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A subject receives a shot in the first-stage safety study clinical trial of Moderna’s potential vaccine in Seattle in March. Photo: AP

Moderna coronavirus vaccine safe, induces immune response, early results show

  • No serious side effects among volunteers tested, but more than half reported mild or moderate reactions such as fatigue, headache, chills or muscle aches
  • US company was first to start human testing of vaccine candidate on March 16. It will start phase 3 trials with 30,000 volunteers on July 27
Moderna Inc’s experimental vaccine for Covid-19 was shown to be safe and provoked immune responses in all 45 healthy volunteers in an ongoing early-stage study, US researchers reported on Tuesday.

No study volunteers experienced a serious side effect, but more than half reported mild or moderate reactions such as fatigue, headache, chills, muscle aches or pain at the injection site.

These were more likely to occur after the second dose and in people who got the highest dose, the team reported in the New England Journal of Medicine.

Moderna shares jumped more than 15 per cent in after-hours trading on Tuesday.

A sign marks the headquarters of Moderna Inc in Cambridge, Massachusetts. Photo: Reuters

Anthony Fauci, director of the US National Institute of Allergy and Infectious Diseases, whose researchers developed Moderna’s vaccine candidate, called the results “good news”, noting that the study found no serious adverse events and the vaccine produced “reasonably high” levels of virus-killing or neutralising antibodies.

“If your vaccine can induce a response comparable with natural infection, that’s a winner,” Fauci said. “That’s why we’re very pleased by the results.”

Moderna was the first to start human testing of a vaccine for the novel coronavirus on March 16, some 66 days after the genetic sequence of the virus was released.

Experts say a vaccine is needed to put an end to the pandemic that has sickened millions and caused more than 575,000 deaths worldwide.

“The world urgently needs vaccines to protect against Covid-19,” said Dr Lisa Jackson of Kaiser Permanente Washington Health Research Institute in Seattle and lead author of the study.

The US federal government is supporting Moderna’s vaccine with nearly half a billion dollars and has chosen it as one of the first to enter large-scale human trials. A successful vaccine could be a turning point for Cambridge, Massachusetts-based Moderna, which has never had a licensed product.

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Moderna’s shot, mRNA-1273, uses ribonucleic acid (RNA) – a chemical messenger that contains instructions for making proteins. When injected into people, the vaccine instructs cells to make proteins that mimic the outer surface of the coronavirus, which the body recognises as a foreign invader, and mounts an immune response against.

The results released on Tuesday involved three doses of the vaccine, tested in groups of 15 volunteers aged 18-55 who got two shots, 28 days apart. The groups tested 25, 100 or 250 micrograms of the vaccine.

The team reported that individuals who got two doses of the vaccine had high levels of virus-killing neutralising antibodies that exceeded the average levels seen in people who had recovered from Covid-19.

Adverse events after the second dose occurred in seven of the 13 volunteers who got the 25-microgram dose, all 15 participants who received the 100 microgram dose and all 14 who got the 250 microgram dose. In the highest-dose group, three patients had severe reactions such as fever, chills, headache or nausea. One of these had a fever of 39.6 degrees Celsius (103.28 Fahrenheit).

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“We didn’t see any events that are characterised as serious adverse events,” Jackson said, referring to reactions that require hospitalisation or result in death.

In June, Moderna said it selected the 100-microgram dose for its late-stage study to minimise adverse reactions.

At that dose, Moderna said the company is on track to deliver about 500 million doses per year, and possibly up to 1 billion doses per year, starting in 2021, from the company’s internal US manufacturing site and strategic collaboration with Swiss drug maker Lonza.

“It’s a good first step,” said Dr William Schaffner, a vaccine expert at Vanderbilt University Medical Centre who was not involved in the study.

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“There’s nothing here that would inhibit one from going ahead to the Phase 2/Phase 3 trials,” he said. “A little fatigue and headache and myalgia [muscle pain] and pain at the injection site is a small price to pay for protection against Covid-19.”

In April, Moderna expanded the Phase 1 trial to include adults over 55, who are more at risk of serious disease, with the aim of enrolling 120 volunteers. Moderna said it will follow study volunteers for a year after the second shot, to look for side effects and check how long immunity lasts.

Moderna started its phase 2 trial in May and expects to start a phase 3 trial on July 27. Phase 1 trials aim to ensure a treatment is safe and help determine an effective dose. Phase 2 trials test a treatment in a larger group and get an early read on effectiveness. Phase 3 trials are conducted in a large group of individuals to confirm efficacy and identify rare side effects. Moderna’s Phase 3 trial will be conducted in 30,000 volunteers.

Meanwhile, Indian pharmaceutical company Zydus said it had started human studies for its potential Covid-19 vaccine, as infections continue to surge in the world’s third worst-hit nation. And life sciences company IQVIA Holdings Inc said it would collaborate with AstraZeneca Plc to speed up clinical studies of the British drugmaker’s potential Covid-19 vaccine in the US.

This article appeared in the South China Morning Post print edition as: Moderna vaccine safe and induces immune response, early results show
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