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市場調查報告書
商品編碼
1371921
2030 年生物製藥市場預測:按產品類型、應用和地區分類的全球分析Biopharmaceuticals Market Forecasts to 2030 - Global Analysis By Product Type, Application and By Geography |
根據 Stratistics MRC 的數據,2023 年全球生物製藥市場規模為 10.4745 億美元,預計預測期內年複合成長率為 14.4%,到 2030 年將達到 26.8605 億美元。
生物製藥,也稱為生物製藥或生技藥品,是由細胞、有機體和蛋白質等活生物體製成的藥物。這些藥物是利用生物技術製造的,對現代醫療保健至關重要。此外,生物製藥也促進了個人化醫療策略的發展。這些藥物有可能針對患者疾病的特定方面,從而可以根據患者的特定遺傳特徵或疾病亞型製定個體化治療計劃。
根據國際癌症研究機構的數據,2020年約有1,930萬人新診斷出癌症,約1,000萬人死亡。從 2020 年到 2040 年,癌症患者數量預計將增加 47%。
結構生物學、基因編輯和高通量篩選方法等不斷發展的科學進步正在改變生物製藥的研究和開發。冷凍電子顯微鏡和尖端成像技術提供的雙分子結構的理解有助於藥物設計。使用人工智慧和機器學習分析大量資料,以對藥物研發做出預測。此外,CRISPR-Cas9 等合成生物學的進步正在使基因治療和基因編輯細胞療法成為可能,從而擴大了生物製藥的範圍。
生物製藥的發展需要在研究、臨床前測試和具有挑戰性的臨床試驗方面進行財務投資。除了這些基本成本之外,生物製藥公司還必須花費在專門的基礎設施上,例如最先進的實驗室設備和專門的生產設施,所有這些都會增加開發成本。此外,生物製藥開發的長期性和資源集中,單一候選藥物的成本往往超過數十億美元,進一步加劇了財務挑戰。
基因組科學和分子診斷的進步使精準醫學成為可能,根據患者的遺傳特徵和特定疾病特徵量身定做治療方法。此策略提高了治療效果,最大限度地減少副作用並最佳化患者的治療效果。此外,腫瘤學是個人化醫療特別有前途的領域,因為生物標記主導的治療正在提高存活率和緩解率。
生物製藥市場的全球性創造了一個複雜的專利、商業機密和專利網路,帶來了新的智慧財產權挑戰。此外,生物相似藥的出現帶來了新的法律複雜性,例如專利糾紛和專利叢林策略,這些策略使用多個專利來涵蓋單一產品並提供擴展的市場獨佔權。
COVID-19大流行在許多方面對生物製藥行業產生了重大影響。對疫苗和治療方法的迫切需求加速了研發工作,同時也導致了臨床試驗的延誤、全球供應鏈的中斷以及資源重新集中到與疫情相關的活動上。此外,疫情凸顯了疫苗開發、抗病毒療法和生物製藥創新的重要性,導致這些領域的投資增加。它也暴露了供應鏈的弱點,迫使公司重新考慮分銷和製造計劃。
疫苗領域通常佔據最大的市場。疫苗可預防多種感染疾病,對公共衛生至關重要。對於當前的威脅(如 COVID-19)和新的威脅(如流感和肝炎),疫苗變得越來越受歡迎。全球對疫苗的需求急劇增加,特別是由於 COVID-19 大流行。然而,由於持續的研發活動,包括創建 mRNA 疫苗等新疫苗平台,疫苗市場對於生物製藥行業的擴張和改善公眾健康的配合措施仍然至關重要。
生物製藥市場年複合成長率最高的預計將出現在腫瘤領域。其主要原因包括全球癌症罹患率上升、標靶治療和免疫療法的進步以及精準醫療技術的持續研究。此外,由於針對各種癌症類型的新型生物藥品的開發以及聯合治療和生物標記主導治療的潛力,腫瘤學市場正在經歷顯著成長。
全球生物製藥市場通常佔據北美地區,尤其是美國的最大佔有率。造成這一優勢的因素包括強大的製藥業、大量的研發支出、發達的醫療保健系統、龐大的患者基礎以及支持生物製藥開發和商業化的法規環境。此外,北美擁有大量生物製藥公司、學術研究中心和生物技術中心,這也有助於提高其市場佔有率。
生物製藥市場年複合成長率最高的是亞太地區。中等收入人口的成長、醫療保健成本的上升、藥品製造能力的提高以及對最先進治療的需求不斷增加只是該行業蓬勃發展的部分原因。對生物製藥和疫苗的研發、臨床試驗以及製造的投資尤其使中國和印度等國家成為生物製藥產業的主要企業。此外,該地區的快速成長也得到了政府的支持政策以及與大型製藥企業的合作夥伴關係的支持。
According to Stratistics MRC, the Global Biopharmaceuticals Market is accounted for $1047.45 million in 2023 and is expected to reach $2686.05 million by 2030 growing at a CAGR of 14.4% during the forecast period. Biopharmaceuticals, also referred to as biologic drugs or biologics, are pharmaceuticals made from living things like cells, organisms, or proteins. These medications are produced using biotechnology techniques and are essential to contemporary healthcare. Moreover, biopharmaceuticals have made it possible to develop personalized medicine strategies. These medications have the potential to target particular molecular aspects of a patient's illness, enabling the development of personalized treatment plans based on the patient's particular genetic profile or disease subtype.
According to the International Agency for Research on Cancer, in the year 2020, around 19.3 million new cases of cancer were diagnosed and around 10 million cancer deaths were recorded. The cancer cases are estimated to grow by 47% from 2020 to 2040.
Biopharmaceutical R&D is being transformed by ongoing scientific advances in structural biology, gene editing, and high-throughput screening methods. Drug design is aided by the understanding of bimolecular structures provided by cryo-electron microscopy and cutting-edge imaging technologies. Massive datasets are analyzed using artificial intelligence and machine learning to make predictions about drug discovery. Additionally, gene therapies and gene-edited cell therapies have been made possible by advances in synthetic biology, such as CRISPR-Cas9, expanding the range of biopharmaceuticals.
Financial investments in research, preclinical studies, and challenging clinical trials are significant in the development of biopharmaceuticals. In addition to these basic costs, biopharmaceutical businesses also have to spend money on specialized infrastructure, such as state-of-the-art lab tools and specialized manufacturing facilities, all of which drive up development costs. Furthermore, the lengthy and resource-intensive nature of biopharmaceutical development, where costs frequently exceed billions of dollars for a single drug candidate, further exacerbates financial difficulties.
Precision medicine, which tailors treatments to a person's genetic profile and particular disease characteristics, is being made possible by developments in genomics and molecular diagnostics. With this strategy, treatment effectiveness is improved, side effects are minimized, and patient outcomes are optimized. Moreover, oncology is a field where personalized medicine holds particular promise because biomarker-driven therapies are increasing survival and response rates.
A complex web of patents, trade secrets, and patent thickets must be negotiated by businesses due to the global nature of the biopharmaceutical market, which presents additional IP challenges. Additionally, the emergence of biosimilars brings with it new legal complexities, such as patent disputes and patent thicket strategies, where multiple patents are used to cover a single product and provide for extended market exclusivity.
The COVID-19 pandemic affected the biopharmaceutical industry significantly and in a variety of ways. In addition to delaying clinical trials, disrupting global supply chains, and refocusing resources on pandemic-related activities, the urgent need for vaccines and treatments accelerated research and development efforts. Moreover, the pandemic highlighted the significance of vaccine development, antiviral therapies, and biopharmaceutical innovation, leading to increased investments in these fields. It also exposed weaknesses in supply chains, forcing businesses to reconsider their distribution and manufacturing plans.
The vaccines segment typically holds the largest share of the market. A wide range of infectious diseases are prevented by vaccines, which are essential to public health. They have become more well-known for both current threats like COVID-19 and emerging ones like influenza and hepatitis. The global demand for vaccines has increased dramatically as a result of the COVID-19 pandemic in particular. However, the vaccine market is still essential to the expansion of the biopharmaceutical industry and efforts to improve public health due to ongoing research and development activities, including the creation of new vaccine platforms like mRNA vaccines.
The biopharmaceutical market's highest CAGR is anticipated in the oncology segment. This is mainly because of a number of things, such as the rising incidence of cancer globally, developments in targeted and immunotherapeutic therapies, and ongoing work on precision medicine methods. Moreover, the oncology market has experienced significant growth as a result of the creation of novel biopharmaceuticals for various cancer types as well as the potential for combination therapies and biomarker-driven treatments.
The global biopharmaceutical market typically holds the largest share in the North American region, in particular the United States. A strong pharmaceutical industry, significant R&D expenditures, a developed healthcare system, a sizable patient base, and a supportive regulatory environment for the development and commercialization of biopharmaceuticals were all cited as contributing factors to this dominance. Additionally, its sizeable market share was influenced by the fact that North America is home to a large number of biopharmaceutical businesses, academic research centers, and biotechnology hubs.
The biopharmaceutical market was growing at the highest CAGR in the Asia-Pacific region. A rising middle-class population, rising healthcare costs, growing pharmaceutical manufacturing capacity, and rising demand for cutting-edge treatments are just a few of the reasons for this industry's rapid growth. Due to their investments in R&D, clinical trials, and the production of biologic drugs and vaccines, nations like China and India in particular were emerging as major players in the biopharmaceutical industry. Moreover, the region's rapid growth was also aided by supportive government policies and partnerships with major pharmaceutical corporations.
Some of the key players in Biopharmaceuticals market include: Merck & Co., Inc. , Novartis AG, Abbott Laboratories., Novo Nordisk A/S, Eli Lilly and Company, AstraZeneca PLC, Bristol-Myers Squibb Company, Biogen Inc. , AbbVie Inc., Pfizer Inc., Bausch Health Companies Inc., F. Hoffmann-La Roche AG, Sanofi, Bayer AG, Allergan plc , Johnson & Johnson and Amgen Inc.
In October 2023, Sanofi has reached an agreement to develop and commercialize an experimental vaccine candidate for extra intestinal pathogenic E. coli developed by Janssen Pharmaceuticals. Under the terms of the deal, Sanofi will pay the Johnson & Johnson unit $175m upfront, followed by development and commercial milestones. Both parties will co-fund current and future research and development costs. Extra intestinal pathogenic E. coli is a common gram-negative bacteria pathogen in humans and a leading cause of sepsis, particularly in older adults.
In October 2023, Bayer AG has entered into an antibody discovery, option, and license agreement with Twist Bioscience Corporation, a company offering high-quality synthetic DNA using its silicon platform. The company's Library of Libraries, a collection of synthetic antibody libraries that harnesses innovative structural and develops ability features to cover a wide range of antibody drug targets, is tailored to address specific challenges in antibody discovery. It has the potential to increase the probability of success of antibody discovery programs across indications and focus areas.
In September 2023, Abbott signs definitive agreement to acquire Bigfoot Biomedical. Abbott has entered a definitive agreement for the acquisition of Bigfoot Biomedical, which develops smart insulin management systems for individuals with diabetes. Together, the companies have worked on connected diabetes solutions since 2017. Developed by Bigfoot Biomedical, Bigfoot Unity is a smart insulin management system. It features connected insulin pen caps that use integrated continuous glucose monitoring (iCGM) data and healthcare provider instructions.
Note: Tables for North America, Europe, APAC, South America, and Middle East & Africa Regions are also represented in the same manner as above.