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市場調査レポート
商品コード
1764754
肝細胞がん治療薬の市場規模、シェア、成長分析、薬剤クラス別、療法タイプ別、治療タイプ別、投与経路別、エンドユーザー別、流通チャネル別、地域別 - 産業予測、2025年~2032年Hepatocellular Carcinoma Drugs Market Size, Share, and Growth Analysis, By Drug Class, By Therapy Type, By Treatment Type, By Route of Administration, By End-Users, By Distribution Channel, By Region - Industry Forecast 2025-2032 |
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肝細胞がん治療薬の市場規模、シェア、成長分析、薬剤クラス別、療法タイプ別、治療タイプ別、投与経路別、エンドユーザー別、流通チャネル別、地域別 - 産業予測、2025年~2032年 |
出版日: 2025年07月02日
発行: SkyQuest
ページ情報: 英文 198 Pages
納期: 3~5営業日
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肝細胞がん治療薬の世界市場規模は、2023年に14億米ドルと評価され、予測期間(2025年~2032年)にCAGR 8.3%で成長し、2024年の15億2,000万米ドルから2032年には28億7,000万米ドルに成長する見通しです。
世界の肝細胞がん(HCC)治療薬市場は、患者の人口動態の進化、腫瘍学に対する政府支出の増加、標的療法の進歩などを背景に、大きな成長を遂げています。医療技術革新への世界の投資により、新しい治療、特に肝がんに特化した精密医療の導入が加速しています。早期診断の増加は、免疫療法や併用療法の導入の増加とともに、ヘルスケア提供システム全体で肝細胞がん治療薬の利用を拡大しています。バイオマーカー誘導治療や次世代チロシンキナーゼ阻害剤(TKI)など、精密腫瘍学における注目すべき技術革新は、肝細胞がん治療のブレークスルーへの道を開いています。さらに、人工知能を活用した創薬プラットフォームが有望な新規免疫療法の迅速な開発を促進し、市場の将来性をさらに高めています。
Global Hepatocellular Carcinoma Drugs Market size was valued at USD 1.4 billion in 2023 and is poised to grow from USD 1.52 billion in 2024 to USD 2.87 billion by 2032, growing at a CAGR of 8.3% during the forecast period (2025-2032).
The global hepatocellular carcinoma (HCC) drugs market is experiencing significant growth, driven by evolving patient demographics, increased government expenditure on oncology, and advancements in targeted therapies. Worldwide investments in health innovation are accelerating the adoption of new treatments, particularly precision medicine dedicated to liver cancer. The rise of early diagnoses, along with the growing implementation of immunotherapies and combination therapies, is expanding the utilization of HCC medications across healthcare delivery systems. Notable innovations in precision oncology, including biomarker-guided therapies and next-generation tyrosine kinase inhibitors (TKIs), are paving the way for breakthroughs in HCC treatment. Additionally, artificial intelligence-driven drug discovery platforms are facilitating the rapid development of promising new immunotherapies, further enhancing the market's prospects.
Top-down and bottom-up approaches were used to estimate and validate the size of the Global Hepatocellular Carcinoma Drugs market and to estimate the size of various other dependent submarkets. The research methodology used to estimate the market size includes the following details: The key players in the market were identified through secondary research, and their market shares in the respective regions were determined through primary and secondary research. This entire procedure includes the study of the annual and financial reports of the top market players and extensive interviews for key insights from industry leaders such as CEOs, VPs, directors, and marketing executives. All percentage shares split, and breakdowns were determined using secondary sources and verified through Primary sources. All possible parameters that affect the markets covered in this research study have been accounted for, viewed in extensive detail, verified through primary research, and analyzed to get the final quantitative and qualitative data.
Global Hepatocellular Carcinoma Drugs Market Segments Analysis
Global Hepatocellular Carcinoma Drugs Market is segmented by Drug Class, Therapy Type, Treatment Type, Route of Administration, End-Users, Distribution Channel and region. Based on Drug Class, the market is segmented into PD-1/PD-L1 Inhibitors and Tyrosine Kinase Inhibitors. Based on Therapy Type, the market is segmented into Targeted Therapy, Immunotherapy and Others. Based on Treatment Type, the market is segmented into Medication, Surgery, Radiotherapy, Chemotherapy and Others. Based on Route of Administration, the market is segmented into Oral, Injectable and Others. Based on End-Users, the market is segmented into Hospitals, Homecare, Specialty Clinics and Others. Based on Distribution Channel, the market is segmented into Hospital Pharmacy, Online Pharmacy and Retail Pharmacy. Based on region, the market is segmented into North America, Europe, Asia Pacific, Latin America and Middle East & Africa.
Driver of the Global Hepatocellular Carcinoma Drugs Market
The global hepatocellular carcinoma (HCC) drugs market is largely driven by the rising incidence of HCC globally, largely due to chronic hepatitis B and C infections that are becoming resistant to treatment. Additionally, increasing alcohol consumption and the prevalence of nonalcoholic fatty liver disease/nonalcoholic steatohepatitis (NAFLD/NASH), which are linked to the growing rates of obesity and diabetes, contribute to this upward trend. With a substantial and expanding patient population requiring effective treatment options, there is a consistent demand for both existing therapies and newly developed drugs to address this pressing health challenge.
Restraints in the Global Hepatocellular Carcinoma Drugs Market
The global hepatocellular carcinoma drugs market faces significant obstacles primarily due to the high costs associated with immunotherapies and targeted treatments, which restrict access for patients, particularly in low- and middle-income nations. Additionally, established markets implement stringent health technology assessment (HTA) policies, such as those from NICE and IQWiG, which require lengthy evaluations before providing reimbursement for expensive therapies. This can further limit patient access and delay the introduction of innovative treatments, despite their proven clinical efficacy, thereby hindering the overall growth and development of the market for hepatocellular carcinoma drugs.
Market Trends of the Global Hepatocellular Carcinoma Drugs Market
The Global Hepatocellular Carcinoma (HCC) drug market is witnessing a significant trend towards the rapid expansion of combination therapies, particularly involving PD-1/PD-L1 inhibitors alongside Tyrosine Kinase Inhibitors (TKIs) and anti-angiogenic agents. Notable combinations, such as Roche's Tecentriq (atezolizumab) with Avastin (bevacizumab), have demonstrated remarkable clinical efficacy, including a 42% reduction in mortality risk as observed in the IMbrave150 trial. This trend is further propelled by accelerated approval processes from regulatory bodies like the FDA and EMA, amplifying market growth potential. As clinical outcomes improve, the demand for effective HCC treatments continues to rise, reshaping the landscape of oncological therapies.