“XOLAIR Drug Insight and Market Forecast - 2032” report provides comprehensive insights about XOLAIR for Nasal Polyposis in the 7MM. A detailed picture of the XOLAIR for Nasal Polyposis 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 XOLAIR for Nasal Polyposis. 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 XOLAIR market forecast, analysis for Nasal Polyposis in the 7MM, descriptive analysis such as SWOT, analyst views, comprehensive overview of market competitors, and brief about emerging therapies in Nasal Polyposis.
The FDA's approval for nasal polyps was based on results from the Phase III POLYP 1 and POLYP 2 trials. Before this approval, XOLAIR had 17 years of patient experience since its initial approval for allergic asthma, then for chronic spontaneous urticarial and chronic idiopathic urticaria (CIU).
Omalizumab inhibits the binding of IgE to the high-affinity IgE receptor (FcεRI) on the surface of mast cells, basophils, and dendritic cells, resulting in FcεRI down-regulation on these cells. In allergic asthmatics, treatment with Omalizumab inhibits IgE-mediated inflammation, as evidenced by reduced blood and tissue eosinophils and reduced inflammatory mediators, including IL-4, IL-5, and IL-13.
XOLAIR 75-600 mg is recommended by subcutaneous injection every 2 or 4 weeks based on serum total IgE level (IU/mL) measure before the start of treatment and by body weight (kg).
Drug Summary
XOLAIR (Omalizumab) is the first biologic for the treatment of nasal polyps that targets and blocks immunoglobulin E (IgE), a key driver of inflammation. Omalizumab is a recombinant DNA-derived humanized IgG1κ monoclonal antibody that selectively binds to human immunoglobulin E (IgE). XOLAIR is administered as a subcutaneous (SC) injection and is available in prefilled syringes and vials (FDA, 2020). Injection form is a lyophilized, white, sterile powder in a 150 mg single-dose vial without preservatives, and prefilled Syringe is available in 75 mg and 150 mg.The FDA's approval for nasal polyps was based on results from the Phase III POLYP 1 and POLYP 2 trials. Before this approval, XOLAIR had 17 years of patient experience since its initial approval for allergic asthma, then for chronic spontaneous urticarial and chronic idiopathic urticaria (CIU).
Omalizumab inhibits the binding of IgE to the high-affinity IgE receptor (FcεRI) on the surface of mast cells, basophils, and dendritic cells, resulting in FcεRI down-regulation on these cells. In allergic asthmatics, treatment with Omalizumab inhibits IgE-mediated inflammation, as evidenced by reduced blood and tissue eosinophils and reduced inflammatory mediators, including IL-4, IL-5, and IL-13.
XOLAIR 75-600 mg is recommended by subcutaneous injection every 2 or 4 weeks based on serum total IgE level (IU/mL) measure before the start of treatment and by body weight (kg).
Scope of the Report
The report provides insights into:- A comprehensive product overview including the XOLAIR description, mechanism of action, dosage and administration, research and development activities in Nasal Polyposis.
- Elaborated details on XOLAIR regulatory milestones and other development activities have been provided in this report.
- The report also highlights the XOLAIR research and development activity in Nasal Polyposis details across the United States, Europe and Japan.
- The report also covers the patents information with expiry timeline around XOLAIR.
- The report contains forecasted sales of XOLAIR for Nasal Polyposis till 2032.
- Comprehensive coverage of the late-stage emerging therapies for Nasal Polyposis.
- The report also features the SWOT analysis with analyst views for XOLAIR in Nasal Polyposis.
Methodology
The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by a 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.XOLAIR Analytical Perspective
In-depth XOLAIR Market Assessment
This report provides a detailed market assessment of XOLAIR in Nasal Polyposis 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 2022 to 2032.XOLAIR Clinical Assessment
The report provides the clinical trials information of XOLAIR for Nasal Polyposis covering trial interventions, trial conditions, trial status, start and completion dates.Report Highlights
- In the coming years, the market scenario for Nasal Polyposis 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 XOLAIR dominance.
- Other emerging products for Nasal Polyposis are expected to give tough market competition to XOLAIR 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 XOLAIR in Nasal Polyposis.
- Our in-depth analysis of the forecasted sales data of XOLAIR from 2022 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the XOLAIR in Nasal Polyposis.
Key Questions Answered
- What is the product type, route of administration and mechanism of action of XOLAIR?
- What is the clinical trial status of the study related to XOLAIR in Nasal Polyposis and study completion date?
- What are the key collaborations, mergers and acquisitions, licensing and other activities related to the XOLAIR development?
- What are the key designations that have been granted to XOLAIR for Nasal Polyposis?
- What is the forecasted market scenario of XOLAIR for Nasal Polyposis?
- What are the forecasted sales of XOLAIR in the 7MM, including the United States, Europe (Germany, France, Italy, Spain, and the United Kingdom), and Japan?
- What are the other emerging products available in Nasal Polyposis and how are they giving competition to XOLAIR for Nasal Polyposis?
- Which are the late-stage emerging therapies under development for the treatment of Nasal Polyposis?
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 Option
2. XOLAIR Overview in Nasal Polyposis
5. XOLAIR Market Assessment
8. Appendix
List of Tables
List of Figures