Joe Palca

Updated at 7:00 a.m. ET

More than 100,000 people are taking part in studies to see if one or more COVID-19 vaccine candidates actually work.

Drugmaker AstraZeneca announced Saturday that its COVID-19 vaccine studies have resumed in the United Kingdom, though not yet in the United States. The vaccine trials had been placed on hold around the world earlier in the week after a U.K. participant in one of the studies developed a neurological illness.

Drugmaker AstraZeneca has announced that it is pausing its COVID-19 vaccine trial because of a "potentially unexplained illness" in one of the trial volunteers.

The vaccine was developed by the University of Oxford in partnership with AstraZeneca. It's being studied in thousands of patients in the United States and the United Kingdom. The illness apparently occurred in a U.K. volunteer.

Scientists and engineers in California are building a unique camera for a unique telescope.

The Rubin Observatory telescope going up on Cerro Pachón in north-central Chile can capture an unusually large swath of sky in a single image.

The camera capable of capturing those images has to be enormous. The one researchers are building at the SLAC National Accelerator Laboratory in Menlo Park, Calif., certainly is.

Several vaccines are currently in large-scale studies to see if they can prevent COVID-19, and more are on the way.

The primary goal of a COVID-19 vaccine is to keep people from getting very sick and dying. But there's another goal — to prevent the spread of the disease — and it's not clear most vaccine candidates currently under development can do that.

Some scientists think they can solve that problem by delivering a vaccine as a nasal spray.

Under normal circumstances, it could take years — if not decades — to bring a new vaccine to market. The COVID-19 pandemic has changed all that. In May, the Trump administration launched Operation Warp Speed with the goal of delivering initial doses of a safe and effective vaccine by January 2021 — shortening the development time from years to months.

There are many approaches to making a vaccine against COVID-19. Some use genetic material from the coronavirus, some use synthetic proteins that mimic viral proteins and some use disabled versions of the virus itself.

But before any of these approaches can generate the antibodies to the coronavirus that scientists say are essential to protecting people from getting sick, the immune system has to be primed to make those antibodies.

That's the job of something called an adjuvant.

Nobody is eager to be stuck by a needle twice, so naturally many would view a COVID-19 vaccine that provides disease protection after a single injection as a good thing.

Two new studies released Thursday suggest that might be possible.

The COVID-19 vaccine candidate made by the U.S. biotech company Moderna and developed in collaboration with the National Institutes of Health starts its final phase of testing Monday.

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Approximately 200 COVID-19 vaccines are being actively developed. All vaccines have one main goal: to prepare a person's immune system to fight off an invading organism should the body encounter it.

It turns out, cows may play an important role in responding to the COVID-19 pandemic.

SAB Biotherapeutics is in the business of making what are known as polyclonal antibodies. These are a collection of different antibodies that a body makes to ward off a specific invading organism.

The company has made polyclonal antibodies to treat influenza and MERS. Now it's making them with the aim of treating or even preventing COVID-19. To make them, SAB uses cows.

A low-cost anti-inflammatory drug appears to reduce the risk of death in patients with COVID-19.

The drug is called dexamethasone. It's been used for decades to treat conditions such as arthritis and asthma. Because patients with advanced COVID-19 disease can have severe lung inflammation, scientists wanted to see if dexamethasone could treat that condition.

It was one of the drugs studied in a large clinical trial in the United Kingdom known as RECOVERY, or Randomized Evaluation of COVID-19 Therapy.

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STEVE INSKEEP, HOST:

Turns out that cows may be helpful to us in the pandemic. There's a biotech company in South Dakota using cows to make antibodies for treating human disease. And lately, they've been making antibodies for COVID-19. Here's NPR's Joe Palca.

The U.S. Food and Drug Administration today withdrew a special status known as emergency use authorization for the drugs chloroquine and hydroxychloroquine.

Emergency use authorization is designed to facilitate the availability of drugs needed during public health emergencies. It allows unapproved medical products or unapproved uses of approved medical products to be used in such emergencies.

Right now, there is only one drug shown by rigorous scientific testing to be helpful for treating COVID-19. That drug is the antiviral medication called remdesivir, made by Gilead Sciences. But remdesivir's proven benefits are modest: reducing hospital stays from 15 to 11 days.

Once upon a time, developing a new vaccine was a step-by-step process that went from concept, to design, to tests in humans, to regulatory approval, to manufacturing.

It was a process that could take a decade or more.

But the urgent need for a COVID-19 vaccine has radically changed all that. Now, the hope is the entire process can be completed in a year or less.

Taking hydroxychloroquine after being exposed to someone with COVID-19 does not protect someone from getting the disease.

That's the conclusion of a study published Wednesday involving 821 participants. All had direct exposure to a COVID-19 patient, either because they lived with one, or were a health care provider or first responder.

A vaccine manufacturer is reporting preliminary data suggesting its COVID-19 vaccine is safe, and appears to be eliciting in test subjects the kind of immune response capable of preventing disease.

Moderna, Inc., of Cambridge, Mass., developed the vaccine in collaboration with the National Institute of Allergy and Infectious Diseases. The results reported Monday come from an initial analysis of a Phase I study primarily designed to see if the vaccine is safe.

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Most health experts agree that the need for a vaccine to prevent COVID-19 is clear.

"To return to a semblance of previous normality, the development of SARS-CoV-2 vaccines is an absolute necessity" is how a perspective in Science magazine puts it.

While authorities across the U.S. struggle to make policy without any hard numbers for how many people are actually infected with the coronavirus, Oregon State University has launched a project to change that — at least for one small city.

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The global race for a coronavirus vaccine is on. And around the world, hopes for a vaccine are high.

(SOUNDBITE OF MONTAGE)

Most public health experts agree that widespread testing will be needed to bring the COVID-19 pandemic under control. But for now, most coronavirus tests require specialized laboratories and high-tech equipment to process them.

Researchers at the McGovern Institute for Brain Research at MIT hope to change that with a simpler test that could conceivably be done in someone's kitchen.

The pharmaceutical giant Pfizer has begun testing a new coronavirus vaccine in the United States. The initial trial will involve 360 volunteers, and the first subjects have already received injections.

The vaccine was developed in a partnership between Pfizer and the German biotech company BioNTech. In addition to the U.S. trials, there will be some 200 patients enrolled in trials in Germany.

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A panel of experts convened by the National Institute of Allergy and Infectious Diseases recommends against doctors using a combination of hydroxychloroquine and azithromycin for the treatment of COVID-19 patients because of potential toxicities.

"The combination of hydroxychloroquine and azithromycin was associated with QTc prolongation in patients with COVID-19," the panel said.

QTc prolongation increases the risk of sudden cardiac death.

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