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Title: | Post-licensure, phase IV, safety study of a live attenuated Japanese encephalitis recombinant vaccine in children in Thailand |
Authors: | Chotpitayasunondh T. Pruekprasert P. Puthanakit T. Pancharoen C. Tangsathapornpong A. Oberdorfer P. Kosalaraksa P. Prommalikit O. Tangkittithaworn S. Kerdpanich P. Techasaensiri C. Korejwo J. Chuenkitmongkol S. Houillon G. |
Keywords: | Japanese encephalitis vaccine live vaccine recombinant vaccine Japanese encephalitis vaccine live vaccine recombinant vaccine acute disseminated encephalomyelitis allergic reaction anaphylaxis Article Bell palsy brain disease bronchitis child child hospitalization congenital malformation convulsion death dengue diarrhea disability drug marketing drug safety dyspepsia encephalitis enteritis epilepsy febrile convulsion female fever food poisoning gastritis gastroenteritis human infant influenza Japanese encephalitis licensing male mouth ulcer multicenter study myelitis neurologic disease normal human open study peripheral neuropathy pharyngitis phase 4 clinical trial pneumonia preschool child priority journal prospective study pyrexia idiopathica rhinopharyngitis side effect single drug dose Thailand urticaria vaccination vaccination reaction vaccine failure viremia virus infection virus pneumonia adverse drug reaction clinical trial Japanese encephalitis pathology Child, Preschool Drug-Related Side Effects and Adverse Reactions Encephalitis, Japanese Female Healthy Volunteers Humans Infant Japanese Encephalitis Vaccines Male Prospective Studies Thailand Vaccines, Attenuated Vaccines, Synthetic |
Issue Date: | 2017 |
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 |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/13164 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85006966243&doi=10.1016%2fj.vaccine.2016.11.062&partnerID=40&md5=5f84f81d084334af01bfa9bd6bb01e7b |
ISSN: | 0264410X |
Appears in Collections: | Scopus 1983-2021 |
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