Novartis Pipeline

Benefiting from our continued focus on innovation,Novartis has one of the industry’smost competitive pipelines.Many of these projects,which include new molecular entities as well as additional indications and different for marketed products, are for medicines that could significantly advance treatment standards for patients worldwide.This table provides an overview of selected projects in development.Please note:the Novartis Pipeline data is updated quarterly。

下载Novartis Pipeline from the 2023 Annual Report(PDF0.1MB)

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Showing103 results
  • YTB323
    rapcabtagene autoleucel
    系统lupus erythematosus
    Immunology Phase2 ≥2027 CD19CART(CD19-targeted chimeric antigen receptor T-cell immunotherapy)
  • YTB323
    rapcabtagene autoleucel
    Adult ALL
    Oncology:Hematology Phase1 CD19CART(CD19-targeted chimeric antigen receptor T-cell immunotherapy)
  • YTB323
    rapcabtagene autoleucel
    1L high-risk large B-cell lymphoma
    Oncology:Hematology Phase2 ≥2027 CD19CART(CD19-targeted chimeric antigen receptor T-cell immunotherapy)
    Lead Indication
Legend

组合abbreviations:
fulv fulvestrant
tmx tamoxifen
gsn goserelin
NSAI Non-steroidal aromatase inhibitor
Taf Tafinlar®(dabrafenib)
中间,中间®(trametinib)

a EU filing,approved in US。
b US filing,approved in EU。
c US filing,submitted in EU。
d US pending submission,approved in EU
e EU filing,submitted in US。

Disclaimer

This information was factually accurate on the date it was published.Novartis assumes no duty to update the information to reflect subsequent developments.Readers should not rely upon the information on this page as current or accurate after its publication date.For the latest information on the Novartis’pipeline, readers should visit the News and Investors sections of our website.This information constitutes forward-looking statements relating to Novartis AG's business,including express or implied discussions regarding potential new products,potential new indications for existing products, orregarding potential future revenues from any such products.Such forward-looking statements reflect the current views of Novartis AG regarding future events,and involve known and unknown risks,uncertainties and other factors that may cause actual restobe materially different from any fultures, performance or achievements expressed or implied by such statements.There can be no guarantee that any new products will be approved for sale in any market,or that any new indications will be approved for existing products in any market,or that such products will achieveany particular revenue levels。

在particular,management's expectations could be affected by,among other things,uncertainties involved in the development of new pharmaceutical products;unexpected clinical trial results, including additional analysis of existing clinical data or unexpected new clinical data;unexpected regulatory actions or delays or government regulation generally;the Novartis Group’s ability to obtain or maintain patent or other proprietary intellectual property保护, including the uncertainties involved in the US litigation process;competition in general;government,industry, and general public pricing and other political pressures;and other risks and factors referred to in Novartis AG's current Form20-F on file with the US Securities and Exchange Commission.Should one or more of these risks or uncertainties materialize,or should underlying assumptions prove incorrect, actual results may vary materially from those described herein as anticipated,believed,estimated or expected。