Johnson & Johnson says that it has 4 million doses of its Covid-19 vaccine able to ship “instantly” as soon as it receives emergency use authorization, which may occur this week.
In an analysis just released, the US Meals and Drug Administration mentioned the corporate’s single-dose vaccine has met the necessities for emergency use authorization.
Nonetheless, regardless of the thrill and anticipation, there are nonetheless a number of steps Johnson & Johnson has to undergo earlier than the vaccine might be out there.
Here is what occurs subsequent:
The FDA’s Vaccines and Associated Organic Merchandise Advisory Committee meets on Friday to evaluation knowledge on the vaccine and determine whether or not to suggest it for emergency use authorization in adults 18 and older.
As soon as the vaccine is permitted, the US Facilities for Illness Management and Prevention Advisory Committee on Immunization Practices, or ACIP, makes suggestions to the CDC on how the vaccine ought to be used, resembling amongst what age teams and on what sort of schedule. An emergency meeting of ACIP is scheduled for Feb. 28 and March 1.
Sometimes, the CDC director accepts the committee’s suggestion. Shortly after that, the vaccine may be distributed, and may begin going into arms.
What everybody desires to know is the place the federal authorities will ship these doses, and who they will be steered towards.
“We’re hoping that ACIP will present some steering on the best use of the J&J one dose vaccine,” Claire Hannan, govt director of the Affiliation of Immunization Managers, wrote in an e-mail to CNN on Tuesday.
“States are in search of steering to be used of the vaccine in populations which could actually profit from the one dose collection full, resembling transient populations,” Hannan mentioned. “We aren’t listening to a lot on this.”
You may learn extra concerning the Johnson & Johnson vaccine here.