ION363 Emerging Drug Insight and Market Forecast – 2032
“ION363, Emerging Drug Insight and Market Forecast – 2032” report provides comprehensive insights about ION363 for Amyotrophic Lateral Sclerosis in the 7MM. A detailed picture of the ION363 for Amyotrophic Lateral Sclerosis in the 7MM, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan, for the study period 2019–2032 is provided in this report along with a detailed description of the ION363 for Amyotrophic Lateral Sclerosis. The report provides insight about mechanism of action, dosage and administration, as well as research and development activity including regulatory milestones, along with other developmental activities. Further, it also consists of future market assessments inclusive of the ION363 market forecast, analysis for Amyotrophic Lateral Sclerosis in the 7MM, descriptive analysis such as SWOT, analyst views, comprehensive overview of market competitors, and brief about other emerging therapies in Amyotrophic Lateral Sclerosis.
Drug Summary
ION363 is an investigational antisense medicine designed to reduce the production of the Fused in Sarcoma (FUS) protein. ION363 is also known as Jacifusen (not an official USAN name) in honor of Jaci Hermstad, the first patient treated with the drug under an expanded access program. It is in development for patients with a rare genetic form of ALS caused by mutations in the FUS gene. Mutant FUS causes motor neuron degeneration through a toxic gain of function mechanism. In patients, mutant FUS protein aggregates in motor neurons. Antisense-mediated reduction of mutant FUS protein in a FUS-ALS mouse model prevents motor neuron loss. It is hypothesized that reduction of FUS protein will reverse or prevent disease progression in FUS-ALS patients. By targeting the root cause of FUS-ALS, ION363 can potentially reduce or prevent disease progression in FUS-ALS patients. The company is currently conducting a Phase III trial of the drug for ALS patients with fused in sarcoma mutations (FUS-ALS), and data from this trial is expected in 2025.
Scope of the Report
The report provides insights into:
A comprehensive product overview including the ION363 description, mechanism of action, dosage and administration, research and development activities in Amyotrophic Lateral Sclerosis.
Elaborated details on ION363 regulatory milestones and other development activities have been provided in this report.
The report also highlights the ION363 research and development activity in Amyotrophic Lateral Sclerosis in detail across the United States, Europe and Japan.
The report also covers the patents information with expiry timeline around ION363.
The report contains forecasted sales of ION363 for Amyotrophic lateral sclerosis till 2032.
Comprehensive coverage of the late-stage emerging therapies for Amyotrophic Lateral Sclerosis.
The report also features the SWOT analysis with analyst views for ION363 in Amyotrophic Lateral Sclerosis.
Methodology
The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by DelveInsight’s team of industry experts. Information and data from the secondary sources have been obtained from various printable and nonprintable sources like search engines, news websites, global regulatory authorities websites, trade journals, white papers, magazines, books, trade associations, industry associations, industry portals and access to available databases.
ION363 Analytical Perspective by DelveInsight
In-depth ION363 Market Assessment
This report provides a detailed market assessment of ION363 in Amyotrophic lateral sclerosis in the 7MM, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan. This segment of the report provides forecasted sales data from 2025 to 2032.
ION363 Clinical Assessment
The report provides the clinical trials information of ION363 in Amyotrophic Lateral Sclerosis covering trial interventions, trial conditions, trial status, start and completion dates.
Report Highlights
In the coming years, the market scenario for Amyotrophic lateral sclerosis is set to change due to the extensive research and incremental healthcare spending across the world; which would expand the size of the market to enable the drug manufacturers to penetrate more into the market.
The companies are developing therapies that focus on novel approaches to treat/improve the disease condition, assess challenges, and seek opportunities that could influence ION363 dominance.
Other emerging products for Amyotrophic Lateral Sclerosis are expected to give tough market competition to ION363 and launch of late-stage emerging therapies in the near future will significantly impact the market.
A detailed description of regulatory milestones, and developmental activities, provide the current development scenario of ION363 in Amyotrophic Lateral Sclerosis.
Our in-depth analysis of the forecasted sales data of ION363 from 2025 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the ION363 in Amyotrophic Lateral Sclerosis.
Key Questions
What is the product type, route of administration and mechanism of action of ION363?
What is the clinical trial status of the study related to ION363 in Amyotrophic lateral sclerosis and study completion date?
What are the key collaborations, mergers and acquisitions, licensing and other activities related to the ION363 development?
What are the key designations that have been granted to ION363 for Amyotrophic Lateral Sclerosis?
What is the forecasted market scenario of ION363 for Amyotrophic Lateral Sclerosis?
What are the forecasted sales of ION363 in the seven major countries, including the United States, Europe (Germany, France, Italy, Spain, and the United Kingdom), and Japan?
What are the other emerging products available in Amyotrophic Lateral Sclerosis and how are they giving competition to ION363 for Amyotrophic Lateral Sclerosis?
Which are the late-stage emerging therapies under development for the treatment of Amyotrophic Lateral Sclerosis?
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