The 7 major myotonic dystrophy markets reached a value of US$ 96.5 Million in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 260.4 Million by 2034, exhibiting a growth rate (CAGR) of 9.45% during 2024-2034.
Report Attribute
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Key Statistics
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Base Year
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2023
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Forecast Years
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2024-2034
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Historical Years
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2018-2023
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Market Size in 2023
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US$ 96.5 Million |
Market Forecast in 2034
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US$ 260.4 Million |
Market Growth Rate 2024-2034 | 9.45% |
The myotonic dystrophy market has been comprehensively analyzed in IMARC's new report titled "Myotonic Dystrophy Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034". Myotonic dystrophy refers to a rare, inherited neuromuscular disorder characterized by muscle weakness and myotonia, a condition in which muscles have difficulty relaxing after contraction. This ailment results from an abnormal expansion of repetitive DNA sequences within specific genes, leading to dysfunctional RNA processing in affected tissues. The symptoms of the illness can vary widely and typically emerge gradually, with the severity often increasing over time. Some common manifestations include muscle stiffness, particularly in the hands and face, causing difficulty with activities, such as releasing handgrips or facial expressions. Weakness in other muscle groups, like the limbs and neck, can also be present, leading to reduced mobility. Additionally, individuals suffering from the disorder might experience heart rhythm abnormalities, cataracts, and cognitive impairment, further complicating the clinical picture. The diagnosis of myotonic dystrophy involves a combination of medical history evaluation, genetic testing, and electromyography (EMG) to measure muscle electrical activity.
The escalating incidences of genetic anomalies affecting the DMPK gene that trigger the abnormal expansion of repetitive DNA sequences, leading to impaired muscle function, are primarily driving the myotonic dystrophy market. In addition to this, the inflating utilization of physical and respiratory therapies on account of their various advantages, such as enhancing muscular function, optimizing respiratory capacity, and promoting overall mobility, is also creating a positive outlook for the market. Moreover, the widespread adoption of non-invasive procedures, including neuromuscular ultrasound, that aid in the visualization of muscle changes and contribute to early diagnosis, is further bolstering the market growth. Apart from this, the rising usage of antisense oligonucleotide therapy, which exhibits promising outcomes by targeting the underlying genetic aberrations responsible for the disorder, is acting as another significant growth-inducing factor. Additionally, the emerging popularity of effective medications, such as anticonvulsants, mexiletine, and cardiac devices, to address the symptoms and reduce complications is also propelling the market growth. Furthermore, numerous technological advancements in the field of gene therapy, including CRISPR-Cas9, for rectifying genetic anomalies and correcting faulty genetic sequences, thereby opening new vistas for potential disease modification, are expected to drive the myotonic dystrophy market during the forecast period.
IMARC Group's new report provides an exhaustive analysis of the myotonic dystrophy market in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom) and Japan. This includes treatment practices, in-market, and pipeline drugs, share of individual therapies, market performance across the seven major markets, market performance of key companies and their drugs, etc. The report also provides the current and future patient pool across the seven major markets. According to the report the United States has the largest patient pool for myotonic dystrophy and also represents the largest market for its treatment. Furthermore, the current treatment practice/algorithm, market drivers, challenges, opportunities, reimbursement scenario and unmet medical needs, etc. have also been provided in the report. This report is a must-read for manufacturers, investors, business strategists, researchers, consultants, and all those who have any kind of stake or are planning to foray into the myotonic dystrophy market in any manner.
Time Period of the Study
Countries Covered
Analysis Covered Across Each Country
This report also provides a detailed analysis of the current myotonic dystrophy marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
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Tideglusib | AMO Pharma |
IONIS-DMPKRX | Ionis Pharmaceuticals |
ERX 963 | Expansion Therapeutics |
DYNE-101 | Dyne Therapeutics |
Pitolisant | Bioprojet |
*Kindly note that the drugs in the above table only represent a partial list of marketed/pipeline drugs, and the complete list has been provided in the report.
Market Insights
Epidemiology Insights
Myotonic Dystrophy: Current Treatment Scenario, Marketed Drugs and Emerging Therapies