|
시장보고서
상품코드
1473015
세계의 PIM 키나아제 표적 치료 시장 : 시장 기회와 임상시험에 관한 인사이트(2024년)Global PIM Kinase Targeted Therapies Market Opportunity & Clinical Trials Insight 2024 |
||||||
PIM 키나아제는 3개의 세린/트레오닌 프로테인키나아제로부터 구성되며, 암 및 기타 질병에서 매우 중요한 역할을 하기 때문에 임상 및 상업적 분야에서 큰 관심을 받고 있습니다. 유망한 치료 표적인 PIM 키나아제는 다양한 질병 영역에서 미충족 의료 수요를 해결하기 위한 표적 치료제 개발에 있으며, 흥미로운 전망을 제시하고 있습니다. 새로운 약물 계열을 통한 치료의 유익한 잠재력을 보여주고 있습니다.
PIM 키나아제(PIM kinase)는 모로니 마우스 백혈병 바이러스의 프로바이러스 삽입부위 키나아제의 약자로, 세포의 생존, 증식 및 분화를 조절하는 데 중요한 역할을 하며, PIM 키나아제 신호전달의 이상은 암, 자가면역질환, 염증성 질환, 심혈관계 질환, 바이러스성 질환 등에 관여하여 치료의 매력적인 타깃이 되고 있습니다. 심혈관 질환, 바이러스성 질환 등에 관여하고 있으며, 그 광범위한 치료 가능성이 강조되고 있습니다. 따라서 PIM 키나아제를 타깃으로 다양한 적응증에 적용할 수 있는 새로운 치료제 개발이 기대되고 있습니다.
PIM 키나아제 억제제의 개발은 표적치료제 분야에서 중요한 이정표가 되고 있습니다. 수년 동안 PIM 키나아제를 표적으로 하는 저분자 억제제가 몇 가지 개발되었는데, 대표적인 예로 SGI-1776, MEN1703, SGI-1776, ETH-155008, JP11646 등이 있습니다. 이들 후보물질은 주로 PIM 키나아제의 ATP 결합 포켓을 선택적으로 표적화하여 촉매 활성을 억제하고, 질병 진행에 관여하는 하류 신호전달 경로를 억제하며, SGI-1776, ETH-155008과 같은 일부 약물이 임상시험에 진입한 것은 PIM 키나아제를 치료 타깃으로 활용하는 것에 대한 관심 치료 타깃으로 PIM 키나아제를 활용하는 것에 대한 관심이 높아지고 있다는 점을 강조하며, PIM 키나아제 억제제의 상용화를 앞당기는 중요한 이정표가 될 것입니다.
임상시험에 진입한 PIM 키나아제 억제제의 수는 제한적이지만, PIM 키나아제 표적 치료제의 전망은 전임상 개발 중인 후보물질의 탄탄한 파이프라인으로 특징지어집니다. 많은 기업과 학술기관들이 효능과 안전성을 개선한 새로운 억제제를 발굴하기 위한 연구개발에 적극 나서고 있습니다. 현재 진행 중인 임상시험은 백혈병, 다발성 골수종, 전립선암 등 다양한 암 적응증과 전신성 홍반성 루푸스 등 염증성 질환에서 PIM 키나아제 억제제의 안전성, 내약성, 유효성을 평가했습니다.
세계의 PIM 키나아제 표적 치료 시장에 대해 조사했으며, 시장의 개요와 적응증별, 기업별, 국가별, 상별 동향, 임상시험 동향 및 시장에 참여하는 기업의 경쟁 동향 등을 제공하고 있습니다.
Global PIM Kinase Targeted Therapies Market Opportunity & Clinical Trials Insight 2024 Report Highlights:
PIM kinases, comprising three serine/threonine protein kinases, have garnered significant attention in both clinical and commercial spheres due to their pivotal roles in cancer and other disease indications. As promising therapeutic targets, PIM kinases offer exciting prospects for the development of targeted therapies aimed at addressing unmet medical needs across various diseases area. Though the market of PIM kinase targeted therapies is still in a budding phase, ongoing research efforts point towards a fruitful future for this emerging drug class.
PIM kinases, standing for Proviral Insertion Site in Moloney Murine Leukemia Virus kinases, play crucial roles in regulating cell survival, proliferation and differentiation, making them attractive targets for therapeutic intervention. Dysregulated PIM kinase signaling has been implicated in cancer, autoimmune disorders, inflammatory conditions, cardiovascular diseases and viral diseases, highlighting their broad therapeutic potential. As such, targeting PIM kinases holds promise for development of novel treatments with potential applications across a diverse range of indications.
The development of PIM kinases inhibitors represents a significant milestone in the field of targeted therapy. Over the years, several small molecule inhibitors targeting PIM kinases have been developed, with notable examples including SGI-1776, MEN1703, SGI-1776, ETH-155008, JP11646. These candidates majorly target the ATP-binding pocket of PIM kinases selectively, inhibiting their catalytic activity and disrupting downstream signaling pathways implicated in disease progression. The advancement of some of these such as SGI-1776, ETH-155008 into clinical trials underscores the growing interest in exploiting PIM kinases as therapeutic targets and represents a key milestone in moving PIM kinase inhibitors towards commercialization.
While only a limited number of PIM kinase inhibitors have progressed to clinical trials, the landscape of PIM kinase targeted therapies is characterized by a robust pipeline of candidates in preclinical development. Numerous companies and academic institutions are actively engaged in research and development efforts aimed at identifying novel inhibitors with improved efficacy and safety profiles. Ongoing clinical trials are evaluating the safety, tolerability and efficacy of PIM kinase inhibitors in various cancer indications, including leukemia, multiple myeloma and prostate cancer, as well as inflammatory conditions like systemic lupus erythematosus.
Collaborations between pharmaceutical companies, academic institutions and research hospitals have been instrumental in driving progress in the development of PIM kinase targeted therapies. Academic institutions like University of Arizona, University of Leipzig, Ludwig Maximilians University Munich, University of Alabama, Ohio State University, Medical University of South Carolina and Pusan National University have over the years contributed valuable insights into the underlying biology of PIM kinases and their role in disease pathogenesis. Companies on the other hand bring expertise in drug discovery and development while hospitals serve as places to conduct clinical trials and additional research.
The development of RF-1302, a novel dual inhibitor of PIM-1 and FLT3 kinases, by the Chinese Academy of Medical Science and Tianjin Medical University General Hospital in partnership with Ruifu Therapeutics, serves as an example of this. The candidate is presently undergoing preclinical studies to treat acute myeloid leukemia. This kind of collaborative spirit encourages innovation and speeds up the translation of fundamental research discoveries into treatment interventions that have practical application. Companies and academic institutions can accelerate the commercialization of PIM kinase targeted therapies and optimize their potential by utilizing complementary capabilities and resources.
The market for PIM kinase targeted therapies looks to have a promising future with lots of scope to grow. Structure-based drug design and high-throughput screening are two examples of how drug discovery technologies are progressing and could lead to the development of new PIM kinase inhibitors with better potency and selectivity. Furthermore, the development of precision medicine strategies and biomarker-driven methodologies may make it possible to implement more individualized and focused treatment plans, improving the therapeutic utility of PIM kinase targeted therapies.
Additionally, novel treatment approaches may be discovered as a result of our growing understanding of PIM kinase biology and its significance in the pathophysiology of disease. PIM kinase targeted therapy development will be accelerated by industry-academia collaborations, which will ultimately benefit patients by offering more individualized and effective treatment alternatives. Because of this, the market for PIM kinase targeted therapies is anticipated to experience rapid expansion and innovation in the years to come, presenting intriguing prospects for players in the pharmaceutical sector.