Following the promising results from trials of the COVID-19 vaccine developed by AstraZeneca PLC and the University of Oxford, the UK company says it will now prepare regulatory submissions around the world, which could result in the vaccine being granted emergency use authorization before the end of the year.
The first interim analysis of the Phase III data showed that AZD1222 achieved a 70% efficacy rate, while an "intriguing" signal suggested that
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