By Carl O’Donnell
(Reuters) – A U.S. Centers for Disease Control and Prevention advisory panel is predicted on Sunday to advocate Johnson & Johnson (NYSE:)’s COVID-19 shot for widespread use, a last clearance for the vaccine after it was approved by U.S. regulators on Saturday.
The Advisory Committee on Immunization Practices (ACIP) has performed a significant function in guiding states on how to allocate scarce doses, although states themselves have the ultimate say in how they allocate photographs.
For earlier COVID vaccines, the CDC panel mentioned scientific issues for sufferers together with pregnant ladies and folks with extreme allergic reactions, who weren’t studied in scientific trials.
A panel vote is scheduled for after 3 p.m. ET (2000 GMT), and the CDC’s director is predicted to approve the suggestions by the panel.
State and native public well being authorities will use Food and Drug Administration and CDC guidance as they administer the primary roughly 4 million doses that the federal authorities, by way of distribution associate McKesson Corp (NYSE:), plans to ship Sunday evening or Monday morning.
J&J’s shot would be the solely one-dose COVID vaccine accessible within the United States. It can be the best to ship and retailer, as it may be saved in a fridge fairly than a freezer.
J&J expects to ship greater than 20 million doses by March and 100 million by mid-year, sufficient to vaccinate almost a 3rd of Americans.
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