Publication:
Efficacy and long-term safety of a dengue vaccine in regions of endemic disease

dc.contributor.authorS. R. Hadinegoroen_US
dc.contributor.authorJ. L. Arredondo-Garcíaen_US
dc.contributor.authorM. R. Capedingen_US
dc.contributor.authorC. Desedaen_US
dc.contributor.authorT. Chotpitayasunondhen_US
dc.contributor.authorR. Dietzeen_US
dc.contributor.authorH. I. Hj Muhammad Ismailen_US
dc.contributor.authorH. Reynalesen_US
dc.contributor.authorK. Limkittikulen_US
dc.contributor.authorD. M. Rivera-Medinaen_US
dc.contributor.authorH. N. Tranen_US
dc.contributor.authorA. Bouckenoogheen_US
dc.contributor.authorD. Chansinghakulen_US
dc.contributor.authorM. Cortésen_US
dc.contributor.authorK. Fanouillereen_US
dc.contributor.authorR. Forraten_US
dc.contributor.authorC. Fragoen_US
dc.contributor.authorS. Gailhardouen_US
dc.contributor.authorN. Jacksonen_US
dc.contributor.authorF. Noriegaen_US
dc.contributor.authorE. Plennevauxen_US
dc.contributor.authorT. A. Wartelen_US
dc.contributor.authorB. Zambranoen_US
dc.contributor.authorM. Savilleen_US
dc.contributor.otherUniversity of Indonesia, RSUPN Dr. Cipto Mangunkusumoen_US
dc.contributor.otherInstituto Nacional de Pediatriaen_US
dc.contributor.otherGokilaen_US
dc.contributor.otherCaribbean Travel Medicine Clinicen_US
dc.contributor.otherQueen Sirikit National Institute of Child Healthen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherSanofi Pasteuren_US
dc.contributor.otherFederal University of Espirito Santoen_US
dc.contributor.otherKuala Lumpur Hospitalen_US
dc.contributor.otherSAS-CAIMEDen_US
dc.contributor.otherSanofi Pasteuren_US
dc.contributor.otherOrganizacion para el Desarrollo y la Investigacion Salud en Honduras (ODIS)en_US
dc.contributor.otherPasteur Institute in Ho Chi Minh Cityen_US
dc.contributor.otherSanofi Pasteuren_US
dc.contributor.otherSanofi S.A.en_US
dc.contributor.otheren_US
dc.contributor.otherSanofi Pasteur SAen_US
dc.contributor.otherSanofi Pasteuren_US
dc.contributor.otherSanofi Pasteuren_US
dc.date.accessioned2018-11-23T10:35:49Z
dc.date.available2018-11-23T10:35:49Z
dc.date.issued2015-09-24en_US
dc.description.abstractCopyright © 2015 Massachusetts Medical Society. Background: A candidate tetravalent dengue vaccine is being assessed in three clinical trials involving more than 35,000 children between the ages of 2 and 16 years in Asian-Pacific and Latin American countries. We report the results of long-term follow-up interim analyses and integrated efficacy analyses. Methods: We are assessing the incidence of hospitalization for virologically confirmed dengue as a surrogate safety end point during follow-up in years 3 to 6 of two phase 3 trials, CYD14 and CYD15, and a phase 2b trial, CYD23/57. We estimated vaccine efficacy using pooled data from the first 25 months of CYD14 and CYD15. Results: Follow-up data were available for 10,165 of 10,275 participants (99%) in CYD14 and 19,898 of 20,869 participants (95%) in CYD15. Data were available for 3203 of the 4002 participants (80%) in the CYD23 trial included in CYD57. During year 3 in the CYD14, CYD15, and CYD57 trials combined, hospitalization for virologically confirmed dengue occurred in 65 of 22,177 participants in the vaccine group and 39 of 11,089 participants in the control group. Pooled relative risks of hospitalization for dengue were 0.84 (95% confidence interval [CI], 0.56 to 1.24) among all participants, 1.58 (95% CI, 0.83 to 3.02) among those under the age of 9 years, and 0.50 (95% CI, 0.29 to 0.86) among those 9 years of age or older. During year 3, hospitalization for severe dengue, as defined by the independent data monitoring committee criteria, occurred in 18 of 22,177 participants in the vaccine group and 6 of 11,089 participants in the control group. Pooled rates of efficacy for symptomatic dengue during the first 25 months were 60.3% (95% CI, 55.7 to 64.5) for all participants, 65.6% (95% CI, 60.7 to 69.9) for those 9 years of age or older, and 44.6% (95% CI, 31.6 to 55.0) for those younger than 9 years of age. Conclusions: Although the unexplained higher incidence of hospitalization for dengue in year 3 among children younger than 9 years of age needs to be carefully monitored during long-term follow-up, the risk among children 2 to 16 years of age was lower in the vaccine group than in the control group.en_US
dc.identifier.citationNew England Journal of Medicine. Vol.373, No.13 (2015), 1195-1206en_US
dc.identifier.doi10.1056/NEJMoa1506223en_US
dc.identifier.issn15334406en_US
dc.identifier.issn00284793en_US
dc.identifier.other2-s2.0-84942436806en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/36320
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942436806&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleEfficacy and long-term safety of a dengue vaccine in regions of endemic diseaseen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942436806&origin=inwarden_US

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