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市场调查报告书
商品编码
1671195
基因治疗的全球市场:市场规模·占有率·趋势,产业分析 (各治疗领域·媒介类别·方法·各给药途径·各地区),未来预测 (2025年~2034年)Gene Therapy Market Size, Share, Trends, Industry Analysis Report: By Therapeutic Area, Vector Type, Approach, Route of Administration, and Region - Market Forecast 2025-2034 |
根据 Polaris Market Research 的最新研究,基因治疗市场预计到 2034 年将达到 272.502 亿美元。该报告对当前的市场动态提供了详细的见解,并对未来的市场成长进行了分析。
基因治疗涉及纠正或替换患者细胞中的不健康基因以治疗或预防疾病。基因工程的快速发展以及对分子生物学认知的不断加深,推动了基因治疗从实验阶段走向实际临床应用。研究人员和生物製药公司正在大力投资开发安全有效的治疗方法,而监管机构正在简化审批流程,以加速基因治疗市场的扩张。
由于杜氏肌肉营养不良症 (DMD)、镰状细胞病、血友病和囊性纤维化等遗传疾病的盛行率不断上升,对基因治疗的需求正在迅速增加。与专注于症状管理的传统治疗不同,基因疗法从基因层面针对这些疾病的根本原因。这种有针对性的方法提高了治疗效果,并有可能带来长期甚至永久的缓解。近年来,CRISPR-Cas9 和锌指核酸酶 (ZFN) 等基因编辑技术的显着进步使得基因修饰更加精确和高效。
越来越多的基因疗法监管部门批准正在推动基因治疗市场的成长。美国食品药物管理局 (FDA) 和欧洲药品管理局 (EMA) 等政府机构已经认识到这些治疗方法的变革潜力。这些机构加快了有前途的候选人的审批流程。 Zolgensma 治疗脊髓性肌肉萎缩症 (SMA) 和 Luxturna 治疗遗传性视网膜疾病等疗法取得了显着的临床成功,为更广泛地应用基因为基础的疗法和程序铺平了道路。
基于治疗领域,肿瘤疾病领域将在 2024 年引领基因治疗市场占有率,因为肿瘤疾病的流行及其治疗对身体和心理产生重大影响。
根据载体类型,病毒部分在基因治疗市场收入占有率中处于领先地位,因为它可以有效且有效率地将基因传递到针对各种癌症、单基因疾病和传染病的目标细胞中。
北美凭藉其强大的研究基础设施、先进的医疗保健系统、大量的临床试验资金以及由 FDA 领导的支持性监管框架引领基因治疗市场,从而实现新型基因疗法的快速开发和批准。
全球主要公司包括abeona·serapyutikku,诺华AG,火花·serapyutikusuLLC,giriado·saienshizu,布里斯托尔·maiyazu·Squibb,adobaumu·baiotekunorojizu,arunairamu·famashutikaruzu,美国的·gene·tekunorojizu,apuraido·jenetikku·tekunorojizu·团体,baiojen,urutorajenikkusu等举出(举行)。
The gene therapy market size is expected to reach USD 27,250.20 million by 2034, according to a new study by Polaris Market Research. The report "Gene Therapy Market Size, Share, Trends, Industry Analysis Report: By Therapeutic Area (Autoimmune Disorders, Cardiovascular Diseases, Dermatological Disorders, Hematological Disorders, Metabolic Disorders, Muscle-Related Diseases, Oncological Disorders, and Others), Vector Type, Approach, Route of Administration, and Region (North America, Europe, Asia Pacific, Latin America, and Middle East & Africa) - Market Forecast, 2025-2034" gives a detailed insight into current market dynamics and provides analysis on future market growth.
Gene therapy involves modifying or replacing unhealthy genes within a patient's cells to treat or prevent disease. Rapid advancements in genetic engineering, along with an increasing understanding of molecular biology, have propelled gene therapy from experimental stages to real-world clinical applications. Researchers and biopharmaceutical companies are investing heavily in developing safe and effective therapies, while regulatory bodies are streamlining approval processes to accelerate gene therapy market expansion.
The demand for gene therapy has surged due to the increasing prevalence of genetic disorders such as Duchenne muscular dystrophy (DMD), sickle cell disease, hemophilia, and cystic fibrosis. Unlike traditional treatment methods that primarily focus on symptom management, gene therapy targets the underlying cause of these diseases at the genetic level. This targeted approach enhances treatment efficacy and offers the potential for long-term or even permanent relief. In recent years, significant breakthroughs in gene-editing technologies, such as CRISPR-Cas9 and zinc finger nucleases (ZFNs), have enabled more precise and efficient gene modifications.
The rising number of regulatory approvals for gene-based treatments is propelling the gene therapy market growth. Government agencies such as the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have recognized the transformative potential of these therapies. They are expediting the approval process for promising candidates. Therapies such as Zolgensma for spinal muscular atrophy (SMA) and Luxturna for inherited retinal disease have demonstrated remarkable clinical success, paving the way for broader adoption of gene-based therapies or treatments.
Based on therapeutic area, the oncological disorders segment leads the gene therapy market share in 2024 due to the prevalence of significant physical and psychological impacts of the disease and its treatment.
By vector type, the viral segment leads gene therapy market revenue share due to its effective and efficient delivering genes to the targeted cells for various cancers, monogenic and infectious diseases.
North America leads the gene therapy market due to its robust research infrastructure, advanced healthcare system, significant funding for clinical trials, and a supportive regulatory framework, particularly from the FDA, which allows for rapid development and approval of new gene therapies.
A few global key market players are Abeona Therapeutic, Novartis AG, Spark Therapeutics LLC, Gilead Sciences Inc., Bristol Myers Squibb, Adverum Biotechnologies, Alnylam Pharmaceuticals, American Gene Technologies, Applied Genetic Technologies Corporation, Biogen, and Ultragenyx.
Polaris Market Research has segmented the gene therapy market report on the basis of therapeutic area, vector type, approach, route of administration, and region: