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市場調査レポート
商品コード
1673492
二重特異性抗体の世界市場:市場の機会、用量、特許、薬価、売上、臨床試験動向(2030年)Global Bispecific Antibody Market Opportunity, Drug Dosage, Patent, Price, Sales & Clinical Trials Insight 2030 |
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二重特異性抗体の世界市場:市場の機会、用量、特許、薬価、売上、臨床試験動向(2030年) |
出版日: 2025年03月01日
発行: KuicK Research
ページ情報: 英文 1000 Pages
納期: 即日から翌営業日
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二重特異性抗体は、絶え間ない技術革新と患者受容の高まりにより、医薬品市場において最も有望かつ商業的に成功したターゲティングアプローチの一つとして台頭してきました。この驚異的な成長の主な要因は、二重特異性抗体の臨床試験数が飛躍的に増加していることであり、2015年には100件未満であったものが、2025年には650件を超えています。この進歩は、医薬品開発者、臨床研究機関、医師、患者といった複数の利害関係者に大きな利益をもたらしています。2025年3月現在、主要市場において17の二特異性抗体が承認されており、最初の二特異性抗体が承認された2015年には7,700万米ドルであったのに対し、累積売上高は350億米ドルを超えています。
二重特異性抗体の市場規模は、2024年に約120億米ドルに達し、2030年までに500億米ドルに急増すると予測されています。この成長軌道は、アンメット・メディカル・ニーズに対応できる革新的な生物製剤に対する需要の高まりを示しています。注目すべきは、HemlibraとVabysmoが世界の二重特異性抗体市場の主役として台頭し、合計で総売上高の75%以上を占めていることです。ロシュが開発した二重特異性抗体ヘムリブラは血友病Aの治療に用いられ、同じくロシュが開発したバビスモは黄斑変性と黄斑浮腫の治療薬です。両剤とも2024年には売上高が40億米ドルを突破し、それぞれの治療領域で主要な参入製品として頭角を現し、二重特異性抗体市場におけるRocheのリーダーシップを確固たるものにしています。
また、現在承認審査中の二重特異性抗体もいくつかあります。特に、治験中の二重特異性抗体であるリンボセルタマブは、多発性骨髄腫の治療薬として米国FDAと欧州医薬品庁(EMA)の審査を受けています。もう一つの有望な候補であるオドロネクスタマブは、様々な血液悪性腫瘍の治療薬として現在FDAの審査を受けています。これらの開発は、二重特異性抗体研究の進行と、がん治療に革命をもたらす可能性を強調するものです。
2025年3月現在、600以上の二特異性抗体が臨床試験中であり、この治療薬が複数の治療領域で計り知れない可能性を秘めていることを示しています。米国は、医薬品の技術革新とヘルスケア支出における主導権を反映し、研究開発(R&D)と売上の両面で二特異性抗体の最大市場であり続けています。
当レポートは、世界の二重特異性抗体市場について調査し、市場の概要とともに、薬剤動向、臨床試験動向、地域別動向、および市場に参入する企業の競合情勢などを提供しています。
Global Bispecific Antibody Market Opportunity, Drug Dosage, Patent, Price, Sales & Clinical Trials Insight 2030 Report findings & Highlights:
Bispecific antibodies have emerged as one of the most promising and commercially successful targeting approaches in the pharmaceutical market, driven by continuous innovations and growing patient acceptance. A major factor contributing to this phenomenal growth is the exponential increase in the number of clinical trials for bispecific antibodies, which has surpassed 650 in 2025 from less than 100 in 2015. This progress has significantly benefited multiple stakeholders like drug developers, clinical research organizations, physicians, and patients. As of March 2025, 17 bispecific antibodies have been approved across key markets, with cumulative sales exceeding US$ 35 Billion as compared to US$ 77 Million in 2015 when the first bispecific antibody was approved.
The bispecific antibody market reached approximately US$ 12 billion in 2024, with projections by Kuick Research suggesting that this market will surge to US$ 50 billion by 2030. This growth trajectory highlights the increasing demand for innovative biologics that can address unmet medical needs. Notably, Hemlibra and Vabysmo have emerged as major contributors to the global bispecific antibodies market, collectively accounting for over 75% of the total sales. Hemlibra, a bispecific antibody developed by Roche, is used to treat hemophilia A, while Vabysmo, also developed by Roche, is a treatment for macular degeneration and macular edema. Both drugs saw sales surpassing US$ 4 Billion in 2024, emerging as key players in their respective therapeutic areas and solidifying Roche's leadership in the market for bispecific antibodies.
There are also several bispecific antibodies currently under regulatory review. Notably, Linvoseltamab, an investigational bispecific antibody, is undergoing review by the US FDA and the European Medicines Agency (EMA) for the treatment of multiple myeloma. Another promising candidate, Odronextamab, is currently under FDA review for the treatment of various hematologic malignancies. These developments underscore the ongoing progress in bispecific antibody research and their potential to revolutionize cancer treatment.
As of March 2025, more than 600 bispecific antibodies are currently undergoing clinical trials, demonstrating the immense potential of these therapeutics across multiple therapeutic areas. The US remains the largest market for bispecific antibodies in terms of both research and development (R&D) and sales, reflecting the country's leadership in pharmaceutical innovation and healthcare spending.
Leading players in the bispecific antibody market include Roche, Gilead, Amgen, Pfizer, Johnson & Johnson (Janssen), and others. These companies are at the forefront of developing innovative bispecific therapies, with a focus on oncology and other high-need areas. For example, Roche has leveraged its expertise in biologics to bring to market Hemlibra and Vabysmo, while Amgen is advancing bispecific T-cell engagers for cancer immunotherapy.
In addition to these leading companies, there have been significant regulatory designations granted to bispecific antibodies, enhancing the overall market landscape. Ivonescimab, a PD-1 x VEGF bispecific antibody developed by Akeso, received FDA Fast Track Designation in October 2024 for the treatment of non-small cell lung cancer (NSCLC) with EGFR mutations in the second-line or beyond setting. This designation accelerates the development process and highlights the growing interest in bispecific antibodies for treating cancer. Akeso is collaborating with Summit Therapeutics in the US and other countries to develop Ivonescimab.
Additionally, Invenra's Novel Antibody INV724 has received both Rare Pediatric Disease and Orphan Drug Designations from the US FDA for the treatment of neuroblastoma, a rare and aggressive cancer affecting children. INV724 targets the GD2 and B7-H3 antigens and has shown promise in early-stage clinical trials, offering hope for more effective treatments for pediatric cancers.
In conclusion, the bispecific antibody market is poised for substantial growth, driven by increasing approvals, ongoing clinical trials, and strong regulatory support. With major players like Roche, Gilead, Amgen, and Pfizer leading the charge, and promising candidates undergoing review, bispecific antibodies are set to transform the landscape of modern therapeutics. The market's rapid expansion from US$ 12 Billion in 2024 to an expected US$ 50 Billion by 2030, reflects the increasing recognition of bispecific antibodies as key solutions for treating complex and life-threatening diseases.
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