We’ll likely have a 3rd COVID vaccine soon; J&J vaccine clears last hurdle

Enlarge / A sign at the Johnson & Johnson campus on August 26, 2019 in Irvine, California. (credit: Getty | Mario Tama)

After a day-long meeting Friday, an advisory panel for the US Food and Drug Administration voted 22 to 0 to recommend issuing an Emergency Use Authorization for Johnson & Johnson’s single-shot, refrigerator-stable COVID-19 vaccine.

If the FDA accepts the panel’s recommendation and grants the EUA—which it likely will—the country will have a third COVID-19 vaccine authorized for use. Earlier this week, FDA scientists released their review of the vaccine, endorsing authorization. Today’s panel, the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) went through the data further.

“It’s a relatively easy call,” Eric Rubin, a Harvard researcher and voting member of the VRBPAC said after the vote. “[The vaccine] clearly gets way over the bar and it’s nice to have a single-dose vaccine… the demand is so large [for vaccines], it clearly has a place.”

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