china lysosomal storage disorders therapeutics market

China Lysosomal Storage Disorders Therapeutics Market: Segmented by Therapy (Enzyme Replacement Therapy, Substrate Reduction Therapy, Gene Therapy), Disease Type (Gaucher, Pompe, Fabry, Mucopolysaccharidosis), Route of Administration (Oral, Intravenous)- Size, Share, Growth, Trends, and Forecasts (2019 2028)

  • Published Date: 2022-12-28
  • Report ID: 139796
  • Pages: 200
  • Format: prudent report format

Report Overview

China Lysosomal Storage Disorders Therapeutics market size stood at around USD xx billion in 2019 and is projected to reach USD $xx billion by 2028, exhibiting a CAGR of 5.2% during the forecast period.

Lysosomal storage diseases are inherited metabolic diseases that are characterized by an abnormal build-up of various toxic materials in the bodys cells as a result of enzyme deficiencies. Although each type of lysosomal storage disease is very rare, as a whole, the global incidence is about 1 in 5000-6000. Taking Shanghai as an example, about 200,000 newborns are born in the city each year, and the number of patients About 10-20.



Market Drivers

China is a growing market for lysosomal storage disorders due to an enormous population, increase in awareness of disease by the establishment of the Chinese Newborns Screening Cooperative Group for Lysosomal Storage Disease and improvement in R&D activities. Development of novel therapeutics and increase in global incidence (1 in 5000-6000) and prevalence rate leads to growth of the China lysosomal Storage Disorders drug market.

However, there are some restraining factors for the growth of lysosomal storage disorders therapeutics market in China such as high cost of treatment, limitations of medical insurance coverage and misdiagnosis of the disease (in 2019 61.9% of Gaucher disease patients have experienced misdiagnosis, and 27.9% of patients need 1-5 years to be diagnosed).


1. China Lysosomal Storage Disorders Therapeutics Market Overview.............
A. Market Size
2. Market Growth Drivers
A. Increase in Awareness of Disease
B. Increase in Prevalence and Incidence Rate
C. Improvement in R&D Activities
D. Adoption of Novel Therapeutics
3. Major Types of Lysosomal Storage Disorders......................
A. Gaucher Disease
B. Fabry Disease
C. Pompe Disease
D. Mucopolysaccharidosis Type I
4. Lysosomal Storage Disorders Therapeutics Market Segmentation
A. By Therapy
I. Enzyme Replacement Therapy
II. Substrate Reduction Therapy
III. Gene Therapy
B. By Disease Type
I. Gaucher Disease
II. Pompe Disease
III. Fabry Disease
IV. Mucopolysaccharidosis
C. By Route of Administration
I. Oral
II. Intravenous
5. Lysosomal Storage Disorders Major Products Market Share
A. Market Analysis, Insights and Forecast By Revenue Type
6. Competitive Landscape.........
A. Major Players
B. Products in Pipeline
7. Key Company Profiles
A. Sanofi Company Overview, Product & Services, Strategies & Financials
B. Takeda Company Overview, Product & Services, Strategies & Financials
C. BioMarin Company Overview, Product & Services, Strategies & Financials
8. Healthcare Policies and Regulatory Landscape.
A. Policy Changes and Reimbursement Scenario
9. Factors Driving Future Growth
A. New Trends and Development of Lysosomal Storage Disorders Therapeutics Market
B. Future Opportunities
10. Conclusion
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