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Dose-sparing effect of two adjuvant formulations with a pandemic influenza A/H7N9 vaccine: a randomized, double-blind, placebo-controlled, phase 1 clinical trial
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DC Field | Value | Language |
---|---|---|
dc.contributor | Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor | (HVB) Hospital Vital Brazil | pt_BR |
dc.contributor | Centro Bioindustrial | pt_BR |
dc.contributor.author | Vanni, Tazio | pt_BR |
dc.contributor.author | Thomé, Beatriz | pt_BR |
dc.contributor.author | Sparrow, Erin | pt_BR |
dc.contributor.author | Mondini, Gabriela | pt_BR |
dc.contributor.author | Silveira, Daniela Haydee Ramos | pt_BR |
dc.contributor.author | Viscondi, Juliana Yukari Koidara | pt_BR |
dc.contributor.author | Braga, Patrícia Emília | pt_BR |
dc.contributor.author | Silva, Anderson da | pt_BR |
dc.contributor.author | Salomão, Maria da Graça | pt_BR |
dc.contributor.author | Piorelli, Roberta de Oliveira | pt_BR |
dc.contributor.author | Santos, Joane do Prado | pt_BR |
dc.contributor.author | Gattás, Vera Lúcia | pt_BR |
dc.contributor.author | Lucchesi, Maria Beatriz Bastos | pt_BR |
dc.contributor.author | Oliveira, Mayra Martho Moura de | pt_BR |
dc.contributor.author | Koike, Marcelo Eiji | pt_BR |
dc.contributor.author | Adami, Eduardo Alfredo | pt_BR |
dc.contributor.author | Akamatsu, Milena Apetito | pt_BR |
dc.contributor.author | Ho, Paulo Lee | pt_BR |
dc.contributor.author | Precioso, Alexander Roberto | pt_BR |
dc.date.accessioned | 2022-10-21T12:37:40Z | - |
dc.date.available | 2022-10-21T12:37:40Z | - |
dc.date.issued | 2022 | pt_BR |
dc.identifier.citation | Vanni T, Thomé B, Sparrow E, Mondini G, Silveira DHR, Viscondi JYK, et al. Dose-sparing effect of two adjuvant formulations with a pandemic influenza A/H7N9 vaccine: a randomized, double-blind, placebo-controlled, phase 1 clinical trial. PloS One. . doi:10.1371/journal.pone.0274943. | pt_BR |
dc.identifier.uri | https://repositorio.butantan.gov.br/handle/butantan/4565 | - |
dc.description.abstract | The emergence of potentially pandemic viruses has resulted in preparedness efforts to develop candidate vaccines and adjuvant formulations. We evaluated the dose-sparing effect and safety of two distinct squalene-based oil-in-water adjuvant emulsion formulations (IB160 and SE) with influenza A/H7N9 antigen. This phase I, randomized, double-blind, placebo-controlled, dose-finding trial (NCT03330899), enrolled 432 healthy volunteers aged 18 to 59. Participants were randomly allocated to 8 groups: 1A) IB160 + 15μg H7N9, 1B) IB160 + 7.5μg H7N9, 1C) IB160 + 3.75μg H7N9, 2A) SE + 15μg H7N9, 2B) SE + 7.5μg H7N9, 2C) SE + 3.75μg H7N9, 3) unadjuvanted vaccine 15μg H7N9 and 4) placebo. Immunogenicity was evaluated through haemagglutination inhibition (HI) and microneutralization (MN) tests. Safety was evaluated by monitoring local and systemic, solicited and unsolicited adverse events (AE) and reactions (AR) 7 and 28 days after each study injection, respectively, whereas serious adverse events (SAE) were monitored up to 194 days post-second dose. A greater increase in antibody geometric mean titers (GMT) was observed in groups receiving adjuvanted vaccines. Vaccinees receiving IB160-adjuvanted formulations showed the greatest response in group 1B, which induced an HI GMT increase of 4.7 times, HI titers ≥40 in 45.2% of participants (MN titers ≥40 in 80.8%). Vaccinees receiving SE-adjuvanted vaccines showed the greatest response in group 2A, with an HI GMT increase of 2.5 times, HI titers ≥40 in 22.9% of participants (MN titers ≥40 in 65.7%). Frequencies of AE and AR were similar among groups. Pain at the administration site and headache were the most frequent local and systemic solicited ARs. The vaccine candidates were safe and the adjuvanted formulations have a potential dose-sparing effect on immunogenicity against influenza A/H7N9. The magnitude of this effect could be further explored. | pt_BR |
dc.description.sponsorship | (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo | pt_BR |
dc.description.sponsorship | (CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico | pt_BR |
dc.format.extent | e0274943 | pt_BR |
dc.language.iso | English | pt_BR |
dc.relation.ispartof | PloS One | pt_BR |
dc.rights | Open access | pt_BR |
dc.rights.uri | https://creativecommons.org/publicdomain/zero/1.0/ | pt_BR |
dc.title | Dose-sparing effect of two adjuvant formulations with a pandemic influenza A/H7N9 vaccine: a randomized, double-blind, placebo-controlled, phase 1 clinical trial | pt_BR |
dc.type | Article | pt_BR |
dc.rights.license | CC0 | pt_BR |
dc.identifier.doi | 10.1371/journal.pone.0274943 | pt_BR |
dc.contributor.external | (WHO-SW) World Health Organization Switzerland | pt_BR |
dc.contributor.external | Infectious Disease Research Institute | pt_BR |
dc.contributor.external | (BARDA) Biomedical Advanced Research and Development Authority | pt_BR |
dc.contributor.external | (USP) Universidade de São Paulo | pt_BR |
dc.contributor.external | (FIOCRUZ) Fundação Oswaldo Cruz | pt_BR |
dc.contributor.external | (IAL) Instituto Adolfo Lutz | pt_BR |
dc.identifier.citationvolume | 17 | pt_BR |
dc.identifier.citationissue | 10 | pt_BR |
dc.relation.ispartofabbreviated | PloS One | pt_BR |
dc.contributor.butantan | Vanni, Tazio|:Desvinculado|:Centro de Ensaios Clínicos e Farmacovigilância|:PrimeiroAutor | pt_BR |
dc.contributor.butantan | Thomé, Beatriz|:Técnico|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Mondini, Gabriela|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Silveira, Daniela Haydee Ramos|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Viscondi, Juliana Yukari Koidara|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Braga, Patrícia Emília|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Silva, Anderson da|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Salomão, Maria da Graça|:Pesquisador|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Piorelli, Roberta de Oliveira|:Outros|:(HVB) Hospital Vital Brazil | pt_BR |
dc.contributor.butantan | Santos, Joane do Prado|:Outros|:Centro Bioindustrial | pt_BR |
dc.contributor.butantan | Gattás, Vera Lúcia|:Pesquisador|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Lucchesi, Maria Beatriz Bastos|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Oliveira, Mayra Martho Moura de|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Koike, Marcelo Eiji|:Especialista|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Adami, Eduardo Alfredo|:Outros|:Centro Bioindustrial | pt_BR |
dc.contributor.butantan | Akamatsu, Milena Apetito|:Outros|:Centro Bioindustrial | pt_BR |
dc.contributor.butantan | Ho, Paulo Lee|:Pesquisador|:Centro Bioindustrial | pt_BR |
dc.contributor.butantan | Precioso, Alexander Roberto|:Pesquisador|:Centro de Ensaios Clínicos e Farmacovigilância|:Autor de correspondência | pt_BR |
dc.sponsorship.butantan | (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2020/07040-1 | pt_BR |
dc.sponsorship.butantan | (CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico¦¦305430/2019-0 | pt_BR |
dc.identifier.bvscc | BR78.1 | pt_BR |
dc.identifier.bvsdb | IBProd | pt_BR |
dc.description.dbindexed | Yes | pt_BR |
item.languageiso639-1 | English | - |
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