Huntington’s Disease Clinical Trial Pipeline Analysis: 20+ Key Companies Shaping the Future of Dopamine Receptor Antagonists Therapeutics | DelveInsight

The Huntington's disease treatment market is poised for significant growth, driven by rising prevalence rates and increased awareness globally. Advancements in gene-targeting and disease-modifying therapies, along with a robust clinical pipeline, are addressing critical unmet needs. Active government support and educational initiatives are further enhancing diagnosis and treatment uptake. Together, these factors create a strong foundation for market expansion in the coming years.

/EIN News/ -- New York, USA, June 03, 2025 (GLOBE NEWSWIRE) -- Huntington’s Disease Clinical Trial Pipeline Analysis: 20+ Key Companies Shaping the Future of Dopamine Receptor Antagonists Therapeutics | DelveInsight

The Huntington's disease treatment market is poised for significant growth, driven by rising prevalence rates and increased awareness globally. Advancements in gene-targeting and disease-modifying therapies, along with a robust clinical pipeline, are addressing critical unmet needs. Active government support and educational initiatives are further enhancing diagnosis and treatment uptake. Together, these factors create a strong foundation for market expansion in the coming years.

DelveInsight’s 'Huntington’s Disease Pipeline Insight 2025' report provides comprehensive global coverage of pipeline Huntington’s disease therapies in various stages of clinical development, major pharmaceutical companies are working to advance the pipeline space and future growth potential of the Huntington’s disease pipeline domain.

Key Takeaways from the Huntington’s Disease Pipeline Report

• DelveInsight’s Huntington’s disease pipeline report depicts a robust space with 20+ active players working to develop 20+ pipeline Huntington’s disease drugs. 
• Key Huntington’s disease companies such as Hoffmann-La Roche, Medibiofarma, PTC Therapeutics, Annexon, Alnylam Pharmaceuticals, Neuvivo, Skyhawk Therapeutics, BPG Bio, and others are evaluating new Huntington’s disease drugs to improve the treatment landscape.
• Promising pipeline Huntington’s disease therapies, such as RG6042, MBF 015, PTC518, ANX-005, ALN-HTT02, NP001, SKY 0515, Research Programme: HDD, and others are in different phases of Huntington’s disease clinical trials.
• In April 2025, the FDA granted a breakthrough therapy designation to AMT-130 (uniQuire) for the treatment of Huntington's disease. Previously, AMT-130 was also granted a regenerative medicine advanced therapy designation and orphan drug designation for this indication.
• In April 2025, Prilenia Therapeutics announced that it had entered into a collaboration and license agreement with Ferrer for the development and commercialization of pridopidine in Europe and other select markets.
• In March 2025, Skyhawk Therapeutics presented their novel SKY-0515 small molecule RNA splicing modulator targeting Huntington's Disease to members of the Huntington's Disease Youth Organization (HDYO), at the biannual HYDO International Congress in Prague, Czech Republic.
• In December 2024, Novartis announced that it had entered into a global licensing and collaboration agreement with PTC Therapeutics for PTC518, an HTT mRNA splice modulator for the treatment of Huntington's disease. Under the terms of the agreement, Novartis will pay USD 1 billion upfront and up to USD 1.9 billion in development, regulatory, and sales milestones. Novartis will also share profits in the US and pay tiered royalties on sales outside the US.
• In September 2024, PTC Therapeutics announced that the FDA had granted Fast Track designation to the PTC518 program for the treatment of Huntington's disease.
• In September 2024, the European Medicines Agency (EMA) accepted the marketing authorization application (MAA) for Prilenia Therapeutics’ pridopidine for the treatment of adults with Huntington's disease.

Request a sample and discover the recent advances in Huntington’s disease drugs @ Huntington’s Disease Pipeline Report

The Huntington’s disease pipeline report provides detailed profiles of pipeline assets, a comparative analysis of clinical and non-clinical stage Huntington’s disease drugs, inactive and dormant assets, a comprehensive assessment of driving and restraining factors, and an assessment of opportunities and risks in the Huntington’s disease clinical trial landscape. 

Huntington’s Disease Overview

Huntington’s disease is a hereditary, progressive neurodegenerative condition marked by the gradual onset of involuntary muscle movements—affecting the hands, feet, face, and trunk—and a steady decline in cognitive abilities and memory. It impacts the central region of the brain, leading to difficulties in movement, emotional regulation, and cognitive functions. Symptoms often appear between ages 30 and 50 but can emerge as early as age 2 or as late as 80. A hallmark feature of the disease is the presence of rapid, uncontrolled movements such as muscle jerks or tics. As the condition advances, patients may experience loss of coordination, speech difficulties, memory deterioration, and worsening choreiform movements, along with personality and behavioral changes.

Huntington’s disease follows an autosomal dominant inheritance pattern, meaning only one copy of the faulty gene is needed to cause the disease. It is triggered by a mutation in a single gene on chromosome 4, which encodes the huntingtin protein. While the exact role of huntingtin remains unclear, its mutated form disrupts normal brain function, leading to involuntary movements, severe cognitive decline, and emotional disturbances such as depression and irritability. The mutation involves an expansion of a CAG repeat segment within the gene. Typically, this segment repeats 17 to 20 times in a healthy gene, but in Huntington’s disease, the number of repeats rises to 40 or more.

Diagnosing Huntington’s disease involves a comprehensive clinical assessment, patient history, and several specialized tests. These may include blood work, genetic testing to detect mutations in the HTT gene, and brain imaging techniques such as CT scans, MRI, and EEG. CT and MRI provide detailed cross-sectional images of the brain, while EEG measures the brain’s electrical activity to support diagnosis.

Currently, there is no cure for Huntington’s disease, and treatment is aimed at alleviating symptoms. The only two FDA-approved medications—Austedo and Xenazine—are indicated specifically for managing chorea related to Huntington’s. Additional symptom management may include antidepressants, antipsychotics, and mood stabilizers to address psychiatric symptoms. Supportive therapies and multidisciplinary care are also critical in improving the quality of life for individuals affected by this condition.

Find out more about Huntington’s disease drugs @ Huntington’s Disease Treatment

A snapshot of the Pipeline Huntington’s Disease Drugs mentioned in the report:

Drugs	Company	Phase	MoA	RoA
MBF 015	Medibiofarma	II	HDAC1/C2 inhibitors	Oral
PTC518	PTC Therapeutics	II	HD protein inhibitors; RNA splicing modulators	Oral
ANX-005	Annexon	II	Complement C1 inhibitors	Intravenous
ALN-HTT02	Alnylam Pharmaceuticals	I	RNA interference	Intrathecal
NP001	Neuvivo	I	Macrophage modulators	Unspecified
SKY 0515	Skyhawk Therapeutics	I	RNA splicing modulators	Oral

Learn more about the emerging Huntington’s disease therapies @ Huntington’s Disease Clinical Trials

Huntington’s Disease Therapeutics Assessment

The Huntington’s disease pipeline report proffers an integral view of the emerging Huntington’s disease therapies segmented by stage, product type, molecule type, route of administration, and mechanism of action.

Scope of the Huntington’s Disease Pipeline Report 

• Coverage: Global 
• Therapeutic Assessment By Product Type: Mono, Combination, Mono/Combination
• Therapeutic Assessment By Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III
• Therapeutics Assessment By Route of Administration: Intra-articular, Intraocular, Intrathecal, Intravenous, Oral, Parenteral, Subcutaneous, Topical, Transdermal
• Therapeutics Assessment By Molecule Type: Oligonucleotide, Peptide, Small molecule
• Therapeutics Assessment By Mechanism of Action: HDAC1/C2 inhibitors, RNA interference, HD protein inhibitors, RNA splicing modulators, Macrophage modulators, Complement C1 inhibitors
• Key Huntington’s Disease Companies: Hoffmann-La Roche, Medibiofarma, PTC Therapeutics, Annexon, Alnylam Pharmaceuticals, Neuvivo, Skyhawk Therapeutics, BPG Bio, and others.
• Key Huntington’s Disease Pipeline Therapies: RG6042, MBF 015, PTC518, ANX-005, ALN-HTT02, NP001, SKY 0515, Research Programme: HDD, and others.

Dive deep into rich insights for new Huntington’s disease treatments, visit @ Huntington’s Disease Drugs

Table of Contents

1.	Huntington’s Disease Pipeline Report Introduction
2.	Huntington’s Disease Pipeline Report Executive Summary
3.	Huntington’s Disease Pipeline: Overview
4.	Analytical Perspective In-depth Commercial Assessment
5.	Huntington’s Disease Clinical Trial Therapeutics
6.	Huntington’s Disease Pipeline: Late-Stage Products (Pre-registration)
7.	Huntington’s Disease Pipeline: Late-Stage Products (Phase III)
8.	Huntington’s Disease Pipeline: Mid-Stage Products (Phase II)
9.	Huntington’s Disease Pipeline: Early-Stage Products (Phase I)
10.	Huntington’s Disease Pipeline Therapeutics Assessment
11.	Inactive Products in the Huntington’s Disease Pipeline
12.	Company-University Collaborations (Licensing/Partnering) Analysis
13.	Key Companies
14.	Key Products in the Huntington’s Disease Pipeline
15.	Unmet Needs
16.	Market Drivers and Barriers
17.	Future Perspectives and Conclusion
18.	Analyst Views
19.	Appendix

For further information on the Huntington’s disease pipeline therapeutics, reach out @ Huntington’s Disease Therapeutics

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