Marker Therapeutics Reports Second Quarter 2020 Operating and Financial Results – PRNewswire

HOUSTON, Aug. 10, 2020 /PRNewswire/ -- Marker Therapeutics, Inc.(Nasdaq:MRKR), a clinical-stage immuno-oncology company specializing in the development of next-generation T cell-based immunotherapies for the treatment of hematological malignancies and solid tumor indications, today provided a corporate update and reported financial results for the second quarter ended June 30, 2020.

"We continue to make progress toward advancing our planned Phase 2 trial with our novel MultiTAA-specific T cell therapy in patients with acute myeloid leukemia, or AML," said Peter L. Hoang, President & CEO of Marker Therapeutics. "While the COVID-19 pandemic has impacted hospital systems globally, we have augmented our process development for our MT-401 product, continued the buildout of our manufacturing facility and added further clinical sites for our Phase 2 AML trial. With a novel cell therapy product candidate that has demonstrated the ability to induce broad and durable immune responses in earlier clinical studies, Marker remains well-positioned to provide a potential treatment option for patients suffering from this devastating disease."

PROGRAM UPDATES

Multi-Antigen Targeted (MultiTAA) T Cell Therapies

Phase 2 AML Trial Update The Company continues to identify and add clinical trial sites in preparation for the Phase 2 AML trial initiation. The study is currently subject to a partial clinical hold on the use of a new reagent in the manufacturing processuntil the FDA reviews and accepts the final data and certificates of analysis for the new reagent. The alternate supplier has been delayed in providing the reagent but expects to ship the reagent to Marker in Q3. Once Marker receives the reagent and completes the required analyses for FDA, the Company will provide additional clarification around the timing of the AML trial enrollment.

USAN Council Approval of "Zelenoleucel" for MT-401Marker recently announced that the United States Adopted Names (USAN) Council approved "zelenoleucel" as the nonproprietary (generic) name for MT-401, a MultiTAA-specific T cell product candidate for the treatment of patients with AML following allogeneic stem cell transplant in both adjuvant and active disease settings.

Pancreatic Cancer Data Presented During ASCO Updated clinical results from an ongoing investigator-sponsored Phase 1 trial led by the Baylor College of Medicine, evaluating the Company's MultiTAA-specific T cell therapy in patients with advanced or metastatic pancreatic adenocarcinoma, were presented during the 2020 American Society of Clinical Oncology (ASCO) Virtual Annual Meeting. Data from a cohort of patients receiving MultiTAA-specific T cell therapy in combination with standard-of-care chemotherapy in the first-line setting (Arm A) were presented.

BUSINESS UPDATES

On June 30, 2020, Marker announced that the Company executed a lease agreement to establish an in-house cGMP manufacturing facility in Houston, TX. The facility is expected to be completed by year-end and operational in 2021. Marker will continue to manufacture its MultiTAA-specific T cell therapy at the Baylor College of Medicine to support the Company-sponsored AML trial until the in-house cGMP manufacturing facility is operational.

SECOND QUARTER 2020 FINANCIAL RESULTS

Cash Position and Guidance:At June 30, 2020, Marker had cash and cash equivalents of $32.1 million. The Company believes that its existing cash and cash equivalents will fund its operating expenses and capital expenditure requirements into Q2 2021.

R&D Expenses:Research and development expenses were$4.3 million for the quarter endedJune 30, 2020, compared to$3.2 million for the quarter ended June 30, 2019.

G&A Expenses:General and administrative expenses were$2.5 million for the quarter endedJune 30, 2020, compared to $2.7 million for the quarter ended June 30, 2019.

Net Loss:Marker reported a net loss of$6.3 millionfor the quarter endedJune 30, 2020, compared to a net loss of$5.6 million for the quarter ended June 30, 2019.

About Marker Therapeutics, Inc.Marker Therapeutics, Inc. is a clinical-stage immuno-oncology company specializing in the development of next-generation T cell-based immunotherapies for the treatment of hematological malignancies and solid tumor indications. Marker's cell therapy technology is based on the selective expansion of non-engineered, tumor-specific T cells that recognize tumor associated antigens (i.e. tumor targets) and kill tumor cells expressing those targets. This population of T cells is designed to attack multiple tumor targets following infusion into patients and to activate the patient's immune system to produce broad spectrum anti-tumor activity. Because Marker does not genetically engineer its T cell therapies, we believe that our product candidates will be easier and less expensive to manufacture, with reduced toxicities, compared to current engineered CAR-T and TCR-based approaches, and may provide patients with meaningful clinical benefit. As a result, Marker believes its portfolio of T cell therapies has a compelling product profile, as compared to current gene-modified CAR-T and TCR-based therapies.

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Forward-Looking Statement Disclaimer This release contains forward-looking statements for purposes of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Statements in this news release concerning the Company's expectations, plans, business outlook or future performance, and any other statements concerning assumptions made or expectations as to any future events, conditions, performance or other matters, are "forward-looking statements." Forward-looking statements include statements regarding our intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things: our research, development and regulatory activities and expectations relating to our non-engineered multi-tumor antigen specific T cell therapies; the effectiveness of these programs or the possible range of application and potential curative effects and safety in the treatment of diseases; the impact of the COVID-19 pandemic; and the timing and success of our clinical trials, as well as clinical trials conducted by our collaborators. Forward-looking statements are by their nature subject to risks, uncertainties and other factors which could cause actual results to differ materially from those stated in such statements. Such risks, uncertainties and factors include, but are not limited to the risks set forth in the Company's most recent Form 10-K, 10-Q and other SEC filings which are available through EDGAR at http://www.sec.gov. Such risks and uncertainties may be amplified by the COVID-19 pandemic and its impact on our business and the global economy. The Company assumes no obligation to update our forward-looking statements whether as a result of new information, future events or otherwise, after the date of this press release.

Marker Therapeutics, Inc.Condensed Consolidated Balance Sheets

June 30,

December 31,

2020

2019

(Unaudited)

(Audited)

ASSETS

Current assets:

Cash and cash equivalents

$ 32,124,187

$ 43,903,949

Prepaid expenses and deposits

2,632,514

1,526,442

Interest receivable

3,440

56,189

Total current assets

34,760,141

45,486,580

Non-current assets:

Property, plant and equipment, net

1,592,094

417,528

Construction in progress

2,629,141

-

Right-of-use assets, net

9,542,228

455,174

Total non-current assets

13,763,463

872,702

Total assets

$ 48,523,604

$ 46,359,282

LIABILITIES AND STOCKHOLDERS' EQUITY

Current liabilities:

Accounts payable and accrued liabilities

$ 4,528,021

$ 1,757,680

Lease liability

456,065

204,132

Warrant liability

-

31,000

Total current liabilities

4,984,086

1,992,812

Non-current liabilities:

Lease liability, net of current portion

9,025,273

280,247

Total non-current liabilities

9,025,273

280,247

Total liabilities

14,009,359

2,273,059

Commitments and contingencies

-

-

Stockholders' equity:

Preferred stock - $0.001 par value, 5 million shares authorized and 0 shares issued and outstanding at June 30, 2020 and December 31, 2019, respectively

-

-

Common stock, $0.001 par value, 150 million shares authorized, 46.6 million and 45.7 million shares issued and outstanding as of June 30, 2020 and December 31, 2019, respectively

46,617

45,728

Additional paid-in capital

374,828,385

371,573,909

Accumulated deficit

(340,360,757)

(327,533,414)

Total stockholders' equity

34,514,245

44,086,223

Total liabilities and stockholders' equity

$ 48,523,604

$ 46,359,282

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Marker Therapeutics Reports Second Quarter 2020 Operating and Financial Results - PRNewswire

University of Minnesota expands clinical investigation of engineered iPSC-derived natural killer cells, opening U.S. clinical trial for the treatment…

The first patient has received treatment in a new clinical trial that has opened at the University of Minnesota to test whether a novel cell therapy currently under clinical investigation as a treatment for acute myeloid leukemia (AML) and lymphoma can be effective as a treatment for COVID-19. The first-of-its-kind, engineered iPSC-derived natural killer (NK) cell product candidate, FT516, may play a role in diminishing viral replication of the novel coronavirus. NK cells have been known to play a role in protecting the body against viral infection; however, it is not known whether NK cells will be able to safely control COVID-19, the infectious disease caused by the virus SARS-CoV-2.

The clinical trial Study of FT516 Safety and Feasibility for the Treatment of Coronavirus Disease 2019 (COVID-19) in Hospitalized Patients with Hypoxia, which is being supported by Fate Therapeutics, Inc., is being run locally by Joshua Rhein, M.D., Assistant Professor of Medicine in the University of Minnesota Medical Schools Division of Infectious Diseases and International Medicine.

The medical research community has been mobilized to meet the unique challenges that COVID-19 presents, said Rhein. There are limited treatment options for COVID-19, and we have been inundated daily with reports of varying quality describing the potential of numerous therapies. We know that NK cells play an important role in responding to SARS-CoV-2, the virus responsible for COVID-19, and that these cells often become depleted in infected patients. Our intent is to replenish NK cells in order to restore a functional immune system and directly target the virus.

Jeffrey Miller, M.D., Deputy Director of the Masonic Cancer Center, and Professor of Medicine in the Medical Schools Division of Hematology, Oncology and Transplantation, is a pioneer in the field of NK cells. As a collaborator on the trial, Dr. Miller will apply his decades of experience in NK cell biology and therapy in cancer to this international challenge.

One of the complexities of treating COVID-19 with cell therapy is the underlying inflammation that coincides with more severe cases of COVID-19 infection. The challenge is to carefully deliver off-the-shelf engineered NK cells at increasing doses to turn off viral replication without overly activating the immune system to make the lungs worse.

The study has been carefully designed with appropriate medical checkpoints to investigate the potential of NK cells in a manner which we believe to be safe in COVID-19 patients, said Miller. We will also track the immune response and duration of viral shedding to see if FT516 decreases shedding of COVID-19 in the respiratory tract. If successful, these off-the-shelf, iPSC-derived NK cells can be batch manufactured and sent nationwide to patients.

FT516 is manufactured from a master human induced pluripotent stem cell (iPSC) line that has been genetically engineered to enhance its binding to therapeutic antibodies. It was initially developed to attack AML and B-cell lymphoma, based on the groundbreaking research on stem cells and NK cells done at the Masonic Cancer Center.

FT516, which is being clinically developed by Fate Therapeutics for the treatment of advanced hematologic malignancies and solid tumors, was produced and manufactured at the U of Ms Molecular and Cellular Therapeutics (MCT) center, which offers full-service development and manufacturing of cell- and tissue-based products, monoclonal antibodies and other therapeutic proteins, as well as active pharmaceutical ingredients for use in Phase I, II or III clinical trials. M Health Fairview, the clinical partner of the Masonic Cancer Center, supports the MCT in the production of these molecules.

###

Read the original release about FT516 here.

About the Masonic Cancer Center, University of MinnesotaThe Masonic Cancer Center, University of Minnesota, is the Twin Cities only Comprehensive Cancer Center, designated Outstanding by the National Cancer Institute. As Minnesotas Cancer Center, we have served the entire state for more than 25 years. Our researchers, educators, and care providers have worked to discover the causes, prevention, detection, and treatment of cancer and cancer-related diseases. Learn more at cancer.umn.edu.

About the University of Minnesota Medical SchoolThe University of Minnesota Medical School is at the forefront of learning and discovery, transforming medical care and educating the next generation of physicians. Our graduates and faculty produce high-impact biomedical research and advance the practice of medicine. Learn how the University of Minnesota is innovating all aspects of medicine by visiting http://www.med.umn.edu.

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University of Minnesota expands clinical investigation of engineered iPSC-derived natural killer cells, opening U.S. clinical trial for the treatment...

Clinical study using mesenchymal stem cells for the treatment of patients with severe COVID-19 – DocWire News

This article was originally published here

Front Med. 2020 Aug 6. doi: 10.1007/s11684-020-0810-9. Online ahead of print.

ABSTRACT

The Coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2 was identified in December 2019. The symptoms include fever, cough, dyspnea, early symptom of sputum, and acute respiratory distress syndrome (ARDS). Mesenchymal stem cell (MSC) therapy is the immediate treatment used for patients with severe cases of COVID-19. Herein, we describe two confirmed cases of COVID-19 in Wuhan to explore the role of MSC in the treatment of COVID-19. MSC transplantation increases the immune indicators (including CD4 and lymphocytes) and decreases the inflammation indicators (interleukin-6 and C-reactive protein). High-flow nasal cannula can be used as an initial support strategy for patients with ARDS. With MSC transplantation, the fraction of inspired O2 (FiO2) of the two patients gradually decreased while the oxygen saturation (SaO2) and partial pressure of oxygen (PO2) improved. Additionally, the patients chest computed tomography showed that bilateral lung exudate lesions were adsorbed after MSC infusion. Results indicated that MSC transplantation provides clinical data on the treatment of COVID-19 and may serve as an alternative method for treating COVID-19, particularly in patients with ARDS.

PMID:32761491 | DOI:10.1007/s11684-020-0810-9

Originally posted here:

Clinical study using mesenchymal stem cells for the treatment of patients with severe COVID-19 - DocWire News

New Report: Regenerative Medicine & Advanced Therapies Sector Thriving Despite COVID-19 – PharmiWeb.com

Cell, Gene & Tissue-Based Therapy Developers Poised to Break Year-Over-Year Global Financing Records

WASHINGTON, D.C. August 6, 2020 The Alliance for Regenerative Medicine (ARM), the leading international advocacy organization dedicated to realizing the promise of regenerative medicines and advanced therapies, today announces the publication of its H1 2020 Global Sector Report, Innovation in the Time of COVID-19. The report provides an in-depth look at trends and metrics in the gene, cell, and tissue-based therapeutic sector in the midst of the pandemic.

As the voice of the sector globally, ARM regularly publishes sector data reports to showcase clinical and scientific progress, as well as advancements and remaining challenges in the policy environment surrounding cell, gene and tissue-based therapies. The report also includes updated metrics on fundraising and clinical trials from more than 1,000 therapeutic developers worldwide.

Highlights from the H1 2020 Global Sector Report include:

Janet Lambert, CEO of ARM, commented: The regenerative medicine and advanced therapy sector has shown remarkable resilience in the face of many new challenges posed by COVID-19. Most importantly, were continuing to see patients benefit from the profound therapeutic effects of both approved products and those currently in clinical development. ARM will continue to work with our membership and with policymakers in the second half of 2020 to further advance these transformative technologies. We are committed to bringing these life-changing therapies to patients in need.

This report is the latest in ARMs series of global regenerative medicine sector reports, providing up-to-date metrics on financings and the clinical landscape, as well as expert commentary on key trends and progress in the field. The full report is available online here, with key sector metrics and infographics available here. For more information, please visit http://www.alliancerm.org or contact Kaitlyn (Donaldson) Dupont at kdonaldson@alliancerm.org.

About the Alliance for Regenerative Medicine

The Alliance for Regenerative Medicine (ARM) is the leading international advocacy organization dedicated to realizing the promise of regenerative medicines and advanced therapies. ARM promotes legislative, regulatory and reimbursement initiatives to advance this innovative and transformative sector, which includes cell therapies, gene therapies and tissue-based therapies. Early products to market have demonstrated profound, durable and potentially curative benefits that are already helping thousands of patients worldwide, many of whom have no other viable treatment options. Hundreds of additional product candidates contribute to a robust pipeline of potentially life-changing regenerative medicines and advanced therapies. In its 11-year history, ARM has become the voice of the sector, representing the interests of 360+ members worldwide, including small and large companies, academic research institutions, major medical centers and patient groups. To learn more about ARM or to become a member, visit http://www.alliancerm.org.

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New Report: Regenerative Medicine & Advanced Therapies Sector Thriving Despite COVID-19 - PharmiWeb.com

UPDATED: After a 4-year sojourn, struggling microbiome pioneer Seres claims a breakout PhIII comeback. And shares respond in frenzied spike -…

Almost exactly 4 years ago, Seres Therapeutics $MCRB experienced one of those soul-crunching failures that can raise big questions about a biotechs future. Out front in their pursuit of a gut punch to C. difficile infection (CDI), the Phase II test was a flat failure, and investors wiped out a billion dollars of equity value that never returned in the years that followed.

Seres, though, pressed ahead, changing out CEOs a year ago bidding Merck vet Roger Pomerantz farewell from the C suite and pushing through a Phase III, hoping that amping up the dosage would make the key difference. And this morning, they unveiled a claim that they had aced the Phase III and positioned themselves for a run at a landmark FDA OK.

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UPDATED: After a 4-year sojourn, struggling microbiome pioneer Seres claims a breakout PhIII comeback. And shares respond in frenzied spike -...

Covid-19 roundup: CureVac beefs up its unicorn IPO dreams as billionaire owner takes this Covid-19 mRNA player on a forced march to Nasdaq; Kodak’s…

Almost exactly 4 years ago, Seres Therapeutics $MCRB experienced one of those soul-crunching failures that can raise big questions about a biotechs future. Out front in their pursuit of a gut punch to C. difficile infection (CDI), the Phase II test was a flat failure, and investors wiped out a billion dollars of equity value that never returned in the years that followed.

Seres, though, pressed ahead, changing out CEOs a year ago bidding Merck vet Roger Pomerantz farewell from the C suite and pushing through a Phase III, hoping that amping up the dosage would make the key difference. And this morning, they unveiled a claim that they had aced the Phase III and positioned themselves for a run at a landmark FDA OK.

Unlock this story instantly and join 86,800+ biopharma pros reading Endpoints daily and it's free.

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Covid-19 roundup: CureVac beefs up its unicorn IPO dreams as billionaire owner takes this Covid-19 mRNA player on a forced march to Nasdaq; Kodak's...

Nearly 70K donated so far towards Wistaston boy’s 120K lifesaving treatment – Cheshire Live

A WIstaston family are overwhelmed by the generosity of people who have donated nearly 70K so far towards the 120K needed for lifesaving treatment for their 11-year-old son.

Georgy Capener was diagnosed with the highly malignant Ewings Sarcoma, a rare form of bone cancer, following a fall in a friends's garden on Easter Sunday in 2018.

He has undergone numerous rounds of high dose aggressive chemotherapy and radiotherapy since then, lost his right arm as a result of the treatment and now has a titanium prosthesis.

Georgy went into remission last March, but the cancer returned in April this year, this time in his left sinus, just under his eye socket and in the back of his nose.

The Wistaston Church Lane pupil is now undergoing chemotherapy and radiotherapy again - but the vital stem cell therapy which is essential to ensure he can live a normal, healthy life and prevent the cancer returning at a later stage costs 130,000 and is not available for Georgy on the NHS.

The money needs to be raised by the beginning of September, when Georgy is due to finish his final round of chemotherapy, as, for the stem cell treatment to be successful, the procedure would have to start immediately after that to ensure the cancer doesnt return straight away,

This week Georgys mum, Helen Capener, was close to tears she was so overwhelmed by the generosity of people who have donated and organised fundraisers.

I just cant believe the total raised so far, she said. Its just so nice. Weve got fundraisers doing things all over the place, my cousins biking from Peterborough to Crewe, weve got people in Cheadle doing stuff, everywhere, its brilliant

Ive been trying to keep up with whos donating. Its so lovely, Im still overwhelmed.

She said money had flooded in from Crewe Chronicle, CheshireLive and Liverpool Echo readers.

Passionate Liverpool fan Georgy has also received a video message of support from the Reds defender Andy Robertson.

It was brilliant, said Helen. Unfortunately I wasnt there when he received it. It was his dads turn to take him to radiotherapy so he saw it in the car so I didnt see his reaction but his dad said he was absolutely over the moon. His little face lit up and he just loves it. As soon as he came back, he ran in to show me.

There are so many fundraising events taking place to raise money for Georgys treatment, it is impossible to list them all here.

They range from an online fitness class which took place on Saturday, to people walking up Snowdon at the end of this month, one person has sold off their vinyl collection, others are making T-shirts and hoodies with the Georgys Fight logo, theres a big raffle and Georgys Fight jewellery being made and sold by another fundraiser.

A Facebook Page set up by a family friend, called Georgys Fight, lists how you can help.

Helen said that she and husband, Richard, cant thank people enough.

Georgy is undergoing his last round of chemotherapy this week.

Speaking earlier this week, Helen said: He finishes his radiotherapy this Friday (August 7) so hes struggling a bit now. Hes been having lots of nosebleeds and hes got an ulcer right at the back of his throat so hes still unable to eat much and hes got ulcers all on the left hand side of his cheek which are stinging.

They did tell us that this would happen and we expected it a bit earlier, so hes done really well to get this far but the last week or so started to take its toll.

Hes got four more sessions after this and its finished.

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He didnt want to go this morning because he knows that at each session its going to hurt even more, but he always bounces back. Once hes finished the radiotherapy, give him a couple of weeks and hell be back to feeling ok again I think.

Georgy has been accepted by a clinic in Thailand to undergo the vital stem cell treatment he needs next month but it is essential the treatment starts in September ensure the cancer doesnt return straight away,

That is why the family set up the JustGiving fundraising page to help save our sons life.

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Nearly 70K donated so far towards Wistaston boy's 120K lifesaving treatment - Cheshire Live

Coronavirus Drug and Treatment Tracker – The New York Times

The Covid-19 pandemic is one of the greatest challenges modern medicine has ever faced. Doctors and scientists are scrambling to find treatments and drugs that can save the lives of infected people and perhaps even prevent them from getting sick in the first place.

Below is an updated list of 20 of the most-talked-about treatments for the coronavirus. While some are accumulating evidence that theyre effective, most are still at early stages of research. We also included a warning about a few that are just bunk.

We are following 20 coronavirus treatments for effectiveness and safety:

Tentative or

mixed evidence

We are following 20 coronavirus treatments

for effectiveness and safety:

Tentative or

mixed evidence

We are following 20 coronavirus treatments

for effectiveness and safety:

There is no cure yet for Covid-19. And even the most promising treatments to date only help certain groups of patients and await validation from further trials. The F.D.A. has not fully licensed any treatment specifically for the coronavirus. Although it has granted emergency use authorization to some treatments, their effectiveness against Covid-19 has yet to be demonstrated in large-scale, randomized clinical trials.

This list provides a snapshot of the latest research on the coronavirus, but does not constitute medical endorsements. Always consult your doctor about treatments for Covid-19.

New additions and recent updates:

Added ivermectin, a drug typically used against parasitic worms that is being increasingly prescribed in Latin America. Aug. 10

Updated descriptions for several treatments. Aug. 10

We will update and expand the list as new evidence emerges. For details on evaluating treatments, see the N.I.H. Covid-19 Treatment Guidelines. For the current status of vaccine development, see our Coronavirus Vaccine Tracker.

WIDELY USED: These treatments have been used widely by doctors and nurses to treat patients hospitalized for diseases that affect the respiratory system, including Covid-19.

PROMISING EVIDENCE: Early evidence from studies on patients suggests effectiveness, but more research is needed. This category includes treatments that have shown improvements in morbidity, mortality and recovery in at least one randomized controlled trial, in which some people get a treatment and others get a placebo.

TENTATIVE OR MIXED EVIDENCE: Some treatments show promising results in cells or animals, which need to be confirmed in people. Others have yielded encouraging results in retrospective studies in humans, which look at existing datasets rather than starting a new trial. Some treatments have produced different results in different experiments, raising the need for larger, more rigorously designed studies to clear up the confusion.

NOT PROMISING: Early evidence suggests that these treatments do not work.

PSEUDOSCIENCE OR FRAUD: These are not treatments that researchers have ever considered using for Covid-19. Experts have warned against trying them, because they do not help against the disease and can instead be dangerous. Some people have even been arrested for their false promises of a Covid-19 cure.

EVIDENCE IN CELLS, ANIMALS or HUMANS: These labels indicate where the evidence for a treatment comes from. Researchers often start out with experiments on cells and then move onto animals. Many of those animal experiments often fail; if they dont, researchers may consider moving on to research on humans, such as retrospective studies or randomized clinical trials. In some cases, scientists are testing out treatments that were developed for other diseases, allowing them to move directly to human trials for Covid-19.

All treatmentsWidely usedPromisingTentative or mixedNot promisingPseudoscience

Antivirals can stop viruses such as H.I.V. and hepatitis C from hijacking our cells. Scientists are searching for antivirals that work against the new coronavirus.

PROMISING EVIDENCE EVIDENCE IN CELLS, ANIMALS AND HUMANSEMERGENCY USE AUTHORIZATIONRemdesivirRemdesivir, made by Gilead Sciences, was the first drug to get emergency authorization from the F.D.A. for use on Covid-19. It stops viruses from replicating by inserting itself into new viral genes. Remdesivir was originally tested as an antiviral against Ebola and Hepatitis C, only to deliver lackluster results. But preliminary data from trials that began this spring suggested the drug can reduce the recovery time of people hospitalized with Covid-19 from 15 to 11 days. (The study defined recovery as either discharge from the hospital or hospitalization for infection-control purposes only.) These early results did not show any effect on mortality, though retrospective data released in July hints that the drug might reduce death rates among those who are very ill.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS, ANIMALS AND HUMANSFavipiravirOriginally designed to beat back influenza, favipiravir blocks a viruss ability to copy its genetic material. A small study in March indicated the drug might help purge the coronavirus from the airway, but results from larger, well-designed clinical trials are still pending.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS, ANIMALS AND HUMANSMK-4482Another antiviral originally designed to fight the flu, MK-4482 (previously known as EIDD-2801) has had promising results against the new coronavirus in studies in cells and on animals. Merck, which has been running clinical trials on the drug this summer, has announced it will launch a large Phase III trial in September.Updated Aug. 6

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS Recombinant ACE-2To enter cells, the coronavirus must first unlock them a feat it accomplishes by latching onto a human protein called ACE-2. Scientists have created artificial ACE-2 proteins which might be able to act as decoys, luring the coronavirus away from vulnerable cells. Recombinant ACE-2 proteins have shown promising results in experiments on cells, but not yet in animals or people.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS AND HUMANS IvermectinFor decades, ivermectin has served as a potent drug to treat parasitic worms. Doctors use it against river blindness and other diseases, while veterinarians give dogs a different formulation to cure heartworm. Studies on cells have suggested ivermectin might also kill viruses. But scientists have yet to find evidence in animal studies or human trials that it can treat viral diseases. As a result, Ivermectin is not approved to use as an antiviral.

In April, Australian researchers reported that the drug blocked coronaviruses in cell cultures, but they used a dosage that was so high it might have dangerous side effects in people. The FDA immediately issued a warning against taking pet medications to treat or prevent Covid-19. These animal drugs can cause serious harm in people, the agency warned.

Since then a number of clinical trials have been launched to see if a safe dose of ivermectin can fight Covid-19. In Singapore, for example, the National University Hospital is running a 5,000-person trial to see if it can prevent people from getting infected. As of now, theres no firm evidence that it works. Nevertheless ivermectin is being prescribed increasingly often in Latin America, much to the distress of disease experts.Updated Aug. 10

NOT PROMISING EVIDENCE IN CELLS AND HUMANS Lopinavir and ritonavirTwenty years ago, the F.D.A. approved this combination of drugs to treat H.I.V. Recently, researchers tried them out on the new coronavirus and found that they stopped the virus from replicating. But clinical trials in patients proved disappointing. In early July, the World Health Organization suspended trials on patients hospitalized for Covid-19. They didnt rule out studies to see if the drugs could help patients not sick enough to be hospitalized, or to prevent people exposed to the new coronavirus from falling ill. The drug could also still have a role to play in certain combination treatments.

NOT PROMISING EVIDENCE IN CELLS, ANIMALS AND HUMANSHydroxychloroquine and chloroquineGerman chemists synthesized chloroquine in the 1930s as a drug against malaria. A less toxic version, called hydroxychloroquine, was invented in 1946, and later was approved for other diseases such as lupus and rheumatoid arthritis. At the start of the Covid-19 pandemic, researchers discovered that both drugs could stop the coronavirus from replicating in cells.

Since then, theyve had a tumultuous ride. A few small studies on patients offered some hope that hydroxychloroquine could treat Covid-19. The World Health Organization launched a randomized clinical trial in March to see if it was indeed safe and effective for Covid-19, as did Novartis and a number of universities. Meanwhile, President Trump repeatedly promoted hydroxychloroquine at press conferences, touting it as a game changer, and even took it himself. The F.D.A. temporarily granted hydroxychloroquine emergency authorization for use in Covid-19 patients which a whistleblower later claimed was the result of political pressure. In the wake of the drugs newfound publicity, demand spiked, resulting in shortages for people who rely on hydroxychloroquine as a treatment for other diseases.

But more detailed studies proved disappointing. A study on monkeys found that hydroxychloroquine didnt prevent the animals from getting infected and didnt clear the virus once they got sick. Randomized clinical trials found that hydroxychloroquine didnt help people with Covid-19 get better or prevent healthy people from contracting the coronavirus. Another randomized clinical trial found that giving hydroxychloroquine to people right after being diagnosed with Covid-19 didnt reduce the severity of their disease. (One large-scale study that concluded the drug was harmful as well was later retracted.) The World Health Organization, the National Institutes of Health and Novartis have since halted trials investigating hydroxychloroquine as a treatment for Covid-19, and the F.D.A. revoked its emergency approval. The F.D.A. now warns that the drug can cause a host of serious side effects to the heart and other organs when used to treat Covid-19.

In July, researchers at Henry Ford hospital in Detroit published a study finding that hydroxychloroquine was associated with a reduction in mortality in Covid-19 patients. President Trump praised the study on Twitter, but experts raised doubts about it. The study was not a randomized controlled trial, in which some people got a placebo instead of hydroxychloroquine. The studys results might not be due to the drug killing the virus. Instead, doctors may have given the drug to people who were less sick, and thus more likely to recover anyway.

Despite negative results, a number of hydroxychloroquine trials have continued, although most are small, testing a few dozen or a few hundred patients. A recent analysis by STAT and Applied XL found more than 180 ongoing clinical trials testing hydroxychloroquine or chloroquine, for treating or preventing Covid-19. Although its clear the drugs are no panacea, its theoretically possible they could provide some benefit in combination with other treatments, or when given in early stages of the disease. Only well-designed trials can determine if thats the case.Updated Aug. 10

Most people who get Covid-19 successfully fight off the virus with a strong immune response. Drugs might help people who cant mount an adequate defense.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS AND HUMANS Convalescent plasmaA century ago, doctors filtered plasma from the blood of recovered flu patients. So-called convalescent plasma, rich with antibodies, helped people sick with flu fight their illness. Now researchers are trying out this strategy on Covid-19. In May, the F.D.A. designated convalescent plasma an investigational product. That means that despite not yet being shown as safe and effective, plasma can be used in clinical trials and given to some patients who are seriously ill with Covid-19. Tens of thousands of patients in the U.S. have received plasma through a program launched by the Mayo Clinic and the federal government.

The Trump administration has praised convalescent plasma, despite the lack of evidence yet that it works. The first wave of trials have been small and the results have been mixed. Large randomized clinical trials are underway, but theyve struggled to enroll enough participants, some of whom worry they will receive a placebo instead of the treatment itself.

Experts say that its vital to complete these trials to determine if convalescent plasma is safe and effective. If these trials are successful, it could serve as an important stopgap measure until more potent therapies become widely available.Updated Aug. 10

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS, ANIMALS AND HUMANSMonoclonal antibodiesConvalescent plasma from people who recover from Covid-19 contains a mix of different antibodies. Some of the molecules can attack the coronavirus, but many are directed at other pathogens. Researchers have sifted through this slurry to find the most potent antibodies against Covid-19. They have then manufactured synthetic copies of these molecules, known as monoclonal antibodies. Researchers have begun investigating them as a treatment for Covid-19, either individually or in cocktails.

Monoclonal antibodies were first developed as a therapy in the 1970s, and since then the F.D.A. has approved them for 79 diseases, ranging from cancer to AIDS. Since the start of the pandemic, researchers have found dozens of monoclonal antibodies that show promise against Covid-19 in preclinical studies on cells and animals. Companies like Eli Lilly and Regeneron recently began clinical trials studying monoclonal antibodies. Several other firms, as well as teams at universities, are slated to enter the race soon as well.Updated Aug. 10

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS, ANIMALS AND HUMANSInterferonsInterferons are molecules our cells naturally produce in response to viruses. They have profound effects on the immune system, rousing it to attack the invaders, while also reining it in to avoid damaging the bodys own tissues. Injecting synthetic interferons is now a standard treatment for a number of immune disorders. Rebif, for example, is prescribed for multiple sclerosis.

As part of its strategy to attack our bodies, the coronavirus appears to tamp down interferon. That finding has encouraged researchers to see whether a boost of interferon might help people weather Covid-19, particularly early in infection. Early studies, including experiments in cells and mice, have yielded encouraging results that have led to clinical trials.

An open-label study in China suggested that the molecules could help prevent healthy people from getting infected. On July 20, the British pharmaceutical company Synairgen announced that an inhaled form of interferon called SNG001 lowered the risk of severe Covid-19 in infected patients in a small clinical trial. The full data have not yet been released to the public, or published in a scientific journal. On August 6, the National Institute of Allergy and Infectious Diseases launched a Phase III trial on a combination of Rebif and the antiviral remdesivir, with results expected by fall 2020.Updated Aug. 10

The most severe symptoms of Covid-19 are the result of the immune systems overreaction to the virus. Scientists are testing drugs that can rein in its attack.

PROMISING EVIDENCE EVIDENCE IN HUMANS DexamethasoneThis cheap and widely available steroid blunts many types of immune responses. Doctors have long used it to treat allergies, asthma and inflammation. In June, it became the first drug shown to reduce Covid-19 deaths. That study of more than 6,000 people, which in July was published in the New England Journal of Medicine, found that dexamethasone reduced deaths by one-third in patients on ventilators, and by one-fifth in patients on oxygen. It may be less likely to help and may even harm patients who are at an earlier stage of Covid-19 infections, however. In its Covid-19 treatment guidelines, the National Institutes of Health recommends only using dexamethasone in patients with COVID-19 who are on a ventilator or are receiving supplemental oxygen.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN HUMANS Cytokine InhibitorsThe body produces signaling molecules called cytokines to fight off diseases. But manufactured in excess, cytokines can trigger the immune system to wildly overreact to infections, in a process sometimes called a cytokine storm. Researchers have created a number of drugs to halt cytokine storms, and they have proven effective against arthritis and other inflammatory disorders. Some turn off the supply of molecules that launch the production of the cytokines themselves. Others block the receptors on immune cells to which cytokines would normally bind. A few block the cellular messages they send. Depending on how the drugs are formulated, they can block one cytokine at a time, or muffle signals from several at once.

Against the coronavirus, several of these drugs have offered modest help in some trials, but faltered in others. Drug companies Regeneron and Roche drug both recently announced that two drugs called sarilumab and tocilizumab, which both target the cytokine IL-6, did not appear to benefit patients in Phase 3 clinical trials. Many other trials remain underway, several of which combine cytokine inhibitors with other treatments.Updated Aug. 10

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN HUMANS EMERGENCY USE AUTHORIZATIONBlood filtration systemsThe F.D.A. has granted emergency use authorization to several devices that filter cytokines from the blood in an attempt to cool cytokine storms. One machine, called Cytosorb, can reportedly purify a patients entire blood supply about 70 times in a 24-hour period. A small study in March suggested that Cytosorb had helped dozens of severely ill Covid-19 patients in Europe and China, but it was not a randomized clinical trial that could conclusively demonstrate it was effective. A number of studies on blood filtration systems are underway, but experts caution that these devices carry some risks. For example, such filters could remove beneficial components of blood as well, such as vitamins or medications.Updated Aug. 10

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN HUMANS Stem cellsCertain kinds of stem cells can secrete anti-inflammatory molecules. Over the years, researchers have tried to use them as a treatment for cytokine storms, and now dozens of clinical trials are under way to see if they can help patients with Covid-19. But these stem cell treatments havent worked well in the past, and its not clear yet if theyll work against the coronavirus.

Doctors and nurses often administer other supportive treatments to help patients with Covid-19.

WIDELY USEDProne positioningThe simple act of flipping Covid-19 patients onto their bellies opens up the lungs. The maneuver has become commonplace in hospitals around the world since the start of the pandemic. It might help some individuals avoid the need for ventilators entirely. The treatments benefits continue to be tested in a range of clinical trials.

WIDELY USEDEMERGENCY USE AUTHORIZATIONVentilators and other respiratory support devicesDevices that help people breathe are an essential tool in the fight against deadly respiratory illnesses. Some patients do well if they get an extra supply of oxygen through the nose or via a mask connected to an oxygen machine. Patients in severe respiratory distress may need to have a ventilator breathe for them until their lungs heal. Doctors are divided about how long to treat patients with noninvasive oxygen before deciding whether or not they need a ventilator. Not all Covid-19 patients who go on ventilators survive, but the devices are thought to be lifesaving in many cases.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN HUMANS AnticoagulantsThe coronavirus can invade cells in the lining of blood vessels, leading to tiny clots that can cause strokes and other serious harm. Anticoagulants are commonly used for other conditions, such as heart disease, to slow the formation of clots, and doctors sometimes use them on patients with Covid-19 who have clots. Many clinical trials teasing out this relationship are now underway. Some of these trials are looking at whether giving anticoagulants before any sign of clotting is beneficial.

False claims about Covid-19 cures abound. The F.D.A. maintains a list of more than 80 fraudulent Covid-19 products, and the W.H.O. debunks many myths about the disease.

WARNING: DO NOT DO THISDrinking or injecting bleach and disinfectantsIn April, President Trump suggested that disinfectants such as alcohol or bleach might be effective against the coronavirus if directly injected into the body. His comments were immediately refuted by health professionals and researchers around the world as well as the makers of Lysol and Clorox. Ingesting disinfectant would not only be ineffective against the virus, but also hazardous possibly even deadly. In July, Federal prosecutors charged four Florida men with marketing bleach as a cure for COVID-19.

WARNING: NO EVIDENCEUV lightPresident Trump also speculated about hitting the body with ultraviolet or just very powerful light. Researchers have used UV light to sterilize surfaces, including killing viruses, in carefully managed laboratories. But UV light would not be able to purge the virus from within a sick persons body. This kind of radiation can also damage the skin. Most skin cancers are a result of exposure to the UV rays naturally present in sunlight.

WARNING: NO EVIDENCESilverThe F.D.A. has threatened legal action against a host of people claiming silver-based products are safe and effective against Covid-19 including televangelist Jim Bakker and InfoWars host Alex Jones. Several metals do have natural antimicrobial properties. But products made from them have not been shown to prevent or treat the coronavirus.

Note: After additional discussions with experts we have adjusted several labels on the tracker. The Strong evidence label has been removed until further research identifies treatments that consistently benefit groups of patients infected by the coronavirus. In its place, Promising evidence will be used for drugs such as remdesivir and dexamethasone that have shown promise in at least one randomized controlled trial, and Widely used for treatments such as proning and ventilators that are often used with severely ill patients, including those with Covid-19. And we may reintroduce the Ineffective label when ongoing clinical trials repeatedly end with disappointing results.

Sources: National Library of Medicine; National Institutes of Health; William Amarquaye, University of South Florida; Paul Bieniasz, Rockefeller University; Jeremy Faust, Brigham & Womens Hospital; Matt Frieman, University of Maryland School of Medicine; Noah Haber, Stanford University; Swapnil Hiremath, University of Ottawa; Akiko Iwaskai, Yale University; Paul Knoepfler, University of California, Davis; Elena Massarotti, Brigham and Womens Hospital; John Moore and Douglas Nixon, Weill Cornell Medical College; Erica Ollman Saphire, La Jolla Institute for Immunology; Regina Rabinovich, Harvard T.H. Chan School of Public Health; Ilan Schwartz, University of Alberta; Phyllis Tien, University of California, San Francisco.

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Coronavirus Drug and Treatment Tracker - The New York Times

World of technology changed forever by the pandemic – TechTarget

jamesteohart/stock.adobe.com

We'll never see a year like 2020 again. Let's hope not, anyway.

We're barely halfway through the year, but it's been chock-full with once-in-a-lifetime or even once-in-a-generation events. We've experienced a pandemic, a major recession, street protests and the occasional riot in major cities around the world.

We've seen major sports seasons interrupted or delayed, only to resume without fans in the stands. Unemployment has spiked to levels of the Great Depression. The U.S. presidential election includes virtual conventions, social-distanced debates and uncertainty as to how ballots will be cast.

The world of technology has changed, too. Working at home is the norm, and we've seen cloud use spiking, buying patterns disrupted and face-to-face communication becoming rare.

Sports fans, economists and political junkies will probably never see another year like this, and they can't wait for life to get back to normal. But for the IT world, many changes will become the new normal.

Some modifications accelerated yearslong trends: a move to the cloud, smaller data center footprints, buying infrastructure as a utility or a service, and a greater emphasis on security and software. But the most sudden change is of a personal nature -- the way we interact. Besides prompting most meetings with co-workers to go virtual, the pandemic changed the way storage and other IT customers interact with vendors.

Call it software-defined sales, where Zoom, Microsoft Teams, Slack and streaming virtual events replace face-to-face on-site meetings and physical user conferences. Fast-tracked due to COVID-19, virtual interactions are the new norm and will only become more so in the coming years.

Gartner predictedthat only 25% of work meetings will take place in person by 2024, down from 60% at the start of 2020.

"We do not see this shift as temporary. In fact, we see the future of work changing permanently," said Nutanix CEO Dheeraj Pandey.

Pandey said the hyper-converged infrastructure vendor experienced no drop-off in lead generation after the first few months of remote work and virtual communications with users due to the new coronavirus. Other storage vendor executives agreed. While business may have suffered because of economic conditions, there has been no lack of interaction internally or between sellers and customers.

"I am remote, yet more connected than ever with a deeper sense of unity," Dell Technologies COO Jeff Clarke said during his company's first post-pandemic earnings call in May. "I'm not traveling, but I'm visiting with more customers, partners, suppliers and team members. And I'm busier than ever."

Pure Storage CEO Charlie Giancarlo said he talks to twice as many customers as he used to while working from home, and his sales team has been more productive.

"So, if anything, I expect that we're going to see sales in a B2B environment permanently take on more of a virtual digital technique," he said on Pure's May earnings call.

We're still not sure what the future holds for in-person industry and vendor events. March and April were filled with decisions to shift vendor conferences to virtual shows. There was a spate of virtual conferences in May and June, while others moved to September and October. Going virtual deprives storage buyers of face-to-face meetings with peers and vendors, hands-on training and roadmap sessions.

We do not see this shift as temporary. In fact, we see the future of work changing permanently. Dheeraj PandeyCEO, Nutanix

However, more people can tune in without having to jump on an airplane and take time away from their day-to-day duties. Expect vendors to continue to tailor shows just as much to virtual attendees even as they ramp up conferences again in the real world.

Many found early virtual conferences had the feel of webinars more than events. Companies that have delayed their virtual shows until later in 2020 -- such as Dell and Nutanix -- have additional time to prepare and, hopefully, come up with more creative ideas.

"Overnight, we can make this a global event, instead of [a regional] event," Pandey said of the virtual .NEXT conference. "We can stream this to anywhere and everywhere. We're thinking real hard about being creative. Virtual doesn't mean copying what you did in the physical world."

Pandey said he didn't want to "spill the beans" about how creative Nutanix will get, but he gave some hints. He wants the show to have short, broadcast-quality sessions like Quibi or TikTok.

"It has to be engaging," he said. "You can stream it to people who don't want to fly to a physical event. You can get people [to watch] for five minutes, [so] it makes for a good break."

As for whether .NEXT and other conferences will go back to being physical events, Pandey said: "It's like public versus private cloud, onshoring versus offshoring. We know the pendulum has to come to rest in the middle."

The IT world pendulum will never swing back to the "old normal" of the pre-2020 world.

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World of technology changed forever by the pandemic - TechTarget

Technology, Innovation Walled Off in US-China Spat – Manufacturing.net

NEW YORK (AP) President Donald Trumps bans ontwo popular Chinese social media apps TikTok and WeChat are the latest moves in an escalating U.S.-China rift, and point to a future where technology and innovation are increasingly walled behind political barriers.

In China, the Communist Party has long limited what foreign tech companies can do. It blocks access to major U.S. internet services, like Google and Facebook, along with thousands of websites operated by news organizations and human rights, pro-democracy and other activist groups.

Those restrictions have helped nurture homegrown tech giants that in recent years have started expanding, and even dominating, outside China.

Now the U.S. and other countries are putting their own limits on China.

The executive orders from the White House are vague. But experts said they appear intended to bar TikTok and WeChat from the app stores run by Apple and Google when the orders take effect in 45 days. That would make them more difficult to use in the U.S.

This is a pretty broad and pretty quick expansion of the technology cold war between the U.S. and China, said Steven Weber, faculty director for the University of California, Berkeley Center for Long-Term Cybersecurity.

The Trump administration has been hawkish against China. A big example is Huawei, the world's biggest maker of smartphones and network equipment, and Chinas first global tech brand. Washington has moved to cut off Huawei Technologies Ltd.'s access to chips and other technology, tried to push allies away from Huawei and barred U.S. government funds from being used to pay for Huawei equipment in U.S. networks, citing security concerns.

The Trump administration has also blocked Chinese buyers from acquiring U.S. companies.

Now it's going after popular services used by millions globally. The effort is driven not only by security concerns but also Trumps anger at Beijing, blaming China for the coronavirus pandemic and for hurting his re-election chances, according to two White House officials not authorized to speak publicly about private deliberations.

We are entering an era of an increasingly bifurcated internet, where it may become more difficult for Chinese information companies to succeed outside of China, said Lindsay Gorman, a fellow specializing in emerging technologies at the Alliance for Securing Democracy.

China's so-called Great Firewall has allowed Chinese internet powerhouses like e-commerce giant Alibaba, social media company Baidu and WeChat owner Tencent, which makes most of its money from online games and entertainment in China, to amass hundreds of millions of users in some cases over a billion. For context, Facebook says it has more than 3 billion users across its various apps, including Instagram and WhatsApp and Messenger.

But Bytedances TikTok has run into obstacles outside China. In the U.S., where TikTok says it has 100 million users, it may have to sell to Microsoft because of the U.S. government's national-security concerns. China's authoritarian government can demand access to data from companies, a concern that has also dogged Huawei. TikTok maintains that it does not share user data with the Chinese government nor censor content at its request. It suggested it would sue to make sure it and its user were treated fairly.

WeChat, which has more than 1 billion users, is less well-known than TikTok to Americans without a connection to China. Mobile research firm Sensor Tower estimates about 19 million U.S. downloads of the app. But it is crucial infrastructure for Chinese students and residents in the U.S. to connect with friends and family in China, as well as for anyone who does business with China.

Within China, WeChat is censored and expected to adhere to content restrictions set by authorities. The Citizen Lab internet watchdog group in Toronto says WeChat monitors files and images shared abroad to aid its censorship in China.

A U.S. ban of on WeChat would deepen the split between the United States and China on a human level by removing the de facto channel of communication for the Chinese diaspora, said Gorman.

Tencent also owns Riot Games, publisher of hit video game League of Legends, and has a big stake in Epic Games, the company behind video game phenomenon Fortnite. It also has a streaming deal with the NBA.

It's not clear what will result from Trump's executive orders, how WeChat and TikTok users will be affected, whether Tencent's other operations are at risk, or whether there is legal authority for what Trump wants to do.

More actions against Chinese technology companies may be coming from the U.S. and other countries, analysts say. China has a reputation for economic espionage and China-backed hackers have been blamed for breaches of U.S. federal databases and the credit agency Equifax.

"I think well only see even further attempts by the U.S. to ban or prohibit Chinese products, services and investment, said Andy Mok, senior research fellow at the Center for China and Globalization in Beijing. He noted U.S. Secretary of State Mike Pompeos statement this week of wanting aclean internetand networks free of Chinese influence.

India has also blocked a slew of Chinese services, citing privacy concerns, amid a border standoff. The U.K. reversed plans for Huawei in its new high-speed mobile phone network. It said U.S. sanctions made it impossible to ensure the security of equipment made by the Chinese company.

You start wondering what will happen in terms of globalization, both economically and politically, if we have every country having completely separate networks, with completely different technology economies, access to information and social spheres, said Tiffany Li, a visiting professor at the Boston University School of Law.

The Chinese foreign ministry accused Washington of political manipulation" but did not indicate how Beijing might respond. Still, the ruling party has used the entirely state-controlled press to encourage public anger at Trumps actions.

I dont want to use American products any more, said Sun Fanyu, an insurance salesperson in Beijing. I will support domestic substitute products.

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Technology, Innovation Walled Off in US-China Spat - Manufacturing.net

Office Depot Unveils ‘powered by CompuCom’ to Provide SMBs with Scalable Technology and Service Solutions – Kankakee Daily Journal

THE NATIONAL WEATHER SERVICE HAS ISSUED SEVERE THUNDERSTORM WATCH426 IN EFFECT UNTIL 7 PM CDT /8 PM EDT/ THIS EVENING FOR THEFOLLOWING AREASIN ILLINOIS THIS WATCH INCLUDES 18 COUNTIESIN CENTRAL ILLINOISLIVINGSTONIN EAST CENTRAL ILLINOISFORD IROQUOISIN NORTH CENTRAL ILLINOISBOONE DE KALB LA SALLELEE OGLE WINNEBAGOIN NORTHEAST ILLINOISCOOK DUPAGE GRUNDYKANE KANKAKEE KENDALLLAKE IL MCHENRY WILLIN INDIANA THIS WATCH INCLUDES 5 COUNTIESIN NORTHWEST INDIANABENTON JASPER LAKE INNEWTON PORTERTHIS INCLUDES THE CITIES OF ALGONQUIN, AURORA, BELVIDERE,BOLINGBROOK, BOURBONNAIS, BUFFALO GROVE, BYRON, CAROL STREAM,CHESTERTON, CHICAGO, COAL CITY, CRYSTAL LAKE, DEKALB, DEMOTTE,DIXON, DOWNERS GROVE, DWIGHT, ELGIN, EVANSTON, FAIRBURY, FOWLER,GARY, GIBSON CITY, GILMAN, GURNEE, HAMMOND, JOLIET, KANKAKEE,KENTLAND, LA SALLE, LEMONT, LOMBARD, MARSEILLES, MCHENRY,MENDOTA, MERRILLVILLE, MINOOKA, MOROCCO, MORRIS, MUNDELEIN,NAPERVILLE, OAK LAWN, OREGON, ORLAND PARK, OSWEGO, OTTAWA,OXFORD, PARK FOREST, PAXTON, PLANO, PONTIAC, PORTAGE, RENSSELAER,ROCHELLE, ROCKFORD, ROSELAWN, SCHAUMBURG, STREATOR, SYCAMORE,VALPARAISO, WATSEKA, WAUKEGAN, WHEATON, WILMINGTON, WOODSTOCK,AND YORKVILLE.

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Office Depot Unveils 'powered by CompuCom' to Provide SMBs with Scalable Technology and Service Solutions - Kankakee Daily Journal

TIG to represent SiliconCore Technology in EMEA – AV Magazine

Technological Innovations Group has announced a strategic partnership with SiliconCore Technology. US-headquartered SiliconCore is an innovator in fine pixel pitch LED display technology, with its Common Cathode technology resulting in displays offering the highest brightness, lowest power consumption and coolest operating temperatures on the market. In addition, its latest technology innovation, LISA, provides a durable surface on the displays without reducing brightness or impacting image reproduction.

The partnership will now allow TIG to offer complete solutions for creating Smart Spaces, including LED displays, control and automation solutions, touch panels, distribution and monitoring solutions, AV furniture and collaboration and management software.

As this exciting new partnership demonstrates, were fully committed to offering our customers the most advanced solutions available, said Robin van Meeuwen, CEO of TIG.With already the best in AV/UC technology in house, adding a brand such as SiliconCore makes our offering complete. We have been looking for a long time to add LED displays to our portfolio and with SiliconCore we feel we have found the perfect partner. Their vision of offering the highest quality and most energy-efficient LED display technology, fits with the TIG vision of being the premium provider of AV and UC technology.

Paul Brown, vice president of sales UK at SiliconCore Technology, commented:The partnership between SiliconCore and TIG is a true testament to the future of the market. Although the global pandemic has had a detrimental impact on project installations, the partnership signifies a positive move towards a stronger future. SiliconCore consistently researches and develops its LED technology, driven to provide the most reliable and sustainable display technology on the market. By joining forces with TIG were able to widen our reach throughout the EMEA and help businesses to implement future-proofing solutions.

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TIG to represent SiliconCore Technology in EMEA - AV Magazine

How Changes in Technology and Law Created the iGaming Industry – UKTN

image source: https://unsplash.com/photos/CT7IWRM7G5k

The iGaming industry was born in 1994 when changes in technology and legislation occurred simultaneously, creating the perfect conditions for online casinos, sports betting, lotteries, and bingo websites to open.

In the 26 years since the industry has grown and matured with several major publicly traded companies building large market shares in Europe and parts of North America. Casino revenues in Europe alone now exceed 20 billion (18 billion) each year, and the industry is expected to become valued at $100 billion (76 billion) by the end of this decade.

So what were these technological and legal changes? And could anything like that happen again?

Free Trade and Processing Zone Act

Spotting an opportunity, lawmakers in Antigua and Barbuda set about passing legislation that would make it possible for businesses to operate casinos from its jurisdiction, even if the customers were resident and present elsewhere.

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The result was the Free Trade and Processing Zone Act, which was adopted on 10th November 1994. Very quickly, companies began scrambling to get a license and develop the software required to operate an online casino.

Microsoft Windows and the Internet

At the same time, Microsoft Windows 3.1 was the most common operating system loaded onto personal computers. It was great at the time, but something much more important was in the pipeline, Windows 95.

It went on sale in August of 1995, around the same time that the first online casinos began opening. It came preinstalled with Internet Explorer, the web browser of choice for most at the time.

Language learning app Memrise scores $15.5m Series B

This was often the first opportunity many people got to use the internet, especially as companies like AOL began aggressively pushing their dial-up services in the US and Europe.

Windows 95 sold 40 million copies in the first year, ten times more than 3.1, significantly increasing the number of people able to access the new online casinos.

It was an exciting time for users who had unprecedented opportunities to explore information, entertainment, and commerce in ways that had never been possible before. And, of course, iGaming companies were a big part of this.

As computers got more powerful and consumer internet connections got faster, iGaming companies improved their offering.

South Yorkshire tech firm Metalysis closes 20m funding round

We have seen this process repeating twice in recent years.

Smartphones

While the legal landscape in Europe remained the same, technology took a big step forward. As consumers began adopting smartphones en-mass in the late 2000s and early 2010s, iGaming companies began making their services available in this new format.

This meant new and more casual players could enjoy casino games without having to use a desktop or laptop computer.

US Legislation Changes

We can see history repeating itself today. In 2018, the US Supreme Court ruled that individual states had the right to set their own rules related to iGaming. Like in 1994, this started a race for companies to launch their services in the states that legalised sports betting and casinos.

Today, there are 12 states that have made it possible to place wagers online in some form, and more are expected to follow suit in the coming years.

As they do, the iGaming companies will vie for market share, just as they did in 1994 and 1995.

Continued here:

How Changes in Technology and Law Created the iGaming Industry - UKTN

Nano One Materials partners with major Asian cathode manufacturer to develop technology for high-performance lithium ion batteries – Proactive…

We are thrilled to be working with a highly respected cathode producer who shares Nano Ones vision to develop and launch a disruptive cathode business,CEO Dan Blondal told shareholders

Nano One Materials Corp () (OTCMKTS:NNOMF) announced Monday a major new agreement that sets the stage to advance its lithium ion battery cathode material technology.

The Vancouver-based company signed a joint development agreement with an unnamed Asian cathode material producer to develop and evaluate materials made with combined technologies.

Nano One has developed a patented technology for the low-cost production of high-performance lithium ion battery cathode materials for electric vehicles, energy storage and consumer electronics.

The technology firm said the agreement completely aligns with Nano Ones vision to develop and license its high-performance lithium ion battery cathode material technology.

We are thrilled to be working with a highly respected cathode producer who shares Nano Ones vision to develop and launch a disruptive cathode business,CEO Dan Blondal told shareholders in a statement.This is a defining moment in our evolution and an important milestone in the advancement of our business.

Nano Ones patented One-Pot process for the production of high-performance coated single crystal cathode powders is included in the agreement, which also lays out a framework to develop a business plan to commercialize the materials.

The development partner, a multibillion-dollar company based outside of China,wishes to remain anonymous due to the competitive nature of the lithium battery supply chain, according to Nano One. The partners may potentially form a joint venture, license the technology or jointly pursue other opportunities.

"We have assembled a valuable portfolio of cathode technologies and our business strategy is designed for opportunities such as this, Blondal added.

We are excited to be working with a global leader in innovation and materials manufacturing who share our vision and we look forward to advancing this partnership and expanding our business opportunities."

Contact Angela at [emailprotected]

Follow her on Twitter @AHarmantas

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Nano One Materials partners with major Asian cathode manufacturer to develop technology for high-performance lithium ion batteries - Proactive...

Being a younger coach helped Texans offensive coordinator Tim Kelly adapt to technology – Texans Wire

Bill OBrien is an old school coach. He likes to get in front of the team and tell them how the cow ate the cabbage.

Offensive coordinator Tim Kelly is a newer school coach. Set to turn 34 years old on Aug. 17, Kelly has a natural inclination to use video conferencing and screen sharing technologies. So when the COVID-19 pandemic forced the NFL into a virtual offseason, there was no learning curve for Kelly.

Not to be too general here, but being a younger coach if you will, being able to get used to FaceTiming and doing all of those things, its become a normal interaction with people, Kelly said. So this isnt than that different than what we usually do on a normal basis.

The second-year offensive coordinator knows on-field instruction during walk-throughs and classroom settings are the ideal when it comes to offseason workouts. However, the Texans, nor any NFL team, had the chance.

Wed much rather be in person, face-to-face, but being able to see each other through the Zoom media, being able to interact with the different technologies that we have was really beneficial, Kelly said.

Though the Texans do have some players who function better in-person than with video conferencing, Kelly nevertheless appreciates the participation from the players.

Said Kelly: Obviously, we would have loved to be in person but I think its a testament to the guys that are in that locker room that I dont think that we skipped a beat there as far as the communication because of the way they approached it, the professionalism of the guys in that room and really their willingness to learn.

The Texans can apply the lessons learned in the virtual offseason to the practice field throughout August.

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Being a younger coach helped Texans offensive coordinator Tim Kelly adapt to technology - Texans Wire

Frost & Sullivan Reveals Innovative Technologies to Revolutionize the Global Building Automation Systems Market – Yahoo Finance

Integration of operational technology with information technology will continue to influence the dynamics of this market

SANTA CLARA, Calif., Aug. 10, 2020 /CNW/ --Frost & Sullivan's recent analysis, Global Building Automation Systems (BAS) Market, Forecast to 2026, reveals that energy-efficiency requisites, energy conservation and favorable government initiatives, rising energy prices, and strict building codes are prominent factors driving the global BAS market. The market is estimated to reach $5.91 billion by 2026 from $4.69 billion in 2019, growing at a compound annual growth rate (CAGR) of 3.4%. However, the market will be restrained by the COVID-19 pandemic in the short term, as some construction projects commissioned by companies and/or governments face delays or cancellations.

For further information on this analysis, please visit: http://frost.ly/4be

"Buildings, infrastructure, and energy will remain the core investment areas for smart city development, which is further expected to drive the demand for advanced and efficient BAS systems," said Neha Tatikota, Energy and Environment Research Analyst at Frost & Sullivan. "Additionally, partnerships and collaborations are becoming increasingly important, as suppliers of all sizes seek to offer a comprehensive, end-to-end market segment solution."

Tatikota added, "Integration of operational technology (OT) control network with information technology (IT) will continue to change the dynamics of the BAS market because this will reduce operating and infrastructure costs and improve the financial optimization of buildings. Further, the adoption of deep learning and machine learning (ML) algorithms for developing voice-over technology and advanced features will be crucial innovation areas for next-generation BAS solutions."

Leveraging the potential of the mixing and matching of BAS products to make them more versatile, compact, and innovative will present tremendous growth opportunities for market participants in:

Global Building Automation Systems (BAS) Market, Forecast to 2026 is the latest addition to Frost & Sullivan's Energy and Environment research and analyses available through the Frost & Sullivan Leadership Council, which helps organizations identify a continuous flow of growth opportunities to succeed in an unpredictable future.

About Frost & SullivanFor over five decades, Frost & Sullivan has become world-renowned for its role in helping investors, corporate leaders and governments navigate economic changes and identify disruptive technologies, Mega Trends, new business models and companies to action, resulting in a continuous flow of growth opportunities to drive future success. Contact us: Start the discussion.

Global Building Automation Systems (BAS) Market, Forecast to 2026MF31

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Frost & Sullivan Reveals Innovative Technologies to Revolutionize the Global Building Automation Systems Market - Yahoo Finance

How mask-makers are using technology to kill viruses left behind on protective face masks – CNBCTV18

They're everywhere now thanks to COVID-19 the protective mask. They come in the highest grade possible, like the N95 mask, which act as a near-foolproof barrier against the novel coronavirus, while the humbler ones are a makeshift handkerchief strung around the wearers nose and mouth. However, at the basic level, a mask is nothing but fabric that attempts to prevent the novel coronavirus from entering one's respiratory body through nasal and oral cavities. However, that simplicity in function could soon change.

A handful of textile companies have started waking up to the need of not just preventing transmission of viral particles to the wearer of a mask, but also destroying the virus in question that would otherwise remain on its surface. The one common link that connects the products of these manufacturers is a Swiss technology called HeiQ Viroblock applied generously in all these anti-viral masks.

Anti-viral masks versus regular masks

Normally a mask or a PPE cover-all are merely barriers that dont let the viruses inside, explains K S Sundararaman, Managing Director of Coimbatore-based Shiva Texyarn, Anti-viral technology, though, kills these viruses that settle on the surface of this barrier.

One of the textile companies to have adopted HeiQ technology, Shiva Texyarn launched its anti-viral masks exactly a month ago. By the time July was done, the Coimbatore textile company sold a whopping 20 lakh pieces. What we made was a washable mask for just 49 rupees, says Sundararaman. But its three-layered mask isnt as simple.

While the HeiQ Viroblock technology attempts to deactivate the viruses that settle on the surface of the mask, another layer of N-95 melt-blown fabric ensures the mask stays washable. Weve used a technique that ensures the virus doesnt penetrate the first layer of the mask, says Sundararaman. The masks third layer is untreated cotton.

Shiva Texyarn's masks come with an N95 melt-blown fabric to ensure that they stay washable. (Image: CNBC-TV18)

How does HeiQ work?

In a nutshell, HeiQ destroys viral particles left behind on the surface of the fabric its technology is used in. In other words, it is constantly self-sanitizing and breaking these viral particles down, says Bharat Subramaniam, Director, Emcee Apparels that is part of the Defend and Protecht initiative, a coming-together of three textile companies using HeiQ Viroblock technology to make anti-viral masks.

When a virus gets attracted onto a silver ion, which is fused to a bio-based lipsome layer, the silver ion destroys the outer layer (protein coat) of the virus, Bharat explains, Once this outer layer is destroyed, the viral RNA is released, which now cannot exist outside a host or the protein coat.

In layman terms, the silver ions and the bio-based liposome layer make the foundation of HeiQ Viroblock, which is the bedrock of the anti-viral technology that these masks come with. The silver ions attract viral particles and use simple osmosis to destroy their protein coats. The surface of the mask has a coating of silver ions and vesicle booster to speed up the process, Bharat says.

Defend and Protecht's mask uses four applications of HeiQ technology in just one mask. (Image: CNBC-TV18)

Mask sales in top gear

Defend and Protecht, Shiva Texyarn, Arvind Ltd and Loyal Textile Mills are some of the textile majors using HeiQ viroblock to equip otherwise basic washable cloth masks. In less than a month since Defend and Protecht launched its top-line of anti-viral masks, priced at Rs 250 per piece, it sold nearly 6,000 pieces. The company is also launching a new Essentials line, priced at between Rs 30 and Rs 60 per mask.

The companys manufacturing footprint, in Chennai, has a capacity of 20,000 pieces per day but only makes around 5,000 to 10,000 masks every day. We can scale up to 75,000 masks, per day with ease, says Bharat, In fact, the machines that weve allotted to manufacture these masks ensure a capacity of 100,000 pieces per day. This isnt surprising especially given that the textile manufacturers that are part of Defend and Protecht Emcee Apparels, Sreekumar Texind Corporation and Dvintex are capable of making an excess of a million shirts every month.

Shiva Texyarn is targeting a sales target of 10 lakh masks this month, in the domestic market alone. We dont foresee the need to scale up further until the export ban is lifted, says Sundararaman, There is a lot of interest from countries as far as Brazil because of our high-level of protection and our competitive price point. While the companys basic product is priced at a very competitive Rs 49, more fancily designed variants are priced at Rs 70.

Value-additions to anti-viral masks

For a relatively steeper price of Rs 250 per piece, Defend and Protechts top-line of anti-viral masks come with some nifty value-additions. In addition to the HeiQ Viroblock technology that exists in all of its masks, HeiQ Pure controls odour that is emanated thanks to bacterial breakdown of sweat, which is fairly common while wearing mask.

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How mask-makers are using technology to kill viruses left behind on protective face masks - CNBCTV18

Apple Watch Likely to Adopt MicroLED Display Technology in 3-4 Years – MacRumors

This year's Apple Watch Series 6 is expected to feature an OLED screen like previous models, but a future model is likely to be the first Apple product to adopt MicroLED display technology, albeit not for another three to four years.

From a DigiTimes' report filed on Monday:

Smartwatches will be the first major applications for micro LED with volume adoption likely to take place 3-4 years from now, according to Epistar chairman Lee Biing-jye.

Epistar has overcome many micro LED technological difficulties, such as mass transfer, and expects to achieve reliable production capability in 2-3 years, and introduce end-market applications in 3-4 years, Lee noted.

Apple is reportedly investing $330 million in the Taiwanese MicroLED factory to manufacture displays for future iPhones, iPads, MacBooks, and other devices. MicroLEDs sized 20-50 microns are too small for PCB substrates that support minimum sizes of 50-100 microns, and therefore glass substrates are used.

Taiwanese LCD panel maker AU Optronics is understood to be supplying the glass substrates for the displays, while Epistar is said to be now focusing on improving yield rates for micro LED epitaxy and reducing cost for mass transfer.

There are several advantages of MicroLED screens over LCD and OLED displays, including being thinner and more energy efficient. For example, the power consumption of MicroLED screens is only one-tenth that of LCD displays, and the color saturation is close to OLED.

Owing to the difficulties involved in developing MicroLED technology, early designs are expected to rely on mini-LEDs that are somewhere in between traditional LED and MicroLED technology. However, Apple still considers MicroLED technology to be the "top priority," according to a previous report.

Apple has six mini-LED products in the works that are set to debut in 2020 and 2021, according to analyst Ming-Chi Kuo. Apple is said to be debuting the technology in a 12.9-inch iPad Pro for launch later this year, followed by a 27-inch iMac Pro, a 14.1-inch MacBook Pro, a 16-inch MacBook Pro, a 10.2.-inch iPad, and a 7.9-inch iPad mini.

Apple has reportedly been testing prototype Apple Watch models with MicroLED displays since 2017. While early rumors suggested an Apple Watch with a microLED display could launch as early as 2020, one leaker poured cold water on that prediction in May by claiming that this year's Apple Watch Series 6 will use the same OLED display as previous models.

There is precedent for new screen technologies showing up in the Apple Watch first. When it was introduced in 2014, the Apple Watch had an OLED screen. The technology then migrated to the iPhone X three years later.

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Apple Watch Likely to Adopt MicroLED Display Technology in 3-4 Years - MacRumors

Is Taiwan Semiconductor Manufacturing Company (TSM) Stock Outpacing Its Computer and Technology Peers This Year? – Yahoo Finance

Investors focused on the Computer and Technology space have likely heard of Taiwan Semiconductor Manufacturing Company (TSM), but is the stock performing well in comparison to the rest of its sector peers? Let's take a closer look at the stock's year-to-date performance to find out.

Taiwan Semiconductor Manufacturing Company is one of 605 individual stocks in the Computer and Technology sector. Collectively, these companies sit at #5 in the Zacks Sector Rank. The Zacks Sector Rank includes 16 different groups and is listed in order from best to worst in terms of the average Zacks Rank of the individual companies within each of these sectors.

The Zacks Rank is a successful stock-picking model that emphasizes earnings estimates and estimate revisions. The system highlights a number of different stocks that could be poised to outperform the broader market over the next one to three months. TSM is currently sporting a Zacks Rank of #2 (Buy).

The Zacks Consensus Estimate for TSM's full-year earnings has moved 12.37% higher within the past quarter. This shows that analyst sentiment has improved and the company's earnings outlook is stronger.

According to our latest data, TSM has moved about 37.75% on a year-to-date basis. At the same time, Computer and Technology stocks have gained an average of 21.42%. As we can see, Taiwan Semiconductor Manufacturing Company is performing better than its sector in the calendar year.

Breaking things down more, TSM is a member of the Semiconductor - Circuit Foundry industry, which includes 1 individual companies and currently sits at #6 in the Zacks Industry Rank. This group has gained an average of 38.88% so far this year, so TSM is slightly underperforming its industry in this area.

Going forward, investors interested in Computer and Technology stocks should continue to pay close attention to TSM as it looks to continue its solid performance.

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 reportTaiwan Semiconductor Manufacturing Company Ltd. (TSM) : Free Stock Analysis ReportTo read this article on Zacks.com click here.Zacks Investment Research

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Is Taiwan Semiconductor Manufacturing Company (TSM) Stock Outpacing Its Computer and Technology Peers This Year? - Yahoo Finance

Virginia launches the first U.S. app using Apple-Google coronavirus notification technology – CNBC

Germany's coronavirus contact-tracing app, Corona-Warn, is displayed on an iPhone in Berlin on Tuesday, June 16, 2020.

Krisztian Bocsi | Bloomberg via Getty Images

Virginia's coronavirus notification app, called Covidwise, launched on Wednesday, just under four months after the Apple-Google partnership was first announced.

Virginia is the first state in the United States to use the Apple-Google technology built into iPhones and Android phones. The exposure notification technology and contact-tracing apps wereonce heralded as a critical part of some countries' strategies to lift their lockdowns, but low adoption and unclear effectiveness in some countries have dampened enthusiasm for the apps.

Virginia's app, like all apps using the Apple-Google framework, uses Bluetooth signals on a smartphone to determine how closely and for how long two phones were nearby, without collecting the location of the contact or the identity of the users. Then, if one of the phone's users were to test positive for Covid-19, the system is able to notify any other phones with the app that they might have been exposed to the virus through a push notification and tell them to get tested or quarantine.

"For the purpose of this app, there wasn't an absolute need to be able to track where you are or who you are," Jeff Stover, director of the Virginia Department of Health, said on a video call with reporters. "The most important thing was that you know whether or not you've potentially been exposed, and that we can all take actions to do whatever prevention is necessary."

When users test positive for Covid-19, they get a six-digit pin number provided by the Virginia Department of Health that they can input into their app. Once that six-digit pin is entered, the Virginia system tells other phones with the app that they that had been close to a person who tested positive, and that they have likely been exposed. That information is delivered in a push notification from the Covidwise app. The Apple-Google system does this by unscrambling random keys that correspond to when phones were in close range with each other.

Virginia's Covidwise app requires a 6-digit PIN number to confirm a positive test result.

Screenshot/CNBC

The app wasn't built by Apple or Google the two tech giants built software into iOS and Android to make it possible.Virginia paid SpringML $229,000 to develop the Covidwise app, and it was funded by the CARES act, Stover said.

Other states in the U.S. have released similar apps, but some of them, such asonein Utah, have used a location-based approach instead of Apple-Google system, which requires apps using it to eschew GPS and emphasizes anonymity. Apple and Google have also said they will turn the system off when the pandemic is over.

One of the most successful exposure notification apps using the Apple-Google system is in Germany. The app, called Corona-Warn-App, was downloaded over 16 million times at the end of July out of a population of 82 million, according to the BBC. In France, which used a different Bluetooth system not backed by the tech giants, only 14 people were notified using the app over its first three weeks.

One issue with the apps is that they will need to be installed by a large percentage of the population to work effectively if a phone isn't running the app, then it will miss potential exposures. One study by researchers at Oxford University suggested that 60% of the population would need to install an exposure notification app to suppress the virus.

"Effective is going to be anyone's guess as how you want to describe that. But they also state in the [Oxford] study that they estimate that for every one to two app users, you will potentially reduce the infection by one," Stover said.

Virginia plans to heavily advertise the app on billboards, digital ads, and through partnerships with schools and workplaces, and Google has offered advertising credits for its search engine and Google Play app store, officials said.

Google said last week in a blog post that 20 states and territories are "exploring" apps based on the system. While the app works outside of Virginia, positive tests require a six-digit pin from the Virginia Department of Health to notify others, effectively limiting its range.

There is no plan for a national coronavirus exposure app, but Virginia officials said that the state is likely to participate in a program building a "national key server" that would enable apps from different states to work together.

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Virginia launches the first U.S. app using Apple-Google coronavirus notification technology - CNBC