Fabry Disease Market to Exhibit Rapid Growth Rate During the Forecast Period (2023-2032), Investigates DelveInsight | Protalix Biotherapeutics, Sanofi Genzyme, Sangamo Therapeutics, Freeline Therapeutics, 4D Molecular Therapeutics

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.

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Some of the key facts of the Fabry Disease Market Report:
• The Fabry Disease market size was valued approximately USD 1,190 million in 2022 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 13,200 total 7MM prevalent instances of Fabry Disease in 2022, with the majority of those cases being found in the US. In 2022, there were 4,700 instances in the EU4 countries and the UK, whereas there were just 430 cases in Japan
• In the United States, 8,000 cases of Fabry disease were reported in 2022
• In 2022, there were 1,680 instances of Fabry disease in the 10-19 age group, 1,560 cases in the 20-29 age group, 1,480 cases in the 30-39 age group, 1,250 cases in the 40-49 age group, and 1,030 cases each in the 10 and 50 age groups
• In 2022, Germany had 1,155 more Fabry Disease cases than the other three EU-4 nations combined. These are anticipated to increase by 2032, according to DelveInsight's projections
• Key Fabry Disease Companies: Protalix Biotherapeutics, Sanofi Genzyme, Sangamo Therapeutics, Freeline Therapeutics, 4D Molecular Therapeutics, Sanofi, Chiesi Farmaceutici S.p.A, Amicus Therapeutics, Idorsia Pharmaceuticals Ltd., Protalix, Shire, Avrobio Inc., BIOSIDUS, and others
• Key Fabry Disease Therapies: PRX-102, Venglustat, ST-920, FLT190, 4D-310, agalsidase beta, pegunigalsidase alfa, migalastat, Lucerastat, PRX-102, 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

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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
• Venglustat: Sanofi Genzyme
• ST-920: Sangamo Therapeutics
• FLT190: Freeline Therapeutics
• 4D-310: 4D Molecular Therapeutics
• agalsidase beta: Sanofi
• pegunigalsidase alfa: Chiesi Farmaceutici S.p.A.
• migalastat: Amicus Therapeutics
• Lucerastat: Idorsia Pharmaceuticals Ltd.
• PRX-102: Protalix
• Agalsidase alfa: Shire

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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 Opportunities
• Development of a potential biomarker that allows for tracking and predicting the severity and potential progress of the disease and the effectiveness of any therapeutic intervention
• Relative lack of enzyme replacement therapy efficacy, partly due to antibody formation, can be alleviated by combining new oral therapy approaches
• Due to patients' poor quality of life with Fabry disease, there is significant patient willingness towards expensive therapies

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, Sanofi Genzyme, Sangamo Therapeutics, Freeline Therapeutics, 4D Molecular Therapeutics, Sanofi, Chiesi Farmaceutici S.p.A, Amicus Therapeutics, Idorsia Pharmaceuticals Ltd., Protalix, Shire, Avrobio Inc., BIOSIDUS, and others
• Key Fabry Disease Therapies: PRX-102, Venglustat, ST-920, FLT190, 4D-310, agalsidase beta, pegunigalsidase alfa, migalastat, Lucerastat, PRX-102, 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

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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

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