市场调查报告书
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1468363
杜氏肌肉营养不良症药物市场按产品类型(皮质类固醇、疼痛管理药物)、治疗方法(突变抑制、外显子跳跃、类固醇治疗)、最终用户(医院、诊所、家庭护理机构)和地区 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,全球杜氏肌肉营养不良症药物市场规模达23亿美元。杜氏肌肉营养不良症在大众中患病率不断上升、新产品批准和上市数量不断增加、政府提供良好报销政策的有利倡议以及推广针对特定目标的治疗方法,是推动市场发展的一些关键因素。
杜氏肌肉营养不良 (DMD) 药物用于治疗严重的 X 连锁遗传性疾病,即进行性肌肉营养不良,主要影响男性群体,很少影响女性。这种疾病的症状包括行走、站立和坐立困难以及言语困难,这可能导致骨骼肌和心肌进行性无力和丧失,也称为萎缩。 DMD 药物透过针对心臟和骨骼肌来增强患者的心肺功能。肌营养不良蛋白是维持肌肉完整性的关键蛋白质,其缺失或异常会导致 DMD。因此,大多数治疗 DMD 的药物都是基于肌肉营养不良蛋白的。 DMD 的其他一些主要治疗策略还包括与特定突变相关的基因疗法,这些突变可恢復肌营养不良蛋白的产生、膜稳定或补偿蛋白的上调,以及减少发炎级联和/或增强肌肉再生。
主要製造商批准和推出的新产品数量不断增加是推动市场成长的重要因素。这可以归因于杜氏肌肉营养不良症在群众中的发生率不断上升。与此一致的是,临床试验的大幅增加以及强大的产品线的存在正在为市场提供动力。此外,由于诊断技术的不断创新,突变特异性疗法的出现也对市场产生了积极影响。除此之外,针对婴儿、女性和非行走患者等服务不足类别的 DMD 准确诊断和治疗的广泛研发 (R&D) 活动正在推动市场发展。然而,药物临床疗效检查标准化程序的缺乏、诊断和预测的延迟以及基因治疗成本的上升正在成为市场成长的限制因素。相反,有利的政府措施提供了良好的报销政策,并推广针对特定目标的治疗,正在促进市场成长。在市场上创造利润丰厚的成长机会的其他一些因素包括快速城市化、医疗基础设施的改善、产品高端化的趋势以及大众可支配收入的增加。
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.