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EU regulator meets to evaluate J&J's one-shot COVID-19 shot

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AMSTERDAM – The European Medicines Agency was meeting Thursday to discuss whether Johnson & Johnson’s one-dose coronavirus vaccine should be authorized, a move that would give the European Union a fourth licensed vaccine to try to curb the pandemic amid a stalled inoculation drive.

The Amsterdam-based EU regulator is scheduled to convene its expert committee in the morning to assess the J&J vaccine data.

A decision on whether the agency recommends that the shot be licensed across the 27-nation bloc could come in the afternoon.

The EMA has already approved COVID-19 vaccines made by Pfizer-BioNTech, Moderna and AstraZeneca. The U.S. Food and Drug Administration approved the J&J shot in late February.

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