In the spotlight
Immunobridging trials: Working to bring medicines to patients faster
COVID-19Home / Our therapy areas / Vaccines and Immune Therapies / Coronavirus (COVID-19) information & research hub
Since the beginning of the pandemic, we have played a significant role in addressing the devastating impact of COVID-19.
The development, manufacture and supply of our COVID-19 vaccine was a principal achievement within our response to the COVID-19 pandemic. In partnership, we built over 25 supply networks across 15 different countries, delivering two billion doses and saving an estimated six million lives in the first year alone. Complementing our vaccines approach, we advanced research efforts into the potential of monoclonal antibodies to provide protection to the immunocompromised.
We are proud that our efforts have been recognised by governments around the world and are widely regarded as being a critical component of ending the global pandemic.
Now in the endemic phase, we remain committed to discovering and developing new approaches to fight COVID-19, with a focus on protecting the most medically vulnerable patients who remain significantly and disproportionally impacted by COVID-19 and are at risk of more severe disease.
While the world moves on from COVID-19, the urgency to protect vulnerable patients from this disease remains at the forefront of our ambitions, as we continue to explore the best and most efficient pathways and processes to support timely access to new preventative therapies.
Health professionals, governments and scientific societies should recognise the ongoing burden of COVID-19 on people who are immunocompromised and their families. Real-world evidence highlights that despite representing about 4% of the population, immunocompromised individuals account for about 25% of COVID-19 hospitalisations, ICU admissions and deaths.1 In addition, these patients also face a considerable economic burden, with data showing that immunocompromised individuals accounted for about one-third (about $310 million US) of the total COVID-19 US hospitalisation costs in 2022.2 We remain committed to exploring innovative solutions to help protect the most vulnerable patients in this ever-changing COVID-19 landscape
Q&A with Ros Hollingsworth, Vice President of Medical, Vaccines & Immune Therapies, AstraZeneca
Absolutely. Despite lower case numbers, COVID-19 hospitalisations and deaths in the general population compared with the height of the pandemic remain a concern. Although the World Health Organization declared an end to the global public health emergency in May 2023, COVID-19 continues to carry a high burden of disease globally.1,3,4 WHO reported substantial increases in COVID-19 hospitalisations and ICU admissions in late 2023.5 COVID-19 remains one of the leading causes of death and respiratory virus hospitalisations in the US, where 2023 ended with about 35,000 weekly hospitalisations and over 2,000 people per week dying from COVID-19.6 New real-word evidence from large-scale studies in England and the US highlight that despite representing a small percentage of the general population, immunocompromised individuals accounted for a disproportionally large percentage of severe COVID-19 outcomes.1 So, we all – health professionals, scientific societies, governments and the public at large – need to remain vigilant and ensure access to effective protection individually and in our communities.
Most people with healthy immune systems now remain well protected against severe outcomes from COVID-19 through vaccination and previous infection. Immunocompromised individuals typically have a diminished immune response to vaccinations, including those for COVID-19, due to their weakened immune system.7 To be effective, vaccines require a healthy immune system to jumpstart the body’s natural ability to produce an infection-fighting response.8 In people who are immunocompromised, the quantity, quality, and durability of protective antibodies produced from COVID-19 vaccinations are lower than in others, and this can leave them at risk of infection and serious outcomes.9-12
Despite vaccination, COVID-19 remains a threat for immunocompromised patients. Immunocompromised individuals carry a disproportionately large proportion of the COVID-19 disease burden compared to the general population.1,2 Their risks for breakthrough infections and severe clinical outcomes remain elevated relative to the rest of the population. A recent study conducted in England showed that despite accounting for about 4% of the population, immunocompromised individuals accounted for around a quarter of all COVID-19 hospitalisations, ICU admissions and deaths, even after receiving repeated doses of COVID-19 vaccines.1 With reduced protection, many in the IC community continue to limit contact with others, practice preventive measures such as mask-wearing and often can’t return to their everyday lives.13,14
Looking beyond the impact for patients and their friends and family, a considerable economic burden also remains. A comprehensive US study showed that immunocompromised individuals accounted for about one-third (about $310 million US) of the total COVID-19 US hospitalisation costs in 2022. More than 60% of costs contributed by immunocompromised individuals were due to hospitalisations for severe COVID-19.2
Discover what living with the continuing threat of COVID-19 has meant to immunocompromised individuals and their families.
While the risk of COVID-19-related hospitalisation is elevated across immunocompromised populations, the risk for people with certain conditions or who take immunosuppressive treatments is particularly high. For example, the risk of hospitalisation is even higher for people with blood/bone marrow cancers, end-stage kidney disease, solid organ transplant recipients and those who take certain medications for autoimmune conditions such as multiple sclerosis.1 Therefore, immunocompromised individuals are advised to get the most recently available COVID-19 vaccines, to use additional preventive measures, such as wearing masks, and be promptly tested and treated at the onset of COVID-19 symptoms.
We believe more needs to be done to protect individuals who are immunocompromised, and we have been committed to this work since the beginning of the COVID-19 pandemic. Immunocompromised patients, and their physicians, need to be aware of the disproportionate risk of COVID-19-related illness and complications, and the fact that vaccination often does not provide adequate protection to immunocompromised individuals.7
Learn more from the International Immunocompromised Advocacy Network, a coalition of more than 40 patient groups that issued a Call to Action outlining the unmet needs and challenges of immunocompromised individuals around COVID-19.
As a supplement to vaccination, monoclonal antibodies may provide additional protection to the immunocompromised as infection-fighting antibodies are given directly to vulnerable individuals who may not generate enough antibodies on their own after vaccination. This approach, known as passive immunisation, may provide near immediate protection against COVID-19.15
COVID-19 is still a threat, especially for immunosuppressed people who continue to face significant and disproportionate health impacts from the virus.1,2 The updated CDC recommendation aims to bring advice for COVID-19 in line with that for other kinds of respiratory infections, such as flu. However, COVID-19 hospitalisations overall in the US remain much higher than for flu.16,17 As such, everyone who tests positive for COVID-19 should be mindful of the potential to cause serious illness in those who are medically vulnerable. The new recommendation also means that immunosuppressed people should take extra precautions to protect themselves from COVID-19 and seek medical advice and care as needed.
To keep pace with rapidly evolving SARS-CoV-2 variants and to be prepared for future pandemics, rapid clinical development and approval pathways are needed to respond in a timely manner. One way that researchers and health authorities are expediting the process is through immunobridging trials, a scientific approach that has paved the way for vaccine approvals across numerous infectious diseases. Immunobridging trials are an established approach used when there is an urgent need for important, new medicines, but full-scale efficacy trials may not be feasible within the timeframe available.22 The trials are designed to demonstrate equivalent activity for an investigational therapy to a similar existing therapy.22 This type of trial has been used since the 1990’s to support the introduction of updated vaccines for a variety of infectious diseases, including COVID-19 boosters, flu, human papillomavirus and pneumococcal pneumonia.18-21
We face an unpredictable world of SARs-CoV-2 variants, and we anticipate that the virus will continue to evolve. What remains true is that immunocompromised patients have few options and need protection in this heterogeneous and ever-changing viral landscape.23 This is a key reason we remain committed to protecting and supporting the immunocompromised community and will continue to do so.
We are all adjusting to a new normal, and health experts anticipate we may have to deal with the disruption of COVID-19 for years to come. Our bold ambition is to create a world where the threat of COVID-19 is eliminated for all people. This is part of our larger mission in AstraZeneca’s Vaccines & Immune Therapies to help protect millions of people where the burden of disease is highest and unmet needs are greatest, ensuring no one is left behind.
Our work continues to support the needs of the immunocompromised as they continue to endure significant and disproportionate burden from COVID-19. Learn more from patients Johanne, Miguel, and Paul/Emma.
From the latest news on antibody testing to our ever-developing covid research, learn about our efforts to combat COVID-19.
1. Evans RA et al. Impact of COVID-19 on immunocompromised populations during the Omicron era: Insights from the observational population-based INFORM study. The Lancet Regional Health – Europe. 2023;0(0):100747. doi:10.1016/J.LANEPE
2. Ketkar A et al. Assessing the burden and dost of COVID-19 across variants in commercially insured immunocompromised populations in the United States: Updated results and trends from the ongoing EPOCH-US study. Adv Ther. 2024. doi:10.1007/s12325-023-02754-0
3. World Health Organization. COVID-19 epidemiological update – 19 January 2024. [cited March 2024]. Available from: http://www.who.int/publications/m/item/covid-19-epidemiological-update---19-january-2024
4. Our World in Data. Coronavirus (COVID-19) hospitalizations. [cited March 2024]. Available from: http://ourworldindata.org/covid-hospitalizations#citation
5. World Health Organization. WHO press conference on global health issues – 10 January 2024. [cited March 2024]. Available from: http://www.who.int/multi-media/details/who-press-conference-on-global-health-issues-10-january-2024
6. Centers for Disease Control. COVID data tracker: Trends by geographic area (hospitalisation). [cited March 2024]. Available from: http://covid.cdc.gov/covid-data-tracker/#trends_weeklyhospitaladmissions_select_00
7. Centers for Disease Control. People who are immunocompromised. [cited March 2024]. Available from: http://www.cdc.gov/coronavirus/2019-ncov/need-extra-precautions/people-who-are-immunocompromised.html
8. Centers for Disease Control and Prevention. Understanding how COVID-19 vaccines work. [cited March 2024]. Available from: http://www.cdc.gov/coronavirus/2019-ncov/vaccines/different-vaccines/how-they-work.html
9. Haidar G et al. Prospective evaluation of coronavirus cisease 2019 (COVID-19) vaccine responses across a broad spectrum of immunocompromising conditions: the COVID-19 vaccination in the immunocompromised study (COVICS). Clin Infect Dis. 2022 75(1):3630-e644. doi: 10:1093/cid/ciac103
10. Obeid M et al. Humoral responses against variants of concern by COVID-19 mRNA vaccines in immunocompromised patients. JAMA Oncol. 2022 May;8(5):E220446. doi:10.1001/jamaoncol.2022.0446
11. Benning L et al. Neutralizing antibody response against the B.1.617.2 (delta) and the B.1.1.529 (omicron) variants after a third mRNA SARS-CoV-2 vaccine dose in kidney transplant recipients. Am J Transplant. 2022;22:1873–83
12. Tartof SY et al. Effectiveness of a third dose of BNT162b2 mRNA COVID-19 vaccine in a large US health system: A retrospective cohort study. Lancet Reg Health Am. 2022 May 9:doi: 10.1016/j.lana.2022.100198
13. All-Party Parliamentary Group on Vulnerable Groups to Pandemics. Covid-19 Inquiry Update and Position Statement, March 2023.
14. Maia T, et al. Post-lockdown behaviors and impacts of avoiding COVID-19 in patients and caregivers of patients at high-risk of severe COVID-19: a qualitative study. Poster at ISPOR 2023, Boston. [cited March 2024]. Available from: http://www.ispor.org/docs/default-source/intl2023/ispor23williamsposter-pdf.pdf?sfvrsn=cbfe579f_0
15. Centers for Disease Control and Prevention. Immunity types. [cited March 2024]. Available from: http://www.cdc.gov/vaccines/vac-gen/immunity-types.htm
16. Centers for Disease Control and Prevention. Laboratory confirmed Influenza Hospitalizations. [cited March 2024]; Available from: http://gis.cdc.gov/grasp/fluview/fluhosprates.html
17. Centers for Disease Control and Prevention. COVID-NET interactive dashboard. [cited March 2024]. Available from:
http://www.cdc.gov/coronavirus/2019-ncov/covidnetdashboard/de/powerbi/dashboard.html
18. Fritzell B. Bridging studies. Dev Biol Stand. 1998 [cited March 2024];95:181–8. Available from: http://pubmed.ncbi.nlm.nih.gov/9855430/
19. Khoury DS et al. Correlates of protection, thresholds of protection, and immunobridging among persons with SARS-CoV-2 Infection. Emerg Infect Dis. 2023;29(2):381–8.
20. PREVNAR 20 Package Insert. [cited March 2024]. Available from: http://labeling.pfizer.com/ShowLabeling.aspx?id=15428
21. Donken R et al. Immunogenicity of 2 and 3 doses of the quadrivalent human papillomavirus vaccine up to 120 months postvaccination: Follow-up of a randomized clinical trial. Clin Infect Dis. 2020;71(4):1022–9
22. Fink D. Immunobridging to evaluate vaccines. [cited March 2024]. Available from: http://cdn.who.int/media/docs/default-source/blue-print/doran-fink_4_immunobridging_vrconsultation_6.12.2021.pdf
23. Lendacki FR, et al. Breakthrough SARS-CoV-2 infections among recipients of tixagevimab-cilgavimab prophylaxis: A citywide real-world effectiveness study. Transpl Infect Dis. 2024;26:314194. doi: 10.1111/tid.14194