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시장보고서
상품코드
1526806
항TIGIT 항체 시장 : 임상시험 및 시장 기회 전망(2028년)Anti TIGIT Antibodies Clinical Trials & Market Opportunity Outlook 2028 |
항TIGIT 항체는 암 면역 치료의 유망한 접근법으로 등장하여 다양한 유형의 암, 특히 고형암 환자에게 새로운 희망을 주고 있습니다. TIGIT(T cell immunoreceptor with Ig and ITIM domains)는 T세포와 자연살해(NK) 세포에 발현하는 억제성 수용체로 면역 반응 조절에 중요한 역할을 하며, TIGIT를 표적으로 삼는 것은 암세포를 인식하고 제거하는 면역체계의 능력을 향상시켜 암 치료 전략에 혁명을 가져올 수 있습니다.
암 면역치료의 표적으로서 TIGIT의 치료적 잠재력은 면역 체크포인트 분자로서의 기능에 있으며, TIGIT가 CD155 및 CD112와 같은 리간드와 상호 작용할 때 T세포 및 NK세포의 활성화를 억제하여 암세포가 면역 감시를 피할 수 있도록 할 수 있습니다. 연구진은 항 TIGIT 치료 접근법으로 이 상호작용을 차단함으로써 종양에 대한 면역반응을 재가동하고 암 환자의 임상결과를 개선할 수 있을 것으로 기대하고 있습니다.
TIGIT를 표적으로 하는 다양한 접근법 중 단클론항체는 가장 널리 사용되고 유망한 약물로 부상하고 있습니다. 이 항체는 TIGIT에 특이적으로 결합하도록 설계되어 TIGIT와 그 리간드와의 상호작용을 억제하여 면역체계의 "단절"을 해제합니다. 항체의 높은 특이성과 상대적으로 낮은 독성은 임상 개발의 매력적인 후보가 될 수 있습니다.
항TIGIT 항체 개발은 빠르게 진행되고 있으며, 현재 50개 이상의 후보물질이 임상 개발 단계에 있습니다. 이 강력한 파이프라인은 암 치료에서 이 접근법에 대한 큰 관심과 잠재력을 뒷받침합니다. 그 중 5가지 이상의 항TIGIT 항체가 임상 3상 시험에 진입해 있으며, 이는 허가 전 임상 개발의 가장 높은 단계에 해당합니다. 여기에는 제약 마커의 선두주자인 머크 제네텍과 베링거인겔하임이 각각 개발한 비보스트리맙, 티라골맙, 오시페리리맙이 포함됩니다.
이 보고서는 세계 항TIGIT 항체 시장에 대해 조사했으며, 시장 개요와 함께 항TIGIT 항체 임상 파이프라인, 적응증별, 국가별 동향, 시장 진입 기업의 경쟁 동향 등을 조사하여 전해드립니다.
Anti TIGIT Antibodies Clinical Trials & Market Opportunity Outlook 2028 Report Highlights:
Anti TIGIT antibodies have emerged a promising approach in cancer immunotherapy, offering new hope for patients with various types of cancers, particularly solid cancers. TIGIT (T cell immunoreceptor with Ig and ITIM domains) is an inhibitory receptor expressed on T cells and natural killer (NK) cells, playing a crucial role in modulating immune responses. By targeting TIGIT, researchers aim to enhance the immune system's ability to recognize and eliminate cancer cells, potentially revolutionizing cancer treatment strategies.
The therapeutic potential of TIGIT as a target for cancer immunotherapy lies in its function as an immune checkpoint molecule. When TIGIT interacts with its ligands, such as CD155 and CD112, it suppresses T cell sand NK cell activation, potentially allowing cancer cells to evade immune surveillance. By blocking this interaction with anti-TIGIT therapeutic approaches, researchers hope to reinvigorate the immune response against tumors, leading to improved clinical outcome for cancer patients.
Among the various approaches for targeting TIGIT, monoclonal antibodies have emerged as the most widely used and promising agents. These antibodies are designed to specifically bind to TIGIT, preventing its interaction with its ligands and thus releasing the "breaks" on the immune system. Their high specificity and relatively low toxicity of antibodies make them attractive candidates for clinical development.
The field of anti-TIGIT antibody development has seen rapid progress, with over 50 candidates currently in clinical development. This robust pipeline underscores the significant interest and potential of this approach in cancer treatment. Among these, more than five anti TIGIT antibodies have advanced to phase 3 clinical trials, representing the most advanced stage of clinical development before potential regulatory approval. These include Vibostolimab, Tiragolumab and Ociperlimab, developed by the pharmaceutical marker leaders, Merck Genentech and BeiGene, respectively.
These phase 3 clinical trials are assessing the safety and efficacy of these anti-TIGIT antibodies in various cancer types, with a particular focus on non-small cell lung cancer (NSCLC). The emphasis on NSCLC is not surprising, given its high prevalence and the need for more effective treatment options. NSCLC represents a significant portion of lung cancer cases and has shown promising responses to immunotherapy approaches in the past.
Several key factors are driving the market potential of anti-TIGIT antibodies. Firstly, there remains a substantial unmet medical need in cancer treatment, especially for patients who do not respond to or develop resistance to existing immunotherapies. Anti-TIGIT antibodies offer a novel mechanism of action that could address these challenges. Moreover, these antibodies show promising results in combination with established therapies like PD-1/L1 inhibitors, potentially expanding the market for both drug classes and improving treatment outcomes. This becomes visible in Merck's vision of developing a coformulation of its anti-TIGIT antibody Vibostolimab with its blockbuster anti-PD-1 antibody pembrolizumab for the treatment of various solid tumors.
The broad applicability of anti-TIGIT antibodies across various cancer forms presents another significant market opportunity. While a majority of clinical trials currently focus on NSCLC, many other ongoing clinical trials are exploring their efficacy in other solid cancers tumors and hematological malignancies, which could lead to multiple approved indications, consequently increasing the anti-TIGIT antibody market size.
As evident from the examples above, the competitive landscape for the anti-TIGIT antibody market is dynamic, with major pharmaceutical companies and biotechnology firms vying for market share. While Vibostolimab leverages the company's strong position in the immuno-oncology market, another, Domvanalimab, being developed by Gilead Sciences and Arcus Biosciences, benefits from a partnership between a major pharmaceutical company and a competent biopharmaceutical company.
In conclusion, anti-TIGIT antibodies not only represent a significant advancement in cancer immunotherapy, but also present many opportunities for drug development and market expansion. With its potential to address unmet medical needs, broad applicability and alignment with personalized medicine, this emerging class of drugs is poised to capture a substantial portion of cancer immunotherapy market.