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FDA to review preventative option for RSV in infants, developers say

Summary by Ground News
The FDA has accepted a biologics license application for a long-acting antibody. If approved, it could be available for use in some infants and toddlers later this year. AstraZeneca and Sanofi, which developed the therapy, say the FDA "has indicated it will work to expedite its review"

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abc12/WJRT broke the news in Flint, United States on Thursday, January 5, 2023.
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