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Alexion Pharmaceuticals

Recent events

Recent events tied to this brand in public sources.

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  1. 2021

    Genomenon and Alexion announce rare-disease genomics collaboration

    Genomenon announced a collaboration with Alexion to produce genomic landscapes and make curated genetic datasets and information on therapies or clinical trials available to doctors, researchers, and clinicians through Genomenon's Mastermind Genomic Search Engine.

  2. 2021

    AstraZeneca completes acquisition of Alexion

    AstraZeneca completed its $39 billion acquisition of Alexion Pharmaceuticals, following regulatory clearances. The deal included cash and newly issued AstraZeneca shares for Alexion shareholders.

  3. 2021

    Alexion highly commended in Treasury Today's Adam Smith Awards

    Alexion Pharmaceuticals was highly commended for “Harnessing the Power of Technology” in Treasury Today's Adam Smith Awards. The article says the recognition took place last week but does not provide a calendar date.

  4. 2020

    AstraZeneca announces plan to acquire Alexion

    AstraZeneca announced plans to acquire Alexion for approximately $39 billion. The boards of both companies approved the acquisition, which was expected to close in the third quarter of 2021 subject to regulatory clearances and shareholder approval.

  5. 2020

    Alexion raises 2020 revenue and earnings guidance

    Alexion said it now expects fiscal 2020 non-GAAP earnings per share of $10.65 to $10.95 and total revenues of $5.55 billion to $5.60 billion, revising both ranges upward.

  6. 2019

    FDA approves Ultomiris for atypical hemolytic uremic syndrome

    The U.S. Food and Drug Administration approved Alexion Pharmaceuticals’ Ultomiris for use in treating atypical hemolytic uremic syndrome (aHUS), according to the company.

  7. 2019

    FDA approves Ultomiris for atypical hemolytic uremic syndrome

    The U.S. Food and Drug Administration approved Alexion Pharmaceuticals' Ultomiris for treating atypical hemolytic uremic syndrome (aHUS), its second rare blood disorder indication.