Press Release

Translational Regenerative Medicine Market to grow with a CAGR of 9.70% During Forecast Period

Increasing healthcare infrastructure and a supportive regulatory environment are the major drivers for the Global Translational Regenerative Medicine Market.


According to TechSci Research report, “Global Translational Regenerative Medicine Market Industry Size, Share, Trends, Competition, Opportunity and Forecast, 2018-2028
”, Global Translational Regenerative Medicine Market has valued at USD 2.72 billion in 2022 and is anticipated to witness an impressive growth in the forecast period with a CAGR of 9.63%. This can be due to collaborations and partnerships among leading companies with a diverse approach to merge the expertise of individual companies and to strengthen their position in the market.


Gene editing technologies are a group of molecular tools and techniques that enable scientists to modify the DNA of living organisms, including humans. These technologies have revolutionized the fields of genetics, biotechnology, and medicine, offering the ability to precisely add, delete, or replace genetic material within an organism's genome. TALENs (Transcription Activator-Like Effector Nucleases) are another gene editing technology that can be used to modify DNA sequences. TALENs are engineered proteins that can be programmed to recognize specific DNA sequences. When combined with a nuclease enzyme, TALENs can be used to induce double strand breaks in the DNA, which can be repaired with desired changes. Zinc Finger Nucleases (ZFNs) are customizable proteins that can be engineered to bind to specific DNA sequences. Like TALENs, they are used in combination with a nuclease enzyme to create double strand breaks in the DNA, facilitating gene editing. In addition to the above techniques, various synthetic biology tools and platforms enable the design and construction of custom genetic circuits and pathways for specific applications, such as metabolic engineering or bioproduction.


Even after approval, monitoring the long-term safety and effectiveness of regenerative therapies is crucial. Post-market surveillance helps identify any unexpected adverse events and ensures ongoing patient safety.
Ensuring that patients have access to regenerative therapies is a key aspect of translational regenerative medicine. This involves addressing issues related to affordability, reimbursement, and equitable access. Healthcare professionals involved in translational regenerative medicine require specialized training and expertise to provide these therapies safely and effectively.


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In April 2023, Institute for Regenerative Medicine Opens at Mount Sinai. The institute, which now has three additional centers, will spearhead research to promote original findings and investigate fresh approaches to treating a variety of illnesses, from leukemia to Alzheimer's disease. Generative medicine, which is the replacement, engineering, or regeneration of human cells, tissues, or organs, holds tremendous promise for the medical industry. In the future, it might be feasible to mend injured nerve cells, create a new kidney in a petri dish, or stop memory loss. Across Mount Sinai's fundamental scientific and clinical departments, the Institute will enhance and organize research and education in broad areas of regenerative biology and medicine. It will also include three centers, each of which will concentrate on a particular group of illnesses and disorders. Alper Centre for Neural Development and Regeneration, Centre for Epithelial and Airway Biology and Regeneration, and Centre for Advancement of Blood Cancer Therapies will also be part of the Institute.


Ethical and moral considerations are significant challenges in the field of global translational regenerative medicine. These considerations encompass a range of ethical dilemmas and moral questions that researchers, healthcare professionals, policymakers, and society at large must grapple with.
One of the most prominent ethical debates in regenerative medicine relates to the use of embryonic stem cells. Harvesting these cells often requires the destruction of human embryos, raising questions about the moral status of embryos and the rights of unborn life. Ensuring that patients fully understand the nature of regenerative therapies, including potential risks and benefits, is critical. Obtaining informed consent, especially in the context of experimental treatments or unproven therapies, can be complex and challenging. Regenerative therapies, especially those involving gene editing and stem cell transplantation, may carry unknown risks. Balancing the potential benefits with the safety of patients is a moral responsibility.


Global Translational Regenerative Medicine Market segmentation is based on Product type, application, and Region

Based on Product type, Global Translational Regenerative Medicine Market is segmented into Cell Based Product, Gene Therapy Product, Tissue Engineered Product. A tissue-engineered product in translational regenerative medicine refers to a biomedical product that has been created by combining living cells, biomaterials, and biologically active molecules to mimic or replace damaged or lost tissues or organs in the human body. These products are designed to promote tissue regeneration and functional restoration, making them a crucial component of regenerative medicine. Tissue-engineered products typically involve the use of various types of cells, such as stem cells, primary cells, or cell lines, depending on the specific application. These cells may be obtained from the patient's own body (autologous) or from other sources (allogeneic or xenogeneic). Scaffolds or matrices made from biomaterials are used as a structural framework to support cell attachment, growth, and tissue formation. These biomaterials are designed to be biocompatible, biodegradable, and capable of providing mechanical support. Growth factors, cytokines, and other signaling molecules are often incorporated into tissue-engineered products to stimulate cell proliferation, differentiation, and tissue regeneration. These molecules play a crucial role in promoting the desired biological responses.


Based on Region,
North America dominated the Global Translational Regenerative Medicine Market. The United States has established a regulatory framework, including the Food and Drug Administration (FDA), that has provided a pathway for the approval and commercialization of regenerative medicine products. Regulatory clarity and guidelines have attracted investment and research efforts. North America has a well-developed system for protecting intellectual property, which has encouraged innovation in the regenerative medicine field. Companies and researchers have been able to secure patents and protect their discoveries. The availability of venture capital and private equity funding in North America has attracted start-ups and emerging companies focused on regenerative medicine, driving market growth. The region has a large and aging population with a high prevalence of chronic diseases and conditions that could benefit from regenerative therapies. The demand for innovative medical solutions has contributed to the growth of the regenerative medicine market in the region.


Asia-pacific
region to fastest growth in the Global Translational Regenerative Medicine Market. The Asia-Pacific region is home to a significant portion of the world's population, including both developed and emerging economies. This large and diverse population creates a substantial patient base for regenerative medicine therapies. Like many other parts of the world, APAC has an aging population with a higher prevalence of age-related diseases and conditions. This demographic shift drives the demand for regenerative therapies that can address these health challenges. Many APAC countries have been increasing their healthcare budgets and investments in medical research and innovation. This includes funding for regenerative medicine research and development. Several countries in APAC, such as China, India, and South Korea, have rapidly growing economies. These emerging economies are investing in biotechnology and life sciences sectors, fostering innovation in regenerative medicine.


Some of the major companies operating in the
Global Translational Regenerative Medicine Market
include:

  • Astellas Pharma Inc.
  • Athersys, Inc.
  • AVITA Medical
  • Axogen Corporation
  • Gamida Cell Ltd.
  • Integra LifeSciences Corporation
  • Medtronic PLC
  • Mesoblast Ltd.
  • Novartis AG
  • Spark Therapeutics Inc.

 

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“Certain areas, particularly in North America, are projected to exert significant demand for gene therapies. The growth in the competitive landscape and the presence of well-established companies in the market, committed to enhance the overall wellbeing of people each year, are expected to contribute to a remarkable growth of the Global Translational Regenerative Medicine Market in the forecast period," said Mr. Karan Chechi, Research Director with TechSci Research, a research-based Global management consulting firm.


Translational Regenerative Medicine Market – Global Industry Size, Share, Trends, Opportunity, and Forecast, 2018-2028, Segmented by Product Type (Cell Based Product, Gene Therapy Product, Tissue Engineered Product), by Application (Cardiovascular, Dermatology, Diabetes, Neurology, Oncology, Orthopedic), by region, and Competition
evaluated the future growth potential of Global Translational Regenerative Medicine Market and provides statistics & information on market size, structure, and future market growth. The report intends to provide innovative market intelligence and help decision makers take sound investment decisions. Besides, the report also identifies and analyzes the emerging trends along with essential drivers, challenges, and opportunities in Global Translational Regenerative Medicine Market.


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