WEBVTT - How Could COVID-19 Vaccines Change the World?

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<v Speaker 1>Welcome to brain Stuff, a production of iHeart Radio, Hey

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<v Speaker 1>brain Stuff, Lauren bog Obam. Here, a medical breakthrough that

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<v Speaker 1>could save thousands of lives and effectively quashed the deadliest

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<v Speaker 1>pandemic in more than a century is eminent, it seems,

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<v Speaker 1>a vaccine for COVID nineteen and all it took to

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<v Speaker 1>reach this point, besides the incalculable pain and suffering of

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<v Speaker 1>millions of people worldwide, was the talent of a veritable

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<v Speaker 1>army of scientists, a push in the back, and some

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<v Speaker 1>crafty maneuvering by the U. S. Government, a good idea

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<v Speaker 1>that wouldn't go away, and billions and billions and billions

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<v Speaker 1>of dollars. We spoke with Jim Richardson, the Senior Scientifical

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<v Speaker 1>Liaison at U S Pharmacopeia, a two hundred year old

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<v Speaker 1>scientific nonprofit that establishes federally enforced quality standards for, among

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<v Speaker 1>other products, vaccines. He said, the amount of resources that

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<v Speaker 1>are being applied to this is just up sedented. Millions

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<v Speaker 1>of dollars have never been in such a short time

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<v Speaker 1>applied to a problem of this magnitude, even with H

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<v Speaker 1>one and one and other things that have happened over

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<v Speaker 1>the years. This has really spurred a lot of a

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<v Speaker 1>variety of different platforms that people have been working on

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<v Speaker 1>for a long time. Dozens of companies, using several different

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<v Speaker 1>scientific methods have been gobbling up those government dollars and

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<v Speaker 1>quite a bit of private capital too, in order to

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<v Speaker 1>create a vaccine to stop the coronavirus that's behind this pandemic.

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<v Speaker 1>It's obviously important work. The virus that causes COVID nineteen

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<v Speaker 1>has infected more than fifty six million people in the

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<v Speaker 1>world and killed more than one point three million. It's

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<v Speaker 1>responsible for more than two hundred and fifty thousand deaths

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<v Speaker 1>in the U s alone. Two of the companies in particular,

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<v Speaker 1>that are trying to create a COVID nineteen vaccine have

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<v Speaker 1>stood out from the competition by employing a bold and

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<v Speaker 1>still unproven process. But this time it just might work.

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<v Speaker 1>Before the coronavirus that causes COVID nineteen reared its spiky

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<v Speaker 1>head early in twenty twenty, creating vaccines was a painstaking,

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<v Speaker 1>years long process. The Mum's vaccine was rolled out in

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<v Speaker 1>nineteen sixty seven in what's considered the fastest implementation in history.

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<v Speaker 1>It took four years. The vaccine for this coronavirus, which

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<v Speaker 1>is officially called the Severe Acute Respiratory syndrome Coronavirus two

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<v Speaker 1>or STARS cove too, is on a much much faster

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<v Speaker 1>track for a few reasons. First, because scientists have sena

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<v Speaker 1>virus like this one before the Star's outbreak in two

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<v Speaker 1>thousand three that infected more than eight thousand people worldwide

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<v Speaker 1>and killed nearly eight hundred. The current virus, as it

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<v Speaker 1>turns out, is eighty percent identical in genetic material to

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<v Speaker 1>the one from two thousand three, so all researchers needed

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<v Speaker 1>this time was to see how this virus was different

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<v Speaker 1>from the last one. The Chinese scientists who discovered the

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<v Speaker 1>current virus back in January mapped its genomes almost immediately

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<v Speaker 1>and provided everyone with a text file of its complete

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<v Speaker 1>set of DNA. Secondly, the pair of companies leading the

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<v Speaker 1>raise for a vaccine, Maderna, which is in partnership with

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<v Speaker 1>the National Institutes of Health, and Visor, which is working

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<v Speaker 1>with a German film bioin Tech, finally seemed to have

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<v Speaker 1>perfected a once dismissed idea for a vaccine to attack

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<v Speaker 1>the virus. This new method of making a vaccine and

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<v Speaker 1>more on that in a moment is simply much quicker

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<v Speaker 1>than the old one. And thirdly, well, those billions and

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<v Speaker 1>billions of dollars certainly lit a fire. To understand these

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<v Speaker 1>new vaccines, it helps to first understand the old ones.

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<v Speaker 1>Traditional vaccines typically use a weekend or attenuated form of

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<v Speaker 1>the offending virus to nudge along a person's natural ability

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<v Speaker 1>to combat microbes. The dead virus is injected into the body,

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<v Speaker 1>the immune system learns what it looks like and how

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<v Speaker 1>to fight it, and so when the real virus tax

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<v Speaker 1>in best case scenarios, our bodies are ready for it

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<v Speaker 1>because they already have the antibodies to fight it. Maderna

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<v Speaker 1>and Fiser are using something different called synthetic messenger ribonucleic

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<v Speaker 1>acid or synthetic mRNA instead of a virus to do

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<v Speaker 1>the same thing. Push our bodies into producing antibodies to

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<v Speaker 1>attack and neutralize the coronavirus before it can hook onto

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<v Speaker 1>healthy cells and make us sick. Potentially, it's game changing,

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<v Speaker 1>life saving, but let's break it down a bit more.

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<v Speaker 1>You've probably heard of DNA, that double helix molecule found

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<v Speaker 1>in every cell that contains your unique genetic code, but

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<v Speaker 1>mRNA as its name flat out states it's a kind

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<v Speaker 1>of messenger that carries bits of genetic code from cells

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<v Speaker 1>nucleus out to the cells ribosomes, which use that code

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<v Speaker 1>to create proteins. Paula Cannon, an associate professor of microbiology

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<v Speaker 1>at the Universe Southern California's Tech School of Medicine, put

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<v Speaker 1>it well when she told NBC News, if DNA is

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<v Speaker 1>the big instruction manual for the cell, then messenger RNA

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<v Speaker 1>is like when you photocopy just one page that you

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<v Speaker 1>need and take that into your workshop. So here's how

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<v Speaker 1>an m RNA vaccine works. The scientists target the spikes

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<v Speaker 1>on the coronavirus, which are actually proteins that enable it

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<v Speaker 1>to latch onto healthy cells. And by the way, it's

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<v Speaker 1>called the coronavirus because these spiky protrusions look like coronas

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<v Speaker 1>something that suggests a halo or a crown. The synthetic

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<v Speaker 1>mRNA in the new vaccine carries the code for the

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<v Speaker 1>spiky protein. When introduced into a healthy body, the m

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<v Speaker 1>RNA takes this code and joins up with the protein

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<v Speaker 1>making ribosomes in cells to manufacture the spiky proteins that

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<v Speaker 1>prompts our bodies to produce antibodies to destroy these strange proteins,

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<v Speaker 1>including when they come attached to a real invading coronavirus.

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<v Speaker 1>Without their spikes, the coronavirus can't live and reproduce, so

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<v Speaker 1>end of story. The advantages of the m r and

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<v Speaker 1>A method are many. On the business end, it's cheaper

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<v Speaker 1>to produce a bunch of m RNA strands than it

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<v Speaker 1>is to grow a bunch of viruses, then kill them off,

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<v Speaker 1>and then build a vaccine around them without all those

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<v Speaker 1>labor intensive and time meeting steps. It's faster too. On

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<v Speaker 1>the health side, m RNA is probably less dangerous than

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<v Speaker 1>dosing people with even a manageable amount of even a

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<v Speaker 1>weekend or dead virus, and best of all, according to

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<v Speaker 1>latest data, it may be more effective. The disadvantages, well,

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<v Speaker 1>there are some. The biggest is that it's never been

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<v Speaker 1>done before. mRNA technology, although it's been around for at

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<v Speaker 1>least a couple of decades, has never been used in

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<v Speaker 1>a vaccine, so it's got a lot of proving to do.

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<v Speaker 1>Late stage testing on Maderna's and Viser's work as of

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<v Speaker 1>early December twenty has been exceedingly promising. Both the fiser

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<v Speaker 1>and Maderna m RNA vaccines have proved better than nine effective. Maderna,

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<v Speaker 1>which enrolled thirty thousand adult participants in the United States,

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<v Speaker 1>reported the just eleven of the hundred ninety six total

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<v Speaker 1>COVID nineteen cases in their study occurred among the vaccinated.

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<v Speaker 1>The other five infections occurred in the placebo group. That

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<v Speaker 1>equates to a ninety four point one percent efficacy rate.

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<v Speaker 1>And Furthermore, none of the infected patients who had received

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<v Speaker 1>the vaccine developed severe symptoms. Viser saw similar results in

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<v Speaker 1>its Phase three trial. In the trials, the vaccines also

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<v Speaker 1>seemed to do more than simply ward off COVID nineteen.

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<v Speaker 1>They've shown that they may reduce the rate of infection too,

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<v Speaker 1>keeping those with the virus from spreading it to others

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<v Speaker 1>around them. Both companies are expected to apply for something

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<v Speaker 1>called an IMMER Agency Use Authorization from the US Food

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<v Speaker 1>and Drug Administration. If granted, they'll ramp up production on

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<v Speaker 1>the vaccines, still testing as they go. If everything goes right,

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<v Speaker 1>the general public might have access to these vaccines by

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<v Speaker 1>the middle of but hurdles do remain. Manufacturing must increase

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<v Speaker 1>at levels never before attempted, Shipping and storing these m

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<v Speaker 1>RNA vaccines must be ironed out. The Fiser m RNA

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<v Speaker 1>vaccine requires it to be stored at negative ninety four

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<v Speaker 1>degrees fahrenheit that's negative thirty four celsius and degrades after

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<v Speaker 1>about five days. The temperatures of just above freezing. Maderna's

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<v Speaker 1>supposedly can be stored at thirty six to forty six

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<v Speaker 1>degrees fahrenheit that's two to eight degrees celsius for up

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<v Speaker 1>to thirty days and remain stable at negative four fahrenheit

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<v Speaker 1>or negative twenties celsius for up to six months. Most

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<v Speaker 1>vaccine candidates now in the late stage trials take two

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<v Speaker 1>doses to be effective, so that has to be planned

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<v Speaker 1>for two and determining who was first in line, what

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<v Speaker 1>countries in which people within those countries is still being

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<v Speaker 1>worked out. In the meantime, other companies are deep in

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<v Speaker 1>research and development, using both m RNA and more traditional

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<v Speaker 1>methods to bring vaccines to market. Some fifty four vaccines

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<v Speaker 1>are in clinical trials and humans, according to The New

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<v Speaker 1>York Times, and at least seven are in pre clinical

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<v Speaker 1>trials and animals. Richardson said the m RNA methods now

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<v Speaker 1>that we have the efficacy numbers are now in the lead,

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<v Speaker 1>but there are many different candidates. There will likely be

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<v Speaker 1>multiple vaccines. They're licensed and available to the public. Who

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<v Speaker 1>knows what the landscape will be In a year. We

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<v Speaker 1>may have five or six more to choose from, just

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<v Speaker 1>like flu vaccines, and because you need so much, you

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<v Speaker 1>need multiple manufacturers. The pace has been breathtaking. Faced with

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<v Speaker 1>one of the deadliest outbreaks of disease in many lifetimes,

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<v Speaker 1>the government and private sector have joined forces to come

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<v Speaker 1>up with a possible answer in record time, and what

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<v Speaker 1>we've learned may help us handle the next virus that

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<v Speaker 1>comes along. Richardson explained the speed, the number of vaccine development,

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<v Speaker 1>corollary effects, bioprocessing, knowing how to scale up, the coordination

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<v Speaker 1>with the regulatory bodies like the f d A and

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<v Speaker 1>other organizations around the world. I think those will pay

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<v Speaker 1>benefits for years to come. Today's episode was written by

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<v Speaker 1>John Donovan and produced by Tyler Klang. For more in

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<v Speaker 1>this amounts of other topics, visit house toffworks dot com.

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<v Speaker 1>Brain Stuff is production of iHeart Radio. Or more podcasts

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