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市場調查報告書

TADEKINIG ALFA-新洞察與市場預測:2030年

TADEKINIG ALFA- Emerging Insight and Market Forecast - 2030

出版商 DelveInsight Business Research LLP 商品編碼 974755
出版日期 按訂單生產 內容資訊 英文 60 Pages
商品交期: 10個工作天內
價格
TADEKINIG ALFA-新洞察與市場預測:2030年 TADEKINIG ALFA- Emerging Insight and Market Forecast - 2030
出版日期: 按訂單生產內容資訊: 英文 60 Pages
簡介

在人類1/1b期臨床試驗和2期臨床試驗中,已證明Tadekinig alfa具有優異的安全性和耐受性。Tadekinig alfa的早期療效跡像已在2期試驗中顯示,該藥在患有難治性成人發作Still病的患者以及NLRC4-MAS,XIAP和全身發作少年特發性關節炎的單例使用案例中顯示。

未來幾年,由於全球對治療適應症的廣泛研究和不斷增加的醫療保健支出,Tadekinig alfa的市場前景將發生變化。這將擴大市場規模,使藥品製造商能夠更擴大滲透到市場中。

這些公司和學者正在努力評估挑戰並尋找可能影響Tadekinig alfa優勢的機會。正在開發的療法集中於治療/改善疾病狀況的新方法。

其他批准用於該疾病的產品正在給Tadekinig alfa帶來市場競爭,並且在不久的將來推出後期新興療法將極大地影響市場。

監管法規里程碑,開發活動以及一些關鍵發現的詳細說明提供了Tadekinig alfa當前的市場情況。

我們將通過對Tadekinig alfa從2017年到2030年銷售數據的深入分析來確定市場上Tadekinig alfa的整體情況,為客戶提供有關其治療產品組合的決策過程的支持。

本報告全面涵蓋7個主要市場上成人史迪爾氏病臨床實驗藥。提供有關2020-2030年調查期間美國,歐洲5個國家(德國,法國,意大利,西班牙,英國)和日本7個主要市場的TADEKINIG 與產品詳細內容一起提供ALFA的詳細概要。產品詳細內容中包含作用機制,劑量管理,合成途徑,法規的里程碑的研究開發活動,以及其他開發活動。再加上市場預測、 SWOT分析,市場上競爭趨勢,及其他新治療方法等未來市場趨勢。

目錄

第1章 藥物概要

  • 產品詳細內容
  • 作用機制
  • 劑量與管理
  • 研究開發活動
    • 臨床開發
    • 安全性和有效性
  • 其他開發活動

第2章 市場評估

  • 主要7個國家市場分析
  • 美國市場
  • 德國市場
  • 法國市場
  • 義大利市場
  • 西班牙市場
  • 英國市場
  • 日本市場

第3章 SWOT分析

第4章 分析師的見解

第5章 市場競爭趨勢

第6章 其他的新治療方法

第7章 附錄

第8章 報告購買選擇

目錄
Product Code: DIDM0136

"TADEKINIG ALFA- Emerging Insight and Market Forecast - 2030" the report provides comprehensive insights about an investigational product for Adult-onset Still's Disease in 7 Major Markets. A detailed picture of the TADEKINIG ALFA in Seven Major Markets, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan, for the study period 2020-2030 is provided in this report along with a detailed description of the product. The product details cover mechanism of action, dosage and administration, route of synthesis, and Research and development activity including regulatory milestones, and other development activities. Further, it also consists of future market assessments inclusive of the market forecast, SWOT analysis, market competitors, and other emerging therapies.

Overview:

Tadekinig alfa is a recombinant interleukin-18 binding protein (r-hIL-18BP), that binds with high affinity to IL-18, a major inflammatory mediator. It is administered subcutaneously. In healthy people, IL-18 and IL-18BP are present constitutively in blood with a large excess of IL-18BP keeping levels of free IL-18 undetectable. However, in patients with inflammatory diseases, the IL-18/IL-18BP balance is disrupted, resulting in high levels of free and active IL-18, which leads to pathological inflammation. While the time-limited inflammatory response is a natural defense mechanism intended to clear pathogens and limit harm to the body, dysregulated and persistent inflammatory processes are the basis of several chronic inflammatory and autoimmune diseases. Administration of Tadekinig alfa restores the IL-18/IL-18BP balance, by removing free IL-18 and thereby reducing inflammation.

Excellent safety and tolerability of Tadekinig alfa have been demonstrated in human subjects in Phase 1/1b clinical trials and a Phase 2 trial. Early signs of efficacy of Tadekinig alfa have been shown in a Phase 2 trial in patients suffering from refractory Adult onset Still's disease, as well in single compassionate use cases in NLRC4-MAS, XIAP, and Systemic onset Juvenile Idiopathic Arthritis.

Scope of the report:

The report provides insights into:

  • A comprehensive product overview including the product description, mechanism of action, dosage and administration, Research and Development activity.
  • Elaborated details on regulatory milestones and other development activities have been provided in this report.
  • The report also highlights the drug research and development activity details across the United States, Europe and Japan.
  • The report also covers the patents information with expiry timeline around TADEKINIG ALFA.
  • The report contains forecasted sales for TADEKINIG ALFA till 2030.
  • Comprehensive coverage of the late-stage emerging therapies (Phase II) for Adult-onset Still's Disease.
  • The report also features the SWOT analysis with analyst insights and key findings of TADEKINIG ALFA.

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.

TADEKINIG ALFA Analytical Perspective by DelveInsight

  • In-depth TADEKINIG ALFA Market Assessment

This report provides a detailed market assessment of TADEKINIG ALFA in Seven Major Markets, 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 2020 to 2030.

  • TADEKINIG ALFA Clinical Assessment

The report provides the clinical trials information of TADEKINIG ALFA covering trial interventions, trial conditions, trial status, start and completion dates.

Report highlights:

  • In the coming years, the market scenario for Adult-onset Still's Disease 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 and academics are working to assess challenges and seek opportunities that could influence TADEKINIG ALFA dominance. The therapies under development are focused on novel approaches to treat/improve the disease condition.
  • Other emerging products for Adult-onset Still's Disease are giving market competition to TADEKINIG ALFA and launch of late-stage emerging therapies in the near future will significantly impact the market.
  • A detailed description of regulatory milestones, development activities, and some key findings provide the current development scenario of TADEKINIG ALFA.
  • Our in-depth analysis of the forecasted sales data of TADEKINIG ALFA from 2020 to 2030 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the TADEKINIG ALFA.

Key Questions:

  • Which company is developing TADEKINIG ALFA along with the phase of the clinical study?
  • What is the technology utilized in the development of TADEKINIG ALFA?
  • What is the product type, route of administration and mechanism of action of TADEKINIG ALFA?
  • What is the clinical trial status of the study and study completion date?
  • What are the key collaborations, mergers and acquisitions, licensing and other activities related to the TADEKINIG ALFA development?
  • What are the key designations that have been granted to TADEKINIG ALFA?
  • What is the forecasted market scenario of TADEKINIG ALFA?
  • What is the history of TADEKINIG ALFA and what is its future?
  • What is the forecasted sales of TADEKINIG ALFA 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 these are giving competition to TADEKINIG ALFA?
  • Which are the late-stage emerging therapies under development for the treatment of the PPD?

Table of Contents

1. Drug Overview

  • 1.1. Product Detail
  • 1.2. Mechanism of Action
  • 1.3. Dosage and Administration
  • 1.4. Research and development activity
    • 1.4.1. Clinical Development
    • 1.4.2. Safety and Efficacy
  • 1.5. Other Development Activities

2. Market Assesment

  • 2.1. 7MM Market Analysis
  • 2.2. The United States Market
  • 2.3. Germany Market
  • 2.4. France Market
  • 2.5. Italy Market
  • 2.6. Spain Market
  • 2.7. United Kingdom Market
  • 2.8. Japan Market

3. SWOT Analysis

4. Analyst Views

5. Market Competitors

6. Other Emerging Therapies

7. Appendix

8. Report Purchase Options

List of Tables

  • Table 1: TADEKINIG ALFA, Description
  • Table 2: TADEKINIG ALFA, Clinical Trial Description
  • Table 3: TADEKINIG ALFA, 7MM Market Size from 2020 to 2030 (in Million USD)
  • Table 4: Market Competitors
  • Table 5: Other Emerging Therapies

List of Figures

  • Figure 1: The Development Timeline of TADEKINIG ALFA
  • Figure 2: Patent Details, TADEKINIG ALFA
  • Figure 3: TADEKINIG ALFA, 7MM Market Size from 2020 to 2030 (in Million USD)
  • Figure 4: TADEKINIG ALFA, US Market Size from 2020 to 2030 (in Millions USD)
  • Figure 5: TADEKINIG ALFA, EU5 Market Size from 2020 to 2030 (in Millions USD)
  • Figure 6: TADEKINIG ALFA, Japan Market Size from 2020 to 2030 (in Millions USD)