市場調查報告書
商品編碼
1417589
全球生物製品市場評估:按產品,應用,藥物類別,採購方式,分銷管道,地區,機會和預測(2017-2031)Biologics Market Assessment, By Product By Application By Drug Classification, By Mode of Purchase By Distribution Channel By Region, Opportunities and Forecast, 2017-2031F |
預計2023年全球生物製品市場規模將達4,013.4億美元,2031年將達6,957.9億美元,2024-2031年預測期間內複合年增長率為7.12%。慢性病的盛行率和診斷率不斷上升,對先進的診斷和治療藥物產生了巨大的需求,從而推動了全球生物製品市場的發展。這些專門的藥物經過基因改造,以針對引起發炎的免疫系統的特定成分。隨著 COVID-19 疾病的出現,世界各國政府正在採取措施加強醫療產業並確保生物製劑的供應。
同時,科學家和研究人員正在探索不同的物種和表現系統,以提高生物製劑的效率。此外,許多製藥公司正在進行旨在提高關節炎口服藥物有效性的研究和開發。由於小分子藥物研發的生產力下降,預計未來幾年生物製劑市場將出現重大飛躍。這些製藥公司正在積極開發各種生物製劑,以維持其市場主導地位。隨著治療克隆氏症和類風濕性關節炎等疾病的口服藥物變得更加有效,預計將有更多的中度疾病患者轉向新品牌的治療。此外,這些新化合物為對傳統治療有抵抗力的患者提供了替代治療,並且通常表現出卓越的安全性和有效性。
全球生物製品市場受到慢性病高盛行率的顯著影響。癌症、糖尿病、自體免疫疾病和心血管疾病等慢性疾病在世界各地變得越來越普遍。生物製劑,即從生物體中提取的藥物,已成為許多此類疾病的重要治療選擇。這些複雜的分子提供標靶治療,並且通常比傳統藥物更有效且副作用更少。
例如,根據世界衛生組織(WHO)2023年9月發布的報告,每年約有4100萬人死於非傳染性疾病(NCD),佔全球死亡總人數的74%。到 %。每年,大約有 1700 萬人在 70 歲之前死於非傳染性疾病,其中 86% 的過早死亡發生在全球。全球每年有超過 4,100 萬人死於慢性病。其中,心血管疾病每年導致1790萬人死亡,其次是癌症、糖尿病和呼吸系統疾病。這四類疾病合計佔慢性病死亡人數的 80%。慢性病的流行正在推動診斷和治療的進步。
市場擴張是由對研發活動的日益重視所推動的,預計將為生物製品市場的成長提供良好的前景。此外,科學家和研究人員正在探索不同的物種和表現系統,以提高生物製劑的生產力。一些製藥公司從事研究和開發活動,旨在提高口服藥物治療類風濕性關節炎和克隆氏症等疾病的有效性。此外,加速藥物審批和推出也支持了市場成長軌跡。
例如,2023年1月,lecanemab透過美國FDA加速審批途徑獲準用於治療阿茲海默症。2022年6月,Alnylam 的 Amvtra 獲得 FDA 批准,這是一種 RNAi 療法,用於治療與遺傳性轉甲狀腺素蛋白介導的澱粉樣變性相關的多發性神經病變。
全球生物製品市場主要參與者的投資持續激增,顯示該行業的成長和潛力。各大製藥公司、生技公司和研究機構都在生物製劑的研究、開發和製造方面投入大量資金。這些注資旨在加強創新、擴大產品組合併改善製造技術,最終滿足對先進個人化醫療解決方案不斷增長的需求。
競爭格局正在迅速演變,該公司計劃推出新的生物製劑,重點關注癌症、自體免疫疾病和傳染病等多種治療領域。不斷增長的投資趨勢表明業界對市場光明的未來充滿信心,推動突破性進展並改善治療方案以應對世界醫療挑戰。
本報告研究和分析了全球生物製品市場,提供市場規模和預測、市場動態、主要參與者趨勢和前景等。
Global biologics market size was valued at USD 401.34 billion in 2023, and is expected to reach USD 695.79 billion in 2031, with a CAGR of 7.12% for the forecast period between 2024 and 2031F. The increasing incidence and diagnosis of chronic diseases have created a significant demand for advanced diagnostics and treatment medications, consequently propelling the global biologics market. These specialized drugs have been genetically altered to target specific components of the immune system that trigger inflammation. With the emergence of coronavirus diseases, governments worldwide are taking measures to fortify the healthcare industry and ensure the availability of biologics.
Simultaneously, scientists and researchers are exploring different species and expression systems to enhance the efficiency of biological products. Moreover, numerous pharmaceutical companies are engaged in research and development efforts aimed at enhancing the effectiveness of oral medications for arthritis. Given the decline in productivity in small molecule medication research and development, a substantial surge in the biologics market is anticipated in the coming years. These pharmaceutical firms are actively pursuing the development of various biologic medications to sustain their market dominance. As oral medications for conditions like Crohn's disease and rheumatoid arthritis become more effective, it is predicted that a larger number of moderately affected patients will transition towards newly branded therapies. Additionally, these new compounds provide therapeutic alternatives for patients who have previously shown resistance to traditional treatments, often displaying superior safety and efficacy.
The global biologics market is witnessing a significant impact due to the high prevalence of chronic diseases. Chronic conditions like cancer, diabetes, autoimmune disorders, and cardiovascular diseases are increasingly becoming prevalent globally. Biologics, which are medicinal products derived from living organisms, have emerged as a critical treatment option for many of these conditions. These complex molecules offer targeted therapies, often with fewer side effects and greater efficacy than traditional pharmaceuticals.
For instance, as per the World Health Organization's report in September 2023, approximately 41 million individuals succumb annually to non-communicable diseases (NCD), representing 74% of the total global deaths. Each year, roughly 17 million people perish from NCDs before reaching the age of 70, with 86% of these untimely fatalities occurring on a global scale. Over 41 million individuals globally succumb to chronic diseases annually. Among these, cardiovascular disease leads, causing 17.9 million deaths per year, followed by cancer, diabetes, and respiratory disorders. Together, these four categories account for 80% of all fatalities attributed to chronic diseases. The prevalence of chronic diseases has spurred the advancement of diagnostics and treatments. Biologics, genetically engineered medications, and target specific components of the immune system are responsible for inflammation.
The expansion of the market is being driven by the increasing emphasis on research and development activities, which is expected to create advantageous prospects for biologics market growth. Moreover, scientists and researchers are exploring various species and expression systems to enhance the productivity of biological products. Several pharmaceutical companies are engaged in research and development activities aimed at improving the effectiveness of oral medications for conditions like rheumatoid arthritis and Crohn's disease. Furthermore, the escalating rate of drug approvals and introductions will continue to accelerate the growth trajectory of the market.
For instance, as an example, in January 2023, Lecanemab received approval from the U.S. FDA via its accelerated approval pathway, specifically intended for addressing Alzheimer's Disease. In June 2022, Alnylam Pharmaceuticals, Inc. obtained FDA approval for its RNAi therapeutic, AMVUTTRA, designed for treating the Polyneuropathy associated with hereditary transthyretin-mediated amyloidosis.
The global biologics market continues to witness a surge in investments by key players, indicative of the sector's growth and potential. Major pharmaceutical companies, biotech firms, and research institutions are channeling substantial investments into research, development, and manufacturing of biologics. The financial commitment aims to bolster innovation, expand product portfolios, and enhance manufacturing technologies, ultimately meeting the rising demand for advanced and personalized healthcare solutions.
The competitive landscape is evolving rapidly as companies are planning to introduce novel biologics, focusing on diverse therapeutic areas like oncology, autoimmune diseases, and infectious diseases. The growing investment trend signifies the industry's confidence in the market's promising future, fostering groundbreaking advancements and improved treatment options for global healthcare challenges. For Instance, in March 2023, Novartis announced the intention of its division, Sandoz to allocate roughly USD 400 million towards establishing a biologics manufacturing plant situated in Slovenia. During March 2023, Eli Lilly disclosed its proposal to invest USD 500 million into expanding its current 500,000 sq. ft. biologics manufacturing site in Limerick.
The global biologics market has witnessed remarkable technological advancements, revolutionizing the landscape of medicine and healthcare. Innovations in biotechnology, particularly in areas like genetic engineering, monoclonal antibodies, and recombinant DNA technology, have significantly enhanced the development and production of biologics industry.
Advanced techniques in cell culture systems, gene editing (like CRISPR), and bioprocessing have streamlined the manufacturing of complex biological molecules. Furthermore, the emergence of personalized medicine has driven a shift towards more tailored and effective treatments, utilizing biologics designed to target specific patient populations. The progress has led to the development of novel biologics, including therapeutic proteins, vaccines, and monoclonal antibodies, fostering breakthroughs in treating various diseases like cancer, autoimmune disorders, and infectious diseases.
For Instance, in February 2022 CARVYKTI, developed by the Janssen Pharmaceutical Companies of Johnson & Johnson obtained approval from the US Food and Drug Administration (FDA) for sale. The biologic medication is designated for individuals with relapsed or refractory multiple myeloma (RRMM) who have undergone four prior lines of therapy, which may include proteasome inhibitor, immunomodulatory agent, and anti-CD38 monoclonal antibody treatments.
The COVID-19 pandemic had a significant impact on the global biologics market. Biologics are complex, large-molecule drugs used to treat a variety of diseases, including autoimmune disorders, cancer, and infectious diseases. The pandemic disrupted supply chains and manufacturing processes, leading to production delays and shortages of some biologics. Additionally, the increased focus on vaccine development and monoclonal antibody therapies to combat the virus diverted resources and attention from other biologic drug development efforts.
On the contrary, the pandemic has highlighted the importance of biotechnology and accelerated innovation in the field. The rapid development of mRNA vaccines, such as the Pfizer-BioNTech and Moderna vaccines, showcased the potential of biologics in responding to infectious diseases. Furthermore, the pandemic has driven investment in research and development of biologics, leading to advancements in bioprocessing and manufacturing technologies. During April 2022, GSK, a British multinational pharmaceutical and biotechnology company, together with SK bioscience, presented a biologics license application for SKYCovione, a COVID-19 vaccine candidate based on recombinant proteins, to the Korean Ministry of Food and Drug Safety (KMFDS).
Prominent industry stakeholders are allocating significant funds to research and development endeavors, aiming to diversify their product portfolios, thereby stimulating the expansion of the global biologics market. The market participants are implementing various strategic measures to enhance their global presence, including pivotal actions such as launching new products, engaging in mergers and acquisitions, forming contractual agreements, amplifying investments, and fostering collaborations with other organizations. In the competitive landscape of the biologics sector, companies must provide cost-effective offerings to broaden their scope and endure in an intensifying, competitive, and burgeoning market environment.
For Instance, the FDA granted approval to Leqembi (lecanemab-irmb) through the Accelerated Approval pathway in January 2023 for addressing Alzheimer's disease. The medication diminishes amyloid-B plaques and moderately retards mild cognitive decline in individuals with early-stage Alzheimer's disease.
All segments will be provided for all regions and countries covered:
Companies mentioned above DO NOT hold any order as per market share and can be changed as per information available during research work.