The Food and Drug Administration (FDA) on Thursday authorized the use of Merck and Ridgeback Biotherapeutics’ molnupiravir pill for treating COVID-19, the second such emergency use authorization in two days.
The FDA on Wednesday authorized Pfizer’s paxlovin drug. Both pills may be taken orally at home, giving health care providers another tool to prevent severe disease amid a wave of omicron variant infections.
the country’s arsenal of COVID-19 therapies using emergency use authorization, while continuing to generate additional data on their safety and effectiveness,” Dr. Patrizia Cavazzoni, director of the FDA’s Center for Drug Evaluation and Research, said in a statement.
The FDA said the treatment pills are not substitutes for approved and authorized COVID-19 vaccines, and that molnupiravir is not a preventative drug.
Cavazzoni said that under the authorization, Merck’s pill will be “limited to situations where other FDA-authorized treatments for COVID-19 are inaccessible or are not clinically appropriate and will be a useful treatment option for some patients with COVID-19 at high risk of hospitalization or death,” Cavazzoni said.
Use of molnupiravir in patients under the age of 18 is not authorized because it may affect bone and cartilage growth in that age group.
The Merck-Ridgeback pill prevents the SARS-CoV-2 virus from replicating by introducing errors into the virus’ genetic code, the FDA said.
During a treatment regiment, patients take a total of 40 pills over the course of five days – four 200 milligram capsules every 12 hours.
The Merck pill was shown to reduce hospitalization and death in a randomized, double-blind, placebo-controlled clinical trial with 709 patients who received the treatment, and 699 who received the placebo. The study participants were all 18 or older, had tested positive for COVID-19 and who had not been vaccinated.