The Department of Health and Human Services’ Office of the Assistant Secretary for Preparedness and Response has stopped distributing the COVID-19 monoclonal antibody sotrovimab because the BA.2 omicron variant now predominates in every U.S. state and territory. The Food and Drug Administration recently revised the emergency use authorization for sotrovimab to exclude regions where the BA.2 variant predominates because the authorized dose was unlikely to be effective against it, and recommends that health care providers use alternative authorized therapies until further notice. 

Headline
The Centers for Disease Control and Prevention Feb. 19 released a report on the low use of COVID-19 antiviral drugs among individuals age 65 and older, a…
Headline
The Centers for Disease Control and Prevention Dec. 11 released a report that found last year’s version of the COVID-19 vaccine was 76% effective in preventing…
Headline
The Advisory Committee on Immunization Practices Sept. 19 recommended that patients should consult their health care provider if they want to receive a COVID-…
Headline
 The Food and Drug Administration July 10 approved Moderna’s Spikevax COVID-19 vaccine for children under 12 with at least one underlying condition that…
Headline
Department of Health and Human Services Secretary Robert F. Kennedy Jr. May 27 announced in a post on X that the Centers for Disease Control and Prevention…
Headline
Leaders of the Food and Drug Administration May 20 announced new guidelines for administering the COVID-19 vaccine in a paper published by the New England…