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Johnson & Johnson Asks for Emergency Use Authorization of Its COVID-19 Vaccine

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Johnson & Johnson Asks for Emergency Use Authorization of Its COVID-19 Vaccine

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Johnson & Johnson asked U.S. regulators Thursday to clear the world’s first single-dose COVID-19 vaccine, an easier-to-use option that could boost scarce supplies. J&J’s vaccine was safe and offered strong protection against moderate to severe COVID-19, according to preliminary results from a massive international study. It didn’t appear quite as strong as two-dose competitors made by Pfizer and Moderna—a finding that may be more perception than reality, given differences in how each was tested. But the Food and Drug Administration is asking its independent advisers to publicly debate all the data behind the single-dose shot—just like its competitors were put under the microscope—before it decides whether to green light a third vaccine option in the U.S. The panel will meet Feb. 26. Dr. Peter Marks, FDA’s vaccine chief, has cautioned against making comparisons before the evidence is all in. “With so much need to get this pandemic under control, I …

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