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ÃÖ±Ù ¹Ì±¹ FDA´Â Finch TherapeuticsÀÇ CP101 ÀÓ»ó½ÃÇè°èȹ(IND) ½Åû¿¡ ´ëÇÑ ÀÓ»ó º¸·ù¸¦ ÇØÁ¦Çß½À´Ï´Ù. ȸ»ç´Â rCDI ¿¹¹æÀ» À§ÇÑ CP101ÀÇ PRISM4(ÀÓ»ó 3»ó) ½ÃÇèÀ» ÁøÇàÇϰí ÀÖÀ¸¸ç, PRISM4ÀÇ Å¾¶óÀÎ µ¥ÀÌÅÍ´Â 2024³â »ó¹Ý±â¿¡ ³ª¿Ã °ÍÀ¸·Î ¿¹»óÇϰí ÀÖ½À´Ï´Ù.
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ÁÖ¿ä 7°³±¹ÀÇ CP101 ½ÃÀå¿¡ ´ëÇØ Á¶»çÇßÀ¸¸ç, ½ÃÀåÀÇ °³¿ä¿Í 2025-2032³â ÆÇ¸Å ¿¹Ãø µ¥ÀÌÅÍ, °æÀï ±¸µµ ¹× ±¹°¡º° µ¿Çâ µîÀ» Á¦°øÇϰí ÀÖ½À´Ï´Ù.
“"CP101 Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about CP101 for clostridium difficile infection (CDI) in the seven major markets. A detailed picture of the CP101 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 CP101 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 CP101 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.
CP101, being developed by Finch Therapeutics, is an investigational, orally administered microbiome drug for conditions linked to microbiome dysfunction. CP101 delivers complete microbiome communities in orally administered, enteric-release capsules. The drug is in late-stage clinical development for the prevention of rCDI. The company is planning to deploy CP101 to other conditions linked to microbiome disruption, starting with the evaluation of CP101 as a treatment for chronic hepatitis B.
Recently, the US FDA removed the clinical hold on Finch's Investigational New Drug (IND) application for CP101. The company has proceeded with patient dosing in the PRISM4 (Phase III) trial of CP101 for the prevention of rCDI, and anticipates topline data from PRISM4 in H1 2024.
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.
CP101 Analytical Perspective by DelveInsight
This report provides a detailed market assessment of CP101 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 2025 to 2032.
The report provides the clinical trials information of CP101 for clostridium difficile infection covering trial interventions, trial conditions, trial status, start and completion dates.