Trends Of Nanoparticles in Biotechnology and Pharmaceuticals Market Reviewed For 2020 With Industry Outlook To 2026 – Cole of Duty

A detailed research study on the Nanoparticles in Biotechnology and Pharmaceuticals Market was recently published by DataIntelo. This is a latest report, covering the current COVID-19 impact on the market. The pandemic of Coronavirus (COVID-19) has affected every aspect of life globally. This has brought along several changes in market conditions. The rapidly changing market scenario and initial and future assessment of the impact is covered in the report. The report puts together a concise analysis of the growth factors influencing the current business scenario across various regions. Significant information pertaining to the industry analysis size, share, application, and statistics are summed in the report in order to present an ensemble prediction. Additionally, this report encompasses an accurate competitive analysis of major market players and their strategies during the projection timeline.

The latest report on the Nanoparticles in Biotechnology and Pharmaceuticals Market consists of an analysis of this industry and its segments. As per the report, the market is estimated to gain significant returns and register substantial y-o-y growth during the forecast period.

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Trends Of Nanoparticles in Biotechnology and Pharmaceuticals Market Reviewed For 2020 With Industry Outlook To 2026 - Cole of Duty

Where Does Intercept Pharmaceuticals Inc (ICPT) Stock Fall in the Biotechnology Field? – InvestorsObserver

Intercept Pharmaceuticals Inc (ICPT) is near the top in its industry group according to InvestorsObserver. ICPT gets an overall rating of 72. That means it scores higher than 72 percent of stocks. Intercept Pharmaceuticals Inc gets a 83 rank in the Biotechnology industry. Biotechnology is number 8 out of 148 industries.

Analyzing stocks can be hard. There are tons of numbers and ratios, and it can be hard to remember what they all mean and what counts as good for a given value. InvestorsObserver ranks stocks on eight different metrics. We percentile rank most of our scores to make it easy for investors to understand. A score of 72 means the stock is more attractive than 72 percent of 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.

Intercept Pharmaceuticals Inc (ICPT) stock is trading at $81.86 as of 10:41 AM on Tuesday, Apr 21, a loss of -$0.75, or -0.91% from the previous closing price of $82.61. The stock has traded between $80.53 and $83.30 so far today. Volume today is less active than usual. So far 80,863 shares have traded compared to average volume of 667,682 shares.

To see InvestorsObserver's Sentiment Score for Intercept Pharmaceuticals Inc click here.

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Where Does Intercept Pharmaceuticals Inc (ICPT) Stock Fall in the Biotechnology Field? - InvestorsObserver

Why Investors Need To Watch Vir Biotechnology, Inc. (VIR)? – The News Heater

Vir Biotechnology, Inc. (NASDAQ:VIR) went up by 3.56% from its latest closing price when compared to the 1-year high value of $75.00 and move down -140.77%, while VIR stocks collected +6.21% of gains with the last five trading sessions. Press Release reported on 04/15/20 that VIR-2218 Demonstrates Dose-Dependent and Durable Reductions of Hepatitis B Surface Antigen in Phase 1/2 Trial

VIR stocks went up by 6.21% for the week, with the monthly drop of -4.89% and a quarterly performance of 83.45%. The simple moving average for the period of the last 20 days is 0.29% for VIR stocks with the simple moving average of 44.30% for the last 200 days.

Many brokerage firms have already submitted their reports for VIR stocks, with JP Morgan repeating the rating for VIR shares by setting it to Underweight. The predicted price for VIR socks in the upcoming period according to JP Morgan is $26 based on the research report published on March 19, 2020.

Goldman, on the other hand, stated in their research note that they expect to see VIR stock at the price of $26. The rating they have provided for VIR stocks is Neutral according to the report published on March 13, 2020.

Robert W. Baird gave Underperform rating to VIR stocks, setting the target price at $17 in the report published on February 27, 2020.

After a stumble in the market that brought VIR to its low price for the period of the last 52 weeks, Vir Biotechnology, Inc. was unable to take a rebound, for now settling with -58.47% of loss for the given period.

The stock volatility was left at 11.09%, however, within the period of a single month, the volatility rate increased by 7.37%, while the shares surge at the distance of +1.30% for the moving average in the last 20 days. In oppose to the moving average for the last 50 days, trading by +70.78% upper at the present time.

In the course of the last 5 trading sessions, VIR went up by +6.21%. In addition, Vir Biotechnology, Inc. saw 147.71% in overturn over the period of a single year with a tendency to cut further gains.

The current profitability levels are settled at -2110.98 for the present operating margin. The net margin for Vir Biotechnology, Inc. stands at -2158.98. Total capital return value is set at -61.54, while invested capital returns managed to touch -62.97.

Based on Vir Biotechnology, Inc. (VIR), the companys capital structure generated 0.27 points for debt to equity in total, while total debt to capital is set at the value of 0.27.

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Why Investors Need To Watch Vir Biotechnology, Inc. (VIR)? - The News Heater

Vir Biotechnology, Inc. (VIR) Plans and Analysts Expectations – The News Heater

Vir Biotechnology, Inc. (NASDAQ:VIR) went down by -9.32% from its latest closing price when compared to the 1-year high value of $75.00 and move down -157.73%, while VIR stocks collected -2.25% of loss with the last five trading sessions. Press Release reported 17 hours ago that Vir Biotechnology to Host Key Opinion Leader Call and Present Update on Phase 1/2 HBV Clinical Trial with siRNA VIR-2218

Vir Biotechnology, Inc. (NASDAQ:VIR) of the analysts out of 0 who provided ratings for Vir Biotechnology, Inc. stocks as a buy while as overweight, rated it as hold and as sell. The average price we get from analysts is $32.00 which is $4.23 above current price. VIR currently has a short float of 1.54% and public float of 100.45M with average trading volume of 892.69K shares.

VIR stocks went down by -2.25% for the week, with the monthly drop of -2.71% and a quarterly performance of 134.11%. The simple moving average for the period of the last 20 days is -20.90% for VIR stocks with the simple moving average of 39.08% for the last 200 days.

Many brokerage firms have already submitted their reports for VIR stocks, with JP Morgan repeating the rating for VIR shares by setting it to Underweight. The predicted price for VIR socks in the upcoming period according to JP Morgan is $26 based on the research report published on March 19, 2020.

Goldman, on the other hand, stated in their research note that they expect to see VIR stock at the price of $26. The rating they have provided for VIR stocks is Neutral according to the report published on March 13, 2020.

Robert W. Baird gave Underperform rating to VIR stocks, setting the target price at $17 in the report published on February 27, 2020.

After a stumble in the market that brought VIR to its low price for the period of the last 52 weeks, Vir Biotechnology, Inc. was unable to take a rebound, for now settling with -61.20% of loss for the given period.

The stock volatility was left at 20.50%, however, within the period of a single month, the volatility rate increased by 15.57%, while the shares sank at the distance of -13.83% for the moving average in the last 20 days. In oppose to the moving average for the last 50 days, trading by +36.56% upper at the present time.

In the course of the last 5 trading sessions, VIR went down by -2.25%, in comparison to the 20-day moving average settled at $36.56. In addition, Vir Biotechnology, Inc. saw 131.41% in overturn over the period of a single year with a tendency to cut further gains.

The current profitability levels are settled at -2110.98 for the present operating margin. The net margin for Vir Biotechnology, Inc. stands at -2158.98. Total capital return value is set at -61.54, while invested capital returns managed to touch -62.97.

Based on Vir Biotechnology, Inc. (VIR), the companys capital structure generated 0.27 points for debt to equity in total, while total debt to capital is set at the value of 0.27.

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Vir Biotechnology, Inc. (VIR) Plans and Analysts Expectations - The News Heater

Vir Biotechnology to Host Key Opinion Leader Call and Present Update on Phase 1/2 HBV Clinical Trial with siRNA VIR-2218 – Yahoo Finance

Company to Host Conference Call onWednesday, April 15, 2020, at2:00 pm PT

SAN FRANCISCO, April 08, 2020 (GLOBE NEWSWIRE) -- Vir Biotechnology, Inc. (VIR), a clinical-stage immunology company focused on treating and preventing serious infectious diseases, today announced that it will host a Key Opinion Leader call and present an update on its Phase 1/2 hepatitis B virus (HBV) clinical trial with small interfering ribonucleic acid (siRNA) VIR-2218 on Wednesday, April 15, 2020 at 2:00 pm PT.

The call will feature a presentation by Dr. Edward J. Gane, Professor of Medicine at the University of Auckland, New Zealand and Chief Hepatologist, Transplant Physician and Deputy Director of the New Zealand Liver Transplant Unit at Auckland City Hospital. Dr. Gane, who also serves as an advisor to Vir, will provide an update on the Phase 1/2 clinical trial of VIR-2218, along with Vir management.

A live webcast of the presentation can be accessed under Events & Presentations in the Investors section of the Vir website at http://www.vir.bio and will be archived there following the presentation for 30 days.

The Company has used, and intends to continue to use, the Investors page of its website as a means of disclosing material non-public information and for complying with its disclosure obligations under Regulation FD. Accordingly, investors should monitor the Companys Investors website, in addition to following the Companys press releases, Securities and Exchange Commission filings, public conference calls, presentations and webcasts.

About VIR-2218VIR-2218 is a subcutaneously administered HBV-targeting siRNA that has the potential to stimulate an effective immune response and have direct antiviral activity against HBV. It is the first siRNA in the clinic to include Enhanced Stabilization Chemistry Plus (ESC+) technology to enhance stability and minimize off-target activity, which potentially can result in an increased therapeutic index. VIR-2218 is the first asset in the companys collaboration with Alnylam Pharmaceuticals, Inc. to enter clinical trials.

About Vir BiotechnologyVir Biotechnology is a clinical-stage immunology company focused on combining immunologic insights with cutting-edge technologies to treat and prevent serious infectious diseases. Vir has assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Its current development pipeline consists of product candidates targeting hepatitis B virus, influenza A, SARS-CoV-2, human immunodeficiency virus, and tuberculosis. For more information, please visit http://www.vir.bio.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as may, will, expect, plan, anticipate, estimate, intend, potential and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements. These forward-looking statements are based on Virs expectations and assumptions as of the date of this press release. Each of these forward-looking statements involves risks and uncertainties. Actual results may differ materially from these forward-looking statements. Forward-looking statements contained in this press release include statements regarding the potential benefits of VIR-2218 and the timing of VIR-2218 data disclosures. Many factors may cause differences between current expectations and actual results including unexpected safety or efficacy data observed during clinical trials and delays or disruptions on our business or clinical trials due to the COVID-19 pandemic. Other factors that may cause actual results to differ from those expressed or implied in the forward-looking statements in this press release are discussed in Virs filings with the U.S. Securities and Exchange Commission, including the section titled Risk Factors contained therein. Except as required by law, Vir assumes no obligation to update any forward-looking statements contained herein to reflect any change in expectations, even as new information becomes available.

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Contact:

Vir Biotechnology, Inc.

InvestorsNeera Ravindran, MDHead of Investor Relations & Strategic Communicationsnravindran@vir.bio+1-415-506-5256

MediaLindy DevereuxScient PRlindy@scientpr.com+1-646-515-5730

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Vir Biotechnology to Host Key Opinion Leader Call and Present Update on Phase 1/2 HBV Clinical Trial with siRNA VIR-2218 - Yahoo Finance

Vir Biotechnology to Host Key Opinion Leader Call and Present Update on Phase 1/2 HBV Clinical Trial with siRNA VIR-2218Company to Host Conference…

SAN FRANCISCO, April 08, 2020 (GLOBE NEWSWIRE) -- Vir Biotechnology, Inc. (Nasdaq: VIR), a clinical-stage immunology company focused on treating and preventing serious infectious diseases, today announced that it will host a Key Opinion Leader call and present an update on its Phase 1/2 hepatitis B virus (HBV) clinical trial with small interfering ribonucleic acid (siRNA) VIR-2218 on Wednesday, April 15, 2020 at 2:00 pm PT.

The call will feature a presentation by Dr. Edward J. Gane, Professor of Medicine at the University of Auckland, New Zealand and Chief Hepatologist, Transplant Physician and Deputy Director of the New Zealand Liver Transplant Unit at Auckland City Hospital. Dr. Gane, who also serves as an advisor to Vir, will provide an update on the Phase 1/2 clinical trial of VIR-2218, along with Vir management.

A live webcast of the presentation can be accessed under Events & Presentations in the Investors section of the Vir website at http://www.vir.bio and will be archived there following the presentation for 30 days.

The Company has used, and intends to continue to use, the Investors page of its website as a means of disclosing material non-public information and for complying with its disclosure obligations under Regulation FD. Accordingly, investors should monitor the Companys Investors website, in addition to following the Companys press releases, Securities and Exchange Commission filings, public conference calls, presentations and webcasts.

About VIR-2218VIR-2218 is a subcutaneously administered HBV-targeting siRNA that has the potential to stimulate an effective immune response and have direct antiviral activity against HBV. It is the first siRNA in the clinic to include Enhanced Stabilization Chemistry Plus (ESC+) technology to enhance stability and minimize off-target activity, which potentially can result in an increased therapeutic index. VIR-2218 is the first asset in the companys collaboration with Alnylam Pharmaceuticals, Inc. to enter clinical trials.

About Vir BiotechnologyVir Biotechnology is a clinical-stage immunology company focused on combining immunologic insights with cutting-edge technologies to treat and prevent serious infectious diseases. Vir has assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Its current development pipeline consists of product candidates targeting hepatitis B virus, influenza A, SARS-CoV-2, human immunodeficiency virus, and tuberculosis. For more information, please visit http://www.vir.bio.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as may, will, expect, plan, anticipate, estimate, intend, potential and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements. These forward-looking statements are based on Virs expectations and assumptions as of the date of this press release. Each of these forward-looking statements involves risks and uncertainties. Actual results may differ materially from these forward-looking statements. Forward-looking statements contained in this press release include statements regarding the potential benefits of VIR-2218 and the timing of VIR-2218 data disclosures. Many factors may cause differences between current expectations and actual results including unexpected safety or efficacy data observed during clinical trials and delays or disruptions on our business or clinical trials due to the COVID-19 pandemic. Other factors that may cause actual results to differ from those expressed or implied in the forward-looking statements in this press release are discussed in Virs filings with the U.S. Securities and Exchange Commission, including the section titled Risk Factors contained therein. Except as required by law, Vir assumes no obligation to update any forward-looking statements contained herein to reflect any change in expectations, even as new information becomes available.

Contact:

Vir Biotechnology, Inc.

InvestorsNeera Ravindran, MDHead of Investor Relations & Strategic Communicationsnravindran@vir.bio+1-415-506-5256

MediaLindy DevereuxScient PRlindy@scientpr.com+1-646-515-5730

Original post:
Vir Biotechnology to Host Key Opinion Leader Call and Present Update on Phase 1/2 HBV Clinical Trial with siRNA VIR-2218Company to Host Conference...

Opinion: Coronavirus outbreak stresses need for One Health and animal biotech advancement – Agri-Pulse

The COVID-19 outbreak is gripping our planet like no other health crisis in recent history. Overt collaboration and policy action are required to meet this challenge and, as importantly, prepare for the future. Elevating and prioritizing the interconnectedness of living things through One Health strategies and modernizing Americas animal biotechnology regulatory approach are two policies Congress and the White House must confront. In fact, they are long overdue.

Sixty percent of human diseases begin in animals.Scientists are confident that the COVID outbreak originated in batsand then was spread through another animal and then to humans, like the 2002-03 SARS outbreak. As the climate changes and populations grow and move, these zoonotic diseases will become more prevalent and potentially more dangerous.

Aside from the dreadful health implications, the resulting economic costs of a pandemic are profound.The World Bank estimates that, between 1997 and 2009, the global costs from six zoonotic outbreaks exceeded $80 billion. While we wont know the total impact for some time, COVID-19 has already producedone of the sharpest economic downturns in U.S. history and is costing the U.S. treasury alone trillions of dollars.

Society was woefully unprepared for this pandemic. We must employ modern approaches to be ready for future outbreaks. One Health collaboration eliminates barriers that often exist between human health, animal health, and environmental health strategies to create smarter, multi-faceted and coordinated efforts.

BIO supports legislation such as the Advancing Emergency Preparedness Through One Health Act of 2019. This bill would direct the U.S. Department of Health and Human Services and the U.S. Department of Agriculture (USDA) to coordinate with other agencies and state and local leaders to advance a national One Health framework to better prevent, prepare for, and respond to zoonotic disease outbreaks like COVID-19. Congress and the White House must factor One Health into their efforts to address future pandemics.

Animal health and wellness is a critical component of One Health strategy. To help the U.S. better prepare for the future, we need changes to the U.S. animal biotechnologyregulatory system.The U.S. governments current approach to regulating animal biotechnology as a new animal drug has all but destroyed investment and blocked market access for a host of beneficial products.

Biotechnology, for example, could armpigs with resistanceto African Swine Fever. Similarly,scientists have developed achickenthat is resistant to contracting and transmitting avian influenza.

Other innovations in animal biotechnology may be able prevent, prepare for, and respond to outbreaks of infectious diseases such as coronavirus, Ebola, MERS, Zika, among others, by providing prevention strategies andtreatments for humans.

Unfortunately, the United States regulatory system for animal biotechnology is not appropriately science- or risk-based, and as a result we are falling behind other countries, such as Brazil, where innovative start-ups are finding more support.

Indeed, despite decades of animal biotechnology research and advances, only one biotech food animal has been approved to date the AquaBounty salmon which languished in the U.S. regulatory system for more than two decades and still has not hit the market because ofpolitical interference.

The current crisis underscores the urgent need to break down roadblocks to progress.

BIO is calling on the White House to direct the U.S. Food and Drug Administration (FDA) and the USDA to clarify within 30 days a plan to overhaul the current regulatory approval process for animal biotechnology.

In alettersent to the President, BIO implores the need for a new approach that 1) more appropriately draws upon existing legal authorities to safeguard animal health, food safety, and the environment; 2) incentivizes research and investment in the technology; and 3) ensures safe and affordable products reach consumers as soon as possible.

A joint agreement between both agencies will help farmers, innovators, and consumers realize the benefits that modern technology can bring to the United States and the world. And just may well prevent the next potential animal to human disease outbreak.

Dana OBrien,Executive Vice President,Food & AgricultureBiotechnology Innovation Organization (BIO)

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Opinion: Coronavirus outbreak stresses need for One Health and animal biotech advancement - Agri-Pulse

We aim to disrupt the biotechnology landscape with out out-of-the-box and innovative product line – Express Healthcare

While promoting hygiene through its products made up of waterless technology, Clensta International has created the first line of defence via shielding human beings from infection of viruses and bacteria, informs Dr Puneet Gupta, Founder and CEO, Clensta International, to Viveka RoyChowdhury

What is the impact of waterless technolgy on sanitation in the public health and sanitation sphere, against the backdrop of the coronavirus infection, which has been declared as a pandemic by the World Health Organization (WHO)?

To minimise the chances of infection and disease and thereby save many lives, we have developed the next generation tech-powered products which directly impact the common population. Besides promoting hygiene, they are also useful in inculcating a behavioural change towards the protection of the environment. This is in line with the Sustainable Development Goal (SDG 6) to ensure availability and sustainable management of water and sanitation for all.

As prevention is always better than cure, our products create the first line of defence via shielding human beings from infection of viruses and bacteria. Over the years, Clensta has been a driver of change to help and protect our loved ones by providing instant hygiene to anyone, anywhere and anytime.0 Hence, we conducted research to understand the new cleanliness regime and mindset. Interestingly, the findings reveal that 70 per cent of mothers believe cleaning is equivalent to germ-free. This waterless hand rub is an ideal offering to ensure cleanliness and underscores our commitment to maintaining a germ-free environment.

Why did you choose to focus on waterless technology for your entrepreneurial journey?

Of late, sustainability has become a new dimension for companies. There has been an emergence of startups working in the area of climate change mitigation and environmental protection. After working closely with the defence personnel, I gained an insight into their challenges. The challenge of not bathing for days, while on duty during extreme weather conditions at locations such as Siachin, Kargil or Drass motivated me towards developing waterless technology products leading to the establishment of Clensta International.

What are the important milestones in this entrepreneurial journey?

The year 2017 marked Clenstas association with IIT Delhi as our research and development centre. This was instrumental in not only providing R&D support, but it also served as a platform for new startups to implement innovative ideas. Another milestone was raising seed and pre-series A fund from Indian Angle Network and notable alumni of IIT Delhi. Clensta International has also received a grant from Biotechnology Industry Research Assistance Council (BIRAC) under BIG Scheme to scale up innovation.

We have also received an appreciation from the President of India Ram Nath Kovind, which boosted the motivation of the entire team. The overwhelming response towards the product truly indicates that people are increasingly becoming conscious of the need to protect the environment and are embracing innovation.

Are there similar products in other geographies?

Currently, there is no company working in the domain of waterless FMCG or personal hygiene space in India as extensively as we are. Hence, it can be said that ours is a one-of-a-kind concept of waterless hygiene products. Though some companies have launched waterless shampoo, we are perhaps the only organisation having waterless technology as the core idea.

What have been the sales and marketing strategies, the sales channels employed?

The marketing strategy plays an instrumental role in gaining a sustainable competitive advantage for the company. We follow a B2B sales channel wherein the product is sold via a distribution network. We deploy the right mix of channels and possess a team with in-depth expertise in healthcare marketing. Their expertise is also instilling a behavioural change towards the innovations. Of late, we have been leveraging digital marketing tools extensively, including social media platforms like Facebook and LinkedIn to connect with our target audience.

Which are the sectors that are being tapped?

Clensta International aims to promote personal hygiene while protecting the environment. The issue is largely unaddressed, especially in rural areas and urban slums. The water resources face unprecedented threat worldwide. Around 2.2 billion people do not have access to safe drinking water and 4.2 billion people lack access to adequate sanitation facilities. Hence, there is an urgent need to scale up innovation geared towards promoting efficiency in water use. If we were to talk about the healthcare sector, a patient undergoing surgery or a bed-ridden person may not bathe for days and survives in unhygienic conditions. Similarly, there is immense potential in the tourism sector as waterless products are handy for travellers. In the defence sector, soldiers deployed in extreme weather conditions such as Siachen does not have access to proper bathing facilities. Adventure enthusiasts and mountaineers too face this issue of poor hygiene. Hence, our products are relevant not only for healthcare, but also for travel and defence sectors.

How are these products being positioned to hospitals and clinics?

Clensta International is working on developing an innovative healthcare product line. Its current products waterless body bath and waterless shampoo cater to the home healthcare and hospital segments. Maintaining hygiene is of utmost importance for patients, especially those in critical situations to minimise the chances of any infection. It is here that our waterless technology comes to the rescue and provides the first line of defence against viruses and bacteria.

It is also noteworthy that alternative means of bathing such as sponging and wet towel bathing increase the chances of microbial load and transfer of bacteria and other viruses to the human body. Thus, our waterless technology comprising a simple formulation that is free of alcohol, SLS and any other harmful ingredients, is useful for maintaining basic hygiene and cleanliness. The products can be directly applied to hair and body, massaged and then can be dried off using a towel. These remove dirt, oil and grease completely. Thus, our innovative healthcare solution enables convenient, on-the-go and quick access to hygiene.

Have there been any studies done to prove that the use of such products decreases the incidence of hospital-acquired infection (HAI), also known as nosocomial infections?

Our product- Clensta Waterless Body Bath is anti-bacterial, antiseptic, and has been approved by the FDA as well as tested dermatologically. All products are being extensively used in defence, hospital and healthcare institutions. The product has also been put at trial at Madras Medical College, Multi- Super Specialty Hospital Tamil Nadu, SRM Institute of Medical Sciences and Indian Navy for antimicrobial testing.

How affordable are such products, given Indias disease burden due to infectious diseases?

Clensta International is continuously striving to make its products affordable through government support. Our products have been deemed for an essential use for the Indian Navy and will soon be a necessity for the Indian Army. We are making efforts to facilitate the availability of our products to the underprivileged section of the society through our Corporate Social Responsibility (CSR) initiative and by joining hands with various governmental institutes and hospitals. Our core idea to disseminate awareness on personal hygiene while protecting the environment is also being encouraged through our marketing strategy and social media awareness campaigns. With our CSR initiative, we are also educating children in rural areas on the significance of maintaining basic hygiene.

As a start-up, what are the policies and regulations which can spur further innovation?

It is commendable that the Indian government has undertaken various initiatives such as Start-up India, Skill India, etc to spur innovation and catalyse entrepreneurship. However, there is a scope of improvement in our existing intellectual property policy framework when it comes to addressing the issue of patent protection. Surely, in comparison to before, multiple processes have been implemented to ease the fund and grant approvals. Moreover, now, we could look forward to expediting the process of granting permissions by instituting a single-window clearance mechanism. Yet, the most daunting challenge ahead for start-ups is to minimise the go-to-market time for products and to attain a sustainable competitive advantage globally.

What are your plans for future products, overseas sales, etc.?

Our focus is to penetrate deeper into the Indian market and expand ourselves in tier II- and tier-III cities. We envision to establish ourselves as a leading player in the B2B space while exploring the possibilities of establishing ourselves in the B2C market as well. Expanding our footprints internationally is on the cards. We have already set up global operations with a subsidiary in The Netherlands and are further exploring business opportunities in Africa, Asia, the European Union, North America as well as South America. We aim to disrupt the biotechnology landscape with out of -the-box and innovative product line. We will be soon foraying into the homecare segment in an endeavour to provide sustainable solutions to Indian households while simultaneously reducing the consumption of plastic.

[emailprotected]

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We aim to disrupt the biotechnology landscape with out out-of-the-box and innovative product line - Express Healthcare

Industry Breakdown: Where Does Oncolytics Biotech, Inc. (ONCY) Stock Fall in the Biotechnology Field? – InvestorsObserver

Oncolytics Biotech, Inc. (ONCY) is around the top of the Biotechnology industry according to InvestorsObserver. ONCY received an overall rating of 85, which means that it scores higher than 85 percent of all stocks. Oncolytics Biotech, Inc. also achieved a score of 99 in the Biotechnology industry, putting it above 99 percent of Biotechnology stocks. Biotechnology is ranked 11 out of the 148 industries.

Analyzing stocks can be hard. There are tons of numbers and ratios, and it can be hard to remember what they all mean and what counts as good for a given value. InvestorsObserver ranks stocks on eight different metrics. We percentile rank most of our scores to make it easy for investors to understand. A score of 85 means the stock is more attractive than 85 percent of stocks.

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.

Oncolytics Biotech, Inc. (ONCY) stock is down -2.44% while the S&P 500 has risen 5.92% as of 2:02 PM on Monday, Apr 6. ONCY is down -$0.04 from the previous closing price of $1.45 on volume of 194,581 shares. Over the past year the S&P 500 is down -8.97% while ONCY is down -24.19%. ONCY lost -$1.05 per share the over the last 12 months.

To see InvestorsObserver's Sentiment Score for Oncolytics Biotech, Inc. click here.

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Industry Breakdown: Where Does Oncolytics Biotech, Inc. (ONCY) Stock Fall in the Biotechnology Field? - InvestorsObserver

Cellect Biotechnology Reports Fourth Quarter and Full Year 2019 Results – BioSpace

TEL AVIV, Israel, April 3, 2020 /PRNewswire/ -- Cellect BiotechnologyLtd. (Nasdaq: APOP), a developer of a novel stem cell production technology, today announced operating and financial results for the fourth quarter and full year ended December 31, 2019.

"We achieved a number of strategic priorities in 2019, including the IND approval to commence our first-ever trial in the U.S.," commented Dr. Shai Yarkoni, Chief Executive Officer."We plan to begin enrolling patients for this trial and completing the trial in Israel when the COVID-19 pandemic is mitigated. While these near-term events are value-enhancers, I believe that our recently announced prospective partnership with Canndoc could be a game-changer for Cellect and change our growth trajectory. It has the potential to significantly enhance our short and long term business prospects and shareholder value. As a player in the fast-growing pain management market, we would anticipate significant revenue opportunities already this year."

Recent Strategic Development

As previously announced, on March 4, 2020, the Company entered into a commercial binding Letter Of Intent (LOI) with Canndoc Ltd, a leading pharma grade medical cannabis pioneer and a wholly owned subsidiary of publicly-traded Intercure Ltd. (TASE: INCR),to acquire from Canndoc all rights to the use and sell Canndoc products for the reduction of opioid usage, including accumulated data, as well as on-going and pipeline of clinical trials. This commercial arrangement is subject to negotiation and approval by each company's board of directors and definitive agreements.

Additionally, the two companies signed a non-binding LOI for a full merger. Under preliminary details, Cellect will acquire from Intercure all of Canndoc outstanding shares, in exchange for additional Cellect ADRs to be in total ~95% (~93% on a fully diluted basis) of the merged company. The proposed merger is subject to independent valuation of both companies, fairness opinion by a third party, negotiation of a definitive agreement, approval of the agreement by the Company's Board of Directors and shareholders, internal approvals by Canndoc and Intercure, and customary closing conditions, including the approval of the IMCA (Israeli Medical Cannabis Agency). Upon the closing of the merger, Cellect and Canndoc will aim to fulfill all of the requirements to ensure the Company's ADRs and warrants continue trading on the Nasdaq Stock Market (Nasdaq) and, for this purpose, Intercure would commit to invest a cash sum of at least $3.0 million in any public offering that is undertaken by the Company, at a price of not less than $4.50 per ADR.

Based on the progress to date, the Company continues to expect the commercial and merger transactions will close in the second quarter of 2020.

Additional Operating Highlights:

Clinical Progress Update:

Due to the ongoing COVID-19 pandemic, the Company is experiencing clinical disruption such as:

The Company continues to take all the necessary precautions advised by global health officials to ensure the health and safety of its employees and partners. The Company is unaware of any impact on employees from pandemic related exposure or illness and is continuing to perform in-house research, including in the opioid/pain management area.

Fourth Quarter and Full Year 2019 Financial Results:

Balance Sheet Highlights:

For the convenience of the reader, the amounts have been translated from NIS into U.S. dollars, at the representative rate of exchange on December 31, 2019 (U.S. $1 = NIS 3.456).

About Cellect Biotechnology Ltd.

Cellect Biotechnology (NASDAQ: APOP) has developed a breakthrough technology, for the selection of stem cells from any given tissue, that aims to improve a variety of stem cell-based therapies.

The Company's technology is expected to provide researchers, clinical community and pharma companies with the tools to rapidly isolate stem cells in quantity and quality allowing stem cell-based treatments and procedures in a wide variety of applications in regenerative medicine. The Company's current clinical trial is aimed at bone marrow transplantations in cancer treatment.

Forward Looking Statements

This press release contains forward-looking statements about the Company's expectations, beliefs and intentions. Forward-looking statements can be identified by the use of forward-looking words such as "believe", "expect", "intend", "plan", "may", "should", "could", "might", "seek", "target", "will", "project", "forecast", "continue" or "anticipate" or their negatives or variations of these words or other comparable words or by the fact that these statements do not relate strictly to historical matters. For example, forward-looking statements are used in this press release when we discuss Cellect's intent regarding the future potential of Cellect's technology. These forward-looking statements and their implications are based on the current expectations of the management of the Company only and are subject to a number of factors and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. In addition, historical results or conclusions from scientific research and clinical studies do not guarantee that future results would suggest similar conclusions or that historical results referred to herein would be interpreted similarly in light of additional research or otherwise. The following factors, among others, could cause actual results to differ materially from those described in the forward-looking statements: the Company's history of losses and needs for additional capital to fund its operations and its inability to obtain additional capital on acceptable terms, or at all; the Company's ability to continue as a going concern; uncertainties of cash flows and inability to meet working capital needs; the Company's ability to obtain regulatory approvals; the Company's ability to obtain favorable pre-clinical and clinical trial results; the Company's technology may not be validated and its methods may not be accepted by the scientific community; difficulties enrolling patients in the Company's clinical trials; the ability to timely source adequate supply of FasL; risks resulting from unforeseen side effects; the Company's ability to establish and maintain strategic partnerships and other corporate collaborations; the scope of protection the Company is able to establish and maintain for intellectual property rights and its ability to operate its business without infringing the intellectual property rights of others; competitive companies, technologies and the Company's industry; unforeseen scientific difficulties may develop with the Company's technology; and the Company's ability to retain or attract key employees whose knowledge is essential to the development of its products. Any forward-looking statement in this press release speaks only as of the date of this press release. The Company undertakes no obligation to publicly update or review any forward-looking statement, whether as a result of new information, future developments or otherwise, except as may be required by any applicable securities laws. More detailed information about the risks and uncertainties affecting the Company is contained under the heading "Risk Factors" in Cellect Biotechnology Ltd.'s Annual Report on Form 20-F for the fiscal year ended December 31, 2019 filed with the U.S. Securities and Exchange Commission, or SEC, which is available on the SEC's website, http://www.sec.gov, and in the Company's periodic filings with the SEC.

Cellect Biotechnology Ltd

Consolidated Statement of Operation

Convenience

translation

Twelvemonths

ended

Twelve months ended

Three months ended

December 31,

December 31,

December 31,

2019

2019

2018

2019

2018

Unaudited

Audited

Audited

Unaudited

Unaudited

U.S. dollars

NIS

(In thousands, except share and pershare data)

Research and development expenses

3,508

12,122

13,513

2,571

4,040

General and administrative expenses

2,954

10,210

15,734

2,378

4,733

Operating loss

6,462

22,332

29,247

4,949

8,773

Financial expenses (income) due towarrants exercisable into ADS

(2,032)

(7,022)

(7,719)

998

(4,784)

Other financial expenses (income), net

433

1,498

(1,415)

129

(238)

Total comprehensive loss

4,863

16,808

20,113

6,076

3,751

Loss per share:

Basic and diluted loss per share

0.023

0.079

0.155

0.027

0.029

Weighted average number of sharesoutstanding used to compute basic anddiluted loss per share

212,642,505

212,6432,505

129,426,091

224,087,799

130,274,953

Cellect Biotechnology Ltd

Consolidated Balance Sheet Data

ASSETS

Convenience

translation

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Cellect Biotechnology Reports Fourth Quarter and Full Year 2019 Results - BioSpace

There are countless reason to get interested in these stocks: :Vir Biotechnology, Inc., (NASDAQ: VIR) – News Align

On Monday, Shares ofVir Biotechnology, Inc., (NASDAQ: VIR), inclined/declined 36.70% and closed at $26.55 in the last trading session.

Arithmetic Moving Averages VIR:

Simple Moving Average (SMA) is easy to calculate and SMA20 one is principally looking at prime trends. The 50-day moving average is more responsive to price changes than the 200-day moving Whereas long-term trend followers generally use SMA200 and most shareholders will look for a cross up or down this average to means if the stock is in a bullish or bearish trend. SMA20 is the last stop on the bus for (ST) short-term traders. The Vir Biotechnology, Inc. having its distance from 20-days simple moving average is -0.26%, and its distance from 50-days simple moving average is 19.04%, while it has a distance of 77.29% from the 200-days simple moving average.

Working over theproductivity proportionsof business stock, the speculator will discover its ROE, ROA, ROI remaining at 0.00%, 0.00% and -41.90%, individually.

ATR remains at 8.38 while Beta component of the stock stands at 0.00. The beta component is used to check the eccentrics of the stock. The VIR stock remained 3.38% unpredictable for the week and -19.69% for the month.

Market capitalization is only an extravagant proclaim for a bright idea: it is the market estimation of an organizations remarkable offers. These Amount and numbers are found by taking the postscript cost and increasing it by the all outnumber of offers remarkable. Understanding the market top isnt merely sign if you nearly putting legitimately in stocks. It is additionally helpful for common reserve speculators, the same number of assets will list the normal or middle showcase capitalization of its property. As the name recommends, this gives the centre-ground of the stores value speculations, filling financial specialists in as to whether the reserve, for the most part, puts resources into large, mid-or little top stocks.

Vir Biotechnology, Inc.Target:

The EPS of the company is strolling at -5.76. The companys Market capitalization is $4.07BBillion.

As stocks have aP/S,P/EandP/Bestimations of 501.93, 0.00 and 1.16 separately. Its P/Cash is esteemed at 10.60.

Development in profit per offer is everything. The healthy future development in profit per share (EPS) is an amazingly significant factor in recognizing an underestimated stock. The effect of income development is exponential. As time goes on, the cost of a stock will typically go up in lockstep with its income (accepting the P/E proportion is steady). Hence stocks with higher profit development should offer the most elevated capital increases. Whats more, doubling-up the growth more than doubles the capital gain, due to the compounding effect.

Volume & Average Volume Shares:

Volume of the Vir Biotechnology, Inc. exchanged hands with 3694738 shares compared to its average daily volume of 815.24K shares. Total volume is the number of shares or deals that point towards the whole activity of a security or market for a same period.

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There are countless reason to get interested in these stocks: :Vir Biotechnology, Inc., (NASDAQ: VIR) - News Align

GE renamed Cytiva upon take-over by Danaher – European Biotechnology

The acquisition of GE Healthcare Life Sciences by Danaher Corporation creates a giant in contract manufacturing and development. While GE Healthcare Life Sciences, will retain its 7,000 staff and multinational operations, the company will change its name to Cytiva, combining its well-known brands and offerings KTA, Amersham, HyClone, MabSelect or Whatman with its new mother companys platform.

The mission of the newly created CDMO, which is set to generate US$3.3bn in annual revenues, is to grow in the expanding biologicals market. Emmanuel Ligner, President of Cytiva, said, "Our commitment remains to provide patients with life-changing therapies and we will continue to bring innovative technologies to market that improve our customers' productivity. The CDMO will not only help companies help outsource their biologics production but also intends to provide services to the scientific community.

According to Danaher, in 2019, more than 75% of FDA-approved biological therapies relied on Cytiva technology for manufacturing including the emerging cell and gene therapy market, a field conducting more than 1,000 regenerative medicine studies at global scale.

As the global demand for personalised medicines, and advanced biological therapies continues to grow, the company will rely on its huge capabilities in instrumentation, cell line and process development together with effective production and purification technologies. Cytiva announced it will continue to drive research collaborations, including with the Center for Advanced Biological Innovation and Manufacturing in Boston, Harvard, MIT, university hospitals and industry partners such as Fujifilm Diosynth Biotechnologies and Alexandria Real Estate Equities Inc.Cytiva's broad portfolio includes well-known brands such as KTA, Amersham, Biacore, FlexFactory, HyClone, MabSelect, Sefia, Whatman, Xcellerex and Xuri.

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GE renamed Cytiva upon take-over by Danaher - European Biotechnology

Animal Biotechnology Market Size Analysis, Top Manufacturers, Shares, Growth Opportunities and Forecast to 2026 – Science In Me

New Jersey, United States: Market Research Intellect has added a new research report titled, Animal Biotechnology Market Professional Survey Report 2020 to its vast collection of research reports. The Animal Biotechnology market is expected to grow positively for the next five years 2020-2026.

The Animal Biotechnology market report studies past factors that helped the market to grow as well as, the ones hampering the market potential. This report also presents facts on historical data from 2011 to 2019 and forecasts until 2026, which makes it a valuable source of information for all the individuals and industries around the world. This report gives relevant market information in readily accessible documents with clearly presented graphs and statistics. This report also includes views of various industry executives, analysts, consultants, and marketing, sales, and product managers.

Market Segment as follows:

The global Animal Biotechnology Market report highly focuses on key industry players to identify the potential growth opportunities, along with the increased marketing activities is projected to accelerate market growth throughout the forecast period. Additionally, the market is expected to grow immensely throughout the forecast period owing to some primary factors fuelling the growth of this global market. Finally, the report provides detailed profile and data information analysis of leading Animal Biotechnology company.

Animal Biotechnology Market by Regional Segments:

The chapter on regional segmentation describes the regional aspects of the Animal Biotechnology market. This chapter explains the regulatory framework that is expected to affect the entire market. It illuminates the political scenario of the market and anticipates its impact on the market for Animal Biotechnology .

The Animal Biotechnology Market research presents a study by combining primary as well as secondary research. The report gives insights on the key factors concerned with generating and limiting Animal Biotechnology market growth. Additionally, the report also studies competitive developments, such as mergers and acquisitions, new partnerships, new contracts, and new product developments in the global Animal Biotechnology market. The past trends and future prospects included in this report makes it highly comprehensible for the analysis of the market. Moreover, The latest trends, product portfolio, demographics, geographical segmentation, and regulatory framework of the Animal Biotechnology market have also been included in the study.

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Table of Content

1 Introduction of Animal Biotechnology Market1.1 Overview of the Market1.2 Scope of Report1.3 Assumptions

2 Executive Summary

3 Research Methodology3.1 Data Mining3.2 Validation3.3 Primary Interviews3.4 List of Data Sources

4 Animal Biotechnology Market Outlook4.1 Overview4.2 Market Dynamics4.2.1 Drivers4.2.2 Restraints4.2.3 Opportunities4.3 Porters Five Force Model4.4 Value Chain Analysis

5 Animal Biotechnology Market, By Deployment Model5.1 Overview

6 Animal Biotechnology Market, By Solution6.1 Overview

7 Animal Biotechnology Market, By Vertical7.1 Overview

8 Animal Biotechnology Market, By Geography8.1 Overview8.2 North America8.2.1 U.S.8.2.2 Canada8.2.3 Mexico8.3 Europe8.3.1 Germany8.3.2 U.K.8.3.3 France8.3.4 Rest of Europe8.4 Asia Pacific8.4.1 China8.4.2 Japan8.4.3 India8.4.4 Rest of Asia Pacific8.5 Rest of the World8.5.1 Latin America8.5.2 Middle East

9 Animal Biotechnology Market Competitive Landscape9.1 Overview9.2 Company Market Ranking9.3 Key Development Strategies

10 Company Profiles10.1.1 Overview10.1.2 Financial Performance10.1.3 Product Outlook10.1.4 Key Developments

11 Appendix11.1 Related Research

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Tags: Animal Biotechnology Market Size, Animal Biotechnology Market Growth, Animal Biotechnology Market Forecast, Animal Biotechnology Market Analysis, Animal Biotechnology Market Trends, Animal Biotechnology Market

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Animal Biotechnology Market Size Analysis, Top Manufacturers, Shares, Growth Opportunities and Forecast to 2026 - Science In Me

Airbus and Koniku Inc. team on biotechnology solutions for aviation security operations – Intelligent Aerospace

TOULOUSE, France - Airbus and Koniku Inc. have made a significant step forward in the co-development of a solution for aircraft and airport security operations, by extending research activities to include biological hazard detection capabilities, as well as chemical and explosive threats.

The disruptive biotechnology solution, which was originally focused on the contactless and automated detection, tracking and location of chemicals and explosives on-board aircraft and in airports, is now being adapted, in light of the COVID-19 crisis, to include the identification of biological hazards.

Based on the power of odor detection and quantification found in nature, the technical solution, developed to meet the rigorous operational regulatory requirements of aircraft and airport security operations, uses genetically engineered odorant receptors that produce an alarm signal when they come into contact with the molecular compounds of the hazard or threat that they have been programmed to detect.

Airbus and Koniku Inc. entered into a cooperation agreement in 2017, leveraging Airbus expertise in sensor integration and knowledge of ground and on-board security operations within the aviation and defense industries as well as Konikus biotechnology know-how for automated and scalable volatile organic compound detection (via their Konikore platform).

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Airbus and Koniku Inc. team on biotechnology solutions for aviation security operations - Intelligent Aerospace

Bayer, Novartis, and Trump convicted by Nature – European Biotechnology

The politically overhyped use of old malaria drugs in combination with COVID-19-specific candidates has been demonstrated to be dangerous, reports Nature Medicine.

In the prestigous paper Nature Medicine, cardiologists under Lior Jankelson report that patients with COVID-19 who were on a regimen of Novartis AGs generic malaria drug hydroxychloroquine and the antibiotic azithromycin experienced electrocardiogram abnormalities. Previous reports demonstrated that the same is true for chloroquine phosphate, an old malaria drug originally developed at Bayer AG. The authorsassessed 84 patients with COVID-19 treated at a centre in New York, USA.

Azithromycin in combination with antimalarial hydroxychloroquine has been touted by President Donald Trump as a possible "game changer" in COVID-19. Former BARDA head Rick Bright was fired because he resisted political interventions to push the use of chloroquine derivatives to treat COVID-19 despite scientific evidence of efficacy and safety according to current authorisation standards. Biocentury reported previously that Trumps preference for the cheap but antiquated malaria treatments looked more like political science than actually based on scientific evidence. Several clinical programmes coordinated by the WHO , the European Union, and the UK promote clinical testing of combinations with either chloroquine phosphate or hydroxychloroquine and may cause thousands of deaths unless they were not updated to include new findings.

Several reports demonstrated that both medications increase the risk of various types of cardiac rhythm abnormalities, such as QTc-interval prolongation and drug-inducedtorsades de pointes, and sudden cardiac death. The QTc interval is measured by an electrocardiogram and represents the time it takes for a heart to recharge between beats. A prolonged QTc interval puts a patient at risk for arrhythmia and sudden cardiac death.

Now, Jankelson and colleagues reviewed the charts and followed the QTc interval of 84 patients with COVID-19 on a 5-day oral regiment of hydroxychloroquine and azithromycin. The patients were, on average, 63 years of age and74% were male. After the patients were administered the drugs, the authors followed up with an electrocardiogram. They observed a prolonged QTc in most patients. The QTc was severely prolonged in 11% of the patients, which put them at high risk of arrhythmia and sudden cardiac death. Four patients in the cohort died from multiple organ failure a characteristic of septic shock without evidence of arrhythmia and without severe QTc prolongation.

Jankelson and colleagues found that most patients with COVID-19 who were treated with hydroxychloroquine and azithromycin experienced QTc prolongation. This may have been exacerbated by other pre-existing conditions and the severity of the SARS-CoV-2 infection. The authors conclude that the QTc in patients with COVID-19 who are treated with hydroxychloroquine and azithromycin should be monitored constantly, especially for patients with additional illnesses and those who are being treated with other QT-prolonging medications.

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Bayer, Novartis, and Trump convicted by Nature - European Biotechnology

Biotechnology Industry: Does Cara Therapeutics Inc (CARA) Stock Beat its Rivals? – InvestorsObserver

The 75 rating InvestorsObserver gives to Cara Therapeutics Inc (CARA) stock puts it near the top of the Biotechnology industry. In addition to scoring higher than 87 percent of stocks in the Biotechnology industry, CARAs 75 overall rating means the stock scores better than 75 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.

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.

Cara Therapeutics Inc (CARA) stock is trading at $15.81 as of 11:14 AM on Wednesday, Apr 22, a rise of $0.39, or 2.53% from the previous closing price of $15.42. The stock has traded between $15.29 and $16.44 so far today. Volume today is below average. So far 328,715 shares have traded compared to average volume of 541,813 shares.

To see InvestorsObserver's Sentiment Score for Cara Therapeutics Inc click here.

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Biotechnology Industry: Does Cara Therapeutics Inc (CARA) Stock Beat its Rivals? - InvestorsObserver

Nanoparticles in Biotechnology and Pharmaceuticals Market Overview by 2026: Verified Market Research Cole Reports – Cole of Duty

Shire

Global Nanoparticles in Biotechnology and Pharmaceuticals Market Segmentation

This market was divided into types, applications and regions. The growth of each segment provides an accurate calculation and forecast of sales by type and application in terms of volume and value for the period between 2020 and 2026. This analysis can help you develop your business by targeting niche markets. Market share data are available at global and regional levels. The regions covered by the report are North America, Europe, the Asia-Pacific region, the Middle East, and Africa and Latin America. Research analysts understand the competitive forces and provide competitive analysis for each competitor separately.

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Global Nanoparticles in Biotechnology and Pharmaceuticals Market Regions and Countries Level Analysis

The regional analysis is a very complete part of this report. This segmentation highlights Nanoparticles in Biotechnology and Pharmaceuticals sales at regional and national levels. This data provides a detailed and accurate analysis of volume by country and an analysis of market size by region of the world market.

The report provides an in-depth assessment of growth and other aspects of the market in key countries such as the United States, Canada, Mexico, Germany, France, the United Kingdom, Russia and the United States Italy, China, Japan, South Korea, India, Australia, Brazil and Saudi Arabia. The chapter on the competitive landscape of the global market report contains important information on market participants such as business overview, total sales (financial data), market potential, global presence, Nanoparticles in Biotechnology and Pharmaceuticals sales and earnings, market share, prices, production locations and facilities, products offered and applied strategies. This study provides Nanoparticles in Biotechnology and Pharmaceuticals sales, revenue, and market share for each player covered in this report for a period between 2016 and 2020.

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We offer state of the art critical reports with accurate information about the future of the market.

Our reports have been evaluated by some industry experts in the market, which makes them beneficial for the company to maximize their return on investment.

We provide a full graphical representation of information, strategic recommendations and analysis tool results to provide a sophisticated landscape and highlight key market players. This detailed market assessment will help the company increase its efficiency.

The dynamics of supply and demand shown in the report offer a 360-degree view of the market.

Our report helps readers decipher the current and future constraints of the Nanoparticles in Biotechnology and Pharmaceuticals market and formulate optimal business strategies to maximize market growth.

Table of Contents:

Study Coverage: It includes study objectives, years considered for the research study, growth rate and Nanoparticles in Biotechnology and Pharmaceuticals market size of type and application segments, key manufacturers covered, product scope, and highlights of segmental analysis.

Executive Summary: In this section, the report focuses on analysis of macroscopic indicators, market issues, drivers, and trends, competitive landscape, CAGR of the global Nanoparticles in Biotechnology and Pharmaceuticals market, and global production. Under the global production chapter, the authors of the report have included market pricing and trends, global capacity, global production, and global revenue forecasts.

Nanoparticles in Biotechnology and Pharmaceuticals Market Size by Manufacturer: Here, the report concentrates on revenue and production shares of manufacturers for all the years of the forecast period. It also focuses on price by manufacturer and expansion plans and mergers and acquisitions of companies.

Production by Region: It shows how the revenue and production in the global market are distributed among different regions. Each regional market is extensively studied here on the basis of import and export, key players, revenue, and production.

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Analysts with a high level of expertise in data collection and governance use industrial techniques to collect and analyze data in all phases. Our analysts are trained to combine modern data collection techniques, superior research methodology, expertise and years of collective experience to produce informative and accurate research reports.

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Tags: Nanoparticles in Biotechnology and Pharmaceuticals Market Size, Nanoparticles in Biotechnology and Pharmaceuticals Market Trends, Nanoparticles in Biotechnology and Pharmaceuticals Market Forecast, Nanoparticles in Biotechnology and Pharmaceuticals Market Growth, Nanoparticles in Biotechnology and Pharmaceuticals Market Analysis

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Nanoparticles in Biotechnology and Pharmaceuticals Market Overview by 2026: Verified Market Research Cole Reports - Cole of Duty

Is SAGE Therapeutics Inc (SAGE) Stock Near the Top of the Biotechnology Industry? – InvestorsObserver

A rating of 18 puts SAGE Therapeutics Inc (SAGE) near the bottom of the Biotechnology industry according to InvestorsObserver. SAGE Therapeutics Inc's score of 18 means it scores higher than 18% of stocks in the industry. SAGE Therapeutics Inc also received an overall rating of 35, putting it above 35% of all stocks. Biotechnology is ranked 10 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.

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.

SAGE Therapeutics Inc (SAGE) stock is trading at $38.00 as of 1:22 PM on Friday, Apr 24, a rise of $1.76, or 4.86% from the previous closing price of $36.24. The stock has traded between $35.62 and $38.03 so far today. Volume today is light. So far 545,172 shares have traded compared to average volume of 1,562,765 shares.

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Is SAGE Therapeutics Inc (SAGE) Stock Near the Top of the Biotechnology Industry? - InvestorsObserver

FDA Clears the Way for Ridgeback Biotherapeutics to begin Human Testing of a Promising Potential Treatment for COVID-19 – BioSpace

EIDD-2801, an oral broad-spectrum antiviral proceeding into Clinical Trials

ATLANTA and MIAMI, April 6, 2020 /PRNewswire/ -- Ridgeback Biotherapeutics LP, a closely held biotechnology company, and Drug Innovations at Emory (DRIVE), LLC, a not-for-profit biotechnology company wholly owned by Emory University, today announced that the U.S. Food and Drug Administration (FDA) has approved an Investigational New Drug application by Drug Innovation Ventures at Emory (DRIVE), LLC, wholly owned by Emory University, for an orally available antiviral compound, EIDD-2801, exclusively licensed to Ridgeback Biotherapeutics, LP (Ridgeback), a closely held biotechnology company. This action by the FDA allows Ridgeback to initiate human clinical testing of EIDD-2801 in the United States.

"We are thankful to FDA Commissioner Dr. Steven Hahn and his team at the Anti-Viral Division for the unprecedented speed in reviewing our submission, the guidance and the highly collaborative process that ensures this promising drug can advance into the clinical development as fast as possible," said Wendy Holman, Chief Executive Officer of Ridgeback. "We also appreciate the guidance we have received from the Assistant Secretary of Preparedness and Response (ASPR), including discussions that occurred months before COVID-19 first emerged, to help Emory/DRIVE advance the development of EIDD-2801 as quickly as possible to address this global pandemic."

EIDD-2801 prevents the replication of SARS-CoV-2, the virus that causes COVID-19, and has shown potent activity against SARS-CoV and MERS-CoV in animal models of infection. In addition to coronaviruses, EIDD-2801 has broad spectrum activity against a number of diseases of public health concern, including influenza, chikungunya, Ebola, and equine encephalitis (VEE and EEE). The antiviral is orally available and, in addition to COVID-19, is being developed for the treatment of seasonal and pandemic influenza under a contract awarded to Emory Institute for Drug Development by the National Institute of Allergy and Infectious Diseases (NIAID) and for Venezuelan and Eastern equine encephalitis virus (VEEV and EEEV) by the Defense Threat Reduction Agency (DTRA).

"FDA's prompt approval of our IND allows us to initiate human testing for EIDD-2801 as quickly as possible," says George Painter, Ph.D., director of the Emory Institute for Drug Development (EIDD) and CEO of DRIVE. "We are grateful to our collaborators for helping us to assemble this application quickly, and to the FDA for expediting the process. An orally available antiviral medication would be a critical weapon for fighting COVID-19."

Ridgeback and DRIVE have established a partnership to advance EIDD-2801 through clinical development and to optimize availability during the current COVID-19 pandemic. EIDD-2801 was exclusively licensed to Ridgeback in March 2020.

"We look forward to our continued work with the highly experienced drug development team at DRIVE and the dedicated medical, public health and governmental personnel who are on the frontlines of this pandemic in the United States and abroad," says Wendy Holman, CEO of Ridgeback Biotherapeutics. "The ability to deliver promising treatments to patients in need is what makes us excited to come to work every day. Ridgeback brings its unique perspective, honed by our success developing an Ebola therapeutic during the 2018-2020 outbreak in the DR Congo, to help advance EIDD-2801 for the treatment of diseases that are critical to pandemics and global health."

About EIDD-2801:

EIDD-2801 is an orally bioavailable form of a highly potent ribonucleoside analog that inhibits the replication of multiple RNA viruses including SARS-CoV-2, the causative agent of COVID-19. In animal studies of two distinct coronaviruses (SARS-CoV1 and MERS), EIDD-2801 has been shown to improve pulmonary function, decrease body weight loss and reduce the amount of virus in the lung. In addition to activity against coronaviruses, EIDD-2801, in laboratory studies, has demonstrated activity against seasonal and bird influenza, respiratory syncytial virus, chikungunya virus, Ebola virus, Venezuelan equine encephalitis virus, and Eastern equine encephalitis virus. The development of EIDD-2801 has been funded in part with Federal funds from the National Institute of Allergy and Infectious Diseases (NIAID), under contract numbers HHSN272201500008C and 75N93019C00058, and from the Defense Threat Reduction Agency (DTRA), under contract numbers HDTRA1-13-C-0072 and HDTRA1-15-C-0075.

About Ridgeback Biotherapeutics LP:

Headquartered in Miami, Florida, Ridgeback Biotherapeutics is a privately held, majority woman-owned biotechnology company focused on orphan and infectious diseases. Initial funding for Ridgeback Biotherapeutics originated from Wayne and Wendy Holman; two individuals committed to investing in and supporting technologies that will make the world a better place. The team at Ridgeback is dedicated to working toward finding life-saving and life-changing solutions for patients and diseases that need champions. Ridgeback is in the process of completing a Biologics Licensing Application with the Food & Drug Administration for mAb114 (ansuvimab) for the treatment of Ebola. Ansuvimab development has been funded in whole or in part with Federal funds from the Department of Health and Human Services; Office of the Assistant Secretary for Preparedness and Response; Biomedical Advanced Research and Development Authority, under Contract No. 75A50119C00059 and 75A50120C0009.

About DRIVE:

DRIVE is a non-profit LLC wholly owned by Emory University and started as an innovative approach to drug development. Operating like an early stage biotechnology company, DRIVE applies focus and industry development expertise to efficiently translate discoveries to address viruses of global concern. DRIVE's mission is to discover and develop antiviral drugs for emerging infections, pandemic threats, and biodefense (e.g. COVID-19, swine flu, bird flu, dengue, chikungunya, Ebola, Zika, and viral encephalitis). Because these diseases are major threats, antiviral drugs are critically needed to treat them; however, they are generally not profitable enough for industry to pursue, and thus are considered neglected diseases. DRIVE is unique in that it brings industry expertise to the assets of a leading research University to develop potential antiviral drugs to a de-risked value inflection point that substantially increases the probability of the potential drug being licensed by industry and developed for the ultimate benefit of the public. DRIVE's executive team, led by George Painter, has over three decades of drug development experience within both large pharmaceutical and biotechnology companies, including leading the development of multiple FDA approved antivirals to treat HIV and Influenza, among other viral diseases, including AZT and Relenza.

About Defense Threat Reduction Agency:

The Defense Threat Reduction Agency (DTRA) was formally established on October 1, 1998. DTRA enables the Department of Defense, the United States Government and International partners to counter and deter weapons of mass destruction and improvised threat networks. As a Combat Support Agency and a Defense Agency, DTRA's mission is to counter the threats posed by the full spectrum of weapons of mass destruction (WMD), including chemical, biological, radiological, nuclear, and high-yield explosives; counter the threats posed by the growing, evolving categories of improvised threats, including improvised explosive devices, car bombs and weaponized consumer drones, as well as the tactics, technologies and networks that put them on the battlefield; and ensure the U.S. military maintains a safe, secure, effective and credible nuclear weapons deterrent.

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SOURCE Ridgeback Biotherapeutics LP

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FDA Clears the Way for Ridgeback Biotherapeutics to begin Human Testing of a Promising Potential Treatment for COVID-19 - BioSpace

Industry Breakdown: Where Does Trillium Therapeutics Inc (TRIL) Stock Fall in the Biotechnology Field? – InvestorsObserver

The 88 rating InvestorsObserver gives to Trillium Therapeutics Inc (TRIL) stock puts it near the top of the Biotechnology industry. In addition to scoring higher than 100 percent of stocks in the Biotechnology industry, TRILs 88 overall rating means the stock scores better than 88 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 88 would rank higher than 88 percent of all stocks.

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.

Trillium Therapeutics Inc (TRIL) stock is trading at $4.23 as of 1:51 PM on Monday, Apr 6, an increase of $0.57, or 15.57% from the previous closing price of $3.66. The stock has traded between $3.76 and $4.31 so far today. Volume today is less active than usual. So far 1,151,186 shares have traded compared to average volume of 3,800,958 shares.

To see InvestorsObserver's Sentiment Score for Trillium Therapeutics Inc click here.

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Industry Breakdown: Where Does Trillium Therapeutics Inc (TRIL) Stock Fall in the Biotechnology Field? - InvestorsObserver