Nanoparticles in Biotechnology and Pharmaceuticals Market Size, Share, Growth, Trends, Outlook, Scope and Forecast to 2027 – The Haitian-Caribbean…

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Global Nanoparticles in Biotechnology and Pharmaceuticals Market: An analysis for future growth

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In market segmentation by manufacturers, the report covers the following companies-

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Nanoparticles in Biotechnology and Pharmaceuticals Market Size, Share, Growth, Trends, Outlook, Scope and Forecast to 2027 - The Haitian-Caribbean...

Reaping the promise of biotechnology – Business Mirror

IT has been nearly two decades since the Philippine government approved the sale and cultivation of genetically modified (GM) corn seeds in local farms. The government issued a permit to commercialize Monsanto Philippiness bacillus thuringiensis (Bt) corn variety dubbed YieldGard on December 5, 2002. With this, the Philippines earned the distinction of being the first in Asia to commercialize Bt corn, a variety that enables corn farmers to save on production cost because they will no longer have to extensively use pesticides to kill the corn borera grain pest, particularly of corn.

Bt corn has been largely instrumental in increasing farmers production in the ensuing years following the issuance of the permit to Monsanto. The increment in output allowed the Philippines to become self-sufficient in corn (See, Yellow corn yield achieved 103 percent self-sufficiency last yearPiol, in the BusinessMirror, March 28, 2018). With the help of the biotech product, farmers were able to earn $642 million from 2003 to 2015, according to the International Service for the Acquisition of Agri-biotech Applications.

Its advantages and its potential to boost incomes have encouraged more farmers to plant the variety in recent years. The United States Department of Agricultures Foreign Agricultural Service in Manila noted that areas planted with Bt corn in the Philippines expanded by 26 percent to 834,617 hectares this year (See, Gain report: GE corn areas in PHL continue to expand, in the BusinessMirror, November 30, 2020). The availability of more yellow corna raw material used in manufacturing animal feedshas also supported the growing livestock and poultry industry.

These developments illustrate the benefits of biotechnology as well as its potential to enable the Philippines to develop other products that will allow farmers to diversify to other crops as well as cope with the ill effects of climate change. Currently, Bt corn is the only biotech product that is being planted in the Philippines. The GM varieties of other crops, like eggplant, are in various stages of development.

It is also worth noting that the Bt corn variety that was approved for commercialization in 2002 was made in the United States. The Philippines has yet to develop its own GM crop, and we urge Philippine researchers and scientists to make biotech products that are tailor fit to local conditions. Government must support these efforts by putting more money in the research initiatives of our local scientists or introduce policies, such as incentives, that will encourage the private sector to partner with them.

The recent successive typhoons that struck the Philippines should serve as a stark reminder of the increasing difficulties being faced by Filipino farmers and the pressing need for government to look for more sustainable means of ensuring food security. We welcome the Department of Agricultures (DA) pronouncement that it will optimize the use of biotechnology and other science-based solutions to increase farm output from limited farmlands and fishing grounds.

We urge Congress to support the DAs initiatives by passing the proposed Modern Biotechnology Act and by increasing the budget for agricultural research and development. Fully supported, our own scientists can harness the power of modern biotechnology.

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Reaping the promise of biotechnology - Business Mirror

Is Cellectar Biosciences Inc (CLRB) Stock Near the Top of the Biotechnology Industry? – InvestorsObserver

A rating of 80 puts Cellectar Biosciences Inc (CLRB) near the top of the Biotechnology industry according to InvestorsObserver. Cellectar Biosciences Inc's score of 80 means it scores higher than 80% of stocks in the industry. Cellectar Biosciences Inc also received an overall rating of 65, putting it above 65% of all stocks. Biotechnology is ranked 35 out of the 148 industries.

Finding the best stocks can be tricky. It isnt easy to compare companies across industries. Even companies that have relatively similar businesses can be tricky to compare sometimes. InvestorsObservers tools allow a top-down approach that lets you pick a metric, find the top sector and industry and then find the top stocks in that sector.

This ranking system incorporates numerous factors used by analysts to compare stocks in greater detail. This allows you to find the best stocks available in any industry with relative ease. These percentile-ranked scores using both fundamental and technical analysis give investors an easy way to view the attractiveness of specific stocks. Stocks with the highest scores have the best evaluations by analysts working on Wall Street.

Cellectar Biosciences Inc (CLRB) stock is trading at $2.29 as of 2:18 PM on Thursday, Dec 3, an increase of $0.34, or 17.18% from the previous closing price of $1.95. The stock has traded between $1.95 and $2.40 so far today. Volume today is high. So far 8,826,004 shares have traded compared to average volume of 928,593 shares.

Click Here to get the full Stock Score Report on Cellectar Biosciences Inc (CLRB) Stock.

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Is Cellectar Biosciences Inc (CLRB) Stock Near the Top of the Biotechnology Industry? - InvestorsObserver

Is Sutro Biopharma Inc (STRO) the Top Pick in the Biotechnology Industry? – InvestorsObserver

Sutro Biopharma Inc (STRO) is near the top in its industry group according to InvestorsObserver. STRO gets an overall rating of 65. That means it scores higher than 65 percent of stocks. Sutro Biopharma Inc gets a 81 rank in the Biotechnology industry. Biotechnology is number 35 out of 148 industries.

Searching for the best stocks to invest in can be difficult. There are thousands of options and it can be confusing on what actually constitutes a great value. Investors Observer allows you to choose from eight unique metrics to view the top industries and the best performing stocks in that industry. A score of 65 would rank higher than 65 percent of all stocks.

Our proprietary scoring system captures technical factors, fundamental analysis and the opinions of analysts on Wall Street. This makes InvestorsObservers overall rating a great way to get started, regardless of your investing style. Percentile-ranked scores are also easy to understand. A score of 100 is the top and a 0 is the bottom. Theres no need to try to remember what is good for a bunch of complicated ratios, just pay attention to which numbers are the highest.

Sutro Biopharma Inc (STRO) stock is trading at $16.67 as of 12:19 PM on Thursday, Dec 3, a gain of $0.32, or 1.96% from the previous closing price of $16.35. The stock has traded between $16.23 and $17.59 so far today. Volume today is 309,465 compared to average volume of 322,449.

Click Here to get the full Stock Score Report on Sutro Biopharma Inc (STRO) Stock.

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Is Sutro Biopharma Inc (STRO) the Top Pick in the Biotechnology Industry? - InvestorsObserver

The vaccines of tomorrow: how to invest in biotechnology – Rask Media

Biotechnology has experienced extraordinary growth in recent times and came to popular attention as companies raced to find vaccines and cures for COVID-19. While investing in this area has obvious appeal from a social and moral perspective, it can also be a highly lucrative space as a growth investment in a portfolio.

Biotechnology specifically refers to technologies that use biological processes, capturing companies that focus on research, development, manufacturing and/or marketing of products based on biological and genetic information. The different types of biotechnology include biological drugs, vaccines, immunotherapy, gene therapy, orphan drugs and genetic engineering.

Biotechnology is predicted to be valued at more than US$833.34bn by 2027, compared to US$447.92 billion at the end of 2019, and will continue to grow, driven by the growing global population and the need for affordable, effective treatments and vaccines.Biotechnology will also be a beneficiary of population aging, particularly in Western countries. The reason for this is that an increase in the volume of older citizens is likely to have an accompanying and proportional increase in the volume of age-related diseases such as cardiovascular disease, dementia or arthritis, all requiring treatment.

Gilead is one example of a company with prospects in this space. Gilead is already well-known for its highly effective HIV treatments but is also targeting US and European approvals to market a drug called Filgotinib to treat rheumatoid arthritis.

In a demonstration of the growth in this industry, this year alone, 30-35 biotechnology companies are anticipated to go public, raising approximately US$3.5 billion.

The healthcare sector as a whole is likely to see greater investment as a result of the COVID-19 pandemic. For example, national health spending growth in the US is expected to average 5.4% annually through 2028, reaching US$6 trillion a year. Biotechnology will also be a beneficiary of this increased investment.

Investment and value from biotechnology is expected to grow in the coming years. While the trend already existed due to continuous tech improvements and the needs of a growing population, the COVID-19 pandemic has created a new spotlight on this area which may accelerate its growth.

Australian investors are likely to already be exposed to this growth segment in the concentrated domestic market. However, they may be missing exposure to the US, which dominates the global market for biotechnology.

Biotechnology could be considered part of a sector allocation to healthcare, or investors might view it as a thematic investment. You can find more information about thematic investing and using it in your portfolio in our latest whitepaper.

There are a range of ways to access the biotechnology industry.Investors could consider direct shares in biotechnology companies or alternatively consider managed funds. Direct shares can be a high-risk approach due to the high failure rates of drug testing and long periods of development (i.e., long periods where there may be no or a limited return on investment). Theres also the element of chance has the investor picked the winner? It could take years to know.

Managed investments, be it actively managed funds or passive options like ETFs, can assist in managing risk by spreading it across a larger number of companies. Investors could choose to invest by taking a sector approach and investing in a fund focusing on broader healthcare, or look at industry-specific options focusing on biotechnology. ETFS S&P Biotech ETF (ASX Code: CURE) is one such example that offers broad exposure to US biotechnology.

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The vaccines of tomorrow: how to invest in biotechnology - Rask Media

Department Of Biotechnology’s Expert Committee Tracking Developments Related To COVID-19 Vaccine: Official | News – Swachh India NDTV

Maharashtra

DistrictCases

Mumbai45,478

Thane13,660

Pune9,920

Mumbai Suburban5,363

Aurangabad1,974

Nashik1,575

Raigad1,462

Palghar1,421

Solapur1,291

Jalgaon1,039

Akola757

Nagpur692

Kolhapur646

Satara629

Ratnagiri350

Amravati291

Dhule228

Hingoli208

Jalna201

Ahmednagar190

Nanded176

Yavatmal150

Sangli145

Latur139

Osmanabad125

Sindhudurg114

Buldhana88

Parbhani78

gondia69

Beed54

Nandurbar42

Gadchiroli42

Bhandara41

Chandrapur32

Washim13

Wardha11

18,52,266 4,757

81,162 2,769

17,23,370 7,486

47,734 40

DistrictCases

Udupi1,176

Kalaburagi669

Yadgir538

Bengaluru Urban529

Raichur369

Mandya346

Belagavi337

Bidar219

Hassan205

Davangere204

Vijayapura201

Dakshina Kannada179

Chikkaballapura149

Mysuru107

Bagalkote103

Uttara Kannada95

Shivamogga67

Dharwad61

Ballari60

Gadag45

Bengaluru Rural40

Tumakuru36

Kolar29

Haveri24

Chikkamagaluru19

Chitradurga14

Koppal5

Kodagu4

Ramanagara3

Chamarajanagara0

8,93,006 1,321

25,400 422

8,55,750 889

11,856 10

DistrictCases

Kurnool795

Krishna557

Guntur511

Anantapur428

East Godavari356

Chittoor319

Sri Potti Sriramulu Nell*296

Y.S.R.205

West Godavari199

Srikakulam183

Prakasam104

Visakhapatnam103

Vizianagaram23

8,71,972 667

5,910 256

8,59,029 914

7,033 9

DistrictCases

Chennai23,324

Chengalpattu1,314

Thiruvallur774

Villupuram509

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Department Of Biotechnology's Expert Committee Tracking Developments Related To COVID-19 Vaccine: Official | News - Swachh India NDTV

Food Biotechnology Industry Market Growth Projection from 2020 to 2026 – Cheshire Media

Market Study Report, LLC adds latest research report on Food Biotechnology Industry Market, which delivers a comprehensive study on current industry trends. The outcome also includes revenue forecasts, statistics, market valuations which illustrates its growth trends and competitive landscape as well as the key players in the business.

This Food Biotechnology Industry market research study is a collection of insights that translate into a gist of this industry. It is explained in terms of a plethora of factors, some of which include the present scenario of this marketplace in tandem with the industry scenario over the forecast timeframe.

Request a sample Report of Food Biotechnology Industry Market at:https://www.marketstudyreport.com/request-a-sample/2727907?utm_source=cheshire.media&utm_medium=Ram

The report is also inclusive of some of the major development trends that characterize the Food Biotechnology Industry market. A comprehensive document in itself, the Food Biotechnology Industry market research study also contains numerous other pointers such as the current industry policies in conjunction with the topographical industry layout characteristics. Also, the Food Biotechnology Industry market study is comprised of parameters such as the impact of the current market scenario on investors.

The pros and cons of the enterprise products, a detailed scientific analysis pertaining to the raw material as well as industry downstream buyers, in conjunction with a gist of the enterprise competition trends are some of the other aspects included in this report.

How has the competitive landscape of this industry been categorized?

, as per the report.

Regional landscape: How will the details provided in the report help prominent stakeholders?

Ask for Discount on Food Biotechnology Industry Market Report at:https://www.marketstudyreport.com/check-for-discount/2727907?utm_source=cheshire.media&utm_medium=Ram

Other pivotal aspects encompassed in the Food Biotechnology Industry market study:

.

.

For More Details On this Report: https://www.marketstudyreport.com/reports/covid-19-outbreak-global-food-biotechnology-industry-market-report-development-trends-threats-opportunities-and-competitive-landscape-in-2020

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Food Biotechnology Industry Market Growth Projection from 2020 to 2026 - Cheshire Media

Where Does Agenus Inc (AGEN) Stock Fall in the Biotechnology Field? – InvestorsObserver

The 62 rating InvestorsObserver gives to Agenus Inc (AGEN) stock puts it near the top of the Biotechnology industry. In addition to scoring higher than 76 percent of stocks in the Biotechnology industry, AGENs 62 overall rating means the stock scores better than 62 percent of all stocks.

Trying to find the best stocks can be a daunting task. There are a wide variety of ways to analyze stocks in order to determine which ones are performing the strongest. Investors Observer makes the entire process easier by using percentile rankings that allows you to easily find the stocks who have the strongest evaluations by analysts.

These scores are not only easy to understand, but it is easy to compare stocks to each other. You can find the best stock in an industry, or look for the sector that has the highest average score. The overall score is a combination of technical and fundamental factors that serves as a good starting point when analyzing a stock. Traders and investors with different goals may have different goals and will want to consider other factors than just the headline number before making any investment decisions.

Agenus Inc (AGEN) stock is down -1.52% while the S&P 500 is higher by 0.15% as of 12:22 PM on Thursday, Dec 3. AGEN is down -$0.06 from the previous closing price of $3.63 on volume of 1,217,123 shares. Over the past year the S&P 500 has risen 18.04% while AGEN is down -9.14%. AGEN lost -$1.09 per share the over the last 12 months.

Click Here to get the full Stock Score Report on Agenus Inc (AGEN) Stock.

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Where Does Agenus Inc (AGEN) Stock Fall in the Biotechnology Field? - InvestorsObserver

Estimating The Fair Value Of Universal Vision Biotechnology Co., Ltd. (GTSM:3218) – Simply Wall St

How far off is Universal Vision Biotechnology Co., Ltd. (GTSM:3218) from its intrinsic value? Using the most recent financial data, we'll take a look at whether the stock is fairly priced by taking the forecast future cash flows of the company and discounting them back to today's value. Our analysis will employ the Discounted Cash Flow (DCF) model. Before you think you won't be able to understand it, just read on! It's actually much less complex than you'd imagine.

Companies can be valued in a lot of ways, so we would point out that a DCF is not perfect for every situation. If you still have some burning questions about this type of valuation, take a look at the Simply Wall St analysis model.

View our latest analysis for Universal Vision Biotechnology

We are going to use a two-stage DCF model, which, as the name states, takes into account two stages of growth. The first stage is generally a higher growth period which levels off heading towards the terminal value, captured in the second 'steady growth' period. To start off with, we need to estimate the next ten years of cash flows. Where possible we use analyst estimates, but when these aren't available we extrapolate the previous free cash flow (FCF) from the last estimate or reported value. We assume companies with shrinking free cash flow will slow their rate of shrinkage, and that companies with growing free cash flow will see their growth rate slow, over this period. We do this to reflect that growth tends to slow more in the early years than it does in later years.

A DCF is all about the idea that a dollar in the future is less valuable than a dollar today, so we need to discount the sum of these future cash flows to arrive at a present value estimate:

("Est" = FCF growth rate estimated by Simply Wall St)Present Value of 10-year Cash Flow (PVCF) = NT$10.0b

After calculating the present value of future cash flows in the initial 10-year period, we need to calculate the Terminal Value, which accounts for all future cash flows beyond the first stage. The Gordon Growth formula is used to calculate Terminal Value at a future annual growth rate equal to the 5-year average of the 10-year government bond yield of 0.9%. We discount the terminal cash flows to today's value at a cost of equity of 6.6%.

Terminal Value (TV)= FCF2030 (1 + g) (r g) = NT$1.7b (1 + 0.9%) (6.6% 0.9%) = NT$31b

Present Value of Terminal Value (PVTV)= TV / (1 + r)10= NT$31b ( 1 + 6.6%)10= NT$16b

The total value is the sum of cash flows for the next ten years plus the discounted terminal value, which results in the Total Equity Value, which in this case is NT$26b. The last step is to then divide the equity value by the number of shares outstanding. Relative to the current share price of NT$286, the company appears about fair value at a 17% discount to where the stock price trades currently. The assumptions in any calculation have a big impact on the valuation, so it is better to view this as a rough estimate, not precise down to the last cent.

Now the most important inputs to a discounted cash flow are the discount rate, and of course, the actual cash flows. You don't have to agree with these inputs, I recommend redoing the calculations yourself and playing with them. The DCF also does not consider the possible cyclicality of an industry, or a company's future capital requirements, so it does not give a full picture of a company's potential performance. Given that we are looking at Universal Vision Biotechnology as potential shareholders, the cost of equity is used as the discount rate, rather than the cost of capital (or weighted average cost of capital, WACC) which accounts for debt. In this calculation we've used 6.6%, which is based on a levered beta of 0.800. Beta is a measure of a stock's volatility, compared to the market as a whole. We get our beta from the industry average beta of globally comparable companies, with an imposed limit between 0.8 and 2.0, which is a reasonable range for a stable business.

Valuation is only one side of the coin in terms of building your investment thesis, and it is only one of many factors that you need to assess for a company. It's not possible to obtain a foolproof valuation with a DCF model. Preferably you'd apply different cases and assumptions and see how they would impact the company's valuation. For example, changes in the company's cost of equity or the risk free rate can significantly impact the valuation. For Universal Vision Biotechnology, we've put together three further elements you should further research:

PS. Simply Wall St updates its DCF calculation for every Taiwanese stock every day, so if you want to find the intrinsic value of any other stock just search here.

PromotedIf you decide to trade Universal Vision Biotechnology, use the lowest-cost* platform that is rated #1 Overall by Barrons, Interactive Brokers. Trade stocks, options, futures, forex, bonds and funds on 135 markets, all from a single integrated account.

This article by Simply Wall St is general in nature. It does not constitute a recommendation to buy or sell any stock, and does not take account of your objectives, or your financial situation. We aim to bring you long-term focused analysis driven by fundamental data. Note that our analysis may not factor in the latest price-sensitive company announcements or qualitative material. Simply Wall St has no position in any stocks mentioned. *Interactive Brokers Rated Lowest Cost Broker by StockBrokers.com Annual Online Review 2020

Have feedback on this article? Concerned about the content? Get in touch with us directly. Alternatively, email editorial-team@simplywallst.com.

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Estimating The Fair Value Of Universal Vision Biotechnology Co., Ltd. (GTSM:3218) - Simply Wall St

Where Does Amarin Corporation plc (AMRN) Stock Fall in the Biotechnology Field? – InvestorsObserver

Amarin Corporation plc (AMRN) is around the bottom of the Biotechnology industry according to InvestorsObserver. AMRN received an overall rating of 34, which means that it scores higher than 34 percent of all stocks. Amarin Corporation plc also achieved a score of 26 in the Biotechnology industry, putting it above 26 percent of Biotechnology stocks. Biotechnology is ranked 35 out of the 148 industries.

Trying to find the best stocks can be a daunting task. There are a wide variety of ways to analyze stocks in order to determine which ones are performing the strongest. Investors Observer makes the entire process easier by using percentile rankings that allows you to easily find the stocks who have the strongest evaluations by analysts.

This ranking system incorporates numerous factors used by analysts to compare stocks in greater detail. This allows you to find the best stocks available in any industry with relative ease. These percentile-ranked scores using both fundamental and technical analysis give investors an easy way to view the attractiveness of specific stocks. Stocks with the highest scores have the best evaluations by analysts working on Wall Street.

Amarin Corporation plc (AMRN) stock is trading at $4.97 as of 12:11 PM on Thursday, Dec 3, a rise of $0.13, or 2.79% from the previous closing price of $4.84. The stock has traded between $4.84 and $5.06 so far today. Volume today is less active than usual. So far 3,157,880 shares have traded compared to average volume of 6,785,044 shares.

Click Here to get the full Stock Score Report on Amarin Corporation plc (AMRN) Stock.

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Where Does Amarin Corporation plc (AMRN) Stock Fall in the Biotechnology Field? - InvestorsObserver

AVM Biotechnology President Selected to Speak at ESWI Conference in Novel and Outstanding Discoveries Track – PRNewswire

I'm honored to be able to present our data, which speaks to the broad and significant potential of AVM0703, Dr. Deisher

Dr. Deisher's presentation entitled "Acute Suprapharmacologic Dexamethasone Mobilizes Natural Killer T and Cytotoxic T cells for Influenza A/B-induced or COVID-19-induced Acute Respiratory Distress Syndrome (ARDS)" will be streamed live during the conference on December 9th.

"I'm honored to be able to present our data, which speaks to the importance of the work being done at the company as well as the broad and significant potential of AVM0703," Dr. Deisher said.

Acute suprapharmacologic dexamethasone sodium phosphate as AVM0703 mobilizes very active Natural Killer T-cells (NKT) and cytotoxic T-cells. Low doses of generic dexamethasone are currently the standard of care in COVID-19 disease and mitigate cytokine release that can trigger ARDS. The high dose of dexamethasone provided by AVM0703 is expected to provide an added benefit to these patients because NKT cells are programmed to eliminate abnormal cells, whether cancer or virus-infected, or autoreactive cells. Rapid elimination of infected monocytes in COVID-19 patients could reduce ICU stays and decrease long-term lung damage as well as provide long term immunity. Since this treatment is microbial strain independent, it could provide an immediate therapy for future pandemics. AVM Biotechnology is currently enrolling patients with Relapsed Refractory Non-Hodgkin's Lymphoma at several US sites, and has received FDA approval to treat moderate to severe ARDS due to COVID-19 or Influenza, enrolling Q1 2021.

AVM0703 is a patent pending, innovative formulation of dexamethasone. This proprietary formulation does not contain excipients such as benzyl alcohol and parabens used in generic formulations which preclude the safe use of generic versions at the acute doses required to mobilize the AVM0703 novel immune cells. AVM0703 is expected to have therapeutic effects in a variety of blood cancers, solid tumors, Type 1 Diabetes, and infectious diseases. Despite the availability of vaccines and anti-virals, influenza continues to lead to ARDS in a substantial number of patients each year. COVID-19 induced ARDS is also likely to continue to be problematic, even after vaccines are available.

AVM Biotechnology is led by Dr. Theresa Deisher, a biotech veteran with a productive history including 47 patents and four discoveries in clinical trials. AVM's COO, Janet R. Rea, has a proven track record working with federal regulators and successfully bringing drugs to market. The Executive Board is comprised of world leaders in the areas of respiratory illness, regulatory affairs, and vaccine development, and AVM is guided by a global Advisory Board that includes well-respected leaders in the areas of cancer and immunology. The company has received two federal SBIR grants and holds eight worldwide patent families protecting its intellectual property. AVM is committed to transforming the future of immunotherapy while reducing the potential for undesirable treatment side effects.

Contact Jena Dalpez Director of Communications and Public Relations [emailprotected]

This contains certain statements that constitute "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. These statements do not relate strictly to historical or current facts and they may be accompanied by words such as "could," "would," "may," "potentially," "suggest," "believes," "expects," "should," and similar words or expressions. These forward-looking statements reflect our current views as of the date this is published, and are subject to risks, uncertainties, assumptions, changes in circumstances, and other factors; drug development and commercialization are highly risky and early clinical results in animals or humans may not reflect the full results from later stage or larger scale clinical trials. These forward-looking statements are subject to risks and uncertainties that could cause our actual results, performance, and expectations to differ materially from those expressed or implied by these statements, including statements about: future and ongoing drug development and timing; the applications of drugs to specific diseases; the potential for ongoing preclinical or clinical trial results; FDA or other regulatory findings and approvals; potential market opportunities; and the occurrence of future events or circumstances. There are risks and uncertainties involving and not limited to our ability to progress in our research and development efforts, complete clinical testing, achieve our expected results, commercialize our products, avoid infringement of patients, trademarks and other proprietary rights of third parties, protect products from competition, navigate the political environment, maintain sufficient capital and funding, avoid problems with our manufacturing processes, maintain our operations, and obtain regulatory approval to sell and market the drugs in the United States and elsewhere. The reader should not place any undue reliance on such forward-looking statements. We have no obligation to release publicly the results of any revisions to any of our forward-looking statements to reflect events or circumstances after the date these statements are made or to reflect the occurrence of unanticipated events, except as may be required by law.

SOURCE AVM Biotechnology, LLC

http://www.avmbiotech.com

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AVM Biotechnology President Selected to Speak at ESWI Conference in Novel and Outstanding Discoveries Track - PRNewswire

Where Does Tauriga Sciences Inc (TAUG) Stock Fall in the Biotechnology Field? – InvestorsObserver

The 5 rating InvestorsObserver gives to Tauriga Sciences Inc (TAUG) stock puts it near the bottom of the Biotechnology industry. In addition to scoring higher than 4 percent of stocks in the Biotechnology industry, TAUGs 5 overall rating means the stock scores better than 5 percent of all stocks.

Searching for the best stocks to invest in can be difficult. There are thousands of options and it can be confusing on what actually constitutes a great value. Investors Observer allows you to choose from eight unique metrics to view the top industries and the best performing stocks in that industry. A score of 5 would rank higher than 5 percent of all stocks.

These rankings allows you to easily compare stocks and view what the strengths and weaknesses are of a given company. This lets you find the stocks with the best short and long term growth prospects in a matter of seconds. The combined score incorporates technical and fundamental analysis in order to give a comprehensive overview of a stocks performance. Investors who then want to focus on analysts rankings or valuations are able to see the separate scores for each section.

Tauriga Sciences Inc (TAUG) stock is unmoved -5% while the S&P 500 is down -0.21% as of 11:20 AM on Wednesday, Dec 2. TAUG is unmoved $0.00 from the previous closing price of $0.03 on volume of 482,338 shares. Over the past year the S&P 500 is higher by 18.16% while TAUG is unmoved 0.00%. TAUG lost -$0.04 per share the over the last 12 months.

Click Here to get the full Stock Score Report on Tauriga Sciences Inc (TAUG) Stock.

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Where Does Tauriga Sciences Inc (TAUG) Stock Fall in the Biotechnology Field? - InvestorsObserver

Agricultural Biotechnology Market Research Report: Overview With Geographical Segmentation By Revenue With Forecast 2026 – The Haitian-Caribbean News…

The researchoffers a comprehensive analysis of the Agricultural BiotechnologyMarket. Bringing out the complete key insights of the industry, the report aims to provide an insight into the latest trends, current market scenario, and technologies related to the market. In addition, it helps the venture capitalists to understand the revenue opportunities across different segments to make better decisions. Global Agricultural Biotechnology market provides a detailed report which covers market analyses before COVID19 & opportunities after this pandemic. With COVID-19 pandemic, many industries are transforming rapidly. The Global Agricultural Biotechnology Market is one of the major industries undergoing changes. This year many industries have vanished entirely from the market and many industries have risen.

Moreover, the government-backed schemes throughout the globe are offering many advantages to businesses. As the governing bodies are supporting the industries, it be a strong pillar to support the market growth of Agricultural Biotechnology in the upcoming decade (2020-2026). Organizations planning to move into new market segments can take the help of market indicators to draw a business plan. With the technological boom, new markets are blossoming across the globe, making it a breeding ground for new businesses.

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Global Agricultural Biotechnology Market 2020: Covering both the industrial and the commercial aspects of the Global Agricultural Biotechnology Market, the report encircles several crucial chapters that give the report an extra edge. The Global Agricultural Biotechnology Market report deep dives into several parts of the report that plays a crucial role in getting the holistic view of the report. The list of such crucial aspects of the report includes company profile, industry analysis, competitive dashboard, comparative analysis of the key players, regional analysis with further analysis country wise.

Global Agricultural Biotechnology Market Analysis by Key Players:

Moreover, one of the uniqueness in the report is that it also covers the country-level analysis of the regulatory scenario, technology penetration, predictive trends, and prescriptive trends. This not only gives the readers of the report the actual real-time insights but also gives country-wise analysis, that plays a vital role in decision making. The inclusion of the report is not limited to the above mention key pointers. The report also emphasizes on the market opportunities, porters five forces, and analysis of the different types of products and application of the Global Agricultural Biotechnology Market.

The report splits by major applications:

Then report analyzed by types:

Any questions or want to Customization on this report, just speak with analyst @ https://www.in4research.com/speak-to-analyst/9515

Global Agricultural Biotechnology Market Report is a professional and in-depth research report on the worlds major regional market conditions of the Agricultural Biotechnology industry, focusing on the main regions and the main countries as Follows:

COVID-19 Impact on Agricultural Biotechnology Market:

The outbreak of COVID-19 has brought along a global recession, which has impacted several industries. Along with this impact COVID Pandemic has also generated few new business opportunities for Agricultural Biotechnology Market. Overall competitive landscape and market dynamics of Agricultural Biotechnology has been disrupted due to this pandemic. All these disruptions and impacts has been analysed quantifiably in this report, which is backed by market trends, events and revenue shift analysis. COVID impact analysis also covers strategic adjustments for Tier 1, 2 and 3 players of Agricultural Biotechnology Market.

Get Brief Information on Pre COVID-19 Analysis and Post COVID-19 Opportunities in Agricultural Biotechnology Market @ https://www.in4research.com/impactC19-request/9515

Table of Contents Includes Major Pointes as follows:

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Agricultural Biotechnology Market Research Report: Overview With Geographical Segmentation By Revenue With Forecast 2026 - The Haitian-Caribbean News...

Gear up for the change! Unity Biotechnology Inc. (UBX) has hit the volume of 830077 – The InvestChronicle

Lets start up with the current stock price of Unity Biotechnology Inc. (UBX), which is $5.97 to be very precise. The Stock rose vividly during the last session to $6.55 after opening rate of $5.74 while the lowest price it went was recorded $5.74 before closing at $6.36.

Recently in News on November 4, 2020, UNITY Biotechnology, Inc. Reports Third Quarter 2020 Financial Results and Clinical Program Updates. UNITY Biotechnology, Inc. (UNITY) [NASDAQ:UBX], a biotechnology company developing therapeutics to slow, halt or reverse diseases of aging, today reported financial results for the third quarter ended September 30, 2020. You can read further details here

Unity Biotechnology Inc. had a pretty Dodgy run when it comes to the market performance. The 1-year high price for the companys stock is recorded $15.44 on 08/10/20, with the lowest value was $2.72 for the same time period, recorded on 08/24/20.

Price records that include history of low and high prices in the period of 52 weeks can tell a lot about the stocks existing status and the future performance. Presently, Unity Biotechnology Inc. shares are logging -61.37% during the 52-week period from high price, and 119.30% higher than the lowest price point for the same timeframe. The stocks price range for the 52-week period managed to maintain the performance between $2.72 and $15.44.

The companys shares, operating in the sector of Healthcare managed to top a trading volume set approximately around 830077 for the day, which was evidently higher, when compared to the average daily volumes of the shares.

When it comes to the year-to-date metrics, the Unity Biotechnology Inc. (UBX) recorded performance in the market was -11.79%, having the revenues showcasing 110.60% on a quarterly basis in comparison with the same period year before. At the time of this writing, the total market value of the company is set at 298.98M, as it employees total of 76 workers.

During the last month, 5 analysts gave the Unity Biotechnology Inc. a BUY rating, 0 of the polled analysts branded the stock as an OVERWEIGHT, 1 analysts were recommending to HOLD this stock, 0 of them gave the stock UNDERWEIGHT rating, and 0 of the polled analysts provided SELL rating.

According to the data provided on Barchart.com, the moving average of the company in the 100-day period was set at 5.37, with a change in the price was noted -1.83. In a similar fashion, Unity Biotechnology Inc. posted a movement of -23.22% for the period of last 100 days, recording 1,269,373 in trading volumes.

Total Debt to Equity Ratio (D/E) can also provide valuable insight into the companys financial health and market status. The debt to equity ratio can be calculated by dividing the present total liabilities of a company by shareholders equity. Debt to Equity thus makes a valuable metrics that describes the debt, company is using in order to support assets, correlating with the value of shareholders equity The total Debt to Equity ratio for UBX is recording 0.25 at the time of this writing. In addition, long term Debt to Equity ratio is set at 0.25.

Raw Stochastic average of Unity Biotechnology Inc. in the period of last 50 days is set at 80.52%. The result represents improvement in oppose to Raw Stochastic average for the period of the last 20 days, recording 76.41%. In the last 20 days, the companys Stochastic %K was 88.45% and its Stochastic %D was recorded 90.89%.

Lets take a glance in the erstwhile performances of Unity Biotechnology Inc., multiple moving trends are noted. Year-to-date Price performance of the companys stock appears to be encouraging, given the fact the metric is recording -11.79%. Additionally, trading for the stock in the period of the last six months notably deteriorated by -32.20%, alongside a downfall of -12.88% for the period of the last 12 months. The shares increased approximately by 34.46% in the 7-day charts and went down by 59.80% in the period of the last 30 days. Common stock shares were driven by 110.60% during last recorded quarter.

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Gear up for the change! Unity Biotechnology Inc. (UBX) has hit the volume of 830077 - The InvestChronicle

Impact of Covid-19 on Biotechnology Separation Systems Market 2020 | Top Business Growing Strategies, Technological Innovation and Emerging Trends of…

Up-To-Date research on Biotechnology Separation Systems Market 2020-2026 :

The Reputed Garner Insights website offers vast reports on different market.They cover all industry and these reports are very precise and reliable. It also offers Biotechnology Separation Systems Market Report 2020 in its research report store. It is the most comprehensive report available on this market. The report study provides information on market trends and development, drivers, capacities, technologies, and on the changing investment structure of the Global Biotechnology Separation Systems Market.

The market is segmented into different sections such as: by product type, by application, by end-users, by deployment mode, and by key geography. The report then employs market breakdown and data triangulation procedures to complete the overall market engineering process and arrive at the exact statistics for all segments and sub-segments. The report on the Global Biotechnology Separation Systems Markethas been curated by analyzing the top players functioning in the market. In order to get an in-depth analysis of the market, the report carried out SWOT analysis, Porters five forces analysis, and Pestel analysis.

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Some of the major geographies included in the market are given below:North America (U.S., Canada)Europe (U.K., Germany, France, Italy)Asia Pacific (China, India, Japan, Singapore, Malaysia)Latin America (Brazil, Mexico)Middle East & Africa

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Components of the Biotechnology Separation Systems Market report:-A detailed assessment of all opportunities and risk in this Market.-Recent innovations and major events-A comprehensive study of business strategies for the growth of the Biotechnology Separation Systems leading market players.-Conclusive study about the growth plot of Biotechnology Separation Systems Market for the upcoming years.-Understanding of Biotechnology Separation Systems Industry-particular drivers, constraints and major micro markets in detail.-An evident impression of vital technological and latest market trends striking theMarket.

The objectives of the study are as follows:

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Utah District Court Dismisses Putative Securities Class Action Against Biotechnology Firm For Failure To Allege Falsity And Loss Causation – JD Supra

On November 22, 2020, Judge Howard C. Nielson, Jr. of the United States District Court for the District of Utah dismissed with prejudice a putative class action asserting claims under the Securities Exchange Act of 1934 against a biotechnology company and certain of its executives. In re PolarityTE, Inc. Sec. Litig., No. 2:18-cv-00510, 2020 WL 6873798 (D. Utah Nov. 22, 2020). Plaintiffs alleged that the company made material misstatements in the course of a reverse merger and in subsequent SEC filings. The Court held that plaintiffs failed to adequately allege falsity with respect to certain challenged statements and failed to establish loss causation for the remainder.

Plaintiffs alleged that the company made misstatements concerning: (1) the companys registration of a product with the FDA under a particular provision of the Public Health Service Act, which the company ultimately abandoned and refiled under a different provision after the FDA disagreed with the companys original approach, id. at *3-4; (2) the quality of the companys manufacturing facilities, in light of violations reported by the FDA, id. at *4; (3) the companys patents, including with respect to an application for which the company had received a non-final rejection a week before the merger closed and subsequently received a final rejection, id. at *2; and (4) the non-existence of any pending or contemplated government proceedings against the company, in light of the company having received a document request from the SEC after reporting to the SEC suspicious trading of its stock. Id. at *5.

The Court first assessed the companys statements regarding its products registration with the FDA and concluded that plaintiffs likely failed to allege a material misstatement, id. at *8, because the challenged statements were either true (to the extent they preceded the companys announcement that it intended to proceed under a different regulatory scheme) or constituted statements of opinion as to whether it was appropriate to pursue registration under the framework originally chosen by the company. Id. at *8. The Court further stated that plaintiffs likely fail[ed] to allege that the company lacked any factual basis for its opinions, thus rendering the opinions nonactionable. Id.

The Court did not, however, definitively determine whether a material misrepresentation had been alleged with regard to the registration issues, relying instead on its conclusion that plaintiffs failed to allege loss causation because the purported corrective disclosures (articles published regarding the company) relied on information previously disclosed to the market. Id. at *9. While noting that the Tenth Circuit had not squarely addressed the issue, the Court observed that other Circuits have held that, to qualify as a corrective disclosure, the disclosure must reveal non-public information. Id. at *6. Here, however, the articles plaintiffs relied upon did not actually reveal any then-undisclosed facts; instead, all the materials the articles referenced were publicly available. Id. at *9. Furthermore, the Court explained that, although some courts have ruled that expert analysis of publicly available information could constitute a corrective disclosure, there was no indication that the authors of the articles relied upon by plaintiffs had any expertise beyond that of careful investors. Id.

The Court next assessed plaintiffs allegations that the companys statements concerning the quality of its manufacturing facilities were materially misleading because the FDA had reported violations in July 2018. Id. at *10. The Court concluded that the challenged statements were either puffery or, in any event, plaintiffs failed to allege how the statements were rendered false by the FDAs findings. Id. While noting that the company had received the FDAs report before the challenged statements were made, the Court emphasized that the FDA had not made a final determination at the time, and that ultimately the FDA closed the inspection indicating that the allegedly objectionable conditions [did] not meet the threshold of regulatory significance. Id. Furthermore, the Court noted that two months passed between the FDAs inspection and the statements in question, during which time it appear[ed] that [the company] had made at least some improvements to its processes in response to the FDAs concerns. Id. at *11. In light of those circumstances, the Court concluded that the FDAs report does not support a reasonable inference that the individual who made the statements did not believe the puffing statements of corporate optimism. Id. at *11.

Turning to statements concerning the companys patents, the Court first noted that statements by the company that its products were subject to pending patent applications were true. Id. To the extent the company erroneously described certain technology as patented, the Court reasoned that those statements were immaterial because other company statements made clear that the technology at issue was not presently protected by existing patents but was rather the subject of pending patent applications. Id. The Court reasoned that, to the extent these statements were conflicting, that would have given a reasonable investor sufficient pause to warrant independent verification. Id. at *12. While the Court thus concluded that plaintiffs likely failed to adequately allege a material misstatement, id. at *11, it held that, regardless, plaintiffs again failed to adequately allege loss causation because the articles relied on as corrective disclosures were based on previously available information. Id. at *12.

Finally, the Court rejected plaintiffs argument that the companys statements about not being subject to any pending or contemplated governmental proceedings were false because the company had received a document request from the SEC. Id. at *13. The Court concluded that an isolated document request is not an investigation, and, in context, it was not reasonable to believe the company should have expected the SEC to conduct an investigation based on the request received. Id. The Court also observed that, even if an investigation had been contemplated, the companys statement was not false because [a]n investigation on its own is not a pending legal proceeding, and the SEC had not informed the company that it was contemplating further action. Id.

Because plaintiffs had not filed a motion seeking leave to amend, the Court dismissed the action with prejudice. Id.

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In re PolarityTE, Inc. Sec. Litig.

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Utah District Court Dismisses Putative Securities Class Action Against Biotechnology Firm For Failure To Allege Falsity And Loss Causation - JD Supra

Vaccines and Approved Antibodies Could Dim Vir Biotechnologys Covid Opportunity – Barron’s

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The tiny Vir Biotechnology was vaulted from obscurity this year, when it said it was developing treatments for Covid-19. Its stock (ticker: VIR) shot from $12 to a March peak of $75, before settling back to the mid-30swhere GlaxoSmithKline (GSK) bought a $250 million stake.

Vir started clinical trials in August for its antibody treatment against Covid-19. But the train has left the station, says Baird analyst Madhu Kumar, and Vir may have missed its Covid business opportunity. Antibodies from Eli Lilly (LLY) and Regeneron Pharmaceutical (REGN) have already gotten emergency use authorizations from regulators and booked orders. Demand for any Covid-19 treatment will start to shrink with the imminent authorization of vaccines from Pfizer (PFE), BioNTech (BNTX) and Moderna (MRNA).

In a Thursday note, Kumar reiterated his Underperform rating for Vir stock, whose shares he thinks should fall to $24 from their recent level near $32.

The Baird analyst went to a sell rating after Virs initial jump in February, and has maintained steady criticism since, in nearly 40 notes. Vir could find success with another treatment it is testing against hepatitis B, says Kumar, but future sales of such a product would only be worth $14 in current value. Ascribing $3.50 in value for Virs other pipeline programs, and counting its $6.50 a share in cash, brings Kumar to his $24 fair value.

Antibodies from Regeneron were among the treatments given to President Donald Trump in October, when he got Covid.

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Virs securities filings say that its Covid-19 antibody trial could produce interim results in January 2021, and a final readout later in that years first quarter. The Baird analyst doesnt expect an authorization and product launch until the springby which point vaccines should be getting into wide supply.

Meanwhile, the bridging opportunity for anti-Covid antibodies is being snapped up by Lilly and Regeneron. The U.S. government arranged to buy 950,000 doses of Lillys treatment, including a deal for 650,000 doses announced Wednesday that will bring $850 million to Lilly.

Write to Bill Alpert at william.alpert@barrons.com

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Pharmacogenomics Market Report 2019 to register a CAGR of 10.8% to reach US$ 20.83 Billion by 2026 | – PharmiWeb.com

Global Pharmacogenomics Market Insights

Pharmacogenomics is the study of how genes affect an individuals response to drugs. This is done by correlating gene expression changes and Single-Nucleotide Polymorphisms (SNPs) with a drugs efficacy or toxicity. It is relatively a new field that combines genomics and pharmacology to develop efficient and safe medications that will customized to an individuals makeup. Growing concerns for the early identification of drug advertises, drug safety, and growing need for timely compliance to regulatory guidelines have led the introduction of new technologies and methods by pharmaceutical manufacturers and other intermediaries. These advancements are expected to fuel adoption of pharmacogenomics technology during the forecast period. Pharmacogenomics has different restorative applications such as cardiology, oncology, neurological disorder, and pain management. In this manner, through further headways in this field, by enhancing drug safety, optimizing drug therapy with increasing patient compliance and further reducing healthcare costs is expected to result in the meteoric growth of the pharmacogenomics market over the forecast period.

Various government agencies are taking proactive initiatives to implement pharmacogenomics in drug development and surveillance, so that patients can benefit from advances in genomic science and technology. The government is also involved in funding companies that work to develop bioinformatics technology for precision medicine research applications. For instance, in 2017, Armonica Technologies, Inc., a U.S.-based company received US$ 1.5 Mn from the states US$ 40 Mn catalyst fund. This fund is intended for seed early stage-companies in New Mexico that are involved in developing novel technologies. Clinically personalized medicine is also expected to provide tools that will enhance the traditional approaches for estimating the risk/benefit of an intervention in patients.

The global pharmacogenomics market was valued at US$8,357.3million in 2017 and is expected to witness a CAGR of10.8%during the forecast period (2018 2026).

Figure 1. Global Pharmacogenomics Market Share, by Technology Type (%)

Market Dynamics- Drivers

Increasing demand for various techniques to pinpointing diagnoses down to the subtype of chronic conditions will drive the pharmacogenomics market

Growing research and development activities related to sequencing and especially generation sequencing is expected to boost the demand for pharmacogenomics tests, which in turn, is expected to drive the global pharmacogenomics market growth during the forecast period. Moreover, significant progress in the aspects of NGS technology, platform, and data analysis solutions is propelling widespread, as it shows validresults for problematic areas that have long plagued the drug development industry.

Furthermore, growing prevalence of several infectious and non-infectious diseases is expected to propel the global pharmacogenomics market over the forecast period, as it is boosting the demand for regulated next-generation sequencing-based clinical trial assays and companion diagnostics. According to U.S. Food and Drug Administration (FDA) statistics, over 100,000 people in the U.S. die each year from injurious responses to drugs that were correctly prescribed by a physician. Additionally, over 2.2 million people endure acute, though not fatal, side effects. Worldwide, BioWorld estimates those figures increase to 200,000 deaths and over 4.5 million people suffering serious side effects.

Pharmacogenomics tests are expected to predict susceptibility to maladies as well as create therapeutics tailored to an individuals specific genetic profile. This in turn, is expected to increase market growth.

Introduction of novel technology leading to new product launch is a prominent factor fueling market growth

Today, screening of known polymorphic drug metabolism enzymes and transporters (DMET) is rapidly becoming routine practice in clinical research. So manufacturers are currently focusing on various approaches to pharmacogenomics analysis to provide rapid and cost-effective solutions for both the screening of known polymorphisms and discovery of novel variants. Few of the advanced technologies already been commercialized like Illumina HiSeq-2000 and HiScan, Roche 454 GSFLX Titanium and the Applied Biosystems SOLiD Analyzer 5500xl. Besides, the combination of goldstandard Applied Biosystems TaqMan Assays with the high-throughput Applied Biosystems Open Array manufactured by Thermo Fisher Scientific Inc., enables analysis of common variants, typically in under four hours with the flexibility to modify array content.

Market Dynamics- Restraints

Lack of proper diagnostic testing due to lack of trained personnel, high costs associated with tests, dearth of laboratory facility, and lack of standardization and validation of the test procedures are expected to restrain the global pharmacogenomics market growth in the near future.

Figure 2. Global Pharmacogenomics Market Share, by Region (%)

Regional Insights

Among regions, North America accounted for the largest market share and is witnessed fastest growth, owing to presence of major key players and strategic collaborations among them. Asia Pacific is expected to register significant growth rate after North America, owing to increased investments in R&D and increasing number of clinical trials. In November 2016, according to the Pharmaceutical Research and Manufacturers of America (PhRMA) data, EFPIA and PhRMA member companies conducted 825 clinical trials for various therapeutic indications across Japan in 2015, showing an increase of 21% in comparison to 2013. Furthermore, Latin America and Africa are expected to exhibit moderate growth rate, as countries in these regions have shown considerable interest in research andcontinuous efforts made by major players to expand their business in these regions. South African Medical Research Council (SAMRC) has collaborated with Beijing Genomics Institute in April 2017, to understand the genetic composition of the population, which is expected to augment growth of the pharmacogenomics in South Africa.

View Press Release For More Information @ https://www.coherentmarketinsights.com/press-release/pharmacogenomics-market-to-surge-past-us-2083-billion-by-2026-468

Competitive Landscape

Key companies in the market are involved in various growth strategies such as collaboration and agreement, in order to gain competitive edge in the market. Objective of these collaborations between the organization and the companies is identification of specific tumor targets by expansion of known mutations associated with defective DNA repair. Companies are engaged in development of single comprehensive tests that can capture a large. amount of relevant content. For instance, in 2017, Qiagen N.V. and Bristol-Myers Squibb signed an agreement for use of Next Generation Sequencing technology to develop gene expression profiles for immuno-oncology therapies.

Major companies operating in the global pharmacogenomics market are Thermo Fisher Scientific Inc., Abbott Laboratories, F. Hoffmann-La Roche AG, Qiagen N.V., Pacific Biosciences of California, Inc., Diatech Pharmacogenetics Srl, and Assurex Health Inc.

Coherent Market Insights is a global market intelligence and consulting organization focused on assisting our plethora of clients achieve transformational growth by helping them make critical business decisions. We are headquartered in India, having office at global financial capital in the U.S. and sales consultants in United Kingdom and Japan. Our client base includes players from across various business verticals in over 150 countries worldwide. We pride ourselves in catering to clients across the length and width of the horizon, from Fortune 500 enlisted companies, to not-for-profit organization, and startups looking to establish a foothold in the market. We excel in offering unmatched actionable market intelligence across various industry verticals, including chemicals and materials, healthcare, and food & beverages, consumer goods, packaging, semiconductors, software and services, Telecom, and Automotive. We offer syndicated market intelligence reports, customized research solutions, and consulting services.

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Pharmacogenomics Market Report 2019 to register a CAGR of 10.8% to reach US$ 20.83 Billion by 2026 | - PharmiWeb.com

Genetic Technologies Secures US and ANZ Distribution Rights for PREDICTIX – BioSpace

MELBOURNE, Australia, Dec. 02, 2020 (GLOBE NEWSWIRE) -- Molecular diagnostics company Genetic Technologies Ltd (ASX: GTG; NASDAQ: GENE, the Company), announced today that they have entered into a three-year partnership agreement with mental health company, Taliaz, for the distribution rights of their PREDICTIX products in Australia, New Zealand and the USA (Agreement).

Key Highlights

The Agreement will support GTG to expand its product offering and establish the mental health vertical by harnessing PREDICTIX, Taliazs pioneering decision-support and management platform to optimize patient treatment for mental health disorders. Starting in the field of depression, this genomic-based, Artificial Intelligence (AI) driven antidepressant selection technology, marks GTGs first foray into pharmacogenomics1.

George Muchnicki, GTGs Interim CEO stated: We are incredibly pleased to have partnered with Taliaz to bring their predictive and personalized mental health product to Australia and New Zealand. GTG are at the forefront of providing personalized and predictive products to empower patients to make informed decisions about their health. This distribution agreement is our first external product partnership and our first product within the mental health vertical. Mental health has remained at the forefront of media discussions and government initiatives within Australia, New Zealand and globally due to the ongoing social and economic impact and given the impact from the current global pandemic. We look forward to working closely with the Taliaz team to deliver their product into these markets at this critical time.

The execution of the Agreement is reliant on product regulatory clearance by the Therapeutic Goods Administration (TGA) in Australia and Food and Drug Administration (FDA) in the USA. Once cleared, GTG has committed to providing a minimum distribution of 8,000 tests over the initial three-year term with an associated minimum cost to GTG of $200,000 over the term, inclusive of licencing fees and a percentage based fee per test paid to Taliaz. Subject to the regulatory clearance process, GTG anticipates that PREDICTIX will be made available for sale and distribution in Australia and New Zealand in Q3 FY21 on GTGs existing Consumer Initiated Testing (CIT) platform, with end-customer pricing to be determined but anticipated to be in line with existing GTG product pricing.

PREDICTIX, developed by the private Israeli company, Taliaz, addresses the growing burden on society from depression, with 1 in 10 Americans2 and 1 in 8 Australians3 prescribed antidepressants per year. PREDICTIX enables a more accurate and rapid treatment plan for patients suffering from depression, reducingtreatment costs and the overall associated economic burden.

PREDICTIX is an algorithmic-based decision support tool that can improve todays antidepressant prescribing accuracy by 47%4. Combining DNA testing with AI, PREDICTIX empowers doctors to improve the assessment, treatment, and management of mental health disorders.

The PREDICTIX technology uses AI to analyse multiple data streams, including patients genomic, clinical history and demographic background, providing doctors with a personalized patient report. The report ranks the statistical efficacy and potential side effects of various antidepressant medication based on each patients genetic makeup andhealth record. This helps doctors optimize prescribing decisions for patients diagnosed with depressive disorder, where there is currently a long and painful trial and error period. PREDICTIX is CE-registered and commercially available in the UK, France and Israel, with the process underway for TGA approval.

Dekel Taliaz, CEO and Co-founder of Taliaz said, We are excited to partner with Genetic Technologies, world-leaders in the genetic risk assessment space. This new partnership will support rapid commercialization of PREDICTIX to help more depression sufferers in Australia, New Zealand and the USA, while adding a complementary and advanced mental health solution to GTGs growing suite of DNA tests.

The Agreement strengthens GTGs mission in creating a suite of tests to enable a holistic and predictive health assessment for patients, which can be adjusted to address the individual patient risks and needs. Establishing the first product within the mental health and pharmacogenetic space continues GTGs progress towards being able to offer a highly comprehensive suite of polygenic risk assessment tests via GTGs CIT platform and additional sales and marketing avenues as these are progressed.

This announcement was approved by the Board of Directors of Genetic Technologies Limited.

About Genetic Technologies Limited

Genetic Technologies Limited (ASX: GTG; Nasdaq: GENE) is a diversified molecular diagnostics company. GTG offers cancer predictive testing and assessment tools to help physicians proactively manage patient health. The Companys lead products GeneType for Breast Cancer for non-hereditary breast cancer and GeneType for Colorectal Cancer are clinically validated risk assessment tests and are first in class. Genetic Technologies is developing a pipeline of risk assessment products.

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

About Taliaz

Taliaz is revolutionizing the treatment and management of mental health disorders with PREDICTIX. PREDICTIX is a CE-registered product that provides an advanced decision support software for psychiatrists and general practitioners. Harnessing artificial intelligence, PREDICTIX can enable easy, effective and rapid patient assessment, improved prescribing precision and management for a wide range of mental health conditions. Starting in the field of depression, the PREDICTIX Genetics and PREDICTIX Digital products can improve todays prescribing accuracy by up to 47%4.

For more information, please visit predictix.ai.

Originally posted here:
Genetic Technologies Secures US and ANZ Distribution Rights for PREDICTIX - BioSpace

Jacob Rees Mogg accused of spreading fake news over claim vaccine approval was down to Brexit – Yahoo Sports

Watch: Jacob Rees-Mogg accused of fake news over Brexit vaccine tweet

Jacob Rees-Mogg has been accused of spreading fake news after he claimed the COVID vaccine was approved quickly in the UK because of Brexit.

On Wednesday, the UKs Medicines and Healthcare products Regulatory Agency (MHRA) approved the jab developed by Pfizer and BioNTech, while the European Medicines Agency (EMA) has yet to do so for the EU.

Rees-Mogg jumped on the news, tweeting: We could only approve this vaccine so quickly because we have left the EU.

Last month we changed the regulations so a vaccine did not need EU approval which is slower.

However, MHRA chief June Raine said the approval was made using provisions under European law, which still binds the UK until the end of the year.

Speaking in the Commons on Thursday morning, deputy leader of the House, Valerie Vaz, urged Rees-Mogg to take back his tweet in light of Raines comments.

She said: We've had fake news. The approval of the vaccine has nothing to do with Brexit.

But Rees-Mogg called the approval of the vaccine a British success and accused the European regulator of being a bit sniffy about it.

He told MPs: The UK should be really proud that our regulator got in first and we notice that the European regulator is a bit sniffy about it, wishes we hadnt done it, and that Germany and France and other European countries havent managed to do the same thing.

We have, were leading, draw your own conclusions, as Im sure the British public will.

We are now free of the dead hand of the European Union and will be even more free from that on 1 January.

Story continues

He added: It is a huge British success of which we should be proud and pleased.

Brexit was also credited as the reason for the speedy approval of the vaccine by health secretary Matt Hancock, who said the Europeans are moving a little bit more slowly.

Hancock told Times Radio: The reason weve been able to move this fast, and the UK is the first country in the world to have a clinically authorised vaccine, the reason is twofold.

Firstly, because the MRHA has done a great job of working with the company to look at that data as its come through and do things in parallel, rather than one after the other as they normally would, thats the first reason.

Watch: Boris Johnson warns against over-optimism following vaccine approval

The second reason is because, whilst until earlier this year we were in the European Medicines Agency (EMA), because of Brexit weve been able to make a decision to do this based on the UK regulator, a world-class regulator, and not go at the pace of the Europeans, who are moving a little bit more slowly.

We do all the same safety checks and the same processes, but we have been able to speed up how theyre done because of Brexit.

Hitting back at Hancocks claims, German MEP Pieter Liese, a member of the European parliaments public health committee, said individual EU member states could have authorised the vaccine but had chosen to wait for the EMA to examine more information rather than follow the hasty UK example.

The EMA suggested that it was imposing more stringent checks than the emergency process used by the MHRA.

A spokeswoman said: The temporary authorisation of the vaccine by the MHRA is not a marketing authorisation.

It differs from marketing authorisations in the level of evidence submitted and checks required.

Downing Street did not back Hancocks claim about Brexit.

The Prime Ministers official spokesman said: It is clear that we are the first country in the world to approve this vaccine and it is incredibly positive news that we will be able to start to distribute it.

Watch: How England's new three-tier COVID system will work

Link:

Jacob Rees Mogg accused of spreading fake news over claim vaccine approval was down to Brexit - Yahoo Sports