Moderna coronavirus vaccine gets US authorisation, second in 8 days

Gulf Today Report

The United States Food and Drug Administration approved Moderna Inc's coronavirus vaccine for emergency use on Friday amid a staggering COVID-19 death toll of over 307,000 lives lost.

Moderna Inc’s vaccine became the second to receive emergency use authorisation (EUA) from the US Food and Drug Administration, paving the way for millions of doses of a second jab to be shipped across the hardest-hit country in the world.

The latest breakthrough came as many governments clamped down on socialising over Christmas and New Year, which is expected to fuel a jump in virus deaths in early 2021.

The FDA announced the authorisation a day after the agency’s panel of outside experts endorsed its use and a week after the FDA authorised a vaccine from Pfizer Inc and German partner BioNTech SE.

A patient arrives in an ambulance due to coronavirus concerns in New York. File/AP

The vaccine from Pfizer and BioNTech, based on similar technology, has been put into the arms of thousands of US healthcare workers this week in a massive nationwide rollout. Moderna injections are expected to begin in the coming days for adults 18 years old and up.

“With the availability of two vaccines now for the prevention of COVID-19, the FDA has taken another crucial step in the fight against this global pandemic that is causing vast numbers of hospitalisations and deaths in the United States each day,” FDA Commissioner Stephen M. Hahn, M D, said in a statement.

The speed of vaccine development is a stunning scientific success, although there is some hesitancy among the public.

“It is my hope that all Americans will protect themselves by getting vaccinated when the vaccine becomes available to them. That is how our country will begin to heal and move forward,” top US infectious disease scientist Anthony Fauci said in a statement.

Older people in long-term health facilities are expected to get vaccines next, with a US Centers for Disease Control and Prevention expert panel on Sunday set to recommend what groups follow, as industries compete to have their workers given precedence.

Moderna said it intended to apply for full US licence in 2021.

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The FDA decision marks the first regulatory authorisation in the world for Moderna’s vaccine and validation of its messenger RNA technology, shown to be nearly 95% effective with no serious safety concerns. It came less than a year after the first COVID-19 case was identified in the United States.

The vaccine, developed in partnership with the National Institutes of Health, had relatively minor side effects including pain around the injection site and swelling.

Emergency Medical Technician members assist a woman who was having difficulty breathing in New York. Reuters

The biotech company has worked with the US government to prepare for the distribution of 5.9 million shots as early as this weekend.

Moderna’s shot is expected to be used in harder-to-reach locations, such as rural hospitals. The vaccine needs to be stored and shipped frozen, but does not require the ultra-cold temperatures of the Pfizer/BioNTech shot.

Once thawed, the Moderna vaccine can be kept at typical refrigerator temperatures. It is administered in two shots 28 days apart.

Between the two vaccines, the United States is expecting 40 million doses before year-end, enough to eventually vaccinate 20 million people, as both require two shots.

US President Donald Trump on Twitter hailed the authorisation. “Congratulations, the Moderna vaccine is now available!” he wrote. The vaccine must be transported to hospitals and other centres before injections begin.

Moderna said it would deliver approximately 20 million doses to the US government this year and expected to have between 100 million and 125 million globally in the first quarter of next year, with 85-100 million of those for the United States.

The firm has deals with the US government to provide a total of 200 million doses by the end of June 2021. Other vaccines still are in testing, including a one-shot injection from Johnson & Johnson, and a two-shot course from AstraZeneca and Oxford University.