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
. 2022 Feb;27(1):1-6.
doi: 10.1136/bmjebm-2020-111507. Epub 2020 Oct 21.

Postmarketing studies: can they provide a safety net for COVID-19 vaccines in the UK?

Affiliations

Postmarketing studies: can they provide a safety net for COVID-19 vaccines in the UK?

Sandeep Dhanda et al. BMJ Evid Based Med. 2022 Feb.

Abstract

In the current era of the COVID-19 pandemic, the world has never been more interested in the process of vaccine development. While researchers across the globe race to find an effective yet safe vaccine to protect populations from the newly emergent SARS-CoV-2 virus, more than one-third of the world has been subjected to either full or partial lockdown measures. With communities having felt the burden of prolonged isolation, finding a safe and efficacious vaccine will yield direct beneficial effects on protecting against COVID-19 morbidity and mortality and help relieve the psychological and economic load on communities living with COVID-19. There is hope that with the extraordinary efforts of scientists a vaccine will become available. However, given the global public health crisis, development of a COVID-19 vaccine will need to be fast tracked through the usual prelicensing development stages and introduced with limited clinical trial data compared with those vaccines that are developed conventionally over more than a decade. In this scenario, surveillance of the vaccine in the real world becomes even more paramount. This responsibility falls to observational researchers who can provide an essential safety net by continuing to monitor the effectiveness and safety of a COVID-19 vaccine after licensing. Postauthorisation observational studies for safety and effectiveness are complementary to prelaunch clinical trials and not a replacement. In this paper, we highlight the importance of postmarketing studies for future newly licensed COVID-19 vaccines and the key epidemiological considerations.

Keywords: public health; vaccination; vaccine-preventable diseases.

PubMed Disclaimer

Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Example of study flow for a COVID-19 active surveillance postmarketing study in the UK. CRN, Clinical Research Networks; HCP, Healthcare professional; GP. General practitioner; NHS, National Health Service; NIHR, National Institute for Health Research.

References

    1. Pronker ES, Weenen TC, Commandeur H, et al. . Risk in vaccine research and development quantified. PLoS One 2013;8:e57755–e55. 10.1371/journal.pone.0057755 - DOI - PMC - PubMed
    1. Mahase E. Covid-19: what do we know so far about a vaccine? BMJ 2020;369:m1679. 10.1136/bmj.m1679 - DOI - PubMed
    1. World Health Organization . Who guidelines on clinical evaluation of vaccines. regulatory expectations. Annex 1, 2001. Available: https://www.who.int/biologicals/publications/clinical_guidelines_ecbs_20...
    1. Lurie N, Saville M, Hatchett R, et al. . Developing Covid-19 vaccines at pandemic speed. N Engl J Med 2020;382:1969–73. 10.1056/NEJMp2005630 - DOI - PubMed
    1. Ferguson NM, Laydon D, Nedjati-Gilani G. Impact of non-pharmaceutical interventions (NPIs) to reduce COVID-19 mortality and healthcare demand. Imperial College London, 2020. - PMC - PubMed

Substances