US FDA authorises Merck’s at-home antiviral Covid-19 pill

December 23

The US Food and Drug Administration on Thursday authorised Merck & Co’s antiviral pill for Covid-19, after giving the go-ahead to a similar treatment from Pfizer Inc a day earlier.

Merck’s drug, molnupiravir, developed with Ridgeback Biotherapeutics, was shown to reduce hospitalizations and deaths by around 30% in a clinical trial of high-risk individuals early in the course of the illness.

The agency authorised the oral drug for the treatment of mild-to-moderate Covid-19 in adults who are at risk for severe disease, and for whom alternative Covid-19 treatments are not accessible or clinically appropriate.

The US government has a contract to buy as many as 5 million courses of the drug for $700 per course.

The drug is not authorised for use in patients younger than 18 because molnupiravir may affect bone and cartilage growth, the FDA said in a statement. —Reuters