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Moderna asking US, European regulators to greenlight COVID-19 vax

Moderna expects to present its data to the US Food and Drug Administration on December 17.

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Moderna Inc, which has reported its Covid-19 vaccine is 94 per cent effective, on Monday announced it is filing with US and European regulators for emergency use authorisation.

Moderna follows barely a week after Pfizer and its German partner BioNTech filed for US regulatory approval. By the end of 2020, Moderna expects to have approximately 20 million doses of its mRNA-1273 vaccine available in the U.S and is "on track to manufacture 500 million to 1 billion doses globally in 2021.

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