Sarepta Therapeutics
Scope of the Report:
As per the , Duchenne muscular dystrophy (DMD) is a genetic disorder characterized by progressive muscle degeneration and weakness. It is a rare muscle disease, which majorly affects males. There are novel drugs and therapies, disease-modifying, and mutation-specific therapies that are some of the emerging major breakthroughs in the DMD treatment market.
The Report Covers:
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Key Market Trends:
Nonsteroidal Anti-inflammatory Drugs (NSAIDs) Segment is Expected to Grow Fastest During the Forecast Period
Corticosteroids are the only known pharmacological treatment for DMD and help to suppress muscle inflammation. This treatment is being limited by its inadequate therapeutic efficacy, and considerable side effects, and hence, non-steroidal anti-inflammatory drugs (NSAIDs) can be used to reduce the inflammation of muscles. The nonsteroidal anti-inflammatory drugs are expected to witness a CAGR of 49.2% over the forecast period.
However, other therapies and treatments include stem cell therapy, repurposing drugs, anti-fibrotics, myostatin inhibition, gene editing (CRISPR/Cas9), etc. Currently, prednisone/prednisolone and deflazacort have been used for the treatment of Duchenne muscular dystrophy, which is expected to drive the growth of the market, over the forecast period.
North American Region holds the Largest Market Share of the Market Currently and is Believed to Follow the Same Trend Over the Forecast Period
North America dominates the global Duchenne muscular dystrophy market, due to new product innovations, high healthcare expenditure, and government awareness programs. The United States has dominated the regional market and is projected to maintain its lead, owing to the rising disease incidence and anticipated launch of promising pipeline candidates. In addition, the market is expected to grow with the increasing clinical trials around the world, especially in the United States and Europe.
Key Questions Answered in This Report:
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Detailed TOC of Duchenne Muscular Dystrophy Treatment Market 2019-2024:
1 INTRODUCTION 1.1 Study Deliverables 1.2 Study Assumptions 1.3 Scope of the Study
2 RESEARCH METHODOLOGY
3 EXECUTIVE SUMMARY
4 MARKET DYNAMICS 4.1 Market Overview 4.2 Market Drivers 4.2.1 Rising Disease Burden of Duchenne Muscular Dystrophy (DMD) 4.2.2 Increasing Investments in Biopharmaceutical R&D to Release Novel Disease Therapies 4.2.3 Increasing Awareness Campaigns for DMD 4.3 Market Restraints 4.3.1 Lack of Standardization to Measure Clinical Efficacy Across All Stages of DMD 4.3.2 Stringent Regulatory Framework with High Product Cost Burden 4.4 Porters Five Forces Analysis 4.4.1 Threat of New Entrants 4.4.2 Bargaining Power of Buyers/Consumers 4.4.3 Bargaining Power of Suppliers 4.4.4 Threat of Substitute Products 4.4.5 Intensity of Competitive Rivalry
5 MARKET SEGMENTATION 5.1 By Therapeutic Approach and Treatment Type 5.1.1 Molecular-based Therapies 5.1.1.1 Mutation Suppression 5.1.1.2 Exon Skipping 5.1.2 Steroid Therapy 5.1.2.1 Corticosteroids 5.1.3 Nonsteroidal Anti-inflammatory Drugs (NSAIDs) 5.1.4 Other Therapeutic Approaches and Treatment Types 5.2 By End User 5.2.1 Hospitals/Clinics 5.2.2 Ambulatory Centers 5.2.3 Other End Users 5.3 Geography 5.3.1 North America 5.3.1.1 United States 5.3.1.2 Canada 5.3.1.3 Mexico 5.3.2 Europe 5.3.2.1 Germany 5.3.2.2 United Kingdom 5.3.2.3 France 5.3.2.4 Italy 5.3.2.5 Spain 5.3.2.6 Rest of Europe 5.3.3 Asia-Pacific 5.3.3.1 China 5.3.3.2 Japan 5.3.3.3 India 5.3.3.4 Australia 5.3.3.5 South Korea 5.3.3.6 Rest of Asia-Pacific 5.3.4 Middle East & Africa 5.3.4.1 GCC 5.3.4.2 South Africa 5.3.4.3 Rest of Middle East & Africa 5.3.5 South America 5.3.5.1 Brazil 5.3.5.2 Argentina 5.3.5.3 Rest of South America
6 COMPETITIVE LANDSCAPE 6.1 Company Profiles 6.1.1 BioMarin 6.1.2 Bristol-Myers Squibb Company 6.1.3 Fibrogen Inc. 6.1.4 Eli Lilly and Company 6.1.5 Nobelpharma Co. Ltd 6.1.6 NS Pharma Inc. 6.1.7 Pfizer Inc. 6.1.8 PTC Therapeutics 6.1.9 Santhera Pharmaceuticals 6.1.10 Sarepta Therapeutics
7 MARKET OPPORTUNITIES AND FUTURE TRENDS
Contact Us:
Name: Ajay More
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