Hunter Syndrome Treatment Market Industry Size, Share Opportunities and Forecast By 2028
Hunter Syndrome Treatment report provides data on patterns, improvements, target business sectors, materials, limits, and advancements. With this market report, it becomes possible to gain a holistic view of the market effectively and then also benchmark all the companies in the ABC industry. Moreover, it works to determine the impact of buyers, substitutes, new entrants, competitors, and suppliers on the market. This gives more accurate understanding of the market landscape, issues that may affect the industry in the future, and how to best position specific brands. Hunter Syndrome Treatment market research document estimates the existing state of the market, market size and market share, revenue generated from the product sale, and necessary changes required in the future products.
Data Bridge Market Research analyses a growth rate in the Hunter syndrome treatment market in the forecast period 2023-2030. The expected CAGR of schistosomiasis diseases market is tend to be around 8.6% in the mentioned forecast period. The market was valued at USD 927.57 million in 2022, and it would grow up to USD 1794.67 million by 2030. In addition to the market insights such as market value, growth rate, market segments, geographical coverage, market players, and market scenario, the market report curated by the Data Bridge Market Research team also includes in-depth expert analysis, patient epidemiology, pipeline analysis, pricing analysis, and regulatory framework.
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Hunter syndrome is a rare, inherited genetic disorder that is caused by missing or malfunctioning of enzyme, iduronate-2-sulfatase. Body does not properly digest or break down sugar molecules in the body. When these molecules build up in organs and tissues over the time, they can cause severe damage, affecting physical and mental development and abilities. The disorder commonly occurs in boys. The condition is one of a group of inherited metabolic disorders known as mucopolysaccharidosis (MPS).
Recent Development:
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In January 2021, GC Pharma and Clinigen K.K. received Japanese manufacturing and marketing approval for Hunterase ICV (intracerebroventricular) Injection 15 mg for the treatment for mucopolysaccharidosis type II (Hunter syndrome)
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In September 2020, CANbridge Pharmaceuticals Inc. announced that it received marketing approval from China’s National Medical Products Administration (NMPA) for Hunterase (Idursulfase beta Injection), an enzyme replacement therapy (ERT) for the long-term treatment of patients with mucopolysaccharidosis II (MPS II or Hunter syndrome).
Key players operating in the Hunter syndrome treatment market include:
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Takeda Pharmaceutical Company Limited (Japan)
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F. Hoffmann-La Roche Ltd (Switzerland)
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Abbott (U.S.)
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Medtronic (Ireland.)
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Abbott (U.S.)
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BD (U.S.)
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Johnson & Johnson Services, Inc.(U.S.)
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GSK Plc. (U.K.)
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Bayer AG (Germany)
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Zimmer Biomet (U.S.)
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