Duchenne Muscular Dystrophy Treatment Market Size, Competitive Analysis, Historical & Forecast Analysis 2023-2030: Cognitive Market Research

Market Overview:
Duchenne muscular dystrophy (DMD) is a genetic disorder characterized by progressive muscle degeneration and weakness. It primarily affects males, with symptoms typically appearing in early childhood. DMD is caused by a mutation in the dystrophin gene, which leads to the absence or dysfunction of the dystrophin protein, an essential component for maintaining muscle integrity.
While there is no known cure for DMD, several treatment approaches aim to manage symptoms, slow disease progression, and improve the quality of life for individuals with the condition. Glucocorticoids, such as prednisone and deflazacort, are commonly prescribed to individuals with DMD. These medications have been shown to slow the progression of muscle degeneration, preserve muscle strength, and improve overall motor function. They work by reducing inflammation and promoting muscle regeneration. However, long-term use of corticosteroids can have side effects, including weight gain, delayed growth, and bone fragility.

Summary:
The Global Duchenne Muscular Dystrophy Treatment market size was $2.48 Billion in 2022.

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Market Dynamics:
• Unmet need has created a strong market demand for innovative DMD treatments
The significant unmet need for Duchenne Muscular Dystrophy (DMD) treatment has created a strong market demand for innovative therapies. DMD is a devastating and progressive genetic disorder that primarily affects young boys, leading to muscle weakness, loss of ambulation, respiratory complications, and reduced life expectancy. Currently, there is no cure for DMD, and available treatments mainly focus on managing symptoms and improving quality of life. The lack of effective treatment options for DMD has resulted in a pressing need for innovative therapies that can address the underlying cause of the disease and provide better outcomes for patients.
Limited efficacy of current treatments while various interventions, such as corticosteroids and physical therapy, can help manage symptoms and slow disease progression to some extent, they do not address the root cause of DMD. These treatments have limitations in terms of their effectiveness, tolerability, and long-term benefits. Therefore, there is a demand for therapies that can more directly target the genetic mutation responsible for DMD and provide more substantial clinical benefits.
DMD significantly impacts the quality of life of patients and their families. Progressive muscle degeneration leads to severe disability, loss of ambulation, respiratory complications, and cardiac dysfunction. The current treatment options only offer partial relief and do not adequately address the overall disease burden. There is a strong market demand for therapies that can halt or slow disease progression, improve muscle function, and extend the lifespan of DMD patients.

• Higher Intake of Corticosteroids eventually boosts the market growth (Access Detailed Analysis in the Full Report Version)

• Growth of Clinical Research significantly fuels the market growth (Access Detailed Analysis in the Full Report Version)

Market Segmentation:
Type:
• Molecular-based Therapies
• Steroid Therapy
• Nonsteroidal Anti-inflammatory Drugs (NSAIDs)
• Other

Application:
• Hospitals/Clinics
• Ambulatory Centers
• Other

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Competitive Analysis for Duchenne Muscular Dystrophy Treatment Market:
• Myers Squibb Company
• NS Pharma Inc.
• Sarepta Therapeutics
• Bristol
• Eli Lilly and Company
• Nobelpharma Co. Ltd
• PTC Therapeutics
• Pfizer Inc.
• BioMarin
• Santhera Pharmaceuticals
• Fibrogen Inc.

Company Profile
• PTC Therapeutics Inc
PTC Therapeutics Inc. is US based company involved in the research and development of drugs and treatments for various health conditions. The company has a presence in different countries like Argentina, Austria, Australia, Brazil, Canada, France, Germany, Italy, Japan, Mexico, and others across the globe. Therapeutic areas of the company include metabolism, neurology, and oncology. Currently, the approved products of the company include, EMFLAZA, EVRYSDI, TEGSEDI, TRANSLARNA, UPSTAZA, and WAYLIVRA.

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