NIH: Halted vaccine study shows ‘no compromises’ on safety

AstraZeneca’s suspension of final testing of its potential COVID-19 vaccine while it investigates a volunteer’s illness shows there will be “no compromises” on safety in developing the shots, the chief of the National Institutes of Health told Congress on Wednesday.

“This ought to be reassuring,” NIH Director Dr. Francis Collins said before a Senate committee. “When we say we are going to focus first on safety and make no compromises, here is Exhibit A of how that is happening in practice.”

Late Tuesday, AstraZeneca announced its final-stage studies are on temporary hold while the company looks into whether a test subject’s illness is a side effect of the shot or a coincidence. The company gave no details on the illness, but Collins said it involved a “spinal problem.”

Behind-the-scenes monitors known as the “data and safety monitoring board” in Britain paused vaccinations while alerting its safety counterparts in the U.S., said Dr. Moncef Slaoui of Operation Warp Speed, the Trump administration’s vaccine development program.

Late last month, AstraZeneca began recruiting 30,000 people in the U.S. for its largest study of the vaccine. It also is testing the vaccine, developed by Oxford University, in thousands of people in Britain and in smaller studies in Brazil and South Africa.

AstraZeneca said the pause in vaccinations covers studies in the U.S. and other countries.

Scientists around the world have been scrambling to develop a vaccine against the coronavirus since the outbreak began. Nearly 900,000 deaths have been reported in the pandemic.

Two other vaccines are in huge, final-stage tests in the United States, one made by Moderna Inc. and the other by Pfizer and Germany’s BioNTech. Those two vaccines work differently than AstraZeneca’s, and the studies already have recruited about two-thirds of the needed volunteers. Three additional experimental vaccines are set to enter huge, late-stage testing later this year.

Earlier-stage studies of AstraZeneca’s vaccine hadn’t revealed any serious side effects.

The company’s announcement comes amid worries that President Donald Trump will pressure the U.S. Food and Drug Administration to approve a vaccine before it’s proven to be safe and effective.

Collins said Wednesday that the decision will be based on science alone and that he will roll up his sleeve to get vaccinated once that happens.

He expressed “cautious optimism” that one of the vaccines being tested will pan out by the end of the year but warned: “Certainly to try to predict whether it happens on a particular week before or after a particular date in early November is well beyond anything that any scientist right now could tell you.”

It’s not uncommon for pauses in research to investigate if an unexpected health complaint is really related to a vaccine or not, he told senators worried about what the AstraZeneca suspension means for that year-end goal.

“The reason we’re investing not in one but six different vaccines is because of the expectation that they won’t all work,” Collins said.

The trial’s suspension came just hours after AstraZeneca and eight other drugmakers issued an unusual pledge, vowing to uphold the highest ethical and scientific standards in developing their vaccines.

The U.S. has invested billions of dollars in efforts to quickly develop multiple vaccines against COVID-19. But public fears that a vaccine is unsafe or ineffective could be disastrous, derailing the effort to vaccinate millions of Americans.


Helpful Coronavirus links

Delaware Division of Health Coronavirus Page
CDC: About the Coronavirus Disease 2019
CDC: What to do if You Are Sick
Johns Hopkins Coronavirus Resource Center
AP News Coronavirus Coverage
Reopening Delaware: Resources for Businesses
Delaware Phase 2 guidance

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