Data validate approved use of Evusheld as COVID-19 blocker
The Lancet has published detailed results from the Phase III TACKLE study, showing the prophylactic benefits of Evusheld (tixagevimab/cilgavimab) in COVID-19.
In the outpatient treatment trial, the long-acting antibody combo showed statistically-significant levels of protection against progression to severe disease, leading to better outcomes.
Developed by British firm AstraZeneca (LSE: AZN), Evusheld is currently approved in the USA, the UK and the European Union to prevent disease caused by the novel coronavirus.
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