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. 2022 Apr 19;75(7):1245–1254. doi: 10.1093/cid/ciac291

Table 1.

Framework for Prioritizing Burden of Disease Data for Vaccine Development and Evaluation Objectives

Vaccine Objective
Element Advocacy Regulatory/Licensure Policy and Post-Licensure Evaluation Financing
Stage of vaccine pipeline All stages Pre-licensure and licensure/pre-qualification stages, with some continuation for post-licensure commitments Post-licensure, but early analyses needed pre-licensure period Required for post-licensure decision making, but evidence needed pre-licensure for 5-year Vaccine Investment Strategy decision making by Gavi and others
Key audience/stakeholders
  • Public and private donors and funding bodies

  • Public figures (eg, politicians and specialist physicians) and advocacy groups, especially in countries with high disease burden

  • Manufacturers/developers (pharmaceutical and biotech companies)

  • Wider community/society (eg, CSOs)

  • National government/regulators (NRAs)

  • WHO vaccines pre-qualification

  • Manufacturers/developers (pharmaceutical and biotech companies, public–private partnerships)

  • Funders and donors

  • Global, regional, and national policy makers and advisors (eg, WHO, SAGE, GNN, RITAGs, NITAGs)

  • Public sector immunization programs (eg, EPI Managers)

  • In-country champions (eg, specialist physicians)

  • Multilateral funders (ie, Gavi and its Vaccine Investment Strategy)

  • National government bodies (NITAGs, Ministries of Health and Finance)

  • Industry/manufacturers

  • Bilateral public and private funders

  • Private medical insurance organizations

Data purpose
  • Quantify overall preventable burden of disease that are comparable across countries/regions

  • Focus on data most likely to influence decision making (including individual vaccinees [and their caregivers]), of greatest public health significance

  • Contextualize in relation to global, regional. or national public health and development goals (eg, SDGs, IA2030)

  • Provide foundation needed to design and plan clinical trials to measure vaccine efficacy and safety for key disease endpoints

  • Measure effectiveness post-licensure (which includes knowledge of disease epidemiology prior to vaccine introduction)

  • Model and predict potential impact pre-licensure

  • Provide evidence to form recommendations

  • Assess return on investment decisions

Overarching data requirements
  • Full disease spectrum

  • Specific and nonspecific disease endpoints

  • Age-specific incidence of specific clinical endpoints as guided by WHO-preferred product characteristics in well-characterized populations

  • Vaccine-preventable disease burden (population-based, where feasible)

  • Specific and nonspecific disease endpoints

  • Cost of vaccination to prevent disease (where feasible)

  • Cost of illness

  • Impact on quality of life (eg, QALYs or DALYs)

  • Time-series data needed for economic modeling

Abbreviations: CSO, civil society organization; DALY, disability-adjusted life-year; EPI, Expanded Programme of Immunisation; Gavi, Gavi, the Vaccine Alliance; GNN, Global NITAG Network; IA2030, Immunization Agenda 2030; NITAG, National Immunization Technical Advisory Group; NRA, National Regulator Agency; QALY, quality-adjusted life-year; RITAG, Regional Immunization Technical Advisory Group; SAGE, Strategic Advisory Group of Experts on Immunization; SDG, Sustainable Development Goal; WHO, World Health Organization.