PUBLISHER: DelveInsight | PRODUCT CODE: 1381074
PUBLISHER: DelveInsight | PRODUCT CODE: 1381074
“"NTCD-M3 Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about NTCD-M3 for clostridium difficile infection (CDI) in the seven major markets. A detailed picture of the NTCD-M3 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 NTCD-M3 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 NTCD-M3 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.
NTCD-M3 (a non-toxigenic strain of C. difficile bacteria- strain M3), previously known as VP 20621, is being developed by Destiny Pharma for the prevention of rCDI. It is an oral formulation of NTCD-M3 spores.
C. difficile NTCD-M3 is a naturally occurring non-toxigenic strain of C. difficile bacteria, which lacks the genes that can express C. difficile toxins. NTCD-M3 temporarily colonizes the human gut without causing any symptoms and the gut microbiome returns to normal a few weeks after treatment. Therefore, it acts as a safe ground cover and prevents the toxic strains of C. difficile from proliferating in the colon after antibiotic treatment.
Phase IIb trials for NTCD-M3 were completed by the Shire and the results were statistically significant confirming efficacy. Destiny Pharma plans to start the Phase III trial by mid of 2023, the design for which was approved by the US FDA in July 2020.
Destiny Pharma is also conducting partnership discussions to co-fund the planned Phase III clinical studies and the subsequent commercialization. It has also received positive scientific advice from EMA on the proposed Phase III study design.
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.
This report provides a detailed market assessment of NTCD-M3 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 2027 to 2032.
The report provides the clinical trials information of NTCD-M3 for clostridium difficile infection covering trial interventions, trial conditions, trial status, start and completion dates.