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Global Cancer Stem Cell Therapy Market 2020: What Are The Key Trends In Market? – Chronicles 99

February 26th, 2020 8:42 pm

The latest version of the 2020 market study on Cancer Stem Cell Therapy Market comprising 97 with market data Tables, Charts, Graphs, and Figures which are easy to understand with showcased in-depth analysis.

The global Cancer Stem Cell Therapy market size is estimated at xxx million USD with a CAGR xx% from 2015-2019 and is expected to reach xxx Million USD in 2020 with a CAGR xx% from 2020 to 2025. The report begins from overview of Industry Chain structure, and describes industry environment, then analyses market size and forecast of Cancer Stem Cell Therapy by product, region and application, in addition, this report introduces market competition situation among the vendors and company profile, besides, market price analysis and value chain features are covered in this report.

Check out sample report at: https://www.amplemarketreports.com/sample-request/global-cancer-stem-cell-therapy-market-1351346.html

As per the research and study, the market has settled its presence worldwide. Cancer Stem Cell Therapy Market Research study offers a comprehensive evaluation of the Market and comprises a future trend, current growth factors, focused opinions, details, and industry certified market data.

Glancing to 2020, the global market expected to be a significant year for Cancer Stem Cell Therapy Market in terms of growth and revenue.

Almost all companies who are listed or profiled are being to upgrade their applications for end-user experience and setting up their permanent base in 2020. This report focused and concentrate on these companies including AVIVA BioSciences, AdnaGen, Advanced Cell Diagnostics, Silicon Biosystems.

Furthermore, the research contributes an in-depth overview of regional level break-up categorized as likely leading growth rate territory, countries with the highest market share in past and current scenario. Some of the geographical break-up incorporated in the study are AVIVA BioSciences, AdnaGen, Advanced Cell Diagnostics, Silicon Biosystems.

With the Cancer Stem Cell Therapy market forecast to expand CAGR% in 2020 and with X-X-X-X supposed to be a big beneficiary, it is better positioned than Z-Z-Z-Z for 2020.

According to the AMR market study, Recent trends in consumer preferences market segments such as type, application will be more challenging. Cancer Stem Cell Therapy market segment sales will traverse the $$ mark in 2020.

Unlike classified segments successful in the industry such as by Type (Autologous Stem Cell Transplants, Allogeneic Stem Cell Transplants, Syngeneic Stem Cell Transplants, Others) and by End-Users/Application (Hospital, Clinic, Medical Research Institution, Others).

The 2020 version of the Cancer Stem Cell Therapy market study is a further split down / narrowed to highlight the latest emerging twist of the industry.

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Due to a change in consumer preferences with a review on the latest sales and revenue report submissions, Major vendors in the Global market are trying to get the attention of end-users or consumers by Offerings and additional services.

With using the latest technology and analysis on demand-side, Key players are getting in consumer behavior and their changing preferences.

Again, big investment firms or giants are willing to put more capital to get a key players performance in the market for new applications or products.

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Research Objectives and Purpose

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Thanks for reading this article, you can also get individual chapter wise section or region wise report versions like North America, Western / Eastern Europe or Southeast Asia.

With the given market data, Research on Global Markets offers customizations according to specific needs. Write to AMR at sales@amplemarketreports.com, or connect via +1-530-868-6979

About Author

Ample Market Research provides comprehensive market research services and solutions across various industry verticals and helps businesses perform exceptionally well. Our end goal is to provide quality market research and consulting services to customers and add maximum value to businesses worldwide. We desire to delivery reports that have the perfect concoction of useful data. Our mission is to capture every aspect of the market and offer businesses a document that makes solid grounds for crucial decision making.

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Global Cancer Stem Cell Therapy Market 2020: What Are The Key Trends In Market? - Chronicles 99

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R3 Stem Cell Heroes Program Performs Complimentary Regenerative Therapies on 70 Veterans in 2019 – PR Web

February 26th, 2020 8:42 pm

R3 Stem Cell Heroes Program - Free Regenerative Procedures for Veterans

LAS VEGAS (PRWEB) February 20, 2020

R3 Stem Cell, the nation's leader in regenerative therapies and provider training, announced that its Heroes Program was able to complete 70 complimentary stem cell procedures on military veterans in 2019. The veterans traveled from all over the US to receive the regenerative therapies at no cost.

At the R3Stem Cell Training Course for doctors, providers of all kinds learn how to perform regenerative procedures in a supervised setting. This includes stem cell and exosome procedures on military veterans of all ages and from all branches of service. Any veteran can be nominated (or nominate themselves), and the pain being experienced does not have to be a result of a service related injury.

According to R3 Stem Cell CEO David Greene, MD, MBA, "When we hear the stories of these Veterans and what they have done for America, it's so exciting to be able to do something to help improve their quality of life. Especially Veterans of the Vietnam War, all they wanted to do was protect our country. To see how well they do afterwards and then refer in their Veteran friends for procedures, it's amazing!"

The chosen Veterans receive an evaluation by the Board Certified doctors who are trainers, and then procedures include whatever amount of regenerative biologic deemed appropriate. The Veteran patients are followed up the R3 staff, and invited back for additional therapies when necessary.

To date over 70 Veterans have successfully receive regenerative therapies in the program. Over a dozen patients are treated at each workshop, with more opportunities upcoming. Added Dr. Greene, "Our stem cell courses are extremely hands on an providers love it. They have been increasing in popularity continuously, which allows us to treat more Veterans!"

For those who would like to nominate a Veteran for the Heroes Program to receive free stem cell therapy, simply visit https://r3stemcell.com/hero or call (844) GET-STEM.

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Radiation, Inflammation and Triple-Negative Breast Cancer: A Study – OncoZine

February 26th, 2020 8:41 pm

Although radiation is successfully used to treat breast cancer, inflammation caused as a side-effect of radiation may have an adverse effect, promoting the survival of triple-negative breast cancer cells.

This is the conclusion of a study by Jennifer Sims-Mourtada, Ph.D., director of Translational Breast Cancer Research at ChristianaCares Helen F. Graham Cancer Center & Research Institute, published online in the International Journal of Radiation Biology.[1]

Triple-negative breast cancer is cancer that tests negative for estrogen receptors, progesterone receptors, and excess human epidermal growth factor receptor 2 (HER2) protein. As a result, the growth of this cancer is not fueled by the hormones estrogen and progesterone, or by the HER2 protein. These cancers tend to be more common in women under age 40, who are African-American, Latina, or who carry a mutated BRCA1 gene.

Triple-negative breast cancer accounts for 15-20% of all breast cancers and is faster growing than other types of breast cancers.

Sims-Mourtadas latest study helps scientists to better understand the mechanisms behind the development of this aggressive and hard-to-treat cancer. It shows that inflammation caused by radiation can trigger stem-cell-like characteristics in non-stem breast cancer cells.[1]

The good and the badThis is the good and the bad of radiation, Sims-Mourtada noted. We know radiation-induced inflammation can help the immune system to kill tumor cells thats good but also it can protect cancer stem cells in some cases, and thats bad.

Whats exciting about these findings is were learning more and more that the environment the tumor is in its microenvironment is very important. Historically, research has focused on the genetic defects in the tumor cells. Were now also looking at the larger microenvironment and its contribution to cancer, she added.

My work focuses on cancer stem cells and their origination. [These cells] exist in many cancers, but theyre particularly elusive in triple-negative breast cancer. Their abnormal growth capacity and survival mechanisms make them resistant to radiation and chemotherapy and help drive tumor growth, Sims-Mourtada explained.

The researchers applied radiation to triple-negative breast cancer stem cells and to non-stem cells. In both cases, they found radiation-induced an inflammatory response that activated the Il-6/Stat3 pathway, which plays a significant role in the growth and survival of cancer stem cells in triple-negative breast cancers. They also found that inhibiting STAT3 blocks the creation of cancer stem cells. As yet unclear is the role IL-6/STAT3 plays in transforming a non-stem cell to a stem-cell.

DelawareFor women living in Delaware, Sims-Mourtadas research is especially urgent: The rates of triple-negative breast cancer in the state are the highest nationwide.

At ChristianaCare, we are advancing cancer research to help people in our community today, while we also advance the fight against cancer nationwide, said Nicholas J. Petrelli, M.D., Bank of America endowed medical director of the Helen F. Graham Cancer Center & Research Institute.

Sims-Mourtadas research is a dramatic step toward better treatments for triple-negative breast cancer, Petrelli concluded.

To advance her research on inflammation, last year Sims-Mourtada received a US $ 659,538 grant from the Lisa Dean Moseley Foundation. The three-year grant will enable her and her team at the Cawley Center for Translational Cancer Research to continue investigating the role of cells immediately around a tumor in spurring the growth of triple-negative breast cancer and possible therapy for this particularly difficult to treat cancer.

Our next step is to understand the inflammatory response and how we might inhibit it to keep new cancer stem cells from developing, Sims-Mourtada said.

The researchers previously identified an anti-inflammatory drug, currently used to treat rheumatoid arthritis, that has the potential to target and inhibit the growth of cancer stem cells and triple-negative breast cancer tumors. That research could set the stage for clinical investigation of the drug, alone or in combination with chemotherapy, to improve outcomes for patients with triple-negative breast cancer.

Reference[1] Arnold KM, Opdenaker LM, Flynn NJ, Appeah DK, Sims-Mourtada J. Radiation induces an inflammatory response that results in STAT3-dependent changes in cellular plasticity and radioresistance of breast cancer stem-like cells [published online ahead of print, 2020 Jan 6]. Int J Radiat Biol. 2020;114. doi:10.1080/09553002.2020.1705423 [Pubmed][Article]

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Radiation, Inflammation and Triple-Negative Breast Cancer: A Study - OncoZine

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Top 5 AJMC Stories of the Week: February 22, 2020 – AJMC.com Managed Markets Network

February 26th, 2020 8:41 pm

The most popular stories of the week onAJMC.

The journalOncogenerecently publishedresultsof an investigation into the drivers behind triple-negativebreast cancer. Because the disease has such high recurrence and low survival rates, investigators from Manchester, Glasgow, and Sheffield universities sought to better understand what triggers, and arrests, the growth of this subtype of breast cancer.

Stem Cells Prove Effective in Treating MS Neural Damage

Several clinical trials have found mesenchymal stem cell therapy effective in treating neural damage in patients with multiple sclerosis (MS), according to a review published inStem Cell Investigation.

Youth Newly Diagnosed With HIV Have Advanced Infection, Higher Viral Loads

Close to 80% of HIV-positive individuals are shown to be virally suppressed through their most recent test results, according to data from 2016 through 2018, as well as 32% to 63% of adults older than 24 years. Youth with a new HIV diagnosis, however, come in at only 12%.

DC Circuit Panel Rejects Arkansas Medicaid Work Rules

Writing for the panel, Judge David Sentelle said HHS Secretary Alex Azar ignored predictions that thousands of people would lose their healthcare coverage.

Much of MS Cost Burden Falls on Patients' Shoulders

A British study shows nonmedical costs make up a significant portion of the annual expense generated by MS. Most of those nonmedical costs are not covered by insurance.

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Magenta Therapeutics to Participate in Cowen Health Care Conference on Monday, March 2nd in Boston – Yahoo Finance

February 26th, 2020 8:41 pm

Magenta Therapeutics (NASDAQ: MGTA), a clinical-stage biotechnology company developing novel medicines to bring the curative power of immune reset to more patients, today announced that the company is scheduled to participate in a fireside chat at the 40th annual Cowen Health Care Conference on Monday, March 2nd, 2020, at 4:10 p.m. ET at the Boston Marriott Copley Place.

A live webcast of the fireside chat can be accessed on the Magenta Therapeutics website at https://investor.magentatx.com/events-and-presentations. The webcast replay will be available for 90 days following the event.

About Magenta TherapeuticsMagenta Therapeutics is a clinical-stage biotechnology company developing medicines to bring the curative power of immune system reset through stem cell transplant to more patients with autoimmune diseases, genetic diseases and blood cancers. Magenta is combining leadership in stem cell biology and biotherapeutics development with clinical and regulatory expertise, a unique business model and broad networks in the stem cell transplant world to revolutionize immune reset for more patients.

Magenta is based in Cambridge, Mass. For more information, please visit http://www.magentatx.com.

Follow Magenta on Twitter: @magentatx.

Forward-Looking StatementThis press release may contain forward-looking statements and information within the meaning of The Private Securities Litigation Reform Act of 1995 and other federal securities laws. The use of words such as "may," "will," "could", "should," "expects," "intends," "plans," "anticipates," "believes," "estimates," "predicts," "projects," "seeks," "endeavor," "potential," "continue" or the negative of such words or other similar expressions can be used to identify forward-looking statements. The express or implied forward-looking statements included in this press release are only predictions and are subject to a number of risks, uncertainties and assumptions, including, without limitation risks set forth under the caption "Risk Factors" in Magentas Registration Statement on Form S-1, as updated by Magentas most recent Quarterly Report on Form 10-Q and its other filings with the Securities and Exchange Commission. In light of these risks, uncertainties and assumptions, the forward-looking events and circumstances discussed in this press release may not occur and actual results could differ materially and adversely from those anticipated or implied in the forward-looking statements. You should not rely upon forward-looking statements as predictions of future events. Although Magenta believes that the expectations reflected in the forward-looking statements are reasonable, it cannot guarantee that the future results, levels of activity, performance or events and circumstances reflected in the forward-looking statements will be achieved or occur. Moreover, except as required by law, neither Magenta nor any other person assumes responsibility for the accuracy and completeness of the forward-looking statements included in this press release. Any forward-looking statement included in this press release speaks only as of the date on which it was made. We undertake no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events or otherwise, except as required by law.

View source version on businesswire.com: https://www.businesswire.com/news/home/20200226005256/en/

Contacts

Manisha Pai, Vice President, Communications & Investor Relations617-510-9193mpai@magentatx.com

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Magenta Therapeutics to Participate in Cowen Health Care Conference on Monday, March 2nd in Boston - Yahoo Finance

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Analysts Estimate Fate Therapeutics (FATE) to Report a Decline in Earnings: What to Look Out for – Yahoo Finance

February 26th, 2020 8:41 pm

The market expects Fate Therapeutics (FATE) to deliver a year-over-year decline in earnings on higher revenues when it reports results for the quarter ended December 2019. This widely-known consensus outlook is important in assessing the company's earnings picture, but a powerful factor that might influence its near-term stock price is how the actual results compare to these estimates.

The stock might move higher if these key numbers top expectations in the upcoming earnings report. On the other hand, if they miss, the stock may move lower.

While management's discussion of business conditions on the earnings call will mostly determine the sustainability of the immediate price change and future earnings expectations, it's worth having a handicapping insight into the odds of a positive EPS surprise.

Zacks Consensus Estimate

This clinical-stage biotech company that develops stem cell treatments is expected to post quarterly loss of $0.39 per share in its upcoming report, which represents a year-over-year change of -56%.

Revenues are expected to be $1.84 million, up 10.8% from the year-ago quarter.

Estimate Revisions Trend

The consensus EPS estimate for the quarter has remained unchanged over the last 30 days. This is essentially a reflection of how the covering analysts have collectively reassessed their initial estimates over this period.

Investors should keep in mind that an aggregate change may not always reflect the direction of estimate revisions by each of the covering analysts.

Price, Consensus and EPS Surprise

Earnings Whisper

Estimate revisions ahead of a company's earnings release offer clues to the business conditions for the period whose results are coming out. Our proprietary surprise prediction model -- the Zacks Earnings ESP (Expected Surprise Prediction) -- has this insight at its core.

The Zacks Earnings ESP compares the Most Accurate Estimate to the Zacks Consensus Estimate for the quarter; the Most Accurate Estimate is a more recent version of the Zacks Consensus EPS estimate. The idea here is that analysts revising their estimates right before an earnings release have the latest information, which could potentially be more accurate than what they and others contributing to the consensus had predicted earlier.

Thus, a positive or negative Earnings ESP reading theoretically indicates the likely deviation of the actual earnings from the consensus estimate. However, the model's predictive power is significant for positive ESP readings only.

A positive Earnings ESP is a strong predictor of an earnings beat, particularly when combined with a Zacks Rank #1 (Strong Buy), 2 (Buy) or 3 (Hold). Our research shows that stocks with this combination produce a positive surprise nearly 70% of the time, and a solid Zacks Rank actually increases the predictive power of Earnings ESP.

Please note that a negative Earnings ESP reading is not indicative of an earnings miss. Our research shows that it is difficult to predict an earnings beat with any degree of confidence for stocks with negative Earnings ESP readings and/or Zacks Rank of 4 (Sell) or 5 (Strong Sell).

How Have the Numbers Shaped Up for Fate Therapeutics?

For Fate Therapeutics, the Most Accurate Estimate is the same as the Zacks Consensus Estimate, suggesting that there are no recent analyst views which differ from what have been considered to derive the consensus estimate. This has resulted in an Earnings ESP of 0%.

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On the other hand, the stock currently carries a Zacks Rank of #3.

So, this combination makes it difficult to conclusively predict that Fate Therapeutics will beat the consensus EPS estimate.

Does Earnings Surprise History Hold Any Clue?

Analysts often consider to what extent a company has been able to match consensus estimates in the past while calculating their estimates for its future earnings. So, it's worth taking a look at the surprise history for gauging its influence on the upcoming number.

For the last reported quarter, it was expected that Fate Therapeutics would post a loss of $0.38 per share when it actually produced a loss of $0.40, delivering a surprise of -5.26%.

The company has not been able to beat consensus EPS estimates in any of the last four quarters.

Bottom Line

An earnings beat or miss may not be the sole basis for a stock moving higher or lower. Many stocks end up losing ground despite an earnings beat due to other factors that disappoint investors. Similarly, unforeseen catalysts help a number of stocks gain despite an earnings miss.

That said, betting on stocks that are expected to beat earnings expectations does increase the odds of success. This is why it's worth checking a company's Earnings ESP and Zacks Rank ahead of its quarterly release. Make sure to utilize our Earnings ESP Filter to uncover the best stocks to buy or sell before they've reported.

Fate Therapeutics doesn't appear a compelling earnings-beat candidate. However, investors should pay attention to other factors too for betting on this stock or staying away from it ahead of its earnings release.

Want the latest recommendations from Zacks Investment Research? Today, you can download 7 Best Stocks for the Next 30 Days. Click to get this free reportFate Therapeutics, Inc. (FATE) : Free Stock Analysis ReportTo read this article on Zacks.com click here.

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Meet 20 European Immuno-Oncology Companies that are Fighting… – Labiotech.eu

February 26th, 2020 8:41 pm

With the success of CAR T-cell therapies and other innovative medicines in this area, immuno-oncology has become a buzzword in biotech, with more and more companies starting up in Europe and elsewhere. With so many players involved, it can be hard to know who is doing what. Here are 20 European companies we think stand out and are leading the revolution in cancer medicine.

Although immunotherapies to treat cancer have been around for decades, new approaches are popping up every other day. After all, enlisting the immune system to fight cancer remains an extremely promising therapeutic strategy. There are so many companies focusing on different kinds of immunotherapies that it was quite a challenge to choose our favorites. We therefore enlisted the help of experts in the industry to select the following 20 immuno-oncology companies in Europe as our top picks. As ever, these are in no particular order.

Founded in Abingdon, UK, in 2008, Adaptimmune develops enhanced T-cell therapies that support the immune system in detecting and targeting cancer cells. Interestingly, its SPEAR T cell technology can target a variety of solid tumors a feat that is not easy to achieve, as solid tumors have a highly complex tumor microenvironment that many immunotherapies find difficult to penetrate.

The companys technology can identify and select T cell receptors (TCRs) that are more likely to improve the patients immune response and result in the effective binding of cancer cells. In January 2020, Adaptimmune and Japanese company Astellas agreed to co-develop and co-commercialize stem-cell-derived allogeneic chimeric antigen receptor (CAR)-T and TCR T cell therapies, which means that they not only treat one specific patient but a large number of patients with a particular cancer type. The deal was worth 806M.

ADC Therapeutics works in the area of antibody-drug conjugates (ADCs). Since being founded in 2011 in Lausanne, Switzerland, ADC Therapeutics has raised 514M ($558M) to advance its immuno-oncology therapies. The companys proprietary ADCs combine monoclonal antibodies that are specific to targets on the surface of tumor cells with a specific class of toxins called pyrrolobenzodiazepine (PBD) dimers.

The PBD dimer is released inside the tumor cells and binds to the tumor DNA, which blocks the division of the tumor cells and eventually kills them. ADC Therapeutics currently has two ADCs for liquid tumors in pivotal phase II studies, and one ADC targeting solid tumors in phase Ib. In January 2020, the company announced the positive results of its phase II trial of its leading ADC in patients with relapsed or refractory diffuse large B cell lymphoma.

Yet another direction in the treatment of cancer via the immune system is taken by Heidelberg-based company Affimed Therapeutics. Founded in 2000, the company focuses on the innate immune system. Using its ROCK platform, Affimed develops multi-specific antibodies called cell engagers.

Innate cell engagers can bind to the patients innate immune cells, including natural killer cells and macrophages, while simultaneously binding to specific tumor cells. As a result, the patients own immune systems can attack and kill the cancer cells. The companys lead candidate is currently in phase II for a number of liquid tumors.

Based in London, UK, and founded in 2014 as a spin-out from the University College London, Autolus Therapeutics uses CARs and TCRs to reprogram T cells so they recognize and consequently kill tumor cells. In January 2020, the company revealed the closure of its public offering on the Nasdaq with net proceeds of 68.4M ($74.2M).

Autolus other news in January was the announcement of the clinical progress of its next-generation programmed T cell therapy. It is currently in Phase I/II for the treatment of adults with relapsed or refractory diffuse large B cell lymphoma. The results showed no neurotoxicity and a manageable safety profile.

BioNTech has a much larger pipeline that contains CARs, TCRs, recombinant cytokines, and optimized mRNA. Founded in Mainz, Germany, in 2008, the company is one of the largest biotechs in Europe. Its pipeline is full to bursting with a variety of immuno-oncology therapies based on mRNA, antibodies, and CAR-T cells.

In July 2019, BioNTech raised one of the biggest ever funding rounds of a European biotech with a whopping 290M Series B. However, in October of that same year, the companys Nasdaq IPO, which was initially estimated to raise around 725M, resulted in pricing at only 141M due to poor market conditions in the US.

Based in Paris, France, and founded in 1999, Cellectis is also focusing on CART-cell therapy. It is working on a novel type of CART therapy known as Universal CARTs (UCARTs). Unlike the two approved CAR-T therapies, Novartis Kymriah and Gileads Yescarta, UCARTs are allogeneic so rather than being personalized, they can treat a large number of patients with a particular cancer type.

In November 2019, Cellectis announced that it had won the European patent challenge for the use of CRISPR-Cas9 for gene editing T cells. This process will help the company further develop its UCART platform. To date, six of its main UCART product candidates are in Phase I clinical trials. For three of these programs, Cellectis has partnered with Servier and Allogene.

As another biotech giant, Celyad is also working in the field of CART-cell therapies but is focusing on the NKG2D receptor. Founded in 2004 in Mont-Saint Guibert, Belgium, the companys lead immuno-oncology candidate uses the NKG2D receptor. NKG2D can bind to eight different ligands that are naturally found on cancer cells present in 80% of solid and liquid malignancies.

Something cool about NKG2D is that the ligands that it recognizes are also expressed by the tumor microenvironment, which comprises the blood vessels that support the tumor and the cells that make sure the tumor can evade the immune system. As a result, the lead candidate can target and kill the tumor as well as cleaning up its microenvironment. The candidate is currently in phase I.

Spun-off from the Babraham Institute in Cambridge, UK, in 2007, Crescendo Biologics develops targeted T-cell enhancing therapeutics with the aim of tackling difficult-to-treat cancers. The companys Humabody therapies are small, multi-specific antibody fragments that can penetrate tumor tissue in a way that conventional antibodies cannot.

Crescendo Biologics lead proprietary candidate is a bispecific T-cell engager targeting the prostate-specific membrane antigen. It can selectively activate tumor-specific T cells within the tumor microenvironment. It is currently advancing towards clinical development.

As a spring chicken among other European immuno-oncology companies, we felt Ervaxx deserved a mention here because it develops cancer vaccines and cell therapies targeting dark antigens normally silent genes that are expressed in cancer cells. Founded in 2017 in London, UK, Ervaxx recently made headlines when it got its hands on the license of an exciting new preclinical stage universal cancer immunotherapy.

In early January 2020, a group of researchers at Cardiff University discovered a new type of T cells that have the potential to attack a wide range of cancers, such as leukemia and melanoma. Ervaxx is continuously expanding its repertoire of Dark Antigens. Using these, the company is working on a pipeline of off-the-shelf cancer vaccines and TCR-based therapies.

Founded in 2008 in Copenhagen, Denmark, Evaxion takes a very different approach to fighting cancer: using artificial intelligence (AI) to develop immunotherapies. The company has developed two AI platforms that can identify and optimize epitopes and antigens that are capable of eliciting strong immune responses against cancer and infectious diseases.

The companys PIONEER platform is used for the development of personalized cancer immunotherapies. In April 2019, it announced the beginning of phase I with the dosing of the first patient with its lead candidate, a therapeutic vaccine. Evaxion closed the year by successfully raising 16M ($17M).

GammaDelta Therapeutics, founded in 2016, takes another approach to immuno-oncology therapies. The London-based company focuses on gamma delta T cells. Unlike alpha beta T cells which are commonly used in CAR-T therapy, gamma delta T cells are a part of the innate immune system. In short, this means that gamma delta T cells are already pre-programmed to identify and kill cells that are modified by cancer. The company is currently advancing its allogeneic gamma delta T cell therapies through preclinical development.

In October 2019, GammaDelta Therapeutics announced the formation of the spinout company Adaptate Biotherapeutics. Adaptate will be developing therapeutic antibodies that can modulate the activity of gamma delta T cells with the aim of triggering an immune response to fight cancer.

Danish biotech Genmab had an exciting start to the new year. In January 2020, one of the companys lead candidates daratumumab, a monoclonal antibody, received marketing authorization by the EMA. Marketed as DARZALEX, it can be used in combination with bortezomib, thalidomide, and dexamethasone to treat multiple myeloma.

Founded in Copenhagen in 1999, Genmab focuses on the development of antibody therapies against cancer. In December 2019, Genmab signed a deal with German biotech CureVac to develop mRNA drugs that can produce antibodies within the patient, which is an exciting development.

Heidelberg Pharma, formerly known as Wilex, was founded in 1997 in Heidelberg, Germany. The company focuses on ADCs. It has an exclusive license agreement with the Max Delbrck Center for Molecular Medicine in the Helmholtz Association in Berlin that includes a number of surface proteins found in multiple myeloma cells called B cell maturation antigen (BCMA).

Heidelberg Pharmas lead candidate targets BCMA and is currently advancing through the preclinical stage. It is an ADC that consists of a BCMA antibody, a specific linker, and the toxin amanitin, one of the deadliest toxins found in several mushroom species.

Founded in 2011, Austrian company Hookipa Pharma engineers arenaviruses to deliver tumor-specific genes to dendritic cells. Dendritic cells naturally activate killer T cells by delivering the tumor-specific antigens to them, which triggers an immune response. HOOKIPA Pharmas co-founder, Rolf Zinkernagel, actually received the Nobel Prize for Physiology or Medicine in 1996 for his work on how killer T cells can recognize virus-infected cells.

Hookipas leading immuno-oncology therapy is currently progressing through phase I. In February 2019, the company closed a Series D financing round for 33.2M ($37.4M). The funding is being used to boost the clinical development of its immunotherapies for cancer and infectious diseases based on its proprietary arenavirus platform.

This French company develops antibody therapies to fight cancer. Marseille-based ImCheck has developed a pipeline of monoclonal antibodies that target specific checkpoint molecules of the butyrophilin (BTN) family, which engage gamma delta T cells. As part of the innate immune system, gamma delta T cells fight cancer cells naturally.

ImChecks lead drug candidate, an anti-BTN3 antibody that targets solid tumors, is expected to enter phase I in 2020. In order to fund this trial and further boost the development of immunotherapies, ImCheck closed a series B funding round in December 2019 worth 48M.

Immatics was founded in 2000 in Tbingen, Germany. The company develops personalized immuno-oncology therapies by engineering patient T cells to express TCRs, which specifically target the patients cancer. Unlike CAR-T therapies that generally target surface proteins, Immatics immunotherapy can also target proteins within cancer cells, which makes the cancer cells more vulnerable and accessible to the immune system.

In August 2019, American company Celgene and Immatics signed a deal worth more than 1.35B ($1.5B) to further develop its immuno-oncology therapies. In three cancer immunotherapy programs, Immatics will develop leading cell immunotherapy candidates for solid tumors, while Celgene has the option to co-develop the candidates or take over the development altogether.

Based in Oxfordshire, UK, and founded in 2008, Immunocore also focuses on TCRs. Its ImmTAC (immune mobilizing monoclonal TCRs against cancer) technology is based on a new class of bi-specific biologics that can activate a specific T cell response in cancer cells.

In December 2019, Immunocore announced the start of the first-in-human clinical trial of its third bispecific, which was developed using the ImmTAC technology platform. Immunocore has collaborations with a number of partners, including AstraZeneca, Genentech, GSK, and Eli Lilli.

Medigene also focuses on TCRs. However, this company develops modified TCRs called TCR-Ts, as well as dendritic cell vaccines (DCs), and T cell-specific antibodies (TABs).

In January 2020, Medigene announced positive results after a two-year phase I/II for its DC vaccine in patients with acute myeloid leukemia (AML). Moreover, its leading TCR-T candidate is currently being prepared for phase II clinical trials. Medigene was founded in 1994 in Martinsried, Germany.

As a neighbor of Medigene, MorphoSys is also based in Martinsried, Germany. It was founded in 1992. The company is one of the very few European biotechs valued at over 1B. MorphoSys develops antibody therapies for numerous conditions.

The companys lead immuno-oncology candidate tafasitamab is a humanized monoclonal antibody that targets CD19, an antigen mainly expressed by various B cell-derived blood cancers, such as non-Hodgkins lymphoma, diffuse large B cell lymphoma, and chronic lymphocytic leukemia. This candidate is being co-commercialized by Incyte. Other partners of MorphoSys include Novartis, Roche, GSK, and Roche.

Another company focusing on ADCs is NBE Therapeutics. This companys goal is to target solid tumors. Based in Basel, Switzerland, and founded in 2012, NBE Therapeutics has developed a technology that uses an enzyme to attach small molecule drugs to monoclonal antibodies. This approach is different from conventional ADCs that are usually generated using a chemical junction, which can be unstable at times.

The companys lead candidate, an ADC for the treatment of triple-negative breast cancer, lung, and ovarian cancer, is expected to reach phase I in 2020.

Images via Elena Resko & Shutterstock.com

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Cell Analysis Market is Expected to See Growth Rate of 6.96% – Nyse Nasdaq Live

February 26th, 2020 8:41 pm

Cells constitute discrete units of biological function and serve as starting points in a myriad of studies to identify and map many of the basic biochemical and physical processes of life. Cell analysis is a wide term that can be applied to a range of different technologies, the technology used depends on experimental needs. Compiling data sets from multiple cell analysis investigations allows scientists to better understand, predict, and ultimately influence the factors that underlie cell health, function, death, and proliferation.

This intelligence report provides a comprehensive analysis of the Global Cell Analysis Market. This includes Investigation of past progress, ongoing market scenarios, and future prospects. Data True to market on the products, strategies and market share of leading companies of this particular market are mentioned. Its a 360-degree overview of the global markets competitive landscape. The report further predicts the size and valuation of the global market during the forecast period. Some of the key players profiled in the study are Thermo Fisher Scientific, Inc. (United States), Danaher Corporation (United States), The Merck KGaA Group (Germany), Becton, Dickinson and Company (United States), GE Healthcare (United States), Agilent Technologies, Inc. (United States), Olympus Corporation (Japan), PerkinElmer, Inc. (United States), Promega Corporation (United States), Sysmex Corporation (Japan) and AbbVie, Inc.(United States) are some of the key players profiled in the study. Additionally, the Players which are also part of the research are Lonza Group (Switzerland), Tecan Group (Switzerland), Miltenyi Biotec (Germany), Stemline Therapeutics, Inc.(United States), Fujifilm Irvine Scientific (United States), STEMCELL Technologies Inc. (Canada), Sino Biological Inc. (United States), BIOTIME, Inc. (United States), Miltenyi Biotec (Germany), PromoCell GmbH (Germany), Carl Zeiss (Germany), Bio-Rad Laboratories Inc (United States), MacroGenics, Inc. (United States), OncoMed Pharmaceuticals, Inc. (United States) and Bionomics (Australia).

Free Sample Report + All Related Graphs & Charts @: https://www.advancemarketanalytics.com/sample-report/124696-global-cell-analysis-market

Market Trend

Market Drivers

Restraints

Opportunities

Each segment and sub-segment is analyzed in the research report. The competitive landscape of the market has been elaborated by studying a number of factors such as the best manufacturers, prices and revenues. Global Cell Analysis Market is accessible to readers in a logical, wise format. Driving and restraining factors are listed in this study report to help you understand the positive and negative aspects in front of your business.

This study mainly helps understand which market segments or Region or Country they should focus in coming years to channelize their efforts and investments to maximize growth and profitability. The report presents the market competitive landscape and a consistent in depth analysis of the major vendor/key players in the market.Furthermore, the years considered for the study are as follows:Historical year 2013-2017Base year 2018Forecast period** 2019 to 2025 [** unless otherwise stated]

**Moreover, it will also include the opportunities available in micro markets for stakeholders to invest, detailed analysis of competitive landscape and product services of key players.The Global Cell Analysis segments and Market Data Break Down are illuminated below:Type (Flow Cytometry Products (Reagents and Consumables, Instruments, Accessories, and Software), QPCR Products (Reagents and Consumables, and Instruments), Cell Microarrays (Consumables, and Instruments), Microscopes (Electron, Inverted, Stereo, and Near-field Scanning Optical), Spectrophotometers (Single-mode Readers, and Multi-mode Readers), Cell Counters (Automated Cell Counters, Hemocytometers, and Manual Cell Counters), HCS Systems, Others)

Application (Cell Culture, Cell Imaging, Cell Isolation and Expansion, Cell Signaling Pathways, Cell Structure, Cell Tracing & Tracking, Cell Function Assays, Stem Cell Research, Others), End Use Verticals (Hospitals and Diagnostic Laboratories, Pharmaceutical & Biotechnology Companies, Research Institutes, Cell Culture Collection Repositories, Others), Process (Cell Identification, Cell Viability, Cell Signaling Pathways/Signal Transduction, Cell Proliferation, Cell Counting and Quality Control, Cell Interaction, Target Identification and Validation, Single-cell Analysis)

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Enquire for customization in Report @ https://www.advancemarketanalytics.com/enquiry-before-buy/124696-global-cell-analysis-marketRegion Included are: North America, Europe, Asia Pacific, Oceania, South America, Middle East & Africa

Country Level Break-Up: United States, Canada, Mexico, Brazil, Argentina, Colombia, Chile, South Africa, Nigeria, Tunisia, Morocco, Germany, United Kingdom (UK), the Netherlands, Spain, Italy, Belgium, Austria, Turkey, Russia, France, Poland, Israel, United Arab Emirates, Qatar, Saudi Arabia, China, Japan, Taiwan, South Korea, Singapore, India, Australia and New Zealand etc.

Objectives of the Study

Read Detailed Index of full Research Study at @ https://www.advancemarketanalytics.com/reports/124696-global-cell-analysis-market

Strategic Points Covered in Table of Content of Global Cell Analysis Market:

Chapter 1: Introduction, market driving force product Objective of Study and Research Scope the Cell Analysis market

Chapter 2: Exclusive Summary the basic information of the Cell Analysis Market.

Chapter 3: Displaying the Market Dynamics- Drivers, Trends and Challenges of the Cell Analysis

Chapter 4: Presenting the Cell Analysis Market Factor Analysis Porters Five Forces, Supply/Value Chain, PESTEL analysis, Market Entropy, Patent/Trademark Analysis.

Chapter 5: Displaying the by Type, End User and Region 2013-2018

Chapter 6: Evaluating the leading manufacturers of the Cell Analysis market which consists of its Competitive Landscape, Peer Group Analysis, BCG Matrix & Company Profile

Chapter 7: To evaluate the market by segments, by countries and by manufacturers with revenue share and sales by key countries in these various regions.

Chapter 8 & 9: Displaying the Appendix, Methodology and Data SourceKey questions answered

Definitively, this report will give you an unmistakable perspective on every single reality of the market without a need to allude to some other research report or an information source. Our report will give all of you the realities about the past, present, and eventual fate of the concerned Market.

Thanks for reading this article; you can also get individual chapter wise section or region wise report version like North America, Europe or Asia.

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Advance Market Analytics is Global leaders of Market Research Industry provides the quantified B2B research to Fortune 500 companies on high growth emerging opportunities which will impact more than 80% of worldwide companies revenues.

Our Analyst is tracking high growth study with detailed statistical and in-depth analysis of market trends & dynamics that provide a complete overview of the industry. We follow an extensive research methodology coupled with critical insights related industry factors and market forces to generate the best value for our clients. We Provides reliable primary and secondary data sources, our analysts and consultants derive informative and usable data suited for our clients business needs. The research study enable clients to meet varied market objectives a from global footprint expansion to supply chain optimization and from competitor profiling to M&As.

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Cell Analysis Market is Expected to See Growth Rate of 6.96% - Nyse Nasdaq Live

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Device inspired by mangroves could help clear up flood water – The Guardian

February 26th, 2020 8:41 pm

A novel approach to removing salt from water, inspired by mangrove trees, has been revealed by researchers who say the system could offer an unusual approach to clearing up flood water.

Mangroves, like other trees, employ a system of water transport: it is thought evaporation of moisture from their leaves produces a negative pressure in their water-conducting tissues that helps to draw water into their roots and up their trunks.

This transport relies on surface tension, the fact that water molecules like to interact with the walls of the tissues, and that water molecules exert a tug on each other.

Salty water can damage most plants, but mangroves can thrive in salty conditions because they have adaptations including cell membranes that prevent salts from passing through in an uncontrolled manner, as well as cell walls that contain a waxy substance.

The upshot is that a mangrove essentially desalinates the water from its surroundings.

Now, writing in the journal Science Advances, researchers say they have reproduced this process in a synthetic system, using a polymer membrane that filters out salts as the root, a finely porous silica filter as the stem, and leaves based on either a hydrogel-filled membrane or aluminium oxide featuring tiny pores.

In our particular demonstration, through simple evaporation, a huge negative pressure was generated to drive water flow through a semi-permeable, reverse-osmosis membrane, thereby desalinating the water, said Dr Jay Werber and Dr Jongho Lee, co-authors of the study, who carried out the work at Yale University. In the industrial process, large, high-pressure pumps and loads of electricity are required to generate these high pressures to drive flow and desalination.

Importantly, they note, their system works without the production of air-bubbles which can block the flow thanks to the use of the membrane and tiny pores in the silica stem.

The team add that replicating the natural process adds support to the theory of how water transport in mangrove trees occurs.

However, they note that the system is not a practical way to desalinate water, not least since a large amount of heat would be needed.

The energy that drives desalination in our device is absorbed from the environment: basically, heat is absorbed to drive evaporation, said Werber and Lee. In a small-scale device, this energy is essentially free, meaning that it isnt provided as electricity or generated heat, similar to how drying clothes on a clothes line doesnt take added energy. However, trying to scale this up to large volumes would be very challenging.

But they offer an alternative suggestion: incorporate the system into buildings to turn them into giant sponges, offering a novel way to handle stormwater and reduce flood damage.

In this scenario, the buildings themselves would soak up excess groundwater and evaporate the water from their walls and roofs, the authors write.

And there is a bonus: The evaporation of water from the building walls would additionally provide passive cooling, the team write.

Prof Marc-Olivier Coppens, director of the UCL Centre for Nature-Inspired Engineering, who was not involved in the study, described the teams synthetic mangrove device as remarkable, but said further developments would be needed.

The proposed device is a creative, exciting development; however, the application of this principle is still early stages, he said. Higher stability for longer times than those tested here, with less salt build-up, but also the possibility to be used for real seawater, containing more [chemical] species, would be necessary for practical use.

He added that the idea of using such synthetic mangroves for stormwater management was exciting. He said: It remains to be seen whether sufficient fluxes and total flows can be achieved for this application, but it is a compelling application.

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Device inspired by mangroves could help clear up flood water - The Guardian

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TG Therapeutics Edges Closer To Commercialization And Potential Share Price Gain – Seeking Alpha

February 26th, 2020 8:41 pm

Investment Thesis

I last posted about TG Therapeutics (TGTX) in November last year after the company published long-awaited positive trial data concerning flagship drugs umbralisib and ublituximab, which caused a small uptick in the share price from ~$5 to ~$9.

I felt that TG was edging closer to commercialising its first drug and recommended its stock as a speculative investment - since then the share price has continued to grow and has reached $16 at the time of posting this update on further positive news flow. The next few months promise to be a critical period for the company.

Data is expected in the coming days from a pivotal trial - UNITY CLL - in which umbralisib and ublituximab are being used in combination (referred to as "U2") to treat chronic lymphocytic leukemia ("CLL"). The randomised trial - which began in November 2015 and has enrolled ~420 patients - compares U2 against a combination of Obinutuzumab and Chlorambucil with the primary outcome measure being progression-free survival ("PFS") assessed over 3 years and the secondary outcome being overall response rates ("ORR"). The company is waiting for the PFS data before deciding whether to push for accelerated approval from the FDA for the treatment.

What makes the data from this trial all the more significant is the impact it will have on a phase 1/2a triple combination trial TG is conducting where U2 is being combined with a third indication targeting CLL, venetoclax. Early data from this trial released in December suggested ORR of 87% after U2 induction and before the use of venetoclax, and the U2 induction was also shown to reduce risk of tumor lysis syndrome. After venetoclax was introduced a 100% ORR was achieved as well as a 44% complete response ("CR"). After 12 cycles of therapy 7 of 9 patients tested had undetectable minimal residue disease and stopped therapy.

According to a recent TG coporate presentation 115,000 Americans are affected by CLL with 20,000 patients being diagnosed with the disease every year. The size of the treatment market for CLL is estimated to reach ~$10bn by 2025 growing at a CAGR of 15%. TG believes that there is significant unmet need in this market and therefore should U2 receive approval as a stand-alone treatment for relapsed patients who have not responded to prior treatment or in combination with other drugs such as venetoclax as a first line treatment then TG's share price is likely to soar on the prospect of global drug sales in the triple-digit millions.

Besides U2 TG is progressing ublituximab through phase 3 trials as a potential treatment for multiple sclerosis ("MS") compared with oral teriflunomide with top line data expected sometime in 2020, and through phase 3 trials in combination with ibrutinib for treatment of high-risk CLL. Umbrasilib could soon win approval as a stand-alone treatment for MZL and FL after management submitted a joint NDA to the FDA in January. Other promising candidates are also in the early phases of clinical testing.

The company recently completed a $50m direct public offering of common stock to a single investor which has eased perennial fears over TG's precarious funding runway, and as such, a stellar 2020 could conceivably be in prospect.

It's worth remembering however that 1 bad trial result could seriously undermine TG's progress and decimate the share price. The fact that TG does not have any development partners for its drug candidates programs in the US and does not seem to be an acquisition target at present can be read either as an encouraging sign (TG can go it alone and earn bigger profits) or as slightly suspicious (do pharma insiders know something investors don't?).

On balance however, just as I did in November, I am prepared to give management the benefit of the doubt. One thing that is for certain is that the company's fortunes (and share price) are about to change significantly whether for better or for worse. After taking a deep breath, I remain bullish.

TG Therapeutics has a somewhat unique approach to drug discovery - founded in 2012 the company is focused on B-cell mediated diseases. B-cells are produced by hematopoietic stem cells in bone marrow from where they migrate to the spleen, lymph nodes or other tissues forming immunocompetent B-cells capable of initiating an immune response when activated by cell antigens. B-cells however can become cancerous causing diseases such as non-Hodgkin's lymphoma ("NHL") or CLL, or become aberrant causing auto-immune diseases such as MS, rheumatoid arthritis ("RA") or systemic lupus erythematosus ("SLE").

TG's strategy is to identify validated targets against B-cell mediated diseases and then conduct global searches for and acquire "best-in-class" drug candidates in early stages of development - preferably with human clinical proof-of-concept ("POC") from a network of academic research centres or biotech drug development companies. Having acquired a candidate the company then looks to use its proprietary technology platform to develop multiple complementary candidates that can be used either as single treatments or in combination.

The 2 drugs are TG's most advanced candidates. Ublituximab is an anti-CD20 monoclonal antibody, similar to commercialised drugs such as Rituximab, Ofatumumab or Obinutuzumab. CD20 tends to be over-expressed in cancerous or malignant B-cells - anti CD20 antibodies can attach themselves to these cells and trigger immune reactions - such as antibody dependent cellular cytotoxicity or phagocytosis - that result in the death of the malignant cell.

TG has bioengineered ublituximab using a process known as glyco-engineering so that certain naturally occurring sugar molecules have been removed from the antibody which the company says increases its potency and shortens drug-infusion times.

Umbralisib is a PI3K delta and CK1 epsilon inhibitor taken orally once a day. PI3K delta is part of a family of enzymes involved in various cell processes such as proliferation and immunity which tends to be implicated in B-cell related lymphomas, whilst inhibiting CK1 epsilon is also suggested to have anti-cancer effects and modulate adverse T-cell activity.

TG initiated this in January after data from a phase 2b study - Unity-NHL - of 72 patients with MZL and 118 with FL showed that the number of positive responses to umbrailsib as a single treatment was above the study threshold of 40%. Preliminary efficacy data from the first 42 patients with MZL also showed 52% of patients who had failed to respond to prior treatment responded to umbralisib and an additional 36% attained stable disease. Overall, umbralisib was well tolerated by patients - 10 patients discontinued treatment due to adverse events ("AEs") possibly related to the drug's side-effects, no deaths were reported and only 3 patients demonstrated grade 3 infections.

A rolling submission allows TG to file sections of the NDA on an ongoing basis, which is an unusual concession from the FDA, as is the permission to file one NDA for 2 separate indications (MZL and FL) - but umbralisib's prior breakthrough drug designation seems to have made this possible. The NDA should be submitted during the first half of 2020 moving the company one step closer to commercialisation.

The data behind TG's NDA submission for umbralisib. Source: TG Therapeutics analyst day presentation Jan 2020.

22,500 new cases of MZL or FL are diagnosed per annum (according to the American Cancer Society, quoted in TG's JPM Healthcare conference presentation), with ~6,000 - 10,000 relapsed indolent patients needing treatment per annum.

Ublituximab is now progressing through 2 fully-enrolled (500 patients) randomised phase 3 trials - ULTIMATE 1 and ULTIMATE 2 - where the drug is being evaluated against oral treatment Teriflunomide (marketed by Sanofi as Aubagio, Teriflunomide makes sales of ~$430m per quarter) with topline data expected in 2H 2020. During its phase 2 MS trials ublituximab patients' annualized relapse rates of 0.05 were favourably comparable to treatments Ocrelizumab (0.13), Rebif (0.36) and the placebo (0.64), whilst no T1 GD-enhancing lesions were present at weeks 24 and 48 of the trial compared to a baseline of 3.63.

TG estimates the global market for MS treatment will exceed $30bn by 2025 with the only other anti-CD20 approved treatment, Ocrelizumab (marketed as Ocrevus by Roche) currently making more than $2bn in annual sales (and on track to reach $4bn by 2025). Should approval be granted to ublituximab the drug will compete in a crowded field (as shown by the table below) but TG management believes that the convenience of the bi-annual, one-hour duration infusion, efficacy and pricing will translate to a $1 - $2bn market opportunity.

MS treatment options. Source: TG Therapeutics analyst day presentation Jan 2020.

TG Therapeutics drug candidate pipeline. Source: TG Website.

TG is progressing a number of other candidates with similar indications to umbrasilib and ublituximab.

TG 1701 is a novel covalent Brutons tyrosine kinase ("BTK") inhibitor that targets the B-cell receptor signalling pathway that helps to proliferate and protect B-lymphocytes. The drug has entered a phase 1 trial where it will be evaluated both as a single agent and in triple combination alongside U2, an interesting prospect for the company since success would enable them to provide an entirely in-house triple combination therapy.

TG-1501, a monoclonal antibody that attaches to Programmed Death-Ligand 1 (PD-L1) blocking the signals that cancerous cells use to protect themselves from the body's natural immune system. Similarly to TG-1701 the drug is in single agent and combination trials with other TG candidates.

Finally, TG-1801 is an ANTI-CD47/CD19 monoclonal antibody. CD47, is expressed by cancerous cells in order to express a "don't eat me" signal to avoid elimination through phagocytosis whilst CD19 is used by B-tumor cells to make up for a loss of CD20 and continue to resist treatment. TG-1801 has also entered a phase 1 trial.

In Q319 TG made a loss of $59.9m compared to a net loss of $34m over the same period in 2018. The difference was put down to manufacturing and CMC costs but the company says they decreased trial costs by $3.8m in the quarter and expect this reduction to continue into 2020. CFO Sean Power told analysts on the Q3 earnings call that management expects to reduce cash burn from Q3's $33m to $25m - $30m per quarter going forward, and that the cash position (at the time) of $96m would be sufficient to see the company through 2020 and the conclusion of the critical ongoing phase 3 trials.

The $50m raise completed in December will probably be viewed by investors as good business since the share price has subsequently risen and therefore the effects of dilution have been minimised. Still management has made repeated use of at-the-market offerings ("ATMs") with the most recent being a $24m raise at the end of Q319 - and further use of their mixed shelf offering may start to try backers' patience.

The upside for investors is that, besides several minor licensing agreements TG has resisted the temptation to enter into collaboration agreements with big-pharma concerns based on development milestones and post commercialisation revenue sharing, and therefore retains exclusive rights to all of its drug candidates.

TG clearly believes that commercialisation is imminent having appointed a new Chief Commercial Officer, Adam Waldman, who joins from Celgene where he was Head of Hematology-Oncology Marketing. Waldman has extensive experience building sales and marketing teams and will be expected to deliver the launch programs that TG will hope are initiated before the end of this year.

The upcoming results, firstly from the UNITY-CLL trial, and subsequently from ublituximab's MS trial will dictate whether or not TG proves to be a good investment or whether investors who have endured years of frustration will have to accept further short-to-medium term disappointment.

Management has done well in my view to progress different drug candidates to the near-conclusion of pivotal trials, win breakthrough drug designations and submit NDAs to the FDA that stand a good chance of success. It has taken time admittedly and the share price has suffered but it feels to me as though the company now has some momentum.

In my view, the signs are promising enough to suggest that TG will have a commercialised drug - and possibly 2 - by the end of the year. Should they be approved both drugs - perhaps ublituximab for MS more so than Umbrasilib for MZL and FL - will have sizeable addressable markets, and the prospect of an approval for treatment of CLL (U2 + venetoclax or even U2 + proprietary TG-1701) is a juicy one given the size of the market.

If the upcoming UNITY-CLL data is positive TG will surely make an attractive acquisition target for a big pharma - and the figures involved could be large - witness the $9.7bn Novartis recently paid Medicines Company for a single RNA therapy. Therefore I would put at least a 25-50% premium on TG's current price and look at a price of $21+, which is below analyst consensus targets of ~$25, and significantly below what TG could achieve if the market, as expected, reacts buoyantly to good news. With more candidates in development and because the company addresses a range of indications, the worst case scenario (in the event of poorly received data) is not catastrophic either.

Long-term, management will have to prove it has what it takes to successfully commercialise an approved drug and generate sales volumes that justify the high cash burn investors have endured for years. But that is for a different day. In the short term I remain bullish and see this as a potentially exciting time to be holding TG stock, although the usual biotech investing caveats still apply. Things can de-escalate quickly when data is not up to scratch.

Disclosure: I am/we are long TGTX. I wrote this article myself, and it expresses my own opinions. I am not receiving compensation for it (other than from Seeking Alpha). I have no business relationship with any company whose stock is mentioned in this article.

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TG Therapeutics Edges Closer To Commercialization And Potential Share Price Gain - Seeking Alpha

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Predicting Immunotherapy Success – BSA bureau

February 25th, 2020 5:46 pm

Overexpression of certain immunoproteasome subunits in melanoma are tied to anti-cancer immune activity

One of the frustrations with anti-cancer therapy is that no one drug fits all: Most work well in some people but have little effect in other patients with the same type of cancer. This is as true of the newer immunotherapy treatments as it is of older types of chemotherapy.

Weizmann Institute of Science researchers have now identified new markers that can help predict which patients have a better chance for a positive response to immunotherapy treatments. Their findings were reported in Nature Communications.

For Prof. Yardena Samuels and her research group partnered with Prof. Eytan Ruppins lab in the National Institutes of Health (USA), basing their research on the understanding that learning to predict which treatments are most likely to work is the first step to creating a personalized approach to curing cancer. The focus of their work is melanoma a collection of skin cancers that are often hard to treat, and which may be made up of varied tumor cells containing hundreds of different mutations. A certain percentage of melanomas have in recent years been successfully treated with immunotherapy drugs known as checkpoint inhibitors, which work by removing internal obstacles that trip up the bodys own immune system and keep it from attacking the cancer. Unfortunately, for others, these drugs remain ineffective.

To understand the differences in response between different people, the research team, led by postdoctoral fellow Dr. Shelly Kalaora in Samuels group and Joo Sang Li in the Ruppin group, first analyzed data from 470 melanoma patients that has been made available in the Cancer Genome Atlas (TCGA). They were particularly interested in differences in survival rates of patients in whom particular subunits of immunoproteasomes are overexpressed compared to those with low expression of these subunits. These are a variation on the proteasome subunits normally expressed in most cells (except for immune cells). Proteasomes are protein complexes that function as cutters, reducing long proteins to short pieces called peptides. These peptides are later presented on the cells surface by molecules called human leucocyte antigens (HLA). HLA peptides are basically bits of information small molecules displayed on the outsides of cells that report about new threats that the immune system needs to assess and address.

The immunoproteasome is assembled out of altered subunits and thus produces a unique collection of HLA peptides. The team thought that a particular change and overexpression in the HLA peptide repertoire might result in better recognition of the tumor cells by the immune system and thus better elimination of cancer cells.

To test this idea, the researchers cultured lines of tumor cells from melanoma patients in which they overexpressed the immunoproteasome subunits and identified the HLA peptides presented in each situation. By testing the response of the immune cells from the same patients, they showed that the newly formed HLA peptides were indeed more reactive compared to the HLA peptides presented by cells without this overexpression.

Could two subunits the research identified in particular and the unique HLA-bound peptides these produce be a predictor of immunotherapy success? The experiments showed that in tumor cells in which the subunits were overexpressed, the various immune system components that directly fight the cancer were more prevalent and more active than average. Indeed, looking back at the details of cancer patients in the database, the team reported that the expression levels of the two subunits were excellent predictors of the outcome better than the tumor mutational burden, a biomarker that is currently used in the clinic. The researchers in Samuelss and Ruppins lab suggest that expression of the immunoproteasome may be used as a biomarker for predicting better outcomes in melanoma and, together with mutational load testing, may improve patient matching to currently available immunotherapy.

Prof. Yardena Samuels is the head of the EKARD Institute for Cancer Diagnosis Research; and head of the Weizmann-Brazil Tumor Bank. Her research is also supported by the Laboratory in the name of M.E.H Fund established by Margot and Ernst Hamburger; the Green Family Charitable Foundation; the Wagner-Braunsberg Family Melanoma Research Fund; the Jean-Jacques Brunschwig Fund for the Molecular Genetics of Cancer; the Comisaroff Family Trust; the Rising Tide Foundation; the Fundacin Ramn Areces; the Meyer Henri Cancer Endowment; Ted and Sylvia Quint; Jean Jacques Roboh; and the European Research Council. Prof Samuels is the incumbent of the Knell Family Professorial Chair.

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Oncology Start-up OncoLens Named to Top 10 List of Innovative Technology Companies in Georgia – PR Web

February 25th, 2020 5:46 pm

ATLANTA (PRWEB) February 24, 2020

OncoLens is pleased to announce it has been named one of the Top 10 Innovative Technology Companies in Georgia by the Technology Association of Georgia (TAG).

Oncology focused, OncoLens is a SaaS-based tumor board platform to help cancer centers connect members of their care teams, as they make treatment decisions for their patients. Centers can increase their referrals and streamline workflows. They can also reduce tumor board prep time by 90% and time to initiate patient treatment from 14 to 2 days.

OncoLens utilizes some of the latest technologies in conjunction with its own proprietary algorithms to identify treatment options for the cancer patient, said Anju Mathew, Co-Founder and CEO, OncoLens. The platform identifies clinical trials, evidence-based guidelines and personalized treatment options based on the tumor genotype. These options are proposed to the multi-disciplinary cancer care team to help them make the best decision possible for the cancer patient.

Better patient outcomes can result from OncoLens robust functionality. Cancer care teams can engage research staff early and automatically screen cases available for clinical trials. Physicians are able to access real time data for clinical decision-making, while the system works in the background to facilitate data/document collection, including EMR clinical data, laboratory and molecular genetics test results and radiology images. The platform also supports regulatory reporting for associations such as the Commission on Cancer (CoC), NAPBC and NAPRC.

The Top 10 were selected from TAGs Top 40 Innovative Technology Companies competition for showing the highest degree of innovation, the broadest scope and financial impact of their innovations, and the greatest effect of such innovation in promoting Georgia's technology industry throughout the U.S. and globally.

As a Top 10 honoree, OncoLens will present at The Summit, hosted by TAG, March 3-4, at Cobb Galleria, in Atlanta. It is Georgias largest technology showcase. We look forward to sharing the future of innovative cancer care at TAGs event, said Mathew.

###About OncoLens OncoLens develops technologies that improve cancer treatment planning, simplify tumor board management, facilitate survivorship care planning, and automate accreditations and quality reporting through an intelligent workflow engine that streamlines business processes and enables more informed clinical decision-making. For more information, visit http://www.oncolens.com.

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Global Molecular Diagnostic Product Market Analysis And Forecast To 2026 By Recent Trends, Developments In Manufacturing Technology And Regional…

February 25th, 2020 5:46 pm

Reportspedia.com in its latest market intelligence study, finds that the Global Molecular Diagnostic Product Market registered a value of ~US$ xx Mn/Bn in 2019 and is observed to grow at CAGR of xx% during the estimative period 2020-2026. In terms of product type, segments holds the significant share, in terms of end use. All the consumption trends and adoption patterns of the Molecular Diagnostic Product are covered in the report.

Download Exclusive Sample of Molecular Diagnostic Product Markets Premium Report at: https://www.reportspedia.com/report/life-sciences/global-molecular-diagnostic-product-market-report-2019,-competitive-landscape,-trends-and-opportunities/29662 #request_sample

Key Players:

SiemensBiotestIlluminaBioMerieuxAbbottTecan GroupFujirebioGrifolsCepheidKreatech/LeicaAffymetrixBiokitLi-Cor BiosciencesSierra MolecularOrtho-Clinical DiagnosticsElitech GroupApplied Gene TechnologiesMyriad GeneticsRocheTakara BioDiadexusBio-RadEnzoProteome SciencesShimadzuPerkin Elmer/CaliperAgilent TechnologiesMonogram Biosciences/LabCorpSequenomDecode GeneticsExact SciencesEikenScienionQiagenBecton DickinsonHologic/Gen-ProbeCellMark Forensics/LabCorpThermo FisherArca BiopharmaBeckman Coulter/Danaher

The Molecular Diagnostic Product industry report offers in-depth analysis and insights into developments impacting businesses and enterprises on a global & regional level. A detailed breakdown of key trends, drivers, restraints, and opportunities influencing revenue growth is presented in this research report. This study focuses on the global Molecular Diagnostic Product market by share, volume, value, and regional appearance along with the types and applications. The market is divided into the below points:

Market by Type/Products:

Type 1Type 2Type 3

Market by Application/End-Use:

Application 1Application 2Application 3

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The geographical analysis covers the following regions:

The Molecular Diagnostic Product market research answers important questions, including the following:

The Molecular Diagnostic Product market research serves a platter of the following information:

In-depth analysis of the drivers, restraints, opportunities and trends influencing the growth of the global Molecular Diagnostic Product market. Critical breakdown of the Molecular Diagnostic Product market as per product type, and end use industry. Exhaustive understanding of the strengths, weaknesses, opportunities and threats of various Molecular Diagnostic Product market players. Precise year-on-year growth of the global Molecular Diagnostic Product market in terms of value and volume.

Key questions answered by this report include:

Table of contents:

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University researchers show how a protein found – Mirage News

February 25th, 2020 5:46 pm

Researchers at the University of Toronto have found that a receptor expression-enhancing protein contributes to normal heart development and function by regulating the sarcoplasmic reticulum, a network of tubules found in cardiac muscle cells.

The sarcoplasmic reticulum is key in the development and progression of heart disease, governing biochemical changes, structural remodeling and deterioration. But how this membrane-bound system organizes itself is still mostly unknown especially in cells with a highly differentiated or diverse network such as heart muscle cells, or cardiomyocytes.

Our findings show that a protein called REEP5 plays a critical role in regulating cellular stress responses in heart muscle cells, says Frank Shin-Haw Lee, a PhD student in the lab of Anthony Gramolini, an associate professor of physiology in U of Ts Faculty of Medicine who is based at the Ted Rogers Centre for Heart Research.

When REEP5 is depleted, it destabilizes the heart and reduces the amount of blood the heart can pump on each contraction, says Lee. When we removed this protein in both mice and zebrafish, it distorted the structure and shape of cardiomyocytes and led to cardiac dysfunction.

The journal Nature Communications published the findings this week.

When cardiomyocytes are under sustained stress from general dysfunction or disease, cellular pathways through the sarcoplasmic reticulum can lead to cell death and heart failure. Lee says that REEP5 is vital to the formation of the sarcoplasmic reticulum and to how it responds to stress and regulates calcium, which is essential for heart health.

A better understanding of how REEP5 functions in the heart may elucidate how heart failure develops amidst a sarcoplasmic reticulum in stress, Lee says.

The Gramolini lab worked with several other Toronto researchers on the study, including Ian Scott, a professor of molecular genetics at U of T and a senior scientist at the Hospital for Sick Children. The work builds on previous collaborative research from the labs of Gramolini, Scott and medical biophysics professor Thomas Kislinger in 2015, which created a blueprint of critical cell-surface and membrane-associated proteins in the heart.

Medical student Sina Hadipour-Lakmehsari was a co-first author on the current paper with Lee, and he says the findings may provide insight into heart disease in patients.

It is clearly an important protein for cardiac development and function and, combined with future human studies, it may help us unearth new potential therapies, Hadipour-Lakmehsari says, adding that the lab can continue to look at REEP5 in genetic studies to help shed light on diseases whose causes remain unknown.

This study is among the first in the world to show that the REEP5 protein plays an essential role in the stress responses that often lead to heart failure, adds Gramolini, who is also a scientist at Toronto General Hospital Research Institute, University Health Network. Deciphering the complex layers of heart function on a cellular level will help us generate new therapeutic and preventative strategies for heart failure.

The study recieved support from the Ted Rogers Centre Innovation Fund, the Natural Sciences and Engineering Research Council of Canada and the Canadian Institutes of Health Research, among others.

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Radiation Kills Cancer Cells, But May Also Protect Some Tumor Stem Cells That Can Spread – MedicalResearch.com

February 25th, 2020 5:45 pm

MedicalResearch.com Interview with:

Jennifer Sims-Mourtada, Ph.D.Senior Rsearch ScientistDirector of Translational Breast Cancer ResearchCenter for Translational Cancer ResearchChristianaCare

MedicalResearch.com: What is the background for this study?

Response: Cancer stem cells are resistant cancer cells that are able to continuously grow and are very resistant to radiation and chemotherapy. Cancer stem cells can also escape to the blood stream and travel to another site causing metastasis.

MedicalResearch.com: What are the main findings?

Response: In this study we show that cancer stem cells depend on radiation induced inflammatory responses to survive radiation. Additionally we show that activation of IL-6-STAT3 pathway after radiation can make even non-cancer stem cells look like and behave as cancer stem cells. Thus any cell that survives radiation in the presence of certain inflammatory signals may be converted to a cancer stem cell.

MedicalResearch.com: What should readers take away from your report?

Response: Although radiation kills tumor cells, it can also activate inflammatory responses that may protect some tumor cells. Co-treatment with anti-inflammatory agents such as inhibitors to the IL-6 STAT 3 pathway may sensitize cancer stem cells to radiation induced death, and may prevent generation of new cancer stem cancer stem cells and improve outcomes in triple negative breast cancer.

MedicalResearch.com: What recommendations do you have for future research as a result of this work?

Response: Agents inhibiting the IL-6-STAT3 pathway are currently in clinical trials for breast cancer. Future work should focus on understanding radiation-induced inflammation in the context of both the immune response and tumor cells, as radiation induced inflammation can activate anti-tumor immunity as well as killing tumor cells. Some studies suggest that inhibition of IL-6 STAT3 signaling may also improve anti-tumor immunity, and thus these agents may target cancer cells by multiple mechanisms. It will be important to understand how these agents work to select which patients will respond to inhibition of this pathway and which ones will not.

MedicalResearch.com: Is there anything else you would like to add?

Response: This is the good and the bad of radiation. We know radiation induced inflammation can help the immune system to kill tumor cells thats good but also it can protect cancer stem cells in some cases, and thats bad. Whats exciting about these findings is were learning more and more that the environment the tumor is in its microenvironment is very important. Historically, research has focused on the genetic defects in the tumor cells. Were now also looking at the larger microenvironment and its contribution to cancer.

There are no disclosures to report

Citation:

Kimberly M. Arnold et al, Radiation induces an inflammatory response that results in STAT3-dependent changes in cellular plasticity and radioresistance of breast cancer stem-like cells,International Journal of Radiation Biology(2019).DOI: 10.1080/09553002.2020.1705423

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Why Some COVID-19 Cases Are Worse than Others – The Scientist

February 25th, 2020 5:45 pm

Like many other respiratory conditions, COVID-19the disease caused by SARS-CoV-2can vary widely among patients. The vast majority of confirmed cases are considered mild, involving mostly cold-like symptoms to mild pneumonia, according to the latest and largest set of data on the new coronavirus outbreak released February 17 by the Chinese Center for Disease Control and Prevention.

Fourteen percent of confirmed cases have been severe, involving serious pneumonia and shortness of breath. Another 5 percent of patients confirmed to have the disease developed respiratory failure, septic shock, and/or multi-organ failurewhat the agency calls critical cases potentially resulting in death. Roughly 2.3 percent of confirmed cases did result in death.

Scientists are working to understand why some people suffer more from the virus than others. It is also unclear why the new coronaviruslike its cousins SARS and MERSappears to be more deadly than other coronaviruses that regularly circulate among people each winter and typically cause cold symptoms. I think its going to take a really, really long time to understand the mechanistic, biological basis of why some people get sicker than others, says Angela Rasmussen, a virologist at Columbia Universitys Mailman School of Public Health.

In the meantime, the latest data from China and research on other coronaviruses provide some hints.

The latest data from China stem from an analysis of nearly 45,000 confirmed cases, and on the whole suggest that the people most likely to develop severe forms of COVID-19 are those with pre-existing illnesses and the elderly.

While less than 1 percent of people who were otherwise healthy died from the disease, the fatality rate for people with cardiovascular disease was 10.5 percent. That figure was 7.3 percent for diabetes patients and around 6 percent for those with chronic respiratory disease, hypertension, or cancer.

While overall, 2.3 percent of known cases proved fatalwhich many experts say is likely an overestimate of the mortality rate, given that many mild cases might go undiagnosedpatients 80 years or older were most at risk, with 14.8 percent of them dying. Deaths occurred in every age group except in children under the age of nine, and, generally speaking, we see relatively few cases among children, World Health Organization Director General Tedros Adhanom Ghebreyesus said last week.

This pattern of increasing severity with age differs from that of some other viral outbreaks, notably the 1918 flu pandemic, for which mortality was high in young children and in people between 20 and 40 years of age. However, its broadly consistent with records of the SARS and MERS coronavirus outbreaks, notes Lisa Gralinski, a virologist at the University of North Carolina at Chapel Hill. If youre over fifty or sixty and you have some other health issues and if youre unlucky enough to be exposed to this virus, it could be very bad, she says.

I think its going to take a really, really long time to understand the mechanistic, biological basis of why some people get sicker than others.

Angela Rasmussen, Columbia University

Scientists dont know what exactly happens in older age groups. But based on research on other respiratory viruses, experts theorize that whether a coronavirus infection takes a turn for the worse depends on a persons immune response. The virus matters, but the host response matters at least as much, and probably more, says Stanley Perlman, a virologist and pediatric infectious disease specialist at the University of Iowa.

Once SARS-CoV-2 gets inside the human respiratory tract, its thought to infect and multiply in cells lining the airway, causing damage that kicks the immune system into action. In most people, it should trigger a wave of local inflammation, recruiting immune cells in the vicinity to eradicate the pathogen. The immune response then recedes, and patients recover.

For reasons that arent entirely clear, some peopleespecially the elderly and sickmay have dysfunctional immune systems that fail to keep the response to particular pathogens in check. This could cause an uncontrolled immune response, triggering an overproduction of immune cells and their signaling molecules and leading to a cytokine storm often associated with a flood of immune cells into the lung. Thats when you end up with a lot of these really severe inflammatory disease conditions like pneumonia, shortness of breath, inflammation of the airway, and so forth, says Rasmussen.

Local inflammation can turn into widespread inflammation of the lungs, which then has ripple effects across all organs of the body. This could also happen if the virus replicates faster than the immune system can respond, so that it then has to play catch-up to contain the pathogena situation that could also cause the immune defense to spiral out of control. With mice, we know that in some cases, particularly for SARS and MERS coronaviruses, virus replication is very rapid and in some cases overwhelming to the immune system, says Perlman.

Its harder to explain why young, healthy people also sometimes die from the diseasefor instance, Li Wenliang, a 34-year-old doctor who first sounded the alarm about the virus. He died a few weeks after contracting the pathogen.

Genetic and environmental risk factors might help explain the severity of infections. Though its clear that genetic factors can strongly determine the outcome of viral infections in miceas some of Rasmussens work has shown for Ebola, for instanceresearchers havent yet been able to tease out specific genes or variants in mice, let alone in people, that are responsible for varying degrees of illness. Environmental factors, such as smoking or air quality, may also play a role in disease severity, Rasmussen adds.

A lot of research has gone into understanding what causes respiratory failure that results from systemic inflammation of the lungsalso called acute respiratory distress syndrome (ARDS)that can occur from coronaviruses and other infections. Yet researchers still dont know how it occurs exactly, let alone how to treat it, Gralinksi notes. Its still a really poorly understood issue.

An intriguing finding in the new data released last week is that although similar numbers of men and women have contracted SARS-CoV-2, more men are dying from the disease. The death rate for males was 2.8 percent and 1.7 percent for women. Rasmussen is quick to caution that although the data encompass nearly 45,000 patients, thats still not that many people to determine if theres really a gender biasyoud have to look at this in a much larger population of patients in a number of different countries, she says.

That said, if there is a bias, it would be consistent with what epidemiologists have observed during the SARS and MERS outbreaks. In the 2003 SARS outbreak in Hong Kong, for instance, nearly 22 percent of infected men died, compared to around 13 percent of women. In an analysis of MERS infections between 2017 and 2018, around 32 percent of men died, and nearly 26 percent of women. The difference could have something to do with the fact that the gene for the ACE-2 receptor, which is used by both SARS-CoV-2 and the SARS virus to enter host cells, is found on the X chromosome, she speculates. If its a particular variant of the protein that makes people more susceptible to the virus, then females could compensate for that one bad variant because theyd have two copies of the X chromosome, whereas men would be stuck with only one copy. Or, it could be that men are more likely to be smokers and so their lungs are already a bit compromised. Theres definitely more to be teased out there, Gralinski says.

Some of Perlmans research, which demonstrated that the sex disparity also holds true in SARS-infected mice, points to the hormone estrogen as possibly having protective effects: Removing the ovaries of infected female mice or blocking the estrogen receptor made the animals more likely to die compared to infected control mice. The effects are probably more pronounced in mice than in people, Perlman tells The New York Times.

Whether patients develop antibodies after SARS-CoV-2 infection that will protect them against future infections is still a mystery. Surveys of SARS patients around five or 10 years after their recovery suggest that the coronavirus antibodies dont persist for very long, Gralinski says. They found either very low levels or no antibodies that were able to recognize SARS proteins.

However, for the new coronavirus, we would expect some immunity, at least in the short term, she says.

There are seven coronaviruses known to infect people. Four of them229E, NL63, OC43, and HKU1typically cause a cold and only rarely result in death. The other threeMERS-CoV, SARS-CoV, and the new SARS-CoV-2have varying degrees of lethality. In the 2003 SARS outbreak, 10 percent of infected people died. Between 2012 and 2019, MERS killed 23 percent of infected people. Although the case fatality rate of COVID-19 is lower, the virus has already killed more people than the other two outbreaks combined, which some have attributed to the pathogens fast transmission.

The cold-causing coronaviruses, as well as many other viruses that cause common colds, are typically restricted to the upper respiratory tract, that is, the nose and sinuses. Both SARS-CoV and SARS-CoV-2, however, are capable of invading deep into the lungs, something that is associated with more severe disease.

One possible reason for this is that the virus binds to the ACE-2 receptor on human cells in order to gain entry. This receptor is present in ciliated epithelial cells in the upper and lower airway, as well as in type II pneumocytes, which reside in the alveoli in the lower airway and produce lung-lubricating proteins. The type II pneumocytes are . . . important for lung function, so this is part of why the lower respiratory disease can be so severe, notes Gralinksi.

The new coronavirus also appears to use the ACE-2 receptor, which may help partially explain why, like SARS, it is more deadly than the other four coronaviruses. Those pathogens use different receptors, except for NL63, which also uses the ACE-2 receptor but binds to it with less affinity, says Gralinski. (MERS is thought to use an entirely different receptor, which is also present in the lower airways.)

To understand these questions fully will take time, research, and consistent funding for long-term studies. Coronavirus funding has been criticized for following a boom-and-bust cycle; viral spillovers from animals to people cause an initial surge of interest that tends to wane until the next outbreak occurs, Rasmussen warns.

Im hopeful that in this case it will be really apparent to everybody in the world that we need to be funding this type of basic science, fundamental science, to understand these mechanisms of disease, she says. Otherwise, were going to be in the same situation when the next outbreak happenswhether its a coronavirus or something else.

Katarina Zimmer is a New Yorkbased freelance journalist. Find her on Twitter@katarinazimmer.

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Precision Medicine Software Market Growing Rapidly with Significant CAGR of +10% by 2026 Syapse, Allscripts, Qiagen, Roper Technologies, Fabric…

February 25th, 2020 5:44 pm

Precision Medicine Software Market research report has been published by A2Z Market Research to give desired insights to drive the growth of businesses. The report initiated with study introduction which is followed by statistical details of the market that reveals the current market status and future forecast. The analysts have scrutinized the market drivers, confinements, risks, and openings present in the overall market.

The Global Precision Medicine Software market size was increased to xx million US$ from xx million US$ in 2015, and it will reach xx million US$ in 2026, growing at CAGR of +10 % between 2020 and 2026.

Precision medicine software enables stakeholders in the healthcare sector to provide personalized treatment plans to patients based on their genetic content. It combines clinical and genetic data to deliver targeted patient care. It also provides a wide range of applications in both the diagnostic and clinical areas of care delivery.

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Some of the Top Companies Profiled in this Report includes: Syapse, Allscripts, Qiagen, Roper Technologies, Fabric Genomics, Foundation Medicine, Sophia Genetics, PierianDx, Human Longevity, Translational Software, Gene42, Lifeomic Health.

This report provides a detailed and analytical look at the various companies that are working to achieve a high market share in the global Precision Medicine Software market. Data is provided for the top and fastest growing segments. This report implements a balanced mix of primary and secondary research methodologies for analysis. Markets are categorized according to key criteria. To this end, the report includes a section dedicated to the company profile. This report will help you identify your needs, discover problem areas, discover better opportunities, and help all your organizations primary leadership processes. You can ensure the performance of your public relations efforts and monitor customer objections to stay one step ahead and limit losses.

Global Precision Medicine Software Market Detail Segmentation:

Market Segment by Type:

Market Segment by Applications:

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The main points which are answered and covered in this Report:

Table of Contents

Global Precision Medicine Software Market Research Report 2020 2026

Chapter 1 Precision Medicine Software Market Overview

Chapter 2 Global Economic Impact on Industry

Chapter 3 Global Market Competition by Manufacturers

Chapter 4 Global Production, Revenue (Value) by Region

Chapter 5 Global Supply (Production), Consumption, Export, Import by Regions

Chapter 6 Global Production, Revenue (Value), Price Trend by Type

Chapter 7 Global Market Analysis by Application

Chapter 8 Manufacturing Cost Analysis

Chapter 9 Industrial Chain, Sourcing Strategy and Downstream Buyers

Chapter 10 Marketing Strategy Analysis, Distributors/Traders

Chapter 11 Market Effect Factors Analysis

Chapter 12 Global Precision Medicine Software Market Forecast

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E.coli bacteria running the Internet of Things – IOL

February 25th, 2020 5:44 pm

Technology/23 February 2020, 3:48pm/Louis Fourie

CAPE TOWN One of the areas of the Fourth Industrial Revolution (4IR) that has seen phenomenal growth over the past few years is that of bioscience and bioengineering. But when bioscience is combined with computer science, it seems that we may one day have biological computing devices that could partly replace the current hard drives, silicon microprocessors and microchips.

At least this is what some scientists firmly belief is possible.

Through the study of genetics we know that all living organisms consists of genes and deoxyribonucleic acid or DNA. These strings of DNA contains huge amounts of data that can last thousands of years as is evident from the 45 000 year old human femur bone from Siberia that was DNA-sequenced or decoded a few years ago.

It is exactly this remarkable data density and longevity of DNA that got scientists interested. Scientists have therefore been researching a synthetic form of DNA sequencing to store large quantities of data for an indefinite period of time. Recently scientists from Microsoft and the University of Washington announced that they were making very good progress. Already in 2018 they were already able to store 200 MB of data in DNA format and were able to retrieve it with zero errors.

Since 2018 much progress has been made and it seems very likely that DNA storage could complement current data storage methods or even replace some of them in the future. Perhaps Microsoft Researchs target of a DNA storage system functioning within a data centre by the turn of the decade is not so far-fetched.

Due to advances in nano- and biotechnology scientists at the Queen Mary University in London are taking research further and are using microbes to network and communicate at nanoscale, which is of particular interest to the Internet of Things (IoT).

In a 2019 paper by Raphael Kim and Stefan Poslad titled The thing with E.coli: Highlighting Opportunities and Challenges of Integrating Bacteria in IoT and HCI the researchers explain that it is not only the minute size, but also the autonomous nature of bacteria that caught their attention and presents interesting possibilities. Bacteria have an embedded, natural propeller motor or whip-like structure, called flagella, that propels them forward.

The research is still at an early stage but the exploitation of similarities between bacteria and computing devices is of great interest to the future of computing. The microbes share interesting similarities with some components of typical IoT devices, which indicate that bacteria could be used as a living form of an IoT device.

A good example would be the field of environmental IoT where bacteria could be programmed and deployed in the sea or in smart cities to detect toxins or pollutants, gather data, and even undertake the biomediation processes.

Likewise, in healthcare and medicine, bacteria could be programmed and deployed to treat specific diseases. The bacteria could swim to a pre-determined destination in the human body, then produce and release encoded hormones when triggered by the microbes internal sensor.

Microbes have exceptional chemical sensing, as well as actuating, communication and processing capabilities typical of a computerised IoT and could even outperform the best electronic devices. Bacteria cannot only detect chemicals, but also electromagnetic fields, light, mechanical stress, and temperature, as is normally done by traditional electronic sensors. The bacteria can also respond to these stimuli through movement using their flagella, or through the production of coloured proteins.

In fact bacteria are better than electronic chip-based sensors, since they are much more sensitive, stable and responsive than their digital counterparts. This superior qualities makes bacteria especially useful as a living form of IoT device and also valuable in the field of Human Computer Interaction (HCI).

Just like a digital control unit, memory and processor, the programmed DNA controls the bacteria and functions as a control unit with regard to the collection (sensing), processing and storing of data. Genomic DNA contains the instructions for the functioning of the bacteria, while the smaller circular plasmids (a form of DNA used to introduce genes into organisms) determine the process functions through gene addition and subtraction, as well as the storage of new data.

According to the team from the Queen Mary University the cellular membrane functions as the transceiver and allows for both the transmission and reception of communication. This molecular communication or the DNA exchange between cells forms the basis of a bacterial nanonetwork or signalling pathway.

This possibility of bacterial networks as an example of molecular communication such as the widely known E.coli bacterium that could act as an information carrier has in particular excited the IoT community.

The research with digital-to-DNA data and back again from DNA-to-digital data is showing great promise for the future. The idea of the researchers is to use the bacteria to create a potential substrate for the Internet of Bio-Nano Things (IoBNT), which entails the networking and communication through nanoscale and biological entities. Some of the often-despised bacteria may indeed change our connected world of sensors and IoT devices in the future.

Interesting is that the researchers from the Queen Mary University, London closes their research paper with a passionate plea for experimentation with do-it-yourself technology by enthusiasts to promote the IoBNT. They refer to the easily obtainable and affordable educational products like the Amino Labs Kit that are widely available to the public and allow, for example, many bioengineering experiments such as the generation of specific colours from bacteria through the programming of K12 E.coli DNA. Tools, data, and materials of biotechnology that enable the broader public to run small-scale experiments with microorganisms are currently easily accessible and affordable.

The Amino Labs Kit, for instance, caters for people who are interesting in manipulating and genetically engineering E.coli bacteria. The kit enables the user to create customised living colours and smells through the building of genetic circuits that can be triggered through a variety of pre-determined environmental stimuli.

This call by the researchers is not so unusual since technology hobbyists that experimented with very affordable Arduino microcontrollers and Rasberry Pi mini-computers were the very people that significantly advanced the traditional IoT. The mini-computers and the building of sensors and IoT controller devices were the learning space of many very successful technologists and scientists.

Due to the hard work of bioscientists around the world, programming of DNA is improving our quality of life in many instances and is keeping diseases at bay. It is therefore logical that the number of genetically engineered products will continue to rise in the future since it is one of of the 4IR.

Biotechnology en bioengineering will play an increasingly important role as major building blocks of the 4IR. Do-it-yourself and educational bio-kits can therefore teach potential future scientists how to effectively program bacteria. And perhaps some of the young bioengineers, learning the skills and concepts of the future, may one day become the scientists that solve the challenges of cancer, hunger, waste and climate change.

Todays adventures in science create tomorrows innovators. And it all starts with a string of DNA and an unpretentious bacterium.

Professor Louis C H Fourie is a futurist and technology strategist.[emailprotected]

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This Dior Serum Is Basically The Fountain Of Youth | BEAUTY/crew – BEAUTYcrew

February 25th, 2020 5:44 pm

The serum can reach deeper into the skin

Besides the star-studded line-up of ingredients, the formula features a clever delivery system that helps it go deeper into your skin. In particular, the formula features a bio-fermented lipopeptide (which is a probiotic to regulate the pH of your skin) which, when combined with the floral and hyaluronic acid ingredients, can improve the rate of penetration by 30 per cent. So, what does this mean? Well, it allows for quicker absorption, making it perfect to use both morning before applying foundation, and at night before going to bed.

The beauty of Dior Capture Totale Super Potent Serum is that it doesnt just do one thing - it actually addresses all aspects of ageing, as proven by 600 women from France, China and Japan*. The panel revealed that after continuous use, their skin looked brighter and smoother, and felt bouncier and stronger. And who doesnt want a complexion that looks and feels seriously healthy?

Like all good skin care products, the Super Potent Serum does its best work when its supported by a great team. There are four other products in the Capture Totale range that are also formulated with natural-origin ingredients. When used as a complete skin care routine the range delivers even more impressive anti-ageing results.

Dior Capture Totale High-Performance Gentle Cleanser: This cleanser can effectively remove dirt and sebum without aggravating skin and can improve skins softness.

Dior Capture Totale High-Performance Serum-Lotion: Pop a few drops of this hydrating product onto a cotton pad or the palms of your hands and press it all over your face for juicy-looking skin. Vitamins C, E and B3 in the formula have brightening and soothing qualities.

Dior Capture Totale Firming & Wrinkle-Correcting Crme: Dont underestimate its lightweight texture; this moisturiser can dial up radiance, fill fine lines and smooth skin in the long run. A special shout-out goes to the bio-fermented ceramides that help improve the skins barrier.

Dior Capture Totale Firming & Wrinkle-Correcting Eye Cream: Want to brighten and strengthen the skin around your eyes? Look no further than this phytosterols-enriched eye cream that works to firm up the delicate area.

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Global Precision Medicine Software Market Research Provides an In-Depth Analysis on the Future Growth Prospects and Market Trends Adopted by the…

February 25th, 2020 5:44 pm

Precision Medicine Software market Research Report 2020 offers a comprehensive analysis of the market growth drivers, trends, opportunities, prospects, drivers and restrictions inside the market. The report emphasizes to meet the requirement of customers by providing complete knowledge of the Precision Medicine Software Industry. This carefully organised report is formulated by industry experts and professional experts, in terms of demand and supply, cost organization, barriers and challenges, product category, crucial market players, technology, regions, and applications.

The Precision Medicine Software market study is based on historical information and present market requirements. As well as includes different business approaches preferred by the decision-makers. That enhanced the Precision Medicine Software industry growth and make a phenomenal stand in the industry. The market will raise with a prominentCAGRby 2020 to 2026.

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Furthermore, it also evaluates the most recent improvements while estimating the growth of theleading playerslike

SyapseAllscriptsQiagenRoper TechnologiesFabric GenomicsFoundation MedicineSophia GeneticsPierianDxHuman LongevityTranslational SoftwareGene42, IncLifeomic Health

Segmentation by Product Type

Cloud-basedOn-premise

Segmentation by Application/ End uses:

Healthcare ProvidersPharmaceutical and Biotechnology CompaniesResearch Centers and Government InstitutesOthers

Regional Analysis for Precision Medicine Software Market:

North America (the United States, Canada & Rest of the countries)

Europe (Germany, The UK, France, Netherlands, Italy, Spain & the rest of the countries)

Asia-Pacific (China, Japan, Korea, India, & rest of the countries)

Middle East & Africa (South Africa, Israel, UAE & rest of the countries)

South America (Brazil, Colombia, Argentina & the rest of the countries)

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What is the regional structure of the market? Our analysis-

The Precision Medicine Software Industry report analyses footprint of every product and its significance analyzes examine each geographical segment of the market with import, export, consumption, and production in these regions to provide a complete understanding of the Precision Medicine Software market

In addition, the Precision Medicine Software Industry report covers an analysis of different products available in the global market built on production, volume, revenue, and cost and price structure. The Precision Medicine Software Market report also highlights key strategies that proved to be profitable for the business in-line with the policies involved in business expansion, partnership deals, composition, and new product/service launches.

YEARS CONSIDERED FOR THIS REPORT:

Historical Years:2015-2019

Base Year:2019

Estimated Year:2020

Forecast Period:2020-2026

DEFINITE SEGMENTS OF GLOBAL Precision Medicine Software INDUSTRY:

The analysis highlights a region-wise as well as a worldwide study of the Precision Medicine Software market. Proportionately, the regional study of the industry comprisesJapan, South East Asia, India, the USA, Europe, and China.Moreover, the report reviews an in-depth market analysis of distinct manufacturers and suppliers. It explainsindustry chain structure, competitive scenario, and study of Precision Medicine Software industry costin detail. It evenly analyzes global industry size pursued by forecast period (2020-2026) and environment.

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The analysis covers basic information about the Precision Medicine Software product likeindustry scope, segmentation, anoverviewof the market. Likewise, it providessupply-demand data, investment feasibleness, and elements that limiting the growth of an industry. Predominantly, it helps product demand, annual revenue and growth prospects of the industry. The foreseen Precision Medicine Software market regions along with the present onesassist leading vendors, decision-makers, and viewers/readersto plan effective business strategies respectively.

KEY TOPIC COVERED

Growth Opportunities

Market Growth Drivers

Leading Market Players

Market Size and Growth Rate

Market Trend and Technological

Company Market Share

TOC OF Precision Medicine Software MARKET REPORT INCLUDES:

1 Industry Overview of Precision Medicine Software

2 Industry Chain Analysis

3 Manufacturing Technology

4 Major Manufacturers Analysis

5 Global Productions, Revenue and Price Analysis of Precision Medicine Software by Regions, Creators, Types, and Applications

6 Global and Foremost Regions Capacity, Production, Revenue and Growth Rate by 2013-2019

7 Consumption Volumes, Consumption Value, Import, Export and Sale Price Analysis by Regions

8 Gross and Gross Margin Analysis

9 Marketing Traders or Distributor Analysis

10 Global and Chinese Economic Impacts on the Precision Medicine Software Industry

11 Development Trend Analysis

12 Contact information

13 New Project Investment Feasibility Analysis

14 Conclusion of the Global Precision Medicine Software Industry 2019 Market Research Report Continued

Finally, the feasibility of new investment projects is assessed, and overall research conclusions are offered.

Key questions answered by the Precision Medicine Software Report:

What are some of the most favourable, high-growth prospects for the global Precision Medicine Software market?

Which products segments will raise at a faster pace throughout the forecast period and why?

What are the foremost factors impacting market prospects?

What are the driving factors, restraints, and challenges in this Precision Medicine Software market?

What are the competitive threats and challenges to themarket?

What are the evolving trends in this Precision Medicine Software market and reasons behind their emergence?

What are some of the changing customer demands in the Precision Medicine Software Industry market?

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https://www.reportspedia.com/report/technology-and-media/global-precision-medicine-software-market-2019-by-company,-regions,-type-and-application,-forecast-to-2024/32812 #table_of_contents

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