Merck seeks emergency-use authorization of oral antiviral for COVID-19

OAN Top News

This undated image provided by Merck & Co. shows their new antiviral medication. The drugmaker has said its experimental pill for people sick with COVID-19 reduced hospitalizations and deaths. (Merck & Co. via AP)

This undated image provided by Merck & Co. shows their new antiviral medication. The drugmaker has said its experimental pill for people sick with COVID-19 reduced hospitalizations and deaths. (Merck & Co. via AP)

This undated image provided by Merck & Co. shows their new antiviral medication. The drugmaker has said its experimental pill for people sick with COVID-19 reduced hospitalizations and deaths. (Merck & Co. via AP)

OAN Newsroom
UPDATED 10:38 AM PT – Monday, October 11, 2021

Drugmakers are seeking FDA authorization for the first oral antiviral medicine for treating COVID-19. Merck and Ridgeback Biotherapeutics announced Monday that they submitted an application with the agency for emergency-use authorization of molnupiravir.

The experimental medication, originally developed for treating influenza, is now demonstrating results in mild-to-moderate COVID-19 cases in at-risk adults. Clinical trials of the pill found that it reduced the risk of hospitalization or death by approximately 50 percent.

The medication is administered as four pills taken twice-a-day for five days. The drug could be made available to Americans by late this year and would be the first authorized oral antiviral medicine for the treatment of COVID-19.

The biotechnology company’s focus revolves around emerging infectious diseases. It’s known to market a treatment for Ebola. The team at Merck and Ridgeback Biotherapeutics noted, they are “dedicated to working toward finding life-saving and life-changing solutions for patients and diseases that need champions.”

MORE NEWS: Neurologist Defends Natural Immunity

Leave a Reply