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  • Media Release
    Mar 13, 2025
    Novartis named first-ever corporate pharmaceutical partner of the National Football League
  • Media Release
    Feb 28, 2025
    Novartis data presentations at AAAAI and AAD underscore commitment to advancing treatment of hidradenitis suppurativa (HS) and chronic spontaneous urticaria (CSU)
  • Media Release
    Jan 28, 2025
    Early detection is a game changer: Novartis makes bold play to prioritize breast health and inspire a new wave of breast cancer screenings
  • Media Release
    Dec 10, 2024
    Longer-term Novartis Kisqali® NATALEE data show durable reduction in distant recurrence in broad population of patients with early breast cancer
  • Media Release
    Dec 08, 2024
    Longer-term data for Novartis Scemblix® reinforce superior efficacy with favorable safety and tolerability profile in adults with newly diagnosed CML
  • Media Release
    Nov 24, 2024
    Novartis highlights new 96-week results from Phase III Scemblix® ASC4FIRST trial at ASH and late-breaking analysis from Phase III Kisqali® NATALEE trial at SABCS
  • Media Release
    Oct 29, 2024
    Novartis Scemblix® FDA approved in newly diagnosed CML, offering superior efficacy, and favorable safety and tolerability profile
  • Media Release
    Oct 26, 2024
    Novartis oral Fabhalta® (iptacopan) sustained clinically meaningful results at one year in Phase III C3 glomerulopathy (C3G) trial
  • Media Release
    Oct 24, 2024
    Novartis ribociclib (Kisqali®) recognized as Category 1 preferred breast cancer adjuvant treatment by NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®)
  • Media Release
    Oct 18, 2024
    Novartis receives positive CHMP opinion for Kisqali® to help reduce risk of recurrence in people with HR+/HER2- early breast cancer
  • Media Release
    Sep 18, 2024
    New Novartis data in relapsing MS reinforce benefits of Kesimpta® for first-line and switch patients
  • Media Release
    Sep 17, 2024
    FDA approves Novartis Kisqali® to reduce risk of recurrence in people with HR+/HER2- early breast cancer

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