The Brighton collaboration standardized module for vaccine benefit-risk assessment
dc.contributor.author | Levitan B. | |
dc.contributor.author | Hadler S.C. | |
dc.contributor.author | Hurst W. | |
dc.contributor.author | Izurieta H.S. | |
dc.contributor.author | Smith E.R. | |
dc.contributor.author | Baker N.L. | |
dc.contributor.author | Bauchau V. | |
dc.contributor.author | Chandler R. | |
dc.contributor.author | Chen R.T. | |
dc.contributor.author | Craig D. | |
dc.contributor.author | King J. | |
dc.contributor.author | Pitisuttithum P. | |
dc.contributor.author | Strauss W. | |
dc.contributor.author | Tomczyk S. | |
dc.contributor.author | Zafack J. | |
dc.contributor.author | Kochhar S. | |
dc.contributor.correspondence | Levitan B. | |
dc.contributor.other | Mahidol University | |
dc.date.accessioned | 2024-02-08T18:19:44Z | |
dc.date.available | 2024-02-08T18:19:44Z | |
dc.date.issued | 2023-01-01 | |
dc.description.abstract | Vaccine Benefit-Risk (B-R) assessment consists of evaluating the benefits and risks of a vaccine and making a judgment whether the expected key benefits outweigh the potential key risks associated with its expected use. B-R supports regulatory and public health decision-making throughout the vaccine's lifecycle. In August 2021, the Brighton Collaboration's Benefit-Risk Assessment of VAccines by TechnolOgy (BRAVATO) Benefit-Risk Assessment Module working group was established to develop a standard module to support the planning, conduct and evaluation of structured B-R assessments for vaccines from different platforms, based on data from clinical trials, post-marketing studies and real-world evidence. It enables sharing of relevant information via value trees, effects tables and graphical depictions of B-R trade-offs. It is intended to support vaccine developers, funders, regulators and policy makers in high-, middle- or low-income countries to help inform decision-making and facilitate transparent communication concerning development, licensure, deployment and other lifecycle decisions. | |
dc.identifier.citation | Vaccine (2023) | |
dc.identifier.doi | 10.1016/j.vaccine.2023.09.039 | |
dc.identifier.eissn | 18732518 | |
dc.identifier.issn | 0264410X | |
dc.identifier.scopus | 2-s2.0-85180589694 | |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/95987 | |
dc.rights.holder | SCOPUS | |
dc.subject | Biochemistry, Genetics and Molecular Biology | |
dc.subject | Medicine | |
dc.subject | Immunology and Microbiology | |
dc.subject | Veterinary | |
dc.title | The Brighton collaboration standardized module for vaccine benefit-risk assessment | |
dc.type | Article | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85180589694&origin=inward | |
oaire.citation.title | Vaccine | |
oairecerif.author.affiliation | Faculty of Tropical Medicine, Mahidol University | |
oairecerif.author.affiliation | Novavax, Inc. | |
oairecerif.author.affiliation | Moderna Therapeutics | |
oairecerif.author.affiliation | GlaxoSmithKline Pharmaceuticals SA/NV | |
oairecerif.author.affiliation | Janssen Research & Development | |
oairecerif.author.affiliation | Public Health Agency of Canada | |
oairecerif.author.affiliation | University of Washington | |
oairecerif.author.affiliation | Sanofi S.A. | |
oairecerif.author.affiliation | Food and Drug Administration | |
oairecerif.author.affiliation | AstraZeneca | |
oairecerif.author.affiliation | Coalition for Epidemic Preparedness Innovations | |
oairecerif.author.affiliation | Independent Consultant | |
oairecerif.author.affiliation | Global Healthcare Consulting | |
oairecerif.author.affiliation | Task Force for Global Health | |
oairecerif.author.affiliation | Independent Consultant |