Spinal Muscular Atrophy Market to Hit US$ 4,823.9 Million by 2031, Coherent Market Insights

According to Coherent Market Insights, the global spinal muscular atrophy market size is estimated to be valued at USD 2,013.5 million in 2024 and is expected to surpass USD 4,823.9 million by 2031, growing at a CAGR of 13.3% from 2024 to 2031.

Growing number of approvals for drugs such as Zolgensma and Evrysdi also boost the market growth. In 2020, the U.S. FDA approved Evrysdi to treat spinal muscular atrophy in adults and children 2 months and older. Rising awareness regarding new treatment options also contributes to the market growth.

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Market Trends

Growing number of gene therapies is a key trend driving market growth. In 2019, Novartis’ Zolgensma became first gene therapy approved by the U.S. FDA for treating pediatric patients under two years old with spinal muscular atrophy (SMA).

Another trend gaining traction is launch of patient assistance programs by pharmaceutical manufacturers. AveXis launched Zolgensma gene treatment. Zolgensma aids insurance verification and financial assistance for eligible patients.

Spinal Muscular Atrophy Market Report Coverage

Report Coverage

Details

Market Revenue in 2024

$2,013.5 million

Estimated Value by 2031

$4,823.9 million

Growth Rate

Poised to grow at a CAGR of 13.3%

Historical Data

2019–2023

Forecast Period

2024–2031

Forecast Units

Value (USD Million/Billion)

Report Coverage

Revenue Forecast, Competitive Landscape, Growth Factors, and Trends

Segments Covered

By Type, By Treatment, By Age Group, By Route of Administration, By Distribution Channel

Geographies Covered

North America, Europe, Asia Pacific, and Rest of World

Growth Drivers

• Increasing prevalence of spinal muscular atrophy

• Increasing research and development activities

• Increased product launches

Restraints & Challenges

• High cost of the treatment

Market Opportunities

Gene therapy is expected to dominate the spinal muscular atrophy market. This is due to one-time treatment and long-term benefits of gene therapy.

Disease-modifying drugs like Spinraza and Evrysdi dominate the SMA treatment market. Spinraza was the first drug approved for SMA. It has proven to prolong survival rates and motor functions. Evrysdi provides an oral alternative and offers comparable efficacy, making it a preferred option.

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Key Market Takeaways

The global spinal muscular atrophy market is anticipated to witness a CAGR of 13.3% during the forecast period 2024-2031. This is owing to increasing research efforts towards the development of gene therapies and disease-modifying drugs.

On the basis of type, Type I segment is expected to hold a dominant position. This is owing to high mortality and morbidity rates associated with this type. Type I SMA accounts for around 60% of total SMA cases.

On the basis of treatment, Gene therapy segment is expected to hold a dominant position over the forecast period. This due to its one-time curative approach and long-term benefits.

On the basis of age group, Infant segment dominates the market. This is due to high diagnosis rates in newborns through screening programs.

On the basis of route of administration, Oral segment is expected to hold a dominant position. This is owing to patient preference for oral drugs over intrathecal injections.

On the basis of distribution channel, Hospital pharmacies segment holds the major share. This is due to a large patient pool.

By Region, North America is expected to hold a dominant position over the forecast period. This is due to established healthcare infrastructure and high treatment rates.

Competitor Insights

- Biogen

- XYROKINETICS

- F. Hoffmann-La Roche Ltd.

- Genentech, Inc.

- PTC Therapeutics, Inc.

- Novartis AG

- Ionis Pharmaceuticals

- Chugai Pharmaceutical Co., Ltd.

- NMD PHARMA A/S

- Astellas Pharma Inc.

Recent Developments 

In June 2023, Biogen Inc. announced new data on SPINRAZA (nusinersen) for spinal muscular atrophy at the Cure SMA Research & Clinical Care Meeting in Orlando, Florida.

In August 2020, the U.S. FDA approved Evrysdi. It is the first at-home orally administered treatment for spinal muscular atrophy. PTC Thearpeutics, Genentech, and Roche co-developed it.

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Detailed Segmentation:

By Type:

    • Type I
    • Type II
    • Type III
    • Type IV

By Treatment:

    • Gene Therapy
    • Disease-modifying drugs

By Age Group:

    • Infant
    • Adult

By Route of Administration:

    • Oral
    • Injectables

By Distribution Channel:

    • Hospital Pharmacies
    • Retail Pharmacies
    • Online Pharmacies

By Region:

    • North America
      • U.S.
      • Canada
    • Latin America
      • Brazil
      • Argentina
      • Mexico
      • Rest of Latin America
    • Europe
      • Germany
      • U.K.
      • Spain
      • France
      • Italy
      • Russia
      • Rest of Europe
    • Asia Pacific
      • China
      • India
      • Japan
      • Australia
      • South Korea
      • ASEAN
      • Rest of Asia Pacific
    • Middle East
      • GCC Countries
      • Israel
      • Rest of Middle East
    • Africa
      • South Africa
      • North Africa
      • Central Africa

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