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Novartis to present new data at AAN, including seven-year disability outcomes and safety analysis of Kesimpta® in people with relapsing multiple sclerosis

In This Article:

Novartis Pharma  AG
Novartis Pharma AG
  • 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

Basel, March 25, 2025 – Novartis will present data from studies across its neuroscience portfolio, including seven-year disability outcomes and safety data from the ALITHIOS open-label extension trial of Kesimpta® (ofatumumab) in people with relapsing multiple sclerosis (RMS), at the American Academy of Neurology (AAN) 2025 Annual Meeting in San Diego from April 5-9, 2025. Additional data on Kesimpta and pipeline assets including remibrutinib and iptacopan will also be highlighted.

“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, Novartis. “As always, we are excited to attend the AAN annual meeting and discuss the latest developments in neuroscience as we work to address some of the most pressing challenges for people living with neurological conditions.”

Data to be presented at AAN include:

Abstract Title      

Abstract Number/ Presentation Details       

Kesimpta

Continuous Ofatumumab Treatment Up to 7 Years Shows a Consistent Safety Profile and Delays Disability Progression in People with Relapsing Multiple Sclerosis

P7.016
Monday,
April 7
5:00 – 6:00 PM PT

Long-Term Ofatumumab Treatment Over 6 Years Did Not Increase the Risk of Serious Infections

P8.017
Tuesday,
April 8
8:00 – 9:00 AM PT

Longer-Term (up to 6 Years) Efficacy and Safety of Ofatumumab in People with Non-highly Active MS Early in the Disease Course

P11.003
Wednesday,
April 9
8:00 – 9:00 AM PT

Real-World Data on Ofatumumab as First-line Treatment in Early RMS (AIOLOS Study)

P7.013
Monday,
April 7
5:00 – 6:00 PM PT

Pipeline Molecules

Remibrutinib Exposure in Cerebrospinal Fluid: Insights from a Study in Healthy Participants

P12.003
Wednesday,
April 9
11:45 AM – 12:45 PM PT

Efficacy and Safety of Iptacopan in Patients with Generalized Myasthenia Gravis: Study Design

P7.027
Monday,
April 7
5:00 – 6:00 PM PT

Biomarkers

Prognostic Value of Baseline Serum Neurofilament Light Chain (sNfL) Levels in People with Relapsing Multiple Sclerosis by Prior Treatment Status and DMT Type

P5.009
Monday,
April 7
8:00 – 9:00 AM PT

NeofiLos – sNfL in Daily Clinical Routine

P5.015
Monday,
April 7
8:00 – 9:00 AM PT

Product Information 
For full prescribing information, including approved indications and important safety information about marketed products, please visit https://www.novartis.com/about/products.