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Covid-19 Effect on Global Semiconductor Laser Therapeutic Equipment Market-Industry Demand, Trends, and Forecast 2028 – The Daily Chronicle

August 21st, 2020 11:56 am

The Impact of COVID-19 on the Semiconductor Laser Therapeutic Equipment Market Report Research Industry, 2020 report has been added to market.biz offering.

Semiconductor Laser Therapeutic Equipment market2020 reportis a research document that comprises of comprehensive data which boosts and helps the appraisal of every aspect of the Semiconductor Laser Therapeutic Equipment businesses withCovid-19 Impact. It deploys an overview of the baseline and structure of the Semiconductor Laser Therapeutic Equipment market, which summarizes its beneficial or prohibitive aspects liable for regional and global evolution. It outlines the ongoing trends and position of Semiconductor Laser Therapeutic Equipment by thoroughly probing several manufacturers, associations, suppliers, organizations, and industries under the Semiconductor Laser Therapeutic Equipment market.

Apart from this, the globalSemiconductor Laser Therapeutic Equipment Market2020 report provides crucial particulars regarding the categorization, assessed growth trends, distribution network, economical or commercial terms, and many other vital elements related to the Semiconductor Laser Therapeutic Equipment. Rapidly increasing spendable income and innovative products offered by manufacturers are expected to boost Semiconductor Laser Therapeutic Equipment industry over the forecast interval. A vast and growing client base of the Semiconductor Laser Therapeutic Equipment industry creates an opportunity for producers to serve to a significant market and make money.

This report considers the Semiconductor Laser Therapeutic Equipment scope (volume and value) by rivals, regions, product categories, and end-users, previous data, and forecast data. The document also examines the international market competition perspective, leading players in the market, and ongoing trends. It even highlights forthcoming opportunities and challenges, ambiguities and import obstructions, sales lines, and vendors. The research document further estimates the Semiconductor Laser Therapeutic Equipment growth scale as well as forthcoming trends worldwide. Even more, it separates Semiconductor Laser Therapeutic Equipment starting from type to purpose and from comprehensive analysis to key market players and predictions.

Whether you need a birds eye view of the Global Semiconductor Laser Therapeutic Equipmentmarket or a deep dive into a niche segment, heres a report ready and waiting for you. Get Sample PDF @https://market.biz/report/global-semiconductor-laser-therapeutic-equipment-market-qy/534384/#requestforsample.

Sirona Dental Systems GmbHLumenis Inc.Dornier MedTech GmbHPHYSIOMED ELEKTROMEDIZIN AGBiolaseIRIDEX CorporationCynosureCuteraQuanta System S.p.AWON TECHShandong ShensiHelsenGuangdunMedicenWuhan HNCL.H.H. MedicalZhengan MedicalShenzhen Tian

OpthalmologyDermatologyGynecologyDentistryUrologyCardiovascularOthers

Family UsingBeauty UsingMedical Using

Semiconductor Laser Therapeutic Equipment report comprises of the manufacturers data, like price, delivery, advantages, net revenue, enterprise allowance, etc. The entire dataset will offer a better understanding of the competitors across the market. Even more, the study covers assessment from a global viewpoint, which shows a regional growth level, along with the scope, disbursement data, market size, and profit.

The report focuses on competitors dominating the sector and outlining Semiconductor Laser Therapeutic Equipment company profile. The analysis relies on SWOT analysis to reveal the competitive environment of the market throughout the world. Even more, the report includes analysis of current Semiconductor Laser Therapeutic Equipment development, market shares, syndicates and grade of investments with other Semiconductor Laser Therapeutic Equipment chief companies, financial agreements affecting the Semiconductor Laser Therapeutic Equipment market.

Geographically, this document is segmented into different chief territories, containing profits, sales, growth rate and market share (percent) of Semiconductor Laser Therapeutic Equipment in the areas listed below,

South America & including countries

The Middle East and Africa

North America

Europe

Asia-Pacific.

& included countries.

This report will provide you following insights-

Dont see what youre looking for? Enquire here. @https://market.biz/report/global-semiconductor-laser-therapeutic-equipment-market-qy/534384/#inquiry

1.The document offers statistical data about the value (US$) and size (units) for the worldwide Semiconductor Laser Therapeutic Equipment industry between 2019 to 2028.

2.The report also traces the leading market rivals that will create and influence the Semiconductor Laser Therapeutic Equipment business to a greater extent.

3.Extensive understanding of the fundamental trends impacting each sector, although greatest threat, latest technologies, and opportunities that could build the global Semiconductor Laser Therapeutic Equipment market both supply and offer.

4.The report helps the customer to determine the substantial results of major market players or rulers of Semiconductor Laser Therapeutic Equipment sector.

5.The study offers a five-year vital prediction for the Semiconductor Laser Therapeutic Equipment developments, separated by basic product type, end-use group, and various regions across the world.

6.The data analysis present in this report relies on and includes extraction from both elementary and secondary assets.

Buy Latest 2020 Edition of This Report

Ultimately, the conclusion section of the Semiconductor Laser Therapeutic Equipment industry report states the opinion of the industry experts.

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Covid-19 Effect on Global Semiconductor Laser Therapeutic Equipment Market-Industry Demand, Trends, and Forecast 2028 - The Daily Chronicle

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Current and Future Trend of Connective Tissue Growth Factor Market Analysis and Forecast 2020-2026 | BLR Bio LLC, FibroGen Inc – Owned

August 21st, 2020 11:56 am

LOS ANGELES, United States: QY Research as of late produced a research report titled, Global and Japan Connective Tissue Growth Factor Market Insights, Forecast to 2026. The research report speak about the potential development openings that exist in the worldwide market. The report is broken down on the basis of research procedures procured from historical and forecast information. The Global and Japan Connective Tissue Growth Factor market is relied upon to develop generously and flourish as far as volume and incentive during the gauge time frame. The report will give a knowledge about the development openings and controls that will build the market. Pursuers can increase important perception about the eventual fate of the market.

Key Companies/Manufacturers operating in the Global and Japan Connective Tissue Growth Factor market include: , BLR Bio LLC, FibroGen Inc, ProMetic Life Sciences Inc, RXi Pharmaceuticals Corp,

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/2080969/global-and-japan-connective-tissue-growth-factor-market

Segmental Analysis

The report incorporates significant sections, for example, type and end user and a variety of segments that decide the prospects of Global and Japan Connective Tissue Growth Factor market. Each type provide data with respect to the business esteem during the conjecture time frame. The application area likewise gives information by volume and consumption during the estimate time frame. The comprehension of this segment direct the readers in perceiving the significance of variables that shape the market development.

Global and Japan Connective Tissue Growth Factor Market Segment By Type:

BLR-200IB-DMDOLX-201PBI-4050Others

Global and Japan Connective Tissue Growth Factor Market Segment By Application:

Hypertrophic ScarsOpthalmologyGenetic DisordersLiver FibrosisOthers

Competitive Landscape

Competitor analysis is one of the best sections of the report that compares the progress of leading players based on crucial parameters, including market share, new developments, global reach, local competition, price, and production. From the nature of competition to future changes in the vendor landscape, the report provides in-depth analysis of the competition in the Global and Japan Connective Tissue Growth Factor market.

Key questions answered in the report:

For Discount, Customization in the Report Drop Your Query Here: https://www.qyresearch.com/customize-request/form/2080969/global-and-japan-connective-tissue-growth-factor-market

TOC

1 Study Coverage1.1 Connective Tissue Growth Factor Product Introduction1.2 Market Segments1.3 Key Connective Tissue Growth Factor Manufacturers Covered: Ranking by Revenue1.4 Market by Type1.4.1 Global Connective Tissue Growth Factor Market Size Growth Rate by Type1.4.2 BLR-2001.4.3 IB-DMD1.4.4 OLX-2011.4.5 PBI-40501.4.6 Others1.5 Market by Application1.5.1 Global Connective Tissue Growth Factor Market Size Growth Rate by Application1.5.2 Hypertrophic Scars1.5.3 Opthalmology1.5.4 Genetic Disorders1.5.5 Liver Fibrosis1.5.6 Others1.6 Study Objectives1.7 Years Considered 2 Executive Summary2.1 Global Connective Tissue Growth Factor Market Size, Estimates and Forecasts2.1.1 Global Connective Tissue Growth Factor Revenue 2015-20262.1.2 Global Connective Tissue Growth Factor Sales 2015-20262.2 Global Connective Tissue Growth Factor, Market Size by Producing Regions: 2015 VS 2020 VS 20262.3 Connective Tissue Growth Factor Historical Market Size by Region (2015-2020)2.3.1 Global Connective Tissue Growth Factor Retrospective Market Scenario in Sales by Region: 2015-20202.3.2 Global Connective Tissue Growth Factor Retrospective Market Scenario in Revenue by Region: 2015-20202.4 Connective Tissue Growth Factor Market Estimates and Projections by Region (2021-2026)2.4.1 Global Connective Tissue Growth Factor Sales Forecast by Region (2021-2026)2.4.2 Global Connective Tissue Growth Factor Revenue Forecast by Region (2021-2026) 3 Global Connective Tissue Growth Factor Competitor Landscape by Players3.1 Global Top Connective Tissue Growth Factor Sales by Manufacturers3.1.1 Global Connective Tissue Growth Factor Sales by Manufacturers (2015-2020)3.1.2 Global Connective Tissue Growth Factor Sales Market Share by Manufacturers (2015-2020)3.2 Global Connective Tissue Growth Factor Manufacturers by Revenue3.2.1 Global Connective Tissue Growth Factor Revenue by Manufacturers (2015-2020)3.2.2 Global Connective Tissue Growth Factor Revenue Share by Manufacturers (2015-2020)3.2.3 Global Connective Tissue Growth Factor Market Concentration Ratio (CR5 and HHI) (2015-2020)3.2.4 Global Top 10 and Top 5 Companies by Connective Tissue Growth Factor Revenue in 20193.2.5 Global Connective Tissue Growth Factor Market Share by Company Type (Tier 1, Tier 2 and Tier 3)3.3 Global Connective Tissue Growth Factor Price by Manufacturers3.4 Global Connective Tissue Growth Factor Manufacturing Base Distribution, Product Types3.4.1 Connective Tissue Growth Factor Manufacturers Manufacturing Base Distribution, Headquarters3.4.2 Manufacturers Connective Tissue Growth Factor Product Type3.4.3 Date of International Manufacturers Enter into Connective Tissue Growth Factor Market3.5 Manufacturers Mergers & Acquisitions, Expansion Plans 4 Market Size by Type (2015-2026)4.1 Global Connective Tissue Growth Factor Market Size by Type (2015-2020)4.1.1 Global Connective Tissue Growth Factor Sales by Type (2015-2020)4.1.2 Global Connective Tissue Growth Factor Revenue by Type (2015-2020)4.1.3 Connective Tissue Growth Factor Average Selling Price (ASP) by Type (2015-2026)4.2 Global Connective Tissue Growth Factor Market Size Forecast by Type (2021-2026)4.2.1 Global Connective Tissue Growth Factor Sales Forecast by Type (2021-2026)4.2.2 Global Connective Tissue Growth Factor Revenue Forecast by Type (2021-2026)4.2.3 Connective Tissue Growth Factor Average Selling Price (ASP) Forecast by Type (2021-2026)4.3 Global Connective Tissue Growth Factor Market Share by Price Tier (2015-2020): Low-End, Mid-Range and High-End 5 Market Size by Application (2015-2026)5.1 Global Connective Tissue Growth Factor Market Size by Application (2015-2020)5.1.1 Global Connective Tissue Growth Factor Sales by Application (2015-2020)5.1.2 Global Connective Tissue Growth Factor Revenue by Application (2015-2020)5.1.3 Connective Tissue Growth Factor Price by Application (2015-2020)5.2 Connective Tissue Growth Factor Market Size Forecast by Application (2021-2026)5.2.1 Global Connective Tissue Growth Factor Sales Forecast by Application (2021-2026)5.2.2 Global Connective Tissue Growth Factor Revenue Forecast by Application (2021-2026)5.2.3 Global Connective Tissue Growth Factor Price Forecast by Application (2021-2026) 6 Japan by Players, Type and Application6.1 Japan Connective Tissue Growth Factor Market Size YoY Growth 2015-20266.1.1 Japan Connective Tissue Growth Factor Sales YoY Growth 2015-20266.1.2 Japan Connective Tissue Growth Factor Revenue YoY Growth 2015-20266.1.3 Japan Connective Tissue Growth Factor Market Share in Global Market 2015-20266.2 Japan Connective Tissue Growth Factor Market Size by Players (International and Local Players)6.2.1 Japan Top Connective Tissue Growth Factor Players by Sales (2015-2020)6.2.2 Japan Top Connective Tissue Growth Factor Players by Revenue (2015-2020)6.3 Japan Connective Tissue Growth Factor Historic Market Review by Type (2015-2020)6.3.1 Japan Connective Tissue Growth Factor Sales Market Share by Type (2015-2020)6.3.2 Japan Connective Tissue Growth Factor Revenue Market Share by Type (2015-2020)6.3.3 Japan Connective Tissue Growth Factor Price by Type (2015-2020)6.4 Japan Connective Tissue Growth Factor Market Estimates and Forecasts by Type (2021-2026)6.4.1 Japan Connective Tissue Growth Factor Sales Forecast by Type (2021-2026)6.4.2 Japan Connective Tissue Growth Factor Revenue Forecast by Type (2021-2026)6.4.3 Japan Connective Tissue Growth Factor Price Forecast by Type (2021-2026)6.5 Japan Connective Tissue Growth Factor Historic Market Review by Application (2015-2020)6.5.1 Japan Connective Tissue Growth Factor Sales Market Share by Application (2015-2020)6.5.2 Japan Connective Tissue Growth Factor Revenue Market Share by Application (2015-2020)6.5.3 Japan Connective Tissue Growth Factor Price by Application (2015-2020)6.6 Japan Connective Tissue Growth Factor Market Estimates and Forecasts by Application (2021-2026)6.6.1 Japan Connective Tissue Growth Factor Sales Forecast by Application (2021-2026)6.6.2 Japan Connective Tissue Growth Factor Revenue Forecast by Application (2021-2026)6.6.3 Japan Connective Tissue Growth Factor Price Forecast by Application (2021-2026) 7 North America7.1 North America Connective Tissue Growth Factor Market Size YoY Growth 2015-20267.2 North America Connective Tissue Growth Factor Market Facts & Figures by Country7.2.1 North America Connective Tissue Growth Factor Sales by Country (2015-2020)7.2.2 North America Connective Tissue Growth Factor Revenue by Country (2015-2020)7.2.3 U.S.7.2.4 Canada 8 Europe8.1 Europe Connective Tissue Growth Factor Market Size YoY Growth 2015-20268.2 Europe Connective Tissue Growth Factor Market Facts & Figures by Country8.2.1 Europe Connective Tissue Growth Factor Sales by Country8.2.2 Europe Connective Tissue Growth Factor Revenue by Country8.2.3 Germany8.2.4 France8.2.5 U.K.8.2.6 Italy8.2.7 Russia 9 Asia Pacific9.1 Asia Pacific Connective Tissue Growth Factor Market Size YoY Growth 2015-20269.2 Asia Pacific Connective Tissue Growth Factor Market Facts & Figures by Country9.2.1 Asia Pacific Connective Tissue Growth Factor Sales by Region (2015-2020)9.2.2 Asia Pacific Connective Tissue Growth Factor Revenue by Region9.2.3 China9.2.4 Japan9.2.5 South Korea9.2.6 India9.2.7 Australia9.2.8 Taiwan9.2.9 Indonesia9.2.10 Thailand9.2.11 Malaysia9.2.12 Philippines9.2.13 Vietnam 10 Latin America10.1 Latin America Connective Tissue Growth Factor Market Size YoY Growth 2015-202610.2 Latin America Connective Tissue Growth Factor Market Facts & Figures by Country10.2.1 Latin America Connective Tissue Growth Factor Sales by Country10.2.2 Latin America Connective Tissue Growth Factor Revenue by Country10.2.3 Mexico10.2.4 Brazil10.2.5 Argentina 11 Middle East and Africa11.1 Middle East and Africa Connective Tissue Growth Factor Market Size YoY Growth 2015-202611.2 Middle East and Africa Connective Tissue Growth Factor Market Facts & Figures by Country11.2.1 Middle East and Africa Connective Tissue Growth Factor Sales by Country11.2.2 Middle East and Africa Connective Tissue Growth Factor Revenue by Country11.2.3 Turkey11.2.4 Saudi Arabia11.2.5 U.A.E 12 Company Profiles12.1 BLR Bio LLC12.1.1 BLR Bio LLC Corporation Information12.1.2 BLR Bio LLC Description and Business Overview12.1.3 BLR Bio LLC Sales, Revenue and Gross Margin (2015-2020)12.1.4 BLR Bio LLC Connective Tissue Growth Factor Products Offered12.1.5 BLR Bio LLC Recent Development12.2 FibroGen Inc12.2.1 FibroGen Inc Corporation Information12.2.2 FibroGen Inc Description and Business Overview12.2.3 FibroGen Inc Sales, Revenue and Gross Margin (2015-2020)12.2.4 FibroGen Inc Connective Tissue Growth Factor Products Offered12.2.5 FibroGen Inc Recent Development12.3 ProMetic Life Sciences Inc12.3.1 ProMetic Life Sciences Inc Corporation Information12.3.2 ProMetic Life Sciences Inc Description and Business Overview12.3.3 ProMetic Life Sciences Inc Sales, Revenue and Gross Margin (2015-2020)12.3.4 ProMetic Life Sciences Inc Connective Tissue Growth Factor Products Offered12.3.5 ProMetic Life Sciences Inc Recent Development12.4 RXi Pharmaceuticals Corp12.4.1 RXi Pharmaceuticals Corp Corporation Information12.4.2 RXi Pharmaceuticals Corp Description and Business Overview12.4.3 RXi Pharmaceuticals Corp Sales, Revenue and Gross Margin (2015-2020)12.4.4 RXi Pharmaceuticals Corp Connective Tissue Growth Factor Products Offered12.4.5 RXi Pharmaceuticals Corp Recent Development12.11 BLR Bio LLC12.11.1 BLR Bio LLC Corporation Information12.11.2 BLR Bio LLC Description and Business Overview12.11.3 BLR Bio LLC Sales, Revenue and Gross Margin (2015-2020)12.11.4 BLR Bio LLC Connective Tissue Growth Factor Products Offered12.11.5 BLR Bio LLC Recent Development 13 Market Opportunities, Challenges, Risks and Influences Factors Analysis13.1 Market Opportunities and Drivers13.2 Market Challenges13.3 Market Risks/Restraints13.4 Porters Five Forces Analysis13.5 Primary Interviews with Key Connective Tissue Growth Factor Players (Opinion Leaders) 14 Value Chain and Sales Channels Analysis14.1 Value Chain Analysis14.2 Connective Tissue Growth Factor Customers14.3 Sales Channels Analysis14.3.1 Sales Channels14.3.2 Distributors 15 Research Findings and Conclusion 16 Appendix16.1 Research Methodology16.1.1 Methodology/Research Approach16.1.2 Data Source16.2 Author Details16.3 Disclaimer

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Current and Future Trend of Connective Tissue Growth Factor Market Analysis and Forecast 2020-2026 | BLR Bio LLC, FibroGen Inc - Owned

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Absorbable and Non Absorbable Sutures Market Projected To Grow At A Significant Rate With Industry Analysis || Major Gaints Curetis., SolGent Co.,…

August 21st, 2020 11:56 am

The research, analysis and estimations about the market have been performed with the steadfast knowledge in this Absorbable and Non Absorbable Sutures Market report. This market report helps to obtain information about all the above factors by giving actionable market insights and comprehensive market analysis. Analysis and discussion of important industry trends, market size, sales volume, and market share are also estimated in this market report. To achieve maximum return on investment (ROI), its very fundamental to figure out market parameters such as brand awareness, market landscape, possible future issues, industry trends & customer behaviour where this Absorbable and Non Absorbable Sutures Market report comes into picture.

Get Sample PDF (including COVID19 Impact Analysis) of Market Report @https://www.databridgemarketresearch.com/request-a-sample/?dbmr=global-absorbable-non-absorbable-sutures-market&rp

Global Absorbable and Non Absorbable Sutures Market report gives clear idea to Healthcare industry in regard with what is already available in the market, what market anticipates, the competitive environment, and what to be get done to surpass the competitor. This market report serves a great purpose of better decision making and achieving competitive advantage. The report supports in evaluating brand awareness, market landscape, possible future issues, industry trends and customer behaviour with which refined business strategies can be fixed. Absorbable and Non Absorbable Sutures Market report has been comprised of a significant data along with future forecast and detailed analysis on a global and regional level.

Market Analysis and Insights: Global Absorbable and Non-Absorbable Sutures Market

Global absorbable and non-absorbable sutures market is expected to gain market growth in the forecast period of 2020 to 2027. Data Bridge Market Research analyses the market to growing at a CAGR of 4% in the above-mentioned forecast period.

The major players operating in theabsorbable and non-absorbable sutures marketreport areThermo Fisher Scientific Inc., Siemens Healthcare GmbH, SeegeneInc, FastSense Diagnostics, Curetis., SolGent Co., Ltd, Mologic, Abbott, altona Diagnostics GmbH, F. Hoffmann-La Roche Ltd, QIAGEN, BioMaxima SA, CTK Biotech, Inc, VivaChek Biotech (Hangzhou) Co., Ltd., Sensing Self, PTE. Ltd, and Hangzhou Biotest Biotech Co., LTD. among other domestic and global players.Market share data is available for global, North America, Europe, Asia-Pacific (APAC), Middle East and Africa (MEA) and South America separately. DBMR analysts understand competitive strengths and provide competitive analysis for each competitor separately.

Get Full TOC, Tables and Figures of Market Report @https://www.databridgemarketresearch.com/toc/?dbmr=global-absorbable-non-absorbable-sutures-market&rp

Sutures are the medical equipments for the usage in cases of surgeries which is in general term known as stitches or surgical threads used insurgeriesfor making connection between the edges of wound which will help to heal it more efficiently. These surgeries can be for either internal or external body system for different tissues healing. There are different sutures available in market according to needs of cases with varying thickness or material as per requirement of surgery. Broadly these sutures are divided into absorbable and non absorbable sutures market. Absorbable suture market is expected to boom in growth rate in forecasted period as it is prove to be better for inner body wound closure whereas in the use of synthetic sources like polymer which are normally manufactured and easily available make market grow. Increase in number of diseases and trauma cases are going to be the driver for the growth of the market whereas rising geriatric population, which is going to be beneficial for market. Moreover Government spending huge amount on healthcare infrastructure development can be opportunity for meeting unmet medical needs in developing regions. However high cost of surgeries and equipment and complicated with other strict regulations on market are restraining factor for the market. There are still some limitations in sutures market which can be a challenge to fulfil market need

This global absorbable and non-absorbable sutures market report provides details of new recent developments, trade regulations, import exportanalysis, production analysis, value chain optimization, market share, impact of domestic and localised market players, analyses opportunities in terms of emerging revenue pockets, changes in market regulations, strategic market growth analysis, market size, category market growths, application niches and dominance, product approvals, product launches, geographic expansions, technological innovations in the market. To gain more info onData Bridge Market ResearchGlobal absorbable and non-absorbable sutures market contact us for anAnalyst Brief, our team will help you take an informed market decision to achieve market growth.

Global Absorbable and Non-Absorbable Sutures Market Scope and Market Size

Global absorbable and non-absorbable sutures market is segmented on the basis of product type, surgery type, and end user. The growth amongst these segments will help you analyse meagre growth segments in the industries, and provide the users with valuable market overview and market insights to help them in making strategic decisions for identification of core market applications.

Global Absorbable and Non-Absorbable Sutures Market Country Level Analysis

Global absorbable and non-absorbable sutures market is analysed and market size insights and trends are provided by country, product type, surgery type, and end user as referenced above.

The countries covered in the absorbable and non absorbable sutures market report are the U.S., Canada and Mexico in North America, Germany, France, U.K., Netherlands, Switzerland, Belgium, Russia, Italy, Spain, Turkey, Rest of Europe in Europe, China, Japan, India, South Korea, Singapore, Malaysia, Australia, Thailand, Indonesia, Philippines, Rest of Asia-Pacific (APAC) in the Asia-Pacific (APAC), Saudi Arabia, U.A.E, South Africa, Egypt, Israel, Rest of Middle East and Africa (MEA) as a part of Middle East and Africa(MEA), Brazil, Argentina and Rest of South America as part of South America.

North America is anticipated to dominate market share during forecast period due high pace in technological advancement and huge government investment to improve healthcare infrastructure whereas increasing demand for efficient and minimal invasive surgery will expand market growth. Moreover increasing cases of chronic disease and trauma surgeries will also fuel region market growth whereas Asia-Pacific (APAC) is anticipated to expand at the most leading germination pace in the coming years due to developing economies like China, Japan, and India

The country section of the absorbable and non-absorbable sutures market report also provides individual market impacting factors and changes in regulation in the market domestically that impacts the current and future trends of the market. Data points such as consumption volumes, production sites and volumes, import export analysis, price trend analysis, cost of raw materials, down-stream and upstream value chain analysis are some of the major pointers used to forecast the market scenario for individual countries. Also, presence and availability of global brands and their challenges faced due to large or scarce competition from local and domestic brands, impact of domestic tariffs and trade routes are considered while providing forecast analysis of the country data.

Healthcare Infrastructure growth Installed base and New Technology Penetration

Absorbable and non-absorbable sutures market also provides you with detailed market analysis for every country growth in healthcare expenditure for capital equipment, installed base of different kind of products for Global absorbable and non-absorbable sutures market, impact of technology using life line curves and changes in healthcare regulatory scenarios and their impact on the Global absorbable and non-absorbable sutures market. The data is available for historic period 2010 to 2018.

Competitive Landscape and Global Absorbable and Non-Absorbable Sutures Market Share Analysis

Absorbable and non-absorbable sutures market competitive landscape provides details by competitor. Details included are company overview, company financials, revenue generated, market potential, investment in research and development, new market initiatives, global presence, production sites and facilities, production capacities, company strengths and weaknesses, product launch, product width and breadth, application dominance. The above data points provided are only related to the companies focus related to Global absorbable and non-absorbable sutures market.

Customization Available: Global Absorbable and Non-Absorbable Sutures Market

Data Bridge Market Research is a leader in advanced formative research. We take pride in servicing our existing and new customers with data and analysis that match and suits their goal. The report can be customised to include price trend analysis of target brands understanding the market for additional countries (ask for the list of countries), clinical trial results data, literature review, refurbished market and product base analysis. Market analysis of target competitors can be analysed from technology-based analysis to market portfolio strategies. We can add as many competitors that you require data about in the format and data style you are looking for. Our team of analysts can also provide you data in crude raw excel files pivot tables (Factbook) or can assist you in creating presentations from the data sets available in the report.

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Data Bridge Market Researchis a versatile market research and consulting firm with over 500 analysts working in different industries. We have catered more than 40% of the fortune 500 companies globally and have a network of more than 5000+ clientele around the globe. Our coverage of industries include Medical Devices, Pharmaceuticals, Biotechnology, Semiconductors, Machinery, Information and Communication Technology, Automobiles and Automotive, Chemical and Material, Packaging, Food and Beverages, Cosmetics, Specialty Chemicals, Fast Moving Consumer Goods, Robotics, among many others.

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Absorbable and Non Absorbable Sutures Market Projected To Grow At A Significant Rate With Industry Analysis || Major Gaints Curetis., SolGent Co.,...

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American Society of Clinical Oncology Exclusively Cites myChoice CDx in New Recommendations for Patients with Advanced Ovarian Cancer – BioSpace

August 21st, 2020 11:55 am

SALT LAKE CITY, Aug. 21, 2020 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc. (NASDAQ: MYGN), a global leader in molecular diagnostics and precision medicine, announced today that the American Society of Clinical Oncology (ASCO) has exclusively included Myriads myChoice CDx test in its new recommendations on the use of PARP inhibitors for the treatment and management of certain patients with advanced ovarian cancer. The new recommendations, based on clinical trial results, were published in the Journal of Clinical Oncology.

The guideline, titled PARP Inhibitors in the Management of Ovarian Cancer: ASCO Guideline, where myChoice CDx was the only named commercial companion diagnostic, states that women with ovarian cancer and germline or somatic mutations in BRCA1 or BRCA2 genes and/or genomic instability as determined by Myriad myChoice CDx are recommended by ASCO for PARP inhibitor therapy. The guideline includes myChoice CDx guided management in both newly diagnosed and recurrent ovarian cancer.

We are thrilled to be a part of the rapidly changing landscape in guiding treatment for patients with ovarian cancer. The new ASCO guidelines highlight the large number of recent studies that have gone into improving ovarian cancer patient outcomes, said Thomas Slavin, M.D., FACMG, DABCC, senior vice president of Medical Affairs for Myriad Oncology.

According to the American Cancer Society, ovarian cancer ranks fifth in cancer deaths among women, accounting for more deaths than any other cancer of the female reproductive system. In the United States, it is estimated there will be 21,750 new cases diagnosed and around 13,940 deaths in 2020. A woman's risk of getting ovarian cancer during her lifetime is about one in 78 and the chance of dying from ovarian cancer is about one in 108.

About Myriad myChoice CDx Myriad's myChoice CDx is the most comprehensive homologous recombination deficiency test, enabling physicians to identify patients with tumors that have lost the ability to repair double-stranded DNA breaks, resulting in increased susceptibility to DNA-damaging drugs such as platinum drugs or PARP inhibitors. The myChoice CDx test comprises tumor sequencing of the BRCA1 and BRCA2 genes and a composite of three proprietary technologies (loss of heterozygosity, telomeric allelic imbalance and large-scale state transitions). For more information, visit: https://myriad-oncology.com/mychoice-cdx/

About Myriad GeneticsMyriad Genetics Inc., is a leading personalized medicine company dedicated to being a trusted advisor transforming patient lives worldwide with pioneering molecular diagnostics. Myriad discovers and commercializes molecular diagnostic tests that: determine the risk of developing disease, accurately diagnose disease, assess the risk of disease progression, and guide treatment decisions across six major medical specialties where molecular diagnostics can significantly improve patient care and lower healthcare costs. Myriad is focused on three strategic imperatives: transitioning and expanding its hereditary cancer testing markets, diversifying its product portfolio through the introduction of new products and increasing the revenue contribution from international markets. For more information on how Myriad is making a difference, please visit the Company's website: http://www.myriad.com.

Myriad, the Myriad logo, BART, BRACAnalysis, Colaris, Colaris AP, myPath, myRisk, Myriad myRisk, myRisk Hereditary Cancer, myChoice, myPlan, BRACAnalysis CDx, Tumor BRACAnalysis CDx, myChoice CDx, Vectra, Prequel, Foresight, GeneSight, riskScore and Prolaris are trademarks or registered trademarks of Myriad Genetics, Inc. or its wholly owned subsidiaries in the United States and foreign countries. MYGN-F, MYGN-G.

Safe Harbor StatementThis press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including statements related to the new ASCO guideline titled PARP Inhibitors in the Management of Ovarian Cancer: ASCO Guideline and the Companys myChoice CDx testings place in such guideline; and the Companys strategic directives under the caption "About Myriad Genetics." These "forward-looking statements" are based on management's current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by forward-looking statements. These risks and uncertainties include, but are not limited to: uncertainties associated with COVID-19, including its possible effects on our operations and the demand for our products and services; our ability to efficiently and flexibly manage our business amid uncertainties related to COVID-19; the risk that sales and profit margins of our molecular diagnostic tests and pharmaceutical and clinical services may decline; risks related to our ability to transition from our existing product portfolio to our new tests, including unexpected costs and delays; risks related to decisions or changes in governmental or private insurers reimbursement levels for our tests or our ability to obtain reimbursement for our new tests at comparable levels to our existing tests; risks related to increased competition and the development of new competing tests and services; the risk that we may be unable to develop or achieve commercial success for additional molecular diagnostic tests and pharmaceutical and clinical services in a timely manner, or at all; the risk that we may not successfully develop new markets for our molecular diagnostic tests and pharmaceutical and clinical services, including our ability to successfully generate revenue outside the United States; the risk that licenses to the technology underlying our molecular diagnostic tests and pharmaceutical and clinical services and any future tests and services are terminated or cannot be maintained on satisfactory terms; risks related to delays or other problems with operating our laboratory testing facilities and our healthcare clinic; risks related to public concern over genetic testing in general or our tests in particular; risks related to regulatory requirements or enforcement in the United States and foreign countries and changes in the structure of the healthcare system or healthcare payment systems; risks related to our ability to obtain new corporate collaborations or licenses and acquire new technologies or businesses on satisfactory terms, if at all; risks related to our ability to successfully integrate and derive benefits from any technologies or businesses that we license or acquire; risks related to our projections about our business, results of operations and financial condition; risks related to the potential market opportunity for our products and services; the risk that we or our licensors may be unable to protect or that third parties will infringe the proprietary technologies underlying our tests; the risk of patent-infringement claims or challenges to the validity of our patents or other intellectual property; risks related to changes in intellectual property laws covering our molecular diagnostic tests and pharmaceutical and clinical services and patents or enforcement in the United States and foreign countries, such as the Supreme Court decisions in Mayo Collab. Servs. v. Prometheus Labs., Inc., 566 U.S. 66 (2012), Assn for Molecular Pathology v. Myriad Genetics, Inc., 569 U.S. 576 (2013), and Alice Corp. v. CLS Bank Intl, 573 U.S. 208 (2014); risks of new, changing and competitive technologies and regulations in the United States and internationally; the risk that we may be unable to comply with financial operating covenants under our credit or lending agreements; the risk that we will be unable to pay, when due, amounts due under our credit or lending agreements; and other factors discussed under the heading "Risk Factors" contained in Item 1A of our most recent Annual Report on Form 10-K for the fiscal year ended June 30, 2020, which has been filed with the Securities and Exchange Commission, as well as any updates to those risk factors filed from time to time in our Quarterly Reports on Form 10-Q or Current Reports on Form 8-K. All information in this press release is as of the date of the release, and Myriad undertakes no duty to update this information unless required by law.

Media Contact:Jared Maxwell(801) 505-5027jmaxwell@myriad.com

Investor Contact:Scott Gleason(801) 584-1143sgleason@myriad.com

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American Society of Clinical Oncology Exclusively Cites myChoice CDx in New Recommendations for Patients with Advanced Ovarian Cancer - BioSpace

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New Study from the Broad Finds PRS is Critical Component to Predicting a Range of Diseases – Clinical OMICs News

August 21st, 2020 11:55 am

Scientists at the Broad Institute have discovered that it isnt enough just to test for mutations to find coronary artery disease, breast cancer or colorectal cancerinstead, its also critical to test for the many small changes across the genome to produce polygenic risk scores (PRS).

The findings are presented in a new study, published Aug. 20 in Nature Communications, and led by the Broad Institute of MIT and Harvard, Massachusetts General Hospital, and by San Francisco-based genetic testing company, Color.

Amit Khera, M.D., associate director of the Broad Institutes Program in Medical and Population Genetics and leader of a research group within the Center for Genomic Medicine at Massachusetts General Hospital and senior author on the study, said he will soon begin offering patients testing based on the findings.

Khera is working with a team of geneticists and genetic counselors in the hospitals Preventive Genomics Clinic to offer a clinical test developed by Color that assesses both monogenic and polygenic risk for heart disease.

This research has real clinical implications for genome interpretation, Khera said. Weve found that the traditional approach of only looking for monogenic risk variants misses an important part of the picture. A persons polygenic risk also plays a crucial role in predicting the development of disease. I suspect that evaluating both will soon become standard in clinical practice.

For the study, researchers focused on breast cancer, coronary artery disease, and colorectal cancer because each disease is associated with what the Centers for Disease Control and Prevention considers a tier 1 genomic condition, meaning there are specific genetic mutations associated with higher risk for developing the condition, according to researchers.

The relationship between the mutations that cause these three genomic conditions and the risk of developing each disease is relatively well understood, authors of the study said. But until now, few researchers have investigated how the interplay between these monogenic variants and someones polygenic risk affects the likelihood of developing disease.

For the study, researchers reviewed genetic information from 80,928 individuals who either participated in case-controlled Color or U.K. Biobank studies, to find the presence of monogenic variants and a patients polygenic risk. The risk score was determined to significantly affect the likelihood of developing a disease associated with a tier 1 genomic condition.

Think about a monogenic variant as a brick, said Julian Homburger, a Color data scientist and co-first author of the paper. A polygenic risk score, then, is like stacking sheets of paper. You can still get to the same sizein this case, the likelihood of developing a diseaseits just a different mechanism. And, what we show is that if you have both of these, they stack on top of each other and contribute to an even greater risk.

Alicia Zhou, CSO at Color and co-author of the paper said the next logical step after testing patients is to monitor them closely, with earlier and more frequent screening. The current approach to screening for genomic conditions is fairly crude, she said. With better information about the risk of genomic diseases, we can refine screening and treatment for people, and hopefully improve patient outcomes.

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Seattle Genetics Appoints Ted W. Love, M.D., to Board of Directors – Business Wire

August 21st, 2020 11:55 am

BOTHELL, Wash.--(BUSINESS WIRE)--Seattle Genetics, Inc. (Nasdaq:SGEN) today announced that Ted W. Love, M.D., has been appointed to the companys Board of Directors. Dr. Love has more than 25 years of global experience in the healthcare and biotechnology/pharmaceutical industry and currently serves as President and Chief Executive Officer of Global Blood Therapeutics.

We are pleased to welcome Ted to our Board of Directors given his distinguished industry expertise and leadership, said Clay Siegall, Ph.D., President and Chief Executive Officer of Seattle Genetics. His extensive experience will be a valued addition at this transformational time for our company, with three marketed products, significant development across our pipeline and an expanding global footprint. We look forward to working with Ted on our quest to improve the lives of people with cancer through innovative medicines that address unmet medical needs.

Concurrent with the appointment of Dr. Love, Srinivas Akkaraju, M.D., Ph.D., has resigned from the companys Board of Directors. Dr. Akkaraju has served as a Director since 2003.

I want to thank Srini for his incredible contributions over more than 17 years, added Dr. Siegall. He has played an instrumental role in building Seattle Genetics to the global, multi-product company that it is today.

Prior to Dr. Loves current role at Global Blood Therapeutics, he held executive positions at a number of biopharmaceutical companies including Onyx Pharmaceuticals, Nuvelo, Inc. and Theravance, Inc. Earlier in his career, Dr. Love held a number of senior management positions at Genentech, where he oversaw the development strategy and execution that led to the approvals of six innovative medicines. Dr. Love holds a B.A. in molecular biology from Haverford College and an M.D. from Yale Medical School. He completed a residency in internal medicine and a fellowship in cardiology at the Massachusetts General Hospital. He currently serves on the board of directors of Royalty Pharma and the Biotechnology Innovation Organization, and has served as a consultant in medicine in the Department of Cardiology at the Massachusetts General Hospital.

About Seattle Genetics

Seattle Genetics, Inc. is a global biotechnology company that discovers, develops and commercializes transformative cancer medicines to make a meaningful difference in peoples lives. ADCETRIS (brentuximab vedotin) and PADCEV (enfortumab vedotin-ejfv) use the Companys industry-leading antibody-drug conjugate (ADC) technology. ADCETRIS is approved in certain CD30-expressing lymphomas, and PADCEV is approved in certain metastatic urothelial cancers. TUKYSA (tucatinib), a small molecule tyrosine kinase inhibitor, is approved in certain HER2-positive metastatic breast cancers. The company is headquartered in the Seattle, Washington area, with locations in California, Switzerland and the European Union. For more information on our robust pipeline, visit http://www.seattlegenetics.com and follow @SeattleGenetics on Twitter.

Forward Looking Statements

Certain of the statements made in this press release are forward looking, such as those, among others, relating to the extent of development across the companys pipeline, the expansion of its global footprint and its efforts to develop additional cancer medicines to address unmet medical needs. Actual results or developments may differ materially from those projected or implied in these forward-looking statements. Factors that may cause such a difference include the difficulty and uncertainty of pharmaceutical product development, the risk of adverse events or safety signals, the inability to show sufficient activity in clinical trials and the possibility of adverse regulatory actions as product candidates are evaluated in clinical trials even after promising results in preclinical research. More information about the risks and uncertainties faced by Seattle Genetics is contained under the caption Risk Factors included in the Companys Quarterly Report on Form 10-Q for the quarter ended June 30, 2020 filed with the Securities and Exchange Commission. Seattle Genetics disclaims any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.

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OpGen Announces CE-IVD Marking and Commercial Launch in Europe of its Own Developed Molecular Diagnostic SARS-CoV-2 Kit with PULB for Detection of the…

August 21st, 2020 11:54 am

- Own developed SARS-CoV-2 Kit with PULB for COVID-19 uses real-time PCR (RT-PCR) technology on open PCR platforms, designed to provide results in approximately one hour

- 100% Sensitivity and 97.3% Specificity demonstrated in isolated RNA

- Inclusion of PCR-Compatible Universal Lysis Buffer (PULB) in the kit as a workflow option allows labs to circumvent the need for extraction equipment and reagents

GAITHERSBURG, Md., and HOLZGERLINGEN, Germany, Aug. 20, 2020 (GLOBE NEWSWIRE) -- OpGen, Inc., Inc. (Nasdaq: OPGN, OpGen), a precision medicine company harnessing the power of molecular diagnostics and bioinformatics to help combat infectious disease, announced today that its subsidiary Curetis GmbH has obtained the CE mark certification in the European Union for its own SARS-CoV-2 Kit with PULB for the detection of SARS-CoV-2, the virus that causes COVID-19.

Developed and manufactured by Curetis team in Germany, the SARS-CoV-2 Kit with PULB uses real-time reverse transcription polymerase chain reaction (RT-PCR) technology for qualitative detection of the SARS-CoV-2 virus isolated from oropharyngeal and nasopharyngeal swab specimens from individuals suspected of COVID-19 by their healthcare provider or for screening of asymptomatic individuals. This kit can be used with RNA isolated by performing standard RNA isolation processes, as well as with oropharyngeal or nasopharyngeal swabs collected in PCR compatible viral transport medium treated with PCR-Compatible Universal Lysis Buffer (PULB) provided in the kit. Including PULB in the kit as a workflow option allows labs to circumvent the need for extraction equipment and extraction kits/reagents, thereby providing operational and workflow efficiencies, time and cost savings. The kit is designed to provide time to results in approximately one hour, and it runs on open real-time PCR instruments such as the QuantStudio 5 Real-Time PCR System and the Bio-Rad CFX96 Real-Time PCR Detection System.

The CE-IVD Marking is an important step in advancing our efforts to support critical COVID-19 testing; the Curetis SARS-CoV-2 Kit with PULB provides additional testing capacity in countries that recognize the CE Mark to test patients, said Johannes Bacher, COO of OpGen.

By launching this new product in Europe, we are committed to helping our distributors and customers to expand the availability of SARS-CoV-2 diagnostic testing, and our own-developed CE-IVD marked SARS-CoV-2 Kit with PULB is expected to help increase availability of these much-needed tests," said Oliver Schacht, PhD, CEO of OpGen. Our customers will benefit from an optimized workflow and a test that delivers great performance and significantly shorter time-to-result at favorable economics compared to many of the commercially available open PCR platform COVID-19 tests including the BGI SARS-CoV-2 kit. Having access to our own SARS-CoV-2 kit allows us to have that product distributed rather than the BGI test kit which we will cease distributing effective immediately.

About OpGen, Inc.OpGen, Inc. (Gaithersburg, MD, USA) is a precision medicine company harnessing the power of molecular diagnostics and bioinformatics to help combat infectious disease. Along with subsidiaries, Curetis GmbH and Ares Genetics GmbH, we are developing and commercializing molecular microbiology solutions helping to guide clinicians with more rapid and actionable information about life threatening infections to improve patient outcomes, and decrease the spread of infections caused by multidrug-resistant microorganisms, or MDROs. OpGens product portfolio includes Unyvero, Acuitas AMR Gene Panel and Acuitas Lighthouse, and the ARES Technology Platform including ARESdb, using NGS technology and AI-powered bioinformatics solutions for antibiotic response prediction.

For more information, please visit http://www.opgen.com.

Forward-Looking Statements by OpGenThis press release includes statements regarding the commercial launch of a SARS-CoV-2 Kit by OpGens subsidiary, Curetis GmbH. These statements and other statements regarding OpGens SARS-CoV-2 test kits, their commercialization and launch, future plans and goals constitute "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934 and are intended to qualify for the safe harbor from liability established by the Private Securities Litigation Reform Act of 1995. Such statements are subject to risks and uncertainties that are often difficult to predict, are beyond our control, and which may cause results to differ materially from expectations. Factors that could cause our results to differ materially from those described include, but are not limited to, our ability to successfully, timely and cost-effectively develop, seek and obtain regulatory clearance for and commercialize our product and services offerings, the rate of adoption of our products and services by hospitals and other healthcare providers, the success of our commercialization efforts, the impact of COVID-19 on the Companys operations, financial results, and commercialization efforts as well as on capital markets and general economic conditions, the realization of expected benefits of our business combination transaction with Curetis GmbH, the effect on our business of existing and new regulatory requirements, and other economic and competitive factors. For a discussion of the most significant risks and uncertainties associated with OpGen's business, please review our filings with the Securities and Exchange Commission. You are cautioned not to place undue reliance on these forward-looking statements, which are based on our expectations as of the date of this press release and speak only as of the date of this press release. We undertake no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events or otherwise.

OpGen Contact:Oliver SchachtCEOInvestorRelations@opgen.com

Press Contact:Matthew BretziusFischTank Marketing and PRmatt@fischtankpr.com

Investor Contact:Megan PaulEdison Groupmpaul@edisongroup.com

Source: OpGen, Inc.

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OpGen Announces CE-IVD Marking and Commercial Launch in Europe of its Own Developed Molecular Diagnostic SARS-CoV-2 Kit with PULB for Detection of the...

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Global Carrier Screening Market COVID-19 Impact Analysis 2020| Competitive Scenario And Dynamics By Myriad Genetics, Inc., Pathway Genomics, Siemens…

August 21st, 2020 11:54 am

Carrier screening marketis expected to gain market growth in the forecast period of 2020 to 2027. Data Bridge Market Research analyses the market to account toUSD 6.47 billion by 2027 growing at a CAGR of 17.40% in the above-mentioned forecast period.

Access Sample Copy Of Carrier Screening Market @https://www.databridgemarketresearch.com/request-a-sample/?dbmr=global-carrier-screening-market

Carrier Screening market research report gives precise idea about the current situation of the worldwide market, ongoing developments,joint endeavors, size, creation worth, mergers and acquisitions dependent on a few market elements. The report helps with deciding and enhancing each phase in the lifecycle of mechanical procedure that incorporates commitment, securing, maintenance, and adaptation. Additionally, the report offers propelled data and situation about the healthcare business which assists with standing separated in the opposition in this relentless business condition. Moreover, organizations can make out the reaction of the customers to a previously existing item in the market.

The major players covered in the carrier screening market report areF. Hoffmann-La Roche Ltd, Abbott, Thermo Fisher Scientific Inc., Agilent Technologies, Inc., BGI Group, Bio-Rad Laboratories, Inc., Illumina, Inc., QIAGEN, Myriad Genetics, Inc., Pathway Genomics, Siemens Healthcare GmbH, Genomic Health, Inc., Admera Health, deCODE geneticsamong other domestic and global players. Market share data is available for global, North America, Europe, Asia-Pacific (APAC), Middle East and Africa(MEA) and South America separately. DBMR analystsunderstand competitive strengths and provide competitive analysis for each competitor separately.

Key benefits of the report

The global Carrier screening market is also presented to the readers as a holistic snapshot of the competitive landscape within the given forecast period. The report also educates about the market strategies that are being adopted by your competitors and leading organizations. The report also focuses on all the recent industry trends. It presents a comparative detailed analysis of the all regional and player segments, offering readers a better knowledge of where areas in which they can place their existing resources and gauging the priority of a particular region in order to boost their standing in the market.

Global Carrier Screening Market:Segmentation

Carrier screening market is segmented onthe basis of test type, disease type, medical condition, technology and end use. The growth amongst these segments will help you analyse meagre growth segments in the industries, and provide the users with valuable market overview and market insights to help them in making strategic decisions for identification of core market applications.

Based on test type, carrier screening market is segmented into molecular screening test, and biochemical screening test.

On the basis of disease type, thecarrier screening marketis segmented into cystic fibrosis, tay-sachs, gaucher disease, sickle cell disease, spinal muscular atrophy, and other autosomal recessive genetic disorders.

On the basis of medical condition, the carrier screening market is segmented into pulmonary conditions, hematological conditions, neurological conditions, and others.

On the basis of technology, the carrier screening market is segmented into DNA sequencing, polymerase chain reaction, microarrays, and others.

Carrier screening markethas also been segmented based onthe end use into hospitals, reference laboratories, physician offices & clinics, and others.

Table of Content:

Chapter 1: Carrier Screening market OverviewChapter 2: Carrier Screening market Economic ImpactChapter 3: Competition by ManufacturerChapter 4: Production, Revenue (Value) by Region (2020-2027)Chapter 5: Supply (Production), Consumption, Export, Import by Regions (2020-2027)

Chapter 6: Production, Revenue (Value), Price Trend by TypeChapter 7: market Analysis by ApplicationChapter 8: Carrier Screening Market by Manufacturing Cost AnalysisChapter 9: Industrial Chain, Sourcing Strategy and Downstream BuyersChapter 10: Marketing Strategy Analysis, Distributors/TradersChapter 11: Carrier Screening Market Geographic AnalysesChapter 11.1: North AmericaChapter 11.2: EuropeChapter 11.3: Asia-PacificChapter 11.4: South AmericaChapter 12: Carrier Screening Market Effect Factors AnalysisChapter 13: Carrier Screening Market Forecast (2020-2027)Chapter 14: Related ReportsChapter 15: Appendix

Get Detailed Table Of[emailprotected]https://www.databridgemarketresearch.com/toc/?dbmr=global-carrier-screening-market

About Us:Data Bridge Market Research set forth itself as an unconventional and neoteric Market research and consulting firm with unparalleled level of resilience and integrated approaches. We are determined to unearth the best market opportunities and foster efficient information for your business to thrive in the market. Data Bridge Market Research provides appropriate solutions to the complex business challenges and initiates an effortless decision-making process.Data Bridge adepts in creating satisfied clients who reckon upon our services and rely on our hard work with certitude. Get Customization and Discount on Report by emailing[emailprotected]. We are content with our glorious 99.9 % client satisfying rate.

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Myriad Genetics Appoints Paul J. Diaz as President and Chief Executive Officer and a Member of the Board of Directors – GlobeNewswire

August 20th, 2020 6:57 am

SALT LAKE CITY, Aug. 13, 2020 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc. (NASDAQ: MYGN, Myriad or the Company), a global leader in molecular diagnostics and precision medicine, today announced the appointment ofPaul J. Diazas President and Chief Executive Officer, effective August 13, 2020. He will also serve on the Companys Board of Directors. Mr. Diaz brings toMyriad Geneticsmore than three decades of executive leadership and business transformation experience in healthcare across a variety of healthcare segments.

Paul is an exceptional leader and executive with extraordinary passion, vision, experience, and operational skills, saidS. Louise Phanstiel, Chair of Myriads Board of Directors. His focus on building high performing teams, and instilling a culture that empowers people to deliver high quality patient care, distinctive customer service and innovation, will be important to supporting Myriads mission and growth. We are excited to have Paul assume the leadership of Myriad Genetics and chart the course to realize the Companys full potential. We look forward to officially introducing Paul during our fourth quarter earnings call. Myriad is dedicated to providing vital information to physicians, patients and their families that enables them to make better decisions about their health and treatment planning. Pauls personal dedication, throughout his career, to patients and their care will be critical in advancing Myriads vision of being a trusted advisor transforming patients lives worldwide with pioneering molecular diagnostics.

I am very excited to join the talented management team and Board of Directors of Myriad Genetics, an organization dedicated to helping patients and physicians identify the risk of developing disease and accurately diagnosing disease and disease progression, commented Paul. Our goal is to empower patients, as consumers, and their physicians and our payer partners with the information and data to help guide their treatment decisions, to improve clinical outcomes and lower healthcare costs.I am equally excited about Myriads potential for innovation and growth.The Company has a tremendous opportunity to transform its business, and strategically position itself for sustainable, profitable growth. We will look to leverage the companys culture of innovation and revitalize our approach to the commercializing of its products and customer service levels.

Mr. Diaz served as the President and Chief Executive Officer and Executive Director and Director of Kindred Healthcare, Inc. for over ten years, where he led the growth, revitalization and diversification of the business that positioned Kindred as the largest provider of post-acute health care services in the United States. Most recently, Mr. Diaz was a Partner at Cressey & Company LP, a private equity firm focusing on healthcare services and HCIT companies. Mr. Diaz is an experienced director and operating executive, having served as an executive and board member of multiple public and private companies. He currently serves on the board of DaVita, Inc. (NYSE: DVA) and is a member of the Board of Trustees of Johns Hopkins Medicine. Mr. Diaz graduated from The American University with a B.S. in Business Administration and with a J.D. from The Georgetown University Law Center.

Heidrick & Struggles led the search process for Myriad.

About Myriad GeneticsMyriad Genetics Inc., is a leading personalized medicine company dedicated to being a trusted advisor transforming patient lives worldwide with pioneering molecular diagnostics. Myriad discovers and commercializes molecular diagnostic tests that: determine the risk of developing disease, accurately diagnose disease, assess the risk of disease progression, and guide treatment decisions across six major medical specialties where molecular diagnostics can significantly improve patient care and lower healthcare costs. Myriad is focused on three strategic imperatives: transitioning and expanding its hereditary cancer testing markets, diversifying its product portfolio through the introduction of new products and increasing the revenue contribution from international markets. For more information on how Myriad is making a difference, please visit the Company's website: http://www.myriad.com.

Myriad, the Myriad logo, BART, BRACAnalysis, Colaris, Colaris AP, myPath, myRisk, Myriad myRisk, myRisk Hereditary Cancer, myChoice, myPlan, BRACAnalysis CDx, Tumor BRACAnalysis CDx, myChoice CDx, Vectra, Prequel, Foresight, GeneSight, riskScore and Prolaris are trademarks or registered trademarks of Myriad Genetics, Inc. or its wholly owned subsidiaries in the United States and foreign countries. MYGN-F, MYGN-G.

Safe Harbor StatementThis press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including statements related to realizing the Companys full potential; officially introducing Paul during the Companys fourth quarter earnings call; advancing Myriads vision of being a trusted advisor transforming patients lives worldwide with pioneering molecular diagnostics; the Companys potential for innovation and growth; the Companys tremendous opportunity to transform its business, and strategically position itself for sustainable, profitable growth; and the Companys strategic directives under the caption "About Myriad Genetics." These "forward-looking statements" are based on management's current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by forward-looking statements. These risks and uncertainties include, but are not limited to: uncertainties associated with COVID-19, including its possible effects on our operations and the demand for our products and services; our ability to efficiently and flexibly manage our business amid uncertainties related to COVID-19; the risk that sales and profit margins of our molecular diagnostic tests and pharmaceutical and clinical services may decline; risks related to our ability to transition from our existing product portfolio to our new tests, including unexpected costs and delays; risks related to decisions or changes in governmental or private insurers reimbursement levels for our tests or our ability to obtain reimbursement for our new tests at comparable levels to our existing tests; risks related to increased competition and the development of new competing tests and services; the risk that we may be unable to develop or achieve commercial success for additional molecular diagnostic tests and pharmaceutical and clinical services in a timely manner, or at all; the risk that we may not successfully develop new markets for our molecular diagnostic tests and pharmaceutical and clinical services, including our ability to successfully generate revenue outside the United States; the risk that licenses to the technology underlying our molecular diagnostic tests and pharmaceutical and clinical services and any future tests and services are terminated or cannot be maintained on satisfactory terms; risks related to delays or other problems with operating our laboratory testing facilities and our healthcare clinic; risks related to public concern over genetic testing in general or our tests in particular; risks related to regulatory requirements or enforcement in the United States and foreign countries and changes in the structure of the healthcare system or healthcare payment systems; risks related to our ability to obtain new corporate collaborations or licenses and acquire new technologies or businesses on satisfactory terms, if at all; risks related to our ability to successfully integrate and derive benefits from any technologies or businesses that we license or acquire; risks related to our projections about our business, results of operations and financial condition; risks related to the potential market opportunity for our products and services; the risk that we or our licensors may be unable to protect or that third parties will infringe the proprietary technologies underlying our tests; the risk of patent-infringement claims or challenges to the validity of our patents or other intellectual property; risks related to changes in intellectual property laws covering our molecular diagnostic tests and pharmaceutical and clinical services and patents or enforcement in the United States and foreign countries, such as the Supreme Court decisions in Mayo Collab. Servs. v. Prometheus Labs., Inc., 566 U.S. 66 (2012), Assn for Molecular Pathology v. Myriad Genetics, Inc., 569 U.S. 576 (2013), and Alice Corp. v. CLS Bank Intl, 573 U.S. 208 (2014); risks of new, changing and competitive technologies and regulations in the United States and internationally; the risk that we may be unable to comply with financial operating covenants under our credit or lending agreements; the risk that we will be unable to pay, when due, amounts due under our credit or lending agreements; and other factors discussed under the heading "Risk Factors" contained in Item 1A of our most recent Annual Report on Form 10-K for the fiscal year ended June 30, 2020, which has been filed with the Securities and Exchange Commission, as well as any updates to those risk factors filed from time to time in our Quarterly Reports on Form 10-Q or Current Reports on Form 8-K. All information in this press release is as of the date of the release, and Myriad undertakes no duty to update this information unless required by law.

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Organigram Joins Medical Cannabis by Shoppers Inc. and TruTrace in Effort to Track Source and Genetics of Cannabis Used by Medical Patients – Business…

August 20th, 2020 6:57 am

MONCTON, New Brunswick--(BUSINESS WIRE)--Organigram Holdings Inc. (NASDAQ: OGI) (TSX: OGI), the parent company of Organigram Inc. (the Company or Organigram), a leading licensed producer of cannabis, is pleased to announce it has partnered with Medical Cannabis by Shoppers(Shoppers) on Phase 2 of Shoppers Pilot Program powered by software partner TruTrace Technologies Inc. (CSE: TTT; OTCQB: TTTSF) (TruTrace).

The program is designed to genetically finger-print all participating cannabis products, tracking them throughout the supply chain, from genome to patient, in order to provide real-time information about the composition of each cannabis product used by Medical Cannabis by Shoppers customers.Organigram will provide cannabis products to Shoppers for use in the tracking program.

Standardized and validated testing of medical cannabis, ensuring consistent quality and efficacy, are critical to the products value as a viable treatment option. Likewise, product information such as strain composition and potency can help healthcare practitioners and patients make more informed and confident decisions about their medical cannabis treatment regimens.

Organigram is proud of our long-standing commitment to our medical cannabis community. From the development of innovative products to the support offered by our patient care team and programs, patients and their needs are at the heart of our medical cannabis business, says Greg Engel, CEO, Organigram. We also recognize how critical consistency is to patients and their healthcare providers so are pleased to partner with Shoppers, providing our products so that they can be followed from raw material to finished product, to offer them important, useable product insights.

Using Trutraces StrainSecure system, the program collects plant testing data and performs genomic verification in plant batches which are then registered in a blockchain-enabled database for intellectual property protection and strain validation. All information gathered from the plants, including their molecular and chemical makeup, can be tracked via the technology.

As jurisdictions around the world have begun to legalize and adopt cannabis as a medical treatment, there has been an influx ofnew breeders and growers and a profusion of new cannabis strains, each with a different representation of at least 500 known metabolites. Subtle changes in the chemical expression of various strains, whether by genetic structure or environmental conditions, may have significant clinical effects on the patients using this treatment option.With so many strains available, and with relatively limitedinformationon strain composition or genetic lineage and their relation to their chemical output, patients havelittleability to control what they aretaking over time.

In the absence of assigned drug identification numbers (DIN)for cannabis products, quantifying the genetics and metabolomics, as well as potency and equivalencies ofcannabis products is of interest to producers, distributors, shippers, government agencies, payers, clinicians and patients.

Maintaining an effective traceability ecosystem about these details throughout the supply chain is a component of providing consistent medicine, says Engel.

Using TruTrace technology, Shoppers has partnered with University Health Network in Toronto (UHN) to launch Medical Cannabis Real World Evidence (MCRWE), a new ground-breaking study on cannabis and health which will track outcomes with TruTrace validated product for the first time in history.

This novel observational study is targeting a minimum of 2,000 patients who will be followed over a 24-week period. Enrolled patients will have access to certain fully verified products on the Medical Cannabis by Shoppers platform, which have been tested for detailed cannabinoid and terpene profiles.More information about the study can be found here.

About Organigram Holdings Inc.

Organigram Holdings Inc. is a NASDAQ Global Select and TSX listed company whose wholly owned subsidiary, Organigram Inc., is a licensed producer of cannabis and cannabis-derived products in Canada.

Organigram is focused on producing high-quality, indoor-grown cannabis for patients and adult recreational consumers in Canada, as well as developing international business partnerships to extend the Company's global footprint. Organigram has also developed a portfolio of legal adult use recreational cannabis brands including The Edison Cannabis Company, AnkrOrganics and Trailblazer. Organigram's facilityis located inMoncton, New Brunswick and the Company is regulated by theCannabis Act and theCannabis Regulations(Canada).

This news release contains forward-looking information. Often, but not always, forward-looking information can be identified by the use of words such as plans, expects, estimates, intends, anticipates, believes or variations of such words and phrases or state that certain actions, events, or results may, could, would, might or will be taken, occur or be achieved. Forward-looking information involves known and unknown risks, uncertainties and other factors that may cause actual results, events, performance or achievements of Organigram to differ materially from current expectations or future results, performance or achievements expressed or implied by the forward-looking information contained in this news release. Risks, uncertainties and other factors involved with forward-looking information could cause actual events, results, performance, prospects and opportunities to differ materially from those expressed or implied by such forward-looking information include factors that change supply quantities; risks associated with international jurisdictions including regulatory risk; receipt of any required permits from Health Canada and other authorities; including general risks related to COVID-19 and risks as disclosed in the Companys most recent annual information form, managements discussion and analysis and other Company documents filed from time to time on SEDAR (see http://www.sedar.com) and filed or furnished to the Securities and Exchange Commission on EDGAR (see http://www.sec.gov). Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. Although the Company believes that the assumptions and factors used in preparing the forward-looking information in this news release are reasonable, undue reliance should not be placed on such information and no assurance can be given that such events will occur in the disclosed time frames or at all. The forward-looking information included in this news release are made as of the date of this news release and the Company disclaims any intention or obligation, except to the extent required by law, to update or revise any forward-looking information, whether as a result of new information, future events or otherwise.

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Organigram Joins Medical Cannabis by Shoppers Inc. and TruTrace in Effort to Track Source and Genetics of Cannabis Used by Medical Patients - Business...

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Will Rice College O-Week moves online after two advisors test positive for COVID-19 – The Rice Thresher

August 20th, 2020 6:57 am

Photo Courtesy Jeff Fitlow

By Rishab Ramapriyan 8/18/20 9:18pm

On Tuesday, Will Rice College announced that the remainder of Orientation Week activities will be conducted fully online. The announcement came after a second Will Rice O-Week advisor tested positive for COVID-19 this morning.

According to the Dean of Undergraduates Bridget Gorman, this decision was not mandated by the Rice University administration, but rather reached locally by the Will Rice magisters and O-Week coordinator team. In their email to the Will Rice advising team and new student cohort, the coordinators said that this decision was made out of an abundance of caution.

We take this action to minimize the risk to your own health and to limit further spread of the virus, the coordinators wrote.

Advisors and new students living on-campus are restricted to their floors as mandated campus-wide, but they are still able to use outdoor spaces, according to Rahul Popat, the Will Rice College President. As long as students follow the guidelines set by the Culture of Care Agreement, they are free to exit their rooms.

Vice President of Administration Kevin Kirby, who chairs the Crisis Management Advisory Committee, said that Rices team of 17 contact tracers promptly responded to both Will Rice cases. Any individuals who met the Centers for Disease Control and Prevention criteria for close contact (within 6 feet for more than 15 minutes) were quarantined and tested using a molecular test (polymerase chain reaction test). A few additional advisors who believed that they had been in contact with the COVID-19-positive students voluntarily quarantined themselves, according to Kirby. All of the quarantined students have tested negative and there have been no additional cases in the Will Rice community as of this morning.

New students and advisors had all received an antigen rapid test from CVS on move-in day, but antigen tests have a lower sensitivity and specificity than molecular tests. As such, all O-Week participants will undergo a follow-up molecular test by the end of this week. However, the entire Will Rice advising team and new student cohort will be tested via the molecular test either today or tomorrow as a precaution, according to Kirby. Results from Rices molecular tests, which are provided by Houston Methodist and Baylor Genetics, are returned within 48 hours, but Kirby said that the tests are often being returned in 24 hours.

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We'll go through the whole college and test everybody, Kirby said. We'll see if there are any [COVID-19 positive students] that have been missed or any new infections and sort of sweep through and get everybody today or tomorrow. And these tests are very accurate.

According to Kirby, there was an additional Will Rice advisor who tested positive for COVID-19, however this student had fully recovered from a previous COVID-19 infection and Student Health Services determined that they did not pose any risk for transmission, according to Kirby. The CDC notes this possibility in their guidance on discontinuing isolation measures.

Recovered persons can continue to shed detectable SARS-CoV-2 RNA in upper respiratory specimens for up to 3 months after illness onset, albeit at concentrations considerably lower than during illness, in ranges where replication-competent virus has not been reliably recovered and infectiousness is unlikely, the CDC writes. Studies have not found evidence that clinically recovered persons with persistence of viral RNA have transmitted SARS-CoV-2 to others.

Following this guidance, Kirby said that this additional Will Rice advisor was not isolated, but continues to be monitored.

Kirby said that 833 new students were given rapid tests on Saturday and Sunday, and three students tested positive. Those who tested positive could either move in to Sid Richardson College, the designated isolation housing, or return home. No more than two students have occupied Sid Rich at any point thus far, Kirby noted.

Campuswide, there have been 4,595 tests administered between August 1 and August 17, and 11 people (3 staff, 7 undergraduates, 1 graduate student) have tested positive, based on a recent update from Crisis Management. Kirby said that Rice will be administering 4,500 tests per week by the first week of classes.

Gorman said that two restrictions have been added to the campuswide O-Week program as precautionary measures. First, all remaining cross-college events have been canceled for the week. Second, students will not be allowed to eat meals together in the college commons, and must eat meals in their dorm rooms or outdoors in a physically-distanced manner.

We're testing everybody this week, as we're doing every week, Gorman said. So we're going to know in the next couple of days whether we're seeing any more spread or whether it's just these two cases at Will Rice.

Gorman said that she hopes to remove the restriction on college commons dining after O-Week, but will decide after more test results are returned.

I think by the weekend after we've gone through and gotten the test results back on everybody on campus and we get a sense about where we're at, we will make a decision at that point, Gorman said. But in preparation, just in case, we are going to ramp up our outside furniture.

Kirby said that while the COVID-19 positivity rate is substantially lower on campus than in Houston, it is important to continue all safety precautions and adapt to changing conditions.

We have to be very careful and wary right about that and we need to not have a false sense of optimism here, Kirby said. That's why it's important that we continue to do all the safety precautions ... and we continue to do our testing rigorously and often. We're prepared to make changes like we already have. I'm sure we'll continue to make changes over the course of the fall semester.

[8/18/2020 at 11:15 p.m.] The story was updated with correct information about the movement of on-campus students. Will Rice President Rahul Popat clarified that on-campus students are not restricted to their rooms.

[8/18/2020 at 11:45 p.m.] The story was updated with information about an additional Will Rice advisor who tested positive for COVID-19, but was determined to not pose any risk for transmission.

[8/19/2020 at 3:10 p.m.] The story was updated with statistics from on-campus COVID-19 testing.

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Will Rice College O-Week moves online after two advisors test positive for COVID-19 - The Rice Thresher

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Whitby student welcomes A-level U-turn – but still left in limbo over his future – Whitby Gazette

August 20th, 2020 6:57 am

A-level student Kilian Robinson.

Kilian Robinson, 18, of Egton, consistently achieved the highest possible grades for his subjects Biology, Chemistry and Maths over the past two years.

But he was horrified on Thursday to discover that his centre assessment grades had been reduced from A*A*A* to ABB by the controversial Government algorithm, despite him not once attaining anything lower than an A.

He said today (Tues) that Imperial College London had indicated they would keep his place on a Biological Scienes course open to him if he successfully appealed.

Yesterday's Governments U-turn means Kilian has attained his grades and fulfilled his side of the bargain.

He is now waiting to hear back from Imperial College London, having emailed them after the dramatic climbdown was announced.

They said they would honour my offer if I got the grades now Ive got them," he said.

The fight isnt over. Everyone is anxious about it and what if the course is full?

Its a massive problem, yes Ive got my grades but its still to be resolved.

Kilian was offered a place on a Molecular Genetics course in Edinburgh, despite not his results being initially downgraded, but he declined as he has set his heart on a place at Imperial College London.

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Whitby student welcomes A-level U-turn - but still left in limbo over his future - Whitby Gazette

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Coronavirus: Cold temperatures are where Covid-19 thrives – Stuff.co.nz

August 20th, 2020 6:57 am

This story was originally published on Newsroom.co.nz and is republished with permission

With investigations into a coolstore and freight as a potential pathway for the latest outbreak of Covid-19, what does science say about surfaces and refrigeration?

Surfaces at a Mount Wellington coolstore are being tested for Covid-19 in an effort to uncover the route of the virus back into the community.

Ryan Anderson/Stuff

Americold in Mount Wellington, Auckland, where a south Auckland man with coronavirus works.

A worker at the coolstore has tested positive for the disease. How he caught it is still a mystery. The possibility it could have come in on overseas freight arriving at the coolstore is being investigated.

Were not ruling that out, said Director-General of Health Ashley Bloomfield, We want to get to the bottom of that.

READ MORE:* Coronavirus: Extension to Covid-19 lockdown likely, says disease modelling expert* Coronavirus: Rapid 'cluster busting' to find Covid-19 outbreak source could nip other clusters in the bud* Coronavirus: Auckland cool storage facility tested over concern Covid-19 entered NZ via freight* Coronavirus: Aucklanders should be wearing masks, experts say

The coolstore environment has been swabbed and test results are expected back today.

Yesterday, three other workers from the coolstore returned positive tests for Covid-19.

It's possible the workers were either infected by contaminated goods, or the virus was brought into the workplace after it was caught elsewhere, possibly by the man who was first diagnosed.

Two branches of the coolstore have been closed. One in Mount Wellington, where the man worked, and another close to Auckland Airport.

Genomic sequencing is still underway, but as of yesterday afternoon there hasnt been a link between genome patterns of cases in border quarantine and the genome pattern of the coolstore-related cases.

University of Auckland professor Shaun Hendy said the fact the source of the outbreak hadnt been identified yet was concerning.

MYTCHALL BRANSGROVE/STUFF

Tests are still ongoing to trace the pandemics source.

To date, the genomic information suggests this cluster is not linked to a managed isolation and quarantine facility. The business itself is linked to international freight, air and sea, which does suggest that this is a possible entry route, whether via packaging, or more likely, via person-to-person.

Like many things Covid-19 related, the science of transmission isnt clear-cut; what studies have been done are often laboratory-based.

Surface transmission is considered a lower risk for virus transmission than person-to-person contact but cold environments, such as meat works, have been at the centre of overseas clusters.

Cant touch this

New Zealands news came as China has again claimed it has found the virus on the outer packaging of frozen prawns imported from Ecuador.

Chinas state television said it was found during a routine inspection of a restaurant in Wuhu city.

Its not the first report of this in China. Since July, several other Chinese cities have also reported cases, including the port cities of Xiamen and Dalian leading to imports from three suppliers being suspended.

After nucleic acid sequence analysis and expert judgment, the test results suggested that the container environment and the outer packaging of the goods of the three companies were at risk of contamination by the new coronavirus, and the companies food safety management system was not in order, the General Administration of Customs said in a statement.

The director of the organisation, Bi Kexi, told reporters: "Experts believe that the results do not mean they are contagious but that the companies' food safety management systems are not well implemented," Bi Kexin, director General Administration of Customs said.

For international packaging to be the cause of this outbreak, a chain of events would need to have taken place. Enough of the virus landing - on packaging - perhaps through a person coughing droplets onto a surface - would be the first step. The droplets would need to remain viable throughout the journey to the New Zealand coolstore.

Then the virus on the packaging would need to find a pathway to a person, possibly through someone touching the package and then touching their face.

Studies have been done on how long the virus survives on different surfaces. Traces of the virus were detected on plastic and steel up to three days after contamination and on cardboard for up to one day.

In chilled conditions, the virus can survive longer. One study looking at the survival time of the virus in a test tube found at 4C, the virus survived for 14 days. At 37C it lasted just one day.

The other factor is the amount of virus on a surface. A recent letter published in The Lancet suggests the risk of surface transmission has been exaggerated.

None of these studies present scenarios akin to real life situations, the letter said.

The Rutgers University professor of microbiology, biochemistry and molecular genetics Emanuel Goldmans issue was that in real life the amount of virus would likely be several orders of magnitude smaller.

While saying he believed in erring on the side of caution, he thought the risk was low.

In my opinion, the chance of transmission through inanimate surfaces is very small, and only in instances where an infected person coughs or sneezes on the surface, and someone else touches that surface soon after the cough or sneeze (within one - two hours).

While the risk is considered low, its still a possibility.

In a Chinese mall, several people caught the virus in January despite not being in direct contact with the one person at the mall who was known to have it. A restroom and elevator buttons were considered to be places where these people may have touched contaminated surfaces.

Covid and chill

Cold work environments have been at the centre of outbreaks. The exact reasons why arent clear, although theres plenty of speculation.

In the US 17,358 cases of coronavirus were recorded from meat and poultry factory workers.

An abattoir in Germany was closed after 1500 workers were infected and in Melbourne at least three abattoirs were closed after outbreaks occurred. Abattoir-related outbreaks have also occurred in the United Kingdom, France, Brazil, Denmark and the Netherlands.

There are a few factors likely to be at play and theyre not related to dead animals.

Physical distancing on a production line can be hard as often people work shoulder-to-shoulder. Shifts are long, and casualised employment can make people less likely to stay home when ill because they cant afford time off.

Background noise can mean shouting is needed to communicate, increasing the risk of droplet spread. Air filtration systems push air around, potentially spreading droplets further.

No sunlight and cold conditions extend the life of the virus.

The conditions at the New Zealand coolstore where cases have emerged may not be identical to overseas abattoirs, but there's a chance cold may play a role in giving any virus in the environment a chance to live longer.

This story was originally published on Newsroom.co.nz and is republished with permission

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Global Nerve Repair and Regeneration Market 2020-2025: The Potential of Stem Cell Therapy in Nerve Repair and Regeneration Fuels Opportunity -…

August 20th, 2020 6:56 am

DUBLIN--(BUSINESS WIRE)--The "Nerve Repair and Regeneration Market by Products (Nerve Conduits, Nerve Wraps, Vagus Nerve Stimulation, Sacral Nerve Stimulation, Spinal Cord Stimulation, TENS, TMS), Application (Neurorrhaphy, Nerve Grafting, Stem Cell Therapy) - Global Forecast to 2025" report has been added to ResearchAndMarkets.com's offering.

The global nerve repair and regeneration market is projected to reach USD 9,781.2 million by 2025 from USD 6,339.7 million in 2020, at a CAGR of 9.1%

The growth in this market is driven by a high incidence of nerve injuries, a growing prevalence of neurological disorders, an increasing geriatric population, and rising government support for neurologic disorder research.

The biomaterial as a segment is anticipated to grow at the fastest growth rate during the forecast period.

Based on product type, the nerve repair and regenerations market is segmented into neurostimulation and neuromodulation devices and biomaterials. The biomaterials segment is expected to grow at the highest growth rate during the forecast period. This can primarily be attributed to the high incidence of nerve injuries. Rising government support for neurologic disorders is also one of the major factors to drive the growth of the biomaterials market globally.

The internal neurostimulation and neuromodulation segment is accounted for the largest share during the analysis period.

Based on the neurostimulation and neuromodulation application, the nerve repair and regeneration market is segmented the neurostimulation and neuromodulation devices market is segmented into internal neurostimulation and neuromodulation applications and external neurostimulation and neuromodulation applications. The internal neurostimulation and neuromodulation segment is accounted for the largest share during the forecast period. This can primarily be attributed to the increasing incidence of neurological disorders across the globe.

Asia Pacific is estimated to register the highest CAGR during the study period.

In this report, the nerve repair and regeneration market is segmented into four major regional segments, namely, North America, Europe, Asia Pacific, and the Rest of the World (RoW). The market in the Asia Pacific is projected to grow at the highest growth rate during the forecast period. Economic growth in the countries of this region, large population base, rising prevalence of neurologic diseases, rising standard of living, growing demand for quality medical care, and increasing healthcare spending will drive the market in the region over the forecast period.

Key Topics Covered

1 Introduction

2 Research Methodology

3 Executive Summary

4 Premium Insights

4.1 Nerve Repair & Regeneration Market Overview

4.2 Nerve Repair & Regeneration Market: Geographic Growth Opportunities

5 Market Overview

5.1 Introduction

5.2 Market Dynamics

5.2.1 Drivers

5.2.1.1 High Incidence of Nerve Injuries

5.2.1.2 Rising Geriatric Population and Subsequent Growth in the Prevalence of Neurological Disorders

5.2.1.3 Rising Government Support for Neurologic Disorder Research

5.2.2 Opportunities

5.2.2.1 Emerging Markets

5.2.2.2 Potential of Stem Cell Therapy in Nerve Repair and Regeneration

5.2.2.3 Rising Research in the Field of Neurology

5.2.3 Challenges

5.2.3.1 Donor-Site Morbidity

5.2.3.2 Difficulties in Treating Large Nerve Gaps

5.2.3.3 Stringent Regulatory Frameworks and Time-Consuming Approval Processes

5.2.3.4 Greater Preference for Drug Therapies Over Nerve Repair and Regeneration Products

5.2.3.5 Dearth of Trained Professionals

5.2.3.6 Product Recalls

5.3 Impact of COVID-19 on the Nerve Repair and Regeneration Market

6 Nerve Repair and Regeneration Market, by Product

6.1 Introduction

6.2 Neurostimulation and Neuromodulation Devices

6.3 Biomaterials

7 Nerve Repair and Regeneration Market, by Application

7.1 Introduction

7.2 Neurostimulation & Neuromodulation Applications

7.3 Nerve Repair & Regeneration Biomaterials Market, by Application

8 Nerve Repair and Regeneration Market, by Region

8.1 Introduction

8.2 North America

8.3 Europe

8.4 Asia-Pacific

8.5 Rest of the World (Row)

9 Competitive Landscape

9.1 Overview

9.2 Market Share Analysis, 2019

9.3 Competitive Scenario

9.3.1 Product Launches and Approvals

9.3.2 Partnerships, Collaborations, Mergers, and Agreements

9.3.3 Expansions

9.3.4 Acquisitions

9.3.5 Other Developments

9.4 Competitive Leadership Mapping (2019)

9.4.1 Visionary Leaders

9.4.2 Innovators

9.4.3 Dynamic Differentiators

9.4.4 Emerging Companies

10 Company Profiles

10.1 Medtronic, plc

10.2 Boston Scientific Corporation

10.3 Abbott Laboratories

10.4 Axogen, Inc.

10.5 Baxter International, Inc.

10.6 Livanova, plc

10.7 Integra Lifesciences

10.8 Polyganics

10.9 Neuropace, Inc.

10.10 Soterix Medical, Inc.

10.11 Nevro Corp.

10.12 Synapse Biomedical, Inc.

10.13 Aleva Neurotherapeutics

10.14 Collagen Matrix, Inc.

10.15 Kerimedical

10.16 Biowave Corporation

10.17 Neurosigma

10.18 Neuronetics, Inc.

10.19 TVNS Technologies GmbH

10.20 Gimer Medical

For more information about this report visit https://www.researchandmarkets.com/r/n8ux49

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Global Nerve Repair and Regeneration Market 2020-2025: The Potential of Stem Cell Therapy in Nerve Repair and Regeneration Fuels Opportunity -...

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Israel and UAE team up on stem cell therapy research for COVID-19 – UPI News

August 20th, 2020 6:56 am

Aug. 17 (UPI) -- Israel and United Arab Emirates stem cell therapy companies signed an agreement Monday to collaborate on researching potential treatment for COVID-19.

The accord between Israel's Pluristem Therapeutics and UAE's Abu Dhabi Stem Cells Center aims to capitalize on each company's expertise to develop therapies and regenerative medicines for the treatment of severe diseases including COVID-19, according to a joint statement.

Both companies have been treating COVID-19 patients with stem cells.

Pluristem has been treating COVID-19 patients with a placenta-based stem cell therapy. The U.S. Food and Drug Administration cleared the Israel stem cell therapy company in May for a Phase II study of the treatment for severe COVID-19 cases. Preliminary results released in May from compassionate-use programs in Israel and the United States were promising, showing that 75 percent of participants no longer needed mechanical ventilation within 28 days.

The Abu Dhabi Stem Cells Center has started a therapy that returns blood-based stem cells back into the patient's lungs as a fine mist through a nebulizer.

"We are extremely proud to partner with our colleagues at the ADSCC by sharing knowledge and expertise that we believe will advance healthcare within and across our borders," Pluristem CEO and President Yaky Yanay said in the statement.

The ADSCC's General Manager Dr. Yendry Ventura also commented on the deal in the statement.

"Pluristem is a major player in the cell therapy field with years of experience, a unique platform and robust clinical pipeline," Ventura said. "We are excited to join forces and to promote the research and development of cell therapies for the best of the patients and the human society as a whole."

The deal is the second cross-border agreement since President Donald Trump brokered a deal to normalize ties between Israel and the UAE. It follows a cross-border deal on Sunday between UAE-based APEX National Investment and Israel's TeraGroup to conduct research on the coronavirus.

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Israel and UAE team up on stem cell therapy research for COVID-19 - UPI News

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Global Stem Cell Therapy Market Growth, Size, Analysis, Outlook by 2020 – Trends, Opportunities and Forecast to 2025 – AlgosOnline

August 20th, 2020 6:56 am

A recent report added by Market Study Report, LLC, on ' Stem Cell Therapy Market' provides a detailed analysis on the industry size, revenue forecasts and geographical landscape pertaining to this business space. Additionally, the report highlights primary obstacles and latest growth trends accepted by key players that form a part of the competitive spectrum of this business.

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The latest document on Stem Cell Therapy market includes a wide-range analysis of this industry along with the thorough division of this vertical. According to the report, the Stem Cell Therapy market is likely to grow and increase a significant return over the estimated time period and will also record an outstanding growth rate y-o-y over the upcoming years.

According to the report, the research study provides valuable estimations about the Stem Cell Therapy market pertaining to the sales capacity, market size, profit projections, and numerous other crucial parameters. The Stem Cell Therapy market document also evaluates details about the industry segmentation as well as the driving forces that impact the remuneration scale of this industry.

Explaining the Stem Cell Therapy market with respect to the geographical landscape:

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The report evaluation of the Stem Cell Therapy market claims that the industry is expected to register a substantial revenue over the given time period. It includes data with respect to the market dynamics such as challenges present in this vertical, the possible growth opportunities, and the factors affecting the business domain.

For More Details On this Report: https://www.marketstudyreport.com/reports/global-stem-cell-therapy-market-2020-by-company-regions-type-and-application-forecast-to-2025

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Global Stem Cell Therapy Market Growth, Size, Analysis, Outlook by 2020 - Trends, Opportunities and Forecast to 2025 - AlgosOnline

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Stem Cell Therapy Market Size By Product Analysis, By Application, By End-Users, By Regional Outlook, By Top Companies and Forecast to 2027 – Bulletin…

August 20th, 2020 6:56 am

New Jersey, United States,- The Stem Cell Therapy Market is predicted by Verified Market Researchs report to find players focusing on new product development to secure a strong position in terms of revenue sharing. Strategic collaboration can be a powerful way to bring new products to the market. The level of competition observed in the market may increase.

This research report categorizes the global market by players/brands, regions, types, and applications. The report also analyzes the global market status, competitive landscape, market share, growth rate, future trends, market drivers, opportunities and challenges, sales channels, five forces of distributors, and porters.

The latest 2020 edition of this report reserves the right to provide further comments on the latest scenarios, recession, and impact of COVID-19 on the entire industry. It also provides qualitative information on when the industry can rethink the goals the industry is taking to address the situation and possible actions.

The report covers extensive analysis of the key market players in the market, along with their business overview, expansion plans, and strategies. The key players studied in the report include:

Stem Cell Therapy Market Segment Analysis-

The research report includes specific segments by Type and Application. Each type provides information about the production during the forecast period of 2015 to 2027. The application segment also provides consumption during the forecast period of 2015 to 2027. Understanding the segments helps in identifying the importance of different factors that aid market growth.

1.Stem Cell Therapy Market, By Cell Source:

Adipose Tissue-Derived Mesenchymal Stem Cells Bone Marrow-Derived Mesenchymal Stem Cells Cord Blood/Embryonic Stem Cells Other Cell Sources

2.Stem Cell Therapy Market, By Therapeutic Application:

Musculoskeletal Disorders Wounds and Injuries Cardiovascular Diseases Surgeries Gastrointestinal Diseases Other Applications

3.Stem Cell Therapy Market, By Type:

Allogeneic Stem Cell Therapy Market, By Application Musculoskeletal Disorders Wounds and Injuries Surgeries Acute Graft-Versus-Host Disease (AGVHD) Other Applications Autologous Stem Cell Therapy Market, By Application Cardiovascular Diseases Wounds and Injuries Gastrointestinal Diseases Other Applications

The study analyses the following key business aspects:

Analysis of Strategies of Leading Players: Market players can use this analysis to gain a competitive advantage over their competitors in the Stem Cell Therapy market.

Study on Key Market Trends: This section of the report offers a deeper analysis of the latest and future trends of the Stem Cell Therapy market.

Market Forecasts:Buyers of the report will have access to accurate and validated estimates of the total market size in terms of value and volume. The report also provides consumption, production, sales, and other forecasts for the Stem Cell Therapy market.

Regional Growth Analysis:All major regions and countries have been covered in the report. The regional analysis will help market players to tap into unexplored regional markets, prepare specific strategies for target regions, and compare the growth of all regional markets.

Segmental Analysis:The report provides accurate and reliable forecasts of the market share of important segments of the Stem Cell Therapy market. Market participants can use this analysis to make strategic investments in key growth pockets of the Stem Cell Therapy market.

Business Opportunities in Following Regions and Countries:

North America (United States, Canada, and Mexico)

Europe (Germany, UK, France, Italy, Russia, Spain, and Benelux)

Asia Pacific (China, Japan, India, Southeast Asia, and Australia)

Latin America (Brazil, Argentina, and Colombia)

How will the report assist your business to grow?

The document offers statistical data about the value (US $) and size (units) for the Stem Cell Therapy industry between 2020 to 2027.

The report also traces the leading market rivals that will create and influence the Stem Cell Therapy business to a greater extent.

Extensive understanding of the fundamental trends impacting each sector, although greatest threat, latest technologies, and opportunities that could build the global Stem Cell Therapy market both supply and offer.

The report helps the customer to determine the substantial results of major market players or rulers of the Stem Cell Therapy sector.

Reason to Buy this Report:

Save and reduce time carrying out entry-level research by identifying the growth, size, leading players, and segments in the global Stem Cell Therapy Market. Highlights key business priorities in order to assist companies to realign their business strategies. The key findings and recommendations highlight crucial progressive industry trends in Stem Cell Therapy Market, thereby allowing players to develop effective long term strategies.

Thank you for reading our report. The report is available for customization based on chapters or regions. Please get in touch with us to know more about customization options, and our team will ensure you get the report tailored according to your requirements.

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Managing Type 2 Diabetes and the Role of Sodium-Glucose Cotransporter 2 Inhibitors – AJMC.com Managed Markets Network

August 20th, 2020 6:54 am

Impact of Type 2 Diabetes

Diabetes is a chronic, progressive disease. It is characterized by elevated blood glucose levels resulting from defects in the body related to insulin secretion, insulin action, or both.1-3 According to the 2020 CDC National Diabetes Statistics Report, an estimated 34.2 million Americans (about 1 in 10) have diabetes; type 2 diabetes (T2D) accounts for 90% to 95% of cases.4,5 Further, an additional 88million American adults (1 in 3) have prediabetes, increasing their risk for T2D.6

T2D most often develops in people aged over 45 years, but children, teens, and young adults are also developing the disease in increasing numbers.4,5 Patients with diabetes often present with and are at a higher risk for comorbidities such as atherosclerotic cardiovascular disease (ASCVD), heart failure (HF), and renal disease.3,7-9 The results of a systematic review of global clinical records from a 10-year period showed that approximately one-third of patients with T2D had cardiovascular disease (CVD) as a comorbidity.10 Further, approximately two-thirds of deaths in people with diabetes are due to CVD, including ischemic heart disease, other forms of heart disease, principally congestive HF, and stroke.11

Additionally, the presence of HF is an independent risk factor for developing diabetes.9 About 12% of patients with T2D have established HF, and approximately 3.3% of patients with T2D develop HF each year.9 Further, the presence and severity of chronic kidney disease (CKD) highlights individuals with a heightened risk for adverse health outcomes, such as HF.12,13 The CDC estimates that approximately 1 in 3 Americans with diabetes may have CKD, with diabetes further accounting for 38% of reported causes of end-stage kidney disease in the United States.14 Further, in patients with diabetes, the presence of albuminuria is an independent risk factor for mortality.15

It is essential that health care providers identify predictors of excess mortality in patients with T2D to optimally target risk-reduction strategies. Patients with T2D would benefit from more aggressive preventive programs to prevent CVD. Programs that set stringent standards are more likely to reduce the incidence of cardiovascular morbidity and mortality.9

Treatment Goals and Guidelines

Treatment goals for T2D center on maintaining a patients quality of life by preventing or delaying associated complications and comorbidities. Treatment goals focus around glycemic control and CVD risk factor management. The American Diabetes Association (ADA) recommends regular patient follow-up and, importantly, a patient-centered approach to optimize treatmentoutcomes.16,17

Lifestyle modifications, including losing weight, increasing physical activity, and adopting a healthy diet, remain first-line strategies for the management of T2D.16,18 However, most patients with T2D are unable to control hyperglycemia with diet and exercise and require pharmacotherapy. Generally, monotherapy with an oral hypoglycemic agent is initiated; however, owing to the progressive nature of the disease, most patients will eventually require combination therapy and ultimately injectable treatments as monotherapy or part of polytherapy.19,20 The ADA states that early combination therapy can be considered in some patients at treatment initiation to extend the time to treatment failure.20 Pharmacologic therapy should take a stepwise approach, taking into account individual patient characteristics and the presence of comorbid diseases andcomplications.20

Prior consensus statements by the ADA and the European Association for the Study of Diabetes focus on efficacy in reducing hyperglycemia, with treatment tolerability and safety being primary factors in glucose-lowering medication selection.16,21 However, an update to treatment recommendations was added to the latest 2020 consensus report. This update is due to new evidence regarding the benefit of specific medications to reduce mortality, HF, and progression of renal disease in the setting of established CVD in patients with T2D.16,20

The ADA has adopted these updates in their 2020 recommendations, Standards of Medical Care: 9. Pharmacologic Approaches to Glycemic Treatment2020 and 10. Cardiovascular Disease and Risk Management2020.17,20 The current ADA T2D treatment guidelines are based on indicators of high risk or established ASCVD, CKD, and HF, with glycated hemoglobin (A1C) target levels also considered (

).20 The ADA has suggested a treatment cascade, initiating with monotherapy treatment (such as metformin) and progressing through dual or triple therapy options depending on patient characteristics and preferences (

).20

T2D Available Drug Treatment Options Per Updated ADA Guidelines

Metformin

The ADA states that metformin is the preferred initial pharmacologic agent for the treatment of T2D and should be started at the time T2D is diagnosed unless there are contraindications.20 However, as stated previously, T2D is a progressive disease and often requires additional therapy with combinations of drugs that have complementary mechanisms of action.22 As such, many patients will require dual combination therapy to achieve their target A1C level.20 Current recommendations are to use a stepwise addition of medications to metformin to maintain A1C at target levels (

).20

DPP4

Dipeptidyl peptidase-4 (DPP4) inhibitors are oral diabetic agents that are placed as an add-on second-line therapy after metformin failure as insulinotropic agents that have no intrinsic hypoglycemia risk.18,23 There are currently four DPP4 inhibitors available in the United States that have been approved by the FDA (

).24-40

All four DPP4 inhibitors appear to have similar efficacy in terms of glucose-lowering ability.40 A notable favorable characteristic of DPP4 inhibitors is their efficacy and safety profile in patients with impaired renal function.23 Further, in phase 3 clinical trials, DPP4 inhibitors have shown good safety and tolerability profiles. The most frequent adverse events (AEs) observed were nasopharyngitis and skin lesions, although 2 studies showed an increased rate of hospitalization due to HF.23,29,41,42 As CVD outcomes and safety are a concern for the T2D patient population, mortality and morbidity associated with therapy options should be considered when making treatment selections.

Several CVD outcomes trials have been completed, comparing DPP4 inhibitors with placebo against the backdrop of standard diabetes care, and the DPP4 inhibitors have been shown to have a neutral effect on CVD outcomes.40,41,43,44 Meta-analyses, however, suggest a possible increased risk of acute HF or hospitalized HF with certain DPP4 inhibitors versus placebo; more research is required to explore these observations.45,46 As DPP4 inhibitors come with the possible heightened risk of negative CVD effects, they are suggested as second-line therapy as an add-on to metformin in patients with T2D who need to control hypoglycemia but have no preexisting CVD.20,23,45

In assessing the cardiovascular safety profiles of antidiabetic drugs, sodium-glucose cotransporter 2 (SGLT2) inhibitor therapies have emerged with robust evidence for reducing the risk of adverse CVD outcomes in people with T2D who have either established CVD or are at risk of developing CVD and HF.8 Additional benefits have also been seen in those at risk of renal decline and progression to CKD.8

SGLT2 Inhibitors

SGLT2 inhibitors are a fast-growing class of diabetes drugs given their convenient oral route of administration, strong A1C efficacy data, observed reductions in body weight, and antihypertensive effects. Importantly, these drugs show similar efficacy from early through late stages of diabetes.47 The FDA has approved four SGLT2 inhibitorbased therapies for use in T2D patients, as they have been shown to convey CVD protective effects and delay the progression of CKD;48-50 clinical trial data are summarized in

and

.48-57 The primary outcomes for all available studies were a combination of composite end points of CVD death, myocardial infarction (MI) or ischemic stroke, and HF or hospitalization due to HF.18,48-50 A reduction in risk of HF, MI, and stroke are the most common CVD benefits noted in SGLT2 inhibitor clinical studies (

and

).48-57 The most common AEs noted in most trials were an increased risk of genital infections in the SGLT2 inhibitor population compared with placebo, although the CANVAS trial also noted a higher incidence of amputations.48-50

Fixed-Dose Treatment Combinations

Although the above treatment options present favorable rationales for the use of each agent, there are current data to support initial combination therapy to more rapidly attain glycemic goals.58,59 Clinical trials have demonstrated that this approach is superior to sequential addition of medications, in terms of extending time to primary and secondary failure and decreasing risk of associatedcomplications.60,61

DPP4 inhibitors and metformin-based fixed-dose combinations are accessible and may safely be used in T2D patients to reach treatment goals (

and

).23,48-57 Fixed-dose combinations of DPP4 and SGLT2 inhibitors can also be used (as dual therapy when metformin is contraindicated or not tolerated, or as triple therapy with metformin) to achieve treatment goals in patients with T2D (

and

).23,48-57 DPP4 and SGLT2 inhibitor combinations have complementary actions that have resulted in additive reductions of glycemic and blood pressure parameters.23,52 Findings of recent clinical trials of triple-therapy combinations with DPP4 and SGLT2 inhibitors have demonstrated significant clinical benefit over the use of each individual component when utilized on a background of metformin (

and

).48-57 A phase 3, randomized, double-blind, parallel-group study by Defronzo et al, examining different treatment combinations of empagliflozin and linagliptin as compared with each ingredient individually, noted more significant reductions in A1C levels from baseline for those patients receiving the combination treatments (P<.001 for all comparisons) (

and

).48-57 Further, SGLT2 inhibitors and metformin-based combinations have demonstrated reductions in glycemia, blood pressure, body weight, and albuminuria in people with diabetes.48,53-55,62 A study by Pratley et al demonstrated that in T2D patients with inadequate glycemic control with metformin, co-administration of ertugliflozin (5 or 15 mg) with sitagliptin (100 mg) provided significantly greater improvements in measures of glycemic control compared with addition of either agent alone (P<.001 for all comparisons).53 Notably, in a phase 3 randomized double-blind, active controlled, parallel group study, patients on a fixed dose treatment of saxagliptin + dapagliflozin + metformin experienced a lower rate of AE compared with those patients on treatments of either saxagliptin or dapagliflozin alone.56

While these results illustrate that a fixed-dose combination treatment can help attain T2D treatment goals, the choice of treatment should be tailored to each individual and their T2D prognosis and comorbidities. For those patients with T2D and no elevated CV risk DPP4 inhibitors, such as sitagliptin, are a safe and effective treatment option and can lead to similar treatment outcomes. A randomized, double-blind, placebo- and active-controlled, parallel group, double-dummy, dose-ranging study by Amin et al demonstrated that a lower dose combination of ertugliflozin (5 mg) plus metformin lead to similar A1C reductions when compared with a higher dose of sitagliptin (100 mg) alone.55 Ultimately a the choice of treatment regimen should be made through an open dialogue taking into consideration patient treatment goals, T2D comorbidities, and patient lifestyle and preferences.

Summary

Despite more than 200 years of research on lifestyle management of diabetes and more than 50 years of comparative-effectiveness research in diabetes, innumerable unanswered questions regarding the management of T2D remain.16 T2D treatment guidelines have evolved to adapt to the larger picture of disease, but T2D still carries a significant burden of illness and unmet need. T2D treatment is further complicated by patient comorbidities and their associated risk factors. Optimizing treatment pathways can help alleviate the burden of disease and reach treatment goals for this patient population.

SGLT2 inhibitors, a new option recommended by the ADA 2020 guidelines either as single agents or in fixed-dose combinations with other treatments, offer patients the option to take advantage of benefits beyond stabilization of A1C levels. SGLT2 inhibitors have shown favorable CVD effects, including a reduction in the risk of hospitalization for HF, predominantly in patients with T2D and established CVD48,49,51; they have also been shown to delay the progression of kidney disease.51

References

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Managing Type 2 Diabetes and the Role of Sodium-Glucose Cotransporter 2 Inhibitors - AJMC.com Managed Markets Network

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Rapper Loses Leg to Diabetes and Friends Rally to Support – The Beet

August 20th, 2020 6:54 am

When a famous rapper loses a leg to diabetes there is little to do but offer sympathy and give to the GoFundMe page set up for his treatment and follow up care. Today, as we listened to The Beet's Creative AdvisorJermaine Dupri being interviewedfor HipHopDX,we learned that Andre "Doctor Dre" Brown, most known for having starred in the MTV show Yo! MTV Raps with Ed Lover inthe late 80s to mid-90s, had his leg amputated earlier this summer, the result of complications from diabetes.

Doctor Dre not to be confused with the west coast producer, co-founder of Beats by Dre headphones and former member of NWA Dr. Dreis credited as having "exposedHip Hop to a whole new audience while introducing the genre into living rooms across the United States," according to a story in HipHopDX.

Doctor Dre made his mark in radio, television, movies and had worked as a DJ, composer, talent scout, program host, actor, critic, and author. But he is best known as co-host with Ed Lover of Yo! MTV Raps,"theTV show that did more than any other to make rap music and hip-hop culture global phenomena," according to ABCnews.com

From 1989 to 1995, Doctor Dr andEd Loverwere the co-hosts of Yo! MTV Raps. Dr had already teamed up with Lover in the early 1990s to co-host a morning radio show as part of the re-launch of Hot 97in New York City.

The pair starred in the1993filmWho's the Man?, directed byYo! MTV Rapsco-creator and co-directorTed Demme. Dr and Ed Lover also recorded an album in 1994 titledBack up off Me! Dr also served as a DJ for theBeastie Boys.Hehad his own clothing line calledBigga Stuffin the early 1990s. In 2003 Dr and Ed Lover participated in theComedy Central Roastof theirWho's the Man?co-star, comedianDenis Leary.

Dre also guest-starred onThe Fresh Prince of Bel-Airin the episode "Ill Will" as a figment ofWill Smith's nightmare of bad doctors. He then appeared on an episode ofThe People's Courtwith JudgeMarilyn Milianas a witness for a talent director suing former colleagues of his.

HisGoFundMe page reads:

Friends,

All of us who lived through the Nineties and care about music know and love Andre "Doctor Dre" Brown. He has made his mark on radio and television, in the movies and in print, working successively as a recording artist (as a founding member of Def Jam's Original Concept), hip-hop DJ (he was the Beastie Boys's DJ during the Raising Hell Tour in 1986) , composer, talent scout, on-air personality, actor, author, and critic. He's undoubtedly best-known as the co-host with Ed Lover of "Yo! MTV Raps" (1989-1995), the tv show that did more than any other to make rap music and hip-hop culture global phenomena. After "Yo!", Dre and Ed duo funneled their chemistry into major market radio. They held down the morning show on New York's Hot 97 (1993-1998), then on L.A.'s The Beat (2000-2001), and finally on New York's Power 105 (2003-2006).

Fans of Doctor Dre (whose real name is Andre Brown) is a big personality and well-loved in the Hip Hop community. He has suffered from type 2 diabetes for years, and when diabetes gets advanced it can cut off circulation to the capillaries that supply oxygen to the toes, eyes and other areas of the body that when damaged can not heal properly. One way to prevent and even reverse symptoms of type 2 diabetes is a plant-based diet, which lowers inflammation and helps keep blood sugar under control.

Even as recently as 10 months ago, he was trying to turn things around.Brownexplained that hes not completely blind, and has undergone retina reattachment surgery. The resulting scar tissue causes his vision to fluctuate. As a result, hes currently more focused on higher factors.

Im learning its better what you put in your mouth to help treat the situation, Brown said. But Ive learned to say I believe in a higher spirit, and he speaks to me all the time.

Now he is alsomostly blinddue to complications stemming from his condition. Back in 2016 when he was awaiting weight loss surgery to help him treat his condition, Doctor Dretold The New York Times:

My stubbornness put me where Im at. Now my energy is going to change that. We got young people, grown people, old, all having this. We can prevent this. We can cure this. I have an idea of how to do it.

Diet and lifestyle changes can help reverse and reduce symptoms of diabetes, as Eric Adams, Brooklyn Borough President, found out when he started to experience declining vision. He was overweight and in poor health until he switched to a vegan diet, lost 35 pounds and got healthier. He's recently written a book about his transformation, due out this fall, called Healthy at Last: A Plant-Based Approach to Preventing and Reversing Diabetes and Other Chronic Illnesses.

A new study just published this month found that a plant-based diet controls blood sugar and helps your body naturally metabolize carbs and fat, to help avoid diabetes. And another review study of diets showed that you reap the benefits of eating more plants when avoiding diabetes is the goal.Thisstudyfound that the more plants, the better.

Our thoughts and prayers are with Doctor Dre and his family. To contribute to his GoFundMe Page click here.

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Rapper Loses Leg to Diabetes and Friends Rally to Support - The Beet

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Sensyne Health launches diabetes app in the UK – – pharmaphorum

August 20th, 2020 6:54 am

UK digital health company Sensyne Health has launched a new smartphone app to help people across the diabetes spectrum manage their condition.

The app called DBm-Health can help users to monitor their blood glucose levels and send readings, notes and medication information to their healthcare practitioner to assess remotely.

It is a follow-on to Sensynes GDm-Health product, which is used for remote monitoring of diabetes during pregnancy and was recently made available for free to all NHS Trusts in the UK for one year to assist with monitoring and managing this high-risk group during the COVID-19 pandemic.

GDm-Health has been a success since launch, says the company, which claims a market share of 47% across all NHS Trusts in England. That has prompted the company to accelerate the roll-out of DBm-Health for the wider diabetic community.

Other uses for DBm Health include cancer patients with pre-diabetes, who are known to be at elevated risk of developing full-blown diabetes if they are given high-dose steroid treatment.

It could also help patients with diabetes who are shielding in order to reduce their risk of coronavirus infection which is important as diabetics are thought to be more vulnerable to severe COVID-19 than non-diabetic people.

There is also evidence suggesting COVID-19 may trigger the onset of diabetes in healthy people and cause poor control for existing diabetes sufferers. Sensyne recently launched a web-based app, CVm-Health, to assist individuals in monitoring coronavirus symptoms.

The new app will be piloted in three NHS Trusts over the next few months, to see if it provides the promised health-economic and operational benefits, and is also due to be launched in the US later this year as part of Sensynes push for overseas expansion.

Sensyne says that unlike other diabetes apps, DBm-Health provides a patients clinician with information on their status and whether any additional treatment may be required.

Managing the 3.9 million people living with diabetes costs the NHS around 9.8 billion a year, according to the charity Diabetes UK. There are also more than 34 million people with diabetes in the US, adding $327 billion to the cost of healthcare.

In light of the coronavirus crisis, the NHS has moved rapidly to offer remote consultations, particularly for those with co-morbidities such as diabetes which puts a person at particular risk of severe infection.

We are responding to the urgent need of NHS Trusts for new digital technologies to optimally care for patients with diabetes, commented Dr Lucy Mackillop, Sensynes chief medical officer.

DBm-Health will help ensure the highest quality information is securely available to clinicians from patients who are particularly vulnerable to COVID-19 and are advised to stay at home during the pandemic, she added.

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Sensyne Health launches diabetes app in the UK - - pharmaphorum

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