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Merck asks EU regulator to authorise its COVID-19 pill

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Merck asks EU regulator to authorise its COVID-19 pill

AMSTERDAM (AP) — The European Medicines Agency said it has received a request from Merck to authorise its coronavirus antiviral, the first pill shown to treat COVID-19

AMSTERDAM (AP) — The European Medicines Agency said it has received a request from Merck to authorise its coronavirus antiviral, the first pill shown to treat COVID-19.

In a statement Tuesday, the EU drug regulator said it had started evaluating molnupiravir, made by Merck and Ridgeback Biotherapeutics, and that a decision could be made within weeks on whether it might be cleared.

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Last week, the EMA issued emergency advice saying that molnupiravir could be used to treat adults infected with the coronavirus who don’t yet need extra oxygen and are at increased risk of developing severe disease.

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The agency said the drug should be given as soon as possible after COVID-19 has been diagnosed and within five days of symptoms starting.

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It is intended to be taken twice a day for five days.

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