JnJ, Moderna COVID vaccine third dose efficacy to be evaluated by USFDA this week
Washington: The US Food and Drug Administration is expected to evaluate the efficacy of Moderna and Johnson & Johnson's third dose of Covid vaccines this week.
The FDA's Vaccines and Related Biological Products Advisory Committee will meet on Thursday and Friday, CNBC reported.
Earlier this month, the US regulators authorised Covid booster shots of Pfizer and BioNTech's vaccine to a wide array of Americans, including the elderly, adults with underlying medical conditions and those who work or live in high-risk settings like health and grocery workers.
More than 7 million Americans have received a booster dose in the US as of Saturday, according to the latest data available from the CDC.
"Even with delta, the current vaccines are holding up quite well as far as hospitalisation and severe disease are concerned," said Norman Baylor, former director of the FDA's vaccines office.
The FDA advisory panel is scheduled to meet on Thursday to discuss data on the safety and effectiveness of a Moderna booster shot in adults. On Friday, the committee will debate J&J booster shots for adults, the report said.
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