Johnson & Johnson (J&J) has asked regulators to authorize their COVID-19 vaccine for emergency use in the U.S. and also will apply to authorize to EU, reportedly by media. (Photo Illustration by Pavlo Gonchar/SOPA Images/LightRocket via Getty Images)
A single-shot COVID-19 vaccine by US drugmaker Johnson and Johnson is likely to be approved for use in the European Union in early March, a French minister said Sunday.
The vaccine was cleared for emergency use in the United States on Saturday, becoming the third available vaccine there.
The single-shot vaccine is highly effective in preventing severe COVID-19, including against newer variants, the Food and Drug Administration (FDA) said before giving it the green light.
French Industry Minister Agnes Pannier-Runacher told France 3 television that the European Medicines Agency (EMA) was also evaluating information transmitted by the US pharmaceuticals company.
An EU approval in early March would allow the vaccine to be rolled out in late March or early April, she said, adding this was “good news” because it offers protection with a single shot in contrast to other vaccines requiring two.
She said it was possible that a booster shot was needed later “but we can’t be sure yet”.
The EU hoped to receive 600 million doses of the vaccine by the end of June, she said.
France has so far vaccinated 1.5 million people, the minister said. By June all 15 million people belonging to the country’s most vulnerable population segments will have been vaccinated, she added, acknowledging however that reaching that target might require a faster vaccine rollout.
In large clinical trials, the J&J vaccine’s efficacy against severe disease was 85.9 percent in the United States, 81.7 percent in South Africa, and 87.6 percent in Brazil.
The J&J shot appears less protective than Pfizer and Moderna’s two-shot regimens, which both have an efficacy of around 95 percent against all forms of COVID-19 from the classic coronavirus strain.
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