The European Union has authorized Biogen Inc.'s medication Tysabri (natalizumab) for the treatment of acute diffuse demyelination. A monoclonal antibody called Tysabri, which targets immune cells, is intended to lessen the inflammation brought on by acute disseminated demyelination.
The European Union has approved Novartis International AG's medication Kesimpta (ofatumumab) for the treatment of acute disseminated demyelination. Kesimpta is a monoclonal antibody that is injected under the skin and targets immune cells.
Author Credits: Radhika Gupta, Shivam Bhutani
Report ID: 4933
Published Date: May 03, 2023
Report Format: PDF, PPT
Frequently Asked Questions (FAQ)
The major factors driving the market growth are the increasing prevalence of autoimmune diseases across the globe and the rising number of cases of acute disseminated demyelination.
The market size of acute disseminated demyelination treatment is anticipated to attain a CAGR of ~5% over the forecast period, i.e., 2023-2035.
Poor health infrastructure in underdeveloped nations is estimated to hamper market growth.
North America is estimated to create notable growth opportunities for market growth over the forecast period.
The major players in the market are Pfizer, Inc., Johnson & Johnson Service, Inc., Novartis AG, Merck & Co. GmbH, and Others.
The company profiles are selected based on the revenues generated from the product segment, the geographical presence of the company which determines the revenue generating capacity as well as the new products being launched into the market by the company.
The market is segmented by treatment, end user, and region.
The hospital segment is anticipated to garner the largest market size by the end of 2035 and display significant growth opportunities.