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市場調査レポート
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1371921
バイオ医薬品市場の2030年までの予測:製品タイプ別、用途別、地域別の世界分析Biopharmaceuticals Market Forecasts to 2030 - Global Analysis By Product Type, Application and By Geography |
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バイオ医薬品市場の2030年までの予測:製品タイプ別、用途別、地域別の世界分析 |
出版日: 2023年10月01日
発行: Stratistics Market Research Consulting
ページ情報: 英文 200+ Pages
納期: 2~3営業日
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Stratistics MRCによると、世界のバイオ医薬品市場は2023年に10億4,745万米ドルを占め、予測期間中にCAGR14.4%で成長し、2030年には26億8,605万米ドルに達すると予測されています。
バイオ医薬品は、生物学的製剤または生物製剤とも呼ばれ、細胞、生物、タンパク質などの生物から作られる医薬品です。これらの医薬品はバイオテクノロジー技術を用いて製造され、現代のヘルスケアに不可欠なものです。さらに、バイオ医薬品は個別化医療戦略の開発を可能にしました。これらの医薬品は、患者の病気の特定の分子的側面を標的とする可能性があり、患者の特定の遺伝的プロファイルや病気のサブタイプに基づいた個別化治療計画の開発を可能にします。
国際がん研究機関によると、2020年には約1,930万人が新たにがんと診断され、約1,000万人が死亡しました。がん患者は2020年から2040年にかけて47%増加すると推定されています。
バイオ医薬品の研究開発は、構造生物学、遺伝子編集、ハイスループットスクリーニング法など、現在進行中の科学の進歩によって変貌を遂げています。医薬品設計は、低温電子顕微鏡や最先端のイメージング技術によってもたらされる二分子構造の理解によって助けられています。膨大なデータセットは、人工知能や機械学習を用いて分析され、創薬に関する予測を行います。さらに、CRISPR-Cas9のような合成生物学の進歩により、遺伝子治療や遺伝子編集細胞治療が可能になり、バイオ医薬品の幅が広がっています。
バイオ医薬品の開発には、調査、前臨床試験、難易度の高い臨床試験への財政投資が重要です。このような基本的なコストに加え、バイオ医薬品企業は、最先端の実験器具や特殊な製造施設といった専門的なインフラにも資金を費やさなければならず、これらすべてが開発コストを押し上げる要因となっています。さらに、バイオ医薬品開発には長期的かつ資源集約的な性質があり、1つの新薬候補に数十億米ドルを超える費用がかかることも多いため、財務上の困難はさらに深刻化しています。
ゲノム科学と分子診断学の発展により、患者の遺伝子プロファイルや特定の疾患特性に合わせた治療を行う精密医療が可能になりつつあります。この戦略により、治療効果が向上し、副作用が最小限に抑えられ、患者の転帰が最適化されます。さらに腫瘍学は、バイオマーカー主導の治療が生存率と奏効率を高めていることから、個別化医療が特に有望視されている分野です。
バイオ医薬品市場は世界に展開されているため、特許、企業秘密、特許の藪が複雑に絡み合い、知的財産に関する新たな課題となっています。さらに、バイオシミラーの出現は、特許紛争や、単一の製品をカバーするために複数の特許を使用し、市場独占権の延長を提供する特許藪戦略など、新たな法的複雑性をもたらします。
COVID-19の大流行は、バイオ医薬品業界に様々な形で大きな影響を与えました。臨床試験の遅延、世界のサプライチェーンの混乱、パンデミック関連活動へのリソースの再集中に加えて、ワクチンと治療薬の緊急の必要性が研究開発の努力を加速させました。さらに、パンデミックはワクチン開発、抗ウイルス療法、バイオ医薬品の技術革新の重要性を浮き彫りにし、これらの分野への投資の増加につながっています。また、サプライチェーンの弱点も露呈し、企業は流通・製造計画の再考を余儀なくされました。
ワクチン分野は通常、市場で最大のシェアを占めています。幅広い感染症がワクチンによって予防されており、公衆衛生に不可欠です。ワクチンは、COVID-19のような現在の脅威と、インフルエンザや肝炎のような新興の脅威の両方で、よりよく知られるようになっています。特にCOVID-19のパンデミックの結果、ワクチンの世界的需要は劇的に増加しました。しかし、ワクチン市場は、mRNAワクチンのような新しいワクチンプラットフォームの創出を含む継続的な研究開発活動により、バイオ医薬品産業の拡大や公衆衛生の向上への取り組みにとって依然として不可欠です。
バイオ医薬品市場のCAGRが最も高いと予想されるのは、がん領域です。その主な理由は、世界のがん罹患率の上昇、標的療法や免疫療法の発展、精密医療手法の継続的な研究などです。さらに、さまざまながん種に対する新規バイオ医薬品の創出、併用療法やバイオマーカー主導型治療の可能性により、がん領域市場は大きな成長を遂げています。
世界のバイオ医薬品市場は通常、北米地域、特に米国で最大のシェアを占めています。強力な製薬産業、多額の研究開発費、発達したヘルスケアシステム、多くの患者基盤、バイオ医薬品の開発・商業化を支援する規制環境などが、この優位性の要因として挙げられています。さらに、北米には多数のバイオ医薬品企業、学術研究センター、バイオテクノロジー拠点があることも、市場シェアの大きさに影響しています。
バイオ医薬品市場のCAGRが最も高いのはアジア太平洋地域です。中間所得層の増加、ヘルスケアコストの上昇、医薬品製造能力の向上、最先端治療に対する需要の高まりは、この業界が急成長している理由のほんの一部に過ぎないです。研究開発、臨床試験、生物学的製剤やワクチンの製造への投資により、特に中国やインドのような国々がバイオ医薬品業界の主要企業として台頭してきています。さらに、この地域の急成長は、政府の支援政策や大手製薬企業との提携も後押ししています。
Note: Tables for North America, Europe, APAC, South America, and Middle East & Africa Regions are also represented in the same manner as above.
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.