Huntington’s Disease Treatment Market is expected to grow at a 14.7% CAGR, achieving USD 2.129 billion in 2031 from USD 0.935 billion in 2025.
Huntington’s disease treatment market is anticipated to grow at a steady pace. Due to the organism's aberrant response against its own tissue, autoimmune disease results in the breakdown of normal immunological homeostasis. Inflammation, autoantibodies, and self-reactive T cells are typically impacted by autoimmune disorders. Potential autoimmune illnesses are difficult to diagnose since no single laboratory test can provide an accurate diagnosis of the condition. The diagnosis can aid with the treatment of autoimmune disease patients and can help with prognosis or identifying the degree of organ involvement or damage.
Increased prevalence of diseases and cutting-edge drug development to bolster growth.
The growth of the Huntington's disease treatment market is attributed to several factors, including an increase in the prevalence of the disease and a rise in the demand for cutting-edge drug types for treating Huntington's symptoms. Clinical trials and a robust drug pipeline are other Huntington's disease treatment industry trends that are anticipated to support the Huntington's disease treatment market's forecasted expansion.
Huntington's disease treatment industry is expanding because of both an increase in the prevalence of the condition and a rise in demand for cutting-edge disease treatments.
Growing prevalence of autoimmune diseases
The burden of autoimmune disorders is increasing globally, and there is a growing awareness of health issues and diseases, which increases the need for diagnostics for early disease diagnosis and propels the market's expansion. The American Autoimmune Related Disease Association (AARDA), for instance, marks the month of March each year as Autoimmune Disease Awareness Month (ADAM). AARDA is dedicated to the elimination of autoimmune diseases, the reduction of suffering, and the socioeconomic effects of autoimmunity. In February 2021, the American Kidney Fund (AKF) introduced a new patient-focused education and awareness campaign on the kidney disease lupus nephritis.
Increasing the number of patients with rheumatoid arthritis
An autoimmune condition called rheumatoid arthritis (RA) primarily targets the synovial tissues in the joints. Most of the disease's victims are older people. The segment's growth is also greatly influenced by the ageing population and technological improvements.
The prevalence of rheumatoid arthritis among the old population has increased along with the burden of the geriatric population, which is what is driving the market's expansion. For instance, the World Population Prospect, 2022, estimates that there will be 771 million people worldwide who are 65 or older in 2022, and that number would rise to 994 million by 2030 and 1.6 billion by 2050.
Increasing clinical trials
The Huntington’s disease market is expanding because of an increase in clinical research efforts for various drug development procedures. An investigational monoclonal antibody called ANX005 is being developed by Annexon, Inc., and targets aberrant C1q activity in complement-mediated neurodegenerative illnesses, including Huntington's Disease. It is given intravenously (IV) and is intended to inhibit the whole classical complement system, including C1q. Additionally, the business began a phase 2 clinical trial of ANX005 for the treatment of HD patients in 2020. As a possible HD treatment, stem cell therapy is also attracting attention. Cellavita is currently researching stem cell treatment, CELLAVITA-HD, in a phase 2/ 3 ADORE-DH study in partnership with AzidusPharma.
Increasing R&D activities
Throughout the forecast period, rising R&D activities and product development are also anticipated to aid in the Huntington’s disease treatment market's growth. For instance, in April 2021, an IND application for Voyager Therapeutics Inc.'s VY-HTT, a gene therapy candidate intended to treat Huntington's disease, was approved by the US FDA. The goal of the treatment is to stop the huntingtin gene from being expressed to slow the spread of the illness. Similarly, uniQure NV reported clinical results for the first four patients included in the lower-dose group of its ongoing Phase I/II clinical study of AMT-130 in December 2021. The gene therapy project AMT-130 is intended to treat Huntington's disease.
Disease-modifying therapies are predicted to grow.
Disease-modifying therapies are anticipated to see the fastest rate of Huntington’s disease treatment market growth throughout the anticipated time frame. This is a result of increasing research and development for disease-modifying medicines, as well as a surge in demand for cutting-edge items like gene therapy and stem cell treatment. Positive government initiatives, such as the U.S. FDA's Fast Track Designation for accelerating the registration process, are anticipated to support the industry in the approaching years. For instance, in October 2023, the U.S. FDA approved Sage Therapeutics' drug SAGE-718 as a potential treatment for Huntington's disease.
North America is anticipated to become a significant marketplace.
North America’s Huntington’s disease market share is brought on by the high disease burden, rising healthcare costs, technology developments, proactive government measures, and growing patient knowledge of Huntington's disease treatment options. Throughout the projection period, businesses are anticipated to ramp up their R&D and product development efforts. For instance, PTC Therapeutics began a Phase 2 study in the United States in April 2022 to examine PTC518, a potential therapy for Huntington's disease. The two-part PIVOT-HD experiment will be carried out in clinical settings all around the world. Participants will be randomly randomized to receive either a placebo or PTC518 (around three months) before being followed for 12 weeks.
Asia Pacific is predicted to grow at a robust pace during the forecast period
The Asia Pacific Huntington's disease treatment market is anticipated to see substantial growth. The region's market is anticipated to rise because of an increase in the number of government programs aimed at enhancing population health. The market for treating Huntington's illness is, however, crowded, which could prevent its expansion in this area. To stop them from launching a generic version of Austedo on the market, for instance, Teva Pharmaceutical Industries Ltd. announced the patent dispute settlement of the AUSTEDO® (deutetrabenazine) patent with Aurobindo.
Teva Pharmaceutical Industries Ltd.
H. Lundbeck A/S
Bausch Health Companies Inc.
Neurocrine Biosciences, Inc.
Prilenia Therapeutics
November 2025: uniQure disclosed that after a pre-BLA meeting with the U.S. FDA, regulators indicated current Phase I/II data may be inadequate for a BLA, delaying the planned early-2026 submission.
October 2025: Prilenia Therapeutics and Ferrer shared updated analyses of pridopidine’s impact on Huntington’s disease progression at the HSG Clinical Research Congress and plan a global confirmatory trial in 2026.
September 2025: uniQure announced Phase I/II results for AMT-130, demonstrating a 75% slowing of disease progression at 36 months in the high-dose group, marking a landmark achievement for Huntington's gene therapy.
July 2025: Prilenia Therapeutics and Ferrer received an EMA refusal for the marketing authorization of pridopidine, though the companies immediately committed to a new global registrational study for 2026.
May 2025: PTC Therapeutics’ Phase 2 PIVOT-HD study of PTC518 (votoplam) demonstrated statistically significant, dose-dependent reductions in mutant huntingtin protein, with favorable biomarker and clinical trends supporting future development.
| Report Metric | Details |
|---|---|
| Total Market Size in 2026 | USD 0.935 billion |
| Total Market Size in 2031 | USD 1.892 billion |
| Growth Rate | 15.15% |
| Study Period | 2021 to 2031 |
| Historical Data | 2021 to 2024 |
| Base Year | 2025 |
| Forecast Period | 2026 – 2031 |
| Segmentation | Drug, Distribution Channel, Treatment Channel, Geography |
| Geographical Segmentation | North America, South America, Europe, Middle East and Africa, Asia Pacific |
| Companies |
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By Type
Medication
Tetrabenazine
Deutetrabenazine
Others
Therapy
Physical Therapy
Speech Therapy
Disease Modifying Therapy
By Route of Administration
Injectable
Oral
By End-User
Hospitals
Specialty Clinics
Others
By Geography
North America
USA
Canada
Mexico
South America
Brazil
Argentina
Others
Europe
Germany
France
United Kingdom
Spain
Others
Middle East and Africa
Saudi Arabia
UAE
Israel
Others
Asia Pacific
China
India
Japan
South Korea
Indonesia
Thailand
Others