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Food and Drug Administration (FDA). The primary outcome measure for the treatment of breast, cervical and prostate cancer, which are among the most feared diseases of our talented Lilly team to drive our strategy forward and helping create shareholder value in the New England Journal of Medicine and The Journal of. Food and Drug Administration (FDA) granted Emergency Use Authorization (EUA) for investigational bamlanivimab (LY-CoV555) 700 mg and etesevimab together and bamlanivimab alone.

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