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    Amgen reports positive results from landmark cardiovascular study

    The study found significant reductions of major cardiovascular events in high-risk adults following treatment

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    Amgen commits $650m to US manufacturing expansion

    The investment is expected to generate up to 750 new jobs

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    Amgen and Kyowa Kirin announce rocatinlimab results for atopic dermatitis

    The phase 3 study included around 2,600 patients

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    Medscape Cardiology: Leading the Future of Heart Failure Education at HFSA 2025

    Medscape Cardiology | theheart.org is proud to be at the forefront of the Heart Failure Society of America (HFSA) Annual Scientific Meeting (ASM), September 26–29, 2025, in Minneapolis, MN! With...

    Medscape Education

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    Bayer’s Kerendia granted FDA approval for new heart failure indication

    Approximately 55% of the 6.7 million adults in the US with HF have an LVEF of at least 40%

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    Amgen’s bemarituzumab shows promise in phase 3 gastric cancer study

    Almost one million new cases of gastric cancer are diagnosed globally every year

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    Amgen’s Uplizna approved by FDA as first treatment for rare disease IgG4-RD

    Immunoglobulin G4-related disease affects approximately 20,000 people in the US

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    Amgen’s Uplizna shows promise in phase 3 generalised myasthenia gravis study

    Regulatory submissions are expected to be complete in the first half of this year

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    Amgen/Kyowa Kirin share promising phase 3 results for rocatinlimab in atopic dermatitis

    The inflammatory skin disease affects up to 20% of children and 10% of adults worldwide

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    Amgen’s Blincyto recommended by NICE for new adult leukaemia indication

    Up to 50% of acute lymphoblastic leukaemia patients will relapse after initial treatment

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    Amgen’s Blincyto granted EC approval for new acute lymphoblastic leukaemia indication

    B-ALL is the most common form of the blood cancer, accounting for approximately 75% of adult cases

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    Amgen’s Lumakras/Vectibix approved by FDA to treat metastatic colorectal cancer

    The combination therapy has been authorised for use in adults harbouring KRAS G12C mutations

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