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市場調查報告書
商品編碼
1371891
到 2030 年的全球生技藥品市場預測:按產品、類型、用途和地區進行的全球分析Biologic Therapeutics Market Forecasts to 2030 - Global Analysis By Product (Gene Therapy, Cell Therapy, Vaccines, Antibody Therapeutics and Other Products), Type, Application and By Geography |
根據 Stratistics MRC 的數據,2023 年全球生技藥品市場規模為 4,575.6 億美元,預計將以 11.3% 的年複合成長率成長,到 2030 年達到 9,680.8 億美元。
專注於生物來源治療藥物的開發、生產和行銷的製藥工業部門被稱為生技藥品市場。這些複雜的化學物質是利用活生物體或活生物體的一部分製成的,例如蛋白質、抗體、核酸和細胞。又稱生技藥品或生物製藥。
據世界衛生組織 (WHO) 稱,疫苗是減輕全球疾病負擔最有力、最具成本效益的方法之一,預計每年可挽救 200-300 萬人的生命。
癌症、自體免疫疾病和代謝性疾病等慢性疾病的增加增加了對有效替代療法的需求。生技藥品提供量身定做的、標靶治療,可以解決許多疾病的根本原因,從而推動市場擴張。此外,生技藥品開發還獲得了製藥和生物技術行業的大量資金。重組蛋白、細胞和基因療法以及單株抗體等生技藥品的發展正在重振市場並刺激創新。
開發和製造生技藥品需要複雜的程序和大量的成本,包括研發、臨床試驗和製造設施。這些高成本可能會限制生技藥品的可得性和可負擔性,特別是在資源有限的醫療保健系統中。然而,由於其複雜性,生技藥品需要專門的生產設施和程序。確保一致的品質、可擴展性和維持強大的供應鏈可能很困難,並且會影響生技藥品治療的可及性和可負擔性。
生物技術、基因工程和重組 DNA 技術的進步正在增加創造創新生物療法的潛力。這些技術的發展使得能夠生產更複雜、更有特異性的生物藥品,擴大了可用治療方法的數量。此外,歐洲藥品管理局(EMA)和美國食品藥物管理局(FDA)等法規機構也為生技藥品的核准制定了精確的規則並加快了核准程序。這些管理體制為生技藥品的開發、評估和行銷提供了有利的環境。
儘管有有利的法律規範,但生技藥品的核准過程複雜且要求嚴格。公司必須進行廣泛的臨床前和臨床試驗來證明安全性、有效性和品質,這需要很長時間並花費大量資金。然而,可能會誘導患者對生物治療的免疫反應,引發對其安全性和免疫抗原性的擔憂。這些免疫反應會不同程度地影響治療的有效性和安全性。有效監測和管理此類問題對於有效使用生物治療至關重要。
COVID-19 的爆發使得高效的疫苗生產和分發變得至關重要。因此,利用 mRNA 和病毒載體疫苗等生物平台進行的疫苗研發顯著增加。 COVID-19疫苗的有效研發和應用凸顯了生物治療的前景,並強調了生物技術領域在感染疾病控制中的重要性。
預測期內,血液製品領域佔據最大佔有率。血液衍生產品,包括免疫球蛋白、凝血因子和血漿衍生蛋白,用於治療各種血液疾病和免疫力缺乏,也被認為是生物療法的一部分。這些物品的使用對於治療許多血液疾病、免疫力缺乏和其他疾病至關重要。
據估計,細胞治療領域在預測期內將出現良好的成長。活細胞用於細胞療法來治療和治癒疾病。細胞療法是一個快速發展的領域,旨在替換、修復和修復受損或患病的細胞和組織。此外,細胞療法在許多治療領域顯示出潛力,包括腫瘤學、心血管疾病、神經退化性疾病疾病和自體免疫疾病。
由於生物治療行業經歷了重大發展和創新,並正在成為一個充滿活力和快速變化的中心,預計亞太地區將在預測期內佔據最大佔有率。該地區與許多擁有自己的醫療保健系統的國家相連,使其成為一個複雜但有吸引力的市場。此外,癌症、糖尿病和自體免疫疾病等慢性疾病的流行增加了對生物治療的需求。
據估計,亞太地區的年複合成長率最高。不斷成長的中等收入人口和不斷上漲的醫療保健費用正在擴大生物療法的可用性。再加上政府鼓勵醫療基礎建設的政策,進一步推動了市場的成長。此外,亞太地區的研發活動蓬勃發展,國內外製藥公司大力投資生技藥品的開發。蓬勃發展的生物技術生態系統吸引人才並促進創新。該地區各國政府也正在努力簡化核准程序,讓生物製藥公司更容易進入市場。
According to Stratistics MRC, the Global Biologic Therapeutics Market is accounted for $457.56 billion in 2023 and is expected to reach $968.08 billion by 2030 growing at a CAGR of 11.3% during the forecast period. The pharmaceutical industry sector that concentrates on the development, production, and marketing of therapeutic medicines generated from biological sources is referred to as the biologic therapeutics market. These complex chemicals are created using living organisms or their parts, such as proteins, antibodies, nucleic acids, or cells. They are also referred to as biologics or biological pharmaceuticals.
According to World Health Organization, vaccines are one of the most powerful and cost-effective ways to reduce the global burden of disease and are estimated to save 2-3 million lives every year.
The need for efficient treatment alternatives is being driven by the increased prevalence of chronic diseases like cancer, autoimmune conditions, and metabolic diseases. Biologic medicines provide customized, targeted treatments that can address the underlying causes of many disorders, spurring market expansion. Additionally, the development of biologic medicines has received significant funding from the pharmaceutical and biotechnology industries. Biologic medication development, including recombinant proteins, cell and gene therapies, and monoclonal antibodies, is boosting the market and spurring innovation.
Complex procedures and high expenditures, such as those associated with research and development, clinical trials, and manufacturing facilities, are involved in the creation and production of biologic therapies. Particularly in healthcare systems with limited resources, these high costs may restrict the availability and affordability of biologic medications. However, due to their complicated nature, biologic pharmaceuticals need specialized production facilities and procedures. It can be difficult to ensure consistent quality, scaleability, and maintain a strong supply chain, which may have an impact on the accessibility and affordability of biologic treatments.
The potential for creating innovative biological therapies has increased as a result of ongoing developments in biotechnology, genetic engineering, and recombinant DNA technology. These technological developments make it possible to produce biological medications that are more sophisticated and specifically targeted, expanding the number of available treatments. Additionally, regulatory organizations have established precise rules and accelerated paths for the approval of biologic therapies, including the European Medicines Agency (EMA) and the U.S. Food and Drug Administration (FDA). These regulatory regimes offer a favorable environment for the creation, assessment, and marketing of biologic medicines.
Despite the existence of favorable regulatory frameworks, the complex and stringent approval procedures for biologic therapies. Extensive preclinical and clinical trials that must be conducted by companies to prove safety, efficacy, and quality can take a long time and cost a lot of funds. However, patients' immune responses to biological therapies may be induced, raising concerns regarding their safety and immunogenicity. The effectiveness and safety of the treatment may be impacted by these immunological reactions, which can range in severity. For biological treatments to be used effectively, it is crucial to provide effective monitoring and management of these problems.
The COVID-19 epidemic made the creation and distribution of efficient vaccinations essential. As a result, vaccine research and development significantly increased, utilizing biological platforms like mRNA and viral vector-based vaccines. The effective creation and application of COVID-19 vaccines highlighted the promise of biological treatments and emphasized the significance of the biotechnology sector in combating infectious diseases.
Blood products segment commanded the largest share over the forecast period. Blood-derived products, including immunoglobulins, clotting factors, and plasma-derived proteins, which are used to treat a variety of blood illnesses and immunological deficiencies, are also considered to be part of biologic therapies. The use of these items is essential in the management of a number of blood diseases, immunological deficiencies, and other ailments.
Cell therapy segment is estimated to witness lucrative growth over the projection period. Living cells are used in cell therapy to treat or cure diseases. It is a fast-developing area that seeks to replace, restore, or fix damaged or sick cells or tissues. Additionally, cell therapy has demonstrated potential in a number of therapeutic fields, including oncology, cardiovascular illness, neurodegenerative disorders, and autoimmune diseases.
Asia Pacific is expected to hold largest share over the forecast period as the biological therapies industry experiences substantial development and innovation, the Asia-Pacific region is emerging as a vibrant and quickly changing hub. This region is connected to numerous nations with distinctive healthcare systems, making it a complex yet attractive market. Additionally, the region's growing need for biological treatments is being driven by the prevalence of chronic diseases like cancer, diabetes, and autoimmune disorders.
Asia Pacific is estimated to hold highest CAGR. The availability of biological therapies has expanded as a result of an expanding middle-class population and rising healthcare costs. This has further propelled the market's growth, along with government policies to encourage the construction of healthcare infrastructure. Additionally, the Asia-Pacific region is experiencing a boom in research and development activity, with both domestic and foreign pharmaceutical firms making significant investments in the development of biologic drugs. A thriving biotechnology ecosystem has resulted in an outcome that draws in talent and encourages innovation. Governments in the area are also making efforts to simplify approval procedures, improving the simplicity of market access for biopharmaceutical firms.
Some of the key players in Biologic Therapeutics Market include: AbbVie Inc, Amgen Inc., AstraZeneca Plc, Aurobindo Pharma Ltd., Baxter International Inc, Biocon Ltd., Celltrion Healthcare Co. Ltd., GlaxoSmithKline Plc, Merck and Co. Inc, Novartis AG, Pfizer Inc , Precision Biologics Inc and Samsung Electronics Co. Ltd.
In May 2022, Precision BioLogic Inc., a leading developer of hemostasis diagnostic products, announceD the launch of its new CRYOcheck Chromogenic Factor IX assay in Canada, the European Union, Australia, and New Zealand following market authorization by Health Canada and respective in-country regulatory authorities. The announcement was made at the World Federation of Hemophilia Congress taking place in Montreal