Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 May-Jun;78(3):293-302.
doi: 10.1016/j.therap.2022.07.003. Epub 2022 Jul 13.

The winding 12-month journey of the AstraZeneca COVID-19 vaccine since its first administration to humans

Affiliations

The winding 12-month journey of the AstraZeneca COVID-19 vaccine since its first administration to humans

Rafael Dal-Ré. Therapie. 2023 May-Jun.

Abstract

The deficiently designed and conducted initial clinical development plan and the occurrence of thrombotic thrombocytopenia cases, have marked the first 12-month journey of the AstraZeneca coronavirus disease 2019 (COVID-19) vaccine after it was first administered to humans. When it was authorized, there were no available efficacy data in the elderly. However, this age group was included in the product labelling based on immunogenicity data. The lack of safety and efficacy data in the elderly that was acknowledged in the product information, triggered most European Union (EU) countries to limit the administration of this vaccine to certain age groups. In February-March/2021, after the results of observational studies supported the vaccine effectiveness in the elderly, several countries broadened its use to this age group. When trust on the vaccine was ramping up, unusual blood clot cases were described in Europe, which led 24 countries around the world to temporarily halt its administration. These cases were first described as thrombotic thrombocytopenia in late March. In mid-April, the UK Medicines and Healthcare products Regulatory Agency (MHRA) and the European Medicines Agency (EMA) updated the product information and confirmed the positive benefit/risk ratio of the vaccine, recommending its use with no age restrictions. The World Health Organization (WHO) coincided with this approach. However, several countries decided to limit its use to certain age groups. The EMA listed thrombotic thrombocytopenia as a "very rare" adverse reaction. Although, the AstraZeneca vaccine was conceived in early 2020 to be a worldwide leader in the fight against COVID-19, its use was abandoned by the African Union, Denmark, and Israel. However, this vaccine has shown its usefulness in many settings across the world.

Keywords: AstraZeneca COVID-19 vaccine; ChAdOx1 nCoV-19; Clinical trials; Effectiveness; Efficacy; Safety; Thrombotic thrombocytopenia.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Bottaro G. AstraZeneca agrees to produce Oxford University's coronavirus vaccine candidate on not-for-profit basis. Proactive. 30 April 2020. https://www.proactiveinvestors.co.uk/companies/news/918534/astrazeneca-a.... [Accessed 25 February 2022].
    1. World Health Organization. COVAX. https://www.who.int/initiatives/act-accelerator/covax. [Accessed 25 February 2022].
    1. Callaway E. The unequal scramble for coronavirus vaccines. Nature. 2020;568:506–507. - PubMed
    1. AstraZeneca. AstraZeneca advances mass global rollout of COVID-19 vaccine through COVAV. 2 March 2021. https://www.astrazeneca.com/media-centre/press-releases/2021/astrazeneca.... [Accessed 25 February 2022].
    1. Dal-Ré R., Banzi R. When is it reasonable to extrapolate during a pandemic? The case of broad UK labelling for AstraZeneca COVID-19 vaccine. Eur J Intern Med. 2021;87:1–2. - PMC - PubMed

Substances