Growth Factors of Hunter Syndrome Treatment Market
The Hunter Syndrome Treatment Market size was valued at USD 70.2 billion in 2023, and the market is now projected tgrow tUSD 159.9 billion by 2032, exhibiting a CAGR of 6.1% during the forecast period of 2023-2030.
The pandemic has been anticipated tbe a bane for the entire industrial developments of various market and fields. This has affected the overall supply and demand chains of the particular market. As a result of the government's lockdown and other steps tstop the coronavirus from spreading, all supply activities were postponed, which decreased the amount of product related tthis domain. These factors affected the Hunter Syndrome Treatment Market growth.
Lack of access tmany medicines for patients and the monopoly of one pharmaceutical, Elaprase, are twimportant market drivers. The cost of elaprase is especially high, and patients in developing nations frequently lack access tthese treatments. People whlack access tappropriate care frequently live far shorter lives than those in developing nations whfrequently have access tthese costly treatments. The only other approved treatment outside Elaprase is Hunterase, which is only authorized in a few nations. It is projected that during the forecast period, the introduction of affordable and efficient therapies will propel the growth of the global market. These particular growth driving factors have been recorded tattribute the Hunter Syndrome Treatment Market Share.
It is necessary for a product market twalk with the trends in order tincreases its lucracy and profits in shares and all over revenue. The growing R&D expenditures made by major players for the creation of innovative treatments are one of the major industry trends currently dominating the Hunter syndrome treatment market. There are several well-known clinical stage biopharmaceutical companies, like ArmaGen and REGENXBIO Inc., whhave promising pipeline candidates at different phases of clinical trials because Hunter syndrome is a major orphan illness. Compared tstandard pharmaceutical portfolios, rare diseases are more likely tsee significant pharmaceutical breakthroughs that result in the development of blockbuster pharmaceuticals, which is why there is growing interest in the treatments of these disorders. During the forecast period, this is anticipated tfurther push the growth of the mucopolysaccharidosis II therapy market.
Comprehensive Analysis of Hunter Syndrome Treatment Market
The segmentation of this particular market has been divided and then further subdivided intvarious categories. The worldwide market is divided intseveral segments based on the type of treatment, including enzyme replacement therapy (ERT). Since Hunter syndrome is a member of the lysosomal storage disorder category, enzyme replacement therapy (ERT) is the main treatment for these disorders. The market is divided intintravenous and intracerebroventricular (ICV)/ intrathecal segments based on the route of administration. Due tthe fact that Elaprase is the most widely used medication for Hunter syndrome, the intravenous form is expected tdominate the route of administration segment. The market for treating hunter syndrome is divided intvarious end-user segments, including hospitals and specialty clinics.
The market for MPS II treatments was worth millions of dollars in North America. Along with appropriate reimbursement policies for these treatments, the region's market is distinguished by greater rates of diagnosis and treatment for these uncommon disorders. Together with increased patient knowledge of new treatment alternatives and the existence of large clinical stage biopharmaceutical businesses as pipeline candidates, these reasons account for the region's dominant market position globally. The region is expected tmaintain a significant proportion during the projected period.
Global markets are fiercely competitive and highly fragmented. Due ttheir creative packaging solutions, a few group of large market companies hold a fair amount of market share. Some of the major Companies includes Shire (Takeda Pharmaceutical Company Limited) (U.S.), Denali Therapeutics (U.S.), ArmaGen (U.S.), Inventiva (France), Green Cross Corp. (GC Pharma) (South Korea), CANbridge Life Sciences Ltd. (U.S.), JCR Pharmaceuticals Co., Ltd. (Japan), REGENXBIO Inc. (U.S.), SangamTherapeutics (U.S.).
In July 2021, This particular company has attributed the market growth in terms of revenue and shares system. Denali Therapeutics Inc. reported encouraging findings from a clinical study assessing the ETV: IDS, an experimental brain-penetrant enzyme replacement medication intended talleviate Hunter Syndrome's peripheral symptoms. Presentations of the findings will take place during the 16th International Symposium on MPS and related disorders.
Segmentation Table
ATTRIBUTE DETAILS
Study Period - 2015-2026
Base Year - 2018
Forecast Period - 2019-2026
Historical Period - 2015-2017
Unit Value (USD million)
Segmentation By Treatment
Learn how to effectively navigate the market research process to help guide your organization on the journey to success.
Download eBook