This “ZILOSUL Emerging Drug Insight and Market Forecast - 2032” report provides comprehensive insights about ZILOSUL for osteoarthritis in the six major markets. A detailed picture of the ZILOSUL for osteoarthritis in the 6MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, along with Canada, and Korea for the study period 2019 -2032 is provided in this report along with a detailed description of the ZILOSUL for osteoarthritis. The report provides insights about mechanism of action, dosage and administration, as well as research and development including regulatory milestones, along with other developmental activities. Further, it also consists of future market assessments inclusive of the ZILOSUL market forecast analysis for osteoarthritis in the 6MM, along with Canada and Korea, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in osteoarthritis.
To achieve European and FDA approval, PPS has been examined in toxicology and safety studies across several species of animals to humans for more than 50 years. It has been ingested orally, infused in the bladder, injected (intravenously, intramuscularly, and subcutaneously), and administered intranasally in a recent company's toxicology study. The prior clinical and commercial experience exceeding 22,000 exposures has informed Paradigm's development program. The company's Phase III study evaluates and identifies the best tolerated and most effective regimen for commercialization.
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Drug Summary
ZILOSUL (Pentosan polysulfate sodium) (PPS) is a semi-synthetic drug manufactured from the wood chips of European beech trees. Extracted glucuronoxylans are sulfated to produce a negatively charged product that mimics glycosaminoglycans (GAGs). GAGs are complex carbohydrates that play a regulatory role in the body by interacting with proteins involved with inflammation. Key features of the activity of PPS are its anti-inflammatory and tissue regenerative properties and its mild antithrombotic activity. Due to PPS having multiple mechanisms of action, the company's broader focus is exploring the use of PPS in treating a wide spectrum of conditions that begin with and are sustained by inflammation, such as OA. The company has a longstanding relationship with bene pharmaChem, the only FDA-approved manufacturer/supplier of PPS. Through the extensive interaction and collaboration with bene pharmaChem and Paradigm's European manufacturers of the injectable formulation of PPS (iPPS). The company is developing PPS for OA under the trademark, ZILOSUL.To achieve European and FDA approval, PPS has been examined in toxicology and safety studies across several species of animals to humans for more than 50 years. It has been ingested orally, infused in the bladder, injected (intravenously, intramuscularly, and subcutaneously), and administered intranasally in a recent company's toxicology study. The prior clinical and commercial experience exceeding 22,000 exposures has informed Paradigm's development program. The company's Phase III study evaluates and identifies the best tolerated and most effective regimen for commercialization.
Scope of the Report
The report provides insights into:
- A comprehensive product overview including the ZILOSUL description, mechanism of action, dosage and administration, research and development activities in osteoarthritis.
- Elaborated details on ZILOSUL regulatory milestones and other development activities have been provided in this report.
- The report also highlights the ZILOSUL research and development activities in osteoarthritis across the United States, Europe, Canada and Korea.
- The report also covers the patents information with expiry timeline around ZILOSUL.
- The report contains forecasted sales of ZILOSUL for osteoarthritis till 2032.
- Comprehensive coverage of the late-stage emerging therapies for osteoarthritis.
- The report also features the SWOT analysis with analyst views for ZILOSUL in osteoarthritis.
Methodology
The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by the 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.ZILOSUL Analytical Perspective
In-depth ZILOSUL Market Assessment
This report provides a detailed market assessment of ZILOSUL for osteoarthritis in the six major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, along with Canada and Korea. This segment of the report provides forecasted sales data from 2025 to 2032.ZILOSUL Clinical Assessment
The report provides the clinical trials information of ZILOSUL for osteoarthritis covering trial interventions, trial conditions, trial status, start and completion dates.Report Highlights
- In the coming years, the market scenario for osteoarthritis 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 ZILOSUL dominance.
- Other emerging products for osteoarthritis are expected to give tough market competition to ZILOSUL 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 ZILOSUL in osteoarthritis.
- This in-depth analysis of the forecasted sales data of ZILOSUL from 2025 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the ZILOSUL in osteoarthritis.
Key Questions
- What is the product type, route of administration and mechanism of action of ZILOSUL?
- What is the clinical trial status of the study related to ZILOSUL in osteoarthritis and study completion date?
- What are the key collaborations, mergers and acquisitions, licensing and other activities related to the ZILOSUL development?
- What are the key designations that have been granted to ZILOSUL for osteoarthritis?
- What is the forecasted market scenario of ZILOSUL for osteoarthritis?
- What are the forecasted sales of ZILOSUL in the six major countries, including the United States, Europe (Germany, France, Italy, Spain) and the United Kingdom, along with Canada and Korea?
- What are the other emerging products available and how are these giving competition to ZILOSUL for osteoarthritis?
- Which are the late-stage emerging therapies under development for the treatment of osteoarthritis?
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Table of Contents
1. Report Introduction3. Competitive Landscape (Marketed Therapies)4. Competitive Landscape (Late-stage Emerging Therapies)6. SWOT Analysis7. Analysts’ Views9. Publisher Capabilities10. Disclaimer11. About the Publisher12. Report Purchase Options
2. ZILOSUL Overview in Osteoarthritis
5. ZILOSUL Market Assessment
8. Appendix
List of Tables
List of Figures