Market Size in 2024 | Market Forecast in 2034 | CAGR (in %) | Base Year |
---|---|---|---|
USD 4.05 Billion | USD 14.04 Billion | 16.80% | 2024 |
FrequentlyAsked Questions
Duchenne muscular dystrophy drugs are dedicated medicines to slowing disease progression, enhancing quality of life, and managing symptoms for individuals suffering from this severe genetic condition. DMD is caused by changes in the dystrophin gene, resulting in progressive muscle weakness and degeneration, especially in boys.
The global Duchenne muscular dystrophy drugs market is projected to grow due to increasing research funding and activities, rising approvals of targeted therapies, and advancements in drug delivery.
According to study, the global Duchenne muscular dystrophy drugs market size was worth around USD 4.05 billion in 2024 and is predicted to grow to around USD 14.04 billion by 2034.
The CAGR value of the Duchenne muscular dystrophy drugs market is expected to be around 16.80% during 2025-2034.
North America is expected to lead the global Duchenne muscular dystrophy drugs market during the forecast period.
The key players profiled in the global Duchenne muscular dystrophy drugs market include Sarepta Therapeutics, PTC Therapeutics, Pfizer Inc., Santhera Pharmaceuticals, Italfarmaco S.p.A., Wave Life Sciences, Capricor Therapeutics, ReveraGen BioPharma, FibroGen, Inc., BioMarin Pharmaceutical Inc., Catalyst Biosciences, Dyne Therapeutics, Avidity Biosciences, Genethon, and Entrada Therapeutics.
The report examines key aspects of the Duchenne muscular dystrophy drugs market, including a detailed analysis of existing growth factors and restraints, as well as an exploration of future growth opportunities and challenges that influence the market.
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