#Graft Versus Host Disease Market Treatment
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Graft Versus Host Disease (GvHD) Treatment Market Types Applications Products Share Growth Insights And Forecasts Report 2032
The global Graft Versus Host Disease (GvHD) Treatment Market is expected to secure US$ 5,655.37 Million in 2032 while expanding at a CAGR of 8.3%.
Graft versus Host disease occurs after a stem cell or bone marrow transplant. High dose treatment destroy cancer cells along with that it simultaneously destroys healthy cells. Stem cell and bone marrow transplant treatments are used in reconstructing damaged cells, surrounding cancer tumors.
Normally after high dose treatment, patient receives bone marrow from a donor through drip which resumes production of blood cells. Graft versus Host Disease occurs when certain types of white blood cells. This is caused due to the transplanted cells (graft) see recipient’s body (host) as exotic, thus transplanted cells attack the host body.
It is tough to diagnose who might develop GvHD after a transplant. Mild form of GvHD is observed in few cases. While in certain cases GvHD may be fatal. GvHD do not occur when recipient receives their own cells through autologous transplant. Prior to a transplant, cells from possible donors are screened to realize how strictly they match the recipient. Chances of GvHD are reduced, or symptoms will be milder, when the match is close.
There are two forms of GvHD:
Acute graft versus host disease (aGvHD).
Chronic graft versus host disease (cGvHD).
Graft Versus Host Disease (GvHD) Treatment Market: Drivers and Restraints
Presently, graft versus host disease (GvHD) market is driven by increase in number of incidence and prevalence of cancer patients which are treated by chemotherapy treatment. Graft versus host disease (GvHD) global market is also fueled by increase in number of bone marrow transplants been carried around the globe to treat specific types of cancers.
Increase in allogeneic hematopoietic stem cell transplant will play key role in global market for graft versus host disease (GvHD). However, cost linked with recent clinical trials and authorizations would acts as a major restraint for graft versus host disease (GvHD) global market.
Graft versus Host Disease (GvHD) Treatment Market: Overview
The global market graft versus host disease (GvHD) treatment is expected to register a healthy CAGR during the forecast period. Innovative development of novel technologies, and increase in the number of cancer patients seeking for chemotherapy treatment is expected to drive the growth of graft versus host disease (GvHD) treatment market in the forecast period (2016-2026).
Graft versus Host Disease (GvHD) Treatment Market: Key Players
Some of the key participating global players in graft versus host disease (GvHD) treatment global market are Sanofi, Novartis AG, Neovii Biotech GmbH, Merck & Co., Astellas Pharma Inc., Soligenix, Inc., Mesoblast Ltd and others.
The research report presents a comprehensive assessment of the market and contains thoughtful insights, facts, historical data, and statistically supported and industry-validated market data. It also contains projections using a suitable set of assumptions and methodologies. The research report provides analysis and information according to categories such as market segments, geographies, types, technology and applications.
Key Segments Profiled In The Global Graft Versus Host Disease (Gvhd) Treatment Market
Graft Versus Host Disease (GvHD) Treatment Market by Product:
Monoclonal antibodies Graft Versus Host Disease (GvHD) Treatment
mTOR inhibitors Graft Versus Host Disease (GvHD) Treatment
Tyrosine kinase inhibitors Graft Versus Host Disease (GvHD) Treatment
Thalidomide Graft Versus Host Disease (GvHD) Treatment
Etanercept Graft Versus Host Disease (GvHD) Treatment
Graft Versus Host Disease (GvHD) Treatment Market by Disease:
Acute Graft Versus Host Disease (a(GvHD))
Chronic Graft Versus Host Disease (c(GvHD))
Graft Versus Host Disease (GvHD) Treatment Market by Region:
North America Graft Versus Host Disease (GvHD) Treatment Market
Latin America Graft Versus Host Disease (GvHD) Treatment Market
Europe Graft Versus Host Disease (GvHD) Treatment Market
Asia Pacific Graft Versus Host Disease (GvHD) Treatment Market
Middle East & Africa Graft Versus Host Disease (GvHD) Treatment Market
#Graft Versus Host Disease (GvHD) Treatment Market Market#Graft Versus Host Disease (GvHD) Treatment Market Market Size#Graft Versus Host Disease (GvHD) Treatment Market Market Growth
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Understanding Chronic Graft-versus-Host Disease: Causes, Symptoms, and Diagnosis
The global Chronic Graft-versus-Host Disease (cGvHD) market size reached USD 3.5 Billion in 2021 and is expected to register a revenue CAGR of 13.3% during the forecast period, according to the latest analysis by Emergen Research. Increasing number of allogenic transplants such as bone marrow transplants, rising regulatory approvals for the treatment of Graft Versus Host Disease (GvHD) as well as increase in prevalence of nephrological leukemia, myeloma, and other forms of cancer are some of the key factors driving revenue growth of the chronic graft-versus-host disease market.
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Competitive Terrain:
The global Chronic Graft versus Host Disease industry is highly consolidated owing to the presence of renowned companies operating across several international and local segments of the market. These players dominate the industry in terms of their strong geographical reach and a large number of production facilities. The companies are intensely competitive against one another and excel in their individual technological capabilities, as well as product development, innovation, and product pricing strategies.
The leading market contenders listed in the report are:
Merck KGaA, Sanofi S.A., Novartis AG, Bristol-Myers Squibb Company, Pfizer, Inc., F. Hoffman-La Roche Ltd, Eli Lilly and Company, Johnson & Johnson, Abbott Laboratories, and Takeda Pharmaceutical Company Limited
Key market aspects studied in the report:
Market Scope: The report explains the scope of various commercial possibilities in the global Chronic Graft versus Host Disease market over the upcoming years. The estimated revenue build-up over the forecast years has been included in the report. The report analyzes the key market segments and sub-segments and provides deep insights into the market to assist readers with the formulation of lucrative strategies for business expansion.
Competitive Outlook: The leading companies operating in the Chronic Graft versus Host Disease market have been enumerated in this report. This section of the report lays emphasis on the geographical reach and production facilities of these companies. To get ahead of their rivals, the leading players are focusing more on offering products at competitive prices, according to our analysts.
Report Objective: The primary objective of this report is to provide the manufacturers, distributors, suppliers, and buyers engaged in this sector with access to a deeper and improved understanding of the global Chronic Graft versus Host Disease market.
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Market Segmentations of the Chronic Graft versus Host Disease Market
This market is segmented based on Types, Applications, and Regions. The growth of each segment provides accurate forecasts related to production and sales by Types and Applications, in terms of volume and value for the period between 2022 and 2030. This analysis can help readers looking to expand their business by targeting emerging and niche markets. Market share data is given on both global and regional levels. Regions covered in the report are North America, Europe, Asia Pacific, Latin America, and Middle East & Africa. Research analysts assess the market positions of the leading competitors and provide competitive analysis for each company. For this study, this report segments the global Chronic Graft versus Host Disease market on the basis of product, application, and region:
Segments Covered in this report are:
Treatment Type Outlook (Revenue, USD Billion; 2019-2030)
Corticosteroids
mTOR inhibitors
Tyrosine Kinase Inhibitors (TKIs)
Monoclonal Antibodies
Photopheresis light treatment (ECP)
Others
Distribution Channel Outlook (Revenue, USD Billion; 2019-2030)
Hospitals Pharmacies
Retail Pharmacies
Online Pharmacies
Regional Outlook (Revenue, USD Billion; 2019-2030)
North America
U.S.
Canada
Mexico
Europe
Germany
France
U.K.
Italy
Spain
Benelux
Rest of Europe
Asia Pacific
China
India
Japan
South Korea
Rest of APAC
Latin America
Brazil
Rest of LATAM
Middle East & Africa
Saudi Arabia
U.A.E.
South Africa
Turkey
Rest of MEA
Browse Full Report Description + Research Methodology + Table of Content + Infographics@ https://www.emergenresearch.com/industry-report/chronic-graft-versus-host-disease-market
Major Geographies Analyzed in the Report:
North America (U.S., Canada)
Europe (U.K., Italy, Germany, France, Rest of EU)
Asia Pacific (India, Japan, China, South Korea, Australia, Rest of APAC)
Latin America (Chile, Brazil, Argentina, Rest of Latin America)
Middle East & Africa (Saudi Arabia, U.A.E., South Africa, Rest of MEA)
ToC of the report:
Chapter 1: Market overview and scope
Chapter 2: Market outlook
Chapter 3: Impact analysis of COVID-19 pandemic
Chapter 4: Competitive Landscape
Chapter 5: Drivers, Constraints, Opportunities, Limitations
Chapter 6: Key manufacturers of the industry
Chapter 7: Regional analysis
Chapter 8: Market segmentation based on type applications
Chapter 9: Current and Future Trends
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Exosome Therapeutics Market Will Grow At Highest Pace Owing To Increasing R&D Investments
Exosome therapeutics involves isolation and characterization of exosomes from various sources like mesenchymal stem cells, immune cells etc and its use in regenerative and immune modulating therapies. Exosomes are being explored as potential delivery vehicles for drugs, genes and other biomolecules owing to their ability to deliver their cargo to specific target sites via surface ligands.
The Exosome Therapeutics Market is estimated to be valued at US$ 32.1 Mn in 2024 and is expected to exhibit a CAGR of 41% over the forecast period 2024-2031.
Key Takeaways
Key players operating in the exosome therapeutics are Aegle Therapeutics,Coya Therapeutics,Evox Therapeutics,Nano 24,ReNeuron. Major players are actively investing in R&D to develop exosome-based treatments for various disease indications such as cancer, neurological disorders. Growing research interest in exploring exosome’s potential role in intercellular communication and biomarker discovery is fueling the demand. Advancements in isolation and characterization methods are enabling better understanding of exosome content and functional impact which is crucial for development of exosome-based clinical applications.
Market Trends
Two major trends driving the exosome therapeutics market are development of exosome isolation techniques and use of mesenchymal stem cell derived exosomes. Significant improvements have been made in development of efficient exosome isolation methods such as ultracentrifugation, size-exclusion chromatography, precipitation, and filtration. These techniques enable high yield and purity isolation which is critical for clinical and research applications. Mesenchymal stem cell derived exosomes possess immuno-regulatory and regenerative properties and are being explored for treatment of conditions such as graft versus host disease, myocardial infarction, lung fibrosis among others.
Market Opportunities
One of the key opportunities is potential use of exosomes as drug delivery vehicles. Exosomes have emerged as attractive drug delivery system due to their natural composition, ability to cross biological barriers and selectively target cells via surface ligands. Exosomes loaded with drugs, proteins or nucleic acids offers safer and more targeted delivery compared to other nanocarriers. Developing exosome-based diagnostics represents another major opportunity. Exosome content profiling can provide valuable insights into various disease states and help develop non-invasive liquid biopsy tests. Significant funding from government and private players is helping advance the promising field of exosome therapeutics.
Impact Of COVID-19 On Exosome Therapeutics Market Growth
The outbreak of COVID-19 pandemic has adversely impacted the growth of exosome therapeutics market globally. Major reasons being restrictions on research activities, disruptions in supply chain and delay in new product launches. During pre-COVID times, the market was growing at a steady pace due to ongoing clinical trials and discovery of new exosome-based therapeutics for various diseases like cancer, diabetes etc. However, post COVID, the market experienced slowdown initially in 2020 due to lockdowns imposed worldwide. Laboratories conducting R&D activities were temporarily shut down impacting overall progress.
Availability of raw materials from overseas suppliers was also hampered globally affecting manufacturing operations of key players. Various clinical trials involving exosome therapeutics had to be either postponed or conducted virtually. The pandemic resulted in diversion of research focus as well as funds towards developing COVID-19 vaccines and therapeutics. Though challenges persisted in initial months, the market is recovering gradually as restrictions are being lifted. Companies are resuming operations with COVID appropriate measures and accelerating clinical research. Telehealth and remote monitoring is also helping drive clinical trials. Going forward, continued investment in R&D, innovations and strategic collaborations would be crucial for the industry to capitalize on the potential of exosome therapeutics.
Geographical Regions With Highest Concentration Of Exosome Therapeutics Market
In terms of value, North America region holds the major share of global exosome therapeutics market, accounting for over 40% share. Presence of top players, ongoing clinical research and availability of latest technologies/infrastructure are driving the market in the region. Within North America, United States represents the largest and fastest growing market. Europe is another lucrative region occupying around 30% share backed by increasing government funding for exosome research. Other emerging regions like Asia Pacific and Latin America are also witnessing rising focus by players to tap growth opportunities.
Fastest Growing Region In Exosome Therapeutics Market
Asia Pacific region is poised to register fastest growth in the Exosome Therapeutics Market during the forecast period. Factors such as rising healthcare expenditure, growing biotech industry, increasing collaborations between foreign players and regional research centers and expanding patient pool are fueling the market growth. Within Asia, China and India have emerged as most promising markets due to presence of skilled labor force and low-cost manufacturing advantages. Moreover, favorable regulatory framework by governments to promote local companies is attracting foreign investments in the region's exosome therapeutics domain.
Get more insights on this topic: https://www.pressreleasebulletin.com/exosome-therapeutics-market-is-estimated-to-witness-high-growth-owing-to-application-in-advanced-cell-free-therapies/
Author Bio:
Money Singh is a seasoned content writer with over four years of experience in the market research sector. Her expertise spans various industries, including food and beverages, biotechnology, chemical and materials, defense and aerospace, consumer goods, etc. (https://www.linkedin.com/in/money-singh-590844163 )
What Are The Key Data Covered In This Exosome Therapeutics Market Report?
:- Market CAGR throughout the predicted period
:- Comprehensive information on the aspects that will drive the Exosome Therapeutics Market's growth between 2024 and 2031.
:- Accurate calculation of the size of the Exosome Therapeutics Market and its contribution to the market, with emphasis on the parent market
:- Realistic forecasts of future trends and changes in consumer behaviour
:- Exosome Therapeutics Market Industry Growth in North America, APAC, Europe, South America, the Middle East, and Africa
:- A complete examination of the market's competitive landscape, as well as extensive information on vendors
:- Detailed examination of the factors that will impede the expansion of Exosome Therapeutics Market vendors
FAQ’s
Q.1 What are the main factors influencing the Exosome Therapeutics Market?
Q.2 Which companies are the major sources in this industry?
Q.3 What are the market’s opportunities, risks, and general structure?
Q.4 Which of the top Exosome Therapeutics Market companies compare in terms of sales, revenue, and prices?
Q.5 Which businesses serve as the Exosome Therapeutics Market’s distributors, traders, and dealers?
Q.6 How are market types and applications and deals, revenue, and value explored?
Q.7 What does a business area’s assessment of agreements, income, and value implicate?
*Note: 1. Source: Coherent Market Insights, Public sources, Desk research 2. We have leveraged AI tools to mine information and compile it
#Exosome Therapeutics Market Trend#Exosome Therapeutics Market Size#Exosome Therapeutics Market Information#Exosome Therapeutics Market Analysis#Exosome Therapeutics Market Demand
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Allogeneic Cell Therapy Market Trends and Opportunities: Global Outlook (2023-2032)
The allogeneic cell therapy market is projected to grow from USD 614.46 million in 2024 to USD 1,806.84 million by 2032, reflecting a compound annual growth rate (CAGR) of 13.90%.
Allogeneic cell therapy is a cutting-edge approach in regenerative medicine that involves the use of cells derived from a donor to treat a patient. Unlike autologous cell therapy, where the patient's own cells are used, allogeneic cell therapy utilizes cells from a genetically different individual of the same species. This method offers several advantages, including the ability to produce cell therapies on a larger scale, as donor cells can be expanded and banked for multiple patients. Allogeneic therapies are particularly promising in the treatment of various conditions, such as hematologic malignancies, autoimmune diseases, and degenerative disorders. One of the most well-known applications is in hematopoietic stem cell transplantation (HSCT), used to treat leukemia and lymphoma.
The primary benefit of allogeneic cell therapy lies in its potential for off-the-shelf availability, allowing for immediate treatment without the need for patient-specific cell harvesting and preparation. This can significantly reduce treatment timelines and make therapies more accessible. However, there are challenges associated with allogeneic cell therapy, including the risk of immune rejection and graft-versus-host disease (GVHD), where the donated cells attack the recipient's body. To mitigate these risks, donors are carefully selected for compatibility, and immunosuppressive therapies are often administered to patients.
Advancements in genetic engineering and immunomodulation are enhancing the safety and efficacy of allogeneic cell therapies. Techniques such as CRISPR-Cas9 are being used to modify donor cells to reduce immunogenicity and improve therapeutic outcomes. Additionally, ongoing research aims to better understand the mechanisms of immune tolerance and develop strategies to prevent adverse immune responses.
The allogeneic cell therapy market is experiencing significant growth, driven by various trending factors that are shaping its development and expansion. These factors include advancements in technology, increasing investment, regulatory progress, and growing clinical applications. Here are the key trending factors in the allogeneic cell therapy market:
Technological Advancements
Genetic Engineering: Innovations in genetic engineering, particularly CRISPR-Cas9 and other gene-editing technologies, are enhancing the safety and efficacy of allogeneic cell therapies by reducing immunogenicity and improving therapeutic outcomes.
Cell Expansion and Manufacturing: Improved techniques for cell expansion and scalable manufacturing processes are enabling the production of large quantities of high-quality allogeneic cells, making therapies more accessible and cost-effective.
Cryopreservation: Advances in cryopreservation methods are ensuring the long-term viability and functionality of allogeneic cells, allowing for the creation of cell banks and off-the-shelf availability.
Increasing Investment and Funding
Venture Capital and Private Equity: Significant investments from venture capital and private equity firms are fueling research and development in the allogeneic cell therapy space, accelerating the pace of innovation and commercialization.
Government and Institutional Funding: Government grants and funding from research institutions are supporting clinical trials and the development of new allogeneic cell therapies, contributing to market growth.
Regulatory Progress
Streamlined Approval Processes: Regulatory agencies such as the FDA and EMA are developing more streamlined approval processes for cell therapies, including expedited pathways like Breakthrough Therapy Designation and Regenerative Medicine Advanced Therapy (RMAT) designation.
Standardization and Guidelines: Efforts to establish standardized guidelines and best practices for the production, testing, and clinical use of allogeneic cell therapies are helping to ensure safety and efficacy, fostering greater acceptance and adoption.
Growing Clinical Applications
Oncology: Allogeneic cell therapies, particularly CAR-T cell therapies, are showing promise in the treatment of various cancers, including hematologic malignancies and solid tumors, driving significant market growth.
Autoimmune Diseases: Increasing research into the use of allogeneic cells for the treatment of autoimmune diseases, such as multiple sclerosis and rheumatoid arthritis, is expanding the therapeutic landscape.
Regenerative Medicine: Allogeneic cell therapies are being explored for their potential in regenerative medicine, including the repair and regeneration of tissues and organs affected by injury, disease, or aging.
Market Dynamics
Strategic Partnerships and Collaborations: Collaborations between biotech companies, pharmaceutical firms, and research institutions are accelerating the development and commercialization of allogeneic cell therapies, leveraging combined expertise and resources.
Mergers and Acquisitions: The market is witnessing a wave of mergers and acquisitions, as larger pharmaceutical companies acquire innovative biotech firms to expand their cell therapy portfolios and capabilities.
Patient and Healthcare Provider Awareness
Education and Advocacy: Increased efforts to educate healthcare providers and patients about the benefits and potential of allogeneic cell therapies are enhancing market acceptance and demand.
Clinical Trial Participation: Growing participation in clinical trials is providing valuable data on the safety and efficacy of allogeneic cell therapies, supporting their approval and integration into clinical practice.
Economic and Market Conditions
Healthcare Expenditure: Rising healthcare expenditure globally is enabling greater investment in advanced therapies, including allogeneic cell therapies.
Market Access and Reimbursement: Efforts to improve market access and reimbursement policies for cell therapies are crucial for their widespread adoption and integration into healthcare systems.
Key Player Analysis
SSM Cardinal Glennon Children’s Medical Center
Cleveland Cord Blood Center
Duke University School of Medicine
New York Blood Center
Clinimmune Labs, University of Colorado Cord Blood Bank
MD Anderson Cord Blood Bank
LifeSouth Community Blood Centers, Inc.
Bloodworks Northwest
JCR Pharmaceuticals Co., Ltd.
Sumitomo Pharma Co., Ltd.
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The allogeneic cell therapy market is highly competitive, characterized by the presence of numerous players ranging from established pharmaceutical companies to innovative biotechnology firms. The competitive landscape is shaped by advancements in technology, strategic collaborations, regulatory approvals, and a focus on expanding clinical applications. Here is an analysis of the competitive dynamics within the allogeneic cell therapy market:
Competitive Strategies
Research and Development: Companies are heavily investing in R&D to advance their allogeneic cell therapy platforms and expand their therapeutic pipelines. Innovations in gene editing, cell engineering, and manufacturing processes are key focus areas.
Strategic Collaborations and Partnerships: Collaborations between biotech firms and large pharmaceutical companies are common, enabling resource sharing, expertise exchange, and acceleration of clinical development. These partnerships often involve joint ventures, co-development agreements, and licensing deals.
Mergers and Acquisitions: The market is witnessing significant M&A activity, with larger companies acquiring smaller, innovative biotech firms to bolster their cell therapy portfolios and capabilities.
Clinical Trials and Regulatory Approvals: Gaining regulatory approval through successful clinical trials is critical for market success. Companies are focusing on advancing their therapies through various phases of clinical trials to demonstrate safety and efficacy.
Expansion of Manufacturing Capabilities: Ensuring scalable and cost-effective manufacturing processes is essential for commercial success. Companies are investing in state-of-the-art manufacturing facilities and adopting single-use technologies to enhance production efficiency and flexibility.
Market Dynamics
Technological Advancements: Innovations in CRISPR-Cas9, TALENs, and other gene-editing technologies are driving the development of more precise and effective allogeneic cell therapies. Improvements in cryopreservation and cell expansion techniques are also enhancing the market.
Regulatory Landscape: Navigating the complex regulatory environment is a significant aspect of market competition. Companies that achieve early regulatory approvals gain a competitive advantage by being first to market.
Therapeutic Diversification: While oncology remains a primary focus, companies are also exploring applications in autoimmune diseases, regenerative medicine, and infectious diseases. Diversifying therapeutic applications can provide a competitive edge.
Patient Access and Reimbursement: Ensuring broad patient access and favorable reimbursement policies is crucial for market penetration. Companies are working to establish value-based pricing models and secure reimbursement from healthcare payers.
Competitive Challenges
Immune Rejection and Safety: Overcoming immune rejection and ensuring the safety of allogeneic cell therapies are significant challenges. Companies are investing in research to develop strategies that minimize immunogenicity and enhance immune tolerance.
High Development Costs: The high costs associated with the development, manufacturing, and clinical testing of allogeneic cell therapies can be a barrier, particularly for smaller biotech firms.
Market Competition: Intense competition from both established players and new entrants necessitates continuous innovation and differentiation to maintain market position.
Segments:
Based on Therapy Type
Stem Cell Therapies
Hematopoietic Stem Cell Therapies
Mesenchymal Stem Cell Therapies
Non-stem Cell Therapies
Keratinocytes & Fibroblast-based Therapies
Others
Based on Therapeutic Area
Hematological Disorders
Dermatological Disorders
Others
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The Rise of Tech-Driven Therapies: Reshaping the Global Graft Versus Host Disease (GvHD) Treatment Market
The global Graft Versus Host Disease (GvHD) Treatments market is set for robust growth, with projections indicating it will reach a valuation of USD 5,960.7 million by 2033. This expansion is expected to occur at a compound annual growth rate (CAGR) of 8.2%.
In 2023, the GvHD treatment market is valued at approximately USD 2,713.6 million. This growth trajectory has been consistent, reflecting an 8.2% CAGR from 2018 to 2022. The market’s steady ascent is attributed to the increasing adoption of corticosteroids and combination therapies for treating graft-versus-host disease in hematopoietic cell transplant (HCT) patients.
Allogeneic hematopoietic cell transplantation (HCT), commonly referred to as stem cell transplantation, is associated with a potentially lethal side effect called Graft Versus Host Disease (GvHD). The global market for GvHD treatments is expanding quickly as a result of improvements in treatment choices and the rising incidence of GvHD.
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In December 2021, the US Food and Drug Administration approved Orencia (abatacept) for the management of GVHD in both adult and pediatric patients. Orencia is used to avoid autoimmune diseases as well as treat them. Through specific attachment to and modification of one of the key costimulation signals sent by these cells, this medicine circumvents the attack of T-cells, which are essential in acute GVHD.
As a result, T-cells are prevented from fully activating, hence preventing acute (GVHD). Surgeons are evaluating several new approaches to prevent (GVHD) in the future.
Key Takeaways:
The global graft versus host disease (GvHD) treatment market is expected to reach US$5.96 billion by 2033, growing at a CAGR of 8.2%.
Rising adoption of combination therapies and advancements in allogeneic hematopoietic cell transplant (HCT) are key growth drivers.
Newer medications like Jakafi and Rezurock offer improved efficacy for chronic GvHD compared to traditional treatments.
Recent improvements in acute graft-versus-host disease (GVHD) severity levels and overall survival rates may be advantageous for allogeneic hematopoietic cell transplant patients; nevertheless, a number of issues still need to be resolved. Furthermore, more recent drug approvals for the prevention and treatment of chronic (GVHD) include Jakafi and Rezurock, which may be more beneficial than earlier ones.
Key Segments Profiled in Market:
By Product:
Monoclonal antibodies
mTOR inhibitors
Tyrosine kinase inhibitors
Thalidomide
Etanercept
By Disease:
Acute Graft Versus Host Disease (aGvHD)
Chronic Graft Versus Host Disease (cGvHD)
By Region:
North America
Latin America
Europe
Asia Pacific
Middle East & Africa
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Immunotherapy Drugs Market to Witness Huge Growth by 2030
Immunotherapy Drugs Market research report deals with many parameters in depth to satisfy the requirements of business or clients. Moreover, it also displays all the information including market definition, classifications, key developments, applications, and engagements along with the detailed actions of key players with respect to product launches, joint ventures, developments, mergers and acquisitions and effects of the same in terms of sales, import, export, revenue and CAGR values. A team of experienced and consummate market research professionals persistently track key industries to spot key developments, unmet needs and possible growth opportunities.
Immunotherapy Drugs Market, By Drug Type (Monoclonal Antibodies, Immunomodulators), By Indication (Infectious Diseases, Cancer) and by Region (North America, Europe, Asia-Pacific, Middle East and Africa and South America). The global Immunotherapy Drugs Market size is projected to reach a CAGR of 11.7% from 2023-2030.
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Immunotherapy drugs are used to enhance or suppress the immune system of the body. They are mostly used in the treatment of cancer and act by stimulating the immune system of the body and generating an immune response aiding the production of antibodies. Antibodies produced against antigens kill the cancerous or tumour cells.
The global immunotherapy market is driven by the increasing adoption of targeted therapies, the increase in the life span of patients, and the high prevalence of lifestyle diseases. Furthermore, rapid approval of drugs and reduction in the recurrence of diseases propel market growth. Additionally, immunotherapy as an alternative to chemotherapy and the use of immunotherapy as the first line of drug for the treatment of cancer provide growth opportunities for the market players shortly.
Immunotherapy Drugs Market Competitive Landscape:
Amgen, Inc.
Novartis AG
AbbVie, Inc.
Pfizer, Inc.
F. Hoffmann-La Roche Ltd.
Johnson & Johnson Services, Inc.
AstraZeneca
GSK
Sanofi
Bayer AG
Immunotherapy Drugs Market Recent Developments:
August 29, 2022 - AbbVie Showcases New Analyses and Real-World Data Across Multiple Immune-Mediated Skin Diseases at the European Academy of Dermatology and Venereology (EADV).
August 24, 2022 - AbbVie announced that the U.S. Food and Drug Administration (FDA) approved the use of IMBRUVICA® (ibrutinib) for the treatment of paediatric patients one year and older with chronic graft versus host disease (cGVHD) after the failure of one or more lines of systemic therapy.
Immunotherapy Drugs Market Key Findings:
Immunotherapy drugs are used to enhance or suppress the immune system of the body. They are mostly used in the treatment of cancer and act by stimulating the immune system of the body and generating an immune response aiding the production of antibodies. Antibodies produced against antigens kill the cancerous or tumour cells.
The indication segment is further fragmented into Cancer, Autoimmune Diseases, Infectious Diseases, and Others. The cancer segment accounted for the largest revenue share owing to the increased prevalence of cancer, coupled with a rise in the launch of cancer immunotherapies.
The drug type segment is further fragmented into monoclonal antibodies, immunomodulators, and vaccines. The monoclonal antibodies segment accounted for the largest share owing to increased R&D in therapeutic monoclonal antibodies coupled with supportive government initiatives.
The market is also divided into various regions such as North America, Europe, Asia-Pacific, South America, and Middle East and Africa. North America dominated the global industry and accounted for the largest share of the overall revenue. The launch and regulatory approval of new immunotherapy drugs and favourable reimbursement policies are projected to aid in the region’s growth.
Immunotherapy Drugs Market Regional Analysis:
North America to Dominate the Market
North America dominated the global industry and accounted for the largest share of the overall revenue.
The launch and regulatory approval of new immunotherapy drugs and favourable reimbursement policies are projected to aid in the region’s growth.
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Scope of the Immunotherapy Drugs Market Report:
Immunotherapy Drugs Market is segmented into various segments such as drug type, indication, and region:
On the basis of drug type
Monoclonal Antibodies
Immunomodulators
Vaccines
On the basis of the indication
Cancer
Autoimmune Diseases
Infectious Diseases
Others
On the basis of region
Asia Pacific
North America
Europe
South America
Middle East & Africa
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Precision in Transplantation: Navigating the HLA Typing for Transplant Market
HLA typing, or human leukocyte antigen typing, plays a critical role in organ and tissue transplantation by assessing the compatibility between the donor and recipient immune systems. As advancements in transplantation techniques and immunogenetics continue to evolve, the HLA typing for transplant market has become increasingly vital in ensuring successful transplant outcomes and improving patient survival rates.
The human leukocyte antigen system, a group of proteins located on the surface of cells, plays a central role in the immune response by distinguishing between self and non-self antigens. HLA typing involves identifying and matching these HLA proteins between the donor and recipient to minimize the risk of rejection and graft-versus-host disease following transplantation.
The demand for HLA typing services is driven by the growing prevalence of end-stage organ failure, autoimmune diseases, and genetic disorders necessitating transplantation as a life-saving treatment option. Additionally, advancements in HLA typing technologies, such as next-generation sequencing and molecular testing methods, have improved the accuracy, efficiency, and turnaround time of HLA typing procedures.
HLA typing for transplantation is crucial not only in solid organ transplantation but also in hematopoietic stem cell transplantation for the treatment of hematologic malignancies and immune disorders. By accurately matching HLA alleles between donors and recipients, healthcare providers can minimize the risk of post-transplant complications and improve patient outcomes.
Furthermore, the HLA typing for transplant market is witnessing increased adoption of advanced informatics tools and software solutions for data analysis, interpretation, and reporting. These tools facilitate comprehensive HLA typing and donor-recipient matching algorithms, enabling healthcare professionals to make informed decisions and optimize transplant outcomes.
In conclusion, the HLA typing for transplant market plays a vital role in ensuring the success and viability of organ and tissue transplantation procedures. With ongoing advancements in technology and immunogenetics, HLA typing services continue to evolve, offering improved accuracy, efficiency, and personalized solutions for patients in need of life-saving transplant therapies.
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Mesenchymal Stem Cells Market is Estimated to Witness High Growth Owing to Rising Awareness About its Therapeutic Benefits
Mesenchymal stem cells are multipotent stromal cells that can differentiate into a variety of cell types, including osteoblasts, chondrocytes, and adipocytes. They are used in research and therapies for various medical conditions such as graft-versus-host disease, Crohn's disease, heart disease, diabetes, and neurological disorders.
Market Dynamics:
Rising awareness about the therapeutic benefits of mesenchymal stem cells and increasing investment in stem cell research are expected to drive the growth of the mesenchymal stem cells market during the forecast period. Mesenchymal stem cells have shown promising results for treatment of various diseases in preclinical and clinical studies. They have immunomodulatory properties and differentiation abilities that allow their use in various regenerative medicine applications.
Furthermore, absence of ethical issues associated with the use of mesenchymal stem cells, as compared to other sources of stem cells, is further expected to support market growth over the forecast period.
Mesenchymal Stem Cells Market Drivers
The growing use of mesenchymal stem cells market in regenerative medicine provides a significant growth opportunity in the market
Mesenchymal stem cells have the potential to regenerate and repair damaged tissues. They are being increasingly used in regenerative medicine applications like treatment of osteoarthritis, cardiovascular diseases, neurological diseases, etc. The robust research activity and growing clinical trials focusing on therapeutic use of MSCs are major factors driving the growth of this market. According to researchers, MSCs have shown promising results for therapies for conditions like myocardial infarction, graft-versus-host disease, Crohn's disease, etc. This is creating substantial demand for MSCs and contributing significantly to market growth.
Increasing investments in stem cell therapy and rising R&D activities
There has been a substantial rise in funding and investments for stem cell research from both public and private sources over the past decade. Government as well as private organizations are investing heavily in R&D activities focused on developing stem cell therapeutics. For instance, the National Institutes of Health (NIH) funding for stem cell research was around $1.45 billion in 2020. Similarly, private equity investments in companies focusing on stem cell therapies have risen considerably. Such increased funding and focus on R&D is supporting the ongoing clinical research as well as development of new applications of MSCs, thereby driving the growth of this market.
Mesenchymal Stem Cells Market Restrain
High costs associated with stem cell therapy and storage of cells
One of the major challenges in the widespread adoption of mesenchymal stem cells is their high treatment and storage costs. The procedure of isolating MSCs from donor tissues and culturing them on a large scale under cGMP conditions is an expensive process. Also, once harvested, MSCs must be cryopreserved for storage and future use. However, cryopreservation and long-term storage in stem cell banks is also costly. These costs often get passed on to patients in the form of high therapy charges making stem cell therapies unaffordable for many. This price sensitivity acts as a major restraint for the mesenchymal stem cells market.
Mesenchymal Stem Cells Market Opportunity
Untapped potential of mesenchymal stem cells in developing novel cell and gene therapies
While majority of current research is focused on using mesenchymal stem cells for regenerative therapies, there remains a huge untapped potential for developing novel cell-based and gene therapies. MSCs have many advantages like low immunogenicity, immunosuppressive properties and easy isolation that make them ideal candidates for applications beyond just regenerative medicine. For instance, MSCs are now being evaluated as potential drug delivery vehicles for targeted cancer therapies. Gene-modified MSCs are being studied for applications in diseases like cystic fibrosis. Overall, the ability of MSCs to serve as effective delivery vectors and assist in developing advanced cell and gene therapies presents a major market opportunity over the coming years.
Mesenchymal Stem Cells Market Trends
Rise in adoption of good manufacturing practices (GMP) for stem cell production and processing
With the growing clinical translation of stem cell therapies, quality standards for stem cell manufacturing are becoming increasingly important. Regulatory authorities worldwide are promoting the adoption of current Good Manufacturing Practices (cGMP) to ensure consistent high quality of cultured stem cell products. More players in the mesenchymal stem cells market are now following cGMP guidelines for isolation, expansion, cryopreservation and characterization of cells. This is helping improve the reproducibility and safety of stem cell products. The trend towards cGMP-compliant stem cell manufacturing using closed and automated processes is expected to continue in the future. This will enhance the therapeutic potential as well as commercial viability of various stem cell-based products.
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Hematopoietic stem cells transplantation (HSCT) market| Analysis and Forecast, 2023 – 2027
Originally published on Technavio: Hematopoietic stem cells transplantation (HSCT) market by Application, Type and Geography - Forecast and Analysis 2023-2027
The Hematopoietic Stem Cells Transplantation (HSCT) Market is poised for significant growth in the forecast period from 2023 to 2027, driven by the increasing prevalence of hematological disorders, advancements in transplantation technologies, and a growing awareness of the potential of hematopoietic stem cells (HSCs) in treating various diseases. This market analysis will explore key aspects such as applications, types of HSCT, and the geographical landscape.
**Applications:** Hematopoietic stem cell transplantation (HSCT) finds applications in the treatment of various hematological disorders, including leukemia, lymphoma, myeloma, and certain genetic blood disorders. The transplantation process involves the infusion of hematopoietic stem cells, either from a donor (allogeneic transplantation) or the patient (autologous transplantation), to replace or repair damaged bone marrow. HSCT is particularly crucial in the management of malignancies and conditions affecting the blood and immune system. The increasing understanding of the regenerative potential of hematopoietic stem cells has expanded the range of applications, with ongoing research exploring their use in non-hematological diseases, including autoimmune disorders and solid organ transplantation.
**Types of HSCT:** The HSCT market encompasses various types based on the source of hematopoietic stem cells. Autologous transplantation involves harvesting the patient's own stem cells before undergoing conditioning therapy, and subsequently reinfusing them to restore hematopoiesis. Allogeneic transplantation utilizes stem cells from a compatible donor, which may be a sibling, unrelated donor, or cord blood source. Allogeneic transplantation is advantageous in certain cases, providing a graft-versus-tumor effect against cancer cells. Umbilical cord blood transplantation involves using stem cells collected from the umbilical cord and placenta after childbirth, offering an alternative source with the potential for reduced graft-versus-host disease (GVHD) and improved accessibility.
**Geographical Landscape:** The HSCT market has a global presence, with key representation in regions such as North America, Europe, Asia-Pacific, Latin America, and the Middle East and Africa. North America, particularly the United States, holds a significant share in the market, driven by the well-established healthcare infrastructure, a high prevalence of hematological disorders, and ongoing research activities. Europe, with countries like Germany and the United Kingdom, is a mature market with advanced transplantation centers and a focus on research and development. The Asia-Pacific region, including China and India, is witnessing significant growth due to the increasing awareness of transplantation as a treatment option and improving healthcare facilities. Latin America and the Middle East and Africa regions are emerging markets, with a rising incidence of hematological disorders and efforts to enhance transplantation capabilities.
**Factors Driving Market Growth:** Several factors contribute to the anticipated growth of the HSCT Market. The rising incidence of hematological disorders, such as leukemia and lymphoma, fuels the demand for transplantation as a therapeutic option. Advancements in transplantation technologies, including improved conditioning regimens, HLA matching, and supportive care, enhance the safety and efficacy of HSCT procedures. Increased awareness among healthcare professionals and patients about the curative potential of HSCT further drives its adoption. Ongoing research exploring the use of HSCT in novel applications, such as treating autoimmune diseases and solid organ transplantation, expands the market's potential. Collaborations between research institutions, transplant centers, and pharmaceutical companies contribute to the development of innovative transplantation approaches.
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In conclusion, the Hematopoietic Stem Cells Transplantation (HSCT) Market presents a dynamic landscape with diverse applications, types, and a global footprint. The forecast period from 2023 to 2027 indicates significant growth, propelled by the increasing prevalence of hematological disorders, advancements in transplantation technologies, and the expanding understanding of the therapeutic potential of hematopoietic stem cells.
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Chronic Graft versus Host Disease Market Future Trends, Growth Factors, Strategy, Price
The global Chronic Graft-versus-Host Disease (cGvHD) market size reached USD 3.5 Billion in 2021 and is expected to register a revenue CAGR of 13.3% during the forecast period, according to the latest analysis by Emergen Research. Increasing number of allogenic transplants such as bone marrow transplants, rising regulatory approvals for the treatment of Graft Versus Host Disease (GvHD) as well as increase in prevalence of nephrological leukemia, myeloma, and other forms of cancer are some of the key factors driving revenue growth of the chronic graft-versus-host disease market.
The report focuses on current and future market growth, technological advancements, volume, raw materials, and profiles of the key companies involved in the market. The report provides valuable insights to the stakeholders, investors, product managers, marketing executives, and other industry professionals.
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Competitive Terrain:
The global Chronic Graft versus Host Disease industry is highly consolidated owing to the presence of renowned companies operating across several international and local segments of the market. These players dominate the industry in terms of their strong geographical reach and a large number of production facilities. The companies are intensely competitive against one another and excel in their individual technological capabilities, as well as product development, innovation, and product pricing strategies.
The leading market contenders listed in the report are:
Merck KGaA, Sanofi S.A., Novartis AG, Bristol-Myers Squibb Company, Pfizer, Inc., F. Hoffman-La Roche Ltd, Eli Lilly and Company, Johnson & Johnson, Abbott Laboratories, and Takeda Pharmaceutical Company Limited
Key market aspects studied in the report:
Market Scope: The report explains the scope of various commercial possibilities in the global Chronic Graft versus Host Disease market over the upcoming years. The estimated revenue build-up over the forecast years has been included in the report. The report analyzes the key market segments and sub-segments and provides deep insights into the market to assist readers with the formulation of lucrative strategies for business expansion.
Competitive Outlook: The leading companies operating in the Chronic Graft versus Host Disease market have been enumerated in this report. This section of the report lays emphasis on the geographical reach and production facilities of these companies. To get ahead of their rivals, the leading players are focusing more on offering products at competitive prices, according to our analysts.
Report Objective: The primary objective of this report is to provide the manufacturers, distributors, suppliers, and buyers engaged in this sector with access to a deeper and improved understanding of the global Chronic Graft versus Host Disease market.
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Market Segmentations of the Chronic Graft versus Host Disease Market
This market is segmented based on Types, Applications, and Regions. The growth of each segment provides accurate forecasts related to production and sales by Types and Applications, in terms of volume and value for the period between 2022 and 2030. This analysis can help readers looking to expand their business by targeting emerging and niche markets. Market share data is given on both global and regional levels. Regions covered in the report are North America, Europe, Asia Pacific, Latin America, and Middle East & Africa. Research analysts assess the market positions of the leading competitors and provide competitive analysis for each company. For this study, this report segments the global Chronic Graft versus Host Disease market on the basis of product, application, and region:
Segments Covered in this report are:
Treatment Type Outlook (Revenue, USD Billion; 2019-2030)
Corticosteroids
mTOR inhibitors
Tyrosine Kinase Inhibitors (TKIs)
Monoclonal Antibodies
Photopheresis light treatment (ECP)
Others
Distribution Channel Outlook (Revenue, USD Billion; 2019-2030)
Hospitals Pharmacies
Retail Pharmacies
Online Pharmacies
Regional Outlook (Revenue, USD Billion; 2019-2030)
North America
U.S.
Canada
Mexico
Europe
Germany
France
U.K.
Italy
Spain
Benelux
Rest of Europe
Asia Pacific
China
India
Japan
South Korea
Rest of APAC
Latin America
Brazil
Rest of LATAM
Middle East & Africa
Saudi Arabia
U.A.E.
South Africa
Turkey
Rest of MEA
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Major Geographies Analyzed in the Report:
North America (U.S., Canada)
Europe (U.K., Italy, Germany, France, Rest of EU)
Asia Pacific (India, Japan, China, South Korea, Australia, Rest of APAC)
Latin America (Chile, Brazil, Argentina, Rest of Latin America)
Middle East & Africa (Saudi Arabia, U.A.E., South Africa, Rest of MEA)
ToC of the report:
Chapter 1: Market overview and scope
Chapter 2: Market outlook
Chapter 3: Impact analysis of COVID-19 pandemic
Chapter 4: Competitive Landscape
Chapter 5: Drivers, Constraints, Opportunities, Limitations
Chapter 6: Key manufacturers of the industry
Chapter 7: Regional analysis
Chapter 8: Market segmentation based on type applications
Chapter 9: Current and Future Trends
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Advancements in Blood Irradiation Technology: Market Expectations By 2023 to 2030
The global blood irradiation market is expected to grow from US$ 1.5 billion in 2023 to US$ 2.5 billion by 2030, at a CAGR of 8.5%. The growth of the market is attributed to the increasing demand for blood irradiation to prevent transfusion-transmitted infections (TTIs), such as graft-versus-host disease (GVHD) and cytomegalovirus (CMV) infection.
Blood irradiation is the process of exposing blood to ionizing radiation to inactivate harmful pathogens, such as bacteria, viruses, and parasites. This process is used to prevent transfusion-transmitted infections (TTIs), which are serious and potentially life-threatening infections that can be transmitted to patients through blood transfusions.
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Blood irradiation market is expected to grow significantly in the coming years, driven by factors such as increasing awareness of TTIs, rising demand for blood transfusions, and growing adoption of blood irradiation technology.
Market drivers:
The key drivers of the blood irradiation market include:
Increasing awareness of TTIs: TTIs are serious and potentially life-threatening infections that can be transmitted to patients through blood transfusions. As awareness of TTIs increases, so too does the demand for blood irradiation services.
Rising demand for blood transfusions: The demand for blood transfusions is rising due to an increasing number of surgeries and medical procedures, as well as an aging population. This is driving the growth of the blood irradiation market.
Growing adoption of blood irradiation technology: Blood irradiation technology is becoming increasingly sophisticated and affordable, making it more accessible to hospitals and blood banks. This is driving the adoption of blood irradiation technology and the growth of the blood irradiation market.
Key Takeaways:
The global blood irradiation market is expected to grow from US$ 1.5 billion in 2023 to US$ 2.5 billion by 2030, at a CAGR of 8.5%.
The growth of the market is attributed to the increasing prevalence of blood-borne diseases, rising demand for blood transfusions, and technological advancements in blood irradiation devices.
North America is the largest market for blood irradiation, followed by Europe and Asia Pacific.
The key players in the blood irradiation market include Terumo Medical Corporation, Haemonetics Corporation, and Mirion Technologies, Inc.
Regional Outlook:
North America is the largest market for blood irradiation, accounting for over 35% of the global market share in 2022. The high prevalence of blood-borne diseases and the rising demand for blood transfusions in the region are the major drivers of the market growth.
Europe is the second-largest market for blood irradiation, accounting for over 30% of the global market share in 2022. The increasing prevalence of cancer and the growing number of organ transplants in the region are driving the market growth.
Asia Pacific is the fastest-growing market for blood irradiation, with a CAGR of over 6% from 2023 to 2030. The increasing prevalence of blood-borne diseases and the rising demand for blood transfusions in the region are the major drivers of the market growth.
Key Players:
Terumo Medical Corporation
Haemonetics Corporation
Mirion Technologies, Inc.
Gammacell, Inc.
Xstrahl, Inc.
Isotope Technologies, Inc.
Nuclear Associates
Rad Source Technologies
X-Ray Products Corporation
SCK CEN
MDS Nordion
Segmentation:
The blood irradiation market is segmented by product, application, and end user.
By product:
Blood irradiators
Blood irradiation indicators and labels
By application:
Prevention of transfusion-associated graft-versus-host disease (TA-GVHD)
Prevention of transfusion-transmitted infections (TTIs)
Cancer treatment
Organ transplant
By end user:
Hospitals
Blood banks
Organ transplant centers
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