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全球癌症基因治疗市场研究报告 - 2024 年至 2032 年产业分析、规模、份额、成长、趋势和预测Global Cancer Gene Therapy Market Research Report - Industry Analysis, Size, Share, Growth, Trends and Forecast 2024 to 2032 |
全球癌症基因治疗市场需求预计将从2023年的31.1亿美元达到近161亿美元的市场规模,2024年至2032年的研究期间复合年增长率为20.05%。
癌症基因治疗利用基因技术,透过标靶参与肿瘤生长、进展和存活的特定基因或细胞途径来治疗癌症。这种治疗方法旨在修改或抑制癌症相关基因,刺激针对癌细胞的免疫反应,或将治疗基因直接传递到肿瘤中以抑制其生长或诱导细胞死亡。这种疗法有望成为包括实体瘤和血液恶性肿瘤在内的各种类型癌症的潜在治疗选择,与传统化疗和放射疗法相比,具有降低毒性的标靶和个人化干预的潜力。
全球范围内癌症的快速流行和传统癌症治疗的有限疗效推动了对基因治疗等新型治疗方法的需求,基因治疗为在基因层面上靶向和精确治疗癌症提供了潜力。随着对癌症生物学、肿瘤异质性和肿瘤发生的分子机制的日益了解,人们越来越重视开发针对特定基因突变、癌基因和与癌症进展有关的信号通路的基因治疗策略。此外,CRISPR/Cas9、TALEN 和锌指核酸酶等基因编辑技术的出现使得能够精确修饰癌症相关基因,为开发破坏致癌途径、增强肿瘤抑制和改善患者预后的基因疗法提供了新的机会。
此外,用于基因传递的病毒和非病毒载体的不断增加、载体工程的进步以及基因转移技术的优化推动了更安全、更有效和有针对性的癌症基因治疗的发展。此外,对癌症研究、临床试验和基因治疗产品监管许可的投资不断增加,促进了癌症基因治疗市场的创新和商业化。基因疗法具有彻底改变癌症治疗模式的潜力,为患有难治性癌症、罕见遗传性疾病和未满足的医疗需求的患者带来了新的希望,推动了人们对这个快速发展的领域的兴趣和投资。
然而,严格的监管要求、临床试验的复杂性和伦理问题可能会挑战癌症基因治疗市场的成长。
研究报告涵盖波特五力模型、市场吸引力分析和价值链分析。这些工具有助于清晰地了解行业结构并评估全球范围内的竞争吸引力。此外,这些工具也对全球癌症基因治疗市场的各个细分市场进行了包容性评估。癌症基因治疗产业的成长和趋势为这项研究提供了整体方法。
癌症基因治疗市场报告的这一部分提供了国家和地区层面细分市场的详细资料,从而帮助策略家确定相应产品或服务的目标人口统计数据以及即将到来的机会。
本节涵盖区域前景,重点介绍北美、欧洲、亚太地区、拉丁美洲以及中东和非洲癌症基因治疗市场当前和未来的需求。此外,该报告重点关注所有主要地区各个应用领域的需求、估计和预测。
该研究报告还涵盖了市场主要参与者的全面概况以及对全球竞争格局的深入了解。癌症基因治疗市场的主要参与者包括Abeona Therapeutics Inc.、Asklepios BioPharmaceutical Inc.、Altor Bioscience Inc.、Bluebird bio Inc.、BioCancell Inc.、Celgene Inc.、Elevate Bio Inc.、GlaxoSmithKline Inc.、Genelux Corporation、 GenVecec 、Introgen Therapeutics Inc.、Merck KGaA、OncoGenex Pharmaceuticals Inc. 本部分包含竞争格局的整体视图,其中包括各种策略发展,例如关键併购、未来产能、合作伙伴关係、财务概览、合作、新产品开发、新产品发布以及其他进展。
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The global demand for Cancer Gene Therapy Market is presumed to reach the market size of nearly USD 16.1 Billion by 2032 from USD 3.11 Billion in 2023 with a CAGR of 20.05% under the study period 2024 - 2032.
Cancer gene therapy uses genetic techniques to treat cancer by targeting specific genes or cellular pathways involved in tumor growth, progression, and survival. This therapeutic approach aims to modify or suppress cancer-related genes, stimulate immune responses against cancer cells, or deliver therapeutic genes directly into tumors to inhibit their growth or induce cell death. This therapy holds promise as a potential treatment option for various types of cancer, including solid tumors and hematological malignancies, offering the potential for targeted and personalized interventions with reduced toxicity compared to traditional chemotherapy and radiation therapy.
The spurring prevalence of cancer worldwide and the limited efficacy of conventional cancer treatments drive the demand for novel therapeutic approaches such as gene therapy, which offers the potential for targeted and precise treatment of cancer at the genetic level. With the growing understanding of cancer biology, tumor heterogeneity, and molecular mechanisms of oncogenesis, there is an increasing emphasis on developing gene therapy strategies that target specific genetic mutations, oncogenes, and signaling pathways implicated in cancer progression. Additionally, the advent of gene editing technologies such as CRISPR/Cas9, TALENs, and zinc finger nucleases enables precise modification of cancer-related genes, offering new opportunities for developing gene therapies that disrupt oncogenic pathways, enhance tumor suppression, and improve patient outcomes.
Moreover, the increasing availability of viral and non-viral vectors for gene delivery, advancements in vector engineering, and optimization of gene transfer techniques drive the development of safer, more efficient, and targeted cancer gene therapy. Furthermore, the growing investment in cancer research, clinical trials, and regulatory clearances for gene therapy products foster innovation and commercialization in the cancer gene therapy market. With the potential to revolutionize cancer treatment paradigms, gene therapy provides new hope for patients with refractory cancers, rare genetic disorders, and unmet medical needs, driving interest and investment in this rapidly evolving field.
However, stringent regulatory requirements, clinical trial complexities, and ethical concerns may challenge the growth of the cancer gene therapy market.
The research report covers Porter's Five Forces Model, Market Attractiveness Analysis, and Value Chain analysis. These tools help to get a clear picture of the industry's structure and evaluate the competition attractiveness at a global level. Additionally, these tools also give an inclusive assessment of each segment in the global market of cancer gene therapy. The growth and trends of cancer gene therapy industry provide a holistic approach to this study.
This section of the cancer gene therapy market report provides detailed data on the segments at country and regional level, thereby assisting the strategist in identifying the target demographics for the respective product or services with the upcoming opportunities.
This section covers the regional outlook, which accentuates current and future demand for the Cancer Gene Therapy market across North America, Europe, Asia-Pacific, Latin America, and Middle East & Africa. Further, the report focuses on demand, estimation, and forecast for individual application segments across all the prominent regions.
The research report also covers the comprehensive profiles of the key players in the market and an in-depth view of the competitive landscape worldwide. The major players in the Cancer Gene Therapy market include Abeona Therapeutics Inc., Asklepios BioPharmaceutical Inc., Altor Bioscience Inc., Bluebird bio Inc., BioCancell Inc., Celgene Inc., Elevate Bio Inc., GlaxoSmithKline Inc., Genelux Corporation, GenVec, Introgen Therapeutics Inc., Merck KGaA, OncoGenex Pharmaceuticals Inc. This section consists of a holistic view of the competitive landscape that includes various strategic developments such as key mergers & acquisitions, future capacities, partnerships, financial overviews, collaborations, new product developments, new product launches, and other developments.
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