EU regulator recommends using J&J’s one-shot vaccine

LONDON (AP) — The European Medicines Agency on Thursday gave the green light to Johnson & Johnson’s one-dose coronavirus vaccine, handing the European Union’s 27 nations a fourth vaccine to try to speed up the bloc’s much-criticised vaccination rollout.

The EU medicines regulator advised that the vaccine be cleared for use in all adults over 18 “after a thorough evaluation” of J&J’s data found the vaccine met the criteria for efficacy, safety and quality.

“With this latest positive opinion, authorities across the European Union will have another option to combat the pandemic and protect the lives and health of their citizens,” said Emer Cooke, EMA’s executive director.

The EMA has already recommended COVID-19 vaccines made by Pfizer-BioNTech, Moderna and AstraZeneca — but all of those vaccines require two doses, several weeks apart. Production delays have also plagued all three vaccine manufacturers.

In its statement Thursday, the EMA said the J&J vaccine was about 67% effective. The most common side effects were pain at the injection site, headache, tiredness, muscle pain and nausea.

The European Commission quickly granted a conditional marketing authorisation to the vaccine.

The U.S. Food and Drug Administration gave an emergency authorisation n to the J&J shot in late February. Health experts hope that having a one-dose vaccine will speed efforts to immunise the world against COVID-19, especially given the recent infection spikes in Europe driven by worrying new variants.

The EU has struggled to quickly roll out shots and immunise its most vulnerable citizens. It ranks far behind countries including Israel, Britain, Chile and the U.S.

J&J said it has committed to providing the EU with its pre-ordered 200 million doses starting in the second quarter.

“The greatest barrier to rolling out the vaccines so far has been the availability of vaccines,” said Dr. Peter English, who previously chaired the British Medical Association’s Public Health Medicine Committee. “This new addition can only add to the quantity of vaccine available in the EU, as well as providing another alternative if there are hitches with the supply or use of other products.”

Europe recorded 1 million new COVID-19 cases last week, an increase of 9% from the previous week and a reversal that ended a six-week decline in new infections. The World Health Organization’s European office blamed that surge partly on virus variants, including one first identified in Britain that is thought to be 50% more transmissible.

J&J is also seeking emergency authorisation of its vaccine in Britain and by the World Health Organization. It has already been approved for use in Bahrain and Canada.

Thomas Mertens, the head of Germany’s independent vaccine advisory panel, said he expected the shot’s use to be recommended in Germany.

However, Mertens wouldn’t rule out that the panel might recommend using the vaccine only for certain groups within the population, as it initially did by limiting the AstraZeneca shot to under 65s - a restriction it later lifted after receiving more data.

J&J has faced production delays in the U.S. and Europe but has recently signed agreements with rival pharmaceuticals who will help make their vaccine. In February, Sanofi Pasteur said it would be able to make about 12 million doses of the J&J vaccine at one of its French production sites once the shot is cleared by the EMA. It is aiming to make 1 billion doses this year.

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