Merck applies for US emergency authorisation of Covid-19 pill

Merck applies for US emergency authorisation of Covid-19 pill

If approved, it will be the first antiviral medication to be administered orally.

Molnupiravir may reduce the risk of mortality or hospitalisation in patients most at risk of severe Covid-19. (Reuters pic)
WASHINGTON:
Merck & Co Inc said on Monday it has applied for emergency use authorisation in the US for its oral drug to treat mild-to-moderate patients of Covid-19.

The treatment, molnupiravir, has been developed with Ridgeback Biotherapeutics. If authorised, it would be the first oral antiviral medication.

Data released last week showed that molnupiravir could halve the chances of death or being hospitalised for those most at risk of contracting severe Covid-19.

Existing drugs include Gilead Sciences Inc’s infused antiviral remdesivir and generic steroid dexamethasone, both of which are generally only given once a patient has already been hospitalised.

Monoclonal antibody drugs have so far seen only limited uptake due to the difficulty in their administration.

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