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The digital press release with multimedia content can be accessed here:Neuroscience
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Basel, October 14, 2021 — Today, Novartis announced data demonstrating the safety of Kesimpta® (ofatumumab) over extended exposure (~3.5 years) in patients with relapsing forms of multiple sclerosis (RMS).1 These data—presented at the 37th Congress of the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) taking place…NeuroscienceNeurodegenerative Disease
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Basel, June 22, 2021 — Today, Novartis disclosed new data showing mean IgG and IgM levels remain unchanged in adults with relapsing multiple sclerosis (RMS) treated with Kesimpta® (ofatumumab) over 3.5 years. The ongoing open label extension of the ALITHIOS study includes 1,703 people living with MS taking Kesimpta for up to 5 years. At the time…NeuroscienceInnovation
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Basel, October 7, 2021 — Novartis announced today it will present 41 abstracts at the upcoming 37th Congress of the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS), taking place digitally on October 13-15, 2021. The data being presented spans a comprehensive MS portfolio, emphasizing the company’s commitment to…NeuroscienceClinical Trials
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Basel, September 8, 2020 — Novartis announced today it will present 48 abstracts at the upcoming MSVirtual2020: 8th Joint ACTRIMS-ECTRIMS Meeting, September 11–13, 2020. The breadth of data being presented highlights the strength and promise of the company’s MS portfolio to improve the lives of patients across the MS spectrum.Reimagine MedicineNeuroscienceInnovation
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The digital press release with multimedia content can be accessed here:Reimagine MedicineNeuroscienceInnovation
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The digital press release with multimedia content can be accessed here:Reimagine MedicineNeuroscienceInnovation
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Basel, October 21, 2020 — Novartis today announced that the US Food and Drug Administration (FDA) has granted Orphan Drug Designation for branaplam (LMI070) in Huntington’s disease (HD). An Orphan Drug Designation grants special status to a drug that treats a rare disease or condition, and provides companies certain benefits to encourage the…Reimagine MedicineNeuroscience
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The digital press release with multimedia content can be accessed here:Reimagine MedicineNeuroscienceLiving With Disease
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The digital press release with multimedia content can be accessed here:Reimagine MedicineNeuroscienceMedical InnovationsLiving With DiseaseAd Hoc
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Basel, February 16, 2021 — Novartis announced today new multicenter survey results showing that people living with multiple sclerosis (MS) and nurses prefer the Sensoready® autoinjector pen for self-administration of Kesimpta® (ofatumumab) over other autoinjectors used for other disease-modifying therapies in MS1. These data, which will be…NeuroscienceInnovation
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Basel, February 16, 2021 — Novartis today announced that the US Food and Drug Administration (FDA) has approved the following expanded indication for Entresto® (sacubitril/valsartan): to reduce the risk of cardiovascular death and hospitalization for heart failure in adult patients with chronic heart failure1. Benefits are most clearly evident in…Reimagine MedicineNeuroscienceMedical InnovationsLiving With DiseaseAd Hoc