HomeNewsWorldCoronavirus vaccine | WHO scientist Soumya Swaminathan expects regulators to cooperate to fast-track approval

Coronavirus vaccine | WHO scientist Soumya Swaminathan expects regulators to cooperate to fast-track approval

Swaminathan, answering questions on social media platforms, also said testing vaccines for safety and efficacy - usually a years-long process - could be accelerated to just six months in the midst of the pandemic, if data satisfied regulators that they have enough information to issue approvals.

July 24, 2020 / 17:36 IST
WHO scientist says trial suspension a 'wake up call': The World Health Organization's chief scientist Soumya Swaminathan said the agency isn't overly worried about the pause in the clinical trials for a coronavirus vaccine developed by Oxford University and AstraZeneca and that the suspension of trial is a wake-up call to the global community to realize there are ups and downs in research.

WHO scientist says trial suspension a 'wake up call': The World Health Organization's chief scientist Soumya Swaminathan said the agency isn't overly worried about the pause in the clinical trials for a coronavirus vaccine developed by Oxford University and AstraZeneca and that the suspension of trial is a wake-up call to the global community to realize there are ups and downs in research.

WHO chief scientist Soumya Swaminathan on July 24 said that regulators that normally work within their own countries or regions will likely harmonize efforts on potential COVID-19 vaccines to speed up their approvals once they become available.

Swaminathan, answering questions on social media platforms, also said testing vaccines for safety and efficacy - usually a years-long process - could be accelerated to just six months in the midst of the pandemic, if data satisfied regulators that they have enough information to issue approvals.

Still, she said, safety would be paramount.

"Whilst speed is important, it cannot be at the cost of compromising on the safety or the efficacy standards," she said.

"It's not the case that the first vaccine is going to be rushed through into injecting millions of people without having established the fact whether it's really protecting you and whether it's safe enough for use in large populations."

COVID-19 Vaccine

Frequently Asked Questions

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How does a vaccine work?

A vaccine works by mimicking a natural infection. A vaccine not only induces immune response to protect people from any future COVID-19 infection, but also helps quickly build herd immunity to put an end to the pandemic. Herd immunity occurs when a sufficient percentage of a population becomes immune to a disease, making the spread of disease from person to person unlikely. The good news is that SARS-CoV-2 virus has been fairly stable, which increases the viability of a vaccine.

How many types of vaccines are there?

There are broadly four types of vaccine — one, a vaccine based on the whole virus (this could be either inactivated, or an attenuated [weakened] virus vaccine); two, a non-replicating viral vector vaccine that uses a benign virus as vector that carries the antigen of SARS-CoV; three, nucleic-acid vaccines that have genetic material like DNA and RNA of antigens like spike protein given to a person, helping human cells decode genetic material and produce the vaccine; and four, protein subunit vaccine wherein the recombinant proteins of SARS-COV-2 along with an adjuvant (booster) is given as a vaccine.

What does it take to develop a vaccine of this kind?

Vaccine development is a long, complex process. Unlike drugs that are given to people with a diseased, vaccines are given to healthy people and also vulnerable sections such as children, pregnant women and the elderly. So rigorous tests are compulsory. History says that the fastest time it took to develop a vaccine is five years, but it usually takes double or sometimes triple that time.

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There are more than 200 COVID-19 vaccines in development, with two dozen in human trials and a handful now entering late-stage studies in thousands of patients. Swaminathan cited Moderna's experimental mRNA vaccine, another which is a collaboration between Oxford University and AstraZeneca , China's Cansino Biologics candidate, and vaccine development project in Russia.

For regulators to approve a vaccine, developers will have to follow trial participants for months and show that there are fewer infections among people given the vaccine than among those given a placebo or control shot.

"We would like to see as high protection as possible - 80 percent, 90 percent - that would be fantastic," she said.

Swaminathan cautioned that only a small number of potential COVID-19 vaccines are likely to make it through all trial stages and be approved for use.

"We have a very robust pipeline of vaccine candidates, which is excellent, because normally the success rate...is around 10 percent," she said.

Asked if the world could fend off the coronavirus pandemic without a vaccine, Swaminathan said pursuing a so-called herd immunity strategy would be deadly. Some 60 percent of a population needs to be infected with COVID-19 to achieve herd immunity, she said, a level which would see many people dying of the disease.

Follow our full coverage of the coronavirus pandemic here.

Reuters
first published: Jul 24, 2020 04:15 pm

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