市場調查報告書
商品編碼
1451738
2024-2032 年按類型(1 型、2 型等)、診斷和治療(診斷、治療)、最終用戶(醫院、家庭護理、專科診所等)和地區分類的法布瑞氏症市場報告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,全球法布瑞氏症市場規模達到20億美元。展望未來, IMARC Group預計到2032年市場規模將達到36億美元,2024-2032年複合年成長率(CAGR)為6.34%。患有法布瑞氏症的患者數量不斷增加,以及對遺傳和酵素替代療法等有效新療法的需求不斷增加,是推動市場發展的一些關鍵因素。
法布瑞氏症或α 半乳糖苷酶A 缺乏症是一種嚴重的X 連鎖溶小體遺傳性疾病,由缺乏代謝各種脂質儲存和脂肪樣成分(包括油、脂肪酸和蠟)所需的酶引起。如果不及時診斷或治療,可能會導致血管和組織阻塞、進行性腎衰竭、神經損傷,甚至中風。目前,法布瑞氏症可以在酵素替代療法(ERT)和輔助療法的支持下進行治療。除此之外,還可以透過基因、血液、腸外檢查進一步確診,抑制腎臟、心臟問題的發生。這些方法可防止發生一級和二級併發症的風險,並糾正潛在的酵素缺乏症。因此,醫院和專科診所廣泛利用各種程序來及時診斷和有效治療法布瑞氏症。
患有法布瑞氏症的患者數量不斷增加,以及對精確有效療法的需求不斷增加,例如遺傳、酵素替代底物減少和穩定個體免受疾病影響的伴侶治療,是推動市場成長的主要動力。與此一致的是,對用於疾病治療的口服藥物和膠囊的需求不斷成長是另一個成長誘導因素。此外,監管機構為投資醫療保健產業以設計突破性疾病治療方案所採取的有利措施正在支持市場成長。此外,重大技術進步,例如用於診斷和治療法布瑞氏症的遠距醫療解決方案和家庭護理設置的引入,有利於市場成長。人們對該疾病的認知不斷提高,也大大推動了市場的發展。醫生和個人對早期診斷和多種預防措施的可用性的認知不斷增強,這有助於市場的成長。老年人口不斷增加,容易患任何慢性病,這是推動市場成長的另一個因素。其他因素,例如醫療保健基礎設施的顯著改善、對遺傳疾病療法進步的更加關注以及擴大治療和藥物組合的持續研發(R&D)活動,正在為市場創造積極的前景。
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.