Your browser doesn't support javascript.
loading
Broad cross-national public support for accelerated COVID-19 vaccine trial designs.
Broockman, David; Kalla, Joshua; Guerrero, Alexander; Budolfson, Mark; Eyal, Nir; Jewell, Nicholas P; Magalhaes, Monica; Sekhon, Jasjeet S.
Afiliação
  • Broockman D; Department of Political Science, University of California, Berkeley, United States.
  • Kalla J; Department of Political Science and Department of Statistics & Data Science, Yale University, United States. Electronic address: josh.kalla@yale.edu.
  • Guerrero A; Department of Philosophy, Rutgers University, United States.
  • Budolfson M; Department of Environmental and Occupational Health and Justice, Rutgers University, United States.
  • Eyal N; Department of Health Behavior, Society and Policy and Center for Population-Level Bioethics, Rutgers University, United States.
  • Jewell NP; London School of Hygiene & Tropical Medicine and Division of Biostatistics, School of Public Health, University of California, Berkeley, United States.
  • Magalhaes M; Center for Population-Level Bioethics, Rutgers University, United States.
  • Sekhon JS; Department of Statistics & Data Science and Department of Political Science, Yale University, United States.
Vaccine ; 39(2): 309-316, 2021 01 08.
Article em En | MEDLINE | ID: mdl-33334616
A vaccine for COVID-19 is urgently needed. Several vaccine trial designs may significantly accelerate vaccine testing and approval, but also increase risks to human subjects. Concerns about whether the public would see such designs as ethical represent an important roadblock to their implementation; accordingly, both the World Health Organization and numerous scholars have called for consulting the public regarding them. We answered these calls by conducting a cross-national survey (n = 5920) in Australia, Canada, Hong Kong, New Zealand, South Africa, Singapore, the United Kingdom, and the United States. The survey explained key differences between traditional vaccine trials and two accelerated designs: a challenge trial or a trial integrating a Phase II safety and immunogenicity trial into a larger Phase III efficacy trial. Respondents' answers to comprehension questions indicate that they largely understood the key differences and ethical trade-offs between the designs from our descriptions. We asked respondents whether they would prefer scientists to conduct traditional trials or one of these two accelerated designs. We found broad majorities prefer for scientists to conduct challenge trials (75%) and integrated trials (63%) over standard trials. Even as respondents acknowledged the risks, they perceived both accelerated trials as similarly ethical to standard trial designs. This high support is consistent across every geography and demographic subgroup we examined, including vulnerable populations. These findings may help assuage some of the concerns surrounding accelerated designs.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Vacinação / Tomada de Decisões / Pandemias / Vacinas contra COVID-19 / SARS-CoV-2 / COVID-19 Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Female / Humans / Male País/Região como assunto: America do norte / Asia / Europa / Oceania Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Vacinação / Tomada de Decisões / Pandemias / Vacinas contra COVID-19 / SARS-CoV-2 / COVID-19 Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Female / Humans / Male País/Região como assunto: America do norte / Asia / Europa / Oceania Idioma: En Ano de publicação: 2021 Tipo de documento: Article