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 Duchenne Muscular Dystrophy Market research evaluates the significant alterations brought about by the outbreak in this commercial environment and takes into account the key market factors that have been significantly impacted. The research elaborates on the fast evolving market environment in the COVID-19 era in an effort to assist companies operating in this industry in overcoming the gripping effects of the pandemic and developing new growth strategies to improve the COVID-19 preparation.
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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:
Segments Covered in this report are:
-
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
- North America
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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