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鎌状赤血球症治療市場レポート:治療タイプ、エンドユーザー、地域別、2024~2032年Sickle Cell Disease Treatment Market Report by Treatment Type (Blood Transfusion, Pharmacotherapy, Bone Marrow Transplant), End User (Hospitals, Diagnostic Centers, and Others), and Region 2024-2032 |
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鎌状赤血球症治療市場レポート:治療タイプ、エンドユーザー、地域別、2024~2032年 |
出版日: 2024年08月10日
発行: IMARC
ページ情報: 英文 140 Pages
納期: 2~3営業日
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世界の鎌状赤血球症治療市場規模は2023年に35億米ドルに達しました。今後、IMARC Groupは、市場は2032年までに119億米ドルに達し、2024~2032年の間に14%の成長率(CAGR)を示すと予測しています。
鎌状赤血球症(SCD)は、全身に酸素を運ぶタンパク質であるヘモグロビンに影響を及ぼす遺伝的な赤血球(RBC)障害です。急性胸部症候群、貧血、血管閉塞性クリーゼ(VOC)など多くの合併症を引き起こします。現在、SCDの治療には血液移植と骨髄移植が一般的に行われています。この移植は、罹患した骨髄をドナーからの健康な骨髄と置き換えるものです。薬剤療法や輸血などの他の効果的な治療法も、特定の症状を軽減し、患者を延命させることができるため、利用されています。
SCDに罹患する患者数が大幅に増加していることは、SCDを効果的に治療できる新薬の需要に影響を与える重要な要因の一つです。その結果、各国の医療規制当局は新しい治療法の早期承認に力を入れています。例えば、米国食品医薬品局(USFDA)は2019年、SCDの成人と小児が経験する痛みを軽減する新薬を承認しました。さらに、政府当局は研究開発(R&D)活動を支援し、研究者や製薬会社に新規治療法の開発を促しています。例えば、米国国立心肺血液研究所(NHLBI)の研究者は、細胞の機能を改善するために、欠損した遺伝子を回復させたり、新しいDNA株を追加したりする遺伝子治療に取り組んでいます。こうした技術革新は、可処分所得の増加や利用可能な医療サービスに対する個人の意識の高まりとともに、市場成長に寄与すると予想されます。
The global sickle cell disease treatment market size reached US$ 3.5 Billion in 2023. Looking forward, IMARC Group expects the market to reach US$ 11.9 Billion by 2032, exhibiting a growth rate (CAGR) of 14% during 2024-2032.
Sickle cell disease (SCD) is a genetic red blood cell (RBC) disorder that affects hemoglobin, a protein that carries oxygen throughout the body. It leads to many complications, such as acute chest syndrome, anemia, and vaso-occlusive crisis (VOC). At present, blood and bone marrow transplant is commonly suggested by doctors for treating SCD. It involves replacing affected bone marrow with a healthy substitute received from a donor. Other effective treatments, such as medications and blood transfusions, are also being utilized as they can reduce specific symptoms and prolong the life of patients.
A considerable increase in the number of individuals suffering from SCD represents one of the significant factors influencing the demand for new medications that can treat the condition effectively. As a result, the health regulatory authorities of numerous countries are focusing on fast-track approval of new treatment methods. For instance, the United States Food and Drug Administration (USFDA) approved a new medicine in 2019 to reduce the pain experienced by adults and children with SCD. Additionally, government authorities are supporting research and development (R&D) activities to encourage researchers and pharmaceutical companies to develop novel treatments. For instance, researchers at the National Heart, Lung, and Blood Institute (NHLBI) in the US are working on genetic therapies that can restore a missing gene or add a new DNA strain to improve the functioning of cells. These innovations, along with the rising disposable incomes and the growing awareness among individuals about the available healthcare services, are anticipated to contribute to market growth.
IMARC Group provides an analysis of the key trends in each sub-segment of the global sickle cell disease treatment market report, along with forecasts at the global, regional and country level from 2024-2032. Our report has categorized the market based on treatment type and end user.
Blood Transfusion
Pharmacotherapy
Bone Marrow Transplant
Hospitals
Diagnostic Centers
Others
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 competitive landscape of the industry has also been examined along with the profiles of the key players being AstraZeneca Plc, Baxter International Inc., bluebird bio Inc., Bristol-Myers Squibb Company, CRISPR Therapeutics, Emmaus Medical Inc., Global Blood Therapeutics Inc., GlycoMimetics Inc., Novartis AG, Pfizer Inc. and Sangamo Therapeutics.