The European regulator evaluates the effectiveness of a booster with the anti-Covid Johnson & Johnson vaccine

November 22, 2021


The EMA is currently evaluating the efficacy of a Johnson & Johnson single-dose Covid vaccine booster.

The European Medicines Agency (EMA) is evaluating a request from the Johnson & Johnson laboratory to allow the injection of a booster dose with the vaccine it has designed against Covid-19 to people aged at least 18 years in the EU.

If the EMA gives the green light, it will be the third vaccine, after those from Pfizer / BioNTech and Moderna, that can be used in the EU as a booster in adults. It will then be administered at least two months after the administration of the single dose of Johnson & Johnson Janssen. A result is “expected in the coming weeks,” the European regulator said.

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The data analyzed by the EMA will include the results of more than 14,000 adults who received a second dose of the Janssen Covid-19 vaccine or a placebo, the agency said. Remember that the EMA has approved the use of four covid vaccines in total: those from Pfizer / BioNTech and Moderna, which are based on messenger RNA technology, and those from AstraZeneca and Johnson & Johnson, which are based on vector technology. virus.

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