FDA panel endorses booster shot for J&J COVID-19 vaccine
The HinduU.S. health advisors endorsed a booster of Johnson & Johnson’s COVID-19 vaccine on Friday, citing concern that Americans who got the single-dose shot aren’t as protected as those given two-dose brands. Unable to settle the best timing, the FDA’s advisory panel voted unanimously that the booster should be offered at least two months after people got their earlier shot. “It would be hard to recommend this as a single-dose vaccine at this point.” The FDA isn’t bound by the recommendation as it makes a final decision – and adding to the debate’s complexity, new research also suggests that J&J recipients might have a stronger immune response if their booster dose is from a competing brand. But J&J’s vaccine has consistently shown lower effectiveness levels across a series of studies – and the FDA panel ultimately settled on another shot for any recipient 18 or older at least two months after their first vaccination. “And that is a finding of concern particularly because that’s been seen in minority communities potentially and others.” As for its booster, J&J presented results from a large study that found giving a second dose just two months after the first bumped protection against symptomatic COVID-19 to 94% from 70% in U.S. recipients.
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