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市場調查報告書
商品編碼
1792333
2025 年至 2033 年腫瘤生物相似藥市場報告(按藥物類型、癌症類型、配銷通路和地區)Oncology Biosimilars Market Report by Drug Type, Cancer Type, Distribution Channel, and Region 2025-2033 |
2024 年全球腫瘤生物相似藥市場規模達 58 億美元。展望未來, IMARC Group預計到 2033 年市場規模將達到 352 億美元,2025-2033 年期間的成長率 (CAGR) 為 21.15%。
癌症是一種生活方式疾病,由細胞異常生長引起,並可能導致腫瘤形成。目前,大多數有效的癌症治療方法是基於生物藥物(也稱為生物製劑),包括標靶治療和免疫療法。這些藥物利用細菌、酵母以及動植物細胞等活體生物體生產,需要複雜的生產過程和較長的研發時間。因此,這些藥物的成本相對較高,增加了癌症治療的費用。為了降低治療費用,人們對開發品牌腫瘤生物製劑的生物相似藥的興趣日益濃厚。這些生物相似藥在有效性和安全性方面與參考生物製劑高度相似,並且由於成本較低,可以幫助顯著降低癌症治療費用。
多年來,老年人口的增加和環境的惡化導致全球癌症的發生率上升。這些因素,加上癌症治療費用的上漲,加重了全球醫療保健系統的負擔。因此,許多國家的管理當局正在推動使用生物相似藥作為成本控制措施。例如,美國食品藥物管理局 (USFDA) 已經為醫生和患者開發了資訊資料,以教育他們有關生物相似藥的知識。除此之外,負擔得起的藥物的可用性也與更早和更廣泛的治療使用以及改善患者獲得藥物的機會有關。此外,腫瘤生物相似藥還可以增加行業競爭,因此它們有可能進一步降低生物藥品的價格。其他一些促進市場成長的因素包括品牌生物製劑專利即將到期以及生物相似藥製造商加強研發力度。
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.