- In March 2024, AstraZeneca's Ultomiris (ravulizumab-cwvz) has received approval from the US Food and Drug Administration (FDA) for the treatment of neuromyelitis optica spectrum disorder, a rare autoimmune condition affecting an estimated 6,000 adults in the United States. This approval marks a significant advancement in therapeutic options for patients living with this challenging disease. By providing a targeted treatment for NMOSD, AstraZeneca aims to improve patient outcomes and quality of life in this underserved population.
- In March 2024, AstraZeneca's Alexion announced that it has gained approval for the fourth indication of Ultomiris, allowing it to be utilized in the treatment of neuromyelitis optica spectrum disorder, a rare autoimmune condition. This milestone underscores the growing versatility of Ultomiris in addressing various severe autoimmune diseases. With this new indication, AstraZeneca aims to enhance treatment options for patients suffering from this challenging disorder, improving their chances for better health outcomes.
- In October 2023, Amgen revealed new findings from the phase 3 N-MOmentum clinical trial, which provide valuable insights into the presence of inflammatory biomarkers associated with neuromyelitis optica spectrum disorder (NMOSD). These findings further reinforce the "durable impact" of Uplizna (inebilizumab) in minimizing disease-related attacks. The study highlights the potential of Uplizna as an effective treatment option, emphasizing its role in managing the condition and improving patient outcomes by targeting the underlying inflammatory processes associated with NMOSD.
Frequently Asked Questions
The market is segmented based on Segmentation, By Types (Neuromyelitis Optica Spectrum Disorder with Aquaporin-4 Antibodies, and Neuromyelitis Optica Spectrum Disorder without Aquaporin-4 Antibodies), Treatment Type (Medication, Plasma Exchange Therapy, and Immunoglobulin Therapy), Drugs (C5 Protein Inhibitor, Oral Corticosteroid, Non-Steroid Immunosuppressive Drugs, and Others), Route of Administration(Oral and Injectable), End- Users (Hospitals, Homecare, Specialty Clinics, and Others) – Industry Trends and Forecast to 2032
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The Global Neuromyelitis Optica Treatment Market size was valued at USD 297.72 USD Million in 2024.
The Global Neuromyelitis Optica Treatment Market is projected to grow at a CAGR of 6.8% during the forecast period of 2025 to 2032.
The market report covers data from the U.S., Canada and Mexico in North America, Germany, France, U.K., Netherlands, Switzerland, Belgium, Russia, Italy, Spain, Turkey, Rest of Europe in Europe, China, Japan, India, South Korea, Singapore, Malaysia, Australia, Thailand, Indonesia, Philippines, Rest of Asia-Pacific (APAC) in the Asia-Pacific (APAC), Saudi Arabia, U.A.E., South Africa, Egypt, Israel, Rest of Middle East and Africa (MEA) as a part of Middle East and Africa (MEA), Brazil, Argentina and Rest of South America as part of South America.
