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Ataxia Pipeline: Advancing Therapeutics and 32+ Leading Companies Shaping the Ataxia Treatment Landscape | DelveInsight

05-08-2025 05:16 PM CET | Health & Medicine

Press release from: DelveInsight

Ataxia Pipeline

Ataxia Pipeline

The therapeutic landscape for Ataxia, a group of rare neurological disorders characterized by impaired coordination and balance, is witnessing significant momentum, driven by advances in genetic research, biomarker development, and a surge in innovative therapies. Biopharmaceutical companies such as Retrotope, Reata Pharmaceuticals, PTC Therapeutics, Metro International Biotech, LLC, and Design Therapeutics are leading the charge, targeting key pathways like mitochondrial dysfunction, cerebellar degeneration, and RNA-based mechanisms to develop disease-modifying treatments for various forms of Ataxia, including Friedreich's Ataxia and Spinocerebellar Ataxias.

DelveInsight's "Ataxia - Pipeline Insight, 2025" delivers a comprehensive evaluation of the clinical and preclinical development pipeline, offering detailed insights into emerging drug candidates, their mechanisms of action, trial progress, and anticipated regulatory timelines. The report highlights investigational therapies ranging from gene therapies and small molecules to novel CNS-targeted agents that aim to slow or halt disease progression.

Additionally, this pipeline assessment provides a 360° view of drug development by analyzing trends across clinical phases, therapeutic classes, administration routes, and trial geographies. It also outlines key unmet needs, strategic partnerships, regulatory designations, and innovations that are expected to reshape the Ataxia treatment paradigm in the near future.

Interested in learning more about the current treatment landscape and the key drivers shaping the ataxia pipeline? Click here: https://www.delveinsight.com/report-store/ataxia-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=jpr

Key Takeaways from the Ataxia Pipeline Report
• DelveInsight's ataxia pipeline analysis depicts a strong space with 32+ active players working to develop 32+ pipeline drugs for ataxia treatment.
• The leading ataxia companies include Retrotope, Reata Pharmaceuticals, PTC Therapeutics, Metro International Biotech, LLC, Design Therapeutics, Larimar Therapeutics, Minoryx Therapeutics, EryDel, Biogen, Matrix Biomed, IntraBio, Biohaven Pharmaceuticals, Inc., Stealth BioTherapeutics Inc., Acasti Pharma, Seelos Therapeutics, Kissei Pharmaceutical, Vico Therapeutics, Q-State Biosciences, Locanabio, Lexeo Therapeutics, Voyager Therapeutics, CRISPR Therapeutics, Capsida Biotherapeutics, AavantiBio, StrideBio, Wave Life Sciences, REPROCELL, SHIONOGI & Co., CORESTEM, Blade Therapeutics, Exicure, Lacerta Therapeutics, Healx Ltd., Uniqure, Ionis Pharmaceuticals, Jupiter Neurosciences, and others are evaluating their lead assets to improve the ataxia treatment landscape.
• Key ataxia pipeline therapies in various stages of development include RT001, Omaveloxolone, Vatiquinone, MIB-626, DT-216, CTI-1601, MIN-102, EryDex, BIIB132, MBM-01, IB1001, Troriluzole, Elamipretide, GTX-102, SLS-005, KPS-0373, VO 659, LX2006, AVB-202, STRX 110, Stemchymal, S-0373, Allo BM-MSC, and others.
• In April 2025, Biohaven secured up to $600 million in financing from Oberland Capital Management, with $250 million expected by April 30. The funding supports the potential U.S. launch of its lead drug, troriluzole, for spinocerebellar ataxia (SCA).
• In February 2025, Biohaven Ltd. announced that the FDA has accepted its New Drug Application (NDA) for troriluzole to treat adult patients with spinocerebellar ataxia (SCA) and granted it Priority Review.
• In January 2025, Solid Biosciences Inc. announced that the FDA approved its Investigational New Drug (IND) application for SGT-212, a gene therapy for Friedreich's ataxia, a progressive disease causing nervous system damage and cardiac dysfunction due to low frataxin production.
• In September 2024, Papillon Therapeutics announced that the U.S. FDA granted Orphan Drug Designation to its experimental treatment, PPL-001, for Friedreich's ataxia. Papillon is a clinical-stage biotech company focused on developing genetic medicines for inherited diseases.

Request a sample and discover the recent breakthroughs happening in the ataxia pipeline landscape @ https://www.delveinsight.com/report-store/ataxia-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=jpr

Ataxia Overview
Ataxia is a degenerative nervous system disorder that causes symptoms similar to intoxication, such as slurred speech, stumbling, falling, and lack of coordination. These symptoms occur due to damage to the cerebellum, the part of the brain responsible for movement coordination. Treatment for Ataxia includes medications to manage symptoms and therapies to enhance the patient's quality of life. Individuals with Ataxia may face difficulties with fine motor skills, walking, speaking, and eye movements. The condition can affect individuals of all ages, with symptoms appearing at various stages, from childhood to late adulthood. Ataxia can lead to severe complications and, in some cases, premature death.

Find out more about ataxia medication @ https://www.delveinsight.com/report-store/ataxia-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=jpr

Ataxia Treatment Analysis: Drug Profile
RT 001: Retrotope
RT001 is an investigational, isotopically stabilized synthetic linoleic acid (LA) under development for various orphan neurodegenerative diseases, including infantile neuroaxonal dystrophy (INAD), Friedreich's ataxia (FA), amyotrophic lateral sclerosis (ALS), and progressive supranuclear palsy (PSP). The compound has been safely administered orally to over 100 patients, with more than 1,000 patient months of experience. RT001 is currently undergoing clinical trials in multiple neurodegenerative conditions, with significant data readouts anticipated by the end of 2021, including pivotal Phase 2/3 trials in INAD, FA, and ALS. RT001 has received key regulatory designations from both the U.S. FDA and the European Medicines Agency (EMA), including rare pediatric disease designations for INAD and FA, Fast Track designation for FA, and orphan drug designations for FA, PSP, and PLA2G6-associated neurodegeneration, which includes INAD. Additionally, RT001 has been granted orphan drug designation for INAD in Europe.

Omaveloxolone: Reata Pharmaceuticals
Omaveloxolone is an investigational oral treatment that activates Nrf2, a transcription factor involved in cellular processes that reduce inflammation, restore mitochondrial function, and inhibit pro-inflammatory signaling. Omaveloxolone has received Orphan Drug and Fast Track Designations from the FDA for Friedreich's ataxia and Orphan Drug Designation from the European Commission for the same condition.

Learn more about the novel and emerging ataxia pipeline therapies @ https://www.delveinsight.com/report-store/ataxia-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=jpr

Ataxia Therapeutics Assessment
By Product Type
• Mono
• Combination
• Mono/Combination.

By Stage
• Late-stage products (Phase III)
• Mid-stage products (Phase II)
• Early-stage product (Phase I) along with the details of
• Pre-clinical and Discovery stage candidates
• Discontinued & Inactive candidates

By Route of Administration
• Inhalation
• Inhalation/Intravenous/Oral
• Intranasal
• Intravenous
• Intravenous/ Subcutaneous
• NA
• Oral
• Oral/intranasal/subcutaneous
• Parenteral
• Subcutaneous

By Molecule Type
• Antibody
• Antisense oligonucleotides
• Immunotherapy
• Monoclonal antibody
• Peptides
• Protein
• Recombinant protein
• Small molecule
• Stem Cell
• Vaccine

Scope of the Ataxia Pipeline Report
• Coverage: Global
• Key Ataxia Companies: Retrotope, Reata Pharmaceuticals, PTC Therapeutics, Metro International Biotech, LLC, Design Therapeutics, Larimar Therapeutics, Minoryx Therapeutics, EryDel, Biogen, Matrix Biomed, IntraBio, Biohaven Pharmaceuticals, Inc., Stealth BioTherapeutics Inc., Acasti Pharma, Seelos Therapeutics, Kissei Pharmaceutical, Vico Therapeutics, Q-State Biosciences, Locanabio, Lexeo Therapeutics, Voyager Therapeutics, CRISPR Therapeutics, Capsida Biotherapeutics, AavantiBio, StrideBio, Wave Life Sciences, REPROCELL, SHIONOGI & Co., CORESTEM, Blade Therapeutics, Exicure, Lacerta Therapeutics, Healx Ltd., Uniqure, Ionis Pharmaceuticals, Jupiter Neurosciences, and others.
• Key Ataxia Pipeline Therapies: RT001, Omaveloxolone, Vatiquinone, MIB-626, DT-216, CTI-1601, MIN-102, EryDex, BIIB132, MBM-01, IB1001, Troriluzole, Elamipretide, GTX-102, SLS-005, KPS-0373, VO 659, LX2006, AVB-202, STRX 110, Stemchymal, S-0373, Allo BM-MSC, and others.

Dive deep into rich insights for drugs used for ataxia treatment; visit @ https://www.delveinsight.com/report-store/ataxia-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=jpr

Table of Contents
1. Introduction
2. Executive Summary
3. Ataxia Pipeline: Overview
4. Analytical Perspective In-depth Commercial Assessment
5. Ataxia Pipeline Therapeutics
6. Ataxia Pipeline: Late-Stage Products (Phase III)
7. Ataxia Pipeline: Mid-Stage Products (Phase II)
8. Ataxia Pipeline: Early Stage Products (Phase I)
9. Therapeutic Assessment
10. Inactive Products
11. Company-University Collaborations (Licensing/Partnering) Analysis
12. Key Companies
13. Key Products
14. Unmet Needs
15. Market Drivers and Barriers
16. Future Perspectives and Conclusion
17. Analyst Views
18. Appendix

Contact Us:
Jatin Vimal
jvimal@delveinsight.com
+14699457679
Healthcare Consulting
https://www.delveinsight.com/consulting-services

About DelveInsight
DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance. Get hassle-free access to all the healthcare and pharma market research reports through our subscription-based platform, PharmDelve.

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