Author Archives: admin


Orchard Therapeutics Announces Orphan Drug and Rare Pediatric Disease Designations for OTL-203 for the Treatment of MPS-I – GlobeNewswire

July 20, 2020 07:00 ET | Source: Orchard Therapeutics (Europe) Limited

BOSTON and LONDON, July 20, 2020 (GLOBE NEWSWIRE) -- Orchard Therapeutics (Nasdaq: ORTX), a global gene therapy leader, today announced that the company has received both orphan drug designation and rare pediatric disease designation from the U.S Food and Drug Administration (FDA) for OTL-203, anex vivoautologous hematopoietic stem cell (HSC) gene therapy in development for the treatment of mucopolysaccharidosis type I (MPS-I).

We are pleased by the FDAs acknowledgement of the critical and urgent need to develop additional treatments for MPS-I given the severe, life-limiting nature of the disease, said Bobby Gaspar, M.D., PhD., chief executive officer of Orchard. The underlying causes of lysosomal storage disorders such as MPS-I have been notably difficult to address, and we are encouraged by the early evidence of our hematopoietic stem cell gene therapys approach to potentially treating this condition. The orphan drug and rare pediatric disease designations provide important momentum for the OTL-203 clinical program, which we remain committed to advancing as quickly as possible for patients in need.

The FDA grants orphan designation, also referred to as orphan status, to drugs intended for the treatment of rare diseases that affect fewer than 200,000 people in the US.1 This designation affords Orchard certain benefits, including tax credits for qualified clinical testing, waiver or partial payment of FDA application fees and seven years of market exclusivity, if approved.2 Separately, rare pediatric disease designations are granted for rare diseases that primarily affect children under 18 years old with recipients of this designation being awarded a priority review voucher, upon approval.3 The priority review voucher may be redeemed, transferred, or sold.4

Orchard recently announced new interim data from an ongoing proof-of-concept clinical trial evaluating the safety and efficacy of OTL-203. The first primary outcome measure was met with all eight patients achieving hematologic engraftment. Additionally, improved motor skills compared to baseline, stable cognitive scores, and normal growth was seen in the first two patients with at least one year of follow-up. Orchard expects to release full proof-of-concept results and initiate the registrational study for OTL-203 in 2021.

About OTL-203 and MPS-I Mucopolysaccharidosis type I (MPS-I) is a rare, inherited neurometabolic disease caused by a deficiency of the alpha-L-iduronidase (IDUA) lysosomal enzyme, which is required to break down sugar molecules called glycosaminoglycans (also known as GAGs). The accumulation of GAGs across multiple organ systems results in symptoms including neurocognitive impairment, skeletal deformity, loss of vision and hearing, and cardiovascular and pulmonary complications. MPS-I occurs at an overall estimated frequency of one in every 100,000 live births. There are three subtypes of MPS-I; approximately 60 percent of children born with MPS-I have the most severe subtype, called Hurler syndrome, and rarely live past the age of 10 when untreated.

Treatment options for MPS-I include hematopoietic stem cell transplant and chronic enzyme replacement therapy, both of which have significant limitations. Though early intervention with enzyme replacement therapy has been shown to delay or prevent some clinical features of the condition, it has only limited efficacy on neurological symptoms. OTL-203 is an ex vivo autologous hematopoietic stem cell gene therapy being studied for the treatment of MPS-I. Orchard was granted an exclusive worldwide license to intellectual property rights to research, develop, manufacture and commercialize the gene therapy program for the treatment of MPS-I developed by the San Raffaele Telethon Institute for Gene Therapy in Milan, Italy.

About Orchard Orchard Therapeutics is a global gene therapy leader dedicated to transforming the lives of people affected by rare diseases through the development of innovative, potentially curative gene therapies. Our ex vivo autologous gene therapy approach harnesses the power of genetically modified blood stem cells and seeks to correct the underlying cause of disease in a single administration. In 2018, Orchard acquired GSKs rare disease gene therapy portfolio, which originated from a pioneering collaboration between GSK and theSan Raffaele Telethon Institute for Gene Therapy in Milan, Italy. Orchard now has one of the deepest and most advanced gene therapy product candidate pipelines in the industry spanning multiple therapeutic areas where the disease burden on children, families and caregivers is immense and current treatment options are limited or do not exist.

Orchard has its global headquarters in London and U.S. headquarters in Boston. For more information, please visit http://www.orchard-tx.com, and follow us on Twitter and LinkedIn.

Availability of Other Information About Orchard Investors and others should note that Orchard communicates with its investors and the public using the company website (www.orchard-tx.com), the investor relations website (ir.orchard-tx.com), and on social media (Twitter andLinkedIn), including but not limited to investor presentations and investor fact sheets,U.S. Securities and Exchange Commissionfilings, press releases, public conference calls and webcasts. The information that Orchard posts on these channels and websites could be deemed to be material information. As a result, Orchard encourages investors, the media, and others interested in Orchard to review the information that is posted on these channels, including the investor relations website, on a regular basis. This list of channels may be updated from time to time on Orchards investor relations website and may include additional social media channels. The contents of Orchards website or these channels, or any other website that may be accessed from its website or these channels, shall not be deemed incorporated by reference in any filing under the Securities Act of 1933.

Forward-Looking Statements This press release contains certain forward-looking statements about Orchards strategy, future plans and prospects, which are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include express or implied statements relating to, among other things, Orchards business strategy and goals, the therapeutic potential of Orchards product candidates, including the product candidate or candidates referred to in this release, and Orchards expectations regarding the timing of clinical trials and announcement of clinical data for its product candidates and the likelihood that such data will be positive and support further clinical development and regulatory approval of these product candidates. These statements are neither promises nor guarantees and are subject to a variety of risks and uncertainties, many of which are beyond Orchards control, which could cause actual results to differ materially from those contemplated in these forward-looking statements. In particular, these risks and uncertainties include, without limitation: the severity of the impact of the COVID-19 pandemic on Orchards business, including on clinical development and commercial programs; the risk that any one or more of Orchards product candidates, including the product candidate or candidates referred to in this release, will not be approved, successfully developed or commercialized; the risk of cessation or delay of any of Orchards ongoing or planned clinical trials; the risk that Orchard may not successfully recruit or enroll a sufficient number of patients for its clinical trials; the risk that prior results, such as signals of safety, activity or durability of effect, observed from preclinical studies or clinical trials will not be replicated or will not continue in ongoing or future studies or trials involving Orchards product candidates; the delay of any of Orchards regulatory submissions; the failure to obtain marketing approval from the applicable regulatory authorities for any of Orchards product candidates or the receipt of restricted marketing approvals; and the risk of delays in Orchards ability to commercialize its product candidates, if approved. Given these uncertainties, the reader is advised not to place any undue reliance on such forward-looking statements.

Other risks and uncertainties faced by Orchard include those identified under the heading "Risk Factors" in Orchards quarterly report on Form 10-Q for the quarter ended March 31, 2020, as filed with the U.S. Securities and Exchange Commission (SEC) on May 7, 2020, as well as subsequent filings and reports filed with the SEC. The forward-looking statements contained in this press release reflect Orchards views as of the date hereof, and Orchard does not assume and specifically disclaims any obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be required by law.

___________________________________ 1 316 Orphan Drug Act & 316.20-21: Verification of orphan-drug status (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=316.20)

2FDA Industry Guidance: Designating an Orphan Product: Drugs and Biological Products (https://www.fda.gov/industry/developing-products-rare-diseases-conditions/designating-orphan-product-drugs-and-biological-products)

3FDA Rare Pediatric Disease Designation Voucher Programs (https://www.fda.gov/industry/developing-products-rare-diseases-conditions/rare-pediatric-disease-rpd-designation-and-voucher-programs)

4360ff Title 21 Food and Drugs (https://www.govinfo.gov/content/pkg/USCODE-2012-title21/pdf/USCODE-2012-title21-chap9-subchapV-partB-sec360ff.pdf)

Contacts

Investors Renee Leck Director, Investor Relations +1 862-242-0764 Renee.Leck@orchard-tx.com

Media Molly Cameron Manager, Corporate Communications +1 978-339-3378 media@orchard-tx.com

Read the original here:
Orchard Therapeutics Announces Orphan Drug and Rare Pediatric Disease Designations for OTL-203 for the Treatment of MPS-I - GlobeNewswire

Growing Infrastructure Development Projects in Asia-Pacific to Fuel Growth of the Animal Stem Cell Therapy Market 2017 2025 – Bulletin Line

According to the latest report published by PMR, the Animal Stem Cell Therapy market is anticipated to grow at a steady pace over the forecast period (2019-2029). The report sheds light on the various trends and restraining factors that are expected to shape the growth of the Animal Stem Cell Therapy in the upcoming years. The report ponders over the various parameters that are expected to impact revenue generation, sales, and demand for the Animal Stem Cell Therapy in the various regional markets.

According to the study, the Animal Stem Cell Therapy market is likely to attain a market value of ~US$ XX by 2019 and grow at a CAGR of ~XX% during the assessment period. The market study introspects the competition landscape of the Animal Stem Cell Therapy market and highlights the key developments and technological innovations witnessed in the current Animal Stem Cell Therapy market landscape.

Request Sample Report @ https://www.persistencemarketresearch.co/samples/14941

Key findings of the Animal Stem Cell Therapy market report:

Animal Stem Cell Therapy Market Segmentation

The report dissects the Animal Stem Cell Therapy market into different segments to provide a fair understanding of the different aspects of the Animal Stem Cell Therapy market.

The regional analysis of the Animal Stem Cell Therapy market sheds light on the growth prospects of the Animal Stem Cell Therapy market in different regions. The current market trends, the impact of regulatory policies, market share, size, and value of each regional market are presented in the report supported by easy-to-understand graphs and tables.

Key Participants

The key participants in the animal stem cell therapy market are Magellan Stem Cells, ANIMAL CELL THERAPIES, Abbott Animal Hospital, VETSTEM BIOPHARMA, Veterinary Hospital and Clinic Frisco, CO, etc. The companies are entering into the collaboration and partnership to keep up the pace of the innovations.

The report covers exhaustive analysis on:

Regional analysis for Market includes

Report Highlights:

Request Report Methodology @ https://www.persistencemarketresearch.co/methodology/14941

Key Questions Related to the Animal Stem Cell Therapy Market Addressed in the Report

Why Choose PMR?

For any queries get in touch with Industry Expert @ https://www.persistencemarketresearch.co/ask-an-expert/14941

Read more:
Growing Infrastructure Development Projects in Asia-Pacific to Fuel Growth of the Animal Stem Cell Therapy Market 2017 2025 - Bulletin Line

Market Share and Size Analysis of Cell Therapy Manufacturing Market till 2029 – 3rd Watch News

Prophecy Market Insights has recently published the Cell Therapy Manufacturing detailed market report which will help retailers, manufacturers, and distributors to understand and realize the market drivers, restraints, and opportunities to generate revenue, and trends that are instrumental in shaping the target market and its revenue.

Cell Therapy Manufacturing market report states the overview, historical data along with size, share, growth, demand, and revenue of the global industry. The report analyses the attractive opportunities in the market by explaining the fastest and largest growing segments across regions.

Comprehensive information pertaining to fire alarm systems and its properties is provided in this section. This section also highlights the inclusions and exclusions, which help readers to understand the scope of the market report.

This segment includes factors that have emerged as key success factors and strategies adopted by key market participants.

The survey report includes a vast investigation of the geographical scene of the Cell Therapy Manufacturing market, which is manifestly arranged into the localities;

Australia, New Zealand, Rest of Asia-Pacific

Regional and Country- level Analysis different geographical areas are studied deeply and an economic scenario has been offered to support new entrants, leading market players, and investors to regulate emerging economies.

Get Sample Copy of This Report @ https://www.prophecymarketinsights.com/market_insight/Insight/request-sample/21

Stakeholders Benefits:

The comprehensive list of Key Market Players along with their market overview, product protocol, key highlights, key financial issues, SWOT analysis, and business strategies. The report dedicatedly offers helpful solutions for players to increase their clients on a global scale and expand their favour significantly over the forecast period. The report also serves strategic decision-making solutions for the clients.

Competitive landscape Analysis provides mergers and acquisitions, collaborations along with new product launches, heat map analysis, and market presence and specificity analysis.

Cell Therapy ManufacturingMarket Key Players:

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.

Request Discount @ https://www.prophecymarketinsights.com/market_insight/Insight/request-discount/21

NOTE: SPECIAL Pandemic offer for our customers: Purchase this Report now by availing up to 40% Discount and free consultation. Limited period offer.

Detailed analysis of the COVID-19 impact will be given in the report, as our analyst and research associates are working hard to understand the impact of COVID-19 disaster on many corporations, sectors and help our clients in taking excellent business decisions. We acknowledge everyone who is doing their part in this financial and healthcare crisis.

Segmentation Overview:

The Cell Therapy Manufacturing research study comprises 100+ market data Tables, Graphs & Figures, Pie Chat to understand detailed analysis of the market. The predictions estimated in the market report have been resulted in using proven research techniques, methodologies, and assumptions. This Cell Therapy Manufacturing market report states the market overview, historical data along with size, growth, share, demand, and revenue of the global industry.

The study analyses the manufacturing and processing requirements, project funding, project cost, project economics, profit margins, predicted returns on investment, etc. With the tables and figures, the report provides key statistics on the state of the industry and is a valuable source of guidance and direction for companies and individuals interested in the market.

Dont Quarantine Research, you keep your social distance and we will provide you with a SPECIAL DISCOUNT due to pandemic crisis. Stay Safe & Sound.

Get In-depth TOC @ https://www.prophecymarketinsights.com/market_insight/Global-Cell-Therapy-Manufacturing-Market-21

About us:

Prophecy Market Insights is specialized market research, analytics, marketing/business strategy, and solutions that offers strategic and tactical support to clients for making well-informed business decisions and to identify and achieve high-value opportunities in the target business area. We also help our clients to address business challenges and provide the best possible solutions to overcome them and transform their business.

Contact Us:

Mr Alex (Sales Manager)

Prophecy Market Insights

Phone: +1 860 531 2701

Email: [emailprotected]

VISIT MY BLOG:- https://prophecyconsumerelectronics.blogspot.com/

Link:
Market Share and Size Analysis of Cell Therapy Manufacturing Market till 2029 - 3rd Watch News

Global Cancer Stem Cells Market 2020 by Key Players, Regions, Type and Application, Forecast to 2025 – Jewish Life News

Global Cancer Stem Cells Market 2020 by Company, Regions, Type and Application, Forecast to 2025 aimed at strengthening players overall growth and offering a strong position in their business, explores facts, events, and possible variations in the market considering regional and global levels. The report contains detailed, accurate research studies that provide an in-depth analysis of global Cancer Stem Cells market dynamics. The report highlights significant insights about the market involving market size, application, fundamental statistics, market share, and growth factors. The research incorporates an exact competitive assessment of industry players and their valuable strategies during the projected timeframe 2020 to 2025.

The report profoundly evaluated in the report covering scope, profitability, demand status, uncertainties, and development forecast. Then report compiles in-depth analysis on critical subjects of the global Cancer Stem Cells industry such as consumption, revenue, sales, production, trends, opportunities, geographic expansion, competition, segmentation, growth drivers, and challenges. The market development and other occurrences are studied to offer detailed and accurate estimates up to 2025. The study report identifies the current and forthcoming opportunities and challenges in the global market.

DOWNLOAD FREE SAMPLE REPORT: https://www.marketandresearch.biz/sample-request/143932

NOTE: This report takes into account the current and future impacts of COVID-19 on this industry and offers you an in-dept analysis of Cancer Stem Cells market.

Key players operating in the market: Thermo Fisher Scientific, Promocell, Bionomics, Abbvie, Miltenyi Biotec, Merck Kgaa, Oncomed Pharmaceuticals, Stemline Therapeutics, Lonza, Macrogenics, Irvine Scientific, Biotime, Stemcell Technologies, Sino Biological

Market segment by product type: Cell Culturing, Cell Separation, Cell Analysis, Molecular Analysis, Others

Market segment by application: , Breast Cancer Diagnosis and Treatment, Prostate Cancer Diagnosis and Treatment, Colorectal Cancer Diagnosis and Treatment, Lung Cancer Diagnosis and Treatment, Others

Regional Segment:

Regional insights on the global Cancer Stem Cells market around several geographies have been covered in this insightful study, coupled with country-level analysis. Influential market dynamics across regional segments are slated in the report, with their magnitudes differing from country to country. Key regions split in this report: North America (United States, Canada and Mexico), Europe (Germany, France, UK, Russia and Italy), Asia-Pacific (China, Japan, Korea, India, Southeast Asia and Australia), South America (Brazil, Argentina, Colombia, Middle East and Africa (Saudi Arabia, UAE, Egypt, Nigeria and South Africa)

The Study Objectives Are:

ACCESS FULL REPORT: https://www.marketandresearch.biz/report/143932/global-cancer-stem-cells-market-2020-by-company-regions-type-and-application-forecast-to-2025

Furthermore, the report sheds light on the leading manufacturers and companies in the report, enfolding assessments of their financial operations, revenue, market size, share, annual growth rates, production cost, sales volume, gross margins, and CAGR. Additionally, the report comprises analysis of their production processes, volume, product specifications, raw material sourcing, key vendors, clients, organizational structure, and global presence. Additionally, the report reveals the overall scope of the global Cancer Stem Cells market in terms of the feasibility of investments in the various segments of the market, as well as the feasibility of new projects that might succeed in the market in the near future.

Customization of the Report: This report can be customized to meet the clients requirements. Please connect with our sales team ([emailprotected]), who will ensure that you get a report that suits your needs. You can also get in touch with our executives on +1-201-465-4211 to share your research requirements.

About Us

Marketandresearch.biz is a leading global Market Research agency providing expert research solutions, trusted by the best. We understand the importance of knowing what global consumers watch and buy, further using the same to document our distinguished research reports. Marketandresearch.biz has worldwide presence to facilitate real market intelligence using latest methodology, best-in-class research techniques and cost-effective measures for worlds leading research professionals and agencies. We study consumers in more than 100 countries to give you the most complete view of trends and habits worldwide. Marketsandresearch.biz is a leading provider of Full-Service Research, Global Project Management, Market Research Operations and Online Panel Services.

Contact Us Mark Stone Head of Business Development Phone: +1-201-465-4211 Email: [emailprotected] Web: http://www.marketandresearch.biz

See the article here:
Global Cancer Stem Cells Market 2020 by Key Players, Regions, Type and Application, Forecast to 2025 - Jewish Life News

3D Cell Culture Market 2020 with Top Countries Data, Global Industry Forecasts Analysis, Top Company Profiles, Competitive Landscape and Key Regions…

3D Biotek

Scope of the 3D Cell Culture Market Report:

The global 3D cell culture market is relatively concentrated; the sales of top nine manufacturers account about 68.23% of total global Production in 2016. The largest manufacture of 3D cell culture is Thermo Fisher Scientific; its Production is 252.73 K Unit in 2016. The next is Corning and Lonza Group.

North America is the largest consumption region of 3D cell culture in 2016. In 2016, the sales of 3D cell culture is about 470 K Unit in North America; its sales proportion of total global sales exceeds 36%.The next is Europe. Asia has a large growth rate of 3D cell culture.

Cancer research is currently the most well established application area and accounts for 40.05% of the present 3D culture market. Drug Discovery has also emerged quite popular with 36.25% of the current market share. Stem cells and regenerative medicine together capture a share of 24.08% in the current 3D culture market and would gradually gain focus as the market matures in the field of therapeutics in 2016. The worldwide market for 3D Cell Culture is expected to grow at a CAGR of roughly 13.5% over the next five years, will reach 970 million US$ in 2024, from 510 million US$ in 2019, according to a new Research study.

This report focuses on the 3D Cell Culture in global market, especially in North America, Europe and Asia-Pacific, South America, Middle East and Africa. This report categorizes the market based on manufacturers, regions, type and application.

Get a Sample Copy of the 3D Cell Culture Market Report 2020

Report further studies the market development status and future 3D Cell Culture Market trend across the world. Also, it splits 3D Cell Culture market Segmentation by Type and by Applications to fully and deeply research and reveal market profile and prospects.

Major Classifications are as follows:

Geographically, this report is segmented into several key regions, with sales, revenue, market share and growth Rate of 3D Cell Culture in these regions, from 2014 to 2024, covering

This 3D Cell Culture Market Research/Analysis Report Contains Answers to your following Questions

Inquire more and share questions if any before the purchase on this report at https://www.360researchreports.com/enquiry/pre-order-enquiry/13964528

Major Points from Table of Contents:

1. Market Overview 1.1 3D Cell Culture Introduction 1.2 Market Analysis by Type 1.3 Market Analysis by Applications 1.4 Market Dynamics 1.4.1 Market Opportunities 1.4.2 Market Risk 1.4.3 Market Driving Force

2.Manufacturers Profiles

2.4.1 Business Overview 2.4.2 3D Cell Culture Type and Applications 2.4.2.1 Product A 2.4.2.2 Product B

3.Global 3D Cell Culture Sales, Revenue, Market Share and Competition By Manufacturer (2019-2020)

3.1 Global 3D Cell Culture Sales and Market Share by Manufacturer (2019-2020) 3.2 Global 3D Cell Culture Revenue and Market Share by Manufacturer (2019-2020) 3.3 Market Concentration Rates 3.3.1 Top 3 3D Cell Culture Manufacturer Market Share in 2020 3.3.2 Top 6 3D Cell Culture Manufacturer Market Share in 2020 3.4 Market Competition Trend

4.Global 3D Cell Culture Market Analysis by Regions

4.1 Global 3D Cell Culture Sales, Revenue and Market Share by Regions 4.1.1 Global 3D Cell Culture Sales and Market Share by Regions (2014-2019) 4.1.2 Global 3D Cell Culture Revenue and Market Share by Regions (2014-2019) 4.2 North America 3D Cell Culture Sales and Growth Rate (2014-2019) 4.3 Europe 3D Cell Culture Sales and Growth Rate (2014-2019) 4.4 Asia-Pacific 3D Cell Culture Sales and Growth Rate (2014-2019) 4.6 South America 3D Cell Culture Sales and Growth Rate (2014-2019) 4.6 Middle East and Africa 3D Cell Culture Sales and Growth Rate (2014-2019)

5.3D Cell Culture Market Forecast (2020-2024) 5.1 Global 3D Cell Culture Sales, Revenue and Growth Rate (2020-2024) 5.2 3D Cell Culture Market Forecast by Regions (2020-2024) 5.3 3D Cell Culture Market Forecast by Type (2020-2024) 5.3.1 Global 3D Cell Culture Sales Forecast by Type (2020-2024) 5.3.2 Global 3D Cell Culture Market Share Forecast by Type (2020-2024) 5.4 3D Cell Culture Market Forecast by Application (2020-2024) 5.4.1 Global 3D Cell Culture Sales Forecast by Application (2020-2024) 5.4.2 Global 3D Cell Culture Market Share Forecast by Application (2020-2024)

6.Sales Channel, Distributors, Traders and Dealers 6.1 Sales Channel 6.1.1 Direct Marketing 6.1.2 Indirect Marketing 6.1.3 Marketing Channel Future Trend 6.2 Distributors, Traders and Dealers

7.Research Findings and Conclusion

8.Appendix 8.1 Methodology 8.2 Data Source

Continued..

Purchase this report (Price3480 USD for a single-user license) https://www.360researchreports.com/purchase/13964528

About Us:

360 Research Reports is the credible source for gaining the market reports that will provide you with the lead your business needs. At 360 Research Reports, our objective is providing a platform for many top-notch market research firms worldwide to publish their research reports, as well as helping the decision makers in finding most suitable market research solutions under one roof. Our aim is to provide the best solution that matches the exact customer requirements. This drives us to provide you with custom or syndicated research reports.

Contact Us: Name: Mr. Ajay More Email: [emailprotected] Organization: 360 Research Reports Phone: +44 20 3239 8187/ +14242530807

For More Related Reports Click Here :

Disposable Stoma Bags Market Size 2020 : Top Countries Data with Global Demand Analysis and Opportunity Outlook 2026

Neonatal Invasive Ventilator Market Size 2020 with Covid 19 Impact Analysis, Top Countries Data, Industry Outlook, Driving Factors by Manufacturers, Growth and Forecast 2026

Fenbendazole (CAS 43210-67-9) Market 2020 : Market Size, Top Countries Data with Global Demand Analysis and Opportunity Outlook 2026

See original here:
3D Cell Culture Market 2020 with Top Countries Data, Global Industry Forecasts Analysis, Top Company Profiles, Competitive Landscape and Key Regions...

Epigenetics Market to Witness an Outstanding Growth by 2025 – Cole of Duty

Global Epigenetics Market: Overview

The global epigenetics market is expected to grow at a fast paced CAGR in the next few years, owing to factors such as extensive use in the research of developmental and disease process, and growing importance of Life Science. Increasing incidences of cancer and other life threatening diseases will also drive the growth of the global epigenetics market. Epigenetic changes are extensively used in cancer research for studying tumor biology as well as to develop therapeutic drugs to fight cancer.

Get Report Sample Copy @https://www.tmrresearch.com/sample/sample?flag=B&rep_id=2705

Global Epigenetics Market: Trends

The recent market trend of increasingly using epigenetics for understanding the development of a disease extensively fuel the growth of this market in the coming years. Another trend that will aid the growth of the global epigenetics market is the escalating demand for personalized medicine. Extensive investments are being made by various organisations, pharmaceutical companies, and governments for the research and development of drugs, and this is another trend that is benefiting the growth of the global epigenetics market. This is because epigenetic techniques enable researchers to compare epigenetic changes between disease samples and normal samples. Public health can thus be analyzed as the changes in epigenetics are influenced by internal biological system and environment directly.

With the economies of developing countries growing faster than that of developed countries, several institutes and research facilities are being set up in the developing countries. The rise in the number of testing and research facilities, particularly in the field of biotechnology and pharmaceuticals, will lead to a rise in demand for epigenetic analysis for diagnosis of diseases and development of therapeutic drugs. This will also drive the growth prospects of the global epienetics market.

Global Epigenetics Market: Market Potential

The rise in the application of epigenetics for cancer prevention as well as cancer diagnosis thanks to technologies such as epigenetics therapy and DNA methylation to control cancer or diagnose cancer respectively, will create new opportunities of growth in the global epigenetics market. New methods such as such as ChIP and next generation sequencing (NGS) are being used to understand gene sequence which are modified due to epigenetic changes. The growing number of retail clinics, companion diagnostics, and the development of whole genome technology are pushing the demand for personalized medicine. This is also acting as a driver for the global epienetics market. As different people react differently to a particular medicine, increasing number of patients and doctors are inclined towards personalized medicine.

Investments in research and development has increased remarkably in the last few years. As investments from the developing economies pricing faster then developed nation where is research facilities is an institution setup in developing companies which is giving rise to testing biotechnology thereby giving rise to a heightened demand for disease diagnosis and development of therapeutic drugs.

Request TOC of the Report @https://www.tmrresearch.com/sample/sample?flag=T&rep_id=2705

Global Epigenetics Market: Regional Outlook

The global epigenetics market is segmented on the basis of geography into Asia Pacific, North America, Europe, and the Rest of the World. Of these, North America has been leading in this market in account of the early adoption of advanced technologies and solutions. Increased investments in research and development as well as growing geriatric population, and the increasing pool patient population are some of the other factors which make North America a key market for epigenetics. In addition to North America, it is estimated the developing economies in Asia Pacific will emerge as lucrative markets for epigenetics.

Global Epigenetics Market: Competitive Landscape

Illumina, Diagenode, Abcam, CellCentric Ltd, Merck, Thermo Fisher Scientific, Zymo research, Qiagen, Chroma Therapeutics Ltd,Syndax Pharmaceuticals, Inc., Sigma-Aldrich Corporation, Eisai Co. Ltd, Oncolys Biopharma Inc., Novartis International AG, and Valirx Plc are some of the leading players within the global epienetics market.

Read the rest here:
Epigenetics Market to Witness an Outstanding Growth by 2025 - Cole of Duty

Biological, clinical and epidemiological features of COVID-19, SARS and MERS and AutoDock simulation of ACE2 – Infectious Diseases of Poverty – BioMed…

Biological, clinical and epidemiologic features of COVID-19

The comparison of features among COVID-19, SARS-CoV and MERS-CoV is summarized in Table1.

With high-throughput sequencing, researchers announced the sequencing of SARS-CoV-2. The genome of SARS-CoV-2 consists of 6 major ORFs that are common to coronaviruses, and the sequence of SARS-CoV-2 has almost 70% similarity to that of SARS-CoV and nearly 40% similarity to that of MERS-CoV [5, 6, 11, 12]. The main differences among SARS-CoV-2, SARS-CoV and MERS-CoV are in ORF1a and the sequence of gene spike coding protein-S [5], which was identified as a key protein that interacts with target cells.

In terms of electron microscopic morphology, SARS-CoV-2 virions are generally spherical, but some are polygonal. The diameter is between 60 and 140nm. The virus particles have prominent spines that are approximately 9 to 12nm, which cause the virus to have a coronal shape. According to the virus morphology observed under the microscope, the virus is consistent with other in the coronavirus family, including SARS-CoV and MERS-CoV [5, 13].

The receptor on the target cells is the factor determining how the virus enters the cell and which tissues are susceptible, and the spike protein initiates the merging of the viral envelope with the host cell cytomembrane. Existing experimental studies have shown that ACE2 is likely to be the cell receptor of SARS-CoV-2, and SARS-CoV-2 does not use other coronavirus receptors. The main receptors of SARS-CoV and MERS-CoV are ACE2 and hDPP4 (human dipeptidyl peptidase 4 or CD26), respectively [1, 5, 14].

Although the study of COVID-19 is still in progress, our summary and comparison of coronaviruses can be useful for further research and clinical applications. The clinical symptoms of COVID-19 are similar to those of SARS and MERS, including fever, cough, myalgia and fatigue. Almost all of the patients have pneumonia, and their chest CT examinations are abnormal [1, 4, 15,16,17]. However, those who are infected with SARS-CoV-2 rarely have significant upper respiratory signs and symptoms, including nosebleed, sneezing or sore throat, which indicates that the target cell may exist in the lower respiratory tract. This is consistent with the autopsy reports of patients with COVID-19 that show that SARS-CoV-2 infection mainly causes deep airway inflammatory reactions and alveolar damage. Some patients may also have headache, hemoptysis, diarrhea, dyspnea and lymphocytopenia, but patients are less likely to have gastrointestinal symptoms [4]. Complications include acute respiratory distress syndrome, acute heart injury, and secondary infections. COVID-19 patients can be divided into those with asymptomatic, mild and severe cases. For most patients, the incubation period of the virus is generally 714days. Typically, COVID-19 gradually progresses and worsens. Thus, each patients condition becomes more serious in the second week.

COVID-19, SARS, and MERS have different mortality rates. Among them, MERS had the highest fatality rate, and COVID-19 has the lowest fatality rate. It is worth noting that watery diarrhea is common in almost 60% of patients who suffer from SARS, and there is a typical biphasic clinical course [10, 18, 19]. In MERS, most patients have symptoms that include dry cough fever, malaise, myalgia, sore throat, headache, nausea, vomiting, and diarrhea, which are similar to the symptoms of SARS, but MERS has an unpredictable and erratic clinical course [19,20,21,22]. Fibrosis and consolidation in COVID-19 are less serious than the lesions caused by SARS, revealing that in COVID-19, the chest lesions are not primarily serous inflammation but rather are exudative reactions. Whether damage to the brain, myocardium, epicardium, kidneys, spleen and digestive organs is associated with viral infection needs further research.

Next-generation sequencing (NGS) and electron microscopy technology play critical roles in the early diagnosis of COVID-19, but their diagnostic values have been weakened by the use of specific nucleic acid detection technology [11, 23]. At present, clinically confirmed patients are usually diagnosed by collecting throat swabs and then detecting the nucleic acid of SARS-CoV-2.

Diagnosis based on clinical manifestations can be an early and rapid screening method. Patients with mild symptoms may not present positive signs. Patients in severe condition may have shortness of breath, moist rales in lungs, weakened breath sounds, dullness on percussion, and changes in voice, and the physical examination can help identify these symptoms. In addition, CT imaging plays an important role in the diagnosis. The imaging features of lesions show characteristic (1) distribution (mainly subpleural, along the bronchial vascular bundles); (2) quantity (often more than three lesions, occasionally single or double lesions); (3) shape (patchy, large block, nodular, lumpy, honeycomb-like or grid-like, cord-like, etc.); (4) density (mostly uneven, crazy-paving pattern mixed with ground glass opacity and interlobular septal thickening, consolidation and thickened bronchial wall, etc.); and (5) concomitant signs (e.g., air bronchogram, rare pleural effusion and mediastinal lymph node enlargement). However, these are not enough. COVID-19 needs to be distinguished from other known viruses that cause pneumonia, such as influenza virus, parainfluenza virus, adenovirus, respiratory syncytial virus, rhinovirus, human metapneumovirus, SARS-CoV, etc. and from Mycoplasma pneumonia, Chlamydia pneumonia, and bacterial pneumonia. In addition, COVID-19 should be distinguished from noninfectious diseases, such as vasculitis, dermatomyositis, and organizing pneumonia.

Research on identifying effective drugs has started, and there have been many in vitro and in vivo experiments being conducted [24]. Vaccines against SARS-CoV-2 are currently in development, and there are at least two kinds currently ready for testing. There are approximately 15 potential vaccine candidates in the pipeline globally using a wide range of approaches (such as messenger RNA, DNA, nanoparticle, and synthetic and modified virus-like particles). The vaccine candidates will be developed by a number of organizations using DNA, recombinant and mRNA vaccine platforms109. On 23 January 2020, The Coalition for Epidemic Preparedness Innovations (CEPI) announced that they will fund vaccine development programmes with Inovio, The University of Queensland and Moderna, Inc., with the target of testing the experimental vaccines clinically. It will likely take approximately a year for most candidates to enter phase 1 clinical trials except for those funded by CEPI. For SARS, the vaccines in development include viral vector-based vaccines, DNA vaccines, subunit vaccines, virus-like particle (VLP)-based vaccines, inactivated whole-virus (IWV) vaccines and live attenuated vaccines, and the latest findings for these vaccines are based on the review by Yong et al. (2019) in August 2019 [25]. There was one SARS vaccine trial conducted by the US National Institute of Allergy and Infectious Diseases. Both Phase I clinical trials reported positive results, but only one will proceed to the Phase 2 trial. For MERS, there is only one published clinical study on a vaccine developed by GeneOne Life Science & Inovio Pharmaceuticals [26]. For therapeutics, there are nine clinical trials registered with the clinical trials registry (ClinicalTrials.gov) investigating therapeutic agents for COVID-19. Five studies on hydroxychloroquine, lopinavir plus ritonavir and arbidol, mesenchymal stem cells, traditional Chinese medicine and glucocorticoid therapy usage have commenced recruitment, and the other four are on antivirals, interferon atomization, darunavir and cobicistat, Arbidol, and remdesivir [24].

COVID-19 patients admitted to a qualified hospital are given chemotherapy, including antiviral treatment, antibiotic therapy, corticosteroid therapy and other medications, such as ibuprofen as an antipyretic, nutrition support treatment, H2 receptor antagonists or proton pump inhibitors for gastrointestinal bleeding, and selective (M1, M3) receptor anticholinergic drugs for dyspnea, coughing, wheezing, and respiratory distress syndrome. Although -interferon atomization inhalation and oral lopinavir/ritonavir can be considered, the effectiveness of the combined use of antivirals is still unknown, given the lack of evidence from a randomized controlled trial (RCT). Given the high risk of adverse effects, there are limitations on the use of corticosteroids. Traditional Chinese medicine has shown a good effect with regard to both prevention and treatment. Fumigating rooms with moxa and wearing perfumed Chinese herb bags can help prevent community transmission. Huoxiang Zhengqi capsules are recommended for hypodynamia accompanied by gastrointestinal upset caused by COVID-19. For hypodynamia and fever, Jinhua Qinggan granules, Lianhua Qingwen capsules, Shufeng Jiedu capsules and Fangfeng Tongsheng pills are recommended [23].

Nursing care is important for isolated and critically ill patients, as classified according to the guidelines. Isolated patients at home should monitor their body temperature and breathing regularly. Patients are given oxygen therapy via a nasal catheter or a mask, antiviral drugs, antibacterial drugs, symptomatic treatments, nutritional support and psychological counselling. Critically ill patients are monitored with regard to their vital signs, water-electrolyte balance, acid-base balance, and the functioning of various organs. In addition to nutritional support and psychological counselling, they need oxygen therapy and some special treatments. For example, if a patient develops moderate to severe ARDS, invasive mechanical ventilation with the patient in a prone position needs to be initiated [23, 27].

According to Yang et al., the case fatality ratio (CFR) during the first weeks of the epidemic ranged from 0.15% (95% confidence interval [CI]: 0.120.18%) in mainland China excluding Hubei t 1.41% (95% CI: 1.381.45%) in Hubei Province excluding the city of Wuhan to 5.25% (95% CI: 4.985.51%) in Wuhan City based on data from the Wuhan Municipal Health Commission and the China and National Health Commission of China [28]. Chen et al. systematically described 99 cases of COVID-19 in Wuhan, China. Critically ill patients died of severe pneumonia, septic shock, respiratory failure and multiple organ failure (MOF). The authors reached a speculative conclusion that SARS-CoV-2 is more likely to infect older adult males with chronic comorbidities as a result of their weaker immune systems. In patients with severe coinfections, immune function is important in addition to the virulence of the pathogens. Old age, obesity, and the presence of comorbidities might be associated with increased mortality. In addition, a substantial decrease in the total number of lymphocytes indicates that SARS-CoV-2 consumes many immune cells and inhibits the bodys cellular immune function; therefore, a low absolute value of lymphocytes could be used as a reference index in the diagnosis of new SARS-CoV-2 infections in the clinic [29].

It is essential to analyze the infection source, transmission route, susceptible population and replication rate, especially the intermediate host and the exact route of transmission, to find the best measures to prevent the further spread of COVID-19.

The infection sources include patients, virus carriers, and infected animals that serve as viral reservoirs. Searching for the hosts of the virus, or for the infection sources, is a vital process in understanding the viral dynamics. SARS-CoV-2 has 96.2% genetic sequence similarity to the previously identified BatCoV RaTG13, suggesting that bats are most likely to be the host of SARS-CoV-2 [1, 3, 30, 31]. The cluster of cases in the seafood market was comprehensively analyzed, and sequence comparison revealed that pangolins are the most likely intermediate host for SARS-CoV-2 [30]. However, SARS-CoV and MERS-CoV were also identified as having zoonotic origins, and the animal reservoirs seemed to be bats [9, 32]. Although bat coronaviruses are genetically related, the intermediate hosts are involved in cross-species transmission, after which human-to-human transmission developed. In contrast to SARS-CoV-2, the intermediate host of SARS-CoV was mainly palm civets [9, 33, 34], and the intermediate host of MERS-CoV was thought to be dromedary camels [22, 35]. All three coronaviruses can be traced to bats, while there are different intermediate hosts involved in cross-species transmission. These three viruses have caused widespread epidemics that originated in animal reservoirs; the high morbidity and mortality levels have caused panic and substantial economic loss.

Viruses can directly infect people but can also infect one or more kinds of animals. Although these animals themselves do not cause disease, they can act as vectors for the virus and transmit it to humans; during this process, some viruses may mutate and evolve new characteristics. According to the experimental results of Peng et al. [5], SARS-CoV-2 can be transmitted through respiratory droplets and direct contact, confirming that while the main transmission route of SARS-CoV-2 is aerosols, other routes of transmission may exist. Moreover, a recent experiment conducted with recovering patients found that SARS-CoV-2 can also exist in the patients stool, suggesting that the fecal-oral route may be a route of transmisson [36]. Li et al. investigated cases of SARS and found that SARS was spread mainly by respiratory droplets [19]. By analyzing case data, Hui et al. also found that direct person-to-person transmission through close contact can also spread SARS-CoV [18]. MERS-CoV was mainly transmitted through close contact with infected family members or infected individuals in the hospital. Xiao et al. identified seven hypothesized transmission modes based on the three main transmission routes (long-range airborne, close contact, and fomite), and the infection risks associated with each hypothesis were estimated using the multiagent modeling framework. This showed that transmission occurred via both the long-range airborne and close contact routes [22]. Based on the available data, all three coronaviruses can be transmitted by breathing respiratory droplets that contain virions, which indicates that wearing masks is an effective means of protecting susceptible people. All three coronaviruses are transmitted from animals to humans and from humans to humans.

There is no evidence that people with certain characteristics are not susceptible to COVID-19. The available data suggest that people of all ages who have close contact with patients can be infected by SARS-CoV-2 [36,37,38]. The general public is susceptible, and the data are still being updated daily. The elderly population and patients with basic diseases are more susceptible to severe illness after infection, and children and infants can also be infected by SARS-CoV-2 [39]. SARS-CoV had a tendency to affect healthier and younger persons, with a mean patient age of 39.9years (range 191), and the male to female ratio was 11.3, with a slight female predominance. MERS-CoV had a tendency to affect the elderly and frail populations, especially males, with a mean age of 56years (range 1494), and the male to female ratio was 3.31 with a male predominance [8, 10, 40].

A commonly used measure of infectivity is the basic reproduction number (R0), which is the average number of people infected who pass the virus on to others without intervention. In other words, the value is equivalent to how many people can be infected by an average patient. The larger the R0 is, the harder it is to control the epidemic. Researchers have estimated the R0 to be in the range of 2.83.9, assuming extreme cases, which means that on average a COVID-19 patient passes the virus on to 2.83.9 healthy persons [28, 41]. In comparison, the R0 of MERS has been reported to be less than 1, and the R0 of SARS is estimated to be 3. Considering that the disease is now widespread around the world, the R0 of COVID-19 may change and could be higher than those of SARS and MERS.

As of May 24, 2020, there were caused 84536 confirmed cases of COVID-19, 4645 deaths and 79757 cured cases in China. A total of 5490640 cases have been diagnosed, and 346328 deaths have occurred worldwide. SARS infected more than 8098 people in 29 countries and caused 916 deaths, with a mortality rate of approximately 10%. MERS was first found in the Arabian Peninsula and infected approximately 2254 people (from 2012 through September 16, 2018) in 27 countries; MERS caused 800 deaths, with a mortality rate of approximately 35%. SARS was characterized by superspreading events, while COVID-19 is unique for its indiscriminate transmission among the general public. However, MERS seemed to be less aggressive [8, 10, 42].

Epidemiological changes have been monitored, taking into account potential routes of transmission and subclinical infections. The official platform updates the public daily on the number of newly diagnosed cases, deaths and cures in each administrative region based on data from the Centers for Disease Control and Prevention and hospitals at all levels. Since the outbreak, many emergency measures have been taken to reduce person-to-person transmission of SARS-CoV-2. For example, public services and facilities provide disinfectants on a routine basis to encourage appropriate hand hygiene, and physical contact with wet and contaminated objects is considered when dealing with the virus, especially fecal and urine samples that can potentially serve as an alternative route of transmission. China and other countries have implemented major prevention and control measures, including screening travelers, to control further spread of the virus [43]. There are many people donating money, vegetables, medical supplies, etc. to the areas affected by the epidemic. In Wuhan, two hospitals, Vulcan Mountain Hospital and Raytheon Mountain Hospital, were built within 10 days, which can contain 1000 and 1300 patients, respectively. According to the Peoples Daily, the National Health and Fitness Commission reported that there are more than 11000 critical care workers and more than 2000 intensive care unit nurses, and there will be more pooling of medical resources in places where they are most needed. The Chinese government has shut down schools and closed businesses to reduce transmission [44].

The outbreak has also caused widespread public concern. Husnayain et al. studied the potential to use Google Trends (GT) to monitor public restlessness regarding the COVID-19 epidemic, and they found that searches related to COVID-19 and face masks increased rapidly [45]. With the advent of 5G and the rapid development of the information age, it may be more convenient for the masses to obtain the latest news from the Internet; thus, Internet-based risk communication is becoming an appropriate strategy. There are many disease control organizations and medical institutions that have played an official role in this outbreak and provided accurate and reliable information to the public in a timely manner. For example, laboratory confirmation of COVID-19 was performed in five different institutions, namely, the China CDC, Chinese Academy of Medical Science, Wuhan Institute of Virology, and Academy of Military Medical Sciences, and Chinese Academy of Sciences [29]. According to the CCTV news, with scientific progress has enabled the use of advanced technologies to control this epidemic. In addition, the health code divides the public into three health situations, namely, green, red and yellow. This provides an effective method of facilitating crowd tracking and monitoring. Furthermore, the geographic information system (GIS), which has long been used by many health professionals when tracking and combating contagion, also plays an important role in the geographical tracking and mapping of epidemics. A range of practical online/mobile GIS and mapping dashboards and applications have come into use for tracking the COVID-19 epidemic [46].

Some treatments have been adopted in clinical practice, and a few have been successful [24, 47]. According to Prashant Pradhan, the first case cured in sevendays in the United States showed that the antiviral medication remdesivir may become one of the specific medicines for COVID-19; however, this remains to be verified through clinical trials [16]. According to the research by Wang, XF, et al. about the clinical manifestations and epidemiology in children with COVID-19 treated with lopinavir and ritonavir and without glucocorticoids and immunoglobulin, all 20 patients improved and were discharged from hospital. This may lead to the conclusion that childrens clinical symptoms of COVID-19 are nonspecific and milder than those in adults, which has significant clinical value [48].

Future research priorities may be focused on biological research on SARS-CoV-2 and clinical research on COVID-19 diagnosis and treatment. According to Pradhan et al., there are four unique insertions, which have similarity to HIV, in the S-protein in COVID-19, which may explain its contagiousness. The gene binding site may become a new target of therapeutics to prevent transmission of the virus [49]. Specifically, virus particles are found in the feces, which suggests that there may exist other routes of transmission, such as fecal-oral transmission. Previously, we focused on cutting off transmission routes mainly by limiting contact and preventing respiratory droplet transmission. This finding emphasizes the significance of dealing with the feces of the patient. Therefore, for patients who already have COVID-19, careful disposal of their feces is an important concern with regard to reducing viral transmission [36]. On the basis of the research by Hongzhou Lu, lopinavir/ritonavir, nucleoside analogs, neuraminidase inhibitors, remdesivir, peptide (EK1), Arbidol, RNA synthesis inhibitors (such as TDF, 3TC), anti-inflammatory drugs (such as hormones and other molecules), Chinese traditional medicine and so on could be therapies for COVID-19, but the effects and safety remain to be tested in clinical trials [27].

3D structures of remdesivir, chloroquine, ciclesonide, niclosamide, and lopinavirus were obtained from NCBI PubChem. The crystal structure of ACE2 (PDB code: 6M17) was obtained from the Protein Data Bank. The ligands within the crystal structure complex were extracted by PyMOL software (San Carlos, CA, USA). AutoDock 4.2 was used for the docking system test. AutoDock tools initialized the ligands by adding gasteiger charges, merging nonpolar hydrogen bonds, and setting rotatable bonds. The ligands were rewritten into PDBQT format, which can be read by Autodock software (AutoDock 4.2, San Carlos, CA, USA). AutoDock Tools were used to add polar hydrogen to the entire receptor. The grid box was set to contain the entire receptor region. The receptor output was also saved in PDBQT format. AutoDock Vina was set with the macromolecule held fixed and the ligands flexible. Affinity maps for all the atom types present, as well as an electrostatic map, were computed, with a grid spacing of 0.375. The structural models were collected from the lowest-energy docking solution of each cluster of autodocks. It is evident from the findings of Fig.2 and Table2 that combinations of antiviral agents are more successful than a single drug.

AutoDock calculations were performed to determine and compare the binding affinities of remdesivir, chloroquine, ciclesonide, niclosamide, and lopinavirus to ACE2. LEU: Leucine, PHE: Phenylalanine, MET: Methionine, VAL: Valine), ILE: Isoleucine, TRP: Ttryptophan, TYR: Tyrosine

The outbreak of SARS renewed interest in this family of viruses and resulted in the development of new drugs, among which remdesivir, chloroquine, ciclesonide, niclosamide, and lopinavirus are the most promising [50,51,52]. In addition, as mentioned above, ACE2 plays a vital role in the development of COVID-19 [53]. With regard to testing the effectiveness of previous medicines used by scientists for the treatment of diseases caused by coronaviruses, AutoDock calculations have been performed to classify specific binding amino acids and thus to determine the likely common cure targets for ACE2. As shown in Table2 and Fig.2, we found that chloroquine and ciclesonide share similar binding amino acid residues (MET124, LEU127, ILE472 and VAL589). Likewise, remdesivir and niclosamide also possess MET124. Taken together, we might therefore hypothesize that MET124 plays a key role in the efficiency of these drugs targeting ACE2. MET24 appears to be a potential target for COVID-19. However, there is no similar amino acid for lopinavir, suggesting that further studies are needed to elucidate the molecular mechanism of lopinavir treatment of COVID-19.

Read more:
Biological, clinical and epidemiological features of COVID-19, SARS and MERS and AutoDock simulation of ACE2 - Infectious Diseases of Poverty - BioMed...

Gene Therapy for Inherited Genetic Disorders Market Qualitative Insights On Application 2028 – 3rd Watch News

Global Gene Therapy for Inherited Genetic Disorders Market: Overview

Rapid advances in mammalian DNA sequencing technologies over the past several years have enabled the identification of the aberrant genes responsible for a vast spectrum of genetic disorders. Gene therapy as a novel approach inarguably holds profound potential in finding universal therapeutic alternatives to treating inherited genetic disorders. Gene therapy for inherited genetic disorders entails introducing a functional copy of the defective gene to make up for the missing function, and can be accomplished using in vivo or ex vivo gene transfer.

Gene therapy for inherited genetic disorders has generated groundswell of interest in the research fraternity in finding cure for or in treatment of Mendelian genetic error causing rare diseases. Particularly, gene therapy in recent years has held promising potential in the treatment of a range of recessive gene disorders most notably sickle cell anemia, hemophilia, muscular dystrophy, cystic fibrosis, and other monogenic disorders. The axes of developments in the gene therapy for inherited genetic disorders market have been in the U.S., Europe, China, and Australia.

Get Sample Copy of the Report @https://www.tmrresearch.com/sample/sample?flag=B&rep_id=5624

Global Gene Therapy for Inherited Genetic Disorders Market: Notable Developments

Growing body of clinical studies done on mice models have unrivalled troves of preclinical data, which bodes well for the effectiveness of gene therapy for inherited genetic disorders. New approaches in the gene therapy for inherited genetic disorders market are being adopted to bring progress in this direction. In this regard, Salmeterol, a medicine approved for asthma, has shone a new light. The vasodilator to be used along with gene therapy has shown potential in increasing the effectiveness of the therapy for Glycogen storage disease type II (Pompe disease).

A team of investigator led by the researcher at Duke University Medical School discussed the preclinical data recently at 2019 annual meeting of the American Society of Gene & Cell Therapy. The preclinical data showed that the Asthma medicine reduces the accumulation of toxic glycogen accumulated in lysosome. The researchers concluded that it holds potential as an adjunctive therapy, and building on that may pave way for novel approaches on gene therapy for inherited genetic disorders.

Efforts to translate the findings of clinical research on gene therapy for inherited disorders to make the therapy a part of standard treatment has caught momentum in recent times. In this regard, vectors containing non-viral vectors have attracted the attention of scientists. A team of researchers at Fred Hutchinson Cancer Research Center in 2019 found that gold nanoparticles enable them to deliver gene-editing tools to blood stem cells in lab models. This might, they opined, pave way for more practicaland accessiblegene therapies for inherited disorders, notably for treating life-threatening blood disorders. Gene therapies were mediated by CRISPR. In the coming years they hope to collaborate with companies with commercial interest to develop the therapy for patient populations.

Some of the bigplayerseyeing promising stakes in the gene therapy for inherited genetic disorders market areSpark Therapeutics Inc., Orchard Therapeutics, Novartis AG, bluebird bio Inc., and BioMarin Pharmaceutical.

Request TOC of the Report @https://www.tmrresearch.com/sample/sample?flag=T&rep_id=5624

Global Gene Therapy for Inherited Genetic Disorders Market: Key Drivers

Since 2000, scores of clinical trials involving patients with inherited genetic disorders have raised hopes of the medical fraternity of the potential of gene therapies. Thus far, more than 5000 clinical trials on gene therapy have been conducted, especially for hard-to-treat diseases. Diseases such as inherited blindness and leukemia have seen the efficacy and safety of gene therapies. Advances in bioengineering are expected to invigorate pre-clinical pipelines. In the not-so-distant future, success of more protocols will catalyze the prospects of the gene therapy for inherited genetic disorders market.

Further, advances have been made in viral and non-viral vectors with the purpose of making gene transfer more efficient, thereby boosting the gene therapy for inherited genetic disorders market. Particularly, new approaches emerged with the aim of making vectors more powerful.

Global Gene Therapy for Inherited Genetic Disorders Market: Regional Assessment

On the regional front, Asia Pacific bears considerable potential in the gene therapy for inherited disorders market. Of note, numerous strategic alliances have shifted their focus on the region, particularly China. The North America market has also been rising at a promising pace, driven by several gene-therapy tools and related drugs in the final stages of clinical trials. Favorable reimbursement models has also encouraged research into the gene therapy for inherited disorders.

Read Comprehensive Overview of Report @https://www.tmrresearch.com/gene-therapy-for-inherited-genetic-disorders-market

About TMR Research:

TMR Research is a premier provider of customized market research and consulting services to business entities keen on succeeding in todays supercharged economic climate. Armed with an experienced, dedicated, and dynamic team of analysts, we are redefining the way our clients conduct business by providing them with authoritative and trusted research studies in tune with the latest methodologies and market trends.

Here is the original post:
Gene Therapy for Inherited Genetic Disorders Market Qualitative Insights On Application 2028 - 3rd Watch News

New Trend: Animal Stem Cell Therapy Market Growth by Top Companies, Trends by Types and Application, Forecast to 2026 | Medivet Biologics LLC, VETSTEM…

LOS ANGELES, United States: The research report published by QYResearch gives the potential headway openings that prevails in the global market. Market study of the global Animal Stem Cell Therapy market is carried out by the analysts in this report, taking into consideration key factors like drivers, challenges, recent trends, opportunities, advancements, and competitive landscape. This report offers a clear understanding of the present as well as future scenario of the global Animal Stem Cell Therapy industry. Research techniques like PESTLE and Porters Five Forces analysis have been deployed by the researchers. They have also provided accurate data on Animal Stem Cell Therapy production, capacity, price, cost, margin, and revenue to help the players gain a clear understanding into the overall existing and future market situation.

Key companies operating in the global Animal Stem Cell Therapy market include _ Medivet Biologics LLC, VETSTEM BIOPHARMA, J-ARM, U.S. Stem Cell, Inc, VetCell Therapeutics, Celavet Inc., Magellan Stem Cells, Kintaro Cells Power, Animal Stem Care, Animal Cell Therapies, Cell Therapy Sciences, Animacel

Get PDF Sample Copy of the Report to understand the structure of the complete report: (Including Full TOC, List of Tables & Figures, Chart) :

https://www.qyresearch.com/sample-form/form/1427718/global-animal-stem-cell-therapy-market

Segmental Analysis

The report has classified the global Animal Stem Cell Therapy industry into segments including product type and application. Every segment is evaluated based on growth rate and share. Besides, the analysts have studied the potential regions that may prove rewarding for the Animal Stem Cell Therapy manufcaturers in the coming years. The regional analysis includes reliable predictions on value and volume, thereby helping market players to gain deep insights into the overall Animal Stem Cell Therapy industry.

Global Animal Stem Cell Therapy Market Segment By Type:

, Dogs, Horses, Others

Global Animal Stem Cell Therapy Market Segment By Application:

, Veterinary Hospitals, Research Organizations Key Players: The Key manufacturers that are operating in the

Competitive Landscape

It is important for every market participant to be familiar with the competitive scenario in the global Animal Stem Cell Therapy industry. In order to fulfil the requirements, the industry analysts have evaluated the strategic activities of the competitors to help the key players strengthen their foothold in the market and increase their competitiveness.

Key companies operating in the global Animal Stem Cell Therapy market include _ Medivet Biologics LLC, VETSTEM BIOPHARMA, J-ARM, U.S. Stem Cell, Inc, VetCell Therapeutics, Celavet Inc., Magellan Stem Cells, Kintaro Cells Power, Animal Stem Care, Animal Cell Therapies, Cell Therapy Sciences, Animacel

Key questions answered in the report:

Enquire Customization in The Report: https://www.qyresearch.com/customize-request/form/1427718/global-animal-stem-cell-therapy-market

TOC

Table of Contents 1 Animal Stem Cell Therapy Market Overview 1.1 Product Overview and Scope of Animal Stem Cell Therapy 1.2 Animal Stem Cell Therapy Segment by Type 1.2.1 Global Animal Stem Cell Therapy Sales Growth Rate Comparison by Type (2021-2026) 1.2.2 Dogs 1.2.3 Horses 1.2.4 Others 1.3 Animal Stem Cell Therapy Segment by Application 1.3.1 Animal Stem Cell Therapy Sales Comparison by Application: 2020 VS 2026 1.3.2 Veterinary Hospitals 1.3.3 Research Organizations 1.4 Global Animal Stem Cell Therapy Market Size Estimates and Forecasts 1.4.1 Global Animal Stem Cell Therapy Revenue 2015-2026 1.4.2 Global Animal Stem Cell Therapy Sales 2015-2026 1.4.3 Animal Stem Cell Therapy Market Size by Region: 2020 Versus 2026 2 Global Animal Stem Cell Therapy Market Competition by Manufacturers 2.1 Global Animal Stem Cell Therapy Sales Market Share by Manufacturers (2015-2020) 2.2 Global Animal Stem Cell Therapy Revenue Share by Manufacturers (2015-2020) 2.3 Global Animal Stem Cell Therapy Average Price by Manufacturers (2015-2020) 2.4 Manufacturers Animal Stem Cell Therapy Manufacturing Sites, Area Served, Product Type 2.5 Animal Stem Cell Therapy Market Competitive Situation and Trends 2.5.1 Animal Stem Cell Therapy Market Concentration Rate 2.5.2 Global Top 5 and Top 10 Players Market Share by Revenue 2.5.3 Market Share by Company Type (Tier 1, Tier 2 and Tier 3) 2.6 Manufacturers Mergers & Acquisitions, Expansion Plans 2.7 Primary Interviews with Key Animal Stem Cell Therapy Players (Opinion Leaders) 3 Animal Stem Cell Therapy Retrospective Market Scenario by Region 3.1 Global Animal Stem Cell Therapy Retrospective Market Scenario in Sales by Region: 2015-2020 3.2 Global Animal Stem Cell Therapy Retrospective Market Scenario in Revenue by Region: 2015-2020 3.3 North America Animal Stem Cell Therapy Market Facts & Figures by Country 3.3.1 North America Animal Stem Cell Therapy Sales by Country 3.3.2 North America Animal Stem Cell Therapy Sales by Country 3.3.3 U.S. 3.3.4 Canada 3.4 Europe Animal Stem Cell Therapy Market Facts & Figures by Country 3.4.1 Europe Animal Stem Cell Therapy Sales by Country 3.4.2 Europe Animal Stem Cell Therapy Sales by Country 3.4.3 Germany 3.4.4 France 3.4.5 U.K. 3.4.6 Italy 3.4.7 Russia 3.5 Asia Pacific Animal Stem Cell Therapy Market Facts & Figures by Region 3.5.1 Asia Pacific Animal Stem Cell Therapy Sales by Region 3.5.2 Asia Pacific Animal Stem Cell Therapy Sales by Region 3.5.3 China 3.5.4 Japan 3.5.5 South Korea 3.5.6 India 3.5.7 Australia 3.5.8 Taiwan 3.5.9 Indonesia 3.5.10 Thailand 3.5.11 Malaysia 3.5.12 Philippines 3.5.13 Vietnam 3.6 Latin America Animal Stem Cell Therapy Market Facts & Figures by Country 3.6.1 Latin America Animal Stem Cell Therapy Sales by Country 3.6.2 Latin America Animal Stem Cell Therapy Sales by Country 3.6.3 Mexico 3.6.3 Brazil 3.6.3 Argentina 3.7 Middle East and Africa Animal Stem Cell Therapy Market Facts & Figures by Country 3.7.1 Middle East and Africa Animal Stem Cell Therapy Sales by Country 3.7.2 Middle East and Africa Animal Stem Cell Therapy Sales by Country 3.7.3 Turkey 3.7.4 Saudi Arabia 3.7.5 U.A.E 4 Global Animal Stem Cell Therapy Historic Market Analysis by Type 4.1 Global Animal Stem Cell Therapy Sales Market Share by Type (2015-2020) 4.2 Global Animal Stem Cell Therapy Revenue Market Share by Type (2015-2020) 4.3 Global Animal Stem Cell Therapy Price Market Share by Type (2015-2020) 4.4 Global Animal Stem Cell Therapy Market Share by Price Tier (2015-2020): Low-End, Mid-Range and High-End 5 Global Animal Stem Cell Therapy Historic Market Analysis by Application 5.1 Global Animal Stem Cell Therapy Sales Market Share by Application (2015-2020) 5.2 Global Animal Stem Cell Therapy Revenue Market Share by Application (2015-2020) 5.3 Global Animal Stem Cell Therapy Price by Application (2015-2020) 6 Company Profiles and Key Figures in Animal Stem Cell Therapy Business 6.1 Medivet Biologics LLC 6.1.1 Corporation Information 6.1.2 Medivet Biologics LLC Description, Business Overview and Total Revenue 6.1.3 Medivet Biologics LLC Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.1.4 Medivet Biologics LLC Products Offered 6.1.5 Medivet Biologics LLC Recent Development 6.2 VETSTEM BIOPHARMA 6.2.1 VETSTEM BIOPHARMA Animal Stem Cell Therapy Production Sites and Area Served 6.2.2 VETSTEM BIOPHARMA Description, Business Overview and Total Revenue 6.2.3 VETSTEM BIOPHARMA Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.2.4 VETSTEM BIOPHARMA Products Offered 6.2.5 VETSTEM BIOPHARMA Recent Development 6.3 J-ARM 6.3.1 J-ARM Animal Stem Cell Therapy Production Sites and Area Served 6.3.2 J-ARM Description, Business Overview and Total Revenue 6.3.3 J-ARM Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.3.4 J-ARM Products Offered 6.3.5 J-ARM Recent Development 6.4 U.S. Stem Cell, Inc 6.4.1 U.S. Stem Cell, Inc Animal Stem Cell Therapy Production Sites and Area Served 6.4.2 U.S. Stem Cell, Inc Description, Business Overview and Total Revenue 6.4.3 U.S. Stem Cell, Inc Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.4.4 U.S. Stem Cell, Inc Products Offered 6.4.5 U.S. Stem Cell, Inc Recent Development 6.5 VetCell Therapeutics 6.5.1 VetCell Therapeutics Animal Stem Cell Therapy Production Sites and Area Served 6.5.2 VetCell Therapeutics Description, Business Overview and Total Revenue 6.5.3 VetCell Therapeutics Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.5.4 VetCell Therapeutics Products Offered 6.5.5 VetCell Therapeutics Recent Development 6.6 Celavet Inc. 6.6.1 Celavet Inc. Animal Stem Cell Therapy Production Sites and Area Served 6.6.2 Celavet Inc. Description, Business Overview and Total Revenue 6.6.3 Celavet Inc. Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.6.4 Celavet Inc. Products Offered 6.6.5 Celavet Inc. Recent Development 6.7 Magellan Stem Cells 6.6.1 Magellan Stem Cells Animal Stem Cell Therapy Production Sites and Area Served 6.6.2 Magellan Stem Cells Description, Business Overview and Total Revenue 6.6.3 Magellan Stem Cells Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.4.4 Magellan Stem Cells Products Offered 6.7.5 Magellan Stem Cells Recent Development 6.8 Kintaro Cells Power 6.8.1 Kintaro Cells Power Animal Stem Cell Therapy Production Sites and Area Served 6.8.2 Kintaro Cells Power Description, Business Overview and Total Revenue 6.8.3 Kintaro Cells Power Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.8.4 Kintaro Cells Power Products Offered 6.8.5 Kintaro Cells Power Recent Development 6.9 Animal Stem Care 6.9.1 Animal Stem Care Animal Stem Cell Therapy Production Sites and Area Served 6.9.2 Animal Stem Care Description, Business Overview and Total Revenue 6.9.3 Animal Stem Care Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.9.4 Animal Stem Care Products Offered 6.9.5 Animal Stem Care Recent Development 6.10 Animal Cell Therapies 6.10.1 Animal Cell Therapies Animal Stem Cell Therapy Production Sites and Area Served 6.10.2 Animal Cell Therapies Description, Business Overview and Total Revenue 6.10.3 Animal Cell Therapies Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.10.4 Animal Cell Therapies Products Offered 6.10.5 Animal Cell Therapies Recent Development 6.11 Cell Therapy Sciences 6.11.1 Cell Therapy Sciences Animal Stem Cell Therapy Production Sites and Area Served 6.11.2 Cell Therapy Sciences Animal Stem Cell Therapy Description, Business Overview and Total Revenue 6.11.3 Cell Therapy Sciences Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.11.4 Cell Therapy Sciences Products Offered 6.11.5 Cell Therapy Sciences Recent Development 6.12 Animacel 6.12.1 Animacel Animal Stem Cell Therapy Production Sites and Area Served 6.12.2 Animacel Animal Stem Cell Therapy Description, Business Overview and Total Revenue 6.12.3 Animacel Animal Stem Cell Therapy Sales, Revenue and Gross Margin (2015-2020) 6.12.4 Animacel Products Offered 6.12.5 Animacel Recent Development 7 Animal Stem Cell Therapy Manufacturing Cost Analysis 7.1 Animal Stem Cell Therapy Key Raw Materials Analysis 7.1.1 Key Raw Materials 7.1.2 Key Raw Materials Price Trend 7.1.3 Key Suppliers of Raw Materials 7.2 Proportion of Manufacturing Cost Structure 7.3 Manufacturing Process Analysis of Animal Stem Cell Therapy 7.4 Animal Stem Cell Therapy Industrial Chain Analysis 8 Marketing Channel, Distributors and Customers 8.1 Marketing Channel 8.2 Animal Stem Cell Therapy Distributors List 8.3 Animal Stem Cell Therapy Customers 9 Market Dynamics 9.1 Market Trends 9.2 Opportunities and Drivers 9.3 Challenges 9.4 Porters Five Forces Analysis 10 Global Market Forecast 10.1 Global Animal Stem Cell Therapy Market Estimates and Projections by Type 10.1.1 Global Forecasted Sales of Animal Stem Cell Therapy by Type (2021-2026) 10.1.2 Global Forecasted Revenue of Animal Stem Cell Therapy by Type (2021-2026) 10.2 Animal Stem Cell Therapy Market Estimates and Projections by Application 10.2.1 Global Forecasted Sales of Animal Stem Cell Therapy by Application (2021-2026) 10.2.2 Global Forecasted Revenue of Animal Stem Cell Therapy by Application (2021-2026) 10.3 Animal Stem Cell Therapy Market Estimates and Projections by Region 10.3.1 Global Forecasted Sales of Animal Stem Cell Therapy by Region (2021-2026) 10.3.2 Global Forecasted Revenue of Animal Stem Cell Therapy by Region (2021-2026) 10.4 North America Animal Stem Cell Therapy Estimates and Projections (2021-2026) 10.5 Europe Animal Stem Cell Therapy Estimates and Projections (2021-2026) 10.6 Asia Pacific Animal Stem Cell Therapy Estimates and Projections (2021-2026) 10.7 Latin America Animal Stem Cell Therapy Estimates and Projections (2021-2026) 10.8 Middle East and Africa Animal Stem Cell Therapy Estimates and Projections (2021-2026) 11 Research Finding and Conclusion 12 Methodology and Data Source 12.1 Methodology/Research Approach 12.1.1 Research Programs/Design 12.1.2 Market Size Estimation 12.1.3 Market Breakdown and Data Triangulation 12.2 Data Source 12.2.1 Secondary Sources 12.2.2 Primary Sources 12.3 Author List 12.4 Disclaimer

About Us:

QYResearch always pursuits high product quality with the belief that quality is the soul of business. Through years of effort and supports from huge number of customer supports, QYResearch consulting group has accumulated creative design methods on many high-quality markets investigation and research team with rich experience. Today, QYResearch has become the brand of quality assurance in consulting industry.

View post:
New Trend: Animal Stem Cell Therapy Market Growth by Top Companies, Trends by Types and Application, Forecast to 2026 | Medivet Biologics LLC, VETSTEM...

Global Biologics Safety Testing Market is expected to grow at a CAGR of 12.2% during the forecast pe – PharmiWeb.com

A new research report published by Fior Markets with the titleBiologics Safety Testing Market by Product Type (Instruments, Services, Kit and Reagents), Test Type (Bioburden tests, Endotoxin, Sterility, Cell Line Authentication, Adventitious Agent Detection Tests, Residual Host Contamination Detection Tests, Characterization Tests and other), Application ( Vaccine Development, Blood Products, Tissue and Tissue related Products testing, Cellular and Gene Therapy and Stem Cell Research), Region, Global Forecast 2020-2027.

Theglobal biologics safety testing marketis expected to grow from USD 3.08 billion in 2019 to USD 7.62 billion by 2027, at a CAGR of 12.2% during the forecast period 2020-2027. Asia-Pacific is expected to increase at the highest CAGR. The rise is healthcare spending, and increasing awareness among the people has anticipated the market growth of the biologics safety testing market. Although, currently North America holds the largest market share as high investments in biotechnology and cancer research has increased the demand for the products. Also, development of vaccines, & drugs and increasing number of R&D investments by many companies has contributed to the market demand. Additionally, increasing number of chronic diseases is anticipated to increase the usage of advanced technologies accelerated the market growth.

DOWNLOAD FREE SAMPLE REPORT:https://www.fiormarkets.com/report-detail/418372/request-sample

Key players in the biologics safety testing market are Toxikon Corporation, Thermo Fisher Scientific Inc., Pace Analytical, Lonza Group, MilliporeSigma, Sartorius Stedim BioOutcome Limited, SGS SA, Merck KFaA, Cytovance Biologics Inc., WuXi Apptec, Charles River Laboratries and others. The companies have been tying up with the research centres in order to adopt the technical advancements and increase the sales margin.

The product type segment includes instruments, services, kit and reagents.Reagents constitutes for the largest market share among all. They can be classified into antibiotics, biological buffers, attachments & matrix factors, etc. The reason for their large market share is the rapid technical advancements and modifications. The test type segment includes bioburden tests, endotoxin, sterility, cell line authentication, adventitious agent detection tests, residual host contamination detection tests, characterization tests and other. Endotoxin dominates the market demand out of all the segments. The rise in use of these tests in sectors such as manufacturing and production of drugs has been the contributing factors. The application segment includes vaccine development, blood products, tissue and tissue related products testing, cellular and gene therapy and stem cell research. Vaccine constitutes of the largest market share as of now in the application segment as because vaccines are made necessary by almost every state. The growing vulnerability to possess disease has increased the use of vaccines over the years which have accelerated the market demand of the biologics safety testing market.

Biologics safety testing prevents bacterial contamination. The products contain serum and blood. The objective of the biologics safety testing devices is to ensure safety of vaccines and biopharmaceuticals by eliminating any bacterial presence. The growing advancement in healthcare sector and continuous innovations in the product have increased the market demand of the product. Also, growing awareness for hygiene among people is the reason why its application has increase over the years.

ACCESS FULL REPORT:https://www.fiormarkets.com/report/biologics-safety-testing-market-by-product-type-instruments-418372.html

About the report:The globalbiologics safety testing market is analyzed on the basis of value (USD Billion), volume (K Units), export (K Units), and import (K Units). All the segments have been analyzed on global, regional and country basis. The study includes an analysis of more than 30 countries for each segment. The report offers in-depth analysis of driving factors, opportunities, restraints, and challenges for gaining the key insight of the market. The study includes porters five forces model, attractiveness analysis, raw material analysis, and competitor position grid analysis.

Customization of the Report: The report can be customized as per client requirements. For further queries, you can contact us onsales@fiormarkets.comor +1-201-465-4211. Our executives will be pleased to understand your requirements and offer you the best-suited reports.

Contact Us Mark Stone Phone:+1-201-465-4211 Email:sales@fiormarkets.com Web:www.fiormarkets.com

This content has been distributed via CDN Newswire press release distribution service. For press release enquires please mail us at contact@cdnnewswire.com.

Continue reading here:
Global Biologics Safety Testing Market is expected to grow at a CAGR of 12.2% during the forecast pe - PharmiWeb.com