市場調查報告書
商品編碼
1422066
再生醫學市場:按成分、按產品、按材料、按應用、按最終用戶、按地區、機會、預測,2017-2031Regenerative Medicine Market Assessment, By Component, By Product, By Material, By Application, By End-user, By Region, Opportunities and Forecast, 2017-2031F |
全球再生醫學市場規模預計將從 2023 年的 249.1 億美元增長到 2031 年的 999.5 億美元,預測期內複合年增長率為 18.97%。
全球再生醫學市場受到人口老化加劇、慢性病盛行率上升、技術進步、投資增加、病患需求增加以及有利的報銷政策等因素的推動。
慢性病的增加是全球再生醫學市場的關鍵驅動力。 世界衛生組織(WHO)強調,心血管疾病、癌症、糖尿病、呼吸道疾病等慢性病正以驚人的速度成長。 如果目前的趨勢持續下去,世界衛生組織預測,到 2050 年,每年 9,000 萬人死亡中的 86% 將死於慢性病。 由於相關的醫療負擔和傳統治療的局限性,慢性病的增加令人擔憂。 再生醫學透過專注於修復和替換受損組織並有效地針對慢性疾病的根本原因,為解決這些健康挑戰提供了一條有前途的途徑。 因此,日益增加的慢性病負擔已成為再生醫學市場成長的強大驅動力,再生醫學市場尋求提供創新和更有效的解決方案。
基因治療解決方案的研發投資在推動全球再生醫學市場方面發揮著至關重要的作用。 基因療法有可能糾正遺傳缺陷、操縱細胞功能並從根源解決各種疾病。 這種有針對性的方法由於其再生和修復受損組織的能力而獲得了大量的財政支持。 投資將促進創新,加速新的再生醫學治療方法的開發,最終為全球再生醫學市場的成長和發展做出貢獻,為以前無法治療的疾病帶來希望,並改善整體醫療保健狀況。
世界各國政府越來越認識到再生醫學領域的巨大潛力,並積極採取措施促進其使用和擴展。 各國政府將透過資助研發、建立安全有效部署治療的監管結構以及加強再生醫學解決方案生產和分配所需的基礎設施來採取這些措施。
在全球再生醫學市場,基因治療的需求正在快速成長。 基因療法因其能夠解決多種遺傳疾病、慢性病和未滿足的醫療需求而獲得發展勢頭。 隨著基因療法研究和技術的不斷進步,其有效性和安全性正在得到保證。 因此,隨著需求的增加以及患者和醫療保健專業人員尋求基因療法的替代療法,基因療法被定位為再生醫學領域的潛在途徑。
本報告調查了全球再生醫學市場,提供了市場定義和概述、市場規模趨勢和預測、各個細分市場和地區的詳細分析、行業結構以及影響市場成長的因素分析、案例研究、競爭格局、主要公司的簡介等等。
Global regenerative medicine market size was valued at USD 24.91 billion in 2023, expected to reach USD 99.95 billion in 2031, with a CAGR of 18.97% for the forecast period between 2024 and 2031. The global regenerative medicine market is driven by factors such as a growing aging population, increasing prevalence of chronic diseases, technological advancements, growing investments, increasing patient demand, and favorable reimbursement policies.
The global regenerative medicine market is undergoing rapid expansion. With an increasing elderly demographic, the prevalence of age-related health issues, chronic diseases, and cases related to tissue degeneration have increased significantly. Conditions such as diabetes, cardiovascular diseases, and neurodegenerative disorders are increasing globally, fuelling the demand for global regenerative medicine market interventions that can repair or replace damaged tissues. Regulatory agencies have recognized regenerative medicine's potential and created pathways and guidelines for product approval and commercialization. Collaborative efforts across various sectors, including pharmaceutical companies, biotechnology firms, academic institutions, and research organizations, have facilitated the development of innovative regenerative medicine products. These partnerships accelerate research and development, resulting in more accessible patient treatments.
Technological advancements in the global regenerative medicine market, such as stem cell research and gene therapy, have expanded the possibilities in regenerative medicine, making treatments more effective and versatile. With patients becoming more aware of regenerative medicine's potential, there is an increasing demand for these innovative therapies. Favorable reimbursement policies and government support in some regions have further encouraged accessibility. Ethical concerns, particularly regarding stem cell research, have hindered the development of alternative methods like induced pluripotent stem cells (iPSCs). The trend toward personalized medicine has reinforced the importance of customizing regenerative medicine treatments based on individual genetic makeup, further enhancing the growth and potential of global regenerative medicine market. These factors collectively propel the regenerative medicine market into a promising and dynamic sector within the healthcare industry, though challenges such as regulatory hurdles and development costs still need to be addressed for sustainable growth.
The increasing prevalence of chronic diseases is a significant catalyst for the global regenerative medicine market. Chronic diseases, as highlighted by the World Health Organization (WHO), including cardiovascular diseases, cancer, diabetes, and respiratory illnesses, have been increasing at an alarming rate. WHO's projections indicate that if the trend persists, by the year 2050, chronic diseases will contribute to a staggering 86% of the estimated 90 million annual deaths. The increase in chronic diseases is a cause for concern due to the associated healthcare burden and the limitations of conventional treatments. Regenerative medicine offers a promising avenue to address these health challenges by focusing on repairing or replacing damaged tissues, effectively targeting the root causes of these chronic conditions. As a result, the escalating burden of chronic diseases is a strong driver for the growth of the regenerative medicine market, as it seeks to provide innovative and more effective solutions.
Investments in research and development in gene therapy solutions have played a pivotal role in propelling the global regenerative medicine market. Gene therapy can potentially correct genetic defects, manipulate cellular functions, and address various diseases at their source. The targeted approach has generated substantial financial support with its ability to regenerate or repair damaged tissues. Investments are driving innovation and accelerating the development of novel regenerative medicine treatments, ultimately contributing to the growth and expansion of the global regenerative medicine market, offering hope for previously untreatable conditions, and enhancing the overall healthcare landscape.
In September 2023, TherageniX, a startup from the University of Nottingham, which specializes in a dry powder gene therapy formulation to enhance bone graft augmentation, received a grant of approx. GBP 995 thousand from Innovate UK, the innovation agency of the United Kingdom, in collaboration with the University of Nottingham. The financial support is earmarked for advancing the company's work on a powder-form non-viral gene delivery system, aimed at enhancing tissue regeneration post-surgery.
Governments around the globe are increasingly acknowledging the substantial potential in the regenerative medicine domain and are actively implementing measures to promote its usage and expansion. The government is taking these measures through financing research and development, establishing regulatory structures for the safe and efficient deployment of treatments, and bolstering the infrastructure required for the production and distribution of regenerative medical solutions. Investment in regenerative medicine catalyzes innovation and positions nations to become leaders in the rapidly growing sector. By nurturing an environment conducive to scientific exploration and commercial advancement, governments aspire to enhance healthcare outcomes, address unmet medical needs, and contribute to advancing the global regenerative medicine market.
In June 2023, the Indian central government inaugurated India's inaugural center dedicated to regenerative therapies for repairing damaged corneas in Delhi. The facility enables patients to receive bioengineered cornea treatment, harnessing tissue-specific exosomes and biomaterials mimicking natural tissues to stimulate the regeneration of robust and functional corneas. The treatment involves applying liquid drops directly onto the cornea, which solidifies in under 10 minutes, seamlessly integrating with the patient's existing corneal tissue.
There has been a notable surge in demand for gene therapy in the global regenerative medicine market. Gene therapy is gaining momentum due to its capacity to tackle various genetic disorders, chronic ailments, and unaddressed medical requirements. As gene therapy research and technologies continue to progress, there is assurance over its efficacy and safety. As a result, demand is increasing, and gene therapy is being positioned as a potential path in the field of regenerative medicine as patients and healthcare professionals are increasingly looking for gene therapy alternatives.
In June 2023, Sarepta Therapeutics, Inc., a frontrunner in precise genetic medicine for rare diseases, unveiled that the U.S. Food and Drug Administration (FDA) approved ELEVIDYS (delandistrogene moxeparvovec-rokl). A gene therapy that utilizes an adeno-associated virus for the treatment of ambulatory pediatric patients between the ages of 4 and 5 years who have been diagnosed with Duchenne muscular dystrophy (DMD) and possess a confirmed mutation in the DMD gene.
The growing demand for regenerative medicines in ophthalmology is proving to be a substantial asset to the global regenerative medicine market. The surge is primarily attributed to the prevalence of ocular conditions like age-related macular degeneration, corneal diseases, and retinal disorders, which can result in vision impairments or blindness. Regenerative medicines present effective solutions by applying stem cells, gene therapies, and tissue engineering to rectify damaged eye tissues and rejuvenate vision. With the aging population continually increasing, the request for these cutting-edge treatments in the ophthalmology is growing rapidly, actively contributing to the overall expansion of the global regenerative medicine market and instilling optimism for enhanced eye health and visual outcomes.
In August 2023, ViGeneron GmbH disclosed that the European Medicines Agency (EMA) had granted its clinical trial application (CTA) approval for the novel gene therapy, VG901. ViGeneron reports that VG901 utilizes an adeno-associated virus (AAV) vector to treat CNGA1-associated retinitis pigmentosa (RP).
The global regenerative medicine market is expected to grow rapidly due to the convergence of multiple influential factors. Primarily, the increasing global aging demographic has led to a higher incidence of chronic illnesses, degenerative ailments, and tissue damage, thereby creating a demand for advanced regenerative therapies. Additionally, breakthroughs in fields such as stem cell research, gene therapy, and tissue engineering have broadened the horizons of regenerative medicine, enhancing the effectiveness and versatility of treatments.
Furthermore, government support and the recognition by regulatory agencies of regenerative medicine's potential have resulted in the establishment of guidelines and pathways for product development and approval. It has instilled greater confidence in investors and expedited research efforts. Collaborative ventures involving pharmaceutical companies, research institutions, and biotechnology firms are expected to spur the innovation ahead.
Companies are progressively establishing strategic partnerships and distribution agreements, which are pivotal in propelling the global regenerative medicine market's expansion. These alliances empower firms to harness each other's strengths, gain access to new markets, and pool resources for research and development endeavors. Distribution agreements enable companies to broaden their market presence and enhance the accessibility of regenerative medicine treatments to a wider patient demographic. These collaborative initiatives promote innovation, expedite product development, and, in the end, contribute to the enduring and robust growth of the regenerative medicine market.
In August 2023, Marrow Access Technologies unveiled a distribution agreement with Spartan Medical. The agreement is set to grant patients in the Department of Veterans Affairs (VA) and Department of Defense (DoD) access to the SmartShot Marrow Access Device. The innovative device offers a unique solution, harnessing the body's inherent stem cells and regenerative potential to address orthopedic soft tissue injuries affecting areas like the knee, hip, shoulder, foot, and ankle.
All segments will be provided for all regions and countries covered:
Companies mentioned above DO NOT hold any order as per market share and can be changed as per information available during research work.