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J&J seeks FDA clearance for COVID-19 booster shot
Johnson & Johnson asks the FDA to authorize boosters for adults who received the one dose vaccine. Data cover two through six month intervals with no formal brand recommendation. Regulators review J&J and Moderna data next week as U S officials push to broaden booster use amid delta variant concerns.
MENTIONED IN THIS ARTICLE
Washington - Johnson & Johnson
Food and Drug Administration
U.S
J&j
FDA
Pfizer
Biden Administration
Moderna
COVID
Mathai Mammen
Janssen
New Brunswick
New Jersey
Baltimore