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ARGX-113 ½Å±Ô ¾àÁ¦ ÀλçÀÌÆ®¿Í ½ÃÀå ¿¹Ãø(2032³â)ARGX-113 Emerging Drug Insight and Market Forecast - 2032 |
Efgartigimod(ARGX-113)´Â IgG¸¦ ¸Å°³·Î ÇÑ ÀÚ°¡¸é¿ªÁúȯ Ä¡·áÁ¦·Î, IgG Ç×ü¿Í ÀçȰ¿ë ¼ö¿ëü FcRnÀÇ ÀÚ¿¬Àû »óÈ£ÀÛ¿ëÀ» ÀÌ¿ëÇϵµ·Ï ¼³°èµÇ¾ú½À´Ï´Ù. ¾ËÁ¨½º´Â ¼øÈ¯ÇÏ´Â Áúº´À» À¯¹ßÇÏ´Â ÀÚ°¡¸é¿ª Ç×ü¸¦ ºÐÇØÇÏ´Â Efgartigimod¸¦ ¼³°èÇÏ¿© ´Ù¹ß¼º °æÈÁõ, ¸é¿ª¼º Ç÷¼ÒÆÇ °¨¼ÒÁõ(ITP), Àü½Å¼º È«¹Ý¼º ·çǪ½º, ÁßÁõ ±Ù¹«·ÂÁõ, ÇǺΠ¼öÆ÷¼º Áúȯ µî ´Ù¼öÀÇ ´ëÇü ¹× Èñ±Í ÀûÀÀÁõ¿¡ ´ëÇÑ ÀáÀç·ÂÀ» °¡Áö°í ÀÖ½À´Ï´Ù.
Efgartigimod´Â ¾ËÁ¨½º¸¸ÀÇ ABDEG ±â¼ú·Î IgG1 Ç×üÀÇ Fc ºÎºÐÀ» º¯Çü½ÃÄÑ FcRn¿¡ ´ëÇÑ Ä£¹Ðµµ¸¦ ÀÏ¹Ý IgG Ç×üº¸´Ù ³ôÀÎ °ÍÀÔ´Ï´Ù. ±× °á°ú, Efgartigimod´Â FcRn °áÇÕ¿¡ ÀÇÇÑ Ç×ü ÀçȰ¿ëÀ» ¾ïÁ¦ÇÏ¿© ÀÚ°¡¸é¿ªÁúȯÀÇ ¿øÀÎÀÌ µÇ´Â IgG ÀÚ°¡Ç×ü¸¦ ºü¸£°Ô °í°¥½ÃŰ´Â È¿°ú¸¦ °¡Á®¿É´Ï´Ù. EfgartigimodÀÇ °³¹ß ¿¬±¸´Â E. Sally Ward ±³¼ö(ÅØ»ç½º ´ëÇб³ »ç¿ì½º¿þ½ºÅÏ ¸ÞµðÄà ½ºÄð ¹× ÅØ»ç½º A&M ´ëÇб³ º¸°Ç°úÇм¾ÅÍ, ÅØ»ç½º A&M ´ëÇб³(TAMHSC)ÀÇ ÀϺÎ)¿ÍÀÇ ±ä¹ÐÇÑ °øµ¿¿¬±¸¸¦ ÅëÇØ ÀÌ·ç¾îÁö°í ÀÖ½À´Ï´Ù. ÀÌ ¾à¹°Àº ÇöÀç ¿ø¹ß¼º ITP ¼ºÀΠȯÀÚ¸¦ ´ë»óÀ¸·Î ÇÑ ÀÓ»ó 3»ó ½ÃÇèÀÌ ÁøÇà ÁßÀÔ´Ï´Ù.
ÁÖ¿ä 7°³±¹ÀÇ ARGX-113 ½ÃÀå¿¡ ´ëÇØ Á¶»çÇßÀ¸¸ç, ½ÃÀåÀÇ °³¿ä¿Í 2024-2032³â ÆÇ¸Å ¿¹Ãø µ¥ÀÌÅÍ, °æÀï ±¸µµ ¹× ±¹°¡º° µ¿Çâ µîÀ» Á¦°øÇϰí ÀÖ½À´Ï´Ù.
“"ARGX-113 Emerging Drug Insight and Market Forecast - 2032" ” report provides comprehensive insights about ARGX-113 for immune thrombocytopenic purpura (ITP) in the seven major markets. A detailed picture of the ARGX-113 for ITP 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 ARGX-113 for ITP. 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 ARGX-113 market forecast analysis for ITP in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in ITP.
Efgartigimod (ARGX-113) is an investigational therapy for IgG-mediated autoimmune diseases and was designed to exploit the natural interaction between IgG antibodies and the recycling receptor FcRn Argenx, designed efgartigimod to degrade circulating disease-causing autoimmune antibodies and has potential in many large and orphan indications, namely multiple sclerosis, ITP, systemic lupus erythematosus, myasthenia gravis, and skin-blistering diseases.
Efgartigimod is the Fc-portion of an IgG1 antibody modified by the Argenx proprietary ABDEG technology to increase its affinity for FcRn beyond normal IgG antibodies. As a result, efgartigimod blocks antibody recycling through FcRn binding and leads to fast depletion of the autoimmune disease-causing IgG autoantibodies. The development work on efgartigimod is conducted in close collaboration with Prof. E. Sally Ward (University of Texas Southwestern Medical and Texas A&M University Health Science Center, a part of Texas A & M University (TAMHSC)). The drug is currently in Phase III trial for adult patients with primary ITP.
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 ARGX-113 for immune thrombocytopenic purpura (ITP) 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 2024 to 2032.
The report provides the clinical trials information of ARGX-113 for ITP covering trial interventions, trial conditions, trial status, start and completion dates.