市場調查報告書
商品編碼
1467741
2024-2032 年按藥物類型、癌症類型、配銷通路和地區分類的腫瘤生物相似藥市場報告Oncology Biosimilars Market Report by Drug Type, Cancer Type, Distribution Channel, and Region 2024-2032 |
IMARC Group年,全球腫瘤生物相似藥市場規模達47億美元。
癌症是一種生活方式疾病,由於細胞異常生長而發生,並可能導致腫瘤的形成。目前,大多數有效的癌症治療都是基於生物藥物,也稱為生物製劑,包括標靶治療和免疫療法。這些藥物是利用活體生物體(包括細菌、酵母和動物或植物細胞)生產的,需要複雜的製造過程和較長的開發時間。因此,這些藥物的成本相對較高,從而增加了癌症治療的費用。為了降低治療價格,人們對開發品牌腫瘤生物製劑的生物相似藥的興趣不斷增加。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,可以幫助顯著減少癌症治療的支出。
多年來,老年人口數量的增加和環境惡化增加了全球癌症的盛行率。這些因素,加上癌症治療成本的不斷上漲,增加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促進生物相似藥的採用,作為成本控制措施。例如,美國食品和藥物管理局 (USFDA) 為醫生和患者開發了資訊材料,以對他們進行生物相似藥的教育。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的可及性有關。除此之外,腫瘤生物相似藥還可以增加產業競爭,因此有可能進一步壓低生物藥的價格。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增加研發 (R&D) 活動。
The global oncology biosimilars market size reached US$ 4.7 Billion in 2023. Looking forward, IMARC Group expects the market to reach US$ 30.3 Billion by 2032, exhibiting a growth rate (CAGR) of 22.3% during 2024-2032.
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.
IMARC Group provides an analysis of the key trends in each sub-segment of the global oncology biosimilars market report, along with forecasts at the global and regional level from 2024-2032. Our report has categorized the market based on drug type, cancer type and distribution channel.
Monoclonal Antibody
Immunomodulators
G-CSF
Hematopoietic Agents
Others
Lung Cancer
Colorectal Cancer
Cervical Cancer
Breast Cancer
Kidney Cancer
Stomach Cancer
Brain Cancer
Others
Hospital Pharmacies
Online Pharmacies
Retail Pharmacies
Others
Europe
Asia Pacific
North America
Middle East and Africa
Latin America
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.