Amyotrophic Lateral Sclerosis Market Outlook: Expanding Therapeutic Pipeline and Novel Drug Launches Propel Growth Throughout Forecast Period (2025-2034) | DelveInsight
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Amyotrophic Lateral Sclerosis Market Summary
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Key Factors Driving the Growth of the Amyotrophic Lateral Sclerosis Market
Rising ALS Prevalence
The global incidence of ALS is on the rise, with nearly 5,000 new cases diagnosed annually in the United States alone. The total prevalent cases of ALS in the 7MM comprised nearly 67K in 2023 which are estimated to reach 75K by 2034. This increase in prevalence is fueling demand for effective treatments and driving market growth.
Regulatory Approvals of RADICAVA
RADICAVA has proven to be a successful treatment for ALS. Approval of oral RADICAVA in the United States and its approval in Japan in December 2022 have enhanced patient compliance.
Technological Innovations in Diagnosis and Treatment
Advancements in diagnostic technologies and treatment methodologies are improving patient outcomes. The development of personalized medicine and targeted therapies is enhancing the efficacy of ALS treatments, contributing to market expansion.
Rising Amyotrophic Lateral Sclerosis Clinical Trial Activities
Some of the drugs in the pipeline include Masitinib (AB Sciences), Prime C (Neurosense Therapeutics), RNS60 (Revalesio), NP001 (Neuvivo), Ibudilast (MediciNova), NurOwn (Brainstorm-Cell Therapeutics' MSC-NTF cells), Pridopidine (Prilenia Therapeutics), and others.
Amyotrophic Lateral Sclerosis Market Analysis
Currently, available drugs for the treatment of ALS include RILUTEK, TIGLUTEK (oral suspension), RADICAVA (IV and oral suspension/ORS), and QALSODY. Approved symptomatic therapies comprise NEUDEXTA, TIGLUTEK, and RILUTEK, along with supportive medications such as anti-epileptic drugs, opioids, nonsteroidal anti-inflammatory drugs (NSAIDs), diuretics, selective serotonin reuptake inhibitors (SSRIs), and various antidepressants.
Following the approval of RADICAVA ORS, sales of the RADICAVA franchise rebounded significantly, reversing the previous decline in IV RADICAVA usage. The oral formulation was rapidly adopted in both the United States and Japan.
RELYVRIO experienced rapid market adoption in the U.S. between 2022 and 2023. However, after the PHOENIX trial failed to meet its primary endpoints, Amylyx Pharmaceuticals upheld its earlier commitment to withdraw the drug. Consequently, RELYVRIO was officially discontinued on April 4, 2024, following consultations with the U.S. FDA and Health Canada.
The anticipated launches of emerging therapies such as IFB-088 (InFlectis BioScience), Ulefnersen (Ionis/Otsuka Pharmaceuticals), Ibudilast (MediciNova), Masitinib (AB Science), NurOwn (BrainStorm Cell Therapeutics), CNM-Au8 (Clene Nanomedicine), NP001 (Neuvivo), and CBT101 (Ceres Brain Therapeutics, early-stage) are expected to expand the ALS market in the coming years, supported by a rising number of diagnosed cases.
Additionally, NDC-011, a novel drug combination developed through DR.NOAH's AI-based drug discovery platform, received Orphan Drug Designation (ODD) from the U.S. FDA in 2023 and IND approval for a Phase I clinical trial in 2024. The therapy aims to slow disease progression, alleviate ALS symptoms, and extend patient survival.
To know more about ALS treatment options, visit @ Approved Amyotrophic Lateral Sclerosis Drugs
Amyotrophic Lateral Sclerosis Competitive Landscape
Some of the ALS drugs in clinical trials include Masitinib (AB Sciences), PrimeC (Neurosense Therapeutics), RNS60 (Revalesio), IFB-088 (InFlectis BioScience), NP001 (Neuvivo), Ibudilast (MediciNova), NurOwn (Brainstorm-Cell Therapeutics' MSC-NTF cells), Pridopidine (Prilenia Therapeutics), CBT101 (CERES Brain Therapeutics), and others.
AB Science's Masitinib (AB1010) is an oral tyrosine kinase inhibitor that regulates the activity of mast cells and macrophages, key immune cells, by selectively targeting a small subset of kinases. Notably, at therapeutic doses, it avoids inhibiting kinases linked to toxicity. The drug is currently undergoing a Phase III confirmatory trial for the treatment of amyotrophic lateral sclerosis (ALS).
NeuroSense's PrimeC is a novel combination of two FDA-approved drugs, ciprofloxacin and celecoxib, formulated at unique doses to work synergistically in slowing the progression of ALS. The therapy has received Orphan Drug Designation (ODD) from both the US FDA and EMA, and NeuroSense is advancing it through regulatory pathways while preparing for a pivotal Phase III trial. Following favorable feedback from the FDA, the company plans to initiate a multinational Phase III study in the second half of 2025.
CERES Brain Therapeutics' CBT101 is a creatine prodrug formulated within a patented composition of matter, representing an innovative drug design. It is currently in a Phase I clinical trial for the treatment of adult patients with ALS.
The anticipated launch of these emerging therapies are poised to transform the ALS market landscape in the coming years. As these cutting-edge therapies continue to mature and gain regulatory approval, they are expected to reshape the ALS market landscape, offering new standards of care and unlocking opportunities for medical innovation and economic growth.
Discover more about therapy for ALS @ Amyotrophic Lateral Sclerosis Clinical Trials
Recent Developments in the Amyotrophic Lateral Sclerosis Market
What is Amyotrophic Lateral Sclerosis?
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord, leading to the gradual loss of muscle control. In ALS, the motor neurons responsible for transmitting signals from the brain to the muscles degenerate and die, resulting in muscle weakness, atrophy, and eventual paralysis. Over time, individuals with ALS lose the ability to speak, swallow, and breathe independently, while cognitive function typically remains intact. Although the exact cause of ALS is not fully understood, a combination of genetic and environmental factors is believed to contribute to its development.
Amyotrophic Lateral Sclerosis Epidemiology Segmentation
The ALS epidemiology section provides insights into the historical and current amyotrophic lateral sclerosis patient pool and forecasted trends for the leading markets. In the US, among mutation-specific cases of ALS in 2024, including C9ORF72, SOD1, FUS, and others such as TARDBP, OPTN, and ANG, non-mutated or unidentified mutations accounted for the largest proportion, representing approximately 75% of cases.
The ALS market report proffers epidemiological analysis for the study period 2020–2034 in the leading markets, segmented into:
Scope of the Amyotrophic Lateral Sclerosis Market Report
Download the report to understand which factors are driving amyotrophic lateral sclerosis therapeutics market trends @ Amyotrophic Lateral Sclerosis Market Trends
Table of Contents
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