AstraZeneca to Present New Data Across its Vaccines and Immune Therapies Portfolio at IDWeek

AstraZeneca will showcase new data across its Vaccines and Immune Therapies portfolio at the 11th annual IDWeek conference, 19 – 23 October 2022, reinforcing its commitment to deliver long-lasting immunity for millions of people globally. The Company is set to present seven abstracts at the event.

AstraZeneca will showcase new data across its Vaccines and Immune Therapies portfolio at the 11th annual IDWeek conference, 19 – 23 October 2022, reinforcing its commitment to deliver long-lasting immunity for millions of people globally. The Company is set to present seven abstracts at the event.

Data featuring Evusheld (tixagevimab and cilgavimab)1-5 and Vaxzevria (ChAdOx1-S [Recombinant], formerly AZD1222)6 in COVID-19 and Beyfortus (nirsevimab), in respiratory syncytial virus (RSV)7 will be presented. Beyfortus has the potential to transform RSV protection as the first and only single-dose preventative option for the broad infant population, including those born healthy, at term, pre-term or with specific medical conditions. In September, Beyfortus received a positive opinion from The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency.

Iskra Reic, Executive Vice-President Vaccines and Immune Therapies, AstraZeneca, said: “In our work in Vaccines and Immune Therapies, AstraZeneca has the ambition to help provide long-lasting immunity for millions. This year at IDWeek, our data for Evusheld, our long-acting antibody for patients at high risk of hospitalisation and death from COVID-19, and Beyfortus, our investigational long-antibody for RSV, demonstrate our commitment to helping protect the most vulnerable, ensuring no one is left behind.”

Evusheld’s role in protecting against COVID-19

Data from three abstracts from the Phase III TACKLE trial of Evusheld in adults with mild to moderate COVID-19 will be presented, which include new analyses on the prevention of hospitalisation and death;1 reduction in the severity and progression of COVID-19 symptoms;2 and the susceptibility of treatment-emergent viral variants to Evusheld.3 Data on the activity of Evusheld against circulating SARS-CoV-2 variants and those identified in the Phase III PROVENT prophylaxis trial will also be presented.

Pursuing a breakthrough in infant RSV care

New viral susceptibility data on Beyfortus data in infants up to 150 days post-dose will be presented during IDWeek.7 Beyfortus is the first investigational passive immunisation with the potential to help protect a broad infant population across the entire RSV season with a single dose.

Additional data on Vaxzevria

AstraZeneca will also present data on Vaxzevria, evaluating its impact on immune responses, viral shedding and symptom burden in breakthrough SARS-CoV-2 infection.

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