The Duchenne Muscular Dystrophy Treatment Market To Flaunt A CAGR Of 48.3% Between 2026

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Duchenne Muscular Dystrophy Treatment Market
Report Id PMRREP12475 Category Life Science
Healthcare
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The Duchenne Muscular Dystrophy Treatment Market
To Flaunt A CAGR Of 48.3 Between 2026

• As per the report by Persistence Market Research
  (PMR), the global duchenne muscular dystrophy
  market is expected to experience strong growth.
  The market is also estimated to expand at a CAGR
  of 48.3 during the forecast period. The global
  duchenne muscular dystrophy market is estimated
  to bring in US 10,664.5 million revenue by the
  end of 2026.
• Duchenne Muscular Dystrophy (DMD) is a type of
  muscular disorder due to which most of the people
  are unable to walk at a very early stage and the
  affected muscles look larger due to the fat
  content. The symptoms include muscle weakness,
  difficulty in walking and breathing and
  intellectual disability.
• Although, the treatment to control and reduce the
  signs and symptoms is available, yet there is no
  cure for DMD. Key players in the market are also
  trying to spread awareness about DMD along with
  the investment in finding a treatment for the
  disease. Meanwhile, human clinical trials are
  also underway to find out effective therapy.

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Increasing Investment in Research and Development
to find a Treatment for DMD to Drive the Market
Growth
Various pharmaceutical companies and
organizations are increasingly investing in the
research and development activities to come up
with an effective treatment for duchenne muscular
dystrophy. Meanwhile, there is an ongoing
research on gene therapy, exon skipping drugs,
and stem cell therapy to treat duchenne muscular
dystrophy in a better way. Current
pharmacological interventions for duchenne
muscular dystrophy include approaches to mitigate
downstream and secondary pathological mechanisms
and solutions targeting primary defect. Patients
with DMD are not able to produce a protein known
as dystrophin. Hence, a variety of new
medications are being developed to replace
dystrophin. Moreover, new therapies aim to
repair muscle damage caused due to the absence of
dystrophin. However, delay in diagnosis and the
high cost of treatment and drugs are some of the
factors restricting the growth of the market.
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