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Innovation

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  • 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
  • Media Release
    Sep 16, 2024
    Novartis Kisqali® shows deepening benefit in new analysis, reducing the risk of recurrence by 28.5% in a broad population of patients with early breast cancer
  • Media Release
    Sep 04, 2024
    Novartis begins construction of two new radioligand therapy facilities in the US, expanding its world-class RLT manufacturing and supply network
  • Media Release
    Aug 07, 2024
    Novartis receives FDA accelerated approval for Fabhalta® (iptacopan), the first and only complement inhibitor for the reduction of proteinuria in primary IgA nephropathy (IgAN)
  • Media Release
    Jul 29, 2024
    Novartis Scemblix® granted FDA Priority Review for the treatment of adults with newly diagnosed CML
  • Media Release
    May 31, 2024
    Novartis Scemblix® Phase III data first to show superior efficacy with a favorable safety and tolerability profile vs. standard-of-care TKIs in adults with newly diagnosed CML
  • Media Release
    May 31, 2024
    Latest analysis of Novartis NATALEE study shows Kisqali® reduces risk of cancer recurrence for early breast cancer patients with high-risk node-negative disease
  • Media Release
    May 25, 2024
    Novartis atrasentan Phase III data show clinically meaningful proteinuria reduction further advancing company's IgA nephropathy (IgAN) portfolio

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