India

FDA Likely To Rule On Virus Pill In December


Washington, Oct 14 (AP) The Food and Drug Administration will ask its outside experts to meet in late November to scrutinise Merck’s pill to treat COVID-19. The November 30 meeting means US regulators likely won’t issue a decision on the drug until December, signalling that the agency will conduct a detailed review of the experimental treatment’s safety and effectiveness. The panelists are likely to vote on whether Merck’s drug should be approved, although the FDA is not required to follow their advice.

Three IV antibody drugs have been authorised since last year but they are expensive, hard to produce and require specialty equipment and health professionals to deliver. If authorised, Merck’s drug, molnupiravir, would be the first that patients could take at home to ease symptoms and speed recovery. If authorised, Merck’s drug is likely the first but not the only pill to treat COVID-19. Pfizer, Roche and Appili Therapeutics are studying similar drugs.(AP) .

Disclaimer: This post has been auto-published from an agency feed without any modifications to the text and has not been reviewed by an editor

Read all the Latest News, Breaking News and Coronavirus News here. Follow us on Facebook, Twitter and Telegram.





Source link

Related Articles

Leave a Reply

Your email address will not be published. Required fields are marked *

Adblock Detected

Turn Off Ad Blocker