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ファブリー病市場レポート:タイプ別、診断・治療別、エンドユーザー別、地域別、2024-2032Fabry 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 |
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ファブリー病市場レポート:タイプ別、診断・治療別、エンドユーザー別、地域別、2024-2032 |
出版日: 2024年03月02日
発行: IMARC
ページ情報: 英文 148 Pages
納期: 2~3営業日
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世界のファブリー病市場規模は2023年に20億米ドルに達しました。今後、IMARC Groupは、2024年から2032年にかけて6.34%の成長率(CAGR)を示し、市場は2032年までに36億米ドルに達すると予測しています。ファブリー病に罹患する患者数の増加と、遺伝子治療や酵素補充療法などの効果的な新規治療に対するニーズの高まりが、市場を牽引する主な要因の一つです。
ファブリー病(αガラクトシダーゼA欠損症)は、重度のx連鎖性リソソーム遺伝性疾患であり、油、脂肪酸、ワックスなど様々な脂質貯蔵成分や脂肪様成分の代謝に必要な酵素の欠乏によって引き起こされます。診断されないまま、あるいは治療されないまま放置されると、血管や組織の詰まり、進行性の腎不全、神経障害、さらには脳卒中を引き起こす可能性があります。現在、ファブリー病は酵素補充療法(ERT)と補助療法によって治療することができます。これとは別に、腎臓や心臓の問題の発生を抑制するために、遺伝子検査、血液検査、非経口検査によってさらに診断することができます。これらのアプローチにより、第一および第二レベルの合併症の発症リスクを防ぎ、根本的な酵素欠乏症を改善することができます。その結果、病院や専門クリニックでは、ファブリー病のタイムリーな診断と効果的な治療のために様々な手技が広く活用されています。
ファブリー病に罹患する患者数の増加と、罹患者を安定させるための遺伝子治療、酵素補充基質減少治療、シャペロン治療などの精密かつ効果的な治療に対するニーズの高まりが、主に市場成長の原動力となっています。これに伴い、疾患治療のための経口投与薬やカプセルの需要が高まっていることも、成長を促す要因となっています。さらに、画期的な疾患治療の選択肢を設計するためにヘルスケア部門に投資する規制機関によって行われている有利なイニシアチブが、市場の成長を支えています。さらに、ファブリー病の診断と治療のための遠隔医療ソリューションや在宅ケア環境の導入など、著しい技術進歩が市場成長を後押ししています。また、ファブリー病に関する意識の高まりも市場を大きく牽引しています。医師や個人の間で、早期診断や複数の予防策が利用可能であるという意識が高まっており、これが市場成長に寄与しています。あらゆる種類の慢性疾患にかかりやすい老年人口が着実に増加していることも、市場成長に寄与している要因です。その他の要因としては、ヘルスケアインフラの大幅な改善、遺伝性疾患治療の進歩に対する重点的な取り組み強化、治療・投薬ポートフォリオを拡充するための継続的な研究開発活動などが挙げられ、市場の明るい見通しを生み出しています。
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.