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市场调查报告书
商品编码
1792333
2025 年至 2033 年肿瘤生物相似药市场报告(按药物类型、癌症类型、配销通路和地区)Oncology Biosimilars Market Report by Drug Type, Cancer Type, Distribution Channel, and Region 2025-2033 |
2024 年全球肿瘤生物相似药市场规模达 58 亿美元。展望未来, IMARC Group预计到 2033 年市场规模将达到 352 亿美元,2025-2033 年期间的成长率 (CAGR) 为 21.15%。
癌症是一种生活方式疾病,由细胞异常生长引起,并可能导致肿瘤形成。目前,大多数有效的癌症治疗方法是基于生物药物(也称为生物製剂),包括标靶治疗和免疫疗法。这些药物利用细菌、酵母以及动植物细胞等活体生物体生产,需要复杂的生产过程和较长的研发时间。因此,这些药物的成本相对较高,增加了癌症治疗的费用。为了降低治疗费用,人们对开髮品牌肿瘤生物製剂的生物相似药的兴趣日益浓厚。这些生物相似药在有效性和安全性方面与参考生物製剂高度相似,并且由于成本较低,可以帮助显着降低癌症治疗费用。
多年来,老年人口的增加和环境的恶化导致全球癌症的发生率上升。这些因素,加上癌症治疗费用的上涨,加重了全球医疗保健系统的负担。因此,许多国家的管理当局正在推动使用生物相似药作为成本控制措施。例如,美国食品药物管理局 (USFDA) 已经为医生和患者开发了资讯资料,以教育他们有关生物相似药的知识。除此之外,负担得起的药物的可用性也与更早和更广泛的治疗使用以及改善患者获得药物的机会有关。此外,肿瘤生物相似药还可以增加行业竞争,因此它们有可能进一步降低生物药品的价格。其他一些促进市场成长的因素包括品牌生物製剂专利即将到期以及生物相似药製造商加强研发力度。
The global oncology biosimilars market size reached USD 5.8 Billion in 2024. Looking forward, IMARC Group expects the market to reach USD 35.2 Billion by 2033, exhibiting a growth rate (CAGR) of 21.15% during 2025-2033.
Cancer is a lifestyle disease that occurs due to the abnormal growth of cells and may result in the formation of a tumor. At present, most of the effective cancer treatments are based on biological drugs, also known as biologics, and include targeted therapies as well as immunotherapies. These drugs are produced using living organisms, including bacteria, yeast, and animal or plant cells, and require complex manufacturing processes and long development time. As a result, the cost of these drugs is relatively higher, which adds to the expense of cancer treatment. To lower the price of treatment, the interest in the development of biosimilars of branded oncology biologics has been increasing. These biosimilars are highly similar to the reference biologics in terms of effectiveness and safety and can help in significantly reducing the expenditure on cancer treatment due to their lower cost.
Over the years, the rising number of geriatric population and environmental degradation have increased the prevalence of cancer across the globe. These factors, along with the inflating cost of cancer care, have increased the burden on healthcare systems worldwide. Consequently, governing authorities in numerous countries are promoting the uptake of biosimilars as a cost-containment measure. For instance, the United States Food and Drug Administration (USFDA) has developed information materials for physicians and patients to educate them about biosimilars. Apart from this, the availability of affordable medication has also been associated with earlier and wider therapy use as well as improved patient access. Besides this, oncology biosimilars can also increase industry competition, owing to which they have the potential to drive down the prices of biological drugs further. Some of the other growth-inducing factors for the market include approaching patent expiries of branded biologics and increasing research and development (R&D) activities by biosimilar manufacturers.
The report has also analyzed the competitive landscape of the market with some of the key players being Biocon Limited, Celltrion Inc., Dr. Reddy's Laboratories Ltd., Intas Pharmaceuticals Ltd., STADA Arzneimittel AG, Pfizer Inc., Apotex Inc., Teva Pharmaceutical Industries Ltd., Sandoz International GmbH, BIOCAD Biotechnology Company, Mylan N.V., F. Hoffmann-La Roche AG, etc.