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市场调查报告书
商品编码
1707942
基因治疗市场规模、份额、成长分析(按基因类型、按治疗类型、按载体类型、按递送方式、按给药途径、按应用、按最终用户、按地区)- 行业预测,2025 年至 2032 年Gene Therapy Market Size, Share, and Growth Analysis, By Gene Type, By Therapy type, By Vector type, By Delivery Method, By Route Of Administration, By Application, By End-user, By Region - Industry Forecast 2025-2032 |
2023 年全球基因治疗市场规模价值为 65 亿美元,预计将从 2024 年的 77.4 亿美元成长到 2032 年的 313.4 亿美元,预测期内(2025-2032 年)的复合年增长率为 19.1%。
由于医疗成本不断上涨、医疗设施日益先进以及报销选择不断增加,全球基因治疗市场呈上升趋势。然而,基因治疗药物的高成本可能在未来几年内在一定程度上阻碍市场成长。基因治疗是一种透过以功能性基因取代缺陷基因来治疗多种疾病(包括血液疾病、癌症、慢性病和感染疾病)的创新治疗方法。这些是体细胞细胞株治疗,针对特定的体细胞来治疗爱滋病或帕金森氏症等疾病,以及生殖系基因治疗,影响生殖细胞株中的遗传 DNA。生物载体有助于治疗基因的传递,包括慢病毒和腺病毒等病毒载体,以及脂质体和质体等非病毒载体。
Global Gene Therapy Market size was valued at USD 6.5 billion in 2023 and is poised to grow from USD 7.74 billion in 2024 to USD 31.34 billion by 2032, growing at a CAGR of 19.1% during the forecast period (2025-2032).
The global gene therapy market is on an uptrend, driven by escalating healthcare costs, state-of-the-art healthcare facilities, and reimbursement options. However, the high cost of gene therapies may somewhat hinder market growth in the coming years. Gene therapy is an innovative treatment modality for various diseases, including blood disorders, cancer, chronic illnesses, and infections, by replacing faulty genes with functional ones. It encompasses two primary types: somatic gene therapy, which targets specific body cells to treat conditions like AIDS and Parkinson's, and germline gene therapy, which affects hereditary DNA in reproductive cells. Delivery of therapeutic genes is facilitated by biological vectors, including viral vectors like lentivirus and adenovirus, as well as non-viral options such as liposomes and plasmids.
Top-down and bottom-up approaches were used to estimate and validate the size of the Global Gene Therapy market and to estimate the size of various other dependent submarkets. The research methodology used to estimate the market size includes the following details: The key players in the market were identified through secondary research, and their market shares in the respective regions were determined through primary and secondary research. This entire procedure includes the study of the annual and financial reports of the top market players and extensive interviews for key insights from industry leaders such as CEOs, VPs, directors, and marketing executives. All percentage shares split, and breakdowns were determined using secondary sources and verified through Primary sources. All possible parameters that affect the markets covered in this research study have been accounted for, viewed in extensive detail, verified through primary research, and analyzed to get the final quantitative and qualitative data.
Global Gene Therapy Market Segments Analysis
Global Gene Therapy Market is segmented by Gene Type, Therapy type, Vector type, Delivery Method, Route Of Administration, Application, End-user and region. Based on Gene Type, the market is segmented into Antigen, Cytokine, Tumor Suppressor, Suicide, Deficiency, Growth factors, Receptors and Others. Based on Therapy type, the market is segmented into Gene silencing therapy, Cell replacement therapy, Gene augmentation therapy and Other therapies. Based on Vector type, the market is segmented into Viral vector and Non-Viral Vector. Based on Delivery Method, the market is segmented into Ex-Vivo and In-Vivo. Based on Route Of Administration, the market is segmented into Intravenous Route, Subcutaneous Route and Others. Based on Application, the market is segmented into Oncological Disorders, Cardiovascular Diseases, Infectious Diseases, Hematology, Rare Diseases, Neurological Disorders and Other Diseases. Based on End-user, the market is segmented into Cancer Institutes, Hospitals, Research institutes and Others. Based on region, the market is segmented into North America, Europe, Asia Pacific, Latin America and Middle East & Africa.
Driver of the Global Gene Therapy Market
The global gene therapy market is experiencing significant growth, driven by swift innovations in gene editing technologies like CRISPR-Cas9. These cutting-edge techniques enhance the precision, effectiveness, and safety of genetic modifications, thereby accelerating the clinical development process and expanding treatment options for patients. Furthermore, the use of vector-based methods coupled with improved delivery systems is contributing to the industry's advancement. As a result, the combination of these factors is fostering an environment ripe for breakthroughs in gene therapy, ultimately leading to enhanced therapeutic outcomes and a broader range of solutions for various genetic disorders on a global scale.
Restraints in the Global Gene Therapy Market
The growth of the global gene therapy market is likely to face challenges stemming from various factors, including potential long-term risks, off-target effects, and a host of ethical and safety considerations. These issues could lead to hesitance among the public and regulatory bodies, resulting in a lack of acceptance for new therapies. Such skepticism may deter investment opportunities and impede overall market expansion, as concerns regarding genetic engineering persist. Therefore, overcoming these reservations is essential for fostering confidence in gene therapy developments and ensuring a sustainable trajectory for the industry in the coming years.
Market Trends of the Global Gene Therapy Market
The global gene therapy market is experiencing remarkable growth driven by rapid advancements in genetic research, the rise of innovative treatment methodologies, and an increasing understanding of gene-based therapies. A significant trend is the focus on rare hereditary disorders, as scientists identify genetic defects that underlie these conditions and develop corresponding gene therapies. This shift not only opens new avenues for treatment but also brings hope to patients with previously incurable diseases, fueling demand for targeted and precise therapies. Furthermore, regulatory advancements and increased investment in biotechnology are expected to propel market expansion, solidifying gene therapy's role in modern medicine.