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Building the concept for WHO Evidence Considerations for Vaccine Policy (ECVP): Tuberculosis vaccines intended for adults and adolescents as a test case.
Kochhar, Sonali; Barreira, Draurio; Beattie, Pauline; Cavaleri, Marco; Cravioto, Alejandro; Frick, Mike W; Ginsberg, Ann M; Hudson, Ian; Kaslow, David C; Kurtz, Sherry; Lienhardt, Christian; Madhi, Shabir A; Morgan, Christopher; Momeni, Yalda; Patel, Deepali; Rees, Helen; Rogalski-Salter, Taryn; Schmidt, Alexander; Semete-Makokotlela, Boitumelo; Voss, Gerald; White, Richard G; Zignol, Matteo; Giersing, Birgitte.
Affiliation
  • Kochhar S; Global Healthcare Consulting, New Delhi, India; Department of Global Health, University of Washington, Seattle, WA, USA. Electronic address: sonalikochhar@yahoo.co.in.
  • Barreira D; UNITAID, Geneva, Switzerland.
  • Beattie P; European & Developing Countries Clinical Trials Partnership (EDCTP), The Hague, the Netherlands.
  • Cavaleri M; European Medicines Agency (EMA), Amsterdam, the Netherlands.
  • Cravioto A; Faculty of Medicine of the National Autonomous University of Mexico, Mexico.
  • Frick MW; Treatment Action Group, NY, USA.
  • Ginsberg AM; Bill & Melinda Gates Foundation, Washington DC, USA.
  • Hudson I; Bill & Melinda Gates Foundation, London, UK.
  • Kaslow DC; PATH, Seattle, USA.
  • Kurtz S; US FDA, Silver Spring, USA.
  • Lienhardt C; Unité Mixte Internationale TransVIHMI (Université de Montpellier, UMI 233 IRD, U1175 INSERM), Institut de Recherche pour le Développement (IRD), Montpellier, France; Epidemiology and Population Health, Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, Lon
  • Madhi SA; South African Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
  • Morgan C; Jhpiego, Baltimore, USA; School of Population and Global Health, University of Melbourne, Victoria, Australia; Burnet Institute, Melbourne, Australia.
  • Momeni Y; UNICEF, Copenhagen, Denmark.
  • Patel D; Gavi, the Vaccine Alliance, Geneva, Switzerland.
  • Rees H; Wits Reproductive Health and HIV Institute, University of Witwatersrand, Johannesburg, South Africa.
  • Rogalski-Salter T; Bill & Melinda Gates Medical Research Institute, Cambridge, MA, United States.
  • Schmidt A; Bill & Melinda Gates Medical Research Institute, Cambridge, MA, United States.
  • Semete-Makokotlela B; South African Health Products Regulatory Authority (SAHPRA), Pretoria, South Africa.
  • Voss G; TuBerculosis Vaccine Initiative (TBVI), Lelystad, the Netherlands.
  • White RG; TB Centre and Centre for the Mathematical Modelling of Infectious Diseases, London School of Hygiene and Tropical Medicine, London, UK.
  • Zignol M; WHO, Geneva, Switzerland.
  • Giersing B; WHO, Geneva, Switzerland.
Vaccine ; 40(12): 1681-1690, 2022 03 15.
Article de En | MEDLINE | ID: mdl-35164990
ABSTRACT
Currently, no formal mechanisms or systematic approaches exist to inform developers of new vaccines of the evidence anticipated to facilitate global policy recommendations, before a vaccine candidate approaches regulatory approval at the end of pre-licensure efficacy studies. Consequently, significant delays may result in vaccine introduction and uptake, while post-licensure data are generated to support a definitive policy decision. To address the uncertainties of the evidence-to-recommendation data needs and to mitigate the risk of delays between vaccine recommendation and use, WHO is evaluating the need for and value of a new strategic alignment tool Evidence Considerations for Vaccine Policy (ECVP). EVCPs aim to fill a critical current gap by providing early (pre-phase 3 study design) information on the anticipated clinical trial and observational data or evidence that could support WHO and/or policy decision making for new vaccines in priority disease areas. The intent of ECVPs is to inform vaccine developers, funders, and other key stakeholders, facilitating stakeholder alignment in their strategic planning for late stage vaccine development. While ECVPs are envisaged as a tool to support dialogue on evidence needs between regulators and policy makers at the national, regional and global level, development of an ECVP will not preclude or supersede the independent WHO's Strategic Advisory Group of Experts on Immunization (SAGE) evidence to recommendation (EtR) process that is required for all vaccines seeking WHO policy recommendation. Tuberculosis (TB) vaccine candidates intended for use in the adolescent and adult target populations comprise a portfolio of priority vaccines in late-stage clinical development. As such, TB vaccines intended for use in this target population provide a 'test case' to further develop the ECVP concept, and develop the first WHO ECVP considerations guidance.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Vaccins antituberculeux Type d'étude: Guideline / Prognostic_studies Limites: Adolescent / Humans Langue: En Journal: Vaccine Année: 2022 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Vaccins antituberculeux Type d'étude: Guideline / Prognostic_studies Limites: Adolescent / Humans Langue: En Journal: Vaccine Année: 2022 Type de document: Article