776230` - Immunogenicity of a Commercial Batch of JEV IC51 up to 24 Months Post Filling	Phase 3
Completed	`NCT00594958` - Comparison of Three Batches of the Japanese Encephalitis Vaccine IC51	Phase 3
Completed	`NCT00596271` - Concomitant Vaccination With the Japanese Encephalitis Vaccine IC51 and HARVIX® 1440	Phase 3
Completed	`NCT00595790` - Rapid Immunization Study of the Japanese Encephalitis Vaccine IC51	Phase 3
Completed	`NCT00604708` - Immunogenicity Study of the Japanese Encephalitis Vaccine IC51	Phase 3
Not yet recruiting	`NCT01954810` - Antibody Response of a Boosted Japanese Encephalitis Chimeric Virus Vaccine (JE-CV) in Children	Phase 4
Completed	`NCT01246479` - Long Term Immunity and Safety Following Vaccination With the JEV IC51 (IXIARO®, JESPECT®) in Pediatric Population In Non Endemic Countries. Uncontrolled, Ph3 FU-Study	Phase 3
Completed	`NCT00605085` - Safety and Tolerability of the Japanese Encephalitis Vaccine IC51	Phase 3
Completed	`NCT00596102` - Longterm Immunogenicity of the Japanese Encephalitis Vaccine IC51	Phase 3
Completed	`NCT00595270` - Long Term Persistence and Effect of a Booster Dose of the Japanese Encephalitis Vaccine IC51	Phase 3
Completed	`NCT00314132` - Safety Study of ChimeriVax™-JE Vaccine to Prevent Japanese Encephalitis.	Phase 3
Active, not recruiting	`NCT01981967` - Post-licensure Safety Study of IMOJEV® in Thailand	Phase 4
Completed	`NCT01466387` - A Phase 3b, Randomized, Open-Label Study to Evaluate the Safety and Immunogenicity of Select Travel Vaccines When Administered Concomitantly With MenACWY in Adults	Phase 3
Completed	`NCT00314145` - A Safety and Efficacy Study of Two Japanese Encephalitis Vaccines ChimeriVax™-JE and JE-VAX	Phase 3
Completed	`NCT00981630` - Study of Live Attenuated ChimeriVax™-Japanese Encephalitis Vaccine	Phase 2
Completed	`NCT01567865` - Lot-to-lot Consistency Trial of Japanese Encephalitis Live Attenuated SA 14-14-2 Vaccine	Phase 4
Completed	`NCT01656200` - A Prospective, Open Label Study of Human T Cell Responses to Live Attenuated Japanese Encephalitis Vaccine SA14-14-2	Phase 4
Unknown status	`NCT01163123` - Seroepidemiology of Japanese Encephalitis Virus Infection in Hualien, Taiwan	N/A