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Global Animal Stem Cell Therapy Market 2020 | Present Status, Share, Future Growth, Past Performance and Forecast Changing Dynamics & Plans …

Global Marketers recently added its expanding repository with a new research study. The research report, entitled Animal Stem Cell Therapy Market mainly includes a complete segmentation of this sector that is expected to generate massive returns by the end of the forecast period, showing a significant growth rate on an annual basis over the coming years. The research study also discusses the need for Animal Stem Cell Therapy Market explicitly.

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A detailed study of the competitive landscape of the Animal Stem Cell Therapy Industry Market has established, providing insights into the corporate profiles, latest developments, mergers, and acquisitions, and therefore the SWOT analysis. This breakdown report will offer a clear program to readers concerns regarding the overall market situation to further choose on this market project.

Key players profiled in the Animal Stem Cell Therapy Market report includes:

VETSTEM BIOPHARMA MediVet Biologic J-ARM Celavet Magellan Stem Cells U.S. Stem Cell Cells Power Japan ANIMAL CELL THERAPIES Animal Care Stem Cell Therapy Sciences VetCell Therapeutics Animacel Aratana Therapeutics

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Geographically, the Animal Stem Cell Therapy report includes the research on production, consumption, revenue, market share and growth rate, and forecast (2020-2026) of the following regions:

United States

Europe (Germany, UK, France, Italy, Spain, Russia, Poland)

China

Japan

India

Southeast Asia (Malaysia, Singapore, Philippines, Indonesia, Thailand, Vietnam)

Central and South America (Brazil, Mexico, Colombia)

Middle East and Africa (Saudi Arabia, United Arab Emirates, Turkey, Egypt, South Africa, Nigeria)

Other Regions

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The global Animal Stem Cell Therapy Market is expected to witness of massive growth in the next few years. The rising level of competition among the players and the increasing focus on the growth of new products are likely to offer promising growth during the forecast period. The research study on the global Animal Stem Cell Therapy Market deals with a complete overview, highlighting the key aspects that are projected to surge the growth of the market in the near future.

Animal Stem Cell Therapy Market Segmentation by Type:

Dogs Horses Others

Animal Stem Cell Therapy Market Segmentation by Application:

Veterinary Hospitals Research Organizations

What To Expect From The Report

Some Major TOC Points:

Chapter 1. Animal Stem Cell Therapy Market Report Overview

Chapter 2. Global Animal Stem Cell Therapy Growth Trends

Chapter 3. Animal Stem Cell Therapy Market Share by Key Players

Chapter 4. Breakdown Data by Type and Application

Chapter 5. Animal Stem Cell Therapy Market by End Users/Application

Chapter 6. COVID-19 Outbreak: Animal Stem Cell Therapy Industry Impact

Chapter 7. Opportunity Breakdown in Covid-19 Crisis

Chapter 9. Animal Stem Cell Therapy Market Driving Force

And Many More

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Conclusively, this report is a one-stop reference point for the industrial stakeholders to get the Free Animal Stem Cell Therapy Market to forecast of till 2026. This report helps to know the predictable market size, market status, future development, growth opportunity, challenges, and growth drivers by analysing the historical overall data of the considered market segments.

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Global Animal Stem Cell Therapy Market 2020 | Present Status, Share, Future Growth, Past Performance and Forecast Changing Dynamics & Plans ...

Lucrative Opportunities in North America to Propel the Growth of the Stem Cell Therapy Market2020 – Owned

In this report, the global Stem Cell Therapy market is valued at USD XX million in 2019 and is projected to reach USD XX million by the end of 2025, growing at a CAGR of XX% during the period 2019 to 2025.

Persistence Market Research recently published a market study that sheds light on the growth prospects of the global Stem Cell Therapy market during the forecast period (20XX-20XX). In addition, the report also includes a detailed analysis of the impact of the novel COVID-19 pandemic on the future prospects of the Stem Cell Therapy market. The report provides a thorough evaluation of the latest trends, market drivers, opportunities, and challenges within the global Stem Cell Therapy market to assist our clients arrive at beneficial business decisions.

The Stem Cell Therapy market report firstly introduced the basics: definitions, classifications, applications and market overview; product specifications; manufacturing processes; cost structures, raw materials and so on. Then it analyzed the worlds main region market conditions, including the product price, profit, capacity, production, supply, demand and market growth rate and forecast etc. In the end, the Stem Cell Therapy market report introduced new project SWOT analysis, investment feasibility analysis, and investment return analysis.

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Resourceful insights enclosed in the report:

The major players profiled in this Stem Cell Therapy market report include:

Some of the major companies operating in the global stem cell therapy market are Mesoblast Ltd., Celgene Corporation, Aastrom Biosciences, Inc. and StemCells, Inc.

Key points covered in the report

For any queries get in touch with Industry Expert @ https://www.persistencemarketresearch.co/ask-an-expert/3253

The market report addresses the following queries related to the Stem Cell Therapy market:

The study objectives of Stem Cell Therapy Market Report are:

To analyze and research the Stem Cell Therapy market status and future forecast in United States, European Union and China, involving sales, value (revenue), growth rate (CAGR), market share, historical and forecast.

To present the Stem Cell Therapy manufacturers, presenting the sales, revenue, market share, and recent development for key players.

To split the breakdown data by regions, type, companies and applications

To analyze the global and key regions Stem Cell Therapy market potential and advantage, opportunity and challenge, restraints and risks.

To identify significant trends, drivers, influence factors in global and regions

To analyze competitive developments such as expansions, agreements, new product launches, and acquisitions in the Stem Cell Therapy market.

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Lucrative Opportunities in North America to Propel the Growth of the Stem Cell Therapy Market2020 - Owned

Cell Therapy Manufacturing Market 2020 Report Including COVID-19 Impact Analysis and Forecast till 2029 – Scientect

The research study on Global Cell Therapy Manufacturing market 2019 presents an extensive analysis of current Cell Therapy Manufacturing market size, drivers, trends, opportunities, challenges, as well as key Cell Therapy Manufacturing market segments. Further, it explains various definitions and classification of the Cell Therapy Manufacturing industry, applications, and chain structure.In continuation of this data, the Cell Therapy Manufacturing report covers various marketing strategies followed by key players and distributors. Also explains Cell Therapy Manufacturing marketing channels, potential buyers and development history. The intent of global Cell Therapy Manufacturing research report is to depict the information to the user regarding Cell Therapy Manufacturing market forecast and dynamics for the upcoming years.The Cell Therapy Manufacturing study lists the essential elements which influence the growth of Cell Therapy Manufacturing industry. Long-term evaluation of the worldwide Cell Therapy Manufacturing market share from diverse countries and regions is roofed within the Cell Therapy Manufacturing report. Additionally, includes Cell Therapy Manufacturing type wise and application wise consumption figures.

The Final Report will cover the impact analysis of COVID-19 on this industry.

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After the basic information, the global Cell Therapy Manufacturing Market study sheds light on the Cell Therapy Manufacturing technological evolution, tie-ups, acquisition, innovative Cell Therapy Manufacturing business approach, new launches and Cell Therapy Manufacturing revenue. In addition, the Cell Therapy Manufacturing industry growth in distinct regions and Cell Therapy Manufacturing R&D status are enclosed within the report.The Cell Therapy Manufacturing study also incorporates new investment feasibility analysis of Cell Therapy Manufacturing. Together with strategically analyzing the key micro markets, the report also focuses on industry-specific drivers, restraints, opportunities, and challenges in the Cell Therapy Manufacturing market.

View Source of RelatedReports :

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Global Cell Therapy Manufacturing Market Segmentation 2019: The study also classifies the entire Cell Therapy Manufacturing market on basis of leading manufacturers, different types, various applications and diverse geographical regions.Overall Cell Therapy Manufacturing market is characterized by the existence of well-known global and regional Cell Therapy Manufacturing vendors. These established Cell Therapy Manufacturing players have huge essential resources and funds for Cell Therapy Manufacturing research as well as developmental activities. Also, the Cell Therapy Manufacturing manufacturers focusing on the development of new Cell Therapy Manufacturing technologies and feedstock. In fact, this will enhance the competitive scenario of the Cell Therapy Manufacturing industry.

The Leading Players involved in global Cell Therapy Manufacturing market are: harmicell, Merck Group, Dickinson and Company, Thermo Fisher, Lonza Group, Miltenyi Biotec GmBH, Takara Bio Group, STEMCELL Technologies, Cellular Dynamics International, Becton, Osiris Therapeutics, Bio-Rad Laboratories, Inc., Anterogen, MEDIPOST, Holostem Terapie Avanazate, Pluristem Therapeutics, Brammer Bio, CELLforCURE, Gene Therapy Catapult EUFETS, MaSTherCell, PharmaCell, Cognate BioServices and WuXi AppTec.

Based on Therapy Type, the Cell Therapy Manufacturing market is categorized into: Allogeneic Cell Therapy Autologous Cell Therapy

Based on Technology, the Cell Therapy Manufacturing market is categorized into: Somatic Cell Technology Cell Immortalization Technology Viral Vector Technology Genome Editing Technology Cell Plasticity Technology 3D Technology

Based on Source, the Cell Therapy Manufacturing market is categorized into: IPSCs Bone Marrow Umbilical Cord Adipose Tissue Neural Stem Cells

Based on Application, the Cell Therapy Manufacturing market is categorized into: Musculoskeletal Cardiovascular Gastrointestinal Neurological Oncology Dermatology Other

Global Cell Therapy Manufacturing Market Regional Analysis: The companies in the world that deals with Cell Therapy Manufacturing mainly concentrate following regions. North America, Europe, Asia Pacific, Latin America, and Middle East & Africa Global Cell Therapy Manufacturing Industry Report Covers following Topics: 01: Cell Therapy Manufacturing Market Overview 02: Global Cell Therapy Manufacturing Sales, Revenue (value) and Market Share by Players 03: Cell Therapy Manufacturing Market Sales, Revenue (Value) by Regions, Type and Application (2014-2018) 04: Region wise Top Players Cell Therapy Manufacturing Sales, Revenue and Price 05: worldwide Cell Therapy Manufacturing Industry Players Profiles/Analysis 06: Cell Therapy Manufacturing Cost Analysis 07: Industrial Chain, Cell Therapy Manufacturing Sourcing Strategy and Downstream Buyers 08: Cell Therapy Manufacturing Marketing Strategy Analysis, Distributors/Traders 09: Cell Therapy Manufacturing Industry Effect Factors Analysis 10: Global Cell Therapy Manufacturing Market Forecast (2019-2026) 11: Cell Therapy Manufacturing Research Findings and Conclusion 12: Appendix

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Worldwide Cell Therapy Manufacturing Market Different Analysis: Competitors Review of Cell Therapy Manufacturing Market: Report presents the competitive landscape scenario seen among top Cell Therapy Manufacturing players, their company profile, revenue, sales, business tactics and forecast Cell Therapy Manufacturing industry situations. Production Review of Cell Therapy Manufacturing Market: It illustrates the production volume, capacity with respect to major Cell Therapy Manufacturing regions, application, type, and the price.

Sales Margin and Revenue Accumulation Review of Cell Therapy Manufacturing Market: Eventually explains sales margin and revenue accumulation based on key regions, price, revenue, and Cell Therapy Manufacturing target consumer.

Supply and Demand Review of Cell Therapy Manufacturing Market: Coupled with sales margin, the report depicts the supply and demand seen in major regions, among key players and for every Cell Therapy Manufacturing product type. Also interprets the Cell Therapy Manufacturing import/export scenario.

Other key reviews of Cell Therapy Manufacturing Market: Apart from the above information, correspondingly covers the company website, number of employees, contact details of major Cell Therapy Manufacturing players, potential consumers and suppliers. Also, the strengths, opportunities, Cell Therapy Manufacturing market driving forces and market restraints are studied in this report.

Highlights of Global Cell Therapy Manufacturing Market Report: * This report provides in detail analysis of the Cell Therapy Manufacturing and provides market size (US$ Million) and Cumulative Annual Growth Rate (CAGR (%)) for the forecast period: 2019 2029. * It also elucidates potential revenue opportunity across different segments and explains attractive investment proposition matrix for world Cell Therapy Manufacturing market. * This study also provides key insights about Cell Therapy Manufacturing market drivers, restraints, opportunities, new product launches, approvals, regional outlook, and competitive strategies adopted by the leading Cell Therapy Manufacturing players. * It profiles leading players in the worldwide Cell Therapy Manufacturing market based on the following parameters company overview, financial performance, product portfolio, geographical presence, distribution strategies, key developments and strategies and future plans. * Insights from Cell Therapy Manufacturing report would allow marketers and management authorities of companies to make an informed decision with respect to their future product launches, market expansion, and Cell Therapy Manufacturing marketing tactics. * The world Cell Therapy Manufacturing industry report caters to various stakeholders in Cell Therapy Manufacturing market. That includes investors, device manufacturers, distributors and suppliers for Cell Therapy Manufacturing equipment. Especially incorporates government organizations, Cell Therapy Manufacturing research and consulting firms, new entrants, and financial analysts. *Various strategy matrices used in analyzing the Cell Therapy Manufacturing market would provide stakeholders vital inputs to make strategic decisions accordingly. Global Cell Therapy Manufacturing Market Report Provides Comprehensive Analysis of Following: Cell Therapy Manufacturing Market segments and sub-segments Industry size & Cell Therapy Manufacturing shares Cell Therapy Manufacturing Market trends and dynamics Market Drivers and Cell Therapy Manufacturing Opportunities Supply and demand of world Cell Therapy Manufacturing industry Technological inventions in Cell Therapy Manufacturing trade Cell Therapy Manufacturing Marketing Channel Development Trend Global Cell Therapy Manufacturing Industry Positioning Pricing and Brand Strategy Distributors/Traders List enclosed in Positioning Cell Therapy Manufacturing Market.

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Moreover, the report organizes to provide essential information on current and future Cell Therapy Manufacturing market movements, organizational needs and Cell Therapy Manufacturing industrial innovations. Additionally, the complete Cell Therapy Manufacturing report helps the new aspirants to inspect the forthcoming opportunities in the Cell Therapy Manufacturing industry. Investors will get a clear idea of the dominant Cell Therapy Manufacturing players and their future forecasts.

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Cell Therapy Manufacturing Market 2020 Report Including COVID-19 Impact Analysis and Forecast till 2029 - Scientect

Cell Therapy Market Opportunities, Threats, Trends, Applications, And Growth Forecast To 2027 | MEDIPOST, Osiris Therapeutics, NuVasive, Cells for…

A new market report by The Insight Partners on the Cell Therapy Market has been released with reliable information and accurate forecasts for a better understanding of the current and future market scenarios. The report offers an in-depth analysis of the global market, including qualitative and quantitative insights, historical data, and estimated projections about the market size and share in the forecast period. The forecasts mentioned in the report have been acquired by using proven research assumptions and methodologies. Hence, this research study serves as an important depository of the information for every market landscape. The report is segmented on the basis of types, end-users, applications, and regional markets.

Cell therapy (CT) is the process of transplanting human cells to replace or repair damaged tissue or cells. Various methods can be used to carry out cell therapy. For instance, hematopoietic stem cell transplantation, also known as bone marrow transplant, is the most widely used cell therapy. It is used to treat a variety of blood cancers and blood-related conditions.

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Key companies Included in Cell Therapy Market:-

Kolon TissueGene, Inc. MEDIPOST JCR Pharmaceuticals Co. Ltd. Stemedica Cell Technologies, Inc. Osiris Therapeutics, Inc. NuVasive, Inc. Fibrocell Science, Inc. Vericel Corporation Cells for Cells Celgene Corporation

The global cell therapy market is segmented on the basis of therapy type, product, technology, application, end user. Based on the therapy type the market is classified as autologous, and allogeneic. Based on product the market is segmented as equipment, consumables, software and services. Based on technology the market is segmented as somatic cell technology, cell immortalization technology, viral vector technology, genome editing technology, cell plasticity technology, and three-dimensional technology. Based on application the market is classified as oncology, cardiology, orthopedic, wound management and others. And based on end user the market is divided into hospitals, regenerative medicine centers, and research institutes.

The report offers key drivers that propel the growth in the global Cell Therapy Market. These insights help market players in devising strategies to gain market presence. The research also outlined the restraints of the market. Insights on opportunities are mentioned to assist market players in taking further steps by determining the potential in untapped regions.

Due to the pandemic, we have included a special section on the Impact of COVID 19 on the Cell Therapy Market which would mention How the Covid-19 is Affecting the Disposable Incontinence Products (DIPs) Industry, Market Trends and Potential Opportunities in the COVID-19 Landscape, Covid-19 Impact on Key Regions and Proposal for Disposable Incontinence Products (DIPs) Players to fight Covid-19 Impact.

Cell Therapy Market: Regional analysis includes:

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Note: Access insightful study with over 150+ pages, list of tables & figures, profiling 10+ companies.

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Cell Therapy Market Opportunities, Threats, Trends, Applications, And Growth Forecast To 2027 | MEDIPOST, Osiris Therapeutics, NuVasive, Cells for...

Grandad and grandson both diagnosed with rare forms of blood cancer – Metro.co.uk

Ted Peel and grandson Romain have both been diagnosed with rare blood cancers (Pictures: MDS UK)

A grandfather and his grandson are set to receive stem cell transplants within weeks of each other after they were both diagnosed with rare forms of blood cancer.

Ted Peel, 71, and his grandson Romain, 18, have faced agonising waits to access the treatment but are now being admitted into hospital at almost the same time for the life-changing procedure.

Retired policeman Ted, whose own grandfather also suffered from a form of the disease, was diagnosed with Myelodysplastic Syndromes (MDS) in 2015 after feeling extremely tired and coughing up blood.

Hes been hospitalised three times with sepsis and at one point his body temperature plummeted to 32C,five degrees lower than average.

Romain, who lives near his grandad in Dover, Kent, began suffering from migraines and fatigue while studying for his A Levels and was prescribed pain medication because doctors thought it was exam stress.

But his condition deteriorated and he received a diagnosis of Acute Lymphoblastic Leukaemia (ALL) in September 2019.

Ted, who is the chairman of MDS UK, a charity set up to support those with blood cancer, told Metro.co.uk: Its been a very difficult time for the family but this is the only type of cure available to both of us and we know we are in the best hands.

When I look at the doctors and nurses in the hospital, I know I am very lucky to be surrounded by such dedicated people and it is the same for Romain.

Ted believes he is one of the oldest people to go in for a stem cell transplant in the UK and his treatment was originally scheduled for the spring but this was postponed due to the coronavirus pandemic.

He was told in July that he was going to be admitted to Kings College Hospital imminently as cases of Covid 19 in London have decreased.

Science-fan Romain is already in hospital just down the road at the Royal Marsden for his treatment. Hes previously had six months of chemotherapy but doctors discovered he had a Philadelphia (Ph+) malignancy which makes this form of treatment much less effective.

He said: Although my specific mutation complicates my treatment, I was really interested in the genetics behind it. Ive learnt a lot going through my diagnosis and treatment.

It was a scary situation, but I was mentally prepared for it. Im aware that most Ph+ cases result in a transplant to prevent relapse scenarios.

Romains 16-year-old sister Sidonie, who today received her GCSE results, was a 12/12 match and donated some of her stem cells to be transfused to her brother.

Ted said: At the moment he is very up and down, Im sure I will be the same. We talk a lot and he tells me what he wants to do when he gets out of hospital. He wants to study science at university and become a doctor.

Hes a very logical person. he knows exactly what his condition is and what is happening. We are keeping everything crossed for him.

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Researchers have identified genes that cause a predisposition to developing forms of blood cancer and believe that, in rare cases, these can be inherited.

The pair are using their experiences to try to encourage others to become stem cell donors and raise money for MDS UK and the Teenage Cancer Trust.

Ted is having to rely on a donor from America because of the shortage of people willing to donate in the UK.

He says his experience with the charity has shown him the tragic consequences of this lack of donors, and has lost several close friends.

He said: We urge more people to become stem cell donors, especially those from ethnic minority communities. We would like to see a future where every blood cancer patient has a donor available and where cost is not an inhibiting factor.

Get in touch with our news team by emailing us at webnews@metro.co.uk.

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Grandad and grandson both diagnosed with rare forms of blood cancer - Metro.co.uk

A bright future for genomics and gene therapy in the UK – Health Service Journal

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So-called scientific breakthroughs are often in the headlines, but in reality, ground-breaking medical innovations adhere to a slow process characterised by cautious clinical experimentation and gradual but continuous improvement before reaching patients. After years of effort, gene therapy looks set to become a routine medical approach to address serious unmet medical need.

Sponsored by

There are two types of gene therapy approved for commercial use today. The first, in vivo, uses a modified virus, administered directly into the body to correct the target cells original genetic defect. The second, ex vivo, takes the patients own cells away from their body for genetic modification with a virus and then puts them back into the patient. Ex vivo gene therapy is dominated by two cell types; CD34+ haematopoietic stem cells (bone marrow stem cells) that can be modified to correct certain genetic disorders, and cytotoxic T-cells that can be altered and trained to kill cancerous cells.

The cell and gene therapy industry in the UK is supported by the formation and growth of many companies with promising assets in clinical development. This thriving biotech community is also supported by a robust and prosperous contingent of specialist manufacturing companies. These companies were key to the recent national covid-19 vaccine manufacturing response because the process for making genetically modified adenovirus such as the SARs-COV-02 vaccine, (as developed at the Oxford University Jenner Institute), is very similar to the process for making viruses for gene therapy.

UK leadership in gene therapy is no accident. As specified in our National Industrial Strategy, the UKs many research councils, in particular the Medicines Research Council, are active in funding the development and translation of treatments. In the UK right now, there are approximately 127 clinical trials testing new cell and gene therapy medicines, which represents 12 per cent of the global total. The government is readying the NHS to support these trials and transition these treatments into more common use through funding of the Advanced Therapy Treatment Centres (ATTC), a multiyear multi-million-pound project coordinated by the Cell and Gene Therapy Catapult and comprising centres of excellence throughout the UK.

In the UK right now, there are approximately 127 clinical trials testing new cell and gene therapy medicines, which represents 12 per cent of the global total. The government is readying the NHS to support these trials

The ATTCs aim to develop and harmonise adoption of the one and done treatment paradigm by developing the appropriate frameworks and systems to support clinical adoption of these novel therapies. The ATTCs and the NHS are also working in partnership to develop novel medicines assessment and reimbursement paradigms which fairly recognise the ultra-long-term medical benefits that can accrue from a one-time gene therapy treatment. Increased adoption of gene therapy, which is proving to be an approach that can reduce the long-term healthcare burden of chronic disease management, has the potential to significantly lighten the NHS resources required for support of several chronic conditions.

As a future example of the UK commitment to gene therapies, we are also leading the practical application of genetic sequencing (genomics). Formation of the National Genomic Test Directory and support for the 100,000 genomes project by Genomics England are critical steps to improve the diagnosis of patients and identification of a new wave of one-off treatments that could be capable of delivering long-term clinical benefit.

Cell and gene therapies are a revolution in medicine and have even been described as the future of the healthcare system. When you consider that 80 per cent of rare diseases have a genetic component, these treatments could transform the prospects of thousands of people living with these conditions, creating a more economically sustainable and brighter future for them and their families.

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A bright future for genomics and gene therapy in the UK - Health Service Journal

Stem Cell Therapy Market by Treatment,Application,End Users and Geography Forecast To 2026 – Good Night, Good Hockey

Stem Cell Therapy Marketis expected to reach 202.77 billion by 2026 from XX billion in 2018 at CAGR of XX %. REQUEST FOR FREE SAMPLE REPORT:https://www.maximizemarketresearch.com/request-sample/522

Stands for use of stem cells to treat or prevent disease or condition.Bone marrow transplant and some therapies derived from umbilical cord blood are mainly used in stem cell therapy. Advancement, in order to establish new sources for stem cells, and to apply stem-cell treatments for neurodegenerative diseases and conditions such as diabetes, heart disease, and other conditions, are increased in recent years.

The report study has analyzed revenue impact of covid-19 pandemic on the sales revenue of market leaders, market followers and disrupters in the report and same is reflected in our analysis.

Stem Cell Therapy Market Researchers are making efforts to discover novel methods to create human stem cells. This will increase the demand as well as supply for stem cell production and potential investigation in disease management. Increasing investment & research grants for developing safe and effective stem cell therapy products, the growing patient base for target diseases, concentrated product pipelines, increasing approval of the new clinical trials, rapid technological advancement in genomics, and the rising awareness about the stem cell are expected to drive the growth of the Stem Cell Therapy solutions market during the forecast period.

However, improper infrastructure, insufficient storage systems, nascent technology in underdeveloped economies, Ethical issues related to an embryonic stem cell, low patient acceptance rate, Difficulty in the preservation of stem cell are expected to restrain the market growth. North America is expected to be the largest growing region by 2026; the reason behind that is extensive funding by Government. However, Emerging countries like India, china, Korea have low growth rate as compared to Developed regions in 2017 but increase in awareness about stem cell therapy will lead the Asia Pacific to generate a significant level of revenue by 2026.

Key Highlights of Stem Cell Therapy Market report

Detailed quantitative analysis of the current and future trends from 2017 to 2026, which helps to identify the prevailing market opportunities. Comprehensive analysis of factors instrumental in changing the market scenario, rising prospective opportunities, market shares, core competencies in terms of market development, growth strategies and identification of key companies that can influence this market on a global and regional scale. Assessment of Market definition along with the identification of key drivers, restraints opportunities and challenges for this market during the forecast period. Complete analysis of micro-markets with respect to individual growth trends, prospects, and contributions to the overall Stem Cell Therapy Solutions market. Stem Cell Therapy market analysis and comprehensive segmentation with respect to the Application, End users, Treatment, and geography to assist in strategic business planning. Stem Cell Therapy market analysis and forecast for five major geographies-North America, Europe, Asia Pacific, Middle East & Africa, Latin America, and their key regions. For company profiles, 2017 has been considered as the base year. In cases, wherein information was unavailable for the base year, the years prior to it have been considered.

Research Methodology:

The market is estimated by triangulation of data points obtained from various sources and feeding them into a simulation model created individually for each market. The data points are obtained from paid and unpaid sources along with paid primary interviews with key opinion leaders (KOLs) in the market. KOLs from both, demand and supply side were considered while conducting interviews to get an unbiased idea of the market. This exercise was done at a country level to get a fair idea of the market in countries considered for this study. Later this country-specific data was accumulated to come up with regional numbers and then arrive at a global market value for the stem cell therapy market. Key Players in the Stem Cell Therapy Market are:

Chiesi Farmaceutici S.P.A Are: Gamida Cell ReNeuron Group, plc Osiris Therapeutics, Inc. Stem Cells, Inc. Vericel Corporation. Mesoblast, Ltd.

Key Target Audience:

Stem Cell Associations and Organizations Government Research Boards and Organizations Research and consulting firms Stem Cell Therapy Market Investors Healthcare Service Providers (including Hospitals and Diagnostic Centers) Stem Cell Therapeutic Product Manufacturing Organizations Research Labs Clinical research organizations (CROs) Stem Cell Therapy Marketing Players Pharmaceutical Product Manufacturing Companies Scope of the Stem Cell Therapy Market Report:

Stem Cell Therapy market research report categorizes the Stem Cell Therapy market based on Application, End users, Treatment, and geography (region wise). Market size by value is estimated and forecasted with the revenues of leading companies operating in the Stem Cell Therapy market with key developments in companies and market trends. Stem Cell Therapy Market, By Treatments:

Allogeneic Stem Cell Therapy Autologous Stem Cell Therapy

Stem Cell Therapy Market, By End Users:

Hospitals Ambulatory Surgical Centers

Stem Cell Therapy Market, By Application:

Oncology Central Nervous System Diseases Eye Diseases Musculoskeletal Diseases Wound & Injuries Metabolic Disorders Cardiovascular Disorders Immune System Disorders Stem Cell Therapy Market, By Geography:

North America Europe Asia Pacific Middle East & Africa Latin America

Available Customization:

With the given market data, Maximize Market Research offers customization of report and scope of the report as per the requirement

Regional Analysis:

Breakdown of the North America stem cell therapy market Breakdown of the Europe stem cell therapy market Breakdown of the Asia Pacific stem cell therapy market Breakdown of the Middle East & Africa stem cell therapy market Breakdown of the Latin America stem cell therapy market

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Stem Cell Therapy Market by Treatment,Application,End Users and Geography Forecast To 2026 - Good Night, Good Hockey

Diabetic patients may find ray of hope in stem cell treatment – The News International

Diabetic patients may find ray of hope in stem cell treatment

TOKYO: Diabetic patients may find a treatment after scientists developed a new technique that grows insulin-producing cells and can protect them from immune attack after they are transplanted.

In type-1 diabetes, the body turns on itself and attacks the so-called beta cells inside clusters in the pancreas called "islets".

These beta cells are responsible for gauging sugar levels in the blood and releasing insulin to keep them stable. Without them, diabetics must rely on insulin injections or pumps.

One treatment devised to end that reliance involves transplanting donor islets into diabetics, but the process is complicated by several obstacles, including a shortage of donors.

Islets also often fail to connect with blood supply, and even when they do, like other transplants, they can come under attack by the recipient's immune system, which views the cells as invaders.

As a result, patients have to take drugs that suppress their immune systems, protecting their transplant but potentially exposing the rest of their body to illness.

In a bid to overcome some of these challenges, a team looked to find another source for islets, by coaxing induced pluripotent stem cells (iPS) to produce what the team called HILOs, or human islet-like organoids.

These HILOs, when grown in a 3D environment mimicking the pancreas and then turbocharged with a "genetic switch", successfully produced insulin and were able to regulate blood glucose when transplanted into diabetic mice.

"In the past, this functionality was only achieved after a month-long maturation in a living animal," said Ronald Evans, director of the Gene Expression Lab at the Salk Institute for Biological Studies.

"This breakthrough allows for the production of functional HILOs which are active on the first day of transplantation, placing us closer to clinical applications," Evans, who led the study, told AFP.

Giving hope

Having found a potential way to solve the supply chain problem, the scientists then sought to tackle the issue of immune rejection.

They focused on something called PD-L1, a so-called checkpoint protein that is known to inhibit the body's immune response.

In cancer treatments, medication is sometimes used to block PD-L1, boosting the body's immune response to cancer cells.

The team effectively reversed that process, and induced the HILOs to express the protein in a bid to outwit the immune system.

"Normally, human cells placed in a mouse would be eliminated within a day or two," said Evans.

"We discovered a way to create an immune shield that makes human cells invisible to the immune system."

While HILOs transplanted into mice without the PD-L1 protection gradually stopped functioning, those induced to express the protein were shielded and continued to help diabetic mice regulate their blood glucose for more than 50 days.

Being able to grow insulin-producing cells and protect them from attack "brings us much closer to having a potential therapy for type-1 diabetic patients," Evans said.

Around 422 million people worldwide were living with diabetes by 2014, according to the World Health Organization, a figure that includes both type-1 and type-2 diabetes.

Islet transplantation is generally considered as a treatment for type-1 diabetics, whose disease is the result of an auto-immune response.

Evans cautioned that the research, already a decade in the making, was still years from being able to treat diabetes in humans.

"To advance HILOs into the clinic, we need to confirm that they work in other animal models, including primates, as well as do longer-term studies in mice," he said.

He hopes that human studies of the technique will be possible in two to five years.

"This is a hard-to-manage disease and insulin is not a cure," he added, noting that 1.6 million children and teenagers are living with type-1 diabetes in the United States alone.

"Good science is not just a discovery it can enrich the world and give hope to those who live with disease."

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Diabetic patients may find ray of hope in stem cell treatment - The News International

Shielded Stem Cells Improve The Cells’ Ability To Heal Heart Injuries – Interesting Engineering

A heart attack survivor's heart might just get fully recovered thanks to this development.

When one experiences a heart attack, it is not certain whether they will fully recover or not. Even if the survivor goes back to his regular life, physical restrictions might be necessary due to heart scarring that occurs after the attack.

Bioengineers and surgeons fromRice University and Baylor College of Medicine (BCM) have developed a biomaterial containing stem cells to help repair the heart tissue damage that forms after a heart attack.

The research was published in the journalBiomaterials Science.

In fact, stem cells have been used to try and repair the heart tissue that was damaged before. A type of adult stem cell produced in blood marrow called mesenchymal stem cells (MSCs) was considered helpful in tissue repair. However, the immune system combatted them.

They thought the cells alone were not to correspond to the immune system.

RELATED: NEW BIOMARKER FINGERPRINT WITH AI TECHNOLOGY CAN NOW PREDICT FUTURE HEART ATTACKS

"The immune system perceives them as foreign. And so very rapidly, the immune system starts chewing at them and clearing them out." saidOmid Veiseh, one of the research leaders.

So basically what they did was to coat the stem cells with a biocompatible hydrogel capsule made of brown algae. Next, they were put in rodents, next to scarred tissue of their hearts. At the end of four weeks, the rodents with shielded stem cells healed 2.5 times better and faster compared to those with non-shielded stem cells.

Samira Aghlara-Fotovat, a graduate student and co-author of the study working in Veiseh's lab, generated 0,05-inch (1.5-millimeter) capsules that each contained around 30,000 MSCs.

"The immune system doesn't recognize our hydrogels as foreign, and doesn't initiate a reaction against the hydrogel," Veiseh added.

In fact, regulations of scarred tissues are operated by a protein called "type 5 collagen." So if one lacks the mentioned collagen or has it in small levels, it is likely that damaged tissue will have a hard time being repaired.

Have the capsules been tried on humans yet? Unfortunately, they haven't. But the thing is that encapsulation technologies designed to be compatible with immune system are already being developed for chronic diseases atSigilon Therapeutics, a Cambridge, Massachusetts-based biotech company. So it is a promising development that most probably will be used on humans soon.

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Shielded Stem Cells Improve The Cells' Ability To Heal Heart Injuries - Interesting Engineering

Steadman Philippon Research Institute (SPRI) Receives Multi-Million-Dollar Matching Grant from the National Institutes of Health – GlobeNewswire

August 20, 2020 15:02 ET | Source: Steadman Philippon Research Institute

VAIL, Colorado, Aug. 20, 2020 (GLOBE NEWSWIRE) -- Steadman Philippon Research Institute (SPRI) has been granted the prestigious Regenerative Medicine Innovation Project Investigator-Initiated Clinical Trials award from the National Institutes of Health (NIH). SPRI Chief Scientific Officer Johnny Huard, Ph.D. will serve as the principal investigator. Marc J. Philippon, M.D., who serves as managing partner of The Steadman Clinic and co-chair of SPRI and Scott Tashman, Ph.D., director of biomedical engineering at SPRI, will serve as co-principal investigators. The clinical trials are expected to begin enrolling in the Fall of 2020.

The award, administered by the National Institute of Arthritis and Musculoskeletal and Skin Diseases, ranks as one of the most significant in SPRIs history, both in size and recognition. Given the potential of regenerative medicine to enhance human health and treat disease, the United States Congress included a provision in the 21st Century Cures Act a law passed in December 2016 to accelerate medical discovery and innovation to support the NIH-established Regenerative Medicine Innovation Project (RMIP). The RMIP aims to accelerate the field by supporting clinical research on adult stem cells while promoting the highest standards for protecting patient safety during the conduct of research.

This is a really great honor for SPRI, said Dr. Huard, who first came to Vail in 2015 and has served as the director of the Center for Regenerative Sports Medicine in addition to his role as the institutes chief scientific officer. Past recipients of these RMIP awards have been Albert Einstein College of Medicine, Boston Childrens Hospital, Columbia University Health Sciences, Childrens Hospital of Philadelphia, Harvard University, University of Colorado Denver and Yale University.So, we are in very good company.

The grant anticipates over $2.8 million from the NIH and requires a 1:1 match from SPRI over the next five years, pending availability of federal funds. The clinical trials and resulting publications and reports will take place over the next five years. A generous SPRI benefactor committed to fund the first year of the match, and Dr. Huard is hopeful that with the NIH matching the funds, more philanthropists will be inspired to become involved in this groundbreaking project.

Our donors have been so generous in supporting all that we do here at SPRI, said Dr. Huard, and I am very grateful and confident that we will raise the funds necessary to complete these trials over the next five years.

The trial is entitled,The Use of Senolytic and Anti-Fibrotic Agents to Improve the Beneficial Effect of Bone Marrow Stem Cells for Osteoarthritis. Huard explains in laypersons terms:

The idea behind the trial is to delay osteoarthritis in the knee, said Huard. Our goal is to delay the need for that first knee replacement in a patient for as long as we can. Over time SPRI intends to expand this area of research to other joints including hip and shoulder.

This clinical trial is designed to determine whether senolytic and/or antifibrotic agents will improve the beneficial effect of Bone Marrow Stem Cells for the treatment of symptomatic knee osteoarthritis. The trial will include four groups, totaling 100 patients, to investigate the teams hypothesis that the use of these agents will improve patient outcomes.

One of the great things that I love about this particular clinical trial is that we are actively involving our orthopaedic surgeons and our biomotion lab staff as well, said Dr. Huard. This will truly be a team effort over the next five years.

Those world-class surgeons are led by Dr. Philippon, considered one of the worlds foremost orthopaedic surgeons. The biomotion lab is under the direction of Dr. Tashman. The contributions of these two leaders and the talented roster of surgeons, clinicians and technicians in their departments will be critical to the success of the upcoming clinical trials. SPRIs Center for Outcomes-Based Orthopaedic Research and its director Grant Dornan are also participating in this project by contributing the statistical outcomes.

Dr. Philippon is not only a world-class surgeon but he is also an innovator, added Dr. Huard. He always wants to improve and is still willing to try new things to enhance patient outcomes. Dr. Tashman is the same way. Like everyone here at SPRI and The Steadman Clinic, they are embracing the cutting-edge technology available to them and finding new and better ways to treat patients and, most importantly, reduce patients recovery time and get them back to their active lives as quickly and safely as possible.

Huard notes that the rare combination of a globally recognized research institute like SPRI and a world-class orthopaedic surgery clinic like The Steadman Clinic in the same building is one of the key factors in the awarding of this RMIP grant.

Weve got something here in Vail that many other research institutes dont have, said Huard. We have one of the worlds finest orthopaedic clinics right next door, working hand-in-hand with us every day.

Dr. Huard and Dr. Tashman along with Suzanne Liv Page, J.D., our director of grants and contracts have worked diligently to prepare and gain acceptance of this grant proposal from the NIH, said Dr. Philippon. Our surgeons here at The Steadman Clinic eagerly await the opportunity to participate in the trial. Johnny, Scott and their staff have put SPRI into position to undertake major trials and studies like this one and we are all very honored that the NIH has given SPRI this incredible opportunity.

For further information or other inquiries about The Steadman Clinic or Steadman Philippon Research Institute, contact Lynda Sampson, Vice President of External Affairs (lsampson@sprivail.org).

Link to current SPRI clinical trials - https://www.sprivail.org/about-us/clinical-trials

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Steadman Philippon Research Institute (SPRI) Receives Multi-Million-Dollar Matching Grant from the National Institutes of Health - GlobeNewswire