![]() |
½ÃÀ庸°í¼
»óǰÄÚµå
1414926
¸é¿ª°ü¹®¾ïÁ¦Á¦ ½ÃÀå - À¯Çüº°, ¿ëµµº° : ¼¼°è ±âȸ ºÐ¼® ¹× »ê¾÷ ¿¹Ãø(2023-2032³â)Immune Checkpoint Inhibitors Market By Type, By Application : Global Opportunity Analysis and Industry Forecast, 2023-2032 |
¸é¿ª°ü¹®¾ïÁ¦Á¦(ICI) ½ÃÀåÀº 2022³â¿¡´Â 401¾ï ´Þ·¯·Î Æò°¡µÇ¾úÀ¸¸ç, 2023³âºÎÅÍ 2032³â±îÁö 16.8%ÀÇ ¿¬Æò±Õ º¹ÇÕ ¼ºÀå·ü(CAGR)·Î ¼ºÀåÇÒ Àü¸ÁÀ̸ç, 2032³â¿¡´Â 1,894¾ï ´Þ·¯¿¡ À̸¦ °ÍÀ¸·Î ÃßÁ¤µË´Ï´Ù.
¾Ï¼¼Æ÷´Â ¸é¿ª ü°èÀÇ °ËÃâ°ú ÆÄ±«¸¦ ÇÇÇϱâ À§ÇØ ÀÌ·¯ÇÑ °ü¹®À» ¾Ç¿ëÇÕ´Ï´Ù. ¸é¿ª°ü¹®¾ïÁ¦Á¦´Â PD-1(ÇÁ·Î±×·¥ ¼¼Æ÷ »ç´Ü¹éÁú 1), PD-L1(ÇÁ·Î±×·¥ »ç¸ê ¸®°£µå 1), CTLA-4(¼¼Æ÷µ¶¼º T ¸²ÇÁ±¸ °ü·Ã ´Ü¹éÁú 4)¿Í °°Àº ƯÁ¤ ´Ü¹éÁúÀ» Ç¥ÀûÈÇÕ´Ï´Ù. ±×¸®°í Â÷´ÜÇÏ¿© ÀÛµ¿ÇÕ´Ï´Ù. ÀÌ·¯ÇÑ ´Ü¹éÁúÀ» ¾ïÁ¦ÇÔÀ¸·Î½á, ÀÌ·¯ÇÑ ¾àÁ¦´Â ¸é¿ª°è°¡ º¸´Ù È¿°úÀûÀ¸·Î ¾Ï¼¼Æ÷¸¦ È®ÀÎÇÏ°í ½Î¿ì´Â °ÍÀ» °¡´ÉÇÏ°Ô ÇÕ´Ï´Ù.
¸é¿ª°ü¹®¾ïÁ¦Á¦ ½ÃÀåÀÇ ¼ºÀåÀ» °¡¼ÓÇÏ´Â ÁÖ¿ä ¿äÀÎÀº ¿¬±¸°³¹ßÀÇ ÁøÀü, ¾Ï ȯÀÚ Áõ°¡, ÀÓ»ó½ÃÇè¼ö Áõ°¡, ¿¬±¸ ÀÌ´Ï¼ÅÆ¼ºêÀÇ È®´ë, Àü·«Àû Á¦ÈÞ, ½Å±Ô ÀûÀÀÁõÀÇ ½ÂÀÎ È®´ë µîÀÔ´Ï´Ù. ¾ÏÀº ¿©ÀüÈ÷ ¼¼°è »ç¸Á ¿øÀÎ 1À§À̸ç, ´Ù¾çÇÑ ¾ÏÁ¾À¸·Î Áø´ÜµÇ´Â Áõ·Ê°¡ °è¼Ó Áõ°¡Çϰí ÀÖ½À´Ï´Ù. ¿¹¸¦ µé¾î ¹Ì±¹ ±¹¸³¾Ï¿¬±¸¼Ò ¾ÏÁ¦¾î ¹× Àα¸°úÇкÎ(DCCPS)¿¡ µû¸£¸é ¹Ì±¹¿¡¼´Â 623,405¸íÀÌ ÀüÀ̼º À¯¹æ¾Ï, Àü¸³¼±¾Ï, Æó¾Ï, ´ëÀå¾Ï ¶Ç´Â ÀüÀ̼º Èæ»öÁ¾À» ¾Î°í ÀÖ½À´Ï´Ù. ¾Ï ºÎ´ãÀÌ Áõ°¡ÇÔ¿¡ µû¶ó, º¸´Ù È¿°úÀûÀÎ Ä¡·á ¿É¼Ç¿¡ ´ëÇÑ ±ä±ÞÇÑ ¿ä±¸°¡ Áõ°¡Çϰí, ¸é¿ª°ü¹®¾ïÁ¦Á¦¿¡ ´ëÇÑ ¼ö¿ä°¡ Áõ°¡Çϰí ÀÖ½À´Ï´Ù.
°Ô´Ù°¡, ¸é¿ª°ü¹®¾ïÁ¦Á¦¿¡ ÃÊÁ¡À» ¸ÂÃá ÀÓ»ó½ÃÇèÀÇ ¼ö°¡ Áõ°¡Çϰí ÀÖ´Â °Íµµ ½ÃÀå ¼ºÀåÀ» µÞ¹ÞħÇÒ °ÍÀ¸·Î ¿¹»óµË´Ï´Ù. Á¦¾àȸ»ç, »ý¸í°øÇбâ¾÷, Çмú±â°ü °£¿¡´Â Àӻ󿬱¸¿¡ ÀÚ¿øÀ» ³ª´©´Â °æÇâÀÌ °ÇØÁö°í ÀÖ½À´Ï´Ù. ÀÌ ÅõÀÚ´Â ´Ù¾çÇÑ ¾ÏÁ¾¿¡¼ ¸é¿ª°ü¹®¾ïÁ¦Á¦ÀÇ ¾ÈÀü¼º, È¿´É ¹× °¡¿ë¼ºÀ» Á¶»çÇÏ´Â °ÍÀ» ¸ñÇ¥·Î ÇÕ´Ï´Ù. ÀÌ·¯ÇÑ ÀÓ»ó½ÃÇèÀº ½Å±Ô¾àÁ¦ Á¶ÇÕÀÇ °ËÅä, Ä¡·á¹ÝÀÀÀÇ Æò°¡, ¿¹Ãø ¹ÙÀÌ¿À¸¶Ä¿ÀÇ ½Äº°¿¡ ÁßÁ¡À» µÎ°í ÀÖÀ¸¸ç, ¸é¿ªÁÖµµÇü Ä¡·áÀÇ ÀÌÇØ¸¦ ³ÐÈ÷´Â µ¥ Å©°Ô ±â¿©Çϰí ÀÖ½À´Ï´Ù. ¿¹¸¦ µé¾î, 2023³â 7¿ù, Merck&Co., Inc. ¹× Moderna, Inc.´Â ÀýÁ¦µÈ °íÀ§Çè(´Ü°è IIB-IV) Èæ»öÁ¾ ȯÀÚ¿¡¼ ¼ö¼ú ÈÄ º¸Á¶ ¿ä¹ýÀ¸·Î ½ÃÇè Áß °³º°ÈµÈ »õ·Î¿î Ç׿ø ¿ä¹ý(INT)ÀÎ V940(mRNA-4157)À» MerckÀÇ Ç×-PD-1 ¿ä¹ýÀÎ KEYTRUDA¿Í º´¿ëÇÏ´Â ¸Å¿ì Áß¿äÇÑ 3»ó ·£´ýÈ V940-001 ÀÓ»ó½ÃÇèÀÇ °³½Ã¸¦ ¹ßÇ¥Çß½À´Ï´Ù. ÀÌ·¯ÇÑ ÀÓ»ó½ÃÇèÀÇ °á°ú´Â ¾à¹°°³Ã´ÀÇ ¿øµ¿·ÂÀÌ µÉ »Ó¸¸ ¾Æ´Ï¶ó Ä¡·á¹æÄ§ÀÇ °áÁ¤¿¡µµ µµ¿òÀÌ µÇ¹Ç·Î ¸é¿ª°ü¹®¾ïÁ¦Á¦ ½ÃÀåÀÇ ¼ºÀåÀ» ´õ¿í µÞ¹ÞħÇÕ´Ï´Ù.
°Ô´Ù°¡ Á¦¾à±â¾÷, »ý¸í°øÇбâ¾÷, Çмú±â°üÀÇ Àü·«Àû Á¦ÈÞ´Â ¸é¿ª°ü¹®¾ïÁ¦Á¦ ½ÃÀåÀÇ ¼ºÀåÀ» °¡¼ÓÇÏ´Â Áß¿äÇÑ ¿äÀÎÀ¸·Î ºÎ»óÇϰí ÀÖ½À´Ï´Ù. ÆÄÆ®³Ê½Ê°ú Á¦ÈÞ´Â Àü¹® Áö½Ä, ÀÚ¿ø, ±â¼úÀÇ ÅëÇÕÀ» ÃËÁøÇϰí â¾à °³¹ß ÇÁ·Î¼¼½º¸¦ °¡¼ÓÈÇÕ´Ï´Ù. ¿¹¸¦ µé¾î, 2020³â 5¿ù, ¼¼°èÀÇ ¹ÙÀÌ¿À ÀǾàǰ ±â¾÷ÀÎ Innovent Biologics, Inc.¿Í ÅØ»ç½º ´ëÇÐ MD ¾Ø´õ½¼ ¾Ï ¼¾ÅÍ´Â À̳뺥ƮÀÇ Ç×PD-1 ´ÜŬ·ÐÇ×üÀÎ TYVYT(½ÅÆ¿¸®¸¿ ÁÖ»çÁ¦)¸¦ Èñ¼Ò¾Ï Ä¡·á ¾àÀ¸·Î ¹Ì±¹¿¡¼ °øµ¿ °³¹ßÇÏ´Â Àü·«Àû Á¦ÈÞ °è¾àÀ» ü°áÇß´Ù°í ¹ßÇ¥Çß½À´Ï´Ù. ÀÌ·¯ÇÑ °øµ¿¿¬±¸¿¡ ÀÇÇØ ¸î°³ÀÇ ¸é¿ª°ü¹®¾ïÁ¦Á¦ °³¹ß ¹× »ó¾÷È¿¡ ¼º°øÇØ, ¾Ï ¿µ¿ª¿¡ ÀÖ¾î¼ÀÇ ¸é¿ª°ü¹®¾ïÁ¦Á¦ÀÇ ÀÀ¿ë ¹üÀ§°¡ ³Ð¾îÁö°í ÀÖ½À´Ï´Ù.
According to a new report published by Allied Market Research, titled, "Immune Checkpoint Inhibitors Market," The immune checkpoint inhibitors market was valued at $40.1 billion in 2022, and is estimated to reach $189.4 billion by 2032, growing at a CAGR of 16.8% from 2023 to 2032.
Cancer cells exploit these checkpoints to evade the immune system's detection and destruction. Immune checkpoint inhibitors work by targeting and blocking specific proteins, such as PD-1 (programmed cell death protein 1), PD-L1 (programmed death-ligand 1), or CTLA-4 (cytotoxic T-lymphocyte-associated protein 4), which are involved in these checkpoints. By inhibiting these proteins, these drugs enable the immune system to more effectively identify and combat cancer cells.
The major factors driving the growth of immune checkpoint inhibitors market are advancements in R&D, increase in prevalence of cancer cases, increase in number of clinical trials, expanding research initiatives, strategic collaborations, and growing approvals for new indications. Cancer remains a leading cause of mortality globally, with continuous rise in diagnosed cases across various cancer types. For instance, National Cancer Institute, Division of Cancer Control & Population Sciences (DCCPS), stated that, 623,405 people are living with metastatic breast, prostate, lung, colorectal cancer, or metastatic melanoma in the U.S. As the burden of cancer grows, there is a pressing need for more effective treatment options, leading to the heightened demand for immune checkpoint inhibitors.
Further, increase in the number of clinical trials focusing on the immune checkpoint inhibitors is expected to fuel the market growth. There is a growing inclination among pharmaceutical companies, biotechnology firms, and academic institutions to allocate more resources toward clinical research. This investment aims to scrutinize the safety, effectiveness, and possible uses of immune checkpoint inhibitors across diverse cancer types. These trials, focused on investigating novel drug combinations, evaluating treatment reactions, and pinpointing predictive biomarkers, significantly contribute to broadening the comprehension of immune-driven treatments. For instance, in July 2023, Merck & Co., Inc., and Moderna, Inc. announced the initiation of the pivotal Phase 3 randomized V940-001 clinical trial evaluating V940 (mRNA-4157), an investigational individualized neoantigen therapy (INT), in combination with KEYTRUDA, Merck's anti-PD-1 therapy, as an adjuvant treatment in patients with resected high-risk (Stage IIB-IV) melanoma. The results from these trials not only drive drug development but also inform treatment decisions, further boosting the growth of the immune checkpoint inhibitors market.
Furthermore, strategic collaborations among pharmaceutical companies, biotechnology firms, and academic institutions have emerged as a key factor propelling the growth of the immune checkpoint inhibitors market. Partnerships and alliances facilitate the consolidation of expertise, resources, and technologies, expediting the drug discovery and development process. For instance, in May 2020, Innovent Biologics, Inc., a world-class biopharmaceutical company that develops, manufactures, and commercializes high-quality medicines for the treatment of cancer, autoimmune, metabolic & other major diseases, and The University of Texas MD Anderson Cancer Center, announced a strategic collaboration agreement to co-develop TYVYT (sintilimab injection), Innovent's anti-PD-1 monoclonal antibody, for treating rare cancers in the U.S. In addition, collaborative efforts facilitate the exploration of diverse therapeutic applications, the conduct of larger clinical trials, and the accelerated translation of research findings into clinical applications. Such collaborations have led to the successful development and commercialization of several immune checkpoint inhibitors, widening their reach and applications in oncology.
The immune checkpoint inhibitors market is segmented on the basis of product type, application, and region. By product type, the market is categorized into CTLA-4 inhibitor, PD-1 inhibitor, and PD-L1 inhibitor. On the basis of application, the market is classified into lung cancer, bladder cancer, melanoma, colorectal cancer, Hodgkin lymphoma, and others. Region-wise, the market is analyzed across North America (the U.S., Canada, and Mexico), Europe (Germany, France, the UK, and rest of Europe), Asia-Pacific (Japan, China, Australia, India, South Korea, and rest of Asia-Pacific), and LAMEA (Brazil, and rest of LAMEA).
Major key players that operate in the global immune checkpoint inhibitors market are Merck & Co., Inc., AstraZeneca plc, F. Hoffmann-La Roche Ltd., Merck KGaA, Regeneron Pharmaceuticals, Inc., Bristol-Myers Squibb Company, BeiGene, Ltd., Shanghai Junshi Biosciences Co., Ltd., GlaxoSmithKline plc, and Innovent Biologics, Inc. The key players have adopted strategies such as acquisition, agreement, strategic alliance, collaboration, clinical trial, expansion, joint venture, new product development, and product approval to expand their product portfolio.
Additional benefits you will get with this purchase are:
Possible Customization with this report (with additional cost and timeline, please talk to the sales executive to know more)