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後天性希少血液疾患治療市場レポート:治療法、疾患適応症、流通チャネル、地域別、2024-2032Acquired Orphan Blood Diseases Therapeutics Market Report by Therapy, Disease Indication, Distribution Channel, and Region 2024-2032 |
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後天性希少血液疾患治療市場レポート:治療法、疾患適応症、流通チャネル、地域別、2024-2032 |
出版日: 2024年03月02日
発行: IMARC
ページ情報: 英文 143 Pages
納期: 2~3営業日
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後天性希少血液疾患治療の世界市場規模は2023年に88億米ドルに達しました。今後、IMARC Groupは、市場は2032年までに172億米ドルに達し、2024年から2032年の間に7.5%の成長率(CAGR)を示すと予測しています。個人における血液関連疾患の有病率の増加、政府の積極的な取り組み、世界のヘルスケアインフラの改善が、市場を牽引する主な要因のひとつです。
後天性希少血液疾患は、赤血球(RBC)の産生不能または血液中の赤血球の不足によって引き起こされる稀な血液疾患です。骨髄異形成症候群(MDS)、特発性血小板減少性紫斑病(ITP)、発作性夜間ヘモグロビン尿症(PNH)、骨髄線維症(MF)、真性多血症(PV)、後天性無顆粒球症など、数多くの疾患が含まれます。これらは骨髄の不適切な機能を引き起こし、血小板の数を減少させます。これらの疾患は、遺伝子組換え因子製剤、免疫グロブリン注入療法、活性化プロトロンビン複合体濃縮製剤、トロンボポエチン受容体作動薬など、いくつかの治療法で治療できるため、後天性希少血液疾患治療の需要は世界中で高まっています。
現在、大衆の間で血液疾患とその治療法に関する認識が高まっており、世界的に個人の所得水準が上昇していることが、市場にプラスの影響を与える主な要因の1つとなっています。さらに、老年人口の増加による血液疾患治療薬の選択肢に対する需要の高まりが、市場の成長を強化しています。これに伴い、様々な国の行政機関や民間団体が、血液関連疾患の発生に関する認識を個人に広めることで血液疾患治療薬の採用を奨励しており、世界中で様々なヘルスケアイニシアチブを提供していることが、市場の成長を後押ししています。これとは別に、世界中の個人の間で様々な血液関連疾患の有病率が増加しているため、血液疾患治療薬の採用が増加しており、市場の見通しが明るくなっています。さらに、世界中のオンラインおよびオフラインの薬局店を通じて後天性希少血液疾患治療が広く入手可能であることも、市場の成長に寄与しています。これに加えて、世界のヘルスケアインフラの改善とともに、個人の間で個別化された医薬品に対する需要が高まっていることも、業界の投資家に有利な成長機会を提供しています。これに加えて、世界中の個人の間で費用対効果が高く質の高いケアソリューションに対する需要が高まっています。このことは、個人の間で蔓延する疾病を回避するための予防ケアやウェルネス・サービスの採用が増加していることと相まって、市場の成長を後押ししています。さらに、主要メーカーは鎌状赤血球貧血の小児患者向けにヒドロキシ尿素ベースの治療を導入しており、これが市場の成長を支えています。
The global acquired orphan blood diseases therapeutics market size reached US$ 8.8 Billion in 2023. Looking forward, IMARC Group expects the market to reach US$ 17.2 Billion by 2032, exhibiting a growth rate (CAGR) of 7.5% during 2024-2032. The growing prevalence of blood-related disorders among individuals, favorable government initiatives, and improving healthcare infrastructure worldwide represent some of the key factors driving the market.
Acquired orphan blood diseases are rare blood conditions that are caused by an inability to produce red blood cells (RBCs) or their insufficiency in the blood. They comprise numerous diseases, such as myelodysplastic syndrome (MDS), idiopathic thrombocytopenic purpura (ITP), paroxysmal nocturnal hemoglobinuria (PNH), myelofibrosis (MF), polycythemia vera (PV), and acquired agranulocytosis. They can cause improper functioning of bone marrow and can decrease the number of platelets. As they can be treated through several therapies, such as recombinant factor, immunoglobulin infusion therapy, activated prothrombin complex concentrate, and thrombopoietin receptor agonists, the demand for acquired orphan blood disease therapeutics is rising across the globe.
At present, the increasing awareness about blood diseases and their treatment options among the masses, along with the inflating income level of individuals worldwide, represents one of the major factors influencing the market positively. Moreover, the rising demand for blood disease therapeutics options due to the increasing geriatric population is strengthening the growth of the market. In line with this, governing agencies and private organizations of various countries are encouraging the adoption of blood disease therapeutics by spreading awareness about the occurrence of blood-associated disorders among individuals and offering several healthcare initiatives around the world is impelling the growth of the market. Apart from this, the growing adoption of blood disease therapeutics due to the increasing prevalence of various blood-related disorders among individuals across the globe is offering a positive market outlook. Additionally, the wide availability of acquired orphan blood disease therapeutics drugs through online and offline pharmacy stores around the world is contributing to the growth of the market. Besides this, the increasing demand for personalized medicines among individuals, along with the improving healthcare infrastructure worldwide, is offering lucrative growth opportunities to industry investors. In addition to this, there is a rise in the demand for cost-effective and quality care solutions among individuals across the globe. This, coupled with the increasing adoption of preventative care and wellness services to avoid widespread disease among individuals, is bolstering the growth of the market. Furthermore, key manufacturers are introducing hydroxyurea-based treatment for pediatric patients with sickle cell anemia, which is supporting the growth of the market.
IMARC Group provides an analysis of the key trends in each segment of the global acquired orphan blood diseases therapeutics market, along with forecasts at the global, regional, and country levels from 2024-2032. Our report has categorized the market based on therapy, disease indication, and distribution channel.
Recombinant Factor
Immunoglobulin Infusion Therapy
Activated Prothrombin Complex Concentrate
Thrombopoietin Receptor Agonists
Others
The report has provided a detailed breakup and analysis of the acquired orphan blood diseases therapeutics market based on the therapy. This includes recombinant factor, immunoglobulin infusion therapy, activated prothrombin complex concentrate, thrombopoietin receptor agonists, and others.
Acquired Agranulocytosis
Acquired Hemophilia
Acquired Von Willebrand Syndrome
Paroxysmal Nocturnal Hemoglobinuria (PNH)
Myelodysplastic Syndrome
Others
A detailed breakup and analysis of the acquired orphan blood diseases therapeutics market based on the disease indication has also been provided in the report. This includes acquired agranulocytosis, acquired hemophilia, acquired von willebrand syndrome, paroxysmal nocturnal hemoglobinuria (PNH), myelodysplastic syndrome, and others. According to the report, acquired hemophilia accounted for the largest market share.
Hospital Pharmacy
Retail Pharmacy
Others
A detailed breakup and analysis of the acquired orphan blood diseases therapeutics market based on the distribution channel has also been provided in the report. This includes hospital pharmacy, retail pharmacy, and others. According to the report, hospital pharmacy 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, which 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 the Middle East and Africa. According to the report, North America was the largest market for acquired orphan blood diseases therapeutics. Some of the factors driving the North America acquired orphan blood diseases therapeutics market included the growing awareness about several treatment options, wide availability of therapeutic drugs, favorable government initiatives, etc.
The report has also provided a comprehensive analysis of the competitive landscape in the global acquired orphan blood diseases therapeutics market. Competitive analysis such as market structure, market share by key players, player positioning, top winning strategies, competitive dashboard, and company evaluation quadrant has been covered in the report. Also, detailed profiles of all major companies have been provided. Some of the companies covered include Alexion Pharmaceuticals Inc. (AstraZeneca plc), Amgen Inc., GSK plc, Novartis AG, Novo Nordisk A/S, Otsuka Pharmaceutical Co. Ltd., Rigel Pharmaceuticals Inc., Roche Holding AG, Sanofi, Takeda Pharmaceutical Company Limited, 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.