市場調查報告書
商品編碼
1468363
杜氏肌肉營養不良症藥物市場按產品類型(皮質類固醇、疼痛管理藥物)、治療方法(突變抑制、外顯子跳躍、類固醇治療)、最終用戶(醫院、診所、家庭護理機構)和地區 2024-2032Duchenne Muscular Dystrophy Drugs Market by Product Type (Corticosteroids, Pain Management Drugs), Therapeutic Approach (Mutation Suppression, Exon Skipping, Steroid Therapy), End User (Hospitals, Clinics, Home Care Settings), and Region 2024-2032 |
IMARC Group年,全球杜氏肌肉營養不良症藥物市場規模達23億美元。杜氏肌肉營養不良症在大眾中患病率不斷上升、新產品批准和上市數量不斷增加、政府提供良好報銷政策的有利舉措以及推廣針對特定目標的治療方法,是推動市場發展的一些關鍵因素。
杜氏肌肉營養不良 (DMD) 藥物用於治療嚴重的 X 連鎖遺傳性疾病,即進行性肌肉營養不良,主要影響男性群體,很少影響女性。這種疾病的症狀包括行走、站立和坐立困難以及言語困難,這可能導致骨骼肌和心肌進行性無力和喪失,也稱為萎縮。 DMD 藥物透過針對心臟和骨骼肌來增強患者的心肺功能。肌營養不良蛋白是維持肌肉完整性的關鍵蛋白質,其缺失或異常會導致 DMD。因此,大多數治療 DMD 的藥物都是基於肌肉營養不良蛋白的。 DMD 的其他一些主要治療策略還包括與特定突變相關的基因療法,這些突變可恢復肌營養不良蛋白的產生、膜穩定或補償蛋白的上調,以及減少發炎級聯和/或增強肌肉再生。
主要製造商批准和推出的新產品數量不斷增加是推動市場成長的重要因素。這可以歸因於杜氏肌肉營養不良症在群眾中的發生率不斷上升。與此一致的是,臨床試驗的大幅增加以及強大的產品線的存在正在為市場提供動力。此外,由於診斷技術的不斷創新,突變特異性療法的出現也對市場產生了積極影響。除此之外,針對嬰兒、女性和非行走患者等服務不足類別的 DMD 準確診斷和治療的廣泛研發 (R&D) 活動正在推動市場發展。然而,藥物臨床療效檢查標準化程序的缺乏、診斷和預測的延遲以及基因治療成本的上升正在成為市場成長的限制因素。相反,有利的政府措施提供了良好的報銷政策,並推廣針對特定目標的治療,正在促進市場成長。在市場上創造利潤豐厚的成長機會的其他一些因素包括快速城市化、醫療基礎設施的改善、產品高階化的趨勢以及大眾可支配收入的增加。
The global Duchenne muscular dystrophy drugs market size reached US$ 2.3 Billion in 2023. Looking forward, IMARC Group expects the market to reach US$ 5.5 Billion by 2032, exhibiting a growth rate (CAGR) of 9.96% during 2024-2032. The rising prevalence of Duchenne muscular dystrophy among the masses, the increasing number of new product approvals and launches, and favorable government initiatives providing good reimbursement policies, along with promoting target-specific treatments, represent some of the key factors driving the market.
Duchenne muscular dystrophy (DMD) drugs are utilized to treat a severe X-linked genetic disorder of a progressive form of muscular dystrophy that primarily affects the male population, and rarely females as well. The symptoms of this disorder include difficulty walking, standing, and sitting, as well as speech difficulties, which can result in progressive weakness and loss, also known as atrophy, in the skeletal and heart muscles. The DMD drugs enhance cardiac and pulmonary functions in patients by targeting cardiac and skeletal muscles. Dystrophin is a key protein that maintains muscular integrity, and its absence or abnormality causes DMD. As a result, most of the drugs for the treatment of DMD are dystrophin-based. Some of the other primary treatment strategies for DMD also include genetic therapies linked to specific mutations which restore dystrophin production, membrane stabilization or upregulation of compensatory proteins, and a reduction of the inflammatory cascade and/or enhancement of muscle regeneration.
The rising number of new product approvals and launches by the major manufacturers is a significant factor driving the growth of the market. This can be attributed to the growing incidences of Duchenne muscular dystrophy among the masses. In line with this, a considerable rise in clinical trials, along with the presence of strong pipeline of products, is providing an impetus to the market. Moreover, the advent of mutation-specific therapies due to continual innovations in diagnostics is also impacting the market positively. Besides this, extensive research and development (R&D) activities focusing on accurate diagnosis and treatment of DMD for underserved categories, such as infants, females, and nonambulant patients, are propelling the market. However, the shortage of standardized procedures for the examination of the clinical efficacy of drugs, delayed diagnosis and prediction, and the rising costs of genetic therapeutics are acting as growth-restraining factors for the market. On the contrary, favorable government initiatives providing good reimbursement policies, along with promoting target-specific treatments, are contributing to the market growth. Some of the other factors creating lucrative growth opportunities in the market include rapid urbanization, improving medical infrastructure, emerging trend of product premiumization, and inflating disposable incomes of the masses.
IMARC Group provides an analysis of the key trends in each segment of the global Duchenne muscular dystrophy drugs market, along with forecasts at the global, regional, and country level from 2024-2032. Our report has categorized the market based on product type, therapeutic approach, and end user.
Corticosteroids
Prednisolone
Prednisone
Deflazacort
Pain Management Drugs
The report has provided a detailed breakup and analysis of the Duchenne muscular dystrophy drugs market based on the product type. This includes corticosteroids (prednisolone, prednisone, and deflazacort) and pain management drugs. According to the report, corticosteroids represented the largest segment.
Mutation Suppression
Exon Skipping
Steroid Therapy
The report has provided a detailed breakup and analysis of the Duchenne muscular dystrophy drugs market based on the therapeutic approach. This includes mutation suppression, exon skipping, and steroid therapy. According to the report, exon skipping represented the largest segment.
Hospitals
Clinics
Home Care Settings
A detailed breakup and analysis of the Duchenne muscular dystrophy drugs market based on the end user has also been provided in the report. This includes hospitals, clinics, and home care settings. According to the report, hospitals 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 the Middle East and Africa. According to the report, North America was the largest market for Duchenne muscular dystrophy drugs. Some of the factors driving the North America Duchenne muscular dystrophy drugs market include the rising number of new product approvals and launches, continual improvements in medical infrastructure, and the presence of several key players in the country.
The report has also provided a comprehensive analysis of the competitive landscape in the global Duchenne muscular dystrophy drugs market. Detailed profiles of all major companies have also been provided. Some of the companies covered include FibroGen Inc., Italfarmaco S.p.A., NS Pharma Inc. (Nippon Shinyaku Co. Ltd.), PTC Therapeutics Inc., Santhera Pharmaceuticals, Sarepta 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.