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市場調査レポート
商品コード
1667965
プラスミノーゲン市場- 世界の産業規模、シェア、動向、機会、予測、タイプ別、用途別、地域別、競合別、2020~2030年Plasminogen Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Type, By Application, By Region and Competition, 2020-2030F |
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プラスミノーゲン市場- 世界の産業規模、シェア、動向、機会、予測、タイプ別、用途別、地域別、競合別、2020~2030年 |
出版日: 2025年02月28日
発行: TechSci Research
ページ情報: 英文 182 Pages
納期: 2~3営業日
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世界のプラスミノーゲン市場は、2024年には26億5,000万米ドルと評価され、2030年にはCAGR5.43%を反映して36億4,000万米ドルに達すると予測されています。
プラスミノーゲンに基づく治療法は、特に創傷治癒や眼疾患など、様々な病態の治療法として認知されつつあり、市場は大きな勢いを増しています。線溶に関与する重要なタンパク質であるプラスミノーゲンは、血栓の分解や創傷治癒の促進に不可欠です。糖尿病性足潰瘍の原因となることが多い糖尿病などの慢性疾患の有病率の上昇が、プラスミノーゲンをベースとした治療に対する需要を牽引しています。さらに、バイオテクノロジーの進歩や、プラスミノーゲン治療に焦点を当てた臨床試験の増加が、その治療可能性への自信を強めています。現在進行中の調査により、その用途が明らかになりつつあり、木部結膜炎や慢性創傷などの症状に多様な治療オプションを提供することで、市場は大きく成長すると予想されます。
市場概要 | |
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予測期間 | 2026-2030 |
市場規模:2024年 | 26億5,000万米ドル |
市場規模:2030年 | 36億4,000万米ドル |
CAGR:2025年~2030年 | 5.43% |
急成長セグメント | 創傷治癒 |
最大市場 | 北米 |
プラスミノーゲン市場の急成長に寄与する主な要因としては、個別化医療の台頭や新興国におけるヘルスケアインフラの拡大などが挙げられます。ヘルスケアの進化に伴い、個別化された治療計画が重視されるようになり、プラスミノーゲン治療の採用が増加すると予想されます。また、特にアジア太平洋やラテンアメリカなどの地域では、ヘルスケアへの投資が市場成長の原動力となっています。世界の外科手術の増加とそれに伴う術後ケアの必要性が、特に創傷ケアや組織再生におけるプラスミノーゲン療法の需要を高めています。さらに、臨床試験での有望な結果が投資家の関心を集め、継続的な技術革新とプラスミノーゲンベースの製品開発に拍車をかけています。
しかし、プラスミノーゲン市場は、その成長軌道を阻害しかねないいくつかの課題に直面しています。主な障害の一つは、プラスミノーゲンに基づく治療薬の製造コストが高いことで、特に低所得国での利用が制限される可能性があります。新しいプラスミノーゲン治療に対する厳格な承認プロセスを含む規制上の課題も、革新的なソリューションを導入しようとする企業にとって障壁となっています。このような課題にもかかわらず、現在進行中の臨床的進歩や効果的な創傷治癒ソリューションに対する需要の高まりは、主要な市場参入企業にとって大きな成長機会となります。治療コストの削減や承認プロセスの合理化への取り組みがこれらの課題に対処し、市場の可能性をさらに高めると期待されます。
血栓関連疾患の有病率の上昇
高い治療費
規制支援と臨床試験
The global plasminogen market was valued at USD 2.65 billion in 2024 and is projected to reach USD 3.64 billion by 2030, reflecting a compound annual growth rate (CAGR) of 5.43%. The market is gaining considerable momentum due to the growing recognition of plasminogen-based therapies for treating a variety of medical conditions, particularly in wound healing and ocular diseases. Plasminogen, a crucial protein involved in fibrinolysis, is essential for breaking down blood clots and promoting wound healing. The rising prevalence of chronic diseases, such as diabetes, which often leads to diabetic foot ulcers, is driving the demand for plasminogen-based treatments. Additionally, advancements in biotechnology and the increasing number of clinical trials focusing on plasminogen therapies are bolstering confidence in its therapeutic potential. With ongoing research highlighting its applications, the market is expected to grow significantly, offering diverse treatment options for conditions like ligneous conjunctivitis and chronic wounds.
Market Overview | |
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Forecast Period | 2026-2030 |
Market Size 2024 | USD 2.65 Billion |
Market Size 2030 | USD 3.64 Billion |
CAGR 2025-2030 | 5.43% |
Fastest Growing Segment | Wound Healing |
Largest Market | North America |
Key factors contributing to the rapid growth of the plasminogen market include the rise of personalized medicine and the expansion of healthcare infrastructure in emerging economies. As healthcare evolves, there is a greater focus on individualized treatment plans, which is anticipated to increase the adoption of plasminogen therapies. Additionally, investments in healthcare, especially in regions such as Asia-Pacific and Latin America, are driving market growth. The global rise in surgical procedures and the subsequent need for post-operative care have increased the demand for plasminogen therapies, particularly in wound care and tissue regeneration. Moreover, promising results in clinical trials have attracted investor interest, fueling continued innovation and the development of plasminogen-based products.
However, the plasminogen market faces several challenges that may impede its growth trajectory. One major obstacle is the high cost of manufacturing plasminogen-based therapies, which could limit their accessibility, particularly in low-income countries. Regulatory challenges, including rigorous approval processes for new plasminogen treatments, also present barriers for companies seeking to introduce innovative solutions. Despite these challenges, ongoing clinical advancements and the growing demand for effective wound healing solutions provide substantial growth opportunities for key market players. Efforts to reduce treatment costs and streamline the approval process are expected to address these challenges and further enhance the market's potential.
Rising Prevalence of Clot-Related Disorders
The increasing prevalence of clot-related disorders is a significant driver of the global plasminogen market. Conditions such as venous thromboembolism (VTE), deep vein thrombosis (DVT), and pulmonary embolism (PE) have become more common due to factors such as sedentary lifestyles, rising obesity rates, and an aging population. In India, the incidence of DVT is reported to be 1% among adults over 40, with 15% to 20% of hospitalized patients affected. These disorders, which result from the abnormal formation of blood clots, can lead to serious complications like stroke, heart attacks, and respiratory failure, making timely treatment essential.
Plasminogen plays a key role in preventing or resolving clot-related complications. A deficiency or dysfunction of plasminogen can impede the body's ability to dissolve clots, increasing the risk of thrombotic events. As these disorders become more prevalent, the demand for plasminogen-based therapies to manage these life-threatening conditions is rising. Treatments involving plasminogen help dissolve existing clots and prevent new ones, improving patient outcomes and reducing complications. The growing number of diagnoses, coupled with improved diagnostic techniques and greater awareness, has expanded the patient base seeking effective treatment. This has led pharmaceutical companies to invest significantly in developing innovative plasminogen therapies, including recombinant plasminogen products, to address the growing demand for safe and effective clot management solutions.
High Treatment Costs
The high treatment costs associated with plasminogen-based therapies present a significant challenge to ensuring equitable access. The complex production of recombinant plasminogen products contributes to their elevated prices. The biotechnology processes involved in synthesizing plasminogen require sophisticated equipment, specialized expertise, and stringent quality control measures. Research, development, and manufacturing costs are substantial, and these expenses are often passed on to patients and healthcare systems.
Additionally, regulatory requirements add to the overall cost. Companies must invest significantly in preclinical and clinical trials to demonstrate the safety and efficacy of plasminogen treatments, meeting the rigorous standards set by regulatory agencies such as the FDA and EMA. These trials involve extensive data collection and monitoring, further contributing to the cost.
The limited patient pool also drives up treatment costs. While clot-related disorders are prevalent, they do not affect as large a population as other medical conditions, preventing the economies of scale that could reduce production costs for plasminogen therapies.
Regulatory Support and Clinical Trials
Regulatory support and clinical trials are crucial drivers for the growth of the global plasminogen market. Regulatory agencies such as the FDA and EMA play an essential role in ensuring the safety and efficacy of plasminogen-based therapies, providing the necessary frameworks for drug approval and market entry. In India, the Central Drugs Standard Control Organization (CDSCO) has expedited the approval of critical therapies, including novel plasminogen replacement treatments for congenital plasminogen deficiency.
Clinical trials form the foundation for the development of plasminogen therapies, providing the evidence needed to validate their safety and effectiveness. As the number of clinical trials increases, so does the confidence in plasminogen's potential, both among healthcare providers and regulatory agencies. In 2024, the Clinical Trials Registry - India (CTRI) reported a 15% increase in registered clinical trials for plasminogen therapies. Notably, a Phase III trial aimed at evaluating recombinant plasminogen for chronic venous leg ulcers is underway, further demonstrating the commitment to advancing plasminogen-based therapies.
The support from regulatory bodies like the FDA, EMA, and CDSCO is instrumental in expediting the approval process and ensuring the continued development and accessibility of plasminogen therapies, ultimately improving patient outcomes.
The report segments the global plasminogen market as follows:
The report provides a detailed analysis of key players in the global plasminogen market. Customizations are available to tailor the report to specific company needs, including additional profiling of up to five market players.