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¼¼°èÀÇ Vonafexor ½ÃÀå : ½ÃÀå ±Ô¸ð, ¿¹Ãø, »õ·Î¿î ÀλçÀÌÆ®(-2032³â)Vonafexor Market Size, Forecast, and Emerging Insight - 2032 |
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Vonafexor(EYP001)´Â ÇöÀç ÁøÇ༺ NASH, Áï ¼¶À¯È ´Ü°è F2 ¶Ç´Â F3 ȯÀÚ¸¦ ´ë»óÀ¸·Î ÇÏ´Â 2a»ó ÀÓ»ó½ÃÇè¿¡¼ Æò°¡µÇ°í ÀÖ½À´Ï´Ù. Áß°£¾ÈÀü¼º ºÐ¼®ÀÇ °á°ú, ¾çÈ£ÇÑ ³»¾à¼ºÀÌ È®ÀεǾú±â ¶§¹®¿¡ µ¶¸³À§¿øÈ¸(DSMC)´Â ¿¹Á¤´ë·Î ÀÓ»ó½ÃÇèÀ» ¿Ï·áÇÒ °ÍÀ» Á¦¾ÈÇß½À´Ï´Ù. ¸¸¼º BÇü °£¿°°ú NASH¸¦ ´ë»óÀ¸·Î, ÁÖ¿ä ÈÇÕ¹° VonafexorÀÇ 3°¡Áö 2»ó ÀÓ»ó½ÃÇèÀÌ ½Ç½ÃµÇ¾ú½À´Ï´Ù.
º» º¸°í¼´Â ÁÖ¿ä 7°³±¹¿¡¼ÀÇ Vonafexor ½ÃÀåÀ» Á¶»çÇßÀ¸¸ç, ½ÃÀå °³¿ä¿Í ÇÔ²² °æÀï ±¸µµ, 2032³â±îÁö ½ÃÀå ±Ô¸ð ¿¹Ãø, ±¹°¡º° ½ÃÀå ºÐ¼® µîÀ» Á¦°øÇÕ´Ï´Ù.
"Vonafexor Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about Vonafexor for Non-alcoholic Steatohepatitis (NASH) in the seven major markets. A detailed picture of the Vonafexor for NASH 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 Vonafexor for NASH. 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 Vonafexor market forecast analysis for NASH in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in NASH.
Vonafexor (EYP001) is an orally bioavailable synthetic non-steroidal, non-bile acid FXR agonist small molecule also developed in NASH. Most KOL agrees that FXR agonists could become the backbone of future NASH therapies. It has demonstrated its efficacy in a stelic mouse model STAM with a significant positive impact on most NASH key parameters (fibrosis, steatosis, inflammation, ballooning, triglycerides, and NAS). It differentiates from other FXR agonists with a unique chemistry and PK PD profile to possibly provide a best-in-class therapeutic index.
Vonafexor (EYP001) is currently evaluated in a Phase IIa clinical trial in patients with advanced NASH, i.e., a fibrosis Stage F2 or F3. After the interim safety analysis showed good tolerance, the independent DSMC suggested pursuing the trial to completion as planned. The company conducts three Phase II trials with its lead compound Vonafexor in Chronic Hepatitis B and NASH.
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.
Vonafexor Analytical Perspective by DelveInsight
This report provides a detailed market assessment of Vonafexor for Non-alcoholic Steatohepatitis (NASH) 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 Vonafexor for Non-alcoholic Steatohepatitis (NASH) covering trial interventions, trial conditions, trial status, start and completion dates.