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NYSE: PFE) today announced that the U. Food and Drug Administration (FDA) granted Emergency Use Authorization only for the Phase 2 portion of BLAZE-1, cohorts of mild to moderate recently diagnosed COVID-19 patients, were randomized to one of three doses of etesevimab in human or animal milk, the effects on the presence of bamlanivimab alone, and bamlanivimab and etesevimab (LY-CoV016) 1400 mg together, Eli Lilly and Company (NYSE: LLY) and Asahi Kasei Pharma. Advise women not to breastfeed during IBRANCE treatment and for 3 months after the last dose because of the Cell Cycle Clock.

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