Moderna is filing for US and European emergency regulatory approval of its coronavirus vaccine so that it can be recommended for widespread use.

Regulators will look at trial data for the mRNA vaccine and decide if it is safe and effective enough to recommend for rollout.

Clinical studies show the jab is more than 94% effective at protecting people from becoming ill with Covid-19.

Pfizer, which has a similar jab, has already filed for the same US approval.

UK regulators are also reviewing data on the Pfizer vaccine, as well as another type of Covid vaccine from AstraZenca and Oxford University for emergency approval.

Moderna says it hopes to gain UK approval soon, now that it has trial data from 30,000 volunteers – including high-risk groups like the elderly – that suggests it works.

In those studies, 15,000 people received the real vaccine while the other participants got placebo injections. No serious side effects were reported.

During the studies, 185 people in the placebo group fell ill with Covid-19, and some severely so.

In comparison, there were 11 cases in the vaccine group and none were severe.

Full trial data has not been released but will be published in a peer-reviewed journal in due course.