Publication:
Post-licensure, phase IV, safety study of a live attenuated Japanese encephalitis recombinant vaccine in children in Thailand

dc.contributor.authorChotpitayasunondh T.
dc.contributor.authorPruekprasert P.
dc.contributor.authorPuthanakit T.
dc.contributor.authorPancharoen C.
dc.contributor.authorTangsathapornpong A.
dc.contributor.authorOberdorfer P.
dc.contributor.authorKosalaraksa P.
dc.contributor.authorPrommalikit O.
dc.contributor.authorTangkittithaworn S.
dc.contributor.authorKerdpanich P.
dc.contributor.authorTechasaensiri C.
dc.contributor.authorKorejwo J.
dc.contributor.authorChuenkitmongkol S.
dc.contributor.authorHouillon G.
dc.date.accessioned2021-04-05T03:22:32Z
dc.date.available2021-04-05T03:22:32Z
dc.date.issued2017
dc.date.issuedBE2560
dc.description.abstractBackground 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). © 2016 The Authors
dc.format.mimetypeapplication/pdf
dc.identifier.citationVaccine. Vol 35, No.2 (2017), p.299-304
dc.identifier.doi10.1016/j.vaccine.2016.11.062
dc.identifier.issn0264410X
dc.identifier.other2-s2.0-85006966243
dc.identifier.urihttps://hdl.handle.net/20.500.14740/4276
dc.rights.holderScopus
dc.subject.otherJapanese encephalitis vaccine
dc.subject.otherLive vaccine
dc.subject.otherRecombinant vaccine
dc.subject.otherJapanese encephalitis vaccine
dc.subject.otherLive vaccine
dc.subject.otherRecombinant vaccine
dc.subject.otherAcute disseminated encephalomyelitis
dc.subject.otherAllergic reaction
dc.subject.otherAnaphylaxis
dc.subject.otherArticle
dc.subject.otherBell palsy
dc.subject.otherBrain disease
dc.subject.otherBronchitis
dc.subject.otherChild
dc.subject.otherChild hospitalization
dc.subject.otherCongenital malformation
dc.subject.otherConvulsion
dc.subject.otherDeath
dc.subject.otherDengue
dc.subject.otherDiarrhea
dc.subject.otherDisability
dc.subject.otherDrug marketing
dc.subject.otherDrug safety
dc.subject.otherDyspepsia
dc.subject.otherEncephalitis
dc.subject.otherEnteritis
dc.subject.otherEpilepsy
dc.subject.otherFebrile convulsion
dc.subject.otherFemale
dc.subject.otherFever
dc.subject.otherFood poisoning
dc.subject.otherGastritis
dc.subject.otherGastroenteritis
dc.subject.otherHuman
dc.subject.otherInfant
dc.subject.otherInfluenza
dc.subject.otherJapanese encephalitis
dc.subject.otherLicensing
dc.subject.otherMale
dc.subject.otherMouth ulcer
dc.subject.otherMulticenter study
dc.subject.otherMyelitis
dc.subject.otherNeurologic disease
dc.subject.otherNormal human
dc.subject.otherOpen study
dc.subject.otherPeripheral neuropathy
dc.subject.otherPharyngitis
dc.subject.otherPhase 4 clinical trial
dc.subject.otherPneumonia
dc.subject.otherPreschool child
dc.subject.otherPriority journal
dc.subject.otherProspective study
dc.subject.otherPyrexia idiopathica
dc.subject.otherRhinopharyngitis
dc.subject.otherSide effect
dc.subject.otherSingle drug dose
dc.subject.otherThailand
dc.subject.otherUrticaria
dc.subject.otherVaccination
dc.subject.otherVaccination reaction
dc.subject.otherVaccine failure
dc.subject.otherViremia
dc.subject.otherVirus infection
dc.subject.otherVirus pneumonia
dc.subject.otherAdverse drug reaction
dc.subject.otherClinical trial
dc.subject.otherJapanese encephalitis
dc.subject.otherPathology
dc.subject.otherChild, Preschool
dc.subject.otherDrug-Related Side Effects and Adverse Reactions
dc.subject.otherEncephalitis, Japanese
dc.subject.otherFemale
dc.subject.otherHealthy Volunteers
dc.subject.otherHumans
dc.subject.otherInfant
dc.subject.otherJapanese Encephalitis Vaccines
dc.subject.otherMale
dc.subject.otherProspective Studies
dc.subject.otherThailand
dc.subject.otherVaccines, Attenuated
dc.subject.otherVaccines, Synthetic
dc.titlePost-licensure, phase IV, safety study of a live attenuated Japanese encephalitis recombinant vaccine in children in Thailand
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85006966243&doi=10.1016%2fj.vaccine.2016.11.062&partnerID=40&md5=5f84f81d084334af01bfa9bd6bb01e7b

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