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Pandion Therapeutics Highlights Potential of Modular Biologics Pipeline for the Treatment of Autoimmune Diseases at FOCIS 2020

October 28th, 2020 10:52 am

WATERTOWN, Mass., Oct. 28, 2020 (GLOBE NEWSWIRE) -- Pandion Therapeutics, Inc. (Nasdaq: PAND), a clinical-stage biotechnology company developing novel therapeutics designed to address the unmet needs of patients living with autoimmune diseases, today announced the presentation of preclinical data highlighting the potential of its modular biologics pipeline for the treatment of autoimmune diseases at the Federation of Clinical Immunology Societies (FOCIS) 2020 virtual annual meeting.

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Scout Bio Advances Novel Gene Therapy for the Treatment of Feline Diabetes

October 28th, 2020 10:52 am

PHILADELPHIA, Oct. 28, 2020 (GLOBE NEWSWIRE) -- Scout Bio, a biotechnology company focused on revolutionizing pet medicine by delivering a pipeline of one-time therapeutics for major chronic pet health conditions, today announced it has initiated two pilot clinical studies to demonstrate effectiveness of an AAV expressing a GLP-1 analog (SB-009) in treating diabetic felines.

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Yield10 Bioscience Announces Start of Field Tests of Winter Camelina Varieties

October 28th, 2020 10:52 am

WOBURN, Mass., Oct. 28, 2020 (GLOBE NEWSWIRE) -- Yield10 Bioscience, Inc. (Nasdaq:YTEN), an agricultural bioscience company, today announced that it has begun field testing to evaluate the emergence and agronomics of winter Camelina sativa varieties. The testing of these winter varieties in the 2020/2021 winter season is part of Yield10’s continued development of Camelina sativa in the medium term for use at commercial scale as a cash cover crop for North America.

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One World’s Dr. Kenneth Perego Joins Montel Williams for Blunt Discussion

October 28th, 2020 10:52 am

LAS VEGAS, NV, Oct. 28, 2020 (GLOBE NEWSWIRE) -- via NewMediaWire -- One World Pharma Inc. (OTC: OWPC), “OWP,” a U.S. based, fully licensed, pure-play hemp and cannabis ingredient producer in Colombia, is pleased to announce that its Executive Chairman, Dr. Kenneth Perego, recently joined television personality and cannabis advocate Montel Williams on his popular podcast “Let’s Be Blunt.”

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AXIM® Biotechnologies Issues Update Letter to Shareholders

October 28th, 2020 10:52 am

SAN DIEGO, Oct. 28, 2020 (GLOBE NEWSWIRE) -- AXIM® Biotechnologies, Inc. (OTCQB: AXIM) (“AXIM® Biotech,” “AXIM” or “the Company”), an international healthcare solutions company targeting oncological and COVID-19 research, announced today that it has issued a letter to its shareholders providing commentary on the Company’s recent announcements and upcoming plans.

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Trading by management and close relations of management

October 28th, 2020 10:52 am

Please read the full announcement in PDF

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Trading by management and close relations of management

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Zenith Confirms Interim Filings on SEDAR

October 28th, 2020 10:52 am

CALGARY, Alberta, Oct. 28, 2020 (GLOBE NEWSWIRE) -- Zenith Capital Corp. (“Zenith” or the “Company”) today announces that, further to its October 9, 2020 press release, it today has filed its interim financial statements and related MD&A for the three months ended July 31, 2020 (the “Interim Filings”). These filings can be found at www.sedar.com under the Company’s profile.

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Tauriga Sciences, Inc. Updates Shareholders on New York State’s Determination to Allow the Sale of CBD Edibles in the Forms of Food & Drink

October 28th, 2020 10:52 am

The Company’s Flagship Brand Tauri-Gum™ is Fully Compliant With the New Rules Set Out This Week by New York State (“New York”)

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Tauriga Sciences, Inc. Updates Shareholders on New York State's Determination to Allow the Sale of CBD Edibles in the Forms of Food & Drink

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In Conversation with John Moore, President of Scientific Bioprocessing Inc. (SBI) – BioBuzz

October 28th, 2020 10:52 am

Scientific Bioprocessing Inc. (SBI) is on a mission to help scientists and engineers de-risk drug development through leading-edge technology that improves the efficiency, effectiveness, and reproducibility of cell culture and bioprocessing.

SBIs single-use optical sensors provide non-invasive, real-time measurement and data monitoring across all form factors from small flasks to the largest bioreactors, enhancing development consistency and scalability. SBI offers a suite of optical sensor products that will be a key component to the biopharma industrys push to standardize processes, reduce development costs, and speed up time to market across cell and gene therapy, tissue engineering, organ-on-a-chip development, and the wider biotech and pharma sectors.

Given the advanced biomanufacturing challenges faced by these industries, and the Food and Drug Administrations (FDA) push for stronger regulatory controls via its Process Analytical Technology (PAT) guidance, we thought it an opportune time to talk with John Moore, SBIs President and the Chairman of the Board of Scientific Industries, Inc., SBIs parent company.

Dr. Govind Rao at the University of Maryland, Baltimore County, and his team from the Center for Advanced Sensor Technology developed optical sensors and licensed them to Fluorometrix, which was then acquired by Scientific Industries in 2011. The sensors were licensed to Sartorius for use in their Ambr and Cultibag systems.

We were in on the ground floor in the very early days of single use technology and the data revolution that is happening in bioprocessing. Since 2011, Sartorius and General Electric have used the licensing of our sensors to sell over $1B worth of products.

The future of personalized medicine is bright. Cell and gene therapy, regenerative medicine, and organ-on-a-chip are virtually untouched by the benefits of optical sensors. Whats really exciting about the market is this: even in biologics only 30% of the 30 approved drugs use single-use bioreactors, yet there are some 1,000 biologic drugs in the clinic right now and 800 are using single-use bioreactors. The industry is really moving away from reusable, stainless steel vessels to disposables. The demand for optical sensors is going to grow dramatically.

I started off as an investment banker in 1987 and our team took Organogenesis, the first regenerative medicine company, public. In 2002, I acquired a portfolio of 16 drug delivery assets from Elan Pharmaceuticals with $148M in funding from the Anglo Irish Bank to buy the portfolio. The transaction occurred over a weekend and was credited with saving Elan Pharmaceuticals from bankruptcy.

What I learned through that process was how some of the most promising companies in our portfolio failed and how some of the most underrated companies ended up having success. I learned how important data and clinical trials are to the success of companies. Wall Street has evolved to understand that the initial scientific insight that created companies is important but not sufficient to create economic value for the shareholders or to benefit society.

As Chairman of Trialogics, a leading clinical trial software provider, I have observed that, remarkably, 50% of clinical trials are still run on paper. I am excited to invest and lead companies like Scientific Industries and SBI that are focused on removing process inefficiencies to improve drug development process and FDA approval chances. The common theme is creating simple, affordable tools to help speed new, safe and effective drugs through approval into the hands of doctors and patients.

SBIs mission is to empower our customers to accelerate the discovery of safe, effective, and affordable solutions in the biotech industry. Our optical sensors can be installed in the smallest scale, early development vessels all the way through clinical trials and downstream manufacturing post-approval. We believe we can deliver the instrumentation and sampling that is required to wring huge inefficiencies out of the development process.

Historically, testing has been done offline and that requires taking samples, risking contamination, and creating an asynchronous effect that runs the risk of losing a million dollar batch of biologics because it wasnt sampled in real-time.

SBIs new generation of sensors empowers bioprocessing engineers to understand the design parameters for an experiment at the earliest conception of the product. The sensors are then placed in the single-use bioreactors and are able to tell the engineers when the batch is going out of the design parameters and they can immediately course-correct by changing what they are feeding the cells or by adjusting the pH of the culture, for example.

In addition, there have been three waves of Artificial Intelligence. The current wave requires accurate, real-time data to be able to make its calculations. The current electrode sensors cant provide this. Our optical sensors are the size of a hole-punch and you can use them to map bioreactors, you can put tens or even hundreds of sensors throughout a bioreactor or deploy them across the process to determine your critical quality attributes. You cant use an electrode or even an optical sensor in a probe format in the earliest stages of development that use multi-well plates and flasks. Our products are available in a variety of form factors within inexpensive kits so that it can be as useful for a cell scientist or a process development person as a telescope is for an astronomer, or a microscope for a microbiologist. We believe all kinds of incredible new insights are going to emerge because of the proliferation and affordable nature of our sensors.

I have a friend that does business development for a large pharmaceutical company; he has personally led over 50 development and licensing deals for biotechs. He told me that they are willing to pay twice as much for an asset that has a strong data package than for an asset that does not. Often scientific researchers focus on the scientific breakthrough and not on documenting the early-stage experiment design and critical quality attributes. Entrepreneurial scientists will see a big benefit by capturing early-stage development data packages because this makes their asset much more attractive to licensors. Strong data packages save years of research work and patent life for the licensors of the technology. Our sensors can help build these strong data packages right from the start.

PAT is guidance from the FDA. What the FDA is trying to do is encourage the voluntary implementation of quality assurance systems as early as possible in the process. The FDA wants consistent QA processes from early-stage experiments through FDA submission and post-marketing.

Just like a good data package is critical for convincing a licensor to take a risk on a project, PAT will improve the likelihood of FDA approval. The FDA doesnt care about whether you have a 10% or 70% yield, they want to know you have the critical quality attributes and monitoring to always deliver that consistent 10% or 70% yield. The FDA wants to know that you have a plan of action for QA.

SBIs sensors and our products can help our clients and partners increase experiment and process repeatability because we offer non-invasive, scalable, automated and real-time data monitoring that is critical to meeting the FDAs PAT guidance for quality assurance.

Biologics drugs today span from large scale, big batch biologics to small scale personalized therapies using autologous cells. One of our partners is the cell therapy company Adva Biotechnology. Advas CEO and Founder Ohad Karnielis vision is to put single-use bioreactors at the point-of-care in hospitals. His vision illustrates the personalized medicine fields aspirations.

The industry will need optical sensors in both large scale manufacturing and for personalized medicine to broadly and affordably deliver its miracles to patients.

One of the less discussed benefits of increased automation and one-touch controls is that cell scientists get to focus on great science and not on just labor intensive sampling and moving liquids. Increased automation and the removal of manual inputs creates more space for the genius of observation and invention in the lab.

It will mean faster FDA approvals, lower costs for patients, and safer therapies. Many cell therapies today cost $500K per patient, and the industry needs to lower this cost to around $100K per patient. Strong quality control and increased repeatability will improve safety, ultimately enabling more drugs to be approved by the FDA faster because of reduced risk and increased regulatory compliance.

A lot of success boils down to three things: credibility, visibility, and understanding the theory of your business. Reinhard brings all three of these to SBI. In our case, the world is full of small companies that have developed individual sensors that dont have the commercial muscle to educate the market. We are creating a company that is poised to redefine cell culture.

Reinhards vision is that there is a big gap in the market. He believes the market doesnt need another small sensor company; the market needs a single, global, one-stop-shop provider for almost any conceivable monitoring and process control modality. He brings a very practical and valuable commercial perspective to SBI.

We are aggressively in-licensing new sensor modalities and are on the acquisition trail. We are part of NIIMBL, ARMI, and ReMDO. What youll be seeing from SBI is collaboration with industry partners at these organizations, and we will be raising non-dilutive funding for adding additional sensing modalities for measuring glucose, lactate, secreted genes, and other key measurables.

There will be some mind-blowing new functionality coming and scientists will be able to design drugs that they never could have dreamed of without the insights they gain from these sensors.

Steve has over 20 years experience in copywriting, developing brand messaging and creating marketing strategies across a wide range of industries, including the biopharmaceutical, senior living, commercial real estate, IT and renewable energy sectors, among others. He is currently the Principal/Owner of StoryCore, a Frederick, Maryland-based content creation and execution consultancy focused on telling the unique stories of Maryland organizations.

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In Conversation with John Moore, President of Scientific Bioprocessing Inc. (SBI) - BioBuzz

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KlaHealth Raises $12.9M in Combined Seed and Series A Financing Round to Deliver AI-Powered, Clinician-Centered Solutions That Improve Surgical Care -…

October 28th, 2020 10:52 am

SAN FRANCISCO, Oct. 28, 2020 /PRNewswire/ --KlaHealth, Inc., a surgical intelligence platform that applies a dynamic cycle of patient-specific predictions, stratified interventions, and outcomes tracking to reduce surgical complications, today announced the closing of a $2.9 million Seed financing and milestone-based $10 million Series A financing led by Sant Ventures and Intuitive Ventures, and inclusive ofgrant funding from the National Science Foundation Small Business Innovation Research (SBIR) Program. These funds will accelerate the expansion of the KlaHealth platform to hospitals and surgical partners across the United States.

A Growing Need for Quality Improvement in Surgical CareIn the U.S., 51 million surgeries are performed annually, with an average complication rate of 15 percent. This results in millions of patients suffering harm and loss after a procedure. Tragically, half of these complications are known to be avoidable, and contribute to $77 billion in wasted healthcare costs each year.[1],[2]

KlaHealth helps to prevent these avoidable complications while enhancing surgical care by delivering stratified patient risk scoring. The company's state-of-the-art platform uses machine learning algorithms to match individual risk levels with graduated pathways of care that align with the unique needs of each surgical patient.

These personalized efforts bring surgery into a new era of precision medicine: with KlaHealth, surgeons can match the right patient with the right procedure with the right precautions at the right time, leading to improved patient outcomes and significant hospital savings.

The Genesis of KlaHealth KlaHealth was founded by CEO, Bora Chang, MD, and advisors Erich Huang MD, PhD, and Zhifei Sun, MD, at Duke University Health System. As practiced clinicians, all of them understood, firsthand, the unique priorities and challenges facing surgical teams.

"As a trained surgeon, I know the complexity of decision-making in caring for surgical patients," said Dr. Huang, Chief Data Officer for Quality at Duke University Health System. "We began this work because we knew that an objective, risk-based stratification tool could help providers deliver the highest levels of care."

Dr. Chang, CEO of KlaHealth added: "Our vision is to apply the lessons learned from millions of previous surgeries for the benefit of every patient undergoing a procedure. Patients and their families, clinicians, and hospitals deserve the assurance that the risks of any surgery will be safely navigated by surgical teams with the best information available to them at every point in the surgical journey. We are thrilled to have a stellar group of surgeons, hospital centers, investors, and advisors working with us to realize the opportunity of precision surgery."

Unlocking Potential Across DisciplinesTo date,KlaHealth's hospital partners have applied the company's AI-powered platform in colorectal, vascular, cardiac, and orthopedics surgical specialties.

"In our cardiac surgery department, our partnership with KlaHealth has identified up to $3 million a year in cost savings by optimizing post-procedure management for our cardiac patients," said Bruce Gewertz, MD, FACS, Surgeon-in-Chief and Chair of Surgery at Cedars-Sinai Medical Center. "Their work showcases the opportunity for improved resource utilization and data-driven clinical best practices across the surgical care continuum."

Citing colliding trends in digital health and care optimization, KlaHealth's investors emphasized the potential of the solution throughout the ecosystem of surgical care:

"KlaHealth's platform represents a powerful solution for providers and medical device partners looking to unlock the potential of data in pursuit of improved outcomes and lowering the cost of care," said Oliver Keown, MD, Director of Intuitive Ventures.

"Data-driven surgery will positively transform the way both hospitals and physicians care for patients, and we are excited to team up with KlaHealth to further innovate surgical care," added Dennis McWilliams of Sant Ventures.

About KlaHealth

KlaHealth is a healthcare data analytics company that delivers patient-specific predictive insight and risk stratification software to help improve surgical quality and prevent complications. The company was founded by a group of surgeon-scientists with a goal of harnessing machine learning algorithms to reduce patient surgical complications and improve outcomes. KlaHealth uses advanced artificial intelligence techniques to deliver a cloud-based software-as-a-service solution to healthcare providers, surgeons, and hospital systems. The company has participated in highly selective accelerator programs such as Cedars-Sinai Techstars Accelerator, Healthbox Studio, and Plug and Play. For more information about KlaHealth, visit http://www.KlaHealth.com.

About Sant Ventures

Founded in 2006, Sant Ventures is a specialized healthcare and life sciences investment firm with over a half-billion dollars in capital under management. The firm invests in early-stage companies developing innovative new medical technologies, biotechnologies, and digitally-enabled healthcare services. Recent Sante successes include Claret Medical (Boston Scientific), TVA Medical (Becton Dickinson), Millipede Medical (Boston Scientific), Molecular Templates (MTEM), AbVitro (Celgene), and Explorys (IBM Corp). Sant invests nationally and is headquartered in Austin, Texas, with additional offices in Houston. For more information, please visit http://www.sante.com.

About Intuitive Ventures

Leveraging Intuitive's entrepreneurial spirit and expansive technological and clinical reach, Intuitive Ventures invests in transformative opportunities advancing positive outcomes in healthcare. The fund is focused on US and international early-stage start-ups and takes a long-term outlook to support portfolio companies reach their major milestones. Through its inaugural $100 million fund and with leadership combining decades of investing and operational experience, the team cultivates strategic resources to drive financial returns and accelerate the future of minimally invasive care. More information and future updates can be found at: http://www.intuitive-ventures.com.

[1]Dimick. J Am Coll Surg. 2004 Oct:199(4)531-7.2004.[2]Healy. JAMA Surg. 2016 Sep 1:151(9)823-30.

Contact: Elissa Baker [emailprotected]

SOURCE KlaHealth

http://www.kelahealth.com/

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KlaHealth Raises $12.9M in Combined Seed and Series A Financing Round to Deliver AI-Powered, Clinician-Centered Solutions That Improve Surgical Care -...

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Imbio Partners with Siemens Healthineers to Deliver Image Analysis Tools to Clinicians Across the Globe – PRNewswire

October 28th, 2020 10:52 am

MINNEAPOLIS, Oct. 27, 2020 /PRNewswire/ -- Imbio, a healthcare technology company developing the leading suite of medical image analysis for pulmonary and cardiothoracic diseases, and Siemens Healthineers, a leading medical technology company, announced they are partnering to expand access to Imbio AI algorithms worldwide. Physicians will now be able to apply Imbio's automated AI for quantitative image analysis directly through the Open Apps interface on Siemens' syngo.via platform.

Imbio provides quantitative and personalized imaging analysis for patients suffering from both acute and chronic diseases. Imbio's fully automated technology transforms chest CT studies into rich visual maps of a patient's lungs with accompanying reports that provide detailed data on the type and extent of abnormalities found in the images. For example, with Imbio Lung Density Analysis and Lung Texture Analysis clinicians can quickly visualize a patient's lungs to support diagnosis and treatment decisions for a variety of patient conditions including COPD/emphysema and fibrotic disease. Imbio products support multiple clinical initiatives such as lung cancer screening, smoking cessation and pulmonary embolism management programs, and can be used in clinical trials and academic research for numerous diseases.

"Delivering our AI solutions requires a reliable and trusted platform like syngo.via. Together with Siemens, we can now offer physicians an easily accessible and cost-effective way of testing and ultimately using our imaging AI applications without adding complexity or investments into existing hospital infrastructure. We look forward to working with Siemens Healthineers to bring our entire portfolio of products to physicians for more personalized care of patients with respiratory and cardiothoracic diseases," says Mike Hostetler, Director - Marketing and Sales at Imbio.

About ImbioImbio is a leader in fully-automated AI image analysis for acute and chronic pulmonary and cardiothoracic conditions. Imbio's solutions transform the way patients are discovered, diagnosed and treated, enabling physician productivity and more personalized care for patients. Imbio's solutions are fully automated, regulatory cleared and available through our global partners. For more information, please visit http://www.imbio.com.

About Siemens Healthineers As a leading medical technology company headquartered in Erlangen, Germany, Siemens Healthineers enables healthcare providers worldwide through its regional companies to increase value by empowering them on their journey towards expanding precision medicine, transforming care delivery, improving the patient experience, and digitalizing healthcare. Siemens Healthineers is continuously developing its product and service portfolio, with AI-supported applications and digital offerings that play an increasingly important role in the next generation of medical technology.

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Human Microbiome Therapeutics Market To Be Worth USD 1,098.4 Million by 2027. Key participants include: Finch Therapeutics, Biotagenics Inc., Commense…

October 28th, 2020 10:52 am

VANCOUVER, BC, Oct. 27, 2020 /PRNewswire/ -- The globalHuman Microbiome Therapeutics Marketis forecast to be worth USD 1,098.4 Million by 2027, according to the latest analysis by Emergen Research.The human microbiome therapeutics market is forecast to augment rapidly due to the rising application of human microbiome therapeutics into personalized medicine and nutrition. Besides, the growing technological advancements in metagenomics and the therapeutic system is anticipated to further propel the market growth over the forecast timeframe.

However, huge infrastructure and equipment costs and complicated laboratory bacteria development and isolation procedures are likely to impede market growth over the forecast timeline.

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Key Highlights From The Report

To get leading market solutions, visit the link below: https://www.emergenresearch.com/industry-report/human-microbiome-therapeutics-market

Emergen Research has segmented the Global Human Microbiome Therapeutics Market based on product, approach, therapeutic area, disease, and region:

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About Emergen Research

At Emergen Research, we believe in advancing with technology. We are a growing market research and strategy consulting company with an exhaustive knowledge base of cutting-edge and potentially market-disrupting technologies that are predicted to become more prevalent in the coming decade.

With market-leading insights and an in-depth understanding of leading and niche technologies, our solutions address the most pertinent questions for your business needs. A major technological shift has been witnessed towards creating a 'Circular Economy,' fuelled by factors, such as the increased adoption of bio-based materials, along with other methods for achieving carbon neutrality. We are conversant in technologies, viz., Artificial Intelligence (AI), Augmented Reality (AR), Virtual Reality (VR), Robotic Process Automation (RPA), Smart Manufacturing, Internet of Things (IoT), Big Data Analytics, Machine learning, Nanotechnology, Edge Computing, Blockchain Technology, Cloud Computing, Vehicle Electrification, Advanced Maintenance Analytics, and Predictive Maintenance, among other prevalent and emergent technologies.

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Eric LeeCorporate Sales SpecialistEmergen Research | Web: https://www.emergenresearch.comDirect Line: +1-(604)-757-9756E-mail: [emailprotected]

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COVID-19 Impact on the Research Antibodies & Reagents Market by Product, Technology, Application, End-user – Global Forecast to 2025 -…

October 28th, 2020 10:52 am

Dublin, Oct. 27, 2020 (GLOBE NEWSWIRE) -- The "Research Antibodies & Reagents Market by Product (Antibodies (Type, Form, Source, Research Area), Reagents), Technology (Western blotting, Flow Cytometry), Application (Proteomics, Drug Development), End User - COVID-19 Impact - Global Forecast to 2025" report has been added to ResearchAndMarkets.com's offering.

The global market projected to reach USD 14.11 billion by 2025 from USD 10.19 billion in 2020, at a CAGR of 6.7% during the forecast period.

The research antibodies and reagents market has evolved owing to factors such as growth in proteomics and genomics research, rising demand for high-quality antibodies for research reproducibility, and increasing R&D activity and expenditure in the life sciences industry. Fueled by the growing demand for personalized medicine and structure-based drug design, the global research antibodies and reagents market is expected to witness significant growth in the coming years.

Based on product, the reagents segment holds the highest market share during the forecast period.

Based on product, the research antibodies and reagents market are segmented into reagent and antibodies. The reagent segment accounted for the larger market share in 2019. The reagents market is experiencing notable growth due to the growing applications of biosciences and biotechnology within the pharmaceutical and healthcare fields.

Based on technology, the flow cytometry segment is expected to register the highest CAGR during the forecast period.

Based on technology, the research antibodies and reagents market is segmented into western blotting, flow cytometry, ELISA, Immunohistochemistry, Immunofluorescence, Immunoprecipitation, and other technologies. The flow cytometry segment is expected to witness the highest growth during the forecast period. This is mainly due to this technique is its ability to perform simultaneous multi-parameter analysis on single cells within a heterogeneous mixture. It offers a high throughput and the automated quantification of cell features. These factors, along with technological innovations in flow cytometry and growing cancer research, are driving the growth of this segment.

By application, the proteomics holds the highest market share during the forecast period.

Based on application, the research antibodies and reagents market is segmented into proteomics, drug development and Genomics. Proteomics held the largest share of the global research antibodies and reagents market in 2019. The growth of the segment is due to as it efficiently maps drug-protein and protein-protein interactions. Moreover, proteomic technologies have minimized the cost, time, and resource requirements for chemical synthesis and biological testing of drugs. Proteomic technologies, such as electrophoresis, ELISA, microarrays, and MS-based proteomics, are highly efficient for analytical laboratory testing.

By end-user, the pharmaceutical & biotechnology holds the highest market share during the forecast period.

The research antibodies and reagents market is segmented into the pharmaceutical & biotechnology companies, academic & research institutions and Contract Research Organizations. The pharmaceutical & biotechnology companies held the largest share of the global research antibodies and reagents end-user market in 2019. The large share of this segment is attributed to the wide use of research antibodies in drug development for the identification and quantification of biomarkers and various analytical procedures.

By Region, The Asia Pacific region is expected to register the highest CAGR during the forecast period.

The Asia Pacific research antibodies and reagents market is expected to grow at the highest CAGR from 2020 to 2025. The growth of this market is primarily due to growing proteomics and genomics research and increasing research funding, investments by pharmaceutical and biotechnology companies, and growing awareness of personalized therapeutics in the region. Also, high-growth countries, such as China, India, Japan, South Korea, Taiwan, Australia, and Singapore are the major contributors to the Asia Pacific research antibodies and reagents market. This region is expected to grow at the highest pace during the forecast period primarily due to growing proteomics and genomics research and increasing research funding, increasing investments by pharmaceutical and biotechnology companies, and growing awareness about personalized therapeutics.Key Topics Covered:

1 Introduction

2 Research Methodology

3 Executive Summary

4 Premium Insights4.1 Research Antibodies and Reagents: Market Overview4.2 Asia-Pacific: Research Antibodies and Reagents Market, by Application4.3 Research Antibodies and Reagents Market: Geographic Growth Opportunities4.4 Research Antibodies and Reagents Market, by Region (2018-2025)4.5 Research Antibodies and Reagents Market: Developed Vs. Developing Markets

5 Market Overview5.1 Introduction5.2 Market Dynamics5.2.1 Drivers5.2.1.1 Increasing Research Activity and Funding for R&D5.2.1.2 Growing Industry-Academia Collaboration5.2.2 Restraints5.2.2.1 Quality Concerns and a Lack of Reproducible Results5.2.3 Opportunities5.2.3.1 Emerging Markets5.2.3.2 Personalized Medicine and Protein Therapeutics5.2.3.3 Growth in Stem Cell and Neurobiology Research5.2.3.4 Increasing Focus on Biomarker Discovery5.2.3.5 Rising Interest in Outsourcing5.2.4 Challenges5.2.4.1 Cost and Time-Intensive Antibody Development Processes5.2.4.2 Pricing Pressure Faced by Prominent Market Players

6 Industry Insights6.1 Introduction6.2 Industry Trends6.2.1 Increasing Research on Therapeutic Antibodies6.2.2 Recombinant Antibodies Are Supporting the Smooth Transition from in Vitro to in Vivo6.2.3 Growing Consolidation of the Life Science Antibodies and Reagents Market6.3 Stakeholder Analysis6.4 Strategic Benchmarking6.5 Impact of COVID-19 on the Research Antibodies and Reagents Market

7 Research Antibodies and Reagents Market, by Product7.1 Introduction7.2 Reagents7.2.1 Media & Sera7.2.1.1 Media & Sera Hold the Largest Share of the Reagents Market7.2.2 Stains & Dyes7.2.2.1 Growth of the Life Science Industry is Driving the Demand and Use of Stains & Dyes7.2.3 Fixatives7.2.3.1 Fixative Agents Are Needed to Preserve the Morphology and Antigenicity of Target Molecules7.2.4 Buffers7.2.4.1 Wide Use in Drug Development Will Drive the Market for Buffers7.2.5 Solvents7.2.5.1 Organic Solvents See Wide Use in Pharmaceutical Processes and Assays Like Ihc7.2.6 Enzymes7.2.6.1 An Increase in Proteomic and Genomic Research Activity Will Ensure Demand for Enzymes7.2.7 Probes7.2.7.1 the Versatility, Sensitivity, and Quantitative Capabilities of Probes Have Ensured Their Use in Research7.2.8 Other Reagents7.3 Antibodies7.3.1 Antibodies, by Type7.3.1.1 Primary Antibodies7.3.1.1.1 Increasing Demand for Accurate and Reliable Antibodies Follows the Rise in R&D Activity and Expenditure7.3.1.2 Secondary Antibodies7.3.1.2.1 Versatility and Low Cost of Production Have Ensured Stable Growth in the Market for Secondary Antibodies7.3.2 Antibodies, by Form7.3.2.1 Monoclonal Antibodies7.3.2.1.1 Monoclonal Antibodies Are Among the Most Common Tools in Biomedical Science7.3.2.2 Polyclonal Antibodies7.3.2.2.1 Thermo Fisher Scientific and Abcam Are Major Players in the Polyclonal Antibodies Market7.3.2.3 Recombinant Antibodies7.3.2.3.1 Recombinant Antibodies Provide a High-Specificity, High-Sensitivity Option7.3.3 Antibodies, by Source7.3.3.1 Mice7.3.3.1.1 Mice Are the Preferred Hosts for Research-Use Antibody Production7.3.3.2 Rabbits7.3.3.2.1 Rabbits Are a Cost-Effective Means of Antibody Production7.3.3.3 Other Sources7.3.4 Antibodies, by Research Area7.3.4.1 Oncology7.3.4.1.1 the High Prevalence of Cancer Has Boosted Research Activity in the Sector7.3.4.2 Infectious Diseases7.3.4.2.1 Rising Awareness and Growing Research Activity Are Key Drivers of the Market7.3.4.3 Immunology7.3.4.3.1 Antibodies Are Used to Identify Protein and Peptides to Understand Infectious Disease Immunology Better7.3.4.4 Neurobiology7.3.4.4.1 Antibody-Based Approaches Are Widely Used in Molecular and Cellular Neuroscience7.3.4.5 Stem Cells7.3.4.5.1 Increasing Funding and the Growing Importance of Stem Cells in Transplantation Are Key Market Drivers7.3.4.6 Other Research Areas

8 Research Antibodies and Reagents Market, by Technology8.1 Introduction8.2 Western Blotting8.2.1 High Accuracy, Ease of Interpretation, and Other Advantages Have Propelled the Use of Western Blotting8.3 Flow Cytometry8.3.1 Flow Cytometry is the Fastest-Growing Technology Segment of the Market8.4 Enzyme-Linked Immunosorbent Assay8.4.1 Elisa Has the Potential to Supersede the Current Gold Standard for COVID-19 Testing8.5 Immunohistochemistry8.5.1 Complexities of Ihc Pose Challenges to Market Growth8.6 Immunofluorescence8.6.1 Immunofluorescence Helps Determine Specific Gene Expressions8.7 Immunoprecipitation8.7.1 Results Obtained by Ip Can be Analyzed Through Other Technologies8.8 Other Technologies

9 Research Antibodies and Reagents Market, by Application9.1 Introduction9.2 Proteomics9.2.1 Proteomics Holds the Largest Share of the Market, by Application9.3 Drug Development9.3.1 the Drug Development Applications Segment is Expected to Grow at the Highest Rate9.4 Genomics9.4.1 Genomics is Currently An Emerging Area of Research Applications and Expected to See Growth in the Coming Years

10 Research Antibodies and Reagents Market, by End-user10.1 Introduction10.2 Pharmaceutical & Biotechnology Companies10.2.1 Pharma & Biotech Companies Dominate the End-User Market10.3 Academic & Research Institutions10.3.1 Growing Government Investments to Propel the Market10.4 Contract Research Organizations10.4.1 Growing Work on Monoclonal Antibodies and Drug Conjugates Among Cros is Aiding Market Growth

11 Research Antibodies and Reagents Market, by Region11.1 Introduction11.2 North America11.3 Europe11.4 Asia-Pacific11.5 Latin America11.6 Middle East and Africa

12 Competitive Landscape12.1 Overview12.2 Matrix Evaluation Framework12.3 Research Antibodies Market Share Analysis12.4 Competitive Leadership Mapping12.4.1 Stars12.4.2 Emerging Leaders12.4.3 Pervasive Companies12.4.4 Emerging Companies12.5 Competitive Situation and Trends12.5.1 Product Launches12.5.2 Expansions12.5.3 Acquisitions12.5.4 Collaborations, Partnerships, and Agreements

13 Company Profiles13.1 Thermo Fisher Scientific13.2 Merck Group13.3 Abcam plc13.4 Becton, Dickinson and Company13.5 Cell Signaling Technology13.6 Bio-Rad Laboratories13.7 F. Hoffmann-La Roche13.8 Agilent Technologies13.9 Danaher Corporation13.10 Lonza13.11 Genscript13.12 PerkinElmer13.13 Biolegend13.14 Illumina13.15 Immunoprecise Antibodies13.16 Fujirebio Diagnostics Ab13.17 Analytik Jena Ag13.18 Omega Bio-Tek13.19 Dovetail Genomics13.20 Atlas Antibodies

14 Appendix14.1 Insights of Industry Experts14.2 Discussion Guide14.3 Knowledge Store: Subscription Portal14.4 Available Customizations14.5 Related Reports14.6 Author Details

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HeartBreast Cancer-on-a-Chip Developed To Monitor Cardiac Toxicity Arising From Chemo – Technology Networks

October 28th, 2020 10:52 am

Breast cancer is the most commonly occurring cancer for women around the world, and much effort has been spent in the development of therapies to treat this disease. Among these treatments, chemotherapy has been shown to be among the most effective methods; however, the drugs used in these therapies can have adverse side effects, the most serious of which is toxicity to the heart. In addition to tissue damage to the heart, chemotherapeutic breast cancer drugs can also affect the heart's pumping ability or result in clinical heart failure.

In order to avoid these problems, efforts are made to monitor the heart of patients who are undergoing chemotherapeutic treatment for breast cancer and to adjust their treatment levels accordingly. Current methods to monitor the heart include the use of echocardiograms and other imaging procedures, as well as taking biopsies of the heart. But the imaging methods only detect late-stage, irreversible cardiac failure and biopsies are highly invasive and are physically painful for the patient.

There are alternative monitoring systems that can be created in the laboratory to mimic what is happening in the body. These organs-on-a-chip models consist of a silicone chip with compartments for culturing specific types of live human tissues. The compartments are connected to microfluidic channels through which oxygen and nutrient media are pumped and circulated. The tissue cells normally secrete molecules called biomarkers into the surrounding medium, which are good indicators of their health and function. The levels of these biomarkers can then be measured in order to determine the condition of the tissues.

Recently, methods have been successful in creating simple systems to monitor heart toxicity from breast cancer drugs in selected patients, but, to date, there have been few attempts to produce such a system in a larger, more comprehensive and reliable model.

A collaborative team, which includes a group from the Terasaki Institute for Biomedical Innovation, has developed an organs-on-a-chip system that more widely examines the responses of breast cancer and heart tissues to therapeutic breast cancer drugs. For their system, they chose to measure two cardiac biomarkers which are produced by healthy heart cells and one biomarker that is produced by actively growing breast cancer cells. Included in the study were tests of both healthy and artificially-induced damaged heart tissues, to mirror the possible heart conditions of breast cancer patients prior to chemotherapy. They also devised added features to the system to enhance its capabilities.

The team designed a chip system with two separate compartments for tissue cultures of breast cancer and either healthy or artificially-induced damaged heart tissues; these compartments were connected by channels which allowed the free flow of fluid between them. To more closely reproduce the mechanical properties of native body tissues, the tissue cultures were prepared by enclosing tiny spheroids of either heart or breast cancer cells in a gelatinous substance. Pre-determined controls for the chip's circulatory fluidic system ensured that the tissues received oxygen, nutrient media and chemotherapeutic drug delivery.

"This work establishes an important model for monitoring cardiac toxicity from breast cancer chemotherapy," said first author Junmin Lee, Ph.D., part of the Terasaki Institute's research team. "We successfully created cardiac and breast cancer tissues that closely mimic bodily tissues, and we developed an improved sensing device and drug delivery system; these are milestones in organs-on-a-chip technology."

In comparison with single-compartment models with either heart or breast cancer tissues, it was found that actively growing breast cancer tissues in communication with heart tissues decreased the levels of healthy heart biomarkers than those found in the single-chip systems. Moreover, the dual-chip system provided evidence that the breast cancer cells' biomarker secretion was affected not only by drug treatment, but by their interaction with cardiac tissues with different levels of damage. This showed that the interplay between the heart and breast cancer tissues had an important influence on indicators of cell function and disease progression.

Although no definitive conclusions could be made on whether pre-damaged heart tissues were more susceptible to cardiac injury when exposed to breast cancer drugs, the results showed that in healthy cardiac tissues, delivery of the breast cancer drug resulted in decreased cellular growth and secretion of healthy heart biomarkers than without the drug.

Further tests may be conducted to explore the use of this model for detecting and predicting cardiac toxicity from chemotherapeutic drugs. The model may be expanded to include observations of tissues cultured on a long-term basis, examination of additional biomarkers, testing the model using tissues derived from several patients and measurements of other, non-biomarker indicators of cardiac damage (electrical and contractive functions, for example). Future possibilities could be the addition of a liver tissue component onto the chip and considerations of the system's scalability to correlate with bodily systems.

"These efforts lay important groundwork that can pave the way to future applications in disease modeling," said Ali Khademhosseini, Ph.D., director and CEO for the Terasaki Institute. "The Personalized Physiological platform that we have at our Institute is one of the many vehicles that we have for bringing personalized medicine to the real world."

Reference:Lee J, Mehrotra S, Zare-Eelanjegh E, et al. A heart-breast cancer-on-a-chip platform for disease modeling and monitoring of cardiotoxicity induced by cancer chemotherapy. Small. 2020;2004258. doi:10.1002/smll.202004258

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.

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Biobanks Market Analysis Growth Opportunities and Trends by Forecast To 2025 – The Think Curiouser

October 28th, 2020 10:52 am

Global Biobanks Market: Snapshot

Biobanks are essentially repositories for storing biological substances derived from humans, which may include organs, bio-specimens, plasma, saliva, and blood. With a vast rise in the number of organ replacement surgeries globally and significant advancements made in the fields of transfusion and replacement technologies, the role of the biobanks market has become more concrete in the healthcare sector in recent years.

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The global biobanks market has witnessed expansion at a significant pace in the recent years owing to the vast rise in prevalence of a number of chronic diseases and the increased demand for personal medicine. The massive rise in incidence rate of conditions such as diabetes, cancer, neurovascular diseases, cardiovascular diseases, and respiratory diseases has compelled government bodies to take stronger actions in terms of investments in biobanks and increasing awareness about them. The global market for biobanks works in coherence with these efforts by adding pace to the process of drug discovery and the treatment of chronic diseases that are caused by activities such as smoking, consumption of alcohol, obesity, and unhealthy lifestyles.

Heavy investment by a proactive government has boosted the North America biobanks market to the leading position in the global biobanks market, followed closely by Europe. Both regions are home to several bioscience companies and host a large number of drug discovery and research activities. Asia Pacific still remains the region with the most promising growth potential as the region shown high promise owing to an increase in investments from both government and non-government organizations, along with a large and increasingly affluent population base that is gaining awareness about the market.

Global Biobanks Market: Overview

The global biobanks market owes its conception to the rising need for replacement organs and the steady advancement in the replacement and transfusion technologies regarding a number of bodily substances. Though the technology and need to store organs and other bio-entities had been available for a long time, the global biobanks market took on a more important role in the healthcare sector following the increasing research in genomics. In the new millennium, the development of the personalized medicine field has been the vital driver for the global biobanks market. The likely advancement of the latter, thanks to helpful government regulations, is likely to make the crucial difference for the global biobanks market in the near future.

The steady technological advancement in the healthcare sector in the last few decades has now led to a scenario where the full potential of biobanks can be harnessed. As a result, the global biobanks market is projected to exhibit steady growth over the coming years.

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Global Biobanks Market: Key Trends

The rising interest in personalized medicine is the prime driver for the global biobanks market. Personalized medicine has only become a viable branch of modern medicine after steady research in genomics and the way various patients react to various medicines. The biobanks market has thus come into the spotlight thanks to their role as a steady supplier of human biomaterials for research as well as direct application. The increasing research in genomics following the findings of the Human Genome Project is thus likely to remain a key driver for the global biobanks market in the coming years.

The utilization of biobanks instem cellresearch has been hampered in several regions by ethical concerns regarding the origin of stem cells. Nevertheless, the potential of stem cells in the healthcare sector is immense, and is likely to have a decisive impact on the trajectory of the global biobanks market in the coming years. Many countries have, in recent years, adopted a supportive stance towards stem cell research, aiding the growth of the biobanks market. Continued government support is thus likely to remain vital for the global biobanks market in the coming years.

Global Biobanks Market: Market Potential

The leading role of the U.S. in the global biobanks market is unlikely to change in the coming years. The easy availability of government-supported healthcare infrastructure and the presence of several industry giants in the region has driven the biobanks market in the U.S.

Northwell Health, the largest healthcare provider in New York State, earlier in 2017 initiated a new biobank aimed at creating precision therapies against various types of cancer. Launched in collaboration with Indivumed, the biobank will provide catalogued biomaterials for research into lung, colorectal, breast, and pancreatic cancer. This would enable targeted, gene-specific studies of a variety of cancer samples, leading to a more comprehensive understanding of cancer. Such well-funded collaboration efforts are crucial for the developing biobanks market.

Global Biobanks Market: Geographical Dynamics

Led by the fertile healthcare research scenario in the U.S., North America is likely to retain a dominant share in the global biobanks market in the coming years. Steady support from institutes such as the NIH is likely to be vital for the North America biobanks market.

Emerging Asia Pacific economies such as India and China could emerge with a significant share in the global biobanks market in the coming years. The healthcare sector in both countries has received steady public or private funding in the last few years. India is also a global leader in medical tourism and is likely to receive an increasing number of patients in the coming years, leading to promising prospects for the global biobanks market in the region.

Global Biobanks Market: Competitive Dynamics

Due to the dynamic nature of the global biobanks market, with advancements in diagnostic fields often determining the direction of the market, the market is heavily fragmented. It is likely to retain a significant degree of fragmentation in the coming years thanks to the diversity in the application segments of the biobanks market. The leading players in the global biobanks market include BioCision, Tecan Group, VWR, Beckman Coulter Inc., and Thermo Fisher Scientific.

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Advancement: Know the Rapid Growth Factors of North America DNA Sequencing Market| Stay Up-To-Date With Emerging Trends Ahead – re:Jerusalem

October 28th, 2020 10:52 am

DNA sequencing is a molecular technique that helps to determine the nucleotide sequence of deoxyribonucleic acid (DNA), which is the fundamental unit of a gene or genome. DNA sequencing has led to a paradigm shift in molecular biology and genomics sectors. The knowledge of DNA sequences of genes and other parts of the genome of organisms has gained prominence in life science research as well as in applied fields, such as forensics, cancer diagnostics, and others. DNA sequencing is used for sequencing DNA strands and whole genomes as well as to study various DNAprotein interactions. Moreover, this technique enables researchers to focus, study, and interpret deep sequence target regions.

Furthermore, it is utilized in various interventions such as oncology, biomarker studies, drug discovery, reproductive health, and personalized genomics. The growth of the global DNA sequencing market is driven by technological advancements in sequencing equipment, surge in applications of DNA sequencing, and increase in genome mapping programs. In addition, rise in awareness pertaining to DNA sequencing and increase in investment in research, development, and innovation have supplemented the market growth. However, dearth of skilled professionals, ethical & legal limitations related to DNA sequencing, and standardization concerns in sequencing procedures impede the market growth.

Based on product, the consumable segment acquired the largest North America DNA sequencing market share in 2018 and constitute a dominant share in 2025 due to the use and necessity in sample preparation and in pre-requisite stages of DNA sequencing. The biomarker and cancer segment is the highest contributor to the North America DNA sequencing as a result of technological advancements and increase in DNA sequencing applications. The personalized medicine segment is anticipated to be a lucrative segment owing to the rise in use of precision medicine wherein the treatment takes in account the individuals variation in the genes, lifestyle and environment. Therefore, these factors contribute toward the growth of the North American DNA sequencing market.

According to technology, the sequencing by synthesis segment was the highest contributor to the North America DNA sequencing market owing to the wide use of DNA sequencing platforms in sequencing protocols and is likely to continue the dominance throughout the forecasting period. Moreover, the research institute segment was the highest contributor to the North America DNA sequencing in 2018 and is occupying the largest share in the North American DNA sequencing market due to the presence of large number of research centers in this region and ongoing research.

In 2018, U.S. occupied the largest share of the North America DNA sequencing market and is expected to maintain its dominance during the forecast period owing to the presence of DNA sequencing giants in this region and the rising incidences of genetic disorders and cancers amongst the population. On the other side, Mexico is estimated to register the fastest growth during the forecast period.

KEY FINDINGS OF THE STUDY-

The pediatrics segment accounted for more than half of the market share in 2018. U.S. and Canada collectively accounted major share of the North America DNA sequencing market in 2018 and is expected to maintain this trend throughout the forecast period. The pharmaceutical company in the end user segment is anticipated to grow at a high CAGR from 2018 to 2025. The biomarker and cancer segment accounted major able share of the market in 2018.

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Prognostic value of plasminogen activator inhibitor-1 in biomarker exploration using multiplex immunoassay in patients with metastatic renal cell…

October 28th, 2020 10:52 am

Vascular endothelial growth factor-directed therapies play a significant role in patients with metastatic renal cell carcinoma (mRCC). Biomarkers for predicting treatment efficacy and resistance are required to develop personalized medicine. We evaluated multiple serum cytokine levels in patients with mRCC treated with axitinib to explore predictive biomarkers.

From September 2012 to October 2015, serum samples were collected from 44 patients with mRCC before treatment and 4weeks after axitinib initiation. Bio-Plex Pro Human Cancer Biomarker Panels 1 and 2 were used to measure levels of 34 serum biomarkers related to angiogenesis and cell proliferation.

Patients with partial response or stable disease had significantly decreased serum plasminogen activator inhibitor-1 (PAI-1) level from pre-treatment to 4weeks after axitinib initiation compared with those with progressive disease (P = .022). The median progression-free survival (PFS) and median overall survival (OS) in patients with increased serum PAI-1 level from pre-treatment to 4weeks after axitinib initiation were significantly shorter than those with decreased serum PAI-1 level (P = .027 and P = .026, respectively). Increased serum PAI-1 level from pre-treatment to 4weeks after axitinib initiation was an independent prognostic marker for shorter PFS and OS in multivariate analyses (P = .015 and P = .032, respectively). The immunohistochemical staining intensity of PAI-1 in tumor specimens was significantly associated with Fuhrman grade and presence of distant metastasis (P = .026 and P = .010, respectively).

The initial change in serum PAI-1 level in the early stage of axitinib treatment could be a useful prognostic biomarker in patients with mRCC.

Health science reports. 2020 Oct 15*** epublish ***

Naoko Honma, Takamitsu Inoue, Norihiko Tsuchiya, Atsushi Koizumi, Ryohei Yamamoto, Taketoshi Nara, Sohei Kanda, Mingguo Huang, Kazuyuki Numakura, Mitsuru Saito, Shintaro Narita, Shigeru Satoh, Tomonori Habuchi

Department of Urology Akita University Graduate School of Medicine Akita Japan., Center for Kidney Disease and Transplantation Akita University Hospital Akita Japan.

PubMed http://www.ncbi.nlm.nih.gov/pubmed/33088925

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OncLive Partners with The Ruesch Center to Host the 11th Annual Ruesch Center Symposium – Business Wire

October 28th, 2020 10:52 am

CRANBURY, N.J.--(BUSINESS WIRE)--OncLive is pleased to announce it has partnered with The Ruesch Center for the Cure of Gastrointestinal (GI) Cancers to host the 11th Annual Ruesch Center Symposium Nov. 20-21.

We are honored to be able to work with The Ruesch Center to help transition their annual symposium into a virtual, interactive learning experience during this uncertain time, said Mike Hennessy Jr., president and CEO of MJH Life Sciences, the parent company of OncLive. The Ruesch Center is part of our exclusive strategic alliance partnership program, and this is a great example of how we can use our state-of-the-art studio to still deliver critical information to the gastrointestinal cancer community.

The educational symposium brings together clinicians, researchers, patients, caregivers, policymakers and industry representatives to network and debate critical issues related to GI cancers. Throughout the two-day virtual meeting, expert speakers will participate in three educational sessions addressing topics such as innovations in therapeutics, cancer genetics and targeted therapies, nuclear imaging and therapy for neuroendocrine tumors, and precision medicine.

The sessions include the following:

As a special highlight, the symposium will offer access to watch the 2020 Luminary Awards in GI Cancers ceremony. The five honorees, Richard M. Goldberg, M.D.; Gayle S. Jameson, MSN, RN, ACNP-BC, AOCN; Stacie C. Lindsey; Tyvin Rich, M.D., FACR; and Diane M. Simeone, M.D., will be presented with their awards and honored for their dedication to improving care for patients and families who are affected by GI cancers.

Finding more cures for GI cancer will only come through innovative research, and we are so proud to be featuring both the most up-to-date science and the projects of tomorrow. And as a bonus, we will be premiering our new POWER program, a short course in precision medicine to close our knowledge gaps in this rapidly evolving field, said John L. Marshall, M.D., director, The Ruesch Center for the Cure of GI Cancers.

This symposium has been approved for up to 11 AMA PRA Category 1 Credits and ANCC contact hours.

For more information and to register, click here.

About OncLive

A digital platform of resources for practicing oncologists, OncLive offers oncology professionals information they can use to help provide the best patient care. OncLive is a brand of MJH Life Sciences, the largest privately held, independent, full-service medical media company in North America dedicated to delivering trusted health care news across multiple channels.

About The Ruesch Center for the Cure of Gastrointestinal Cancers

The Ruesch Center for the Cure of Gastrointestinal Cancers is part of the Georgetown Lombardi Comprehensive Cancer Center. It focuses on personalized patient care and fighting against gastrointestinal cancers. The Ruesch Center provides the highest standard of care and individualized cures through clinical trials and research, education and advocacy, and regional and global alliances.

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DayTwo Science Cited in 10-Year $150 Million National Institutes of Health Precision Nutrition Strategic Plan – PRNewswire

October 28th, 2020 10:52 am

The NIH Strategic plan focuses on "Precision Nutrition What to Eat to Stay Healthy." NIH in conjunction with the Nutrition Research Task Force will partner with private and public organizations to accelerate nutrition science with the focus on precision medicine. The ambitious initiative looks to push forward the concept of individualized dietary recommendations to maximize health as well as prevent and combat disease.

"We are thrilled to be recognized by NIH as a pioneer in the field of precision nutrition. We look forward to supporting and participating in the ongoing research effort toward new discoveries," said Lihi Segal, CEO and founder of DayTwo.

Metabolic disease (diabetes, prediabetes, clinical obesity and NASH) impacts almost 3/4 of U.S. adults and costs the U.S. economy almost $700 billion a year. In the era of COVID-19, people with diabetes rank first and second at risk for hospitalizations and death if they contract the disease. Poor nutrition is a root cause of metabolic disease and according to the American Diabetes Association, food choices are the greatest stressor and have the greatest impact on daily life for people with diabetes.

DayTwo was founded as a result of a clinical trial published in Cell in 2015 entitled, "Personalized Nutrition by Prediction of Glycemic Responses." A follow-up clinical trial was published in the Journal of the American Medical Association in 2019 entitled, "Assessment of a Personalized Approach to Predicting Postprandial Glycemic Responses to Food." Both studies demonstrated that people respond differently to the same food, and the personalized response can be predicted using machine learning algorithms based on high resolution, gut microbiome profiling and additional clinical and personal parameters.

Employers and payers looking to learn more can contact Robert Boyer, vice president of Enterprise Solutions, at [emailprotected]. Or, visit http://www.daytwo.com/employers.

About DayTwo DayTwo is the only precision nutrition solution that enables a path to remission for metabolic disease. DayTwo's telehealth-centric, high touch / high tech solution employs machine learning algorithms based high resolution gut microbiome profiling and additional clinical and personal parameters, a care team of Certified Diabetes Care and Educational Specialists / Registered Dietitian Nutritionists skilled in behavioral coaching and a digital app to achieve outcomes. DayTwo offers up to 100% fees at risk for its solution.

For questions or comments about this release please contact [emailprotected] 415-426-4767.

SOURCE DayTwo

https://www.daytwo.com

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COVID-19 Is Redefining Healthcare Innovation – D Healthcare Daily

October 28th, 2020 10:52 am

COVID-19 has led to rapid changes in health care innovation: telemedicine, artificial intelligence, payment models, and a host of other digital analytics tools have morphed from experimental to borderline conventional.

At a panel during the 2020 North Texas State of Reform Virtual Health Policy Conference, health executives Tom Banning, chief executive officer of Texas Academy of Family Physicians,Dr. Andrew Masica, senior vice president of Texas Health Resources, and Dr. Steve Miff, president of Parkland Center for Clinical Innovation, met to discuss which of these developments will last beyond the pandemic.

Before COVID-19, telemedicine accounted for about one percent of health care visits, approximately 1.4 million visits. According to Tom Banning, seven months later, the nation has seen a three-fold increase in the use of telemedicine, accounting for about 35 million virtual visits.

I dont think theres any question that telemedicine is here to stay, Banning says. Its proven its effectiveness. Patients now expect to be able to connect with their doctors, and doctors see value in connecting with their patients.

Despite the high reliance on telehealth during the pandemic, health executives like Banning acknowledge that there are still workflow and payment methodologies to develop for telemedicine to become a scalable and viable innovation long term.

I dont think theres any question that telemedicine is here to stay.

Through partnerships and collaboration across healthcare organizations, leaders have rapidly applied predictive analytics to engage with the surrounding community.Its kind of ironic. Data and computers are helping deliver more personalized medicine, Dr. Andrew Masica says. If we do it the right way, thats a possibility for health systems.

The pandemic laid bare the need for high-speed data reports that allow primary care physicians to understand and digest patient information quickly. Through this innovation, healthcare providers and physicians can better leverage data, creating more personal interactions with patients.

There has been a paradigm shift, Masica says. We know the market and patient expectations are going to be different. Our challenge is to adapt to whats at hand. The underlying theme of where digital tools and innovation can help us is the push towards a more consumer and patient-centered health system with the ability to leverage data in real-time.

The development of proximity data has been crucial to understanding the viruss spread and defining vulnerability indexes. Initially, health officials attempted to track the virus by monitoring Americans international travel. With the virus rapid spread across the nation and relatively high case counts months later, these data tools have provided health experts with predictive tools to anticipate the virus and critical areas of concern.

It gives us something very actionable to do, Dr. Miff says. Predictive modeling is pretty simple. Based on a patients address, we can geo-map every single positive case, and then use a sophisticated machine learning formula to calculate distances to those positive cases and the density.

As the industry adapts to changes in innovation, health leaders are regularly evaluating the outcomes of these new measures to determine their effectiveness outside of controlled trials. Moving beyond the pandemics initial peak, further study will be necessary for defining these tools future use.Proof of efficacy isnt proof of effectiveness, Masica says. We need to be adopting and pushing digital innovations that are shown to be effective and rigorously assessing the outcomes of these technologies.

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