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

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dc.contributor.author Chotpitayasunondh T.
dc.contributor.author Pruekprasert P.
dc.contributor.author Puthanakit T.
dc.contributor.author Pancharoen C.
dc.contributor.author Tangsathapornpong A.
dc.contributor.author Oberdorfer P.
dc.contributor.author Kosalaraksa P.
dc.contributor.author Prommalikit O.
dc.contributor.author Tangkittithaworn S.
dc.contributor.author Kerdpanich P.
dc.contributor.author Techasaensiri C.
dc.contributor.author Korejwo J.
dc.contributor.author Chuenkitmongkol S.
dc.contributor.author Houillon G.
dc.date.accessioned 2021-04-05T03:22:32Z
dc.date.available 2021-04-05T03:22:32Z
dc.date.issued 2017
dc.identifier.issn 0264410X
dc.identifier.other 2-s2.0-85006966243
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/13164
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-85006966243&doi=10.1016%2fj.vaccine.2016.11.062&partnerID=40&md5=5f84f81d084334af01bfa9bd6bb01e7b
dc.description.abstract 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). © 2016 The Authors
dc.subject Japanese encephalitis vaccine
dc.subject live vaccine
dc.subject recombinant vaccine
dc.subject Japanese encephalitis vaccine
dc.subject live vaccine
dc.subject recombinant vaccine
dc.subject acute disseminated encephalomyelitis
dc.subject allergic reaction
dc.subject anaphylaxis
dc.subject Article
dc.subject Bell palsy
dc.subject brain disease
dc.subject bronchitis
dc.subject child
dc.subject child hospitalization
dc.subject congenital malformation
dc.subject convulsion
dc.subject death
dc.subject dengue
dc.subject diarrhea
dc.subject disability
dc.subject drug marketing
dc.subject drug safety
dc.subject dyspepsia
dc.subject encephalitis
dc.subject enteritis
dc.subject epilepsy
dc.subject febrile convulsion
dc.subject female
dc.subject fever
dc.subject food poisoning
dc.subject gastritis
dc.subject gastroenteritis
dc.subject human
dc.subject infant
dc.subject influenza
dc.subject Japanese encephalitis
dc.subject licensing
dc.subject male
dc.subject mouth ulcer
dc.subject multicenter study
dc.subject myelitis
dc.subject neurologic disease
dc.subject normal human
dc.subject open study
dc.subject peripheral neuropathy
dc.subject pharyngitis
dc.subject phase 4 clinical trial
dc.subject pneumonia
dc.subject preschool child
dc.subject priority journal
dc.subject prospective study
dc.subject pyrexia idiopathica
dc.subject rhinopharyngitis
dc.subject side effect
dc.subject single drug dose
dc.subject Thailand
dc.subject urticaria
dc.subject vaccination
dc.subject vaccination reaction
dc.subject vaccine failure
dc.subject viremia
dc.subject virus infection
dc.subject virus pneumonia
dc.subject adverse drug reaction
dc.subject clinical trial
dc.subject Japanese encephalitis
dc.subject pathology
dc.subject Child, Preschool
dc.subject Drug-Related Side Effects and Adverse Reactions
dc.subject Encephalitis, Japanese
dc.subject Female
dc.subject Healthy Volunteers
dc.subject Humans
dc.subject Infant
dc.subject Japanese Encephalitis Vaccines
dc.subject Male
dc.subject Prospective Studies
dc.subject Thailand
dc.subject Vaccines, Attenuated
dc.subject Vaccines, Synthetic
dc.title Post-licensure, phase IV, safety study of a live attenuated Japanese encephalitis recombinant vaccine in children in Thailand
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Vaccine. Vol 35, No.2 (2017), p.299-304
dc.identifier.doi 10.1016/j.vaccine.2016.11.062


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