DelveInsight’s “Fabry Disease Market Insights, Epidemiology, and Market Forecast-2032″ report offers an in-depth understanding of the Fabry Disease, historical and forecasted epidemiology as well as the Fabry Disease market trends in the United States, EU4 (Germany, Spain, Italy, France) the United Kingdom and Japan.
To Know in detail about the Fabry Disease market outlook, drug uptake, treatment scenario and epidemiology trends, Click here; Fabry Disease Market Forecast
Some of the key facts of the Fabry Disease Market Report:
- The Fabry Disease market size was valued approximately USD 1,167.8 million in 2020 and is anticipated to grow with a significant CAGR during the study period (2019-2032)
- By aggregating the instances in the various nations, the total prevalence cases in the 7MM were determined. There were 13,053 Fabry Disease instances in the 7MM population overall in 2020, with the majority of those cases being found in the US. In contrast to Japan, which had 437 instances in 2020, the EU5 countries had 4,708 cases
- Germany had the most Fabry Disease cases per 100,000 people among the EU5 nations in 2020 (1,158 cases). These are anticipated to increase by 2032, according to DelveInsight’s projections
- In the US, males were more likely than females to have Fabry disease. 4,099 males and 3,809 females were affected by Fabry disease in 2020. According to DelveInsight, the number will rise by 2032
- Key Fabry Disease Companies: Protalix Biotherapeutics, AVROBIO, Sanofi Genzyme, Sangamo Therapeutics, Freeline Therapeutics, 4D Molecular Therapeutics, Idorsia Pharmaceuticals, Greenovation Biotech GMBH, ICON plc, Chiesi Farmaceutici S.p.A., Amicus Therapeutics, Shire, and others
- Key Fabry Disease Therapies: PRX-102, AVR-RD-01, Venglustat, ST -920, FLT190, 4D-310, Lucerastat, Moss-aGal, PRX-102, pegunigalsidase alfa, migalastat, Agalsidase alfa, and others
- The Fabry Disease epidemiology based on gender analyzed that Fabry Disease is more prevalent in males than females in the United States
- The Fabry Disease market is expected to surge due to the disease’s increasing prevalence and awareness during the forecast period. Furthermore, launching various multiple-stage Fabry Disease pipeline products will significantly revolutionize the Fabry Disease market dynamics.
Fabry Disease Overview
Alpha-galactosidase A (-Gal A), a lysosomal storage disorder that is hereditary, is the primary culprit in Fabry disease. The accumulation of enzyme substrates (Gb3 and lyso-Gb3) caused by decreased -Gal A activity in lysosomes leads to cellular damage in tissues all over the body.
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Fabry Disease Epidemiology
The epidemiology section provides insights into the historical, current, and forecasted epidemiology trends in the seven major countries (7MM) from 2019 to 2032. It helps to recognize the causes of current and forecasted trends by exploring numerous studies and views of key opinion leaders. The epidemiology section also provides a detailed analysis of the diagnosed patient pool and future trends.
Fabry Disease Epidemiology Segmentation:
The Fabry Disease market report proffers epidemiological analysis for the study period 2019–2032 in the 7MM segmented into:
- Total Prevalence of Fabry Disease
- Prevalent Cases of Fabry Disease by severity
- Gender-specific Prevalence of Fabry Disease
- Diagnosed Cases of Episodic and Chronic Fabry Disease
Download the report to understand which factors are driving Fabry Disease epidemiology trends @ Fabry Disease Epidemiology Forecast
Fabry Disease Drugs Uptake and Pipeline Development Activities
The drugs uptake section focuses on the rate of uptake of the potential drugs recently launched in the Fabry Disease market or expected to get launched during the study period. The analysis covers Fabry Disease market uptake by drugs, patient uptake by therapies, and sales of each drug.
Moreover, the therapeutics assessment section helps understand the drugs with the most rapid uptake and the reasons behind the maximal use of the drugs. Additionally, it compares the drugs based on market share.
The report also covers the Fabry Disease Pipeline Development Activities. It provides valuable insights about different therapeutic candidates in various stages and the key companies involved in developing targeted therapeutics. It also analyzes recent developments such as collaborations, acquisitions, mergers, licensing patent details, and other information for emerging therapies.
Fabry Disease Therapies and Key Companies
- PRX-102: Protalix Biotherapeutics
- AVR-RD-01: AVROBIO
- Venglustat: Sanofi Genzyme
- ST-920: Sangamo Therapeutics
- FLT190: Freeline Therapeutics
- 4D-310: 4D Molecular Therapeutics
- Lucerastat: Idorsia Pharmaceuticals
- Moss-aGal: Greenovation Biotech GMBH
- PRX-102: ICON plc
- pegunigalsidase alfa: Chiesi Farmaceutici S.p.A.
- migalastat: Amicus Therapeutics
- Agalsidase alfa: Shire
Discover more about therapies set to grab major Fabry Disease market share @ Fabry Disease Treatment Market
Fabry Disease Market Strengths
- Important progress has been made regarding understanding disease pathology, diagnosis, and treatment effects in Fabry disease.
- Newborn screening for Fabry disease has been implemented in several countries, enabling the early detection of individuals with Fabry mutations.
- Many therapies are under investigation in various phases of clinical trials. These include pegylated forms of α-GAL, gene therapy, and substrate reduction therapy.
Fabry Disease Market Unmet Needs
- Challenges in diagnoses
- Development of novel therapies
- Limitations in gene therapy
- Poor disease understanding
- Clinical biomarkers
Scope of the Fabry Disease Market Report
- Study Period: 2019–2032
- Coverage: 7MM [The United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan]
- Key Fabry Disease Companies: Protalix Biotherapeutics, AVROBIO, Sanofi Genzyme, Sangamo Therapeutics, Freeline Therapeutics, 4D Molecular Therapeutics, Idorsia Pharmaceuticals, Greenovation Biotech GMBH, ICON plc, Chiesi Farmaceutici S.p.A., Amicus Therapeutics, Shire, and others
- Key Fabry Disease Therapies: PRX-102, AVR-RD-01, Venglustat, ST-920, FLT190, 4D-310, Lucerastat, Moss-aGal, PRX-102, pegunigalsidase alfa, migalastat, Agalsidase alfa, and others
- Fabry Disease Therapeutic Assessment: Fabry Disease current marketed and Fabry Disease emerging therapies
- Fabry Disease Market Dynamics: Fabry Disease market drivers and Fabry Disease market barriers
- Competitive Intelligence Analysis: SWOT analysis, PESTLE analysis, Porter’s five forces, BCG Matrix, Market entry strategies
- Fabry Disease Unmet Needs, KOL’s views, Analyst’s views, Fabry Disease Market Access and Reimbursement
To know more about Fabry Disease companies working in the treatment market, visit @ Fabry Disease Clinical Trials and Therapeutic Assessment
Table of Contents
1. Fabry Disease Market Report Introduction
2. Executive Summary for Fabry Disease
3. SWOT analysis of Fabry Disease
4. Fabry Disease Patient Share (%) Overview at a Glance
5. Fabry Disease Market Overview at a Glance
6. Fabry Disease Disease Background and Overview
7. Fabry Disease Epidemiology and Patient Population
8. Country-Specific Patient Population of Fabry Disease
9. Fabry Disease Current Treatment and Medical Practices
10. Fabry Disease Unmet Needs
11. Fabry Disease Emerging Therapies
12. Fabry Disease Market Outlook
13. Country-Wise Fabry Disease Market Analysis (2019–2032)
14. Fabry Disease Market Access and Reimbursement of Therapies
15. Fabry Disease Market Drivers
16. Fabry Disease Market Barriers
17. Fabry Disease Appendix
18. Fabry Disease Report Methodology
19. DelveInsight Capabilities
20. Disclaimer
21. About DelveInsight
About DelveInsight
DelveInsight is a leading Healthcare Business Consultant, and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance.
It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate the business growth and overcome challenges with a practical approach.
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