Explainer: When will COVID-19 vaccines be generally
available in the United States?
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[October 17, 2020]
By Carl O'Donnell and Michael Erman
(Reuters) - U.S. President Donald Trump and the head of the Centers for
Disease Control and Prevention (CDC) have disagreed about when a
COVID-19 vaccine would become widely available. Trump has said enough
vaccine would be available for every American by April, while the CDC
director said vaccines were likely to reach the general public around
mid-2021, an assessment more in line with most experts.
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Pfizer Inc <PFE.N> said on Friday it could file for U.S.
authorization of the COVID-19 vaccine it is developing with German
partner BioNTech <22UAy.F> in late November, suggesting it is
possible a vaccine could be available in the United States this
year.
WHAT DOES IT MEAN FOR A VACCINE TO BE GENERALLY AVAILABLE?
General availability is when every American who wants the vaccine
can get it. There are currently no COVID-19 vaccines approved by
U.S. regulators, although a handful are in late-stage trials to
prove they are safe and effective.
Experts estimate that at least 70% of roughly 330 million Americans
would need to be immune through a vaccine or prior infection to
achieve what is known as herd immunity, which occurs when enough
people are immune to prevent the spread of the virus to those unable
to get a vaccine.
HOW LONG BEFORE VACCINE PRODUCTION IS FULLY RAMPED UP?
The CDC anticipates that up to 700 million doses of vaccine will be
available in April of 2021, enough to vaccinate all Americans
because most vaccines in development require two doses per person.
It has forecast that 35 million to 45 million doses of vaccines will
be available in the United States by the end of this year from the
first two companies to receive authorization. The current
front-runners are Pfizer and Moderna Inc <MRNA.O>.
Though 35 million to 45 million doses sounds like a lot, obtaining
enough doses to inoculate everyone in the United States will likely
take until later in 2021. CDC Director Robert Redfield told a
congressional hearing in September that most Americans will be
vaccinated by July, not April.
Drugmakers have been more ambitious with their calculations. Pfizer
and BioNTech SE have said they expect to have 100 million doses
available worldwide by the end of 2020, but did not specify how much
of that was earmarked for the United States. Moderna has said it is
on track to make around 20 million doses by the end of the year and
between 500 million and 1 billion doses a year beginning in 2021.
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AstraZeneca Plc <AZN.L> has said it could deliver as many as 300 million doses
of its experimental vaccine in the United States as early as October but its
U.S. trial has been on hold since September.
WHO WOULD GET AN APPROVED VACCINE FIRST?
The CDC has said that if supplies are limited, the earliest inoculations may go
to healthcare workers, people at increased risk for severe COVID-19, people aged
65 years and older and essential workers.
It is unclear when a vaccine will be available for children as major drugmakers
have yet to include them in late-stage trials. Pfizer and BioNTech have approval
from regulators to start recruiting volunteers as young as 12 for vaccine
studies.
WHICH COMPANIES WILL LIKELY ROLL OUT A VACCINE QUICKLY?
Pfizer/BioNTech said it may have data as early as October and Moderna says it
could have similar evidence in November. The vaccines would first need to be
approved or authorized for emergency use by U.S. regulators, and Pfizer says it
expects to have the safety data it needs in the third week of November to file
with the U.S. Food and Drug Administration.
Drugmakers have already started manufacturing supplies of their vaccine
candidates to be ready as soon as they get the go-ahead. The U.S. Department of
Defense and the CDC plan to start distribution of vaccines within 24 hours of
regulatory authorization.
Several drugmakers including Pfizer, AstraZeneca, Johnson & Johnson <JNJ.N> and
Novavax Inc <NVAX.O> have said they expect to produce at least 1 billion doses
of their vaccines next year if they get regulatory authorization.
Sanofi SA <SASY.PA> and GlaxoSmithKline Plc <GSK.L> are also working on
developing a vaccine they say could be authorized next year.
(Reporting by Carl O'Donnell, Michael Erman and Caroline Humer in New York;
Editing by Bill Berkrot and Matthew Lewis)
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