British regulator 1st to authorize Moderna's updated COVID booster

British drug regulators have become the first in the world to authorize an updated version of Moderna's coronavirus vaccine that aims to protect against the original virus and the Omicron variant.

In a statement on Monday, the Medicines and Healthcare Regulatory Agency said it had given the green light to Moderna's combination "bivalent" vaccine, which will be used as an adult booster shot.

Each dose of the booster shot will target both the original COVID-19 virus that was first detected in 2020 and the Omicron BA.1 variant that was first picked up in November. British regulators said the side effects were similar to those seen for Moderna's original booster shot and were typically "mild and self-resolving."

"What this [combination]vaccine gives us is a sharpened tool in our armoury to help protect us against this disease as the virus continues to evolve," said Dr June Raine, the head of Britain's health-care and medicines regulator.

Such an approach is used with flu shots, which are adjusted each year depending on the variants that are circulating and can protect against four influenza strains.

Stephane Bancel, Moderna'schief executive, said in a statement that it was the first regulatory authorization for a vaccine aiming to fight the Omicron variant, predicting the booster would have an "important role" to play in protecting people against COVID-19 in the winter.

Fall vaccines

Britain's health officials have not yet decided whether the tweaked vaccine will be used in its fall strategy. In July, the government said everyone 50 and over would be able to get a COVID booster in the fall.

On Friday, Germany's health minister said the European Medicines Agency might clear tweaked COVID-19 boosters next month.

In June, Canada'sNational Advisory Committee on Immunization (NACI) recommended that only those with an increased risk of severe illness from COVID-19 should be offered a booster shot this fall in anticipation of a future wave, regardless of how many boosters they've previously received.

That recommendation applies to everyone age 65 and older. NACI said people age 12 to 64 "may be offered" additional doses in the fall.

Many provinces and territories have already moved to offer four doses this summer of the original vaccines. NACIsaid it will provide recommendations on the type ofboosterto be given whenevidence about multivalent vaccinesbecomes available.

In June, the U.S. Food and Drug Administration told vaccine makers that any booster shots tweaked for the fall would have to include protection against the newest Omicron variants, meaning BA.4 and BA.5, not the BA.1 subvariant included in Moderna's latest shot.

Last month, the FDA said it was no longer considering authorizing a second COVID-19 booster for all adults but would instead focus on revamped vaccines for the autumn that target the newest viral subvariants.

Both Moderna and Pfizer are currently brewing updated versions of their vaccine to include BA.5 in addition to the original COVID-19 virus.

According to the World Health Organization, the latest global surge of COVID-19 has been driven by Omicron subvariant BA.5, which is responsible for about 70 per centof the virus samples shared with the world's largest public virus database.

The subvariant BA.5 is even more infectious than the original version of Omicron and has some genetic differences that earlier vaccines might not address.

Scientists have warned that the continued genetic evolution of COVID-19 means drugmakers will likely be one step behind the virus in their efforts to tailor their vaccines.

"The virus is unlikely to stand still and Omicron-targeted immunitymight push the virus down other evolutionary paths," warned Jonathan Ball, a professor of virology at Britain's University of Nottingham. Still, he said the new Moderna vaccine would likely still be protective.

"Unless there is a major shift in the virus, immunity will continue to protect the vast majority from serious disease caused by emerging variants," he said in a statement.