
Ataxia Market Report and Forecast 2025-2034
Description
The ataxia market size was valued at USD 37.70 Billion in 2024, driven by intensive research activities to develop effective drugs and therapies across the 8 major markets. The market is expected to grow at a CAGR of 9.72% during the forecast period of 2025-2034, with the values likely to reach USD 95.32 Billion by 2034.
Ataxia Market Overview
Ataxia is a neurological condition characterized by loss of muscle control in the arms and legs of a patient. Lack of balance and coordination often results in trouble walking. The condition can also affect fingers, speech, and eye movements in the patients. Ataxia may appear suddenly due to some head injury, stroke, infections, etc., or develop gradually due to alcohol abuse, hypothyroidism, exposure to certain drugs, etc. It can be sporadic, hereditary, or acquired, with Friedreich ataxia being the most common hereditary form, affecting one in every 50,000 people in the United States.
Ataxia has a prevalence of 26 cases per 100,000 children , while hereditary ataxias affect 10 per 100,000 individuals. The increasing incidence is anticipated to boost the ataxia market share in the forecast period. Moreover, the regions with consanguinity (mating between blood relatives) as a common practice show a high prevalence of the disorder. In addition, a surge in drug approvals by the health authorities and robust research activities to find treatment options are driving the growth of the market.
Surge in Drug Approvals to Offer Advanced Treatment Alternatives
The increasing number of drug approvals by the health authorities to address ataxia-associated morbidities is contributing to the ataxia market growth. In February 2023, the United States Food and Drug Administration (FDA) approved Reata Pharmaceuticals, Inc.'s Skyclarys (omaveloxolone), developed by as the first treatment for Friedreich’s ataxia. The efficacy of the drug was tested in a 48-week randomized, placebo-controlled, and double-blind study of 103 patients with the neuromuscular condition, which yielded positive results.
Skyclarys reached another milestone in December 2023 when the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) issued a positive response to its marketing authorization in the European Union. Upon the approval by the European Commission (EC), Skyclarys will be the first authorized treatment within the region for people aged 16 years or more, which can slow the progression of Friedreich’s ataxia.
Intensive Research Activities to Address Increasing Ataxia Market Demand
As Friedreich’s ataxia is the most common type of inherited ataxia, research activities aimed at finding promising therapeutic treatments are being promoted to reduce ataxia-associated healthcare burden. In April 2023 , an investigative study on the role of adenosine (a widely distributed nucleoside in the central nervous system) was conducted to evaluate its role in mitigating mitochondrial impairment in patients with Friedreich’s ataxia. The results demonstrated that adenosine could counter the deleterious effects of mitochondrial dysfunction and oxidative stress by regulating mitochondrial function and biogenesis in the fibroblasts of a patient with Friedreich’s ataxia. The results of the study support adenosine as a potential therapeutic in the treatment of this neuromuscular disease.
Other interventions such as stem cell therapy are also receiving attention from researchers for ataxia treatment. In addition, the treatment of spinocerebellar ataxia with mesenchymal stem cells is under investigation, projected to contribute to boost the market size in the forecast period.
Ataxia Market Segmentation
“Ataxia Market Report and Forecast 2025-2034” offers a detailed analysis of the market based on the following segments:
Market Breakup by Type
The United States is anticipated to lead the ataxia market, owing to the presence of prominent biopharmaceutical companies, working to offer better treatment alternatives. In May 2023 , a Biohaven Ltd. announced the submission of a new drug application (NDA) for troriluzole to the United States FDA. The novel drug was designed to treat Spinocerebellar Ataxia Type 3 (SCA3) in patients.
Europe is also witnessing increased funding and investments by various sectors to accommodate the growing ataxia market demand. In January 2024 , Vico Therapeutics B.V., a clinical-stage genetic medication company based in the Netherlands, announced USD 60 million Series B financing. The funding is aimed to support the ongoing Phase 1/2a clinical trial of its intrathecally administered product VO659, designed to treat patients affected with spinocerebellar ataxia type 3 and type 1, among other neurological diseases.
Ataxia Market: Competitor Landscape
In July 2023, a global biotechnology company Biogen Inc. acquired Reata Pharmaceuticals, Inc. to accelerate the commercialization of the drug Skyclarys to patients with Friedreich’s ataxia around the world. Biogen agreed to buy Reata for USD 172.50 per share in cash, equivalent to a total enterprise value of around USD 7.3 billion. The market has been witnessing similar events of collaborations and acquisitions to deliver innovative therapies in the areas of unmet medical needs. Consequently, this is expected to propel ataxia market share in the coming years.
The key features of the market report include patent analysis, grants analysis, clinical trials analysis, funding and investment analysis, partnerships, and collaborations analysis by the leading key players. The major companies in the market are as follows:
*Please Note:* The report will take 5 business days to complete, after order confirmation.
Ataxia Market Overview
Ataxia is a neurological condition characterized by loss of muscle control in the arms and legs of a patient. Lack of balance and coordination often results in trouble walking. The condition can also affect fingers, speech, and eye movements in the patients. Ataxia may appear suddenly due to some head injury, stroke, infections, etc., or develop gradually due to alcohol abuse, hypothyroidism, exposure to certain drugs, etc. It can be sporadic, hereditary, or acquired, with Friedreich ataxia being the most common hereditary form, affecting one in every 50,000 people in the United States.
Ataxia has a prevalence of 26 cases per 100,000 children , while hereditary ataxias affect 10 per 100,000 individuals. The increasing incidence is anticipated to boost the ataxia market share in the forecast period. Moreover, the regions with consanguinity (mating between blood relatives) as a common practice show a high prevalence of the disorder. In addition, a surge in drug approvals by the health authorities and robust research activities to find treatment options are driving the growth of the market.
Surge in Drug Approvals to Offer Advanced Treatment Alternatives
The increasing number of drug approvals by the health authorities to address ataxia-associated morbidities is contributing to the ataxia market growth. In February 2023, the United States Food and Drug Administration (FDA) approved Reata Pharmaceuticals, Inc.'s Skyclarys (omaveloxolone), developed by as the first treatment for Friedreich’s ataxia. The efficacy of the drug was tested in a 48-week randomized, placebo-controlled, and double-blind study of 103 patients with the neuromuscular condition, which yielded positive results.
Skyclarys reached another milestone in December 2023 when the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) issued a positive response to its marketing authorization in the European Union. Upon the approval by the European Commission (EC), Skyclarys will be the first authorized treatment within the region for people aged 16 years or more, which can slow the progression of Friedreich’s ataxia.
Intensive Research Activities to Address Increasing Ataxia Market Demand
As Friedreich’s ataxia is the most common type of inherited ataxia, research activities aimed at finding promising therapeutic treatments are being promoted to reduce ataxia-associated healthcare burden. In April 2023 , an investigative study on the role of adenosine (a widely distributed nucleoside in the central nervous system) was conducted to evaluate its role in mitigating mitochondrial impairment in patients with Friedreich’s ataxia. The results demonstrated that adenosine could counter the deleterious effects of mitochondrial dysfunction and oxidative stress by regulating mitochondrial function and biogenesis in the fibroblasts of a patient with Friedreich’s ataxia. The results of the study support adenosine as a potential therapeutic in the treatment of this neuromuscular disease.
Other interventions such as stem cell therapy are also receiving attention from researchers for ataxia treatment. In addition, the treatment of spinocerebellar ataxia with mesenchymal stem cells is under investigation, projected to contribute to boost the market size in the forecast period.
Ataxia Market Segmentation
“Ataxia Market Report and Forecast 2025-2034” offers a detailed analysis of the market based on the following segments:
Market Breakup by Type
- Spinocerebellar Ataxias
- Ataxia-Telangiectasia
- Episodic Ataxia
- Others (Multiple System Atrophy (MSA)
- Treatment
- Diagnosis
- Solid
- Liquids
- Others
- Adult
- Child
- Geriatric
- Hospitals
- Clinics
- Others
- United States
- United Kingdom
- Germany
- France
- Italy
- Spain
- Japan
- China
The United States is anticipated to lead the ataxia market, owing to the presence of prominent biopharmaceutical companies, working to offer better treatment alternatives. In May 2023 , a Biohaven Ltd. announced the submission of a new drug application (NDA) for troriluzole to the United States FDA. The novel drug was designed to treat Spinocerebellar Ataxia Type 3 (SCA3) in patients.
Europe is also witnessing increased funding and investments by various sectors to accommodate the growing ataxia market demand. In January 2024 , Vico Therapeutics B.V., a clinical-stage genetic medication company based in the Netherlands, announced USD 60 million Series B financing. The funding is aimed to support the ongoing Phase 1/2a clinical trial of its intrathecally administered product VO659, designed to treat patients affected with spinocerebellar ataxia type 3 and type 1, among other neurological diseases.
Ataxia Market: Competitor Landscape
In July 2023, a global biotechnology company Biogen Inc. acquired Reata Pharmaceuticals, Inc. to accelerate the commercialization of the drug Skyclarys to patients with Friedreich’s ataxia around the world. Biogen agreed to buy Reata for USD 172.50 per share in cash, equivalent to a total enterprise value of around USD 7.3 billion. The market has been witnessing similar events of collaborations and acquisitions to deliver innovative therapies in the areas of unmet medical needs. Consequently, this is expected to propel ataxia market share in the coming years.
The key features of the market report include patent analysis, grants analysis, clinical trials analysis, funding and investment analysis, partnerships, and collaborations analysis by the leading key players. The major companies in the market are as follows:
- Novartis AG
- Merck KGaA
- Aurobindo Pharma
- Pfizer Inc.
- Sanofi
- Teva Pharmaceutical
- Acorda Therapeutics
- Viatris Inc.
- Design Therapeutics Inc.
- Lupin
- Apotex Inc.
- Biohaven Pharmaceuticals
- Amneal Pharmaceuticals LLC.
- Biovista
- Intrabio
*Please Note:* The report will take 5 business days to complete, after order confirmation.
Table of Contents
350 Pages
- 1 Preface
- 1.1 Objectives of the Study
- 1.2 Key Assumptions
- 1.3 Report Coverage – Key Segmentation and Scope
- 1.4 Research Methodology
- 2 Executive Summary
- 3 Ataxia Overview
- 3.1 Guidelines and Stages
- 3.2 Pathophysiology
- 3.3 Screening and Diagnosis
- 3.4 Treatment Pathway
- 4 Patient Profile
- 4.1 Patient Profile Overview
- 4.2 Patient Psychology and Emotional Impact Factors
- 4.3 Risk Assessment and Treatment Success Rate
- 5 Ataxia Epidemiology Analysis – 8 Major Markets
- 5.1 8MM Epidemiology Scenario Overview (2018-2034)
- 5.2 United States Ataxia Epidemiology Forecast (2018-2034)
- 5.3 EU-4 and United Kingdom Ataxia Epidemiology Forecast (2018-2034)
- 5.3.1 Germany Ataxia Epidemiology Forecast (2018-2034)
- 5.3.2 France Ataxia Epidemiology Forecast (2018-2034)
- 5.3.3 Italy Ataxia Epidemiology Forecast (2018-2034)
- 5.3.4 Spain Ataxia Epidemiology Forecast (2018-2034)
- 5.3.5 United Kingdom Ataxia Epidemiology Forecast (2018-2034)
- 5.4 Japan Ataxia Epidemiology Forecast (2018-2034)
- 5.5 China Ataxia Epidemiology Forecast (2018-2034)
- 6 Ataxia Market Overview – 8 Major Markets
- 6.1 Ataxia Market Historical Value (2018-2024)
- 6.2 Ataxia Market Forecast Value (2025-2034)
- 7 Ataxia Market Landscape – 8 Major Markets*
- 7.1 Ataxia Developers Landscape
- 7.1.1 Analysis by Year of Establishment
- 7.1.2 Analysis by Company Size
- 7.1.3 Analysis by Region
- 7.2 Ataxia Product Landscape
- 7.2.1 Analysis by Type
- 7.2.2 Analysis by Service
- 7.2.3 Analysis by Dosage Form
- 8 Ataxia Challenges and Unmet Needs
- 8.1 Treatment Pathway Challenges
- 8.2 Compliance and Drop-Out Analysis
- 8.3 Awareness and Prevention Gaps
- 9 Cost of Treatment
- 10 Ataxia Market Dynamics
- 10.1 Market Drivers and Constraints
- 10.2 SWOT Analysis
- 10.2.1 Strengths
- 10.2.2 Weaknesses
- 10.2.3 Opportunities
- 10.2.4 Threats
- 10.3 Porter’s Five Forces Model
- 10.3.1 Bargaining Power of Suppliers
- 10.3.2 Bargaining Power of Buyers
- 10.3.3 Threat of New Entrants
- 10.3.4 Threat of Substitutes
- 10.3.5 Degree of Rivalry
- 10.4 Key Demand Indicators
- 10.5 Key Price Indicators
- 10.6 Industry Events, Initiatives, and Trends
- 10.7 Value Chain Analysis
- 11 Ataxia Market Segmentation – 8 Major Markets
- 11.1 Ataxia Market by Type
- 11.1.1 Market Overview
- 11.1.2 Spinocerebellar Ataxias
- 11.1.3 Ataxia-Telangiectasia
- 11.1.4 Episodic Ataxia
- 11.1.5 Others (Multiple System Atrophy (MSA)
- 11.2 Ataxia Market by Service
- 11.2.1 Market Overview
- 11.2.2 Treatment
- 11.2.3 Diagnosis
- 11.3 Ataxia Market by Dosage Form
- 11.3.1 Market Overview
- 11.3.2 Solid
- 11.3.3 Liquids
- 11.3.4 Others
- 11.4 Ataxia Market by Age Group
- 11.4.1 Market Overview
- 11.4.2 Adult
- 11.4.3 Child
- 11.4.4 Geriatric
- 11.5 Ataxia Market by End User
- 11.5.1 Market Overview
- 11.5.2 Hospitals
- 11.5.3 Clinics
- 11.5.4 Others
- 11.6 Ataxia Market by Region
- 11.6.1 Market Overview
- 11.6.2 United States
- 11.6.3 EU-4 and the United Kingdom
- 11.6.3.1 Germany
- 11.6.3.2 France
- 11.6.3.3 Italy
- 11.6.3.4 Spain
- 11.6.3.5 United Kingdom
- 11.6.4 Japan
- 11.6.5 China
- 12 United States Ataxia Market
- 12.1 Ataxia Market Historical Value (2018-2024)
- 12.2 Ataxia Market Forecast Value (2025-2034)
- 12.3 Ataxia Market by Type
- 12.4 Ataxia Market by Service
- 13 EU-4 and United Kingdom Ataxia Market
- 13.1 Ataxia Market Historical Value (2018-2024)
- 13.2 Ataxia Market Forecast Value (2025-2034)
- 13.3 Germany Ataxia Market Overview
- 13.3.1 Ataxia Market by Type
- 13.3.2 Ataxia Market by Service
- 13.4 France Ataxia Market Overview
- 13.4.1 Ataxia Market by Type
- 13.4.2 Ataxia Market by Service
- 13.5 Italy Ataxia Market Overview
- 13.5.1 Ataxia Market by Type
- 13.5.2 Ataxia Market by Service
- 13.6 Spain Ataxia Market Overview
- 13.6.1 Ataxia Market by Type
- 13.6.2 Ataxia Market by Service
- 13.7 United Kingdom Ataxia Market Overview
- 13.7.1 Ataxia Market by Type
- 13.7.2 Ataxia Market by Service
- 14 Japan Ataxia Market
- 14.1 Ataxia Market Historical Value (2018-2024)
- 14.2 Ataxia Market Forecast Value (2025-2034)
- 14.2.1 Ataxia Market by Type
- 14.2.2 Ataxia Market by Service
- 15 China Ataxia Market
- 15.1 Ataxia Market Historical Value (2018-2024)
- 15.2 Ataxia Market Forecast Value (2025-2034)
- 15.2.1 Ataxia Market by Type
- 15.2.2 Ataxia Market by Service
- 16 Regulatory Framework
- 16.1 Regulatory Overview
- 16.1.1 US FDA
- 16.1.2 EU EMA
- 16.1.3 Japan PMDA
- 16.1.4 Others
- 17 Patent Analysis
- 17.1 Analysis by Type of Patent
- 17.2 Analysis by Publication Year
- 17.3 Analysis by Issuing Authority
- 17.4 Analysis by Patent Age
- 17.5 Analysis by CPC Analysis
- 17.6 Analysis by Patent Valuation
- 17.7 Analysis by Key Players
- 18 Grants Analysis
- 18.1 Analysis by Year
- 18.2 Analysis by Amount Awarded
- 18.3 Analysis by Issuing Authority
- 18.4 Analysis by Grant Application
- 18.5 Analysis by Funding Institute
- 18.6 Analysis by NIH Departments
- 18.7 Analysis by Recipient Organization
- 19 Clinical Trials Analysis
- 19.1 Analysis by Trial Registration Year
- 19.2 Analysis by Trial Status
- 19.3 Analysis by Trial Phase
- 19.4 Analysis by Therapeutic Area
- 19.5 Analysis by Geography
- 20 Funding Analysis
- 20.1 Analysis by Funding Instances
- 20.2 Analysis by Type of Funding
- 20.3 Analysis by Funding Amount
- 20.4 Analysis by Leading Players
- 20.5 Analysis by Leading Investors
- 20.6 Analysis by Geography
- 21 Partnership and Collaborations Analysis
- 21.1 Analysis by Partnership Instances
- 21.2 Analysis by Type of Partnership
- 21.3 Analysis by Leading Players
- 21.4 Analysis by Geography
- 22 Supplier Landscape
- 22.1 Novartis AG
- 22.1.1 Financial Analysis
- 22.1.2 Product Portfolio
- 22.1.3 Demographic Reach and Achievements
- 22.1.4 Mergers and Acquisition
- 22.1.5 Certifications
- 22.2 Merck KGaA
- 22.2.1 Financial Analysis
- 22.2.2 Product Portfolio
- 22.2.3 Demographic Reach and Achievements
- 22.2.4 Mergers and Acquisition
- 22.2.5 Certifications
- 22.3 Aurobindo Pharma
- 22.3.1 Financial Analysis
- 22.3.2 Product Portfolio
- 22.3.3 Demographic Reach and Achievements
- 22.3.4 Mergers and Acquisition
- 22.3.5 Certifications
- 22.4 Pfizer Inc.
- 22.4.1 Financial Analysis
- 22.4.2 Product Portfolio
- 22.4.3 Demographic Reach and Achievements
- 22.4.4 Mergers and Acquisition
- 22.4.5 Certifications
- 22.5 Sanofi
- 22.5.1 Financial Analysis
- 22.5.2 Product Portfolio
- 22.5.3 Demographic Reach and Achievements
- 22.5.4 Mergers and Acquisition
- 22.5.5 Certifications
- 22.6 Teva Pharmaceutical
- 22.6.1 Financial Analysis
- 22.6.2 Product Portfolio
- 22.6.3 Demographic Reach and Achievements
- 22.6.4 Mergers and Acquisition
- 22.6.5 Certifications
- 22.7 Acorda Therapeutics
- 22.7.1 Financial Analysis
- 22.7.2 Product Portfolio
- 22.7.3 Demographic Reach and Achievements
- 22.7.4 Mergers and Acquisition
- 22.7.5 Certifications
- 22.8 Viatris Inc.
- 22.8.1 Financial Analysis
- 22.8.2 Product Portfolio
- 22.8.3 Demographic Reach and Achievements
- 22.8.4 Mergers and Acquisition
- 22.8.5 Certifications
- 22.9 Design Therapeutics Inc.
- 22.9.1 Financial Analysis
- 22.9.2 Product Portfolio
- 22.9.3 Demographic Reach and Achievements
- 22.9.4 Mergers and Acquisition
- 22.9.5 Certifications
- 22.10 Lupin
- 22.10.1 Financial Analysis
- 22.10.2 Product Portfolio
- 22.10.3 Demographic Reach and Achievements
- 22.10.4 Mergers and Acquisition
- 22.10.5 Certifications
- 22.11 Apotex Inc.
- 22.11.1 Financial Analysis
- 22.11.2 Product Portfolio
- 22.11.3 Demographic Reach and Achievements
- 22.11.4 Mergers and Acquisition
- 22.11.5 Certifications
- 22.12 Biohaven Pharmaceuticals
- 22.12.1 Financial Analysis
- 22.12.2 Product Portfolio
- 22.12.3 Demographic Reach and Achievements
- 22.12.4 Mergers and Acquisition
- 22.12.5 Certifications
- 22.13 Amneal Pharmaceuticals LLC.
- 22.13.1 Financial Analysis
- 22.13.2 Product Portfolio
- 22.13.3 Demographic Reach and Achievements
- 22.13.4 Mergers and Acquisition
- 22.13.5 Certifications
- 22.14 Biovista
- 22.14.1 Financial Analysis
- 22.14.2 Product Portfolio
- 22.14.3 Demographic Reach and Achievements
- 22.14.4 Mergers and Acquisition
- 22.14.5 Certifications
- 22.15 Intrabio
- 22.15.1 Financial Analysis
- 22.15.2 Product Portfolio
- 22.15.3 Demographic Reach and Achievements
- 22.15.4 Mergers and Acquisition
- 22.15.5 Certifications
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