市場調査レポート
商品コード
1377974
FLU-v新薬の考察と市場予測 - 2032年FLU-v Emerging Drug Insight and Market Forecast - 2032 |
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FLU-v新薬の考察と市場予測 - 2032年 |
出版日: 2023年11月01日
発行: DelveInsight
ページ情報: 英文 30 Pages
納期: 1~3営業日
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当レポートでは、FLU-v新薬の主要7市場(米国、ドイツ、フランス、イタリア、スペイン、英国、日本)について調査分析し、作用機序、用法と用量、研究開発活動に関する考察や、市場予測などを提供しています。
“"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.
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.
The report provides insights into:
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.
FLU-v Analytical Perspective by DelveInsight
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.
The report provides the clinical trials information of FLU-v for seasonal influenza covering trial interventions, trial conditions, trial status, start and completion dates.
Key Questions