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Assessing vaccine introduction and uptake timelines in Gavi-supported countries: are introduction timelines accelerating across vaccine delivery platforms?
Luthra, Karuna; Zimmermann Jin, Anna; Vasudevan, Prarthana; Kirk, Karen; Marzetta, Carol; Privor-Dumm, Lois.
  • Luthra K; International Vaccine Access Center, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Zimmermann Jin A; Vaccines & Sustainability, GAVI Alliance, Geneva, Geneva, Switzerland.
  • Vasudevan P; (Formerly Applied Strategies), Strategic Decisions Group, Palo Alto, California, USA.
  • Kirk K; Skoll Foundation, Palo Alto, California, USA.
  • Marzetta C; International Vaccine Access Center, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Privor-Dumm L; Center for Health Security, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA.
BMJ Glob Health ; 6(5)2021 05.
Article in English | MEDLINE | ID: covidwho-1476468
ABSTRACT

BACKGROUND:

Previous studies identified factors influencing regulatory approval to introduction timelines for individual vaccines. However, introduction and uptake timelines have not been comprehensively assessed across the portfolio of Gavi-supported vaccines.

METHODS:

We analysed median times between introduction milestones from vaccine licensure to country introduction and uptake across six vaccine-preventable diseases (VPDs), three delivery platforms and 69 Gavi-supported countries. Data were gathered from public, partner and manufacturer records. VPDs and prequalified vaccines analysed included Haemophilus influenzae type b (DTwP-HepB-Hib, pentavalent), pneumococcal disease (pneumococcal conjugate vaccine, PCV), rotavirus diarrhoea (rotavirus vaccine, RVV), cervical cancer (human papillomavirus vaccine, HPV), polio (inactivated polio vaccine, IPV) and meningococcal meningitis (meningococcal group A conjugate vaccine, MenA).

RESULTS:

Median time from first vaccine licensure to first Gavi-supported country introduction across VPDs at a 'global level' (Gavi-supported countries) was 5.4 years. Once licensed, MenA vaccines reached first introduction fastest (campaign=0.6 years; routine immunisation (RI)=1.7 years). Most introductions were delayed. Country uptake following first introduction was accelerated for more recently Gavi-supported RI vaccines compared with older ones.

CONCLUSION:

Factors accelerating timelines across delivery platforms included rapid product prequalifications by WHO, strong initial recommendations by the WHO Strategic Advisory Group of Experts (SAGE) on Immunization, achieving target product profiles on first vaccine licensure within a VPD and completing several VPD milestones at a global level prior to licensure. Milestones required for introduction in Gavi-supported countries should start prior or in parallel to licensure to accelerate uptake of vaccines delivered through diverse delivery platforms.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Rotavirus Vaccines Topics: Vaccines Limits: Humans Language: English Year: 2021 Document Type: Article Affiliation country: Bmjgh-2021-005032

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Rotavirus Vaccines Topics: Vaccines Limits: Humans Language: English Year: 2021 Document Type: Article Affiliation country: Bmjgh-2021-005032