This “FLU-v Emerging Drug Insight and Market Forecast - 2032” report provides comprehensive insights about FLU-v for seasonal influenza in the seven major markets. A detailed picture of the FLU-v for seasonal influenza in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and 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 FLU-v for seasonal influenza. 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 FLU-v market forecast analysis for seasonal influenza in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in seasonal influenza.
Working closely with the National Institute of allergy and infectious disease in the United States (NIAID), Imutex leveraged the hVIVO and National Institute of Allergy and Infectious Diseases (NIAID) platforms to conduct Phase IIb clinical studies of FLU-v to evaluate the efficacy and safety of this novel vaccine. Both the field study and challenge study achieved the primary endpoints. It has demonstrated efficacy in animals and safety and immunogenicity in Phase I and Phase Ib trials, the latter demonstrating cellular immune responses to FLU-v correlated with reduced viral shedding and reduced symptoms after the H3N2 influenza challenge. It is expected to eliminate the sensitivity to strain variability seen with traditional vaccines and promote single-vaccine coverage for all flu strains.
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Drug Summary
Imutex is leveraging technology licensed from PepTcell (trading as SEEK) to develop a broad-spectrum ‘universal' influenza vaccine (BIV), called FLU-v, against multiple flu strains. FLU-v works by targeting conserved internal proteins common to all flu viruses to activate T- and B-cell, key components of the human immune system response. FLU-v, is a peptide vaccine derived from conserved regions of internal proteins aiming to provide a broadly protective immune response against influenza A and B through viral clearance by cytotoxic T-cell release of pro-inflammatory cytokines and perforin and granzyme.Working closely with the National Institute of allergy and infectious disease in the United States (NIAID), Imutex leveraged the hVIVO and National Institute of Allergy and Infectious Diseases (NIAID) platforms to conduct Phase IIb clinical studies of FLU-v to evaluate the efficacy and safety of this novel vaccine. Both the field study and challenge study achieved the primary endpoints. It has demonstrated efficacy in animals and safety and immunogenicity in Phase I and Phase Ib trials, the latter demonstrating cellular immune responses to FLU-v correlated with reduced viral shedding and reduced symptoms after the H3N2 influenza challenge. It is expected to eliminate the sensitivity to strain variability seen with traditional vaccines and promote single-vaccine coverage for all flu strains.
Scope of the Report
The report provides insights into:
- A comprehensive product overview including the FLU-v description, mechanism of action, dosage and administration, research and development activities in seasonal influenza.
- Elaborated details on FLU-v regulatory milestones and other development activities have been provided in this report.
- The report also highlights the FLU-v research and development activities in seasonal influenza across the United States, Europe and Japan.
- The report also covers the patents information with expiry timeline around FLU-v.
- The report contains forecasted sales of FLU-v for seasonal influenza till 2032.
- Comprehensive coverage of the late-stage emerging therapies for seasonal influenza.
- The report also features the SWOT analysis with analyst views for FLU-v in seasonal influenza.
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.FLU-v Analytical Perspective
In-depth FLU-v Market Assessment
This report provides a detailed market assessment of FLU-v for seasonal influenza in the seven major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan. This segment of the report provides forecasted sales data from 2026 to 2032.FLU-v Clinical Assessment
The report provides the clinical trials information of FLU-v for seasonal influenza covering trial interventions, trial conditions, trial status, start and completion dates.Report Highlights
- In the coming years, the market scenario for seasonal influenza 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 FLU-v dominance.
- Other emerging products for seasonal influenza are expected to give tough market competition to FLU-v 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 FLU-v in seasonal influenza.
- This in-depth analysis of the forecasted sales data of FLU-v from 2026 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the FLU-v in seasonal influenza.
Key Questions
- What is the product type, route of administration and mechanism of action of FLU-v?
- What is the clinical trial status of the study related to FLU-v in seasonal influenza and study completion date?
- What are the key collaborations, mergers and acquisitions, licensing and other activities related to the FLU-v development?
- What are the key designations that have been granted to FLU-v for seasonal influenza?
- What is the forecasted market scenario of FLU-v for seasonal influenza?
- What are the forecasted sales of FLU-v 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 and how are these giving competition to FLU-v for seasonal influenza?
- Which are the late-stage emerging therapies under development for the treatment of seasonal influenza?
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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. FLU-v Overview in seasonal influenza
5. FLU-v Market Assessment
8. Appendix
List of Tables
List of Figures