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市場調査レポート
商品コード
1397170
薬剤溶出バルーンの世界市場:洞察、競合情勢、市場予測:2028年Drug Eluting Balloons - Market Insights, Competitive Landscape, and Market Forecast - 2028 |
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薬剤溶出バルーンの世界市場:洞察、競合情勢、市場予測:2028年 |
出版日: 2023年12月18日
発行: DelveInsight
ページ情報: 英文 150 Pages
納期: 1~3営業日
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世界の薬剤溶出バルーンの市場規模は、2023年から2028年の予測期間中に8.31%のCAGRで拡大すると予測されています。薬剤溶出バルーンの需要は、主に末梢動脈疾患や冠動脈疾患を含む数多くの心臓疾患の有病率の増加が後押ししています。さらに、低侵襲治療への嗜好の高まり、薬剤溶出ステントに対するバルーンカテーテルの優位性、高齢者人口の増加などが、今後数年間の薬剤溶出バルーンの需要を押し上げると思われます。また、新興国を中心としたヘルスケア支出の増加、製品の発売と承認の増加、主要企業による研究開発活動の急増などが、2023年~2028年の予測期間における薬剤溶出バルーン市場全体の成長に寄与しています。
薬剤溶出バルーン市場は、さまざまな要因によって製品需要が伸びていますが、その主な要因の1つは、末梢動脈疾患と冠動脈疾患を含む心臓疾患の数値が上昇していることです。
例えば、米国心臓協会(American Heart Association)によると、2020年には世界全体で2億4,410万人が冠動脈疾患として知られる虚血性心疾患(IHD)に罹患していると推定されています。同じ出典によると、女性よりも男性の方が多く、それぞれ1億4,100万人と1億310万人でした。
さらに、British Heart Foundation 2023は、2019年には末梢動脈(血管)疾患が世界で1億1,000万症例を占めると推定しています。
このように、冠動脈および末梢動脈疾患の有病率の増加は、疾患の治療および管理に頻繁に使用されるため、薬剤溶出バルーンの需要を増加させます。
さらに、これらのカテーテルは、薬剤溶出ステントと比較して、標的薬剤デリバリーにおけるさまざまな利点があるため、多くの心血管適応症に対する血管形成術での使用が増加しています。これらのデバイスは、ステントや開腹手術と比較して、より優れた血管造影と臨床結果をもたらします。また、薬剤コーティングバルーンは、最小限の副作用を含む様々な利点により、冠動脈疾患に対する最も適応性の高い治療アプローチとなっています。さらに、薬剤コーティングバルーンカテーテルを用いた低侵襲手術は、リスクの高いステント治療に代わる心筋梗塞治療法として注目されています。
また、市場参入企業は知名度を高めるために頻繁に新製品を開発しています。例えば、2023年6月、医療機器および体外診断技術をヘルスケア業界に提供する大手プロバイダーであるSurmodics, Inc.は、SurVeil(TM)薬剤コーティングバルーン(DCB)の米国食品医薬品局(FDA)承認を取得しました。
したがって、上記の要因は、2023年から2028年の予測期間における薬剤溶出バルーン市場の成長に寄与しています。
しかし、副作用や製品回収、厳しい規制手続きなどが薬剤溶出バルーン市場の成長を制限する可能性があります。
当レポートでは、世界の薬剤溶出バルーン市場について調査し、市場の概要とともに、製品タイプ別、エンドユーザー別、地域別動向、および市場に参入する企業のプロファイルなどを提供しています。
Drug-Eluting Balloon Market By Product Type (Coronary Drug-Eluting Balloon, Peripheral Drug-Eluting Balloon, And Others), End-User (Hospitals, Ambulatory Surgical Centers, And Others), and geography is expected to grow at a steady CAGR forecast till 2028 owing to the increasing prevalence of peripheral and coronary artery diseases and rising demand for minimally invasive procedures across the globe.
Global drug-eluting balloon market is estimated to grow at a CAGR of 8.31% during the forecast period from 2023 to 2028. The demand for drug-eluting balloons is primarily being boosted by the increasing prevalence of numerous heart diseases including peripheral and coronary artery diseases. Furthermore, the increasing preference for minimally invasive procedures, the advantages of balloon catheters over drug-eluting stents, the rising elderly population base, and others will propel the demand for drug-eluting balloons in the upcoming years. In addition, growing healthcare spending, especially in emerging countries, rising product launches and approvals, and surging research and developmental activities by the key players, among others are thereby contributing to the overall growth of the drug-eluting balloon market during the forecast period from 2023-2028.
The drug-eluting balloon market is witnessing a growth in product demand owing to various factors, one of the key factors being the rising figures of heart diseases comprising peripheral and coronary artery disease.
For instance, according to the American Heart Association 2022, globally, it was estimated that in 2020, 244.1 million people were living with ischemic heart disease (IHD), also known as coronary heart or coronary artery disease. The same source estimated that it was more prevalent in males than in females, 141.0 and 103.1 million people, respectively.
Further, British Heart Foundation 2023 estimated that the peripheral arterial (vascular) disease accounted for 110 million cases in 2019, globally.
Thus, the increasing prevalence of coronary and peripheral artery disease will increase the demand for drug-eluting balloons as they are frequently used to treat and manage the disease.
Additionally, various advantages of these catheters over drug-eluting stents in targeted drug delivery have increased their use in angioplasty surgeries for a number of cardiovascular indications. These devices provide better angiographic and clinical outcomes as compared to stents or open surgeries. Also, the drug-coated balloons are the most adaptive therapeutics approach for coronary disease due to their various advantages including minimal side effects. Further, drug-coated balloon catheter usage with minimally invasive procedures is a preferable replacement over risky stent treatment for myocardial infarction.
Also, market participants frequently develop new products to increase their visibility. For instance, in June 2023, Surmodics, Inc., a leading provider of medical devices and in vitro diagnostic technologies to the healthcare industry, received the US Food and Drug Administration (FDA) approval for the SurVeil™ drug-coated balloon (DCB).
Therefore, the above-mentioned factors are contributing to the growth of the drug-eluting balloon market during the forecast period from 2023-2028.
However, adverse effects and product recalls, stringent regulatory procedures and others may restrict the drug-eluting balloon market growth.
Drug-eluting Balloon Market by Product Type (Coronary Drug-Eluting Balloon, Peripheral Drug-Eluting Balloon, and Others), End-User (Hospitals, Ambulatory Surgical Centers, and Others), and Geography (North America, Europe, Asia-Pacific, and the Rest of the World).
In the product type segment of the drug-eluting balloon market, the peripheral drug-eluting balloon category is expected to amass a significant revenue share in the year 2022. This was primarily owing to the benefits that various the segment and the rising figures of peripheral artery disease (PAD) across the globe.
According to DelveInsight estimates, the US accounted for approximately 9 million cases, which was the highest diagnosed prevalent cases of peripheral artery disease, followed by EU4 and the UK with 5 million cases, and Japan with 2 million cases in 2022. Further, among the European countries, Germany had the highest diagnosed prevalent population of peripheral artery disease (approximately 2 million cases), followed by Italy (approximately 1 million cases) in 2022. On the other hand, Spain (0.7 million cases) had the lowest diagnosed prevalent population in EU4 and the UK countries and the 7MM.
Thus, the above statistics show that PAD is increasing at a faster pace, which is ultimately driving the segment for peripheral drug-eluting balloons.
Numerous businesses and key players in this field are also working to create technologically advanced peripheral drug-eluting balloons. For instance, in August 2022, BD (Becton, Dickinson, and Company), a leading global medical technology company, announced the start of enrollment in a first-in-human trial of a peripheral sirolimus drug-coated balloon (DCB). The PREVISION trial is a prospective, multicenter, single-arm, non-randomized study designed to evaluate the safety of the BD sirolimus DCB in the treatment of peripheral arterial disease in the femoropopliteal arteries.
Also, in November 2020, Boston Scientific received US Food and Drug Administration (FDA) approval for the Ranger™ Drug-Coated Balloon, developed for the treatment of patients with peripheral artery disease (PAD) in the superficial femoral artery (SFA) and proximal popliteal artery (PPA).
Thus, the above-mentioned factors are likely to propel the demand for peripheral drug-eluting balloons, thereby contributing to the growth of the drug-eluting balloon market during the forecast period from 2023-2028.
Among all the regions, North America is estimated to account for the largest share in the drug-eluting balloon market in the year 2022. This domination is due to the increasing application of drug-eluting balloons in the treatment and management of peripheral and coronary artery disease, increasing sedentary lifestyle lacking physical activity, lack of proper diet, anxiety, and stress resulting in chronic diseases, such as diabetes and obesity, leading to an increase in the prevalence of multiple cardiovascular diseases, rising product launch and approvals, presence of favorable regulatory authority, among others will propel the market of drug-eluting balloon in North America.
For instance, as per the study conducted by the Centre for Disease Control and Prevention (CDC) in 2023, it was stated that in 2021, about 1 in 20 adults age 20 and older have coronary artery disease (CAD). Coronary heart disease is the most common type of heart disease in the US, killing 375,476 people in 2021. In 2021, about 2 in 10 deaths from CAD happen in adults less than 65 years old. Thus, the high burden of cardiovascular diseases in the region demands the availability of drug-eluting balloons.
The American Heart Association in the latest study estimated that over 500,000 percutaneous coronary intervention (PCI) procedures are carried out annually in the US. Percutaneous coronary intervention with a drug-coated balloon (DCB) is a novel treatment that seeks to acutely dilate coronary stenosis and deliver an anti-proliferative drug to the vessel wall. Thus, the surging number of PCI procedures in the region will increase the demand for drug-eluting balloons.
Further, the availability of various major manufacturers, the launch and approval of new and technologically advanced devices, and favorable reimbursement regulations are all important factors responsible for driving the demand for drug-eluting balloons in the region. For instance, in November 2022, Genesis MedTech Group announced that the Food and Drug Administration (FDA) has approved the Chocolate Touch® Drug-coated Balloon PTA Catheter, developed by TriReme Medical LLC, for the treatment of patients with peripheral artery disease in the superficial femoral artery and the popliteal artery.
Thus, all the above-mentioned factors will lead to an increase in the North America drug-eluting balloon market growth during the forecasting period of 2023-2028.
Some of the key market players operating in the drug-eluting balloon market include: Boston Scientific Corporation, BD, Terumo Corporation, Medtronic, Koninklijke Philips N.V., M.A. Med Alliance SA., Cook, BIOTRONIK, SurModics Inc., B. Braun SE, Aachen Resonance Entwicklungsgesellschaft mbH, Biosensors International Group, Ltd., Eurocor GmbH, iVascular, Innvolution, Cardiovascular Systems, Inc., Genesis Medtech, Concept Medical, Cardionovum GmbH, YINYI (LIAONING) BIOTECH CO., LTD., and others.