Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/56810
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dc.contributor.authorTawee Chotpitayasunondhen_US
dc.contributor.authorPornpimol Pruekpraserten_US
dc.contributor.authorThanyawee Puthanakiten_US
dc.contributor.authorChitsanu Pancharoenen_US
dc.contributor.authorAuchara Tangsathapornpongen_US
dc.contributor.authorPeninnah Oberdorferen_US
dc.contributor.authorPope Kosalaraksaen_US
dc.contributor.authorOlarn Prommalikiten_US
dc.contributor.authorSuwimon Tangkittithawornen_US
dc.contributor.authorPhirangkul Kerdpanichen_US
dc.contributor.authorChonnamet Techasaensirien_US
dc.contributor.authorJoanna Korejwoen_US
dc.contributor.authorSunate Chuenkitmongkolen_US
dc.contributor.authorGuy Houillonen_US
dc.date.accessioned2018-09-05T03:30:33Z-
dc.date.available2018-09-05T03:30:33Z-
dc.date.issued2017-01-05en_US
dc.identifier.issn18732518en_US
dc.identifier.issn0264410Xen_US
dc.identifier.other2-s2.0-85006966243en_US
dc.identifier.other10.1016/j.vaccine.2016.11.062en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85006966243&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/56810-
dc.description.abstract© 2016 The Authors Background Japanese encephalitis is a mosquito-borne viral disease endemic in most countries in Asia. A recombinant live, attenuated Japanese encephalitis virus vaccine, JE-CV, is licensed in 14 countries, including Thailand, for the prevention of Japanese encephalitis in adults and children. Methods This was a prospective, phase IV, open-label, multicentre, safety study of JE-CV conducted from November 2013 to April 2015, to evaluate rare serious adverse events (AEs). JE-CV was administered to 10,000 healthy children aged 9 months to <5 years in Thailand as a primary (Group 1) or booster (Group 2) vaccination. Serious AEs (SAEs), including AEs of special interest, up to 60 days after administration were evaluated. Immediate Grade 3 systemic AEs up to 30 min after JE-CV administration were also described. Results The median age of participants was 1.1 years in Group 1 and 3.8 years in Group 2. SAEs were reported in 204 (3.0%) participants in Group 1 and 59 (1.9%) participants in Group 2. Among a total of 294 SAEs in 263 participants, only three events occurring in two participants were considered related to vaccination. All three cases were moderate urticaria, none of which met the definition of AEs of special interest for hypersensitivity. AEs of special interest were reported in 28 (0.4%) participants in Group 1 and 4 (0.1%) participants in Group 2; none were considered related to vaccination. Febrile convulsion was the most frequently reported AE of special interest: 25 (0.4%) participants in Group 1; and 2 (<0.1%) in Group 2. There were no cases of Japanese encephalitis reported. No Grade 3 immediate systemic AEs were reported after any JE-CV vaccination. Conclusions Our study did not identify any new safety concerns with JE-CV and confirms its good safety profile. This study was registered on www.clinicaltrials.gov (NCT01981967; Universal Trial Number: U1111-1127-7052).en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.subjectVeterinaryen_US
dc.titlePost-licensure, phase IV, safety study of a live attenuated Japanese encephalitis recombinant vaccine in children in Thailanden_US
dc.typeJournalen_US
article.title.sourcetitleVaccineen_US
article.volume35en_US
article.stream.affiliationsQueen Sirikit National Institute of Child Healthen_US
article.stream.affiliationsPrince of Songkla Universityen_US
article.stream.affiliationsChulalongkorn Universityen_US
article.stream.affiliationsFaculty of Medicine, Thammasat Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsSrinagarind hospitalen_US
article.stream.affiliationsSrinakharinwirot Universityen_US
article.stream.affiliationsPhramongkutklao College of Medicineen_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsSanofi Pasteur SAen_US
article.stream.affiliationsSanofi Pasteuren_US
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