WASHINGTON (AP) — Drugmaker Merck has asked U.S. regulators to authorize its promising antiviral pill against COVID-19, setting the stage for a decision within weeks. If cleared by the Food and Drug Administration, it would be the first pill shown to treat COVID-19, adding a new, easy-to-use weapon to the world’s arsenal against the pandemic. The FDA will scrutinize company data on the drug’s safety and effectiveness before rendering a decision. All COVID-19 drugs now authorized by the FDA require an IV or injection.
Photo: FILE – In this Dec. 18, 2014, file photo, a person walks through a Merck company building in Kenilworth, N.J. (AP Photo/Mel Evans, File)
