查看購物車
  • Simplified Chinese
  • English
  • Japanese
  • Korean
封面
市場調查報告書
商品編碼
1383639

法布瑞氏症治療市場 - 2018-2028 年全球產業規模、佔有率、趨勢、機會和預測，按藥物、治療、給藥途徑、配銷通路、地區和競爭細分

Fabry Disease Treatment Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, 2018-2028 Segmented by Drugs, By Treatment, By Route of Administration, By Distribution Channel, by region, and Competition
出版日期: | 出版商: TechSci Research | 英文 190 Pages | 商品交期: 2-3個工作天內

價格

We offer 8 hour analyst time for an additional research. Please contact us for the details.

簡介目錄

2022年，全球法布瑞氏症治療市場價值為18.625億美元，預計在預測期內將出現令人印象深刻的成長，到2028年CAGR為6.30%。法布瑞氏症，也稱為安德森-法布瑞氏症，是一種罕見的遺傳性疾病屬於溶小體貯​​積症一群疾病的遺傳性疾病。這種疾病是由 GLA 基因突變引起的，該基因編碼一種稱為 α-半乳糖苷酶 A (α-Gal A) 的酶。這種酵素的缺乏會導致一種特定類型的脂肪物質在全身細胞內積聚，稱為三醯基神經醯胺（Gb3 或 GL-3）。 Gb3 的累積主要影響血管、腎臟、心臟和神經系統的細胞，導致多種症狀和併發症。法布瑞氏症的症狀通常出現在兒童期或青春期，儘管受影響個體的症狀出現年齡及其嚴重程度可能存在很大差異。法布瑞氏症的徵兆症狀之一是神經性疼痛，這種疼痛可能是嚴重且慢性的。這種疼痛通常會影響四肢，例如手和腳，通常被描述為灼熱感或刺痛感。

醫療保健專業人員、患者和護理人員對法布瑞氏症的認知不斷提高，從而提高了診斷率。認知的提升是市場的重要驅動力，因為早期診斷對於開始治療至關重要。診斷工具和基因檢測的進步使得法布瑞氏症的識別變得更加容易，即使在早期階段也是如此。診斷能力的提高導致更多病例得到診斷和治療。全球醫療保健支出一直在增加，使得對法布瑞氏症等罕見疾病治療的投資增加。醫療保健預算的增加支持了研究和開發工作，並改善了患者獲得治療的機會。製藥公司一直在投資研發，以開發法布瑞氏症的新療法。這包括基因療法、伴侶療法和其他創新治療方案，擴大了市場。生物技術和藥物輸送方法的進步提高了法布瑞氏症治療的安全性和有效性，使其對患者和醫療保健提供者更具吸引力。

主要市場促進因素

市場概況
預測期 2024-2028
2022 年市場規模 186250萬美元
2028 年市場規模 268885萬美元
2023-2028 年CAGR 6.30%
成長最快的細分市場 網路藥局
最大的市場 北美洲

診斷的進步

目錄

第 1 章：產品概述

  • 市場定義
  • 市場範圍
    • 涵蓋的市場
    • 研究年份
    • 主要市場區隔

第 2 章：研究方法

  • 研究目的
  • 基線方法
  • 主要產業夥伴
  • 主要協會和二手資料來源
  • 預測方法
  • 數據三角測量與驗證
  • 假設和限制

第 3 章：執行摘要

  • 市場概況
  • 主要市場細分概述
  • 主要市場參與者概述
  • 重點地區/國家概況
  • 市場促進因素、挑戰、趨勢概述

第 4 章：客戶之聲

第 5 章：全球法布瑞氏症治療市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 依藥物分類（Agalsidase Beta、Migalastat 等）
    • 依治療方式（酵素替代療法 (ERT)、伴侶治療、底物減少療法 (SRT) 等）
    • 依給藥途徑（口服、腸胃外、其他）
    • 按配銷通路（醫院藥房、零售藥房、網路藥房）
    • 按地區
    • 按公司分類 (2022)
  • 市場地圖

第 6 章：亞太地區法布瑞氏症治療市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 按藥物分類
    • 按治療
    • 依給藥途徑
    • 按配銷通路
    • 按國家/地區
  • 亞太地區：國家分析
    • 中國法布瑞氏症治療
    • 印度法布瑞氏症治療
    • 澳洲法布瑞氏症治療
    • 日本法布瑞氏症治療
    • 韓國法布瑞氏症治療

第 7 章：歐洲法布瑞氏症治療市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 按藥物分類
    • 按治療
    • 依給藥途徑
    • 按配銷通路
    • 按國家/地區
  • 歐洲：國家分析
    • 法國
    • 德國
    • 西班牙
    • 義大利
    • 英國

第 8 章：北美法布瑞氏症治療市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 按藥物分類
    • 按治療
    • 依給藥途徑
    • 按配銷通路
    • 按國家/地區
  • 北美：國家分析
    • 美國
    • 墨西哥
    • 加拿大

第 9 章：南美洲法布瑞氏症治療市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 按藥物分類
    • 按治療
    • 依給藥途徑
    • 按配銷通路
    • 按國家/地區
  • 南美洲：國家分析
    • 巴西
    • 阿根廷
    • 哥倫比亞

第 10 章：中東和非洲法布瑞氏症治療市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 按藥物分類
    • 按治療
    • 依給藥途徑
    • 按配銷通路
    • 按國家/地區
  • MEA：國家分析
    • 南非法布里病治療
    • 沙烏地阿拉伯法布瑞氏症治療
    • 阿拉伯聯合大公國法布瑞氏症治療

第 11 章：市場動態

  • 促進要素
  • 挑戰

第 12 章：市場趨勢與發展

  • 最近的發展
  • 產品發布
  • 併購

第 13 章：全球法布瑞氏症治療市場：SWOT 分析

第 14 章：波特的五力分析

  • 產業競爭
  • 新進入者的潛力
  • 供應商的力量
  • 客戶的力量
  • 替代產品的威脅

第 15 章：大環境分析

第16章：競爭格局

  • 賽諾菲（健贊公司）
    • Business Overview
    • Company Snapshot
    • Products & Services
    • Financials (In case of listed companies)
    • Recent Developments
    • SWOT Analysis
  • 武田藥品工業株式會社
    • Business Overview
    • Company Snapshot
    • Products & Services
    • Financials (In case of listed companies)
    • Recent Developments
    • SWOT Analysis
  • Amicus 治療公司
    • Business Overview
    • Company Snapshot
    • Products & Services
    • Financials (In case of listed companies)
    • Recent Developments
    • SWOT Analysis
  • JCR製藥有限公司
    • Business Overview
    • Company Snapshot
    • Products & Services
    • Financials (In case of listed companies)
    • Recent Developments
    • SWOT Analysis
  • Protalix 生物治療公司
    • Business Overview
    • Company Snapshot
    • Products & Services
    • Financials (In case of listed companies)
    • Recent Developments
    • SWOT Analysis
  • 基耶西農莊公司
    • Business Overview
    • Company Snapshot
    • Products & Services
    • Financials (In case of listed companies)
    • Recent Developments
    • SWOT Analysis
  • Freeline 治療控股有限公司
    • Business Overview
    • Company Snapshot
    • Products & Services
    • Financials (In case of listed companies)
    • Recent Developments
    • SWOT Analysis
  • 宇瀚株式會社
    • Business Overview
    • Company Snapshot
    • Products & Services
    • Financials (In case of listed companies)
    • Recent Developments
    • SWOT Analysis
  • M6P 療法
    • Business Overview
    • Company Snapshot
    • Products & Services
    • Financials (In case of listed companies)
    • Recent Developments
    • SWOT Analysis
  • ISU Abxis 有限公司
    • Business Overview
    • Company Snapshot
    • Products & Services
    • Financials (In case of listed companies)
    • Recent Developments
    • SWOT Analysis

第 17 章：策略建議

第 18 章：關於我們與免責聲明

簡介目錄
Product Code: 18737

Global Fabry Disease Treatment Market has valued at USD 1862.50 million in 2022 and is anticipated to witness an impressive growth in the forecast period with a CAGR of 6.30% through 2028. Fabry disease, also known as Anderson-Fabry disease, is a rare and inherited genetic disorder that belongs to a group of conditions known as lysosomal storage disorders. This disease is caused by mutations in the GLA gene, which encodes an enzyme called alpha-galactosidase A (alpha-Gal A). The deficiency of this enzyme results in the accumulation of a specific type of fatty substance, known as globotriaosylceramide (Gb3 or GL-3), within cells throughout the body. This buildup of Gb3 primarily affects the cells of blood vessels, kidneys, heart, and nervous system, leading to a wide range of symptoms and complications. Symptoms of Fabry disease often appear in childhood or adolescence, although the age of symptom onset and their severity can vary widely among affected individuals. One of the hallmark symptoms of Fabry disease is neuropathic pain, which can be severe and chronic. This pain typically affects the extremities, such as the hands and feet, and is often described as burning or tingling.

Growing awareness among healthcare professionals, patients, and caregivers about Fabry disease has led to improved diagnosis rates. Increased awareness is a significant driver for the market, as early diagnosis is critical for initiating treatment. Advances in diagnostic tools and genetic testing have made it easier to identify Fabry disease, even in its early stages. Improved diagnostic capabilities have led to more cases being diagnosed and treated. Global healthcare expenditure has been increasing, allowing for greater investment in rare disease treatments like Fabry disease. Increased healthcare budgets have supported research and development efforts and improved patient access to treatments. Pharmaceutical companies have been investing in research and development to develop novel therapies for Fabry disease. This includes gene therapy, chaperone therapy, and other innovative treatment options, expanding the market. Advances in biotechnology and drug delivery methods have improved the safety and efficacy of Fabry disease treatments, making them more attractive to patients and healthcare providers.

Key Market Drivers

Market Overview
Forecast Period2024-2028
Market Size 2022USD 1862.50 Million
Market Size 2028USD 2688.85 Million
CAGR 2023-20286.30%
Fastest Growing SegmentOnline Pharmacies
Largest MarketNorth America

Advancements in Diagnosis

Genetic testing has become a cornerstone in the diagnosis of Fabry disease. Advances in genetic sequencing technology have made it more accessible and cost-effective to identify specific mutations in the GLA gene, which is responsible for the disease. Genetic testing can confirm the presence of Fabry disease and provide information about the specific genetic mutations involved. In some regions, newborn screening programs have been implemented to identify Fabry disease in infants shortly after birth. This early detection allows for prompt intervention and treatment, potentially preventing or delaying the onset of symptoms and organ damage. Researchers have been investigating biomarkers associated with Fabry disease. Biomarkers are measurable substances in the body that can indicate the presence of a disease or its progression. Biomarker research can aid in early diagnosis and monitoring the effectiveness of treatment. Clinical diagnostic criteria for Fabry disease have been refined and standardized. Healthcare professionals now have clearer guidelines and criteria to assist in diagnosing disease based on clinical symptoms and genetic testing results.

Advanced imaging techniques, such as magnetic resonance imaging (MRI) and echocardiography, can help visualize organ damage caused by Fabry disease. These non-invasive methods allow for the assessment of heart, kidney, and other organ involvement. Enzyme activity assays, which measure the activity of alpha-galactosidase A, the deficient enzyme in Fabry disease, have become more precise and widely available. These assays can confirm the enzyme deficiency in individuals suspected of having the disease. Telemedicine and telehealth technologies have expanded access to Fabry disease specialists, allowing patients to receive consultations and diagnostic evaluations remotely. This is especially important for individuals in underserved or remote areas. Collaboration among healthcare professionals, researchers, and patient advocacy groups on a global scale has facilitated the sharing of diagnostic knowledge and best practices, leading to more accurate and consistent diagnosis. Healthcare providers are increasingly educated about Fabry disease, leading to better recognition and diagnosis of the condition. Continuing medical education programs and resources have contributed to this improvement. Fabry disease patients and their families have become more informed and proactive in seeking a diagnosis. Online resources and patient advocacy groups have empowered individuals to advocate for their healthcare needs. This factor will help in the development of the Global Fabry Disease Treatment Market.

Rising Pharmaceutical Innovation

Pharmaceutical companies invest in research and development to create novel and more effective treatments for Fabry disease. These innovations can lead to therapies that are better at managing the disease, reducing symptoms, and improving the quality of life for patients. Pharmaceutical innovation leads to a broader range of treatment options for Fabry disease. This diversification of therapies allows healthcare providers and patients to choose the most appropriate treatment based on individual needs, preferences, and disease characteristics. Advancements in pharmaceutical research enable the development of targeted therapies. These treatments are designed to address the specific molecular and genetic mechanisms underlying Fabry disease. Targeted therapies can be more effective and have fewer side effects than traditional treatments. Pharmaceutical innovation supports the concept of personalized medicine, where treatments are tailored to an individual's genetic profile and disease characteristics. This approach can lead to more precise and effective treatments, optimizing patient outcomes. Innovations in drug delivery technology can enhance the convenience and effectiveness of Fabry disease treatments. For example, advancements in enzyme replacement therapy (ERT) delivery methods can make it easier for patients to receive treatment. Pharmaceutical research can lead to the development of therapies that require less frequent administration. This can improve patient adherence to treatment regimens and reduce the burden of frequent hospital visits.

Many pharmaceutical companies pursue orphan drug designations for Fabry disease treatments. These designations provide incentives and regulatory support for the development of treatments for rare diseases, increasing investment in this area. Pharmaceutical companies conduct clinical trials to test the safety and efficacy of new Fabry disease treatments. These trials provide valuable data on the benefits and risks of innovative therapies and help bring them to market. Competition among pharmaceutical companies can drive innovation by encouraging the development of new and improved Fabry disease treatments. This competition can lead to better treatment options and potentially lower costs for patients. As pharmaceutical companies expand their presence in global markets, access to Fabry disease treatments improves for patients in different regions, increasing demand for these therapies. Patient advocacy groups and organizations often collaborate with pharmaceutical companies in research and development efforts. This collaboration can accelerate the development and availability of innovative treatments. This factor will pace up the demand of the Global Fabry Disease Treatment Market.

Increasing Disease Awareness

Disease awareness campaigns educate healthcare providers and the public about Fabry disease, its symptoms, and risk factors. This knowledge can lead to earlier diagnosis, enabling patients to access treatment before the disease progresses to more severe stages. Improved awareness can help reduce delays in diagnosis. Fabry disease is often underdiagnosed or misdiagnosed because its symptoms can mimic other conditions. Increased awareness among healthcare professionals can lead to more accurate and timely diagnoses. When people become more aware of Fabry disease, they may seek medical advice and testing if they exhibit symptoms or have a family history of the disease. This can result in more individuals being tested for Fabry disease, potentially leading to earlier identification and treatment. Awareness campaigns are often driven by patient advocacy groups and organizations. These groups work to raise awareness about Fabry disease, support affected individuals, and advocate for better access to treatment and resources. Disease awareness initiatives often include educational programs for healthcare providers. These programs help physicians recognize the signs and symptoms of Fabry disease and consider it as a potential diagnosis when evaluating patients.

Disease awareness efforts provide patients and their families with accurate information about Fabry disease, available treatments, and support services. Informed patients are more likely to seek appropriate care and treatment options. Raising awareness can reduce the stigma associated with rare diseases like Fabry disease. This can encourage individuals to discuss their symptoms openly with healthcare providers and seek help without fear of judgment. Increased awareness can lead to greater interest from pharmaceutical companies and researchers in developing new and improved Fabry disease treatments. As the demand for treatments grows, so does the incentive for innovation in the field. Public awareness campaigns can garner support from policymakers and government agencies. This support can lead to increased funding for research, improved healthcare policies, and better access to treatment. Disease awareness is not limited by geographical boundaries. Global collaboration among healthcare organizations, advocacy groups, and researchers can further drive awareness and foster international efforts to combat Fabry disease. This factor will accelerate the demand of the Global Fabry Disease Treatment Market.

Key Market Challenges

Limited Patient Population

The small patient population with Fabry disease results in a limited market size for pharmaceutical companies. This can make it less economically attractive for these companies to invest in research and development of treatments for disease. Developing and gaining regulatory approval for new treatments, including clinical trials and research, is costly. In the case of rare diseases like Fabry disease, the small number of potential patients can make it challenging to recoup these expenses. Due to the small market size, the revenue potential for treatments for Fabry disease may be limited compared to drugs for more common conditions. This can affect the profitability of drug development efforts. Limited patient populations can result in challenges related to patient access to treatments and affordability. Even if effective treatments exist, they may not be accessible to all patients due to cost or availability. The rarity of Fabry disease can lead to delayed diagnosis or misdiagnosis, as healthcare providers may not be familiar with the condition. This can result in patients not receiving appropriate treatment until the disease has progressed. Limited patient populations can also result in a scarcity of clinical data on the disease and its treatment. This can make it challenging for healthcare providers to make informed treatment decisions. Recognizing the challenges posed by rare diseases, some regulatory agencies provide incentives for orphan drug development. These incentives can include extended market exclusivity and reduced regulatory fees.

Supply Chain Vulnerabilities

The primary treatment for Fabry disease involves enzyme replacement therapy, which can be costly. ERT drugs are typically administered intravenously every two weeks, and the cost of these treatments can accumulate significantly over time. Fabry disease is a chronic condition that requires lifelong treatment. The long-term nature of treatment can result in a substantial financial burden on patients and healthcare systems. Access to ERT and other Fabry disease treatments may be limited in some regions. Even when treatments are available, not all patients may have adequate insurance coverage to offset the costs, leading to disparities in access to care. Patients with Fabry disease often require ongoing medical care, including monitoring for complications in various organs (e.g., heart, kidneys) and managing associated symptoms. These additional healthcare expenses can further contribute to the overall cost of treatment. From a pharmaceutical industry perspective, developing and bringing Fabry disease treatments to market can be expensive due to the need for extensive research, clinical trials, and regulatory approvals. These costs can influence the pricing of therapies. Fabry disease is a rare condition, and the limited patient population can result in higher treatment costs per patient. Pharmaceutical companies may need to recover development costs from a smaller pool of patients, which can lead to higher drug prices. Many Fabry disease treatments receive orphan drug designation, which provides certain incentives to pharmaceutical companies but can also result in higher drug prices.

Key Market Trends

Biomarker Development

Biomarkers can aid in the early diagnosis of Fabry disease, allowing for timely intervention and treatment initiation. Early diagnosis is essential for preventing or delaying the onset of symptoms and organ damage. Biomarkers can be used to monitor disease progression and assess the effectiveness of treatment over time. This enables healthcare providers to tailor treatment plans to individual patients' needs. Certain biomarkers may be associated with the severity of Fabry disease. Identifying these biomarkers can help predict disease outcomes and guide treatment decisions. Biomarkers can help determine how well a patient is responding to treatment. If treatment is effective, biomarkers may show improvements in disease-related indicators. Biomarkers can serve as valuable endpoints in clinical trials of new Fabry disease treatments. They provide objective measures of treatment efficacy and safety. The development of biomarkers supports the concept of personalized medicine, where treatments are tailored to individual patients based on their biomarker profiles. This approach can optimize treatment outcomes. Biomarkers provide insights into the underlying molecular and genetic mechanisms of Fabry disease. This knowledge can inform drug development efforts, leading to more targeted and effective therapies. Biomarkers can be used to stratify Fabry disease patients into different subgroups based on disease characteristics. This stratification can guide treatment decisions and improve patient outcomes. Biomarkers can help reduce diagnostic delays by providing objective evidence of Fabry disease. This is particularly important because Fabry disease is often underdiagnosed or misdiagnosed.

Segmental Insights

Drugs Insights

In 2022, the Global Fabry Disease Treatment Market largest share was held by Agalsidase Beta segment and is predicted to continue expanding over the coming years. Agalsidase Beta has been available for Fabry disease treatment for an extended period. Its long history in the market has contributed to its recognition and use among healthcare providers. Clinical studies have demonstrated the efficacy of Agalsidase Beta in reducing symptoms and slowing the progression of Fabry disease. It works by replacing the deficient enzyme alpha-galactosidase A in patients with the condition. Many Fabry disease patients have received treatment with Agalsidase Beta and have reported positive outcomes, such as a reduction in pain, improved kidney function, and enhanced overall quality of life. Healthcare professionals, including specialists in Fabry disease, are familiar with Agalsidase Beta and its administration. Their experience with this therapy contributes to its continued use.

Treatment Insights

In 2022, the Global Fabry Disease Treatment Market largest share was held by Enzyme Replacement Therapy (ERT) segment and is predicted to continue expanding over the coming years. Enzyme Replacement Therapy (ERT) was one of the earliest and most established treatment options for Fabry disease. It has been used for many years to manage the symptoms and complications of the disease. ERT has demonstrated efficacy in stabilizing and improving the health of individuals with Fabry disease by replacing the deficient enzyme (alpha-galactosidase A). Clinical studies have shown that ERT can reduce pain, improve kidney function, and slow the progression of organ damage. Many Fabry disease patients have had positive experiences with ERT in terms of symptom relief and improved quality of life. This has contributed to its continued use and market dominance. Healthcare providers, particularly specialists in Fabry disease, have extensive experience with ERT. They are familiar with its administration and monitoring, making it a preferred choice for treatment.

Route of Administration Insights

In 2022, the Global Fabry Disease Treatment Market largest share was held by Oral segment and is predicted to continue expanding over the coming years. Oral medications are generally more convenient for patients compared to other routes of administration, such as intravenous (IV) infusions. Fabry disease patients may prefer oral treatments, as they can take these medications at home without the need for frequent hospital visits. Oral medications can enhance patient adherence to treatment regimens. Patients are more likely to consistently take oral medications as prescribed, which is crucial for managing a chronic condition like Fabry disease effectively. Advancements in drug development have led to the creation of oral medications that are effective in managing Fabry disease. These medications can stabilize and improve patients' health by addressing the underlying enzyme deficiency.

Distribution Channel Insights

In 2022, the Global Fabry Disease Treatment Market largest share was held by Hospital Pharmacies segment in the forecast period and is predicted to continue expanding over the coming years. Fabry disease is a rare genetic disorder that requires specialized medications, such as enzyme replacement therapy (ERT), for treatment. These medications are typically administered under the supervision of healthcare professionals in hospital settings. Hospital pharmacies are well-equipped to handle the storage, preparation, and administration of these specialized drugs. Patients with Fabry disease often require close monitoring of their treatment and health status. Hospitals have the resources and expertise to provide comprehensive patient care and monitor treatment efficacy, including managing potential side effects or complications. Fabry disease patients are typically under the care of specialized physicians, such as geneticists or metabolic disease specialists, who work closely with hospital-based healthcare teams. Hospital pharmacies are integrated into the healthcare system, facilitating collaboration among healthcare professionals to ensure optimal patient care.

Regional Insights

The North America region dominates the Global Fabry Disease Treatment Market in 2022. North America, particularly the United States and Canada, has a well-developed and advanced healthcare infrastructure. This infrastructure includes a network of hospitals, clinics, and research institutions with access to cutting-edge medical technology and expertise. North America has a relatively high level of awareness about rare diseases, including Fabry disease. Healthcare providers in the region are more likely to recognize and diagnose rare diseases, which can lead to earlier treatment and better outcomes. North America is a hub for clinical research and pharmaceutical development. Many clinical trials for Fabry disease treatments are conducted in the region, attracting global pharmaceutical companies and researchers. The United States has a well-established regulatory framework for drug approvals through the Food and Drug Administration (FDA). This facilitates the development and approval of Fabry disease treatments, making them available to patients more quickly.

Key Market Players

Sanofi (Genzyme Corporation)

Takeda Pharmaceutical Company Limited

Amicus Therapeutics, Inc

ISU ABXIS Co Ltd.

JCR Pharmaceuticals Co., Ltd.

Protalix BioTherapeutics Inc.

Chiesi Farmaceutici S.p.A.

Freeline Therapeutics Holdings PLC

Yuhan Corporation

M6P Therapeutics

Report Scope:

In this report, the Global Fabry Disease Treatment Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:

Fabry Disease Treatment Market, By Drugs:

  • Agalsidase Beta
  • Migalastat
  • others

Fabry Disease Treatment Market, By Treatment:

  • Enzyme Replacement Therapy (ERT)
  • Chaperone Treatment
  • Substrate Reduction Therapy (SRT)
  • Others

Fabry Disease Treatment Market, By Route of Administration:

  • Oral
  • Parenteral
  • Others

Fabry Disease Treatment Market, By Distribution Channel:

  • Hospital pharmacies
  • Retail pharmacies
  • Online Pharmacies

Global Fabry Disease Treatment Market, By region:

  • North America
  • United States
  • Canada
  • Mexico
  • Asia-Pacific
  • China
  • India
  • South Korea
  • Australia
  • Japan
  • Europe
  • Germany
  • France
  • United Kingdom
  • Spain
  • Italy
  • South America
  • Brazil
  • Argentina
  • Colombia
  • Middle East & Africa
  • South Africa
  • Saudi Arabia
  • UAE

Competitive Landscape

  • Company Profiles: Detailed analysis of the major companies present in the Global Fabry Disease Treatment Market.

Available Customizations:

  • Global Fabry Disease Treatment Market report with the given market data, Tech Sci Research offers customizations according to a company's specific needs. The following customization options are available for the report:

Company Information

  • Detailed analysis and profiling of additional market players (up to five).

Table of Contents

1. Product Overview

  • 1.1. Market Definition
  • 1.2. Scope of the Market
    • 1.2.1. Markets Covered
    • 1.2.2. Years Considered for Study
    • 1.2.3. Key Market Segmentations

2. Research Methodology

  • 2.1. Objective of the Study
  • 2.2. Baseline Methodology
  • 2.3. Key Industry Partners
  • 2.4. Major Association and Secondary Sources
  • 2.5. Forecasting Methodology
  • 2.6. Data Triangulation & Validation
  • 2.7. Assumptions and Limitations

3. Executive Summary

  • 3.1. Overview of the Market
  • 3.2. Overview of Key Market Segmentations
  • 3.3. Overview of Key Market Players
  • 3.4. Overview of Key Regions/Countries
  • 3.5. Overview of Market Drivers, Challenges, Trends

4. Voice of Customer

5. Global Fabry Disease Treatment Market Outlook

  • 5.1. Market Size & Forecast
    • 5.1.1. By Value
  • 5.2. Market Share & Forecast
    • 5.2.1. By Drugs (Agalsidase Beta, Migalastat, others)
    • 5.2.2. By Treatment (Enzyme Replacement Therapy (ERT), Chaperone Treatment, Substrate Reduction Therapy (SRT), others)
    • 5.2.3. By Route of Administration (Oral, Parenteral, others)
    • 5.2.4. By Distribution Channel (Hospital pharmacies, Retail pharmacies, Online Pharmacies)
    • 5.2.5. By Region
    • 5.2.6. By Company (2022)
  • 5.3. Market Map

6. Asia Pacific Fabry Disease Treatment Market Outlook

  • 6.1. Market Size & Forecast
    • 6.1.1. By Value
  • 6.2. Market Share & Forecast
    • 6.2.1. By Drugs
    • 6.2.2. By Treatment
    • 6.2.3. By Route of Administration
    • 6.2.4. By Distribution Channel
    • 6.2.5. By Country
  • 6.3. Asia Pacific: Country Analysis
    • 6.3.1. China Fabry Disease Treatment Market Outlook
      • 6.3.1.1. Market Size & Forecast
        • 6.3.1.1.1. By Value
      • 6.3.1.2. Market Share & Forecast
        • 6.3.1.2.1. By Drugs
        • 6.3.1.2.2. By Treatment
        • 6.3.1.2.3. By Route of Administration
        • 6.3.1.2.4. By Distribution Channel
    • 6.3.2. India Fabry Disease Treatment Market Outlook
      • 6.3.2.1. Market Size & Forecast
        • 6.3.2.1.1. By Value
      • 6.3.2.2. Market Share & Forecast
        • 6.3.2.2.1. By Drugs
        • 6.3.2.2.2. By Treatment
        • 6.3.2.2.3. By Route of Administration
        • 6.3.2.2.4. By Distribution Channel
    • 6.3.3. Australia Fabry Disease Treatment Market Outlook
      • 6.3.3.1. Market Size & Forecast
        • 6.3.3.1.1. By Value
      • 6.3.3.2. Market Share & Forecast
        • 6.3.3.2.1. By Drugs
        • 6.3.3.2.2. By Treatment
        • 6.3.3.2.3. By Route of Administration
        • 6.3.3.2.4. By Distribution Channel
    • 6.3.4. Japan Fabry Disease Treatment Market Outlook
      • 6.3.4.1. Market Size & Forecast
        • 6.3.4.1.1. By Value
      • 6.3.4.2. Market Share & Forecast
        • 6.3.4.2.1. By Drugs
        • 6.3.4.2.2. By Treatment
        • 6.3.4.2.3. By Route of Administration
        • 6.3.4.2.4. By Distribution Channel
    • 6.3.5. South Korea Fabry Disease Treatment Market Outlook
      • 6.3.5.1. Market Size & Forecast
        • 6.3.5.1.1. By Value
      • 6.3.5.2. Market Share & Forecast
        • 6.3.5.2.1. By Drugs
        • 6.3.5.2.2. By Treatment
        • 6.3.5.2.3. By Route of Administration
        • 6.3.5.2.4. By Distribution Channel

7. Europe Fabry Disease Treatment Market Outlook

  • 7.1. Market Size & Forecast
    • 7.1.1. By Value
  • 7.2. Market Share & Forecast
    • 7.2.1. By Drugs
    • 7.2.2. By Treatment
    • 7.2.3. By Route of Administration
    • 7.2.4. By Distribution Channel
    • 7.2.5. By Country
  • 7.3. Europe: Country Analysis
    • 7.3.1. France Fabry Disease Treatment Market Outlook
      • 7.3.1.1. Market Size & Forecast
        • 7.3.1.1.1. By Value
      • 7.3.1.2. Market Share & Forecast
        • 7.3.1.2.1. By Drugs
        • 7.3.1.2.2. By Treatment
        • 7.3.1.2.3. By Route of Administration
        • 7.3.1.2.4. By Distribution Channel
    • 7.3.2. Germany Fabry Disease Treatment Market Outlook
      • 7.3.2.1. Market Size & Forecast
        • 7.3.2.1.1. By Value
      • 7.3.2.2. Market Share & Forecast
        • 7.3.2.2.1. By Drugs
        • 7.3.2.2.2. By Treatment
        • 7.3.2.2.3. By Route of Administration
        • 7.3.2.2.4. By Distribution Channel
    • 7.3.3. Spain Fabry Disease Treatment Market Outlook
      • 7.3.3.1. Market Size & Forecast
        • 7.3.3.1.1. By Value
      • 7.3.3.2. Market Share & Forecast
        • 7.3.3.2.1. By Drugs
        • 7.3.3.2.2. By Treatment
        • 7.3.3.2.3. By Route of Administration
        • 7.3.3.2.4. By Distribution Channel
    • 7.3.4. Italy Fabry Disease Treatment Market Outlook
      • 7.3.4.1. Market Size & Forecast
        • 7.3.4.1.1. By Value
      • 7.3.4.2. Market Share & Forecast
        • 7.3.4.2.1. By Drugs
        • 7.3.4.2.2. By Treatment
        • 7.3.4.2.3. By Route of Administration
        • 7.3.4.2.4. By Distribution Channel
    • 7.3.5. United Kingdom Fabry Disease Treatment Market Outlook
      • 7.3.5.1. Market Size & Forecast
        • 7.3.5.1.1. By Value
      • 7.3.5.2. Market Share & Forecast
        • 7.3.5.2.1. By Drugs
        • 7.3.5.2.2. By Treatment
        • 7.3.5.2.3. By Route of Administration
        • 7.3.5.2.4. By Distribution Channel

8. North America Fabry Disease Treatment Market Outlook

  • 8.1. Market Size & Forecast
    • 8.1.1. By Value
  • 8.2. Market Share & Forecast
    • 8.2.1. By Drugs
    • 8.2.2. By Treatment
    • 8.2.3. By Route of Administration
    • 8.2.4. By Distribution Channel
    • 8.2.5. By Country
  • 8.3. North America: Country Analysis
    • 8.3.1. United States Fabry Disease Treatment Market Outlook
      • 8.3.1.1. Market Size & Forecast
        • 8.3.1.1.1. By Value
      • 8.3.1.2. Market Share & Forecast
        • 8.3.1.2.1. By Drugs
        • 8.3.1.2.2. By Treatment
        • 8.3.1.2.3. By Route of Administration
        • 8.3.1.2.4. By Distribution Channel
    • 8.3.2. Mexico Fabry Disease Treatment Market Outlook
      • 8.3.2.1. Market Size & Forecast
        • 8.3.2.1.1. By Value
      • 8.3.2.2. Market Share & Forecast
        • 8.3.2.2.1. By Drugs
        • 8.3.2.2.2. By Treatment
        • 8.3.2.2.3. By Route of Administration
        • 8.3.2.2.4. By Distribution Channel
    • 8.3.3. Canada Fabry Disease Treatment Market Outlook
      • 8.3.3.1. Market Size & Forecast
        • 8.3.3.1.1. By Value
      • 8.3.3.2. Market Share & Forecast
        • 8.3.3.2.1. By Drugs
        • 8.3.3.2.2. By Treatment
        • 8.3.3.2.3. By Route of Administration
        • 8.3.3.2.4. By Distribution Channel

9. South America Fabry Disease Treatment Market Outlook

  • 9.1. Market Size & Forecast
    • 9.1.1. By Value
  • 9.2. Market Share & Forecast
    • 9.2.1. By Drugs
    • 9.2.2. By Treatment
    • 9.2.3. By Route of Administration
    • 9.2.4. By Distribution Channel
    • 9.2.5. By Country
  • 9.3. South America: Country Analysis
    • 9.3.1. Brazil Fabry Disease Treatment Market Outlook
      • 9.3.1.1. Market Size & Forecast
        • 9.3.1.1.1. By Value
      • 9.3.1.2. Market Share & Forecast
        • 9.3.1.2.1. By Drugs
        • 9.3.1.2.2. By Treatment
        • 9.3.1.2.3. By Route of Administration
        • 9.3.1.2.4. By Distribution Channel
    • 9.3.2. Argentina Fabry Disease Treatment Market Outlook
      • 9.3.2.1. Market Size & Forecast
        • 9.3.2.1.1. By Value
      • 9.3.2.2. Market Share & Forecast
        • 9.3.2.2.1. By Drugs
        • 9.3.2.2.2. By Treatment
        • 9.3.2.2.3. By Route of Administration
        • 9.3.2.2.4. By Distribution Channel
    • 9.3.3. Colombia Fabry Disease Treatment Market Outlook
      • 9.3.3.1. Market Size & Forecast
        • 9.3.3.1.1. By Value
      • 9.3.3.2. Market Share & Forecast
        • 9.3.3.2.1. By Drugs
        • 9.3.3.2.2. By Treatment
        • 9.3.3.2.3. By Route of Administration
        • 9.3.3.2.4. By Distribution Channel

10. Middle East and Africa Fabry Disease Treatment Market Outlook

  • 10.1. Market Size & Forecast
    • 10.1.1. By Value
  • 10.2. Market Share & Forecast
    • 10.2.1. By Drugs
    • 10.2.2. By Treatment
    • 10.2.3. By Route of Administration
    • 10.2.4. By Distribution Channel
    • 10.2.5. By Country
  • 10.3. MEA: Country Analysis
    • 10.3.1. South Africa Fabry Disease Treatment Market Outlook
      • 10.3.1.1. Market Size & Forecast
        • 10.3.1.1.1. By Value
      • 10.3.1.2. Market Share & Forecast
        • 10.3.1.2.1. By Drugs
        • 10.3.1.2.2. By Treatment
        • 10.3.1.2.3. By Route of Administration
        • 10.3.1.2.4. By Distribution Channel
    • 10.3.2. Saudi Arabia Fabry Disease Treatment Market Outlook
      • 10.3.2.1. Market Size & Forecast
        • 10.3.2.1.1. By Value
      • 10.3.2.2. Market Share & Forecast
        • 10.3.2.2.1. By Drugs
        • 10.3.2.2.2. By Treatment
        • 10.3.2.2.3. By Route of Administration
        • 10.3.2.2.4. By Distribution Channel
    • 10.3.3. UAE Fabry Disease Treatment Market Outlook
      • 10.3.3.1. Market Size & Forecast
        • 10.3.3.1.1. By Value
      • 10.3.3.2. Market Share & Forecast
        • 10.3.3.2.1. By Drugs
        • 10.3.3.2.2. By Treatment
        • 10.3.3.2.3. By Route of Administration
        • 10.3.3.2.4. By Distribution Channel

11. Market Dynamics

  • 11.1. Drivers
  • 11.2. Challenges

12. Market Trends & Developments

  • 12.1. Recent Developments
  • 12.2. Product Launches
  • 12.3. Mergers & Acquisitions

13. Global Fabry Disease Treatment Market: SWOT Analysis

14. Porter's Five Forces Analysis

  • 14.1. Competition in the Industry
  • 14.2. Potential of New Entrants
  • 14.3. Power of Suppliers
  • 14.4. Power of Customers
  • 14.5. Threat of Substitute Product

15. PESTLE Analysis

16. Competitive Landscape

  • 16.1. Sanofi (Genzyme Corporation)
    • 16.1.1. Business Overview
    • 16.1.2. Company Snapshot
    • 16.1.3. Products & Services
    • 16.1.4. Financials (In case of listed companies)
    • 16.1.5. Recent Developments
    • 16.1.6. SWOT Analysis
  • 16.2. Takeda Pharmaceutical Company Limited
    • 16.2.1. Business Overview
    • 16.2.2. Company Snapshot
    • 16.2.3. Products & Services
    • 16.2.4. Financials (In case of listed companies)
    • 16.2.5. Recent Developments
    • 16.2.6. SWOT Analysis
  • 16.3. Amicus Therapeutics, Inc
    • 16.3.1. Business Overview
    • 16.3.2. Company Snapshot
    • 16.3.3. Products & Services
    • 16.3.4. Financials (In case of listed companies)
    • 16.3.5. Recent Developments
    • 16.3.6. SWOT Analysis
  • 16.4. JCR Pharmaceuticals Co., Ltd.
    • 16.4.1. Business Overview
    • 16.4.2. Company Snapshot
    • 16.4.3. Products & Services
    • 16.4.4. Financials (In case of listed companies)
    • 16.4.5. Recent Developments
    • 16.4.6. SWOT Analysis
  • 16.5. Protalix BioTherapeutics Inc.
    • 16.5.1. Business Overview
    • 16.5.2. Company Snapshot
    • 16.5.3. Products & Services
    • 16.5.4. Financials (In case of listed companies)
    • 16.5.5. Recent Developments
    • 16.5.6. SWOT Analysis
  • 16.6. Chiesi Farmaceutici S.p.A.
    • 16.6.1. Business Overview
    • 16.6.2. Company Snapshot
    • 16.6.3. Products & Services
    • 16.6.4. Financials (In case of listed companies)
    • 16.6.5. Recent Developments
    • 16.6.6. SWOT Analysis
  • 16.7. Freeline Therapeutics Holdings PLC
    • 16.7.1. Business Overview
    • 16.7.2. Company Snapshot
    • 16.7.3. Products & Services
    • 16.7.4. Financials (In case of listed companies)
    • 16.7.5. Recent Developments
    • 16.7.6. SWOT Analysis
  • 16.8. Yuhan Corporation
    • 16.8.1. Business Overview
    • 16.8.2. Company Snapshot
    • 16.8.3. Products & Services
    • 16.8.4. Financials (In case of listed companies)
    • 16.8.5. Recent Developments
    • 16.8.6. SWOT Analysis
  • 16.9. M6P Therapeutics
    • 16.9.1. Business Overview
    • 16.9.2. Company Snapshot
    • 16.9.3. Products & Services
    • 16.9.4. Financials (In case of listed companies)
    • 16.9.5. Recent Developments
    • 16.9.6. SWOT Analysis
  • 16.10. ISU Abxis Co Ltd
    • 16.10.1. Business Overview
    • 16.10.2. Company Snapshot
    • 16.10.3. Products & Services
    • 16.10.4. Financials (In case of listed companies)
    • 16.10.5. Recent Developments
    • 16.10.6. SWOT Analysis

17. Strategic Recommendations

18. About Us & Disclaimer