CNBCのインスタグラム(cnbc) - 2月25日 00時18分


The Food and Drug Administration’s staff endorsed Johnson & Johnson’s Covid-19 vaccine for emergency use, a critical step in bringing a third shot to the U.S. marketplace.⁠

The FDA staff said it determined that the clinical trial results and safety data were “consistent with the recommendations set forth in FDA’s guidance Emergency Use Authorization for Vaccines to Prevent COVID-19.” The staff report released Wednesday is meant to brief the FDA’s Vaccines and Related Biological Products Advisory Committee, which will meet Friday to review J&J’s request for emergency use authorization. ⁠

During similar requests by Pfizer and Moderna, the agency authorized those companies’ vaccinations one day after the committee of outside medical advisors backed emergency use authorization. The committee is expected to recommend J&J’s vaccine. The FDA doesn’t have to follow the committee’s recommendation, but it often does.⁠

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