The market’s growth can be attributed to the increasing cases of Huntington’s disease and rapid advancements in early disease detection technologies and gene therapies.
Home>Industry Reports>Global Huntington’s Disease Treatment Market Assessment, Opportunities and Forecast, 2018-2032F
Global Huntington’s disease treatment market is projected to witness a CAGR of 12.45% during the forecast period 2025-2032, growing from USD 509.56 million in 2024 to USD 1302.78 million in 2032. The market’s growth is supported by the rising cases of Huntington’s disease, increasing investments towards pharmaceutical products and therapies, rising initiatives to increase awareness about the condition, and rapid advancements in medical research. As per the estimates of UC Davis Health (University of California), Huntington’s disease affects about 1 in 10,000 people across the globe. Recent advancements in gene therapies and RNA therapeutics are also supporting the market’s expansion.
Report Attribute |
Details |
Base Year of the Analysis |
2024 |
Historical Period |
2018-2023 |
Forecast Period |
2025-2032 |
Projected Growth Rate |
CAGR of 12.45% between 2025 and 2032 |
Revenue Forecast in 2032 |
USD 1302.78 million |
Additionally, government and nonprofit organizations are fostering collaborations and clinical trial awareness among patients and caregivers. These efforts are not only improving trial participation rates but also accelerating drug development timelines. The market’s growth is also driven by the increasing awareness among medical professionals about the ongoing clinical research and advancements in neurodegenerative diagnostics. Increasing investments in disease-modifying therapies coupled with the rising government support for the management of rare diseases is also contributing towards the market’s expansion.
Early diagnosis and intervention are essential for the management of neurodegenerative disorders such as Huntington’s disease. Modern testing techniques aid in the identification of individuals carrying Huntington’s disease gene mutation, even before the occurrence of symptoms. This early identification for genetic counseling, clinical monitoring, and enrollment in clinical trials in a time-efficient manner. This in turn is allowing pharmaceutical companies to develop novel drugs, that are able to halt or slow the progression of the disease, providing lucrative growth opportunities for the market. For instance, in February 2025, Latus Bio, Inc. released data in support of its preclinical gene therapy program for Huntington’s disease. The company introduced a new computational model for predicting the effects of the knockdown of MSH3 on reducing somatic instability. The company aims to use its AAV-DB-3 capsid variant for delivering an engineered mRNA to reduce the MSH3 in the cells that are affected by Huntington’s disease.
Regulatory Approvals Support Market Expansion
Increasing regulatory support and approvals are propelling the market’s expansion as they accelerate the adoption and accessibility of new therapeutic solutions. Regulatory bodies such as the European Medicines Agency (EMA) and the United States Food and Drug Administration (US FDA) are granting regenerative medicine advanced therapy and breakthrough therapy to promising candidates to ensure the availability of advanced therapies and incentivize the leading pharmaceutical companies to invest in Huntington’s disease treatments. The provision of such designations facilitates faster drug development and review, ensuring the entry of innovative treatments. For instance, in April 2025, the US FDA granted breakthrough therapy designation to AMT-130 for treating Huntington’s disease. Unlike current therapies available in the market, AMT-130 aims to address the underlying genetic cause of the condition and provide long-term solutions for Huntington’s. As new drugs and gene therapies progress through clinical stages, the market is expected to expand rapidly, due to improved clinical outcomes and patient access.
The segment’s dominance is supported by the central role played by hospital pharmacies in the management of complex diseases such as Huntington’s disease. A large portion of Huntington’s disease medications, including deutetrabenazine and tetrabenazine, often necessitate close medical supervision and are prescription-only. Hospital pharmacies are well-equipped to ensure that both outpatients and inpatients have access to the necessary drugs and are often under the care of multidisciplinary teams such as genetic counselors, neurologists, and psychiatrists. Moreover, hospital pharmacies offer comprehensive services including medication monitoring, management of side effects, and adjustments to treatment regimens, which are crucial for Huntington’s disease patients who may experience rapid changes in symptoms.
Meanwhile, leading hospital pharmacies are focusing on expanding their market presence, contributing to the segment’s expansion. For instance, in March 2025, Apollo HealthCo Ltd, operator of the online platform Apollo 24/7 and Apollo Pharmacy, announced the expansion of its offline hospital pharmacy network in Bengal, India.
North America Holds a Major Market Share
The region’s dominance can be attributed to the strong presence of leading pharmaceutical companies, high investments in research activities, and increasing cases of Huntington’s disease in countries such as the United States and Canada. As per the estimates of the Huntington’s Disease Society of America, approximately 41,000 Americans have Huntington’s, and 200,000 Americans are at risk of inheriting the disease.
The market also benefits from favorable reimbursement policies and high levels of awareness among clinicians and the general population. The US FDA’s stance on gene therapies and orphan drugs incentivizes companies to pursue treatments for Huntington’s disease. Furthermore, organizations such as Huntington’s Disease Society of America and the Hereditary Disease Foundation play a key role in advocacy, funding, and education. Canada, too, is witnessing a rise in Huntington’s disease research with several centers of excellence and registry programs promoting real-world data collection. The region also benefits from numerous clinical trials and significant investments in neurodegenerative diseases.
Impact of the U.S. Tariffs on Global Huntington’s Disease Treatment Market
The financial strain from the tariffs may divert resources away from research and development activities, forcing companies to scale back on or postpone clinical trials for Huntington’s disease therapies due to rising operational costs. This could result in delays in the availability of novel therapeutic solutions and could slow the progress of promising treatments, including gene therapies, which are currently under various stages of development. In response to the tariffs, leading pharmaceutical companies are considering reshoring their manufacturing sites to the United States and diversifying their supply chains. The uncertainties surrounding the trade policies are also deterring investments in Huntington’s research, impacting the market’s expansion.
Report Scope
“Global Huntington’s Disease Treatment Market Assessment, Opportunities and Forecast, 2018-2032F”, is a comprehensive report by Markets and Data, providing in-depth analysis and qualitative and quantitative assessment of the current state of global Huntington’s disease treatment market, industry dynamics, and challenges. The report includes market size, segmental shares, growth trends, opportunities, and forecasts between 2025 and 2032. Additionally, the report profiles the leading players in the industry, mentioning their respective market share, business models, competitive intelligence, etc.
Report Attribute |
Details |
Segments Covered |
Drug Type, Distribution Channel |
Regions Covered |
North America, Europe, South America, Asia-Pacific, Middle East and Africa |
Key Companies Profiled |
H. Lundbeck A/S, Bausch Health Companies Inc., Sun Pharmaceutical Industries Ltd., Teva Pharmaceuticals Industries Ltd., Dr. Reddy’s Laboratories Ltd., Pfizer Inc., Neurocrine Biosciences, Inc., Hikma Pharmaceuticals PLC, Lupin Limited, and Prilenia Therapeutics B.V. |
Customization Scope |
15% free report customization with purchase |
Pricing and Purchase Options |
Avail the customized purchase options to fulfill your precise research needs |
Delivery Format |
PDF and Excel through email (subject to the license purchased) |
In the report, global Huntington’s disease treatment market has been segmented into the following categories:
Key Players Landscape and Outlook
The key players in the market are actively focusing on developing novel therapeutic solutions that target the root cause of the disease and its progression and provide symptomatic relief. Additionally, the companies are also engaging in mergers and acquisitions to enhance their neurodegenerative pipeline. For instance, in December 2024, H. Lundbeck A/S completed the acquisition of Longboard Pharmaceuticals, Inc., allowing the company to expand its Huntington’s portfolio. With Lundbeck's established expertise in neurology and global reach, Longboard’s neflamapimod can be efficiently developed, commercialized, and made accessible to a broader patient base. Such acquisitions are expected to support the leading players in the market in expanding their customer base and strengthening their position in the market.
Key Players Operating in Global Huntington’s Disease Treatment Market are:
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