Merck seeks first US FDA authorisation for Covid-19 tablet
WASHNGTON — Merck & Co said on Monday (Oct 11) it has applied for US emergency use authorization for its tablet to treat mild-to-moderate patients of Covid-19, putting it on course to become the first oral antiviral medication for the disease.
WASHNGTON — Merck & Co said on Monday (Oct 11) it has applied for US emergency use authorisation for its tablet to treat mild-to-moderate patients of Covid-19, putting it on course to become the first oral antiviral medication for the disease.
Its authorisation could help change clinical management of Covid-19 as the pill can be taken at home.
The treatment, molnupiravir, could halve the chances of death or being hospitalised for those most at risk of contracting severe Covid-19, according to the drugmaker.
Viral sequencing done so far have showed it is effective against all coronavirus variants, including Delta, Merck said.
The interim efficacy data on the drug, which has been developed with Ridgeback Biotherapeutics, had heavily impacted the shares of Covid-19 vacine makers when it was released last week.
Existing drugs include Gilead Sciences' infused antiviral remdesivir and generic steroid dexamethasone, both of which are generally only given once a patient has already been hospitalised.
Meanwhile, monoclonal antibody drugs from Regeneron Pharmaceuticals and Eli Lilly have so far seen only limited uptake due to the difficulty in administering them. REUTERS