AstraZeneca COVID-19 drug neutralizes Omicron sub-variants in lab study | Inquirer News

AstraZeneca COVID-19 drug neutralizes Omicron sub-variants in lab study

/ 05:23 PM March 21, 2022

AstraZeneca

The logo of AstraZeneca is seen on medication packages in a pharmacy in London April 28, 2014. REUTERS

AstraZeneca (AZN.L) said on Monday its antibody-based cocktail to prevent and treat COVID-19 retained neutralising activity against Omicron coronavirus variants, including the highly contagious BA.2 sub-variant, in an independent lab study.

This is the first data looking at the impact of AstraZeneca’s Evusheld treatment on “cousins” of the Omicron variant following a recent global spike in cases. The Anglo-Swedish drugmaker said in December that another lab study found that Evusheld retained neutralising activity against Omicron.

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Data from the latest study by Washington University in the United States showed the therapy reduced the amount of virus detected in samples – viral load – of all tested Omicron sub-variants in mice lungs, AstraZeneca said. The study has yet to be peer reviewed.

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Evusheld was tested against the BA.1, BA.1.1, and BA.2 sub-variants of Omicron and it was also shown in the study to limit inflammation in the lungs – a critical symptom in severe COVID-19 infections.

“The findings further support Evusheld as a potential important option to help protect vulnerable patients such as the immunocompromised who could face poor outcomes if they were to become infected with COVID-19,” John Perez, head of Late Development, Vaccines & Immune Therapies at AstraZeneca, said.

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Last week the World Health Organization said figures showing a global rise in COVID-19 cases could herald a much bigger problem, as the Omicron and BA.2 variants spread amid the easing of restrictions and testing.

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Evusheld was found to cut the risk of developing symptomatic COVID-19 by 77% in trials, Britain’s drug regulator said last week, after approving the therapy for preventing infections in adults with poor immune response.

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Evusheld has also been shown to save lives and prevent disease progression when given within a week of first symptoms.

While vaccines rely on an intact immune system to develop targeted antibodies and infection-fighting cells, Evusheld contains lab-made antibodies designed to linger in the body for months to contain the virus in case of an infection.

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The therapy is currently under a European review. It has already been authorized in the United States.

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