市场调查报告书
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2024-2032 年按药物类型、癌症类型、配销通路和地区分類的肿瘤生物相似药市场报告Oncology Biosimilars Market Report by Drug Type, Cancer Type, Distribution Channel, and Region 2024-2032 |
IMARC Group年,全球肿瘤生物相似药市场规模达47亿美元。
癌症是一种生活方式疾病,由于细胞异常生长而发生,并可能导致肿瘤的形成。目前,大多数有效的癌症治疗都是基于生物药物,也称为生物製剂,包括标靶治疗和免疫疗法。这些药物是利用活体生物体(包括细菌、酵母和动物或植物细胞)生产的,需要复杂的製造过程和较长的开发时间。因此,这些药物的成本相对较高,从而增加了癌症治疗的费用。为了降低治疗价格,人们对开髮品牌肿瘤生物製剂的生物相似药的兴趣不断增加。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,可以帮助显着减少癌症治疗的支出。
多年来,老年人口数量的增加和环境恶化增加了全球癌症的盛行率。这些因素,加上癌症治疗成本的不断上涨,增加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促进生物相似药的采用,作为成本控制措施。例如,美国食品和药物管理局 (USFDA) 为医生和患者开发了资讯材料,以对他们进行生物相似药的教育。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的可及性有关。除此之外,肿瘤生物相似药还可以增加产业竞争,因此有可能进一步压低生物药的价格。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增加研发 (R&D) 活动。
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.