A second coronavirus vaccine, made by Moderna, has gotten a key endorsement from an advisory committee to the FDA. The regulatory agency will now decide whether it will be authorized.

Now the FDA will decide whether to authorize the COVID-19 vaccine
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An independent committee of experts recommended that the Food and Drug Administration authorize the Moderna COVID-19 vaccine for people 18 and older. This is the second COVID-19 vaccine to go before the committee the first, made by Pfizer and BioNTech, was authorized last week. The agency is expected to issue an authorization for Modernas vaccine within a day or two.
This is a really opportune time for us to move science forward, said Hayley Gans, a committee member and professor of pediatrics at Stanford University Medical Center, during the committees deliberations. The evidence available for benefits of the vaccine outweighs any issues, she said. That really supports us being able to, with the pandemic in the background, really move forward, and finally provide a safe and effective way to get to herd immunity.
The FDAs review of the vaccine ahead of the meeting confirmed that its safe and 94 percent effective at preventing symptomatic COVID-19, all but guaranteeing a vote of confidence. The Vaccines and Related Biological Products Advisory Committee (VRBPAC), which met to discuss the data, spent the day discussing the additional questions remaining around the vaccine, and how Moderna should handle vaccinations in the placebo group of their clinical trial.
Moderna said during its presentation that the company plans to offer vaccines to people in the placebo arm quickly. Pfizer and BioNTech, on the other hand, plan to wait for participants in the placebo group to become eligible under their vaccine prioritization plans before telling them of their placebo status. Moderna would vaccinate this group with doses set aside for the clinical trial, which the company argues means study participants arent cutting in line.
Telling the placebo group that they did, in fact, receive a placebo limits the ability to continue to study the vaccine in a blinded clinical trial which worries the VRBPAC, which would want to collect data for as long as possible. The pharmaceutical companies, though, both said they think they have a responsibility to offer vaccine to the placebo group.
The committee also pointed to a handful of issues the clinical trials still havent addressed. Moderna still doesnt know, for example, if the vaccine can protect against asymptomatic cases of COVID-19 stopping infection with the coronavirus entirely or if it just prevents symptoms. Early data from Moderna hints that it could block asymptomatic infection. Trial participants who didnt have symptoms were tested for the coronavirus between their first and second dose. People who took the vaccine were less likely to test positive than people in the placebo group. More answers on that question are coming in January, Moderna said.
Moderna is still analyzing data collected after it submitted the vaccine for authorization. There were 450 more cases of disease reported in the trial after that submission, and that will add to the understanding of the vaccines efficacy.
As this vaccine and the Pfizer and BioNTech vaccine are distributed throughout the country, the pharmaceutical companies and federal agencies will track how well they work and how safe they are in the real world. Already, regulators are finding effects that werent seen in clinical trials a handful of allergic reactions and cases of anaphylaxis were reported in the US and United Kingdom in people vaccinated with the Pfizer and BioNTech vaccine, for example. The FDA is investigating the US incidents.
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