This “MGB-BP-3 Emerging Drug Insight and Market Forecast - 2032” report provides comprehensive insights about MGB-BP-3 for clostridium difficile infection (CDI) in the seven major markets. A detailed picture of the MGB-BP-3 for clostridium difficile infection 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 MGB-BP-3 for clostridium difficile infection. 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 MGB-BP-3 market forecast analysis for clostridium difficile infection in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in clostridium difficile infection.
The positive Phase II data showed that MGB-BP-3 provides high rates of sustained cure from CDI. In January 2021, MGB Biopharma announced the successful completion of its End-of-Phase II (EOP2) meeting with the US FDA. At the meeting, the US FDA confirmed that the design and the endpoints of the company's two prospective Phase III studies were appropriate. The Phase III studies, which are expected to recruit approximately 900 patients, will include the superiority of MGB-BP-3 against vancomycin in the critical measure of sustained clinical response as one of their endpoints.
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Drug Summary
MGB-BP-3, being developed by MGB Biopharma, is a potent oral bactericidal antibiotic with a novel mode of action for the treatment of Clostridium difficile-associated disease (CDAD). MGB-BP-3 has a fast bactericidal effect which can kill C. difficile in its vegetative form before it forms spores, thus achieving an initial cure and preventing the disease from recurring and reducing the total burden of C. difficile. Moreover, MGB-BP-3 has strong bactericidal activity against the BI/NAP1/027 strain, the most virulent strain that is largely resistant to current therapy.The positive Phase II data showed that MGB-BP-3 provides high rates of sustained cure from CDI. In January 2021, MGB Biopharma announced the successful completion of its End-of-Phase II (EOP2) meeting with the US FDA. At the meeting, the US FDA confirmed that the design and the endpoints of the company's two prospective Phase III studies were appropriate. The Phase III studies, which are expected to recruit approximately 900 patients, will include the superiority of MGB-BP-3 against vancomycin in the critical measure of sustained clinical response as one of their endpoints.
Scope of the Report
The report provides insights into:
- A comprehensive product overview including the MGB-BP-3 description, mechanism of action, dosage and administration, research and development activities in clostridium difficile infection.
- Elaborated details on MGB-BP-3 regulatory milestones and other development activities have been provided in this report.
- The report also highlights the MGB-BP-3 research and development activities in clostridium difficile infection across the United States, Europe and Japan.
- The report also covers the patents information with expiry timeline around MGB-BP-3.
- The report contains forecasted sales of MGB-BP-3 for clostridium difficile infection till 2032.
- Comprehensive coverage of the late-stage emerging therapies for clostridium difficile infection.
- The report also features the SWOT analysis with analyst views for MGB-BP-3 in clostridium difficile infection.
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.MGB-BP-3 Analytical Perspective
In-depth MGB-BP-3 Market Assessment
This report provides a detailed market assessment of MGB-BP-3 for clostridium difficile infection 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 2028 to 2032.MGB-BP-3 Clinical Assessment
The report provides the clinical trials information of MGB-BP-3 for clostridium difficile infection covering trial interventions, trial conditions, trial status, start and completion dates.Report Highlights
- In the coming years, the market scenario for clostridium difficile infection 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 MGB-BP-3 dominance.
- Other emerging products for clostridium difficile infection are expected to give tough market competition to MGB-BP-3 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 MGB-BP-3 in clostridium difficile infection.
- This in-depth analysis of the forecasted sales data of MGB-BP-3 from 2028 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the MGB-BP-3 in clostridium difficile infection.
Key Questions
- What is the product type, route of administration and mechanism of action of MGB-BP-3?
- What is the clinical trial status of the study related to MGB-BP-3 in clostridium difficile infection and study completion date?
- What are the key collaborations, mergers and acquisitions, licensing and other activities related to the MGB-BP-3 development?
- What are the key designations that have been granted to MGB-BP-3 for clostridium difficile infection?
- What is the forecasted market scenario of MGB-BP-3 for clostridium difficile infection?
- What are the forecasted sales of MGB-BP-3 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 MGB-BP-3 for clostridium difficile infection?
- Which are the late-stage emerging therapies under development for the treatment of clostridium difficile infection?
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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. MGB-BP-3 Overview in Clostridium difficile infection
5. MGB-BP-3 Market Assessment
8. Appendix
List of Tables
List of Figures