By Joe Hoppe

 

AstraZeneca PLC said Tuesday that its Evusheld long-acting antibody combination has been approved in the European Union for the treatment of patients with Covid-19.

The Anglo-Swedish pharmaceutical giant said that the European Commission's approval is based on the Tackle Phase 3 treatment data, which proved that Evusheld statistically significantly reduced the risk of severe Covid-19 or death, and that the drug was well tolerated.

The company's drug would be used for patients aged 12 years old and older who don't require supplemental oxygen but who are at increased risk of severe Covid-19, it added.

Evusheld was granted marketing authorization in the EU for the prevention of coronavirus in March, and is already available in the majority of countries in Europe.

 

Write to Joe Hoppe at joseph.hoppe@wsj.com

 

(END) Dow Jones Newswires

September 20, 2022 02:27 ET (06:27 GMT)

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