Huntington’s Disease Treatment Market by Drug (Tetrabenazine, Deutetrabenazine, Valbenazine, Others), by Distribution Channel (Hospital Pharmacies, Drug Stores & Retail Pharmacies, Online Pharmacies), by North America (U.S., Canada) Forecast 2024-2032
The Huntington’s Disease Treatment Marketsize was valued at USD 945.8 USD million in 2023 and is projected to reach USD 2924.59 USD million by 2032, exhibiting a CAGR of 17.5 % during the forecast period.Huntington’s disease (HD) is a type of neurodegenerative disorder which is caused by the genetic mutation that consecutively depletes the nerve cells in the brain resulting in different types of symptoms including malfunctions of movement, cognition, and psychiatric disorders. The disease is due to the presence of a point mutation in the HTT gene, wherein the synthesis of an abnormal huntingtin protein starts that is characterized by also a progression of aggregation within neurons and consequently the neuronal dysfunction and cell death. The cardinal features of the disease consist of chorea (involuntary movements), pain caused by muscle rigidity, impaired coordination of movement, memory loss, executive dysfunction, depression, anxiety, irritability and psychosis. The disease usually makes its appearance in the later stages of life, but it can also begin at any stage. There is significant variability in terms of the severity and progression of the disease for different people. The comprehensive influence of Huntington's disease is often unsightly, impairing the motoric functions, mental capabilities and psychological attitude as well as the general welfare. People with HD continually have their motor skills compromised as well as mental functions, emotional problems together with the inability to perform daily routines. Caregivers also encounter significant disadvantages in the process of giving guiding and managing a wide range of needs of persons with Huntington's disease.Genetic testing and counselling are two crucial elements of HD management; they secures the people genetic status to avoid the predictable injury and provide scientifically based information regarding the future of their family and, if appropriate, outsource for support services, and maybe take part in research projects. Although as yet there is no cure for Huntington's disease, scientists are excavating modes of death for the identified genes and the mechanisms are being explored for their potential to both hinder the progression, alleviate its symptoms and optimize the patient outcomes.
Rising awareness about Huntington's disease, advancements in gene therapy approaches, and the emergence of novel drugs are shaping market trends. Personalized treatment and multi-disciplinary approaches are gaining popularity.
Drug:
Distribution Channel:
Aspects | Details |
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Study Period | 2018-2032 |
Base Year | 2023 |
Estimated Year | 2024 |
Forecast Period | 2024-2032 |
Historical Period | 2018-2023 |
Growth Rate | CAGR of 17.5% from 2018-2032 |
Segmentation |
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Aspects | Details |
---|---|
Study Period | 2018-2032 |
Base Year | 2023 |
Estimated Year | 2024 |
Forecast Period | 2024-2032 |
Historical Period | 2018-2023 |
Growth Rate | CAGR of 17.5% from 2018-2032 |
Segmentation |
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Note* : In applicable scenarios
Primary Research
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