“EB05 Emerging Drug Insight and Market Forecast - 2032” report provides comprehensive insights about EB05 for Acute Respiratory Distress Syndrome in seven major markets. A detailed picture of the EB05 for Acute Respiratory Distress Syndrome in 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 EB05 for Acute Respiratory Distress Syndrome. 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 EB05 market forecast analysis for Acute Respiratory Distress Syndrome in 7MM, SWOT, analyst views, comprehensive overview of market competitors, and brief about other emerging therapies in Acute Respiratory Distress Syndrome.
The company received approval from Health Canada to test EB05 as a rescue therapy for critically ill patients in the Phase III part of a Phase II/III clinical study. Approval of the company's Phase III study design followed favorable Phase II results, which demonstrated compelling preliminary evidence of EB05's ability to reduce mortality in the sickest patients. Edesa has filed similar protocol amendments with the US FDA as well as other jurisdictions. In the US, the company is currently in discussions with the FDA on the design of the final Phase III protocol.
The company is also developing an EB06 monoclonal antibody in Phase II for the treatment of ARDS according to the company's pipeline. It acts by inhibiting the signaling protein CXCL10.
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Drug Summary
EB05 is an experimental monoclonal antibody that Edesa believes could regulate the overactive and dysfunctional immune response associated with ARDS. Specifically, the drug inhibits toll-like receptor 4 (TLR4) signaling - an important mediator of inflammation responsible for acute lung injury that is activated by SARS-CoV2, SARS-CoV1, and Influenza viruses.The company received approval from Health Canada to test EB05 as a rescue therapy for critically ill patients in the Phase III part of a Phase II/III clinical study. Approval of the company's Phase III study design followed favorable Phase II results, which demonstrated compelling preliminary evidence of EB05's ability to reduce mortality in the sickest patients. Edesa has filed similar protocol amendments with the US FDA as well as other jurisdictions. In the US, the company is currently in discussions with the FDA on the design of the final Phase III protocol.
The company is also developing an EB06 monoclonal antibody in Phase II for the treatment of ARDS according to the company's pipeline. It acts by inhibiting the signaling protein CXCL10.
Scope of the Report
The report provides insights into:
- A comprehensive product overview including the EB05 description, mechanism of action, dosage and administration, research and development activities in Acute Respiratory Distress Syndrome.
- Elaborated details on EB05 regulatory milestones and other development activities have been provided in this report.
- The report also highlights the EB05 research and development activities in Acute Respiratory Distress Syndrome across the United States, Europe and Japan.
- The report also covers the patents information with expiry timeline around EB05.
- The report contains forecasted sales of EB05 for Acute Respiratory Distress Syndrome till 2032.
- Comprehensive coverage of the late-stage emerging therapies for Acute Respiratory Distress Syndrome.
- The report also features the SWOT analysis with analyst views for EB05 in Acute Respiratory Distress Syndrome.
Methodology
The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by the publisher'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.EB05 Analytical Perspective
In-depth EB05 Market Assessment
This report provides a detailed market assessment of EB05 for Acute Respiratory Distress Syndrome 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 2025 to 2032.EB05 Clinical Assessment
The report provides the clinical trials information of EB05 for Acute Respiratory Distress Syndrome covering trial interventions, trial conditions, trial status, start and completion dates.Report Highlights
- In the coming years, the market scenario for Acute Respiratory Distress Syndrome 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 EB05 dominance.
- Other emerging products for Acute Respiratory Distress Syndrome are expected to give tough market competition to EB05 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 EB05 in Acute Respiratory Distress Syndrome.
- The in-depth analysis of the forecasted sales data of EB05 from 2025 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the EB05 in Acute Respiratory Distress Syndrome.
Key Questions Answered
- What is the product type, route of administration and mechanism of action of EB05?
- What is the clinical trial status of the study related to EB05 in Acute Respiratory Distress Syndrome and study completion date?
- What are the key collaborations, mergers and acquisitions, licensing and other activities related to the EB05 development?
- What are the key designations that have been granted to EB05 for Acute Respiratory Distress Syndrome?
- What is the forecasted market scenario of EB05 for Acute Respiratory Distress Syndrome?
- What are the forecasted sales of EB05 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 EB05 for Acute Respiratory Distress Syndrome?
- Which are the late-stage emerging therapies under development for the treatment of Acute Respiratory Distress Syndrome?
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Table of Contents
1. Report Introduction3. Competitive Landscape (Late-stage Emerging Therapies)5. SWOT Analysis6. Analysts’ Views8. Publisher Capabilities9. Disclaimer10. About the Publisher11. Report Purchase Options
2. EB05 Overview in Acute Respiratory Distress Syndrome
4. EB05 Market Assessment
7. Appendix
List of Tables
List of Figures