“Typically, one or two companies are working on a vaccine to prevent [infection by] a particular bacteria or virus,” says Dr. Paul Offit, director of the Vaccine Education Center at the Children’s Hospital of Philadelphia.
But in this case, dozens of companies are working on options to prevent Covid-19. They’re trying every strategy that’s worked in developing vaccines in the past. In some instances, they’re creating completely new approaches. And nations are investing billions of dollars in their work.
“When you have this level of interest and resources and expertise and money to make a vaccine, there’s every reason that we can make it more quickly than usual,” Offit says.
In fact, researchers have already started human testing for several potential coronavirus vaccines. Such tests show whether a vaccine is effective in preventing people from contracting the virus. They also reveal possible side effects and help determine how large a dose will be needed to create an immune response. In August, Russian President Vladimir Putin announced that his country had approved a vaccine for use in Russia. But the nation had done so without first finishing testing to be sure of its safety. It’s an approach that many of the world’s scientists denounced as too risky.
In the U.S., a vaccine has to be successful in several rounds of human testing before it’s advanced. At that point, it goes to the Food and Drug Administration (FDA) for a safety review.
That process can take a year. But because of Covid-19’s high death toll, President Trump and some U.S. lawmakers are urging scientists and the FDA to speed up the process. And they want things to move quicker without compromising safety. Some companies are doing so by running multiple rounds of human testing at the same time. Under normal conditions, they would wait to see whether a vaccine succeeds in one round before moving on to the next.
The U.S. government is also starting to manufacture vaccines that appear the most promising before their final rounds of testing are finished. That way, doses will be ready if they gain approval.