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Junshi Biosciences Announces Dosing of First Patient in Phase I Study of Anti-TROP2 Antibody -TUB196 Conjugate

SHANGHAI, China, Dec. 01, 2020 (GLOBE NEWSWIRE) -- Junshi Biosciences (HKEX: 1877; SSE: 688180), an innovation-driven biopharmaceutical company dedicated to the discovery, development and commercialization of novel therapies, is pleased to announce that the Phase I clinical study (NCT04601285) of a recombinant humanized anti-TROP2 monoclonal antibody - Tub196 conjugate (JS108), has completed the dosing of the first patient.

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Junshi Biosciences Announces Dosing of First Patient in Phase I Study of Anti-TROP2 Antibody -TUB196 Conjugate

New Drug Could Improve Effectiveness of Stem Cell Therapy – Pain News Network

By Pat Anson, PNN Editor

Scientists have developed an experimental drug that can lure stem cells to damaged tissues and help them heal -- a discovery being touted as a major advancement in the field of regenerative medicine.

The findings, recently published in the Proceedings of the National Academy of Sciences (PNAS), could improve the effectiveness of stem cell therapy in treating spinal cord injuries, stroke, amyotrophic lateral sclerosis(ALS), Parkinsons disease and other neurodegenerative disorders. It could also expand the use of stem cells to treat conditions such as heart disease and arthritis.

The ability to instruct a stem cell where to go in the body or to a particular region of a given organ is the Holy Grail for regenerative medicine, said lead authorEvan Snyder, MD, director of theCenter for Stem Cells & Regenerative Medicineat Sanford Burnham Prebys Medical Discovery Institute in La Jolla, CA. Now, for the first time ever, we can direct a stem cell to a desired location and focus its therapeutic impact.

Over a decade ago, Snyder and his colleagues discovered that stem cells are drawn to inflammation -- a biological fire alarm that signals tissue damage has occurred. However, using inflammation as a therapeutic lure for stem cells wasnt advisable because they could further inflame diseased or damaged organs, joints and other tissue.

To get around that problem, scientists modified CXCL12 -- an inflammatory molecule that Snyders team discovered could guide stem cells to sites in need of repair to create a drug called SDV1a. The new drug works by enhancing stem cell binding, while minimizing inflammatory signals.

Since inflammation can be dangerous, we modified CXCL12 by stripping away the risky bit and maximizing the good bit, Snyder explained. Now we have a drug that draws stem cells to a region of pathology, but without creating or worsening unwanted inflammation.

To demonstrate its effectiveness, Snyders team injected SDV1a and human neural stem cells into the brains of mice with a neurodegenerative disease called Sandhoff disease. The experiment showed that the drug helped stem cells migrate and perform healing functions, which included extending lifespan, delaying symptom onset, and preserving motor function for much longer than mice that didnt receive the drug. Importantly, the stem cells also did not worsen the inflammation.

Researchers are now testing SDV1as ability to improve stem cell therapy in a mouse model of ALS, also known as Lou Gehrigs disease, which is caused by a progressive loss of motor neurons in the brain. Previous studies conducted by Snyders team found that broadening the spread of neural stem cells helps more motor neurons survive so they are hopeful that SDV1a will improve the effectiveness of neuroprotective stem cells and help slow the onset and progression of ALS.

We are optimistic that this drugs mechanism of action may potentially benefit a variety of neurodegenerative disorders, as well as non-neurological conditions such as heart disease, arthritis and even brain cancer, says Snyder. Interestingly, because CXCL12 and its receptor are implicated in the cytokine storm that characterizes severe COVID-19, some of our insights into how to selectively inhibit inflammation without suppressing other normal processes may be useful in that arena as well.

Snyders research is supported by the National Institutes of Health, U.S. Department of Defense, National Tay-Sachs & Allied Disease Foundation, Childrens Neurobiological Solutions Foundation, and the California Institute for Regenerative Medicine (CIRM).

Thanks to decades of investment in stem cell science, we are making tremendous progress in our understanding of how these cells work and how they can be harnessed to help reverse injury or disease, says Maria Millan, MD, president and CEO of CIRM. This drug could help speed the development of stem cell treatments for spinal cord injury, Alzheimers, heart disease and many other conditions for which no effective treatment exists.

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New Drug Could Improve Effectiveness of Stem Cell Therapy - Pain News Network

Are stable producer cells the future of viral vector manufacturing and when will allogeneic cell therapy take hold? – BioPharma-Reporter.com

The publication, based on data generated from a questionnaire with 150 industry representatives, explores the challenges and solutions facing cell and gene therapy (CGT) companies over the next few years.

The top six trends identified in the CRB survey were:

We got the inside track from Noel Maestre, director of SlateXpace, a CRB solution focused on suite-based manufacturing platforms for the Advanced Therapy Medicinal Products (ATMP) and Peter Walters, CRBs director of ATMP, on how the CGT landscape is likely to develop in the short-term.

In a recent report, the MITs Center for Biomedical Innovationprojected that around 500,000 patients will have been treated with 40-60 approved gene therapies by 2030.

Going from the current scenario whereby only a few gene therapies are approved to 60 launches in a decade would represent an extraordinary leap forward and would dramatically change how medicine is actually perceived, said Maestre.

But as regards CGT production today, especially autologous cell therapy (ACT) work, he said that while the science exists the technology - process equipment, facility design and automation platforms - is really still trying to catch up, endeavoring to address a sector that has exploded in the past five years, he commented.

Looking ahead at the CGT landscape over the next few years, he expects a significant amount of change. The science is evolving we see the industry moving away from old cell lines to new cell lines or moving away from viral vectors altogether and using cleavage enzymes as a gene editing tool.

A new host cell line stable producer lines is gaining momentum, he said.

We are seeing the industry moving towards suspension cell culture from less than optimal cell lines, and then further going into producer cell lines.

A full 65% of respondents to the CRB poll said they are developing or intend to develop this type of vector host cell, drawn by the potential for a less expensive, more scalable process.

CRB: Our survey findings provide a data-driven snapshot of an industry whose intellectual capital and cutting-edge science is too often betrayed by outdated technology and applications ill-suited for commercial scale at a time when demand for urgent therapies is rising.

Once the industry gets to the point where producer cell lines are more like a name brand, easier to pull off the shelf and use, it will be a much more cost-effective way to produce viral vectors.

But we are right on the cusp - a lot of companies are recognizing the opportunity and are investing the time and money into producing these. And we also see a lot of contract development and manufacturing organizations (CDMOs) producing their own cell lines in house and using those as a lure to [attract the clinical material work] of their clients, said Walters.

According to Maestre, and the CRB survey data backs him up, the product pipelines of companies operating in the CGT space are going to get more complex, for the next five years at least.

More than half of those polled indicated they expect to adopt a multimodal solution within the next two years, with flexibility, scalability, operational efficiency, and speed to market as the top drivers.

Every company is going to be dealing with this dilemma of whether they build dedicated spaces for each of their different modalities, or whether they build highly flexible facilities that can allow them to accommodate whatever is coming next, said Maestre.

He also sees a lot more companies wanting to integrate their supply chain, bringing a lot of manufacturing in-house whereas before they would have been reliant on a whole set of different CDMOs and manufacturers.

Project delivery is also where change is occurring.

We are seeing the industry really moving away from the way projects were executed in the past into a much more integrated model; they are looking for turnkey facility delivery and they want turnaround to be faster. COVID-19 has only accentuated that, with project timelines compressed by 30-40%, and I dont think that it is ever going back to the way it was I think that is going to become the standard, commented Maestre.

And another major trend over the next few years will be around the cost of therapies. As they become more commonplace and there are more and more CGT licensed products, the costs will come down.

Projecting forward, Walters sees an eventual shift away from autologous to allogeneic cell therapy.

As the technology continues to develop and the science continues to improve and new and better ways are found to use and leverage cells, we will see companies moving to a scalable allogeneic model, getting away from having to do that point-of-care, personalized tracking and more towards a classic manufacturing model that allows them to produce cells in advance in a way that they can be scaled up.

The idea, evidently, is to process cells for not one but dozens of patients at a time.

We see the industry moving towards donated cells for allogeneic therapy and we are also seeing the beginnings of a shift to using stem cells that can be genetically modified and scaled up and differentiated to become T-Cells or NK cells. I dont think industry has settled on a course yet but there are a lot of companies trying to find that pathway, trying to find the edge to move their manufacturing platform that way, remarked Walters.

Right now, though, all facets of CGT manufacturing are under pressure from COVID-19 vaccine production, they said.

There is significant shortage of cleanroom manufacturing space to manufacture and develop the almost 1,200 CGT products in clinical trials currently.

What we are seeing is that CDMOs have so much demand - they have 12-18 months of backlog in terms of contracts for product development so they are building [new facilities] very rapidly.

As owner operator companies are stuck with that delay in getting their products into development, they are also developing a significant amount of manufacturing space on their own. But while both branches are building as fast as they can, it still isnt enough.

We are constantly hearing from our clients that they are concerned about their supply chains and being able to secure their material. Right now, a lot of companies are moving towards a combination of using CDMOs and manufacturing in-house, said Maestre.

CRB is a provider of engineering, architecture, construction and consulting solutions to the global life sciences and advanced technology industries, with over 1,300 employees.

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Are stable producer cells the future of viral vector manufacturing and when will allogeneic cell therapy take hold? - BioPharma-Reporter.com

How Stem Cell Therapy Market Will Dominate In Coming Years? Report Covering Products, Financial Information, Developments, Swot Analysis And…

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How Stem Cell Therapy Market Will Dominate In Coming Years? Report Covering Products, Financial Information, Developments, Swot Analysis And...

The Promise of Using Cell Cultures To Fight SARS-CoV-2 – Technology Networks

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The COVID-19 pandemic has significantly disrupted scientific activities. Labs have been forced to shut down. Researchers have been placed on furloughs and advised to work from home. Animal facilities have also been scaled down and shipping of research supplies has been delayed. However, despite these challenges, many researchers remain undeterred and are applying their scientific expertise in the fight against SARS-CoV-2, the coronavirus responsible for COVID-19. Portable diagnostic kits with short turnaround time have been invented to facilitate timely and on-field viral detection. Masks made of different materials have been tested for their ability to prevent aerosol transmission and re-usable masks that can be disinfected with electrical fields/heat have been commercialized. Furthermore, the pandemic has significantly accelerated vaccine development and in an unprecedented case, motivated companies with competing interests to work together in efforts to address this global health crisis. In order to fully win the fight against SARS-CoV-2, it is paramount to understand the biological mechanisms of COVID-19 viral infection. A variety of models have been used, but none as frequently as cell culture. Cell cultures, including immortalized cell lines, stem cell lines and primary cells from patients, are being used as in vitro models to understand viral entry into human cells. They are useful for drug screening purposes and as cellular factories to generate viral particles for testing. This article highlights the promising research being conducted using cell cultures and illustrates how these models are contributing to the fight against COVID-19. Cell cultures A variety of in vitro cell cultures exist and depending on the purpose of the experiments, they each have their pros and cons. Immortalized cell lines The most common cell cultures are immortalized cell lines, such as HeLa, CHO and Vero cells. As the name suggests, these are cells that either by natural mutation or genetic engineering, have become immortal, enabling them to be grown in culture indefinitely. These cells divide at a relatively fast rate, are cheaper to obtain and maintain, and are generally more homogenous in their biological properties. Cell lines are most suitable for use when there is a demand for high cell numbers such as in an initial phase of high-throughput COVID-19 drug screening to identify a target. Stem cell lines Stem cell lines, such as mesenchymal and induced pluripotent stem cells (iPSCs), on the other hand, have the inherent ability to proliferate indefinitely, provided that they receive the appropriate growth signals. Stem cells can either be obtained directly from their sources or have been treated with a de-differentiation chemical cocktail to revert them to a stem-like state. As they bear more similar biological characteristics to cells in vivo, they are better models for biological testing. However, primary stem cells can be difficult and expensive to maintain. For instance, some primary stem cells require feeder cells to maintain their stemness and most can only grow on surfaces coated with specific biomaterials. In cases where patientscells are not easily obtainable, iPSCs can also be differentiated to diverse lineages including neurons, cardiomyocytes, and immune cells for applications like COVID-19 drug testing to investigate potential adverse effects of drugs. iPSCs have also been used to construct 3D cell cultures known as organoids to facilitate biological investigations in a 3D environment in efforts to more closely recapitulate the in vivo setting. Primary cells The final type of cell cultures are primary cells from patients. It remains extremely challenging to grow these cells because commercially available products like media are not optimized for them, and thus these cells do not proliferate well ex vivo. Thus far, the exception may be primary leukocytes from patients which can be cultured efficiently ex vivo. This is also partly driven by developments in Chimeric Antigen Receptor (CAR) T-cell therapy to manufacture engineered T cells for cancer immunotherapy. Ex vivo culture of primary immune cells has been particularly useful to study the immune repertoire involved in antigen recognition and antibody production against SARS-CoV-2. Cell culture for understanding disease One of the most important questions regarding COVID-19 is the mechanism of viral entry into host cells. Cell culture has been an invaluable tool for discovering the role of the human angiotensin-converting enzyme 2 (hACE2) cell surface receptor in facilitating viral entry into human cells. Shang and colleagues at the University of Minnesota made use of a variety of immortalized cell lines (HEK293T, HeLa, Calu-3 and MRC-5) and found that a viral surface spike protein binds to hACE2 through its receptor-binding domain (RBD) and is proteolytically activated by human host proteases. The coronavirus membrane fusion S2 protein was also discovered as an essential protein for viruscell membrane fusion. This study suggests that antibody-based therapeutics with high affinity to hACE2 or RBD could inhibit SARS-CoV-2 from associating with the host cell, therefore preventing its entry. Finally, compounds that can inhibit host cell membrane and lysosomal proteases responsible for activating viral entry, may also be useful as therapeutics. These findings were also supported by a subsequent study by Dr Markus Hoffman and colleagues which showed that an inhibitor for the serine protease TMPRSS2 (a cell surface protein) was able to block SARS-CoV-2 infection in lung cells. We identified the cellular protein TMPRSS2 as a crucial factor for SARS-CoV-2 infection and showed that an existing drug that is approved in Japan for treatment of pancreatitis, camostat mesylate, can inhibit TMPRSS2 activity and thus block SARS-CoV-2 infection in cell culture experiments, said Hoffman. Hoffman added that we are currently exploring the antiviral effects of camostat mesylate and related drugs in culture systems that represent the human respiratory tract, and we are collecting data on the required dosage and longevity of the drugs. Finally, we are planning to do efficacy testing of the most promising drugs in non-human primates that have been experimentally infected with SARS-CoV-2. Studies using cell cultures have also provided insights into symptoms of COVID-19 infection. To understand why COVID-19-positive patients suffer from a persistent cough and other respiratory effects, Jia and colleagues analyzed ACE2 receptor expression in cell cultures of primary human airway epithelia, and found high receptor expression in these airway cells, as well as a correlation between ACE2 expression and susceptibility to SARS-CoV-2 infection. Researchers have also identified high ACE2 expression on human neurons, particularly the olfactory neuronal cells, possibly explaining the loss of smell experienced in some patients. Recently, a greater ratio of ACE2 positive cells were found to be present in the digestive tract compared to the lungs, and the receptor expression was higher in gastric cancer cells, potentially explaining the symptom of diarrhea. This myriad of COVID-19 related symptoms has motivated the search for cellular tropism by SARS-CoV-2. For instance, Chu and colleagues systematically investigated the replication rate and cellular damage due to SARS-CoV-2 in cells from different species (humans, non-human primates, cats, rabbits, and pigs) and organs. Their study revealed the range of cells that SARS-CoV-2 is able to infect efficiently for generating physiologically relevant animal models for studying the disease. To better generate policies for managing the spread of SARS-CoV-2, scientists also made use of cell cultures to understand the possible routes of virus entry into the body. For instance, Xu and co-workers made use of a bulk RNA sequencing technique and found that ACE2 was highly expressed on the mucosa of the oral cavity, especially in epithelial cells on tongue tissue derived from patients. This finding suggests that the oral cavity is a susceptible route for SARS-CoV-2 entry, in addition to the lungs. Cell culture for drug screening Cell cultures are invaluable tools for high-throughput drug screening to identify therapeutics capable of inhibiting entry and replication of SARS-CoV-2. Touret and colleagues screened 1,520 US Food and Drug Administration (FDA)-approved drugs in vitro for their anti-viral properties using VeroE6 and Caco-2 immortalized cell lines. From this study, they identified 90 compounds spanning different drug categories such as antibiotics and proton pump inhibitors, that may be therapeutically relevant. Similarly, Ianevski and co-workers made use of VeroE6 cell lines and found that a combination of orally-available virus-directed nelfinavir and host-directed amaodiaquine exhibited the best therapeutic effects against SARS-CoV-2 across 136 broad spectrum antiviral products. Recently, Daniloski and colleagues also performed a knock-out screening of genes in the human genome to identify which are needed for SARS-CoV-2 infection of human alveolar epithelial cell lines. They discovered that the most important genes included those encoding the vacuolar ATPase proton pump and Arp2/3 complex which they also validated using RNA interference knock-out and small molecule inhibitors. Going a step further, by using both in vitro cell culture and computational analysis approaches, Prof. Tudor Oprea and his team screened almost 4,000 approved drugs and identified those with structural similarity to hydroxychloroquine. In their study, they discovered that zuclopenthixol and nebivolol blocked COVID-19 infection at a low concentration with minimal side effects, and proposed that these drugs may be further tested for their therapeutic value. Critical to our work was not just the computer-guided effort, but also the dual (independent) experimental confirmation of these drugs in vitro. Experiments conducted first at University of New Mexico Health Sciences Center (Steven Bradfute lab) were later confirmed at the University of Tennessee Health Sciences Center (Colleen Jonsson lab), said Oprea. Given the documented cases of reinfection, it is possible that vaccines may not work against SARS-CoV-2, so we need to keep pursuing effective therapeutic approaches. Combining drugs with synergistic effects may be the best way to go forward. The thought behind this is to give a lower dose of each drug which can be safer and accessible because some drugs are in shortages. At the same time, this approach delivers a two-pronged attack against virus which is prone to develop drug resistance when subjected to monotherapy, Oprea added. Cell culture for producing viral particles To study SARS-CoV-2 transmission and infection, such as testing how different mask materials block transmission of SARS-CoV-2, it is necessary to obtain samples of the virus. Attributing to their lower costs of maintenance and fast cell division, immortalized cell lines have been used as factories to generate viral particles. This facilitates high-throughput production of viruses for testing and greatly enhances scientific study when it is challenging to access patients samples for extracting viruses. Kaye and co-workers showed that viral replication of severe acute respiratory syndromeassociated coronavirus (SARS-CoV) occurs efficiently in different cell lines. The viruses could then be isolated at high titers in the absence of specific cytopathic effects. Similar technology can likely be applied to SARS-CoV-2 as it belongs to the same virus family. Conclusion Cell cultures have facilitated studies investigating the biology of SARS-CoV-2 infection and have been harnessed for drug screening, they are also useful as a means for producing viral particles and therapeutics. Cell cultures have been an invaluable tool for biological studies and will be a key contributor in the ongoing fight against COVID-19.

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The Promise of Using Cell Cultures To Fight SARS-CoV-2 - Technology Networks

Coronavirus Updates: The Latest Treatments and Vaccines – GovTech

(TNS) - Scientists at Bay Area universities, laboratories, biotechnology companies and drug manufacturers are fashioning drug concoctions out of blood plasma, chimpanzee viruses and cells taken from bone marrow in the race to rid the world of COVID-19.

The microbial treasure hunt is not just to find a cure which may not be possible but to control the debilitating health problems caused by the coronavirus.

Major progress has been made this year. The antiviral drug remdesivir, produced in Foster City, has improved recovery times, and the steroid dexamethasone has cut the number of deaths in severely ill patients.

What follows is a list of some of the most promising medications and vaccines with ties to the Bay Area:

Antibodies

and Immunity

Mesenchymal stem cells / UCSF and UC Davis Medical Center:

UCSF Dr. Michael Matthay is leading a study of whether a kind of stem cell found in bone marrow can help critically ill patients with severe respiratory failure, known as ARDS. Matthay hopes the stem cells can help reduce the inflammation associated with some of ARDS' most dire respiratory symptoms, and help patients' lungs recover.

In all, 120 patients are being enrolled at UCSF Medical Center, Zuckerberg San Francisco General Hospital, the UC Davis Medical Center in Sacramento and hospitals in Oregon and Texas. He said the trial, which includes a small number of ARDS patients who don't have COVID-19, should have results by summer or fall 2021. So far, 28 patients are enrolled in San Francisco.

Lambda-interferon / Stanford University:

Lambda-interferon is a manufactured version of a naturally occurring protein that had been used to treat hepatitis, and researchers hoped it would help patients in the early stages of COVID-19.

Stanford researchers completed their trial of lambda-interferon and found that it did not boost the immune system response to coronavirus infections.

"That trial did not find any difference in outcomes between the treatment and placebo," said Yvonne Maldonado, chief of pediatric infectious diseases at Lucile Packard Children's Hospital at Stanford, where 120 patients were enrolled in the trial. "It didn't work."

Antiviral drugs

Remdesivir / Gilead Sciences ( Foster City):

Remdesivir, once conceived as a potential treatment for Ebola, was approved by the Food and Drug Administration in October for use on hospitalized COVID-19 patients.

Trademarked under the name Veklury, the drug interferes with the process through which the virus replicates itself. It was one of the drugs given to President Trump and has been used regularly in hospitals under what is known as an emergency use authorization.

It was approved after three clinical trials showed hospitalized coronavirus patients who received remdesivir recovered five days faster on average than those who received a placebo. Patients who required oxygen recovered seven days faster, according to the studies.

Gilead now plans to conduct clinical trials to see how remdesivir works on pediatric patients, from newborns to teenagers, with moderate to severe COVID-19 symptoms. Remdesivir is also being studied with steroids and other drugs to see if it works better as part of a medicinal cocktail. An inhalable form of the drug is also being developed.

Favipiravir / Fujifilm Toyama Chemical ( Stanford University):

This antiviral drug, developed in 2014 by a subsidiary of the Japanese film company to treat influenza, is undergoing numerous clinical studies worldwide, including a trial involving 180 patients at Stanford University.

Stanford epidemiologists are testing favipiravir to see if it prevents the coronavirus from replicating in human cells, halts the shedding of the virus and reduces the severity of infection. Unlike remdesivir, it can be administered orally, so it can be used to treat patients early in the disease, before hospitalization is necessary.

The Stanford study has so far enrolled about 90 patients, who are given the drug within 72 hours of when they were first diagnosed with COVID-19. Half of them get a placebo. People can enroll by emailing treatcovid@stanford.edu.

Monoclonal antibodies

REGN-COV2 / Regeneron Pharmaceuticals / Stanford School of Medicine:

The REGN-COV2 cocktail is the same one Trump received, and Stanford is one of dozens of locations nationwide where clinical trials are being held. Two separate trials are under way at Stanford one for hospitalized patients, the other for outpatients. A third trial is about to begin for people who aren't sick but are in contact with carriers of the virus.

Regeneron halted testing on severely ill patients requiring high-flow oxygen or mechanical ventilation after the independent Data and Safety Monitoring Board determined that the drug was unlikely to help them.

The drug is a combination of two monoclonal antibodies lab-made clones of the antibodies produced naturally in people who have recovered from COVID-19. The antibodies bind to the virus' spike protein and block the virus' ability to enter cells.

Dr. Aruna Subramanian, professor of infectious diseases at Stanford and lead investigator for the inpatient trial, said the 21 hospitalized patients in the study receive a high dose like Trump, a lower dose or a placebo. Subramanian plans to expand the inpatient trial to 45 patients. The outpatient study has enrolled a little more than 40 of the 60 patients researchers intend to sign up.

"There's enough promising evidence that it helps people early in the infection," Subramanian said. "What we don't know is whether it helps people who are pretty sick but not critically ill."

Bamlanivimab / Eli Lilly / Stanford and UCSF:

Stanford and UCSF are testing the Eli Lilly monoclonal antibodies on outpatients after the pharmaceutical company halted trials on hospitalized COVID-19 patients because of adverse results.

Dr. Andra Blomkalns, chair of emergency medicine at Stanford and the lead in the Eli Lilly outpatient trial, said she is now enrolling older people with comorbidities like heart disease, chronic lung disease, a history of strokes and severe obesity shortly after they test positive.

The hypothesis is that the bamlanivimab monotherapy, which is very similar to the Regeneron monoclonals, might work best early in the infection. Although about 400 patients have been enrolled in the Lilly phase 3 trials nationwide, to date fewer than 10 have been enrolled at Stanford and UCSF.

Matthay, who headed up the Lilly monoclonal study with LY-CoV555 at UCSF, said the cancellation of this inpatient trial was disappointing, but "just because this one did not work, doesn't mean another one won't work for hospitalized patients."

Blomkalns said the testing criteria has been changing. She expects the outpatient trial to open soon to adolescents ages 12 and up to determine whether the drug can be used as a preventive.

Designer monoclonal antibodies / Vir Biotechnology, San Francisco:

Scientists at Vir are studying several types of monoclonal antibodies, including a type engineered to activate T cells, which can search out and destroy cells infected with the coronavirus. A study published in the journal Nature in October found that monoclonals, modified to bind with certain receptors, stimulated T cells and improved the human immune response.

"By observing and learning from our body's powerful natural defenses, we have discovered how to maximize the capacity of antibodies through the amplification of key characteristics that may enable more effective treatments for viral diseases," said Herbert Virgin, the chief scientific officer at Vir and co-author of the study.

A similarly modified monoclonal antibody, leronlimab, is being studied in coronavirus clinical trials by its Washington state drugmaker, CytoDyn, which has developed drugs to treat HIV. The company's chief medical officer is in San Francisco, and the company that does laboratory tests of leronlimab is in San Carlos.

Anti-inflammatory drugs

Colchicine / UCSF ( San Francisco and New York):

The anti-inflammatory drug commonly used to treat gout flare-ups is being studied by scientists at UCSF and New York University. The drug short-circuits inflammation by decreasing the body's production of certain proteins, and researchers hope that it will reduce lung complications and prevent deaths from COVID-19.

Preliminary results from a clinical trial found that "Colchicine can be effective in reducing systemic symptoms of COVID-19 by inhibiting inflammatory biomarkers."

Selinexor / Kaiser Permanente:

Kaiser hospitals in San Francisco, Oakland and Sacramento are studying selinexor, an anticancer drug that blocks a key protein in the cellular machinery for DNA processing. Preliminary findings during the trials indicated that low doses of selinexor helped hospitalized patients with severe COVID-19. The drug has both antiviral and anti-inflammatory properties, and it's administered orally, according to Kaiser's Dr. Jacek Skarbinski.

Vaccines

VXA-COV2-1 / Vaxart, South San Francisco:

The biotechnology company Vaxart is testing VXA-COV2-1, the only potential vaccine in pill form. It uses the genetic code of the coronavirus to trigger a defensive response in mucous membranes. The hope is that the newly fortified membranes will prevent the virus from entering the body.

"It's the only vaccine (candidate) that activates the first line of defense, which is the mucosa," said Andrei Floroiu, Vaxart's chief executive. He said intravenous vaccines kill the virus after it is inside the body, but this one stops it beforehand.

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Coronavirus Updates: The Latest Treatments and Vaccines - GovTech

HCT Deemed More Favorable for MDS That Is High Risk – Cancer Therapy Advisor

Hematopoietic stem cell transplant (HCT) treatment of myelodysplastic syndromes (MDS) resulted in a lower risk of death if performed early after diagnosis or among patients with high-risk disease, according to results of an observational study published in Leukemia.

HCT is the only potentially curative treatment for MDS. However, the disease primarily occurs among older patients in whom myoablative conditioning regimens are associated with an increased risk of mortality. The aim of this study was to evaluate mortality after transplant in a real-world population of patients with MDS.

The prospective, observational study included 290 patients with advanced MDS aged 60 to 75 years from the MDS Transplant-Associated Outcomes study who were determined to be fit to undergo HCT. All patients had disease that warranted consideration of HCT, including patients with intermediate- to high-risk disease or those with standard risk and severe cytopenia. The primary endpoint was overall survival (OS).

At baseline, the median age was 69 years, and the majority of patients had intermediate-risk disease (78%) and good cytogenetic risk (53%). Mutations in TP53, JAK2, or in the RAS pathway were either not present or unknown in most patients.

HCT was performed in 113 patients (39%) with a median time to HCT of 5 months (range, 1-58 months).

The median OS of the entire cohort was 29 months (95% CI, 19-39.5 months), which translated to a 3-year OS of 46%. Overall, there was no difference in the risk of death between the cohort who underwent HCT and those who did not (hazard ratio [HR], 0.75; 95% CI, 0.52-1.09; P =.13), in a multivariate analysis. However, landmark analyses showed a survival benefit with HCT at 5 (P =.04) and 9 months (P =.01), but not at 12 months or 24 months.

HCT performed earlier, within 5 months from study entry, was significantly associated with a lower risk of death than transplants performed later (HR, 0.53; 95% CI, 0.33-0.83; P =.006). HCTs performed after 5 months did not result in a survival benefit between the HCT and non-HCT cohorts.

Transplant also lowered the risk of death among patients with adverse-risk disease compared with patients with standard-risk MDS with severe cytopenia (HR, 0.57; 95% CI, 0.37-0.88; P =.01).

Other characteristics associated with a survival benefit with HCT included patients with poor cytogenetic risk, an Eastern Cooperative Oncology Group performance status of 1, and patients of male sex.

The authors concluded that these data showed that there were also significant benefits for those receiving HCT within 5 months and for those with adverse disease risk factors as compared to standard risk with severe cytopenias.

Reference

Abel GA, Kim HT, Hantel A, et al. Fit older adults with advanced myelodysplastic syndromes: who is most likely to benefit from transplant? Leukemia. Published November 17, 2020. doi:10.1038/s41375-020-01092-2

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HCT Deemed More Favorable for MDS That Is High Risk - Cancer Therapy Advisor

Mini kidneys bioprinted in the lab – Lab + Life Scientist

Researchers from the Murdoch Childrens Research Institute (MCRI) and biotech company Organovo have used cutting-edge technology to bioprint miniature human kidneys in the lab, paving the way for new treatments for kidney failure and possibly lab-grown transplants. Their study has been published in the journal Nature Materials.

Like squeezing toothpaste out of a tube, extrusion-based 3D bioprinting uses a bioink made from a stem cell paste, squeezed out through a computer-guided pipette to create artificial living tissue in a dish. According to MCRI Professor Melissa Little, a world leader in modelling the human kidney, this new bioprinting method is faster and more reliable than previous methods, allowing the whole process to be scaled up. 3D bioprinting could now create about 200 mini kidneys in 10 minutes without compromising quality.

From larger than a grain of rice to the size of a fingernail, bioprinted mini kidneys fully resemble a regular-sized kidney, including the tiny tubes and blood vessels that form the organs filtering structures called nephrons. Prof Little said the mini organs will be used to screen drugs to find new treatments for kidney disease or to test if a new drug was likely to injure the kidney.

Drug-induced injury to the kidney is a major side effect and difficult to predict using animal studies; bioprinting human kidneys are a practical approach to testing for toxicity before use, she said.

In the study, researchers tested the toxicity of aminoglycosides a class of antibiotics that commonly damage the kidney. Prof Little said, We found increased death of particular types of cells in the kidneys treated with aminoglycosides.

By generating stem cells from a patient with a genetic kidney disease, and then growing mini kidneys from them, also paves the way for tailoring treatment plans specific to each patient, which could be extended to a range of kidney diseases.

Prof Little said the study also showed that 3D bioprinting of stem cells can produce large enough sheets of kidney tissue needed for transplants. She noted, 3D bioprinting can generate larger amounts of kidney tissue but with precise manipulation of biophysical properties, including cell number and conformation, improving the outcome.

Prof Little said prior to this study the possibility of using mini kidneys to generate transplantable tissue was too far away to contemplate, but that may no longer be the case.

The pathway to renal replacement therapy using stem cell-derived kidney tissue will need a massive increase in the number of nephron structures present in the tissue to be transplanted, she said.

By using extrusion bioprinting, we improved the final nephron count, which will ultimately determine whether we can transplant these tissues into people.

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Mini kidneys bioprinted in the lab - Lab + Life Scientist

Canine Stem Cell Therapy Market Analysis, Overview, Growth, Demand and Forecast Research Report to 2026 – The Haitian-Caribbean News Network

The global Canine Stem Cell Therapy market was valued at US$ 118.5 Mn in 2018 and is expected to reach US$ 240.7 Mn in 2026, growing at a CAGR of 9.3% during the forecast period.

Global Canine Stem Cell Therapy Market would reach to a substantial size by 2026. Comprehensive coverage of the market classification can be availed in this report where the type, application and geography are the main segmentation. Also, analysis has been covered the scope of the Canine Stem Cell Therapy Market along with the market size and forecast of current and future trends and analysis.

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The Following key players are covered in this Report:

The report analyses their product offerings, key strategies, sales and revenues, and prospects going forward.

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Market segments of the global Canine Stem Cell Therapy have been provided below to understand the bifurcation of the Market. The segments help the reader to understand the market from all the aspects.

The Report Splits by Major Applications:

The Report Analysed by Types:

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

COVID-19 Impact on Canine Stem Cell Therapy Market:

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

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Mon Nov 30 , 2020

New Jersey, United States: Market Research Intellect has added a new report to its huge database of research reports, entitled Consumer Healthcare Market Size and Forecast to 2027. The report offers a comprehensive assessment of the market including insights, historical data, facts, and industry-validated market data. It also covers the []

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Canine Stem Cell Therapy Market Analysis, Overview, Growth, Demand and Forecast Research Report to 2026 - The Haitian-Caribbean News Network

Stem Cell Therapy Market Size, Share & Trends Analysis Report By Product Types, And Applications Forecast To 2026 – Cheshire Media

Latest released the research study on the Global Stem Cell Therapy Market offers a detailed overview of the factors influencing the global business scope. Stem Cell Therapy Market research report shows the latest market insights, current situation analysis with upcoming trends, and breakdown of the products and services. The report provides key statistics on the market status, size, share, growth factors of the Stem Cell Therapy. It also explains what the market definition, classifications, applications, engagements, and global industry trends are. The report puts light on the entire market trends and analyses the effect of buyers, consumers, substitutes, new entrants, competitors, and suppliers on the market. Stem Cell Therapy market research report delivers a comprehensive analysis of the market structure along with estimations of the various segments and sub-segments of the market.

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Market Overview of Global Stem Cell Therapy

If you are involved in the Global Stem Cell Therapy industry or aim to be, then this study will provide you inclusive point of view. Its vital you keep your market knowledge up to date segmented by Product Types and major players. If you have a different set of players/manufacturers according to geography or needs regional or country segmented reports we can provide customization according to your requirement.

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 along with impact of economic slowdown due to COVID.

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This report provides pinpoint analysis for changing competitive dynamics. It offers a forward-looking perspective on different factors driving or limiting market growth. It provides a five-year forecast assessed on the basis of how they Conversational Stem Cell Therapy Market is predicted to grow. It helps in understanding the key product segments and their future and helps in making informed business decisions by having complete insights of market and by making in-depth analysis of market segments.

Stem Cell Therapy Market Segmentation

Type Analysis of Stem Cell Therapy Market:

Based on cell source, the market has been segmented into,

Adipose Tissue-Derived Mesenchymal SCs Bone Marrow-Derived Mesenchymal SCs Embryonic SCs Other Sources

Applications Analysis of Stem Cell Therapy Market:

Based on therapeutic application, the market has been segmented into,

Musculoskeletal Disorders Wounds & Injuries Cardiovascular Diseases Gastrointestinal Diseases Immune System Diseases Other Applications

Key questions answered in the report include:

1. What will the market size and the growth rate be in 2025? 2. What are the key factors driving the Global Conversational Stem Cell Therapy Market? 3. What are the key market trends impacting the growth of the Global Conversational Stem Cell Therapy Market? 4. What are the challenges to market growth? 5. Who are the key vendors in the Global Conversational Stem Cell Therapy Market? 6. What are the market opportunities and threats faced by the vendors in the Global Stem Cell Therapy Market?

Browse the complete report Along with TOC @ https://www.adroitmarketresearch.com/industry-reports/stem-cell-therapy-market?utm_source=Pallavi

1 Stem Cell Therapy Market Overview 2 Global Stem Cell Therapy Market Competition by Manufacturers 3 Global Stem Cell Therapy Capacity, Production, Revenue (Value) by Region) 4 Global Stem Cell Therapy Supply (Production), Consumption, Export, Import by Region 5 Global Stem Cell Therapy Production, Revenue (Value), Price Trend by Type 6 Global Stem Cell Therapy Market Analysis by Application 7 Global Stem Cell Therapy Manufacturers Profiles/Analysis 8 Stem Cell Therapy Manufacturing Cost Analysis 9 Industrial Chain, Sourcing Strategy and Downstream Buyers 10 Marketing Strategy Analysis, Distributors/Traders 11 Market Effect Factors Analysis 12 Global Stem Cell Therapy Market Forecast 13 Research Findings and Conclusion 14 Appendix

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Stem Cell Therapy Market Size, Share & Trends Analysis Report By Product Types, And Applications Forecast To 2026 - Cheshire Media