Here’s Exactly Where We Are with Vaccines and Treatments for COVID-19

Scientists around the world are working on potential treatments and vaccines for the new coronavirus disease known as COVID-19.
  • Several companies are working on antiviral drugs, some of which are already in use against other illnesses, to treat people who already have COVID-19.
  • Other companies are working on vaccines that could be used as a preventive measure against the disease.

With confirmed COVID-19 cases worldwide surpassing 2.7 million and continuing to grow, scientists are pushing forward with efforts to develop vaccines and treatments to slow the pandemic and lessen the disease’s damage.

Some of the earliest treatments will likely be drugs that are already approved for other conditions, or have been tested on other viruses.

“People are looking into whether existing antivirals might work or whether new drugs could be developed to try to tackle the virus,” Dr. Bruce Y. Lee, a professor at the CUNY Graduate School of Public Health & Health Policy, said in March.

Antiviral drugs were a topic of a March 18 White House briefing on the COVID-19 outbreak.

President Trump said he was pushing the Food and Drug Administration (FDA) to eliminate barriers to get treatments to people with COVID-19.

A few days later, the FDA issued an emergency use declaration for the anti-malaria drugs hydroxychloroquine and chloroquine.

About 30 million doses of hydroxychloroquine and 1 million doses of chloroquine were donated to the nation’s Strategic National Stockpile.

The medications can be distributed and prescribed by doctors for adults and teens hospitalized with COVID-19 when a clinical trial isn’t available.

However, the following week, officials from the European Union said there’s no evidence that hydroxychloroquine was effective in treating COVID-19.

The use of these medications was also questioned in an opinion pieceTrusted Source in the journal Annals of Internal Medicine.

The authors raised questions about recent studies done on the anti-malaria drugs and whether there’s been a “rush to judgement” on getting them through the approval pipeline.

In late April, the FDA issued a warningTrusted Source against the use of both hydroxychloroquine and chloroquine outside of medical facilities. The agency stated there were “serious and potentially life-threatening heart rhythm problems” connected with the drugs.

In addition, the Journal of the American Medical Association (JAMA) reportedTrusted Source on the same day that a clinical study on chloroquine had been ended because some participants had developed irregular heartbeats, and nearly two dozen had died after taking daily doses of the medication.

Indeed, don’t expect these two drugs or other medications to be available at your pharmacy anytime soon.

FDA officials have stated it could still be a year before any drugs are available to the general public for COVID-19 treatment, because the agency needs to make sure the medications are safe for this particular use and what the proper dosage should be.

Indeed, there’s only so much that vaccine and drug development can be sped up, even with improvements in genetic sequencing and other technologies.

“Even though technological advances allow us to do certain things more quickly,” Lee told Healthline, “we still have to rely on social distancing, contact tracing, self-isolation, and other measures.”

Here’s a rundown of the latest COVID-19 vaccine and drug developments.

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Treatment

Several companies are developing or testing antivirals against SARS-CoV-2, the virus that causes COVID-19.

Antivirals target the virus in people who already have an infection. They work in different ways, sometimes preventing the virus from replicating, other times blocking it from infecting cells.

Lee says antivirals work better if you administer them sooner, “before the virus has a chance to multiply significantly.”

And also before the virus has caused significant damage to the body, such as to the lungs or other tissues.

Dr. Robert Amler, dean of the School of Health Sciences and Practice at New York Medical College and a former chief medical officer at the Centers for Disease Control and Prevention (CDC) Agency for Toxic Substances and Disease Registry (ATSDR), says both antivirals and vaccines will be valuable tools in combating COVID-19.

However, he told Healthline that “antivirals are likely to be developed and approved before a vaccine, which typically takes longer.”

Drug development is sometimes described as a pipeline with compounds moving from early laboratory development to laboratory and animal testing to clinical trials in people.

It can take a decade or more for a new compound to go from initial discovery to the marketplace. Many compounds never even make it that far.

That’s why antivirals being eyed as treatments for COVID-19 are drugs that already exist.

Antivirals

Remdesivir

Developed a decade ago, this drug failed in clinical trials against Ebola in 2014. But it was found to be generally safe in people. Research with MERS showed that the drug blocked the virus from replicating.

In April, it was being tested in five COVID-19 clinical trialsTrusted Source. The first results weren’t encouraging. In mid-April, the Department of Veterans Affairs reported that the drug produced no noticeable benefits in patients at veterans’ hospitals. They also noted that the death rate among this group was higher than among patients who were given standard medical care.

In late April, Gilead Sciences announced one of its trials had been “terminated” due to low enrollment. Gilead officials said the results of that trial had been “inconclusive” when it was ended.

A few days later, they company announced that another trial of remdesivir overseen by the National Institute of Allergy and Infectious Diseases had “met its primary endpoint.”

Dr. Anthony FauciTrusted Source, the institute’s director, told reporters the trial produced a “clear cut positive effect in diminishing time to recover.” He said people taking the drug recovered from COVID-19 in 11 days compared to 15 days to people who didn’t take remdesivir. More details will be released after the trial is peer reviewed and published.

At the same time, another studyTrusted Source published in The Lancet, reported that participants in a clinical trial who took remdesivir showed no benefits compared to people who took a placebo.

Despite the conflicting results, the FDA will reportedly issue an emergency approval for remdesivir in the near future.

Kaletra

This is a combination of two drugs that work against HIV. Clinical trials are planned to see whether it works against SARS-CoV-2.

Favipiravir

This drug is approved in some countries outside the United States to treat influenza. Some reports from China suggest it may work as a treatment for COVID-19. These results, though, haven’t been published yet.

Arbidol

This antiviral was tested along with the drug lopinavir/ritonavir as a treatment for COVID-19. Researchers reported in mid-April that the two drugs didn’t improve the clinical outcomes for people hospitalized with mild to moderate cases of COVID-19.

Other drugs

Scientists are also looking at other ways to target the virus or treat the complications of COVID-19, such as:

Monoclonal antibodies

These drugs trigger the immune system to attack the virus. Vir Biotechnology has isolated antibodies from patients who survived SARS.

The company is working with Chinese firm WuXi Biologics to test them as a treatment for COVID-19. AbCellera has isolated 500 unique antibodies from a person who recovered from COVID-19 and is set to start testing them.

Blood plasma transfers

Along the same lines, the FDA has announcedTrusted Source a process for medical facilities to conduct trials on an experimental treatment that uses blood plasma from people who have recovered from COVID-19.

The theory is that the plasma contains antibodies that will attack this particular coronavirus. In late March, the New York Blood Center began collecting plasma from people who have recovered from COVID-19.

Stem cells

Athersys Inc. released preliminary data last year showing that its stem cell treatment could potentially benefit people with acute respiratory distress syndrome (ARDS).

This condition occurs in some people with severe COVID-19. MesoblastTrusted Source tested its stem cell product in a small group of people with COVID-19 with positive results.

Immune suppressants

In some people with COVID-19, the immune system goes into overdrive, releasing large amounts of small proteins called cytokines. Scientists think this “cytokine storm” may be the reason certain people develop ARDS and need to be put on a ventilator.

Several immune suppressants are being tested in clinical trials to see whether the drugs can quell the cytokine storm and reduce the severity of ARDS.

These include baricitinib, a drug for rheumatoid arthritis; CM4620-IE, a drug for pancreatic cancer; and IL-6 inhibitors. The FDA has also approved a device that filters cytokinesTrusted Source out of the blood of patients.

Next steps

While a lot of the focus is on developing new treatments for COVID-19, improvements in how doctors care for patients using existing technology are also crucial.

“The things that we have to worry about with the novel coronavirus is that it can cause pneumonia and acute respiratory distress syndrome,” Lee said. “There are ways of treating those things that can reduce the effects, so doctors are trying to use those as well.”

No company has offered a timeline for when its drug might be used more widely to treat COVID-19. This isn’t an easy thing to estimate.

After laboratory and animal testing, drugs have to pass through several clinical trial stagesTrusted Source before they can be approved for widespread use in people.

It’s also difficult to speed things up, because scientists have to enroll enough people in each stage to have useful results. They also have to wait long enough to see whether there are harmful side effects of the drug.

However, drugs can sometimes be given to people outside a clinical trial through the FDA’s “compassionate useTrusted Source” program. For this to happen, people must have an “immediately life-threatening condition or serious disease or condition.”

Doctors at the University of California, Davis were able to secure this type of approval for a woman with severe COVID-19 to receive remdesivir. They report she’s now doing well.

Many will take this as a sign that the drug works. But because the drug was given outside of a clinical trial to just one person, it’s not possible to know for certain. Also, other people may not have the same response to the drug.