BRUSSELS – Vaccines specially adapted for the new Omicron coronavirus variant could be approved in three to four months if needed, the head of the European Union’s (EU) drug regulator said yesterday.
The decision on whether new shots are required would, however, have to be made by other bodies, European Medicines Agency (EMA) executive director Emer Cooke said.
“Were there a need to change the existing vaccines, we could be in a position to have those approved within three to four months,” Cooke told a European Parliament committee.
“That’s from the start of the time when they would start to change.”
Her comments come after the head of United States vaccine maker Moderna was quoted as saying that existing jabs will struggle against the heavily mutated Omicron.
Moderna has already said it is working on an Omicron-specific vaccine, as is US rival Pfizer.
Cooke said EU regulators “don’t know” yet whether the current vaccines remain effective against Omicron – which she said would take about two weeks to find out – or whether new ones are needed.
“A decision needs to be made first whether that’s necessary, and that’s not a decision for EMA,” Cooke said.
The agency has so far approved four vaccines for use for adults in the EU – Pfizer-BioNTech, Moderna, AstraZeneca, and Johnson & Johnson.
A decision on a fifth by US firm Novavax is expected “within a matter of weeks”, Cooke said. – AFP, December 1, 2021
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