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市場調査レポート
商品コード
1574655
がん抗体薬物複合体の世界市場:市場規模、薬剤承認、薬価、販売、臨床試験に関する洞察(2030年)Global Cancer Antibody Drug Conjugates Market Size, Drugs Approval, Price, Sales & Clinical Trials Insight 2030 |
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がん抗体薬物複合体の世界市場:市場規模、薬剤承認、薬価、販売、臨床試験に関する洞察(2030年) |
出版日: 2024年10月01日
発行: KuicK Research
ページ情報: 英文 1300 Pages
納期: 即日から翌営業日
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抗体薬物複合体(ADC)は、モノクローナル抗体の特異性と細胞毒性薬剤の効能を併せ持つ、がん治療において革新的な治療薬として登場しました。この革新的な治療法は、安定したリンカーを介して細胞毒性薬剤と結合した抗体から構成されており、周囲の健康な組織へのダメージを最小限に抑えながら、がん細胞に標的を絞って送達することができます。抗体薬物複合体の急速な進化は、その臨床的・商業的成功を反映しており、現在、さまざまな市場で16製品が承認され、販売高は2023年に100億米ドル、2024年の最初の6ヵ月で70億米ドルを突破しています。この成長は、抗体薬物複合体がより広範ながん治療薬市場において商業的に実行可能なセグメントであることを浮き彫りにし、より効果的で安全な候補化合物の創製に向けた研究開発の活発化を促しています。
2024年10月現在、世界の規制当局は16種類の抗体薬物複合体を承認しており、現在13種類がさまざまながん種に対して臨床使用可能です。このうち、代表的なものにはパドセブ、カドサイラ、エンヘルツがあり、2023年の抗体薬物複合体売上高全体の約60%を占めています。Enhertuは複数のHER2陽性固形がんの治療に適応がありますが、PadcevとKadcylaはそれぞれ膀胱がんと乳がんの治療にのみ承認されています。これらの製品タイプは、治療の可能性だけでなく、さまざまながん種を管理するADCの有効性に対する市場の信頼が高まっていることを示しています。
世界のがん抗体薬物複合体市場は競合情勢に特徴があり、固形がんや血液悪性腫瘍を含む複数のがんを標的とした開発が活発に行われています。しかし、その中でも肺がんは現在最も広範な開発活動が行われており、CAB-AXL-ADC、TQB2102、MYTX-011を含む60以上の候補が臨床試験段階にあり、Enhertuが1つ臨床での使用が承認されています。これは、依然として世界のがん死亡の主要原因のひとつである肺がんにおいて、アンメットメディカルニーズの高い治療薬への戦略的転換を反映したものです。抗体薬物複合体は、より効果的で毒性の低い治療選択肢を提供する可能性があり、この治療領域では特に魅力的です。
特徴 | 詳細 |
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主要セグメント | 用途:がんタイプ別、地域別、技術プラットフォーム |
対象となる適応症 | 対象疾患:肺がん、乳がん、子宮頸がん、膵臓がん、食道がん、その他 |
主要対象国 | 米国、中国、韓国、カナダ、インドなど |
対象薬剤 | Enhertu、Adcetris、Polivy、Kadcylaなど |
レポート対象範囲 | 作用機序、ADC世代、パイプラインと承認薬の洞察、販売洞察、現在の動向、将来の機会、市場促進要因・課題 |
対象企業 | Biocytogen、Merck、AstraZeneca、Pfizer、Daiichi Sankyo、ADC Therapeuticsなど |
当レポートは、世界のがん抗体薬物複合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 Cancer Antibody Drug Conjugates Market Size, Drugs Approval, Price, Sales & Clinical Trials Insight 2030" Report Finding and Inclusions:
Features | Details |
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Key Segments: | Application by Cancer Type, By Region, Technology Platforms |
Indications Covered: | Lung Cancer, Breast Cancer, Cervical Cancer, Pancreatic Cancer, Pancreatic Cancer, Esophageal Cancer, among others |
Key Countries Covered: | US, China, South Korea, Canada, India, among others |
Drugs Covered: | Enhertu, Adcetris, Polivy, Kadcyla, among others |
Report Coverage: | Mechanism of Action, ADC Generations, Pipeline & Approved Drugs Insight, Sales Insight, Current Trends, Future Opportunities, Market Drivers & Challenges |
Companies Covered: | Biocytogen, Merck, AstraZeneca, Pfizer, Daiichi Sankyo, ADC Therapeutics, among others |
Antibody drug conjugates (ADCs) have emerged as a transformative class of therapeutics in the cancer treatment landscape, integrating the specificity of monoclonal antibodies with the potency of cytotoxic drugs. These innovative therapies consist of an antibody linked to a cytotoxic agent through a stable linker, allowing targeted delivery to cancer cells while minimizing damage to surrounding healthy tissues. The rapid evolution of antibody drug conjugates reflects their clinical and commercial success, with 16 products currently approved across various markets and sales surpassing US$ 10 Billion in 2023 and US$ 7 Billion in the first 6 months of 2024. This growth highlights antibody drug conjugates as a commercially viable segment of the broader cancer therapeutics market, prompting increased research and development efforts to create more effective and safer candidates.
As of October 2024, regulatory authorities around the world have approved 16 antibody drug conjugates, with 13 currently available for clinical use for different cancer types. Among these, prominent examples include Padcev, Kadcyla, and Enhertu, which collectively accounted for approximately 60% of the total antibody drug conjugates sales in 2023. While Enhertu is indicated for the treatment of several HER2-positive solid cancers, Padcev and Kadcyla are solely approved for the treatment of bladder cancer and breast cancer, respectively. The commercialization of these products demonstrates not only their therapeutic potential but also the market's growing confidence in the effectiveness of ADCs in managing various cancer types.
Global cancer antibody drug conjugates market is characterized by a competitive landscape, with substantial development efforts targeting multiple cancers, including both solid tumors and hematological malignancies. However, out of all these, lung cancer is currently witnessing the most extensive development activity, with over 60 candidates in clinical trials, including CAB-AXL-ADC, TQB2102, and MYTX-011, and one Enhertu, approved for use in clinical setting. This reflects a strategic shift towards addressing the high-unmet medical need in lung cancer, which remains one of the leading causes of cancer mortality worldwide. The potential for antibody drug conjugates to provide more effective and less toxic treatment options makes them particularly attractive in this therapeutic area.
In contrast, however, breast cancer has experienced the highest number of antibody drug conjugates approvals to date, with four approved candidates, contributing significantly to the market's commercial success. Two key players in this domain are the aforementioned Kadcyla and Enhertu, both of which have demonstrated remarkable efficacy and have achieved significant sales milestones. The promising pipeline also includes AstraZeneca and Daiichi Sankyo's Datopotamab Deruxtecan, a TROP2-directed antibody drug conjugate that is currently under review for its use in breast cancer treatment. This continued investment in research and development underscores the critical role antibody drug conjugates play in advancing cancer care.
Regionally, the cancer antibody drug conjugates market is primarily led by the US and China, two of the largest and most dynamic pharmaceutical markets globally. In the US, robust healthcare infrastructure, high R&D expenditure, and a favorable regulatory environment foster innovation and accelerate the approval process for new therapies. Additionally, the presence of major pharmaceutical companies, such as Regeneron, Gilead, Merck and Pfizer, bolsters the competitive landscape, enabling rapid development and commercialization of antibody drug conjugates.
In China, the growing demand for advanced cancer treatments, coupled with increasing government support for biotechnology and pharmaceutical research, has catalyzed significant growth in the antibody drug conjugates sector. Local players like Mabwell, Miracogen, Chia Tai Tianqing Pharmaceutical, Hansoh BioMedical, Sichuan Baili Pharmaceuticals, Biocytogen and Affinity Biopharma are emerging as significant contributors to the market, developing novel Antibody drug conjugates tailored to the specific needs of the Chinese patient population, and out licensing promising candidates to their international counterparts through license agreements.
The global market for cancer antibody drug conjugates represents a dynamic and rapidly evolving segment of the cancer therapeutics landscape. With ongoing clinical trials, innovative research, and increasing regulatory support, antibody drug conjugates are poised to play an increasingly pivotal role in cancer treatment. As efforts continue to address existing challenges and expand the range of approved indications, the future of antibody drug conjugates appears promising, offering hope to patients worldwide in the fight against cancer. The collaborative efforts among pharmaceutical companies, regulatory bodies, and research institutions will be crucial in shaping the next wave of advancements in this exciting therapeutic field.