Novartis to present new data at AAN, including seven-year disability outcomes and safety analysis of Kesimpta® in people with relapsing multiple sclerosis
-
Long-term disability and safety data from
ALITHIOS open-label extension study on continuous treatment with Kesimpta vs. later switch from teriflunomide in relapsing multiple sclerosis (RMS) patients to be presented
-
Additional presentations highlight the
Novartis neuroscience pipeline, including remibrutinib for RMS and iptacopan for generalized myasthenia gravis
"We look forward to sharing several clinical and real-world studies on Kesimpta in people living with RMS as well as additional studies across our neuroscience portfolio," said Norman Putzki, M.D., Ph.D., Development Unit Head, Neuroscience & Gene Therapy, Development,
Data to be presented at AAN include:
Abstract Title |
Abstract Number/ |
Kesimpta |
|
Continuous Ofatumumab Treatment Up to 7 Years Shows a |
P7.016 Monday,
5:00 – |
Long-Term Ofatumumab Treatment Over 6 Years Did Not |
P8.017 Tuesday,
8:00 – |
Longer-Term (up to 6 Years) Efficacy and Safety of |
P11.003 Wednesday,
8:00 – |
Real-World Data on Ofatumumab as First-line Treatment in |
P7.013 Monday,
5:00 – |
Pipeline Molecules |
|
Remibrutinib Exposure in Cerebrospinal Fluid: Insights from |
P12.003
|
Efficacy and Safety of Iptacopan in Patients with |
P7.027 Monday,
5:00 – |
Biomarkers |
|
Prognostic Value of Baseline Serum Neurofilament Light |
P5.009 Monday,
8:00 – |
NeofiLos – sNfL in Daily Clinical Routine |
P5.015 Monday,
8:00 – |
Product Information
For full prescribing information, including approved indications and important safety information about marketed products, please visit https://www.novartis.com/about/products.
At
Disclaimer
This press release contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements can generally be identified by words such as "potential," "can," "will," "plan," "may," "could," "would," "expect," "anticipate," "look forward," "believe," "committed," "investigational," "pipeline," "launch," or similar terms, or by express or implied discussions regarding potential marketing approvals, new indications or labeling for the investigational or approved products described in this press release, or regarding potential future revenues from such products. You should not place undue reliance on these statements. Such forward-looking statements are based on our current beliefs and expectations regarding future events, and are subject to significant known and unknown risks and uncertainties. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those set forth in the forward-looking statements. There can be no guarantee that the investigational or approved products described in this press release will be submitted or approved for sale or for any additional indications or labeling in any market, or at any particular time. Nor can there be any guarantee that such products will be commercially successful in the future. In particular, our expectations regarding such products could be affected by, among other things, the uncertainties inherent in research and development, including clinical trial results and additional analysis of existing clinical data; regulatory actions or delays or government regulation generally; global trends toward health care cost containment, including government, payor and general public pricing and reimbursement pressures and requirements for increased pricing transparency; our ability to obtain or maintain proprietary intellectual property protection; the particular prescribing preferences of physicians and patients; general political, economic and business conditions, including the effects of and efforts to mitigate pandemic diseases; safety, quality, data integrity or manufacturing issues; potential or actual data security and data privacy breaches, or disruptions of our information technology systems, and other risks and factors referred to in
About Novartis
Reimagine medicine with us: Visit us at https://www.novartis.com and https://www.novartis.us and connect with us on LinkedIn, LinkedIn US, Facebook, X/Twitter, X/Twitter US and Instagram.
# # #
E-mail: media.relations@novartis.com |
|
|
|
|
|
Central investor relations line: +41 61 324 7944 E-mail: investor.relations@novartis.com |
|
SOURCE