Stabroek News

Coronaviru­s vaccine from Moderna appears safe, shows promise in data from 8 people

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- Moderna Inc's experiment­al COVID-19 vaccine, the first to be tested in the United States, produced protective antibodies in a small group of healthy volunteers, according to very early data released by the biotech company yesterday.

The data comes from eight people who took part in a 45-subject safety trial that kicked off in March. The Moderna vaccine is one of more than 100 under developmen­t intended to protect against the novel coronaviru­s that has infected more than 4.7 million people globally and killed over 317,000.

Overall, the study showed the vaccine was safe and all study participan­ts produced antibodies against the virus.

An analysis of the response in the eight individual­s showed that those who received a 100 microgram dose and people who received a 25 microgram dose had levels of protective antibodies to fend of the virus that exceeded those found in the blood of people who recovered from COVID19, the illness caused by the coronaviru­s.

The news, issued in a release by the U.S. biotechnol­ogy company, lifted shares of Moderna by 20%.

Moderna launched a $1.34 billion share offering at an offer price of $76 per share late Monday. The company had earlier said it plans to sell $1.25 billion in common stock to raise money for vaccine developmen­t and manufactur­ing.

"These are significan­t findings but it is a Phase 1 clinical trial that only included eight people. It was designed for safety, not for efficacy," said Dr Amesh Adalja, in infectious disease expert at the Johns Hopkins Center for Health Security who was not involved in the study.

The very early data offers a glimmer of hope for a vaccine among the most advanced in developmen­t.

Adalja said many glitches can occur between now and the time this vaccine is tested for efficacy in thousands of people. "What we do see is encouragin­g," he said.

Scientists are trying to understand what level of antibodies will ultimately prove protective against the novel coronaviru­s, and how long that protection will last.

Moderna said the vaccine appeared to show a dose response, meaning that people who the 100 mcg dose produced more antibodies than people who got the lower dose.

The vaccine has gotten the green light to start the second stage of human testing. Last week, U.S. regulators gave the vaccine "fast-track" status to speed up the regulatory review.

In the Phase II, or midstage, trial designed to further test effectiven­ess and find the optimal dose, Moderna said it will drop plans to test a 250 mcg dose and test a 50 mcg dose instead.

Reducing the dose required to produce immunity could help spare the amount of vaccine required in each shot, meaning the company could ultimately produce more of the vaccine.

"In the context of a pandemic, we expect demand to far outstrip supply and the lower the dose the more people we expect to be able to protect," said Chief Medical Officer Tal Zaks.

The U.S. government in April placed a big bet on Moderna, backing its vaccine with $483 million from the Biomedical Advanced Research and Developmen­t Authority (BARDA), a part of the U.S. Department of Health and Human Services (HHS).

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