Press release
Duchenne Muscular Dystrophy Treatment Market t to Witness Remarkable Growth by 2025 | BioMarin, Fibrogen Inc., Nobelpharma Co. Ltd
Latest released, the research study on Global Duchenne Muscular Dystrophy Treatment Market Report Forecast 2021 - 2025, offers a detailed overview of the factors influencing the global business scope. Duchenne Muscular Dystrophy Treatment Market research report shows the latest market insights, current situation analysis with upcoming trends and breakdown of the products and services. The report provides key statistics on the market status, size, share, growth factors of the Duchenne Muscular Dystrophy Treatment. The study covers emerging player's data, including competitive landscape, sales, revenue and global market share of top manufacturers are: BioMarin, Fibrogen Inc., Nobelpharma Co. Ltd, NS Pharma Inc., Pfizer Inc., PTC Therapeutics, Santhera Pharmaceuticals, Sarepta Therapeutics, F. Hoffmann-La Roche AG, ReveraGen BioPharmaClick the link to Get a Free Exclusive Sample Copy of the Report:
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Covid-19 Impact and Recovery Analysis:
The global Duchenne Muscular Dystrophy Treatment market report also includes the impact of the Covid-19 pandemic. Moreover, it offers an exhaustive analysis of aspects that will encounter the development of the market pre & post Covid-19 pandemic.
Key Market Trends
Exon-skipping Segment is Expected to Dominate Duchenne Muscular Dystrophy Treatment Market
Duchenne muscular dystrophy is mostly caused by the internal deletions in the gene for dystrophin, a protein essential for maintaining muscle cell membrane integrity. One of the potential therapeutic method is to mask an exon close to the site where the others are missing, so that the remaining exons can join together. Exon-skipping approach signifies one of the most capable therapeutic approaches that aim to restore the expression of a shorter but functional dystrophin protein.
Moreover, market players are focusing on frequent launches in exon skipping technology which is a significant factor driving the segment thereby propelling the market growth. For instance, In December 2019, Sareptas exon skipping drug, VYONDYS 53 (golodirsen) has been approved by the Food and Drug Administration (FDA) for the treatment of Duchenne muscular dystrophy.
Regional Analysis:
North America (United States, Canada and Mexico)
Europe (Germany, France, UK, Russia and Italy)
Asia-Pacific (China, Japan, Korea, India, Southeast Asia and Australia)
South America (Brazil, Argentina, Colombia)
Middle East and Africa (Saudi Arabia, UAE, Egypt, Nigeria and South Africa)
North American Region holds the Largest Market Share 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 increasing clinical trials around the world, especially in the United States and Europe. According to the FDA in 2017, the Emflaza (deflazacort) tablets and oral suspension were approved to treat DMD patients aged 5 years and above. Emflaza is a corticosteroid that works by decreasing inflammation and reducing the activity of the immune system.
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-Competitive landscape involving the market share of major players, along with the new projects and strategies adopted by players in the past five years
-Comprehensive company profiles covering the product offerings, key financial information, recent developments, SWOT analysis, and strategies employed by the major market players
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