市场调查报告书
商品编码
1451738
2024-2032 年按类型(1 型、2 型等)、诊断和治疗(诊断、治疗)、最终用户(医院、家庭护理、专科诊所等)和地区分類的法布瑞氏症市场报告Fabry Disease Market Report by Type (Type 1, Type 2, and Others), Diagnosis and Treatment (Diagnosis, Treatment), End User (Hospitals, Homecare, Specialty Clinics, and Others), and Region 2024-2032 |
2023年,全球法布瑞氏症市场规模达到20亿美元。展望未来, IMARC Group预计到2032年市场规模将达到36亿美元,2024-2032年复合年增长率(CAGR)为6.34%。患有法布瑞氏症的患者数量不断增加,以及对遗传和酵素替代疗法等有效新疗法的需求不断增加,是推动市场发展的一些关键因素。
法布瑞氏症或α 半乳糖苷酶A 缺乏症是一种严重的X 连锁溶小体遗传性疾病,由缺乏代谢各种脂质储存和脂肪样成分(包括油、脂肪酸和蜡)所需的酶引起。如果不及时诊断或治疗,可能会导致血管和组织阻塞、进行性肾衰竭、神经损伤,甚至中风。目前,法布瑞氏症可以在酵素替代疗法(ERT)和辅助疗法的支持下进行治疗。除此之外,还可以透过基因、血液、肠外检查进一步确诊,抑制肾臟、心臟问题的发生。这些方法可防止发生一级和二级併发症的风险,并纠正潜在的酵素缺乏症。因此,医院和专科诊所广泛利用各种程序来及时诊断和有效治疗法布瑞氏症。
患有法布瑞氏症的患者数量不断增加,以及对精确有效疗法的需求不断增加,例如遗传、酵素替代底物减少和稳定个体免受疾病影响的伴侣治疗,是推动市场成长的主要动力。与此一致的是,对用于疾病治疗的口服药物和胶囊的需求不断增长是另一个增长诱导因素。此外,监管机构为投资医疗保健产业以设计突破性疾病治疗方案所采取的有利措施正在支持市场成长。此外,重大技术进步,例如用于诊断和治疗法布瑞氏症的远距医疗解决方案和家庭护理设置的引入,有利于市场成长。人们对该疾病的认识不断提高,也大大推动了市场的发展。医生和个人对早期诊断和多种预防措施的可用性的认识不断增强,这有助于市场的成长。老年人口不断增加,容易患任何慢性病,这是推动市场成长的另一个因素。其他因素,例如医疗保健基础设施的显着改善、对遗传疾病疗法进步的更加关注以及扩大治疗和药物组合的持续研发(R&D)活动,正在为市场创造积极的前景。
The global fabry disease market size reached US$ 2.0 Billion in 2023. Looking forward, IMARC Group expects the market to reach US$ 3.6 Billion by 2032, exhibiting a growth rate (CAGR) of 6.34% during 2024-2032. The increasing number of patients suffering from fabry disease and the escalating need for effective novel therapies, such as genetic and enzyme replacement therapy, represent some of the key factors driving the market.
Fabry disease, or alpha galactosidase-A deficiency, represents a severe x-linked lysosomal inherited disorder that is caused by the lack of enzymes that are required to metabolize various lipid storage and fat-like components, including oils, fatty acids, and waxes. If left undiagnosed or untreated, it might result in clogging of blood vessels and tissue, progressive kidney failures, nerve damage, and even strokes. Currently, fabry disease can be treated with the support of enzyme replacement therapies (ERT) and adjunct therapy. Apart from this, it can be further diagnosed through genetic, blood, and parenteral examinations to inhibit the occurrence of kidney and heart problems. These approaches prevent the risk of developing first and second-level complications and correct underlying enzyme deficiency. Consequently, hospitals and specialty clinics widely utilize various procedures for the timely diagnosis and effective treatment of the Fabry disease.
The increasing number of patients suffering from fabry disease and the escalating need for precise and effective therapies, such as genetic, enzyme replacement substrate reduction, and chaperone treatments to stabilize individuals from suffering disease, are primarily driving the market growth. In line with this, the rising demand for orally administered medications and capsule for disease treatment is acting as another growth-inducing factor. Additionally, the favorable initiatives being undertaken by regulatory bodies to invest in the healthcare sector for the designing of breakthrough disease treatment options are supporting the market growth. Moreover, significant technological advancements, such as the introduction of telemedicine solutions and home care settings for the diagnosis and treatment of Fabry disease, are favoring the market growth. The market is also significantly driven by the rising awareness regarding the disease. There is an increasing consciousness regarding the availability of early-stage diagnosis and multiple preventive measures amongst physicians and individuals, which is contributing to the market growth. The steadily increasing geriatric population, which is susceptible to any kind of chronic ailments, is another factor contributing to the market growth. Other factors, such as significant improvements in the healthcare infrastructure, an enhanced focus on the advancement of the genetic disease therapies, and continuous research and development (R&D) activities to expand treatment and medication portfolios, are creating a positive outlook for the market.
IMARC Group provides an analysis of the key trends in each segment of the global fabry disease market, along with forecasts at the global, regional, and country level from 2024-2032. Our report has categorized the market based on type, diagnosis and treatment, and end user.
Type 1
Type 2
Others
The report has also provided a detailed breakup and analysis of the fabry disease market based on the type. This includes Type 1, Type 2 and others.
Diagnosis
Blood Test
Genetic Test
Parenteral Test
Others
Treatment
Enzyme Replacement Therapy
Oral Therapy
Adjunct Therapy
Others
A detailed breakup and analysis of the fabry disease market based on the diagnosis and treatment has also been provided in the report. This includes diagnosis (blood test, genetic test, parental test, and others) and treatment (enzyme replacement therapy, oral therapy, adjunct therapy, and others).
Hospitals
Homecare
Specialty Clinics
Others
A detailed breakup and analysis of the fabry disease market based on the end user has also been provided in the report. This includes hospitals, homecare, specialty clinics and others. According to the report, specialty clinics accounted for the largest market share.
North America
United States
Canada
Asia Pacific
China
Japan
India
South Korea
Australia
Indonesia
Others
Europe
Germany
France
United Kingdom
Italy
Spain
Russia
Others
Latin America
Brazil
Mexico
Others
Middle East and Africa
The report has also provided a comprehensive analysis of all the major regional markets that include North America (the United States and Canada); Asia Pacific (China, Japan, India, South Korea, Australia, Indonesia, and others); Europe (Germany, France, the United Kingdom, Italy, Spain, Russia, and others); Latin America (Brazil, Mexico, and others); and Middle East and Africa. According to the report, North America was the largest market for Fabry disease. Some of the factors driving the North America fabry disease market included the increasing prevalence of fabry disease and the ongoing approvals of advanced therapeutics by regional governments for the disorder treatment.
The report has also provided a comprehensive analysis of the competitive landscape in the global fabry disease market. Detailed profiles of all major companies have also been provided. Some of the companies covered include Amicus Therapeutics, Freeline, Idorsia Pharmaceuticals Ltd, JCR Pharmaceuticals Co. Ltd, Protalix BioTherapeutics, Sangamo Therapeutics Inc., etc. Kindly note that this only represents a partial list of companies, and the complete list has been provided in the report.
Kindly, note that this only represents a partial list of companies, and the complete list has been provided in the report.