According to the most recent analysis by Emergen Research, the market for duchenne muscular dystrophy in the world reached $1.03 billion in 2021 and is projected to grow at a rate of 40.7% over the forecast period. The prevalence of duchenne muscular dystrophy is rising, and there are more clinical trials and studies being conducted in the area of duchenne muscular dystrophy-based treatments, which are key contributors in the market's expansion. Additionally, the market for drugs to treat Duchenne muscular dystrophy has shown tremendous revenue increase in recent years due to the quick development of these drugs in clinical trials.
The Global Duchenne Muscular Dystrophy Market Research Report added by Emergen Research to its expanding repository is an all-inclusive document containing insightful data about the Duchenne Muscular Dystrophy market and its key elements. The report is formulated through extensive primary and secondary research and is curated with an intent to offer the readers and businesses a competitive edge over other players in the industry.
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Competitive Terrain:
The section on the competitive landscape offers valuable and actionable insights related to the business sphere of the Duchenne Muscular Dystrophy market, covering extensive profiling of the key market players. The report offers information about market share, product portfolio, pricing analysis, and strategic alliances such as mergers and acquisitions, joint ventures, collaborations, partnerships, product launches and brand promotions, among others. The report also discusses the initiatives taken by the key companies to combat the impact of the COVID-19 pandemic.
The leading market contenders listed in the report are:
PTC Therapeutics, Eli Lilly and Company, Sarepta Therapeutics, Bristol-Myers Squibb Company, Nippon Shinyaku, Acceleron Pharma Inc., BioMarin Pharmaceutical, Inc., Pfizer, Ltd., Tahio Pharmaceutical Co. Ltd., and Lexicon Pharmaceuticals, Inc.
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Emergen Research has segmented the global Duchenne Muscular Dystrophy market on the basis of type, application, end-use, and region:
Treatment Type Outlook (Revenue, USD Million; 2019-2030)
Corticosteroid therapy
Exon-Skipping Therapy
Mutation Suppression
Gene Therapy
End-Use Outlook (Revenue, USD Million; 2019-2030)
Hospitals & Clinics
Home-Care
Others
Regional Outlook (Revenue, USD Million; 2019-2030)
North America
U.S.
Canada
Mexico
Europe
Germany
France
U.K.
Italy
Spain
Benelux
Rest of Europe
Asia Pacific
China
India
Japan
South Korea
Rest of APAC
Latin America
Brazil
Rest of LATAM
Middle East & Africa
Saudi Arabia
UAE
South Africa
Turkey
Rest of MEA
The various regions analyzed in the report include:
North America (U.S., Canada)
Europe (U.K., Italy, Germany, France, Rest of EU)
Asia Pacific (India, Japan, China, South Korea, Australia, Rest of APAC)
Latin America (Chile, Brazil, Argentina, Rest of Latin America)
Middle East & Africa (Saudi Arabia, U.A.E., South Africa, Rest of MEA)
Key Objectives of the Report:
Analysis and estimation of the Duchenne Muscular Dystrophy Market size and share for the projected period of 2022-2030
Extensive analysis of the key players of the market by SWOT analysis and Porter’s Five Forces analysis to impart a clear understanding of the competitive landscape
Study of current and emerging trends, restraints, drivers, opportunities, challenges, growth prospects, and risks of the global Duchenne Muscular Dystrophy Market
Analysis of the growth prospects for the stakeholders and investors through the study of the promising segments
Strategic recommendations to the established players and new entrants to capitalize on the emerging growth opportunities
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