CRISPR trial shows promising results for sickle cell and thalassaemia – BioNews

22 June 2020

CRISPRgenome editing has been successfully used to treat three patients with blood disorders in a clinical trial.

Two US patients with beta-thalassaemia and one with sickle cell disease had their bone marrow stem cells edited to produce a different form of haemoglobin, which is normally only found in fetuses and newborns.

'The results [demonstrate] that CRISPR/Cas9 gene editing has the potential to be a curative therapy for severe genetic diseases like sickle cell and beta-thalassaemia,' said Dr Reshma Kewalrami, CEO and President of Vertex, which is running the study jointly with another US pharmaceutical company, CRISPR Therapeutics.

Both sickle cell and beta-thalassaemia are caused by mutations in a gene that produces haemoglobin, the protein in red blood cells that carries oxygen throughout the body. With limited treatment options, patients are often dependent on blood transfusions.

However, the human body is able to make another form of haemoglobin, encoded in a completely separate gene, which is normally only expressed during fetal development and is switched off soon after birth.

In the clinical trial, blood stem cells were removed from the patients and a control gene that turns off the production of fetal haemoglobin was inactivated. Patients were given chemotherapy to remove remaining bone marrow stem cellsbefore they were replaced by the editedcells. The patients were then able to make fetal haemoglobin as adults.

The results of the ongoing trial, presented at the virtual Annual European Hematology Association Congress, reported that two beta-thalassaemia patients were transfusion independent at five and fifteen months after treatment, and the sickle cell patient was free from painful crises at nine months after treatment.

All three patients suffered significant side effects (from which they all recovered), but these were thought to be as a result of the chemotherapy rather than genome editing. Chemotherapy can also have long-term effects including infertility.

It is hoped that this treatment will have long-lasting and durable effects in patients with inherited blood diseases, and early clinical data appear promising. However, patients will need to be followed up throughout their lives to record any changes.

'These highly encouraging early data represent one more step toward delivering on the promise and potential of CRISPR/Cas9 therapies as a new class of potentially transformative medicines to treat serious diseases,' said Dr Samarth Kulkarni, CEO of CRISPR Therapeutics.

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CRISPR trial shows promising results for sickle cell and thalassaemia - BioNews

Stem Cell Therapy Designed To Treat Severely Ill Coronavirus Patients Being Tested In Maryland – CBS Baltimore

BALTIMORE (WJZ) A stem cell therapy trial for the most critically ill coronavirus patients is underway in Maryland.

Researchers at the University of Maryland School of Medicine are trying to save the maximum number of patients who are significantly sickened by the virus and reduce the mortality rate.

Thanks to a sponsorship by Australian regenerative medicine company Mesoblast, the stem cell therapy trial is underway at several sites across the U.S., including in Maryland.

The therapy involves 300 people hospitalized with COVID-19 with moderate to severe acute respiratory distress syndrome.

These are patients that are intubated, requiring great support for their lung function, Dr. Sunjay Kaushal with the University of Maryland said.

CORONAVIRUS RESOURCES:

COVID-19 patients often become very ill from an escalated immune response referred to as a cytokine storm, which creates high levels of inflammation that can be fatal. The experimental stem cell therapy called remestemcel-L, which has been developed for various inflammatory conditions like what is being seen with the coronavirus, aims to block or mitigate that response, Kaushal said.

Were trying to extrapolate from what they have been shown to be efficacious in trying to treat before and trying to use that type of therapy now for COVID-19 patients, he said.

Once the final results from the trial are available, which could take between six and eight months, researchers hope to reach even more patients.

Were excited, weve seen some early signs that these cells may be efficacious, Kaushal said.

Ultimately, their hope is to provide a new treatment for those suffering from the worst cases of COVID-19.

Were hoping we can save a lot of patients lives, Kaushal said.

For the latest information on coronavirus go to the Maryland Health Departments website or call 211. You can find all of WJZs coverage on coronavirus in Maryland here.

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Stem Cell Therapy Designed To Treat Severely Ill Coronavirus Patients Being Tested In Maryland - CBS Baltimore

R3 International Offering New Stem Cell Therapy Program for Kidney Disease in Mexico – PR Web

Stem Cell Therapy for Kidney Disease (888) 988-0515

SAN DIEGO (PRWEB) June 09, 2020

R3 Stem Cell International, the leading regenerative clinic in Mexico, announced a new stem cell program for kidney disease. The program involves upwards of 200 million live stem cells and starts at only $8975.

R3's world renowned center has helped hundreds of patients over the past years for such conditions as kidney failure, autoimmune disease, COPD, stroke, diabetes, arthritis, ALS, MS and many more ailments. While stem cell therapy for kidney disease in Mexico works fantastic on a single visit, the new program provides significantly increased cell counts.

According to R3 International Medical Director Ramon De La Puerta MD, "We have seen so many patients avoid dialysis and get back to desired activities with our newest protocol. The key is the large numbers of quality stem cells and exosomes provided during treatment, and it's extremely affordable!"

The two options for the kidney failure stem cell treatment in Mexico include several therapies in a five day visit or four visits over a one year period. The total stem cell counts for either option range from 150 to 200 million.

The treatment programs start at only $8975, with interested patients starting with a free phone consultation. The experienced, licensed, stem cell doctor will review any medical records and provide a recommendation.

According to R3 CEO David Greene, MD, MBA, "Achieving treatment in the US with this many stem cells would be prohibitively expensive. So I created R3 International where treatment is not only affordable, but amazingly safe and effective. The biologics our Center uses undergo quality assurance testing that actually exceeds FDA standards in the US!"

R3 Stem Cell International assists patients with travel logistics, and offers concierge escorted transportation from San Diego to the treatment center. Phone consultations are free, and the stem cell biologics have a perfect safety record. Call (888) 988-0515 to set up the consultation, and visit https://stemcelltreatmentclinic.com/the-process/ to see how the process works to receive treatment.

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Evera, A Harvard Consumer Biotech Company, Brings Stem Cell Banking To You – Forbes

Throughout the past decade, consumer biology tests have been all the rage. Companies such as 23andMe and Ancestry DNA have made their test kits accessible to every day Americans. One can screen for anomalies in their genetic code or identify their lineage. With recent advances in stem cell research, a new opportunity within the consumer biology market has appeared. Nabeel Quryshi, Michael Chen and Zeel Patel are three Harvard undergraduates who observed the unmet, rising demand of control over ones stem cells. They worked together to create Evera, the first at-home stem cell banking company. The three Harvard students are joined by the schools world-renowned biology professor, Dr. George Church. The Cambridge, Massachusetts-based company was incubated at the Harvard Innovation Lab, and has former NASA astronaut Scott Kelly as a investor.

Evera cofounders from left to right: Nabeel Quryshi, Michael Chen and Zeel Patel.

Kelly says, "I did a lot of my independent research, consulted with NASA physicians and scientists, and experts in the stem cell for cancer treatment fields. All those discussions and research indicated that this technology has merit."

Frederick Daso: What led you and your team to identify that stem cells could be potentially used to prevent neurodegenerative disease?

Nabeel Quryshi: I wouldn't single out a focus on neurodegenerative diseases. However, over the last decade, there has been a flurry of research around the use of stem cells to treat conditions such as Parkinson's, Dementia, Alzheimer's, etc. People are working on prevention, but there are two main use cases of stem cells currently. One is for treatment (replacement of damaged or lost cells), and the other is disease modeling (being able to model diseases and test the effects of new drugs completely in vitro without having to get a biopsy).

Daso: In the same ways that blood banks function, how did you manage to apply that concept to the storage of stem cells over a long time?

Quryshi: Cord blood banks and academic stem cell banks that use standardized cryopreservation protocols have been around for a while. The main innovation behind Evera was developing technology around the collection and preservation of urine-derived cells.

Daso: Why don't more mothers store their children's cord blood in stem cell banks? Is it mostly due to a price issue, or is there some other factor at play?

Quryshi: From the countless interviews we've done, it seems to be a price issue. Additionally, it's hard to make a sale around the time of birth as families have countless other things to worry about that are more immediate to the birth of a child.

Daso: What would be driving the growth of this market both now and in the future?

Quryshi: The growth of new cutting edge cell therapies is certainly further demonstrating the need for personal cell biobanking. Furthermore, the success of the direct to consumer genetic testing industry (23andMe, Ancestry, etc.) is a significant driver of growth. From the research we've conducted and the customers we have spoken to, individuals who have already taken 23andMe or another genetic test and know what they are at risk for genetically are looking for ways to take tangible action. Evera is that next step. Instead of just understanding what your future genetic risk is, Evera allows you to make a real biological investment in your future health and wellbeing. While knowing you're at risk for saying Parkinson's is excellent, being able to set aside your youngest cells so that one day you may be able to combat the effects of such a disease is terrific.

However, one should note that although the growth and technology coming from the cell therapy and stem cell therapy industry is astonishing, these are still projections. We have yet to see a fully FDA approved therapy that utilizes the specific types of stem cells we use (induced pluripotent stem cells). Nevertheless, by the time such treatments make it to the clinic, your cells will have aged significantly, and thus it makes sense to save them away now.

Daso: Could you walk me through the thought process of figuring out how to extract stem cells from urine? (From what I know, stem cells usually come from other parts of your body!)

Quryshi: Until around 2011/2012, you would have been right. However, utilizing the fantastic technology that comprised Dr. Yamanaka's 2006 Nobel Prize, scientists have been able to convert any cell in the human body to a kind of stem cell called an induced pluripotent stem cell. This cell has the capability of being able to differentiate into any cell type in the human body. We have advanced tech around the conversation of urine-derived cells to these iPSCs.

Daso: How have you designed your D2C service to ensure that a customer's DNA and associated data are not at risk?

Quryshi: We take data and privacy extremely seriously. We are well aware of the concerns people already have to D2C genetics products. To ensure the confidentiality and privacy of your data and sample, we separate your personally identifiable information from sample information and simultaneously use multiple layers of encryption and cryptography. Your sample and associated data cannot be associated with you individually. Furthermore, our facility is monitored 24/7 with top of the line security measures. We believe that your sample is your property.

Daso: What was the turning point during your undergrad to pursue this idea?

Quryshi: Having worked at 23andMe, I was able to get the lucky opportunity to be a part of arguably the world's most successful consumer genetics company. I saw first hand the benefits of providing customers with their genetic risk. Yet, I discovered that merely providing such risk predictions may not be enough led me to found Evera on the notion that tangibly investing in one's future health and wellbeing through cell banking will propel us into the age of personalized medicine.

Daso: How do you leverage your advisory board to navigate regulations and moral hazards in this space?

Quryshi: We have assembled a dream team consisting of experts in stem cell banking and cell therapy. Our co-founders and advisors comprise of professors from Harvard and Stanford, executives from companies such as Verily as well as top grad students and postdocs in stem cell biology from Harvard and Stanford. We work collaboratively to make sure we adhere to all regulations and ensure the secure preservation of our customer's cells.

If you enjoyed this article, feel free to check out my other work onLinkedInand my personal website,frederickdaso.com. Follow me on Twitter@fredsoda, on Medium@fredsoda, and on Instagram@fred_soda.

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Evera, A Harvard Consumer Biotech Company, Brings Stem Cell Banking To You - Forbes

Here’s Why Fate Therapeutics Rose 18.4% in May – Motley Fool

What happened

Shares of Fate Therapeutics (NASDAQ:FATE) gained over 18% last month, according to data provided by S&P Global Market Intelligence. Most of the stock's gains in May can be traced to a single announcement by the cell-therapy developer.

On May 20, the development-stage company announced the U.S. Food and Drug Administration (FDA) cleared a new drug candidate to begin clinical trials. Identified as FT538, the drug candidate is the first cell therapy that has been both engineered with CRISPR gene-editing tools and derived from induced pluripotent stem cells (iPSC). The combination could lead to safer, more effective, and significantly lower-cost drug products.

Investors cheered the latest sign of progress for the early stage pipeline -- and the momentum hasn't waned. In fact, a public offering of common stock on June 9 triggered additional gains for the pharma stock. Apparently, investors are content with dilution so long as Fate Therapeutics maintains a well-funded balance sheet.

Image source: Getty Images.

Fate Therapeutics has one of the most ambitious pipelines in cell therapy, spanning 13 unique programs and multiple cell types. Until recently, investors had few tangibles to analyze, but promising (very) early-stage data and a multi-billion-dollar partnership with Johnson & Johnson subsidiary Janssen have de-risked the stock.

It might be a bit silly to get excited about a preclinical asset moving to clinical trials, but FT538 could prove to be an important bellwether for Fate Therapeutics. If researchers prove that gene-editing tools can be used with reproducible results on cells grown from master cell lines, such as iPSCs, then it would be a big step forward for the field of cell therapy. The capabilities would enable the relatively quick engineering of cell therapies, both for efficacy and safety, and allow living drug products to be manufactured at scales and costs simply not possible today.

Including cash on hand at the end of March and the expected proceeds from the stock offering on June 9, Fate Therapeutics should begin the second half of 2020 with at least $350 million in cash. That should be enough to generate results from a handful of ongoing clinical trials, but investors shouldn't forget that the company's ambitious pipeline will require many hundreds of millions of dollars to develop.

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Here's Why Fate Therapeutics Rose 18.4% in May - Motley Fool

Animal Stem Cell Therapy Sales Market 2019 Break Down by Top Companies, Countries, Applications, Challenges, Opportunities and Forecast 2026 – Cole of…

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Who’s to blame? These three scientists are at the heart of the Surgisphere COVID-19 scandal – Science Magazine

By Charles PillerJun. 8, 2020 , 7:00 PM

Sciences COVID-19 reporting is supported by the Pulitzer Center.

Three unlikely collaborators are at the heart of the fast-moving COVID-19 research scandal, which led to retractions last week by The Lancet and The New England Journal of Medicine (NEJM), and the withdrawal of an online preprint, after the trove of patient data they all relied on was challenged. The three physician-scientists never were at the same institution nor had they ever before written together, but they are the only authors in common on the disputed papers, and the other co-authors all have ties to at least one of them. Their partnership, which seized a high-impact role during a global public health crisis, has now ended disastrously.

The first author for both retracted papers was cardiac surgeon Mandeep Mehra, an eminent Harvard University professor who works at Brigham and Womens Hospital (BWH) and is known internationally for cardiovascular medicine and heart transplants. He provided the kind of gravitas that can fast-track papers to leading journals. In a statement provided by BWH, Mehra said he had met another of the trio, cardiac surgeon Amit Patel, in academic and medical circles, and that Patel had introduced him to Sapan Desai, a vascular surgeon and founder of Surgisphere, the tiny company that supplied the data. Journal disclosures, however, also indicate Mehra received compensation from Triple-Gene, a gene therapy company Patel co-founded to develop cardiovascular treatments.

Desai publicly aspired to combine big data and artificial intelligence (AI) in ways that he said can replace randomized controlled clinical trials. For a brief moment, it seemed that Surgispheres enticing data set, said to include nearly 100,000 detailed patient records from about 700 hospitals on six continents, would settle questions about the possible benefits of various drugsincluding the controversial antimalarial hydroxychloroquinefor COVID-19 patients.

Patel once apparently headed cardiac surgery at the University of Miami Miller School of Medicine. A university press release announcing his arrival in 2016 is no longer posted on the university website, however, and the school has not confirmed his job duties there. More recently, he has been a volunteer adjunct professor at the University of Utah. But, as STAT first reported yesterday, Patel tweeted on Friday that he had severed his relationship with the university, which a school spokesperson confirmed. In recent years Patel has developed and commercialized experimental stem cell therapies purported to cure heart problems, reverse aging, or treat sexual dysfunction. He is also part of a network of physicians that just launched a trial to use stem cells from umbilical cord blood to treat COVID-19 patients.

Normally co-authors of high-profile papers share subject area expertise or have clear professional ties, says Jerome Kassirer, chief editor ofNEJMduring the 1990s. He calls the collaboration of the apparently disparate individuals completely bizarre, and a red flag that the studies warranted intensive scrutiny that the journals failed to provide.

None of the three co-authors responded to requests for comment. Patel spoke with aSciencereporter initially but said he wanted to wait for audits of the Surgisphere data to comment, and Desais spokesperson stopped communicating after the retractions. Still, interviews with former colleagues and a long paper trail shed some light on each of them.

Desai had a history of convincing respected researchers of his skill and integrity. One of them, Gilbert Upchurch, department of surgery chair at the University of Florida, wrote last year in a journal commentary that he had never met Desai but had nonetheless mentored him remotely and developed an online friendship with him. Upchurch placed the scientist in a group of amazing and talented young vascular surgeons.

Illinois court records show Desai is facing two medical malpractice lawsuits filed last year. He told The Scientist that he deems any lawsuit naming him to be unfounded.

Desai has a history of big aspirations and entrepreneurial venturessome short-lived. His science-fiction blog, corewardfront.com, was meant to find the most parsimonious route for mankind to establish a meaningful presence in space. In 2009, he wrote that the site would publish fiction grounded in facts and reality, adding, the scientific method must be followed religiously. The blog is no longer published.

As a student, Desai won several small National Institutes of Health (NIH) grants for studies of the vestibular system. He started Surgisphere in 2007, when he was a medical resident at Duke University. Surgispheres initial products were medical guides and textbooks, although Desai has said he was working on big data projects for the company from its birth. In 2010, under the firms auspices, he founded the Journal of Surgical Radiologywhose editors included researchers with well-established publishing records. It folded in January 2013. Articles from the journal were cited only 29 times in its history, according to Scimago, a journal rating service. Yet an undated Surgisphere web page, no longer accessible online, said the online-only publication had 50,000 subscribers and nearly 1 million page views monthlywhich would have placed it in elite company in academic publishing.

Surgisphere appears over time to have shifted its efforts into developing a database of hospital records that could be used for research. When the pandemic erupted, Desai declared that his data set could answer key questions about the efficacy and safety of treatments. Speaking about the finding that hydroxychloroquine increases mortality in COVID-19 patients, the main finding from the now retracted Lancet paper, he told a Turkish TV reporter, with data like this, do we even need a randomized controlled trial? Soon after, the World Health Organization temporarily suspended enrolling patients for its COVID-19 trial of the drug.

Immediately after the Lancet and NEJM studies appeared, however, critics identified anomalies in the data. And they doubted that a tiny firmwith a scant public track record in AI, few employees, and no publicly named scientific boardcould convince hundreds of unidentified hospitals in dozens of nations to share complex, protected, and legally fraught patient data. Ultimately, despite Desai promising repeatedly to allow an independent audit of Surgisphere, the firm refused to release the raw patient data and agreements with hospitals for an audit, so no one could validate the authenticity of its database.

No hospitals have come forward to acknowledge working with Surgisphere. Indeed, NHS Scotland, which is mentioned as a case study on the companys website, says none of its hospitals worked with Surgisphere and that it would ask the firm to remove an image of a Glasgow hospital from its website.

Science contacted several of Desais current or former employees or colleagues. Most would not comment. But Fred Rahimi, an Illinois podiatrist and co-author of a paper with Desai, praises the surgeon as highly capable for salvaging limbs, and easy to work with. Through his publicist, Desai cited Mark Melin, a University of Minnesota, Twin Cities, vascular surgeon, as a supporter. Before the retractions, Melin called Desai a gentleman of the highest integrity who has nothing to cover up.

But one physician-scientist who worked closely with Desai several years ago, says, Just about everyone who knew him would say: I just didnt have a good feeling about him. After theyd been with him, most people dissociated themselves from him, the scientist says, declining to be named to avoid personal and institutional embarrassment.

In the decade since completing his medical residency, Desai moved from job to jobat Duke, the University of Texas, Southern Illinois University, and two private Illinois hospitals, according to his LinkedIn profile. You might say we should have stopped him, which now seems obvious, Desais former colleague says. We should have found a way to get together and say, Whats going on here? rather than allowing him to move from place to place. We should have done better as a medical community. We looked the other way.

Before and after his stint at the University of Miami, which appears to have started in late 2016 or early 2017, Patels academic home was the University of Utah. He started as a full-time faculty member at Utah in 2008 and kept that position until he left for Miami. The website for Foldax, a heart valve company that he serves as medical adviser, describes him as a Tenured Professor of Surgery in the Division of Cardiothoracic Surgery at the University of Utah School of Medicine and Director of Clinical Regenerative Medicine and Tissue Engineering at the University of Utah.

The university confirmed Patel had tenure there, but says the directorship was an unofficial title. And among more than 100 publications listed on his University of Utah profile, nearly two-thirds were actually co-authored by other scientists who share the same surname. The page was removed from the university website after inquiries from Science. A university spokesperson said the timing, late Friday last week, was when Patel and the school agreed to separate.

According to the NIH database, Patel has never received funding from the agency. Before the recent COVID-19 papers, one of his most notable publications was a 2016 paper in The Lancet, which reported that extracting stem cells from the bone marrow of a person with end-stage heart failure and then reinjecting them could reduce the number of cardiac events that produced deaths or hospital admissions by 37%. The 126 patient, 31-site, phase II trial was billed in a press release, now not available on the University of Utah website but stored elsewhere, as the largest cell therapy trial for heart failure to date. Despite the apparent positive results, the sponsoring company Vericel no longer is developing stem cells for heart disease and, according to its webpage, is focused on advanced cell therapies for the sports medicine and severe burn care markets.

Patel left Miami under unclear circumstances, but has retained ties with Camillo Ricordi, an influential stem cell researcher at the University of Miami School of Medicine who is also the founder of a nonprofit called the Cure Alliance. The alliance previously focused on testing whether stem cells derived from umbilical cord blood could treat diabetes or Alzheimers, but has now pivoted to fighting COVID-19, according to its website. Ricordi is the principal investigator on a multisite trial to see whether the stem cells can treat lung inflammation in severe COVID-19 patients and Patel is listed in various references to the trial as a key contributor or coprincipal investigator. Ricordi says Patel is an upaid collaborater on the trial and praises Patel's work in regenerative medicine.

Patel recently tweeted that he is related to Dr. Desai by marriage but called that old news and added, Despite this I still do not have the information of what happened at Surgisphere. In addition to apparently connecting Mehra and Desai, Patel had prior connections with other authors of the NEJM paper and the preprint. David Grainger, co-author of the preprint, is a professor of biomedical engineering at the University of Utah and also works with Foldax. Grainger declined to comment.

Timothy Henry, a cardiovascular clinician and scientist at the Christ Hospital in Cincinnati and a co-author on the NEJM article, has written several scholarly articles with Patel, including the 2016 Lancet paper. Henry, who also declined to comment, advises Patels Triple-Gene, which develops cardiovascular gene therapy treatments. Henry and Patel adviseand Patel is a board member ofCreative Medical Technology Holdings, a Phoenix company that develops and markets stem cell therapies, including treatments purported to reverse aging and cure sexual disfunction.

Creative Medicals CaverStem and FemCelz kits are distributed to physicians who use them to extract stem cells from a patients bone marrow, then inject the cells into the penis or clitoral area to stimulate blood flow, according to a statement filed with the U.S. Securities and Exchange Commission. (As of the market close Friday, the publicly traded firms shares were valued at one-third of 1 cent.) The CaverStem treatments are advertised by the company as successful in more than 80% of patients, based on a 40-person phase I clinical trial that was not randomized or controlled, and on observations of 100 other patients. Phase I trials typically measure safety, not health benefits of a potential treatment.

Science contacted multiple colleagues or co-authors of Patel. None would comment. Before the retractions, two high-profile researchersDeepak Bhatt, who directs interventional cardiovascular programs at BWH; and Peter Gruber, a pediatric cardiothoracic surgeon at Yale Universityendorsed Patel on his LinkedIn page. Bhatt says he doesnt know Patel and attempted to remove his endorsement after being contacted by Science. Gruber says he overlapped with Patel at the University of Utah about a decade ago, but doesnt know his work in detail.

In contrast, Mehraauthor of more than 200 scholarly articles, editor ofThe Journal of Heart and Lung Transplantation, and head of the cardiology division of theUniversity of Maryland before moving to BWH in 2012enjoys considerable support even after the unraveling of the recent studies. Obviously, you dont rise to the position hes risen to without being ambitious, but Ive never had any indication whatsoever that he would do anything unethical, says Keith Aaronson, a cardiologist at the University of Michigan, Ann Arbor, who collaborated with Mehra on several studies, including a clinical trial of a mechanical pump for heart failure patients.

Mehra, the first author on both retracted papers, was the only one to issue a personal statement of apology, for failing to ensure that the data source was appropriate for this use. BWH and Harvard declined to say whether further investigation of Mehras roles in the papers would occur. (Mehra has written papers recently with another co-author of the Lancet paper, Frank Ruschitzka of University Hospital Zrich.)

I think he just fell into thisperhaps a little navely, says another former collaborator, cardiothoracic surgeon Daniel Goldstein of the Albert Einstein College of Medicine. Given the amount of data that was in the [Surgisphere] database, its just hard to believe someone would [fabricate] something like this.

Kassirer offers a harsher view: If youre a scientist and youre going to sign on to a project, by God you should know what the data are.

With reporting by Kelly Servick and John Travis.

This story was supported by theScienceFund for Investigative Reporting.

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Who's to blame? These three scientists are at the heart of the Surgisphere COVID-19 scandal - Science Magazine

Stem Cell Therapy Market Size, Share 2020 Globally Industry Demand, Trends, Regional Overview, Top Manufacture, Business Growth and Forecast to 2025 -…

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Stem Cell Therapy market research report delivers a close watch on leading competitors with strategic analysis, micro and macro market trend and scenarios, pricing analysis and a holistic overview of the market situations in the forecast period. It is a professional and a detailed report focusing on primary and secondary drivers, market share, leading segments and geographical analysis. Further, key players, major collaborations, merger & acquisitions along with trending innovation and business policies are reviewed in the report. The report contains basic, secondary and advanced information pertaining to the Stem Cell Therapy Market global status and trend, market size, share, growth, trends analysis, segment and forecasts from 2020-2025.

Read complete report with TOC at: https://www.adroitmarketresearch.com/industry-reports/stem-cell-therapy-market

The report includes a detailed segmentation study of the global Stem Cell Therapy market, where all of the segments are analyzed in terms of market growth, share, growth rate, and other vital factors. It also provides the attractiveness index of segments so that players can be informed about lucrative revenue pockets of the global Stem Cell Therapy market. The extensive evaluation of segments provided in the report will help you to direct your investments, strategies, and teams to focus on the right areas of the global Stem Cell Therapy market.

Global Stem Cell Therapy market is segmented based by type, application and region.

Based on Type, the market has been segmented into:

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

Adipose Tissue-Derived Mesenchymal SCsBone Marrow-Derived Mesenchymal SCsEmbryonic SCsOther Sources

Based on application, the market has been segmented into:

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

Musculoskeletal DisordersWounds & InjuriesCardiovascular DiseasesGastrointestinal DiseasesImmune System DiseasesOther Applications

Geographically, global Stem Cell Therapy market is segmented into five major regions including North America, Europe, Asia Pacific, Latin America and Middle East & Africa region. Among these regions, North America has been the dominating region the global Stem Cell Therapy market with highest percentage share. Further, North America region is expected to witness a robust growth during the forecast period. Moreover, Asia Pacific region is anticipated to be fastest growing market for Stem Cell Therapy during the forecast period.

Finally, researchers throw light on the pinpoint analysis of Global Stem Cell Therapy market dynamics. It also measures the sustainable trends and platforms which are the basic roots behind the market growth. The degree of competition is also measured in the research report. With the help of SWOT and Porters five analysis, the market has been deeply analyzed. It also helps to address the risk and challenges in front of the businesses. Furthermore, it offers extensive research on sales approaches.

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Stem Cell Therapy Market Size, Share 2020 Globally Industry Demand, Trends, Regional Overview, Top Manufacture, Business Growth and Forecast to 2025 -...

Using big data approaches to develop cell therapies – Drug Target Review

An area where stem cell biology and medicine are combining effectively is the establishment of new cell therapies. However, current therapies are limited to a narrow set of cell types that can be isolated or created and expanded in vitro. Dr Owen Rackham discusses how utilising computational approaches will further enhance applications of stem-cell-derived therapies in the future.

For decades (or perhaps centuries) the approach in cell biology has remained relatively unchanged. We isolate cells and with our confined knowledge of their endogenous conditions, begin to experiment until we can sustain them in vitro. Once established, we can conduct further investigation to assess a cells response to different conditions, changes over time or response to manipulation. This is especially true of stem cell biology, established from tireless efforts to incrementally improve culture conditions or differentiation protocols based on fragmented knowledge of developmental processes. Despite this, the promise of stem-cell therapies is already being realised in the clinic, but the breadth of cell types being used is still relatively narrow. Recent technological advances in the field have been focused on the safe and scalable manufacture of therapies. While these are revolutionary breakthroughs, the applications are largely limited to T cells, haematopoietic- and pluripotent-stem cells (HSCs and PSCs), a small fraction in the grand heterogeneity of cell types. Consequently, the lack of cell source diversity prevents cell therapy from fulfilling its clinical potential, pointing to the need for new means to isolate or generate source cells.

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Using big data approaches to develop cell therapies - Drug Target Review

Stem cell treatment during COVID-19? This story will give your tear ducts a workout – Sydney Morning Herald

TUESDAY

Foreign Correspondent: Pirates of the Caribbean ABC, 8pmPirates, we generally assume, are a thing of the past, and when they rear their heads in the modern era it's disappointing just how far from the romantic cliches of the Spanish Main they are just look at Captain Phillips. This report from Foreign Correspondent's Andy Park reveals dark doings in the gorgeous surrounds of Trinidad and Tobago, where the waters once fictionally plied by impish rogues like Jack Sparrow are terrorised by brutal criminals.

Kidnapping, robbery, murder: it's all here, and it's all deeply disturbing. The episode was shot during the islands' festival of Carnival, well-planned to showcase the juxtaposition of party atmosphere and high-seas marauding. Although even the party part is calculated to freak a newcomer out a little.

Doctor and TV presenter Andrew Rochford, influencer Ellie Gonsalves, comedian Ciaran Lyons, restaurateur Pauline Nguyen, and Melbourne's deputy lord mayor, Arron Wood, appear in this season of Filthy Rich and Homeless. Credit:SBS

Filthy Rich & HomelessSBS, 8.30pmFive prominent Australians swap their privileged lifestyles for 10 days sleeping rough on the streets. The premise feels like an uneasy mixture of reality-show stunt and earnest social-issues documentary, a concept that can easily slip into poverty porn. The question mark over the celeb-driven approach to social justice hangs heavy here: it's easy for the likes of Dr Andrew Rochford and Ellie Gonsalves to forsake all their worldly goods for a week and a half, knowing full well they're getting it all back.

Filthy Rich and Homeless never quite shakes off a feeling of self-consciously performative compassion, but that's not to say there's nothing of value here. Indira Naidoo was a wise choice for host, her credentials both journalistic and charitable impeccable, and the gravitas she brings vital. There's also no doubting the sincerity of the temporarily homeless five, who are genuine, committed, and clearly moved by what they observe on the streets.

At its best, it shakes off its gimmicky origins to bring poignant insight to the plight of Australia's homeless: at its worst it feels like homelessness tourism, not so much cutting off the participants' privilege as highlighting it. Whether the show achieves its stated purpose to drive change by shining a light and putting a human face on a growing crisis remains to be seen.

This week on Dateline, Michael shares his story about receiving treatment for MS during COVID-19 shutdowns.Credit:SBS

DatelineSBS, 9.30pm Things are tough all over in the season of COVID-19, but it's also provided new opportunities, not least for current affairs TV producers hungry for unique stories. In Melbourne, a suburban dad, diagnosed with multiple sclerosis, is due to fly to Russia to undergo stem cell treatment when the pandemic throws a spanner in the works. At the same time, in Russia, another Australian who has just had the treatment is due to fly home, when the world suddenly starts locking down.

The difficulties of getting to where they need to be combine with the fact that the treatment compromises their immune system while a deadly virus is running rampant across the world. It's a hell of a pickle to find oneself in, and there is a high likelihood your tear ducts will get a workout if you give it a squiz. The stories are compelling, by turns inspiring and heartbreaking, and the sober, anti-sensationalist telling of them only serves to heighten the emotions involved. Not for anyone looking to relax on a Tuesday night.

WEDNESDAY

The Weekly with Charlie Pickering ABC, 8.30pmCharlie Pickering is the smooth, handsome, articulate face of topical comedy in this country or at least a reasonable stand-in between series of Mad as Hell. With a crack team of comedic correspondents including Tom Gleeson, Judith Lucy and Luke McGregor, it's the kind of reasonably amusing news-gaggery that gives the ABC's left-leaning audience a chuckle and a feeling of superiority while never risking making anyone uncomfortable. It's satire at its safest, but at a time like this that's a blessing not to be sneezed at.

Family Guy7Mate, 9pmThere are those who scoff at the comedic stylings of Seth MacFarlane, and refuse to recognise his towering genius, but there's no need to worry about them, because he's got one show currently in its 19th season and another in its 15th and is presumably richer than God. The former is his original opus, Family Guy, and it's as good as ever. In fact it's much better than in its first few seasons, if perhaps not quite at the heights of three or four years back.

It remains a relentless blitz of pop-culture references, wilful surrealism and delightfully bad taste, and is so clever and so silly in equal measure that it achieves a kind of lunatic brilliance. This is one of the notorious "Meg episodes", in which the Griffin family's long-suffering daughter is wrongly presumed dead, giving her a shot at a new life. This means plenty of time showcasing the vocal talents of Mila Kunis, an impressive actress even when you can't see her ridiculously perfect face.

THURSDAY

Tin Star SBS, 11.05pmThe amazing thing about the western is that a genre of film and TV based on a narrow band of about 30 years of American history came to dominate the cultural landscape, and even today, creatives can't stop finding new ways to adapt, subvert and update the form. And so to Tin Star, a modern western saga set in the Canadian Rockies, where Tim Roth's British ex-detective brings his family for a peaceful life, only to find like so many western heroes before him that it's up to him to clean up this stinking town. Violence, betrayal, murder and moral murk naturally follow: the second season begins with blood on the snow and things aren't going to lighten up any time soon.

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FRIDAY

BaptisteABC, 8.30pmTcheky Karyo's Julien Baptiste, the battered but unbowed French police detective at the centre of missing child anthology series The Missing, gets his own spin-off courtesy of prolific thriller creators Harry and Jack Williams. Claiming to have changed after a health scare, Baptiste is seconded to a missing person's investigation in Amsterdam, where the supporting cast of the European mystery includes the reliably unsettling Tom Hollander. As Friday night crime fare on the ABC goes, this is decidedly darker than normal. Death in Paradise never had near this much dismemberment.

The Graham Norton ShowTen, 8.30pmZoom meeting chat shows are a dicey proposition and it's fair to say that one host who's suffering from lockdown restrictions is Britain's reigning talk and tease champ Graham Norton. While he can expertly draw out amusing isolation details from his famous guests the lack of group interaction on the studio couch inhibits Norton's usual dynamic. This pre-lockdown highlights show with the likes of Robert Downey Jr., Margot Robbie and Michael B. Jordan is a reminder of what Norton would like to get back to. It's a greatest hits package and a reminder of how he makes such a contrived format enjoyable viewing.

This week, we're down to the top 10 on MasterChef. Pictured here are judges Jock Zonfrillo, Melissa Leong and Andy Allen.Credit:Network 10

SATURDAY

Alaska: The Last Frontier9Rush, 9pmIf you can endure the overblown narrative and the jingoistic theme song, then there's at least a facsimile of farming life in Alaska to enjoy in this typically American frontier reality series. Situated 300 kilometres south of Anchorage, the Kilcher clan are cattle farmers whose herd are at regular risk from damning winters and hungry bears. There are genuine challenges to be surmounted, which means that the producers don't have to invent so many storylines. And even photographed quickly on the cheap, the vast and rugged landscape fills the screen nicely.

MasterChefTen, 7.30pmThe social distancing age has caught up with MasterChef, with gloves, individual dishes, and no more rubbing shoulders the new norm in the reality show kitchen. Given that the show already survived Katy Perry's freeform guest judging appearance, they should be fine. And emotionally at least, the rejigged series continues to lean in, with a connection between the new judges, the veteran contestants, and the heritage-laden food they make that has proven to be nourishing even if the complexity of the dishes executed is high. With the top 10 now locked in, a street food challenge sets the tone for this episode. Let the tastiness continue.

Craig Mathieson is a TV, film and music writer for The Age and The Sydney Morning Herald.

Excerpt from:

Stem cell treatment during COVID-19? This story will give your tear ducts a workout - Sydney Morning Herald

Stem Cell Therapy Market 2019 Break Down by Top Companies, Countries, Applications, Challenges, Trends, Opportunities and Forecast 2026 – Cole of Duty

A new market report by Verified Market Research on the Stem Cell Therapy Market has been released with reliable information and accurate forecasts for a better understanding of the current and future market scenarios. The report offers an in-depth analysis of the global market, including qualitative and quantitative insights, historical data, and estimated projections about the market size and share in the forecast period. The forecasts mentioned in the report have been acquired by using proven research assumptions and methodologies. Hence, this research study serves as an important depository of the information for every market landscape. The report is segmented on the basis of types, end-users, applications, and regional markets.

The research study includes the latest updates about the COVID-19 impact on the Stem Cell Therapy sector. The outbreak has broadly influenced the global economic landscape. The report contains a complete breakdown of the current situation in the ever-evolving business sector and estimates the aftereffects of the outbreak on the overall economy.

Get Sample Copy with TOC of the Report to understand the structure of the complete report @ https://www.verifiedmarketresearch.com/download-sample/?rid=24113&utm_source=COD&utm_medium=007

The report also emphasizes the initiatives undertaken by the companies operating in the market including product innovation, product launches, and technological development to help their organization offer more effective products in the market. It also studies notable business events, including corporate deals, mergers and acquisitions, joint ventures, partnerships, product launches, and brand promotions.

Leading Stem Cell Therapy manufacturers/companies operating at both regional and global levels:

The report also inspects the financial standing of the leading companies, which includes gross profit, revenue generation, sales volume, sales revenue, manufacturing cost, individual growth rate, and other financial ratios.

The report also focuses on the global industry trends, development patterns of industries, governing factors, growth rate, and competitive analysis of the market, growth opportunities, challenges, investment strategies, and forecasts till 2026. The Stem Cell Therapy Market was estimated at USD XX Million/Billion in 2016 and is estimated to reach USD XX Million/Billion by 2026, expanding at a rate of XX% over the forecast period. To calculate the market size, the report provides a thorough analysis of the market by accumulating, studying, and synthesizing primary and secondary data from multiple sources.

To get Incredible Discounts on this Premium Report, Click Here @ https://www.verifiedmarketresearch.com/ask-for-discount/?rid=24113&utm_source=COD&utm_medium=007

The market is predicted to witness significant growth over the forecast period, owing to the growing consumer awareness about the benefits of Stem Cell Therapy. The increase in disposable income across the key geographies has also impacted the market positively. Moreover, factors like urbanization, high population growth, and a growing middle-class population with higher disposable income are also forecasted to drive market growth.

According to the research report, one of the key challenges that might hinder the market growth is the presence of counter fit products. The market is witnessing the entry of a surging number of alternative products that use inferior ingredients.

Key factors influencing market growth:

Reasons for purchasing this Report from Verified Market Research

Customized Research Report Using Corporate Email Id @ https://www.verifiedmarketresearch.com/product/Stem-Cell-Therapy-Market/?utm_source=COD&utm_medium=007

Customization of the Report:

Verified Market Research also provides customization options to tailor the reports as per client requirements. This report can be personalized to cater to your research needs. Feel free to get in touch with our sales team, who will ensure that you get a report as per your needs.

Thank you for reading this article. You can also get chapter-wise sections or region-wise report coverage for North America, Europe, Asia Pacific, Latin America, and Middle East & Africa.

To summarize, the Stem Cell Therapy market report studies the contemporary market to forecast the growth prospects, challenges, opportunities, risks, threats, and the trends observed in the market that can either propel or curtail the growth rate of the industry. The market factors impacting the global sector also include provincial trade policies, international trade disputes, entry barriers, and other regulatory restrictions.

About us:

Verified Market Research is a leading Global Research and Consulting firm servicing over 5000+ customers. Verified Market Research provides advanced analytical research solutions while offering information enriched research studies. We offer insight into strategic and growth analyses, Data necessary to achieve corporate goals and critical revenue decisions.

Our 250 Analysts and SMEs offer a high level of expertise in data collection and governance use industrial techniques to collect and analyse data on more than 15,000 high impact and niche markets. Our analysts are trained to combine modern data collection techniques, superior research methodology, expertise and years of collective experience to produce informative and accurate research.

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Stem Cell Therapy Market 2019 Break Down by Top Companies, Countries, Applications, Challenges, Trends, Opportunities and Forecast 2026 - Cole of Duty

KOCO 5’s Zach Rael heading to California to help cousin with rare form of blood cancer – KOCO Oklahoma City

KOCO 5 reporter and anchor Zach Rael is heading to California to help his cousin in a battle against a rare form of blood cancer called myelofibrosis.Raels cousin reached out to him about eight months ago for him for help, saying her brother had been diagnosed with myelofibrosis. Rael said his cousin is doing well and there is an up-and-coming treatment that requires a healthy person to donate their stem cells from their blood.Ideally, the donor is a family member because there is a high chance of a match and a positive result, Rael posted on social media.Tests revealed that many family members were not suitable donors, so the family reached out to Rael and others with the hopes that someone would be a match. Rael submitted his DNA and, a few weeks later, learned he was a match.Rael took a flight Tuesday to California, where he will be for the next 10 days as part of the donation process.Over the next few days, I will be documenting my experience, he wrote. I plan on posting daily updates on my social media accounts and will be putting together a special story for air on KOCO when Im done.You can read Raels full story below:Hello everyone! I hope you are doing well on this Tuesday. Im writing this while on board an airplane somewhere over Arizona, on my way to Los Angeles, California. This is my first time flying post-pandemic. Besides the face masks - its been relatively normal.Unfortunately, this is not a vacation or a trip for fun.About 8 months ago my cousin Kathy (2nd cousin on my moms side) reached out to me asking for help. Her brother, my cousin Don, is battling Myelofibrosis, a rare form of blood cancer. While any type of cancer is scary, he is doing as well as he can and luckily there is an up and coming treatment used to treat it. The treatment essentially requires a healthy person to donate their stem cells from their blood to the person with cancer (Ill explain more on that later). Ideally, the donor is a family member because there is a high chance of a match and a positive result.Don and Kathy had already asked all their extended family to submit their DNA, but to no luck. No one came back as a suitable donor. So, they opened the search to extended family and I happily agreed to submit my DNA. Basically, I got a tube in the mail and was asked to spit in it. A few weeks later and I got a call from my cousins that I came back as a match to submit my stem cells to my cousin Don!Truth be told, before all of this, I was not very close with this side of my family. As it happens with extended family - we would only see each other at special family events like weddings, graduations, or funerals. So, I was a little surprised that I came back as a match. But I could not be more thrilled I did! This will be the best possible shot of giving cousin Don a chance to beat this thing!Flash forward to today. Ill be in California for the next 10 days as part of the donation process.A quick breakdown of what is to come: once I land, I will be going straight to City of Hope, the hospital system that is performing the donation and treating Don. They will be running some final tests on me this afternoon, including taking 20 of my vitals (Im told this is normal). Later this week I will have to take a COVID-19 test, an information class, and receive a few dosages of special shots. Ill be taking these shots once a day for 5 days before the donation. They help generate my stem cells so they are more easily extracted. One week from today will be my actual donation. It is a 6-8 hour process where I will be hooked up to a machine. They will take my blood from one arm, run it through a machine, and put my blood back in me through my other arm. Im told its just like giving blood.Over the next few days I will be documenting my experience (see the pic with all my equipment). I plan on posting daily updates on my social media accounts and will be putting together a special story for air on KOCO when Im done. My bosses at KOCO have been so understanding and willing to do what they can so I was able to come out to California for nearly two weeks. Im so thankful.Anyway this post is getting long. I hope you follow along and I hope to shed some light on what it is like to become a stem cell donor. There is a HUGE need for them.Talk soon. Cheers!-Zach

KOCO 5 reporter and anchor Zach Rael is heading to California to help his cousin in a battle against a rare form of blood cancer called myelofibrosis.

Raels cousin reached out to him about eight months ago for him for help, saying her brother had been diagnosed with myelofibrosis. Rael said his cousin is doing well and there is an up-and-coming treatment that requires a healthy person to donate their stem cells from their blood.

Ideally, the donor is a family member because there is a high chance of a match and a positive result, Rael posted on social media.

Tests revealed that many family members were not suitable donors, so the family reached out to Rael and others with the hopes that someone would be a match. Rael submitted his DNA and, a few weeks later, learned he was a match.

Rael took a flight Tuesday to California, where he will be for the next 10 days as part of the donation process.

Over the next few days, I will be documenting my experience, he wrote. I plan on posting daily updates on my social media accounts and will be putting together a special story for air on KOCO when Im done.

You can read Raels full story below:

Hello everyone! I hope you are doing well on this Tuesday. Im writing this while on board an airplane somewhere over Arizona, on my way to Los Angeles, California. This is my first time flying post-pandemic. Besides the face masks - its been relatively normal.

Unfortunately, this is not a vacation or a trip for fun.

About 8 months ago my cousin Kathy (2nd cousin on my moms side) reached out to me asking for help. Her brother, my cousin Don, is battling Myelofibrosis, a rare form of blood cancer. While any type of cancer is scary, he is doing as well as he can and luckily there is an up and coming treatment used to treat it. The treatment essentially requires a healthy person to donate their stem cells from their blood to the person with cancer (Ill explain more on that later). Ideally, the donor is a family member because there is a high chance of a match and a positive result.

Don and Kathy had already asked all their extended family to submit their DNA, but to no luck. No one came back as a suitable donor. So, they opened the search to extended family and I happily agreed to submit my DNA. Basically, I got a tube in the mail and was asked to spit in it. A few weeks later and I got a call from my cousins that I came back as a match to submit my stem cells to my cousin Don!

Truth be told, before all of this, I was not very close with this side of my family. As it happens with extended family - we would only see each other at special family events like weddings, graduations, or funerals. So, I was a little surprised that I came back as a match. But I could not be more thrilled I did! This will be the best possible shot of giving cousin Don a chance to beat this thing!

Flash forward to today. Ill be in California for the next 10 days as part of the donation process.

A quick breakdown of what is to come: once I land, I will be going straight to City of Hope, the hospital system that is performing the donation and treating Don. They will be running some final tests on me this afternoon, including taking 20 of my vitals (Im told this is normal). Later this week I will have to take a COVID-19 test, an information class, and receive a few dosages of special shots. Ill be taking these shots once a day for 5 days before the donation. They help generate my stem cells so they are more easily extracted. One week from today will be my actual donation. It is a 6-8 hour process where I will be hooked up to a machine. They will take my blood from one arm, run it through a machine, and put my blood back in me through my other arm. Im told its just like giving blood.

Over the next few days I will be documenting my experience (see the pic with all my equipment). I plan on posting daily updates on my social media accounts and will be putting together a special story for air on KOCO when Im done. My bosses at KOCO have been so understanding and willing to do what they can so I was able to come out to California for nearly two weeks. Im so thankful.

Anyway this post is getting long. I hope you follow along and I hope to shed some light on what it is like to become a stem cell donor. There is a HUGE need for them.

Talk soon. Cheers!

-Zach

Here is the original post:

KOCO 5's Zach Rael heading to California to help cousin with rare form of blood cancer - KOCO Oklahoma City

Adipose Tissue-derived Stem Cell Therapy Market 2020 | by Manufacturers | by Countries | by Types and by Applications | by Forecasts to 2026 – Farmers…

The Adipose Tissue-derived Stem Cell Therapy Market report we provide to our readers contains comprehensive data on a specific product/service, available in this industry. We want to perform in-depth analysis, to obtain a comprehensive understanding of the Adipose Tissue-derived Stem Cell Therapy Market. It starts off by going to the basics of the product/service, which is to take a look at the industry definition. The Adipose Tissue-derived Stem Cell Therapy Market report identifies and analyzes the factors which contribute and hamper the growth of this line of business. At the same time, we identify the current value of the Adipose Tissue-derived Stem Cell Therapy Market, with the estimated financial worth, at the end of the forecast period, 2020-2026.

One metric we use to understand the potential growth of the Adipose Tissue-derived Stem Cell Therapy Market is to calculate the CAGR. It helps provide accurate data, improving the quality of the data collected for this report. We make sure to analyze all the information available in this document, to ensure it meets our standards. In this report, the reader will learn which elements are responsible for creating demand for the product/service under observation. At the same time, the reader will also get to know about product/service types that boost the popularity of this industry.

The key players covered in this study > AlloCure, Antria, Celgene Corporation, Cellleris, Corestem, Cytori Therapeutics, Intrexon, Mesoblast, Pluristem Therapeutics, Tissue Genesis, BioRestorative Therapies, Celltex Therapeutics Corporation, iXCells Biotechnologies, Pluristem Therapeutics, Cyagen, Lonza.

The final report will add the analysis of the Impact of Covid-19 in this report Adipose Tissue-derived Stem Cell Therapy industry.

Get a Sample Copy @ https://www.reportsandmarkets.com/sample-request/covid-19-impact-on-global-adipose-tissue-derived-stem-cell-therapy-market-size-status-and-forecast-2020-2026-one

Market Segmentation

For the purpose of making the information available on Adipose Tissue-derived Stem Cell Therapy Market comprehensive, we segmented the industry. The reason is that it helps our readers learn in-depth about this line of business. The segmentation of the Adipose Tissue-derived Stem Cell Therapy Market is as follows distribution channel, product type, region, and application. When it comes to application, it deals with end-users, who are responsible for generating demand for the product/service. Product type refers to the different variants available in the Adipose Tissue-derived Stem Cell Therapy Market. We use distribution channel, to understand the various sources companies use to supply the product/service to the consumers.

Regional Overview

In the regional overview portion, the Adipose Tissue-derived Stem Cell Therapy Market report has data from countries all over the world. Each region is responsible for contributing to the growth of this industry. From the available data, we will identify which area has the largest share of the market. At the same time, we will compare this data to other regions, to understand the demand in other countries. North and South America, Asia Pacific, Middle East and Africa, and Europe are the areas of interest in this Adipose Tissue-derived Stem Cell Therapy Market report.

Table Of Content

1 Report Overview

2 Global Growth Trends

3 Market Share by Key Players

4 Breakdown Data by Type and Application

5 North America

6 Europe

7 China

8 Japan

9 Southeast Asia

10 India

11 Central & South America

12 International Players Profiles

13 Market Forecast 2020-2026

14 Analysts Viewpoints/Conclusions

15 Appendix

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Latest Industry News

We will cover government policies, which favor or go against the Adipose Tissue-derived Stem Cell Therapy Market, as we believe this can change the level of growth. At the same time, technological advancements which have the power to influence the growth will appear in the latest industry news.

Any special requirements about this report, please let us know and we can provide custom report.

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Adipose Tissue-derived Stem Cell Therapy Market 2020 | by Manufacturers | by Countries | by Types and by Applications | by Forecasts to 2026 - Farmers...

Stem Cell And Platelet Rich Plasma (PRP) Alopecia Therapies Market 2019 Break Down by Top Companies, Countries, Applications, Challenges,…

A new market report by Market Research Intellect on the Stem Cell And Platelet Rich Plasma (PRP) Alopecia Therapies Market has been released with reliable information and accurate forecasts for a better understanding of the current and future market scenarios. The report offers an in-depth analysis of the global market, including qualitative and quantitative insights, historical data, and estimated projections about the market size and share in the forecast period. The forecasts mentioned in the report have been acquired by using proven research assumptions and methodologies. Hence, this research study serves as an important depository of the information for every market landscape. The report is segmented on the basis of types, end-users, applications, and regional markets.

The research study includes the latest updates about the COVID-19 impact on the Stem Cell And Platelet Rich Plasma (PRP) Alopecia Therapies sector. The outbreak has broadly influenced the global economic landscape. The report contains a complete breakdown of the current situation in the ever-evolving business sector and estimates the aftereffects of the outbreak on the overall economy.

Get Sample Copy with TOC of the Report to understand the structure of the complete report @ https://www.marketresearchintellect.com/download-sample/?rid=174132&utm_source=COD&utm_medium=888

The report also emphasizes the initiatives undertaken by the companies operating in the market including product innovation, product launches, and technological development to help their organization offer more effective products in the market. It also studies notable business events, including corporate deals, mergers and acquisitions, joint ventures, partnerships, product launches, and brand promotions.

Leading Stem Cell And Platelet Rich Plasma (PRP) Alopecia Therapies manufacturers/companies operating at both regional and global levels:

Sales and sales broken down by Product:

Sales and sales divided by Applications:

The report also inspects the financial standing of the leading companies, which includes gross profit, revenue generation, sales volume, sales revenue, manufacturing cost, individual growth rate, and other financial ratios.

The report also focuses on the global industry trends, development patterns of industries, governing factors, growth rate, and competitive analysis of the market, growth opportunities, challenges, investment strategies, and forecasts till 2026. The Stem Cell And Platelet Rich Plasma (PRP) Alopecia Therapies Market was estimated at USD XX Million/Billion in 2016 and is estimated to reach USD XX Million/Billion by 2026, expanding at a rate of XX% over the forecast period. To calculate the market size, the report provides a thorough analysis of the market by accumulating, studying, and synthesizing primary and secondary data from multiple sources.

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The market is predicted to witness significant growth over the forecast period, owing to the growing consumer awareness about the benefits of Stem Cell And Platelet Rich Plasma (PRP) Alopecia Therapies. The increase in disposable income across the key geographies has also impacted the market positively. Moreover, factors like urbanization, high population growth, and a growing middle-class population with higher disposable income are also forecasted to drive market growth.

According to the research report, one of the key challenges that might hinder the market growth is the presence of counter fit products. The market is witnessing the entry of a surging number of alternative products that use inferior ingredients.

Key factors influencing market growth:

Reasons for purchasing this Report from Market Research Intellect

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To summarize, the Stem Cell And Platelet Rich Plasma (PRP) Alopecia Therapies market report studies the contemporary market to forecast the growth prospects, challenges, opportunities, risks, threats, and the trends observed in the market that can either propel or curtail the growth rate of the industry. The market factors impacting the global sector also include provincial trade policies, international trade disputes, entry barriers, and other regulatory restrictions.

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Stem Cell And Platelet Rich Plasma (PRP) Alopecia Therapies Market 2019 Break Down by Top Companies, Countries, Applications, Challenges,...

Magenta Therapeutics to Participate in Upcoming Healthcare Investor Conferences – Business Wire

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Magenta Therapeutics (Nasdaq: MGTA), a clinical-stage biotechnology company developing novel medicines to bring the curative power of immune reset to more patients, today announced that the company will participate in a fireside chat and hold investor meetings at the 41st annual Goldman Sachs Healthcare Conference on June 11th, 2020. The Company will also hold investor meetings and participate in a panel discussion on novel approaches for gene therapy on Monday, June 15th at the Raymond James Human Health Innovation Conference.

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

About Magenta Therapeutics

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

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

Follow Magenta on Twitter: @magentatx.

Forward-Looking Statement

This press release may contain forward-looking statements and information within the meaning of The Private Securities Litigation Reform Act of 1995 and other federal securities laws. The use of words such as may, will, could, should, expects, intends, plans, anticipates, believes, estimates, predicts, projects, seeks, endeavor, potential, continue or the negative of such words or other similar expressions can be used to identify forward-looking statements. The express or implied forward-looking statements included in this press release are only predictions and are subject to a number of risks, uncertainties and assumptions, including, without limitation risks set forth under the caption Risk Factors in Magentas Annual Report on Form 10-K filed on March 3, 2020, as updated by Magentas most recent Quarterly Report on Form 10-Q and its other filings with the Securities and Exchange Commission. In light of these risks, uncertainties and assumptions, the forward-looking events and circumstances discussed in this press release may not occur and actual results could differ materially and adversely from those anticipated or implied in the forward-looking statements. You should not rely upon forward-looking statements as predictions of future events. Although Magenta believes that the expectations reflected in the forward-looking statements are reasonable, it cannot guarantee that the future results, levels of activity, performance or events and circumstances reflected in the forward-looking statements will be achieved or occur. Moreover, except as required by law, neither Magenta nor any other person assumes responsibility for the accuracy and completeness of the forward-looking statements included in this press release. Any forward-looking statement included in this press release speaks only as of the date on which it was made. We undertake no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events or otherwise, except as required by law.

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Magenta Therapeutics to Participate in Upcoming Healthcare Investor Conferences - Business Wire

Biopharma Develops Antibody and Stem Cell Therapies in the Fight Against COVID-19 – JD Supra

Updated: May 25, 2018:

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Biopharma Develops Antibody and Stem Cell Therapies in the Fight Against COVID-19 - JD Supra

This startup aims to treat coronavirus using stem cell research – YourStory

In its fourth week now, C-CAMPs Covid Innovation Deployment Accelerator (C-CIDA) continues to select top startups across India innovating to fight the coronavirus pandemic. It has managed to select and showcase 30 startups in 30 days that are solving gaps and needs across screening, monitoring, and diagnostics.

Several of these are usingstem cell research. One of them is Bengaluru-based cell therapy startup Eyestem. Founded by Jogin Desai, Rajani Battu, and Dhruv Sareen, the startup aims to develop scalable cell replacement therapies for the world.

Hence, Eyestem believes that the easiest way forward is to repurpose existing drugs and has built an Anti-Covid screening (ACS) platform, which aims to provide the research community with a resource to determine the efficacy of a drug or a vaccine using the closest human host cell population.

Led by Rajarshi Pal, Chief Scientist of Eyestem, the startup had been working on lung cells for a couple of years now, publishing papers on the same. However, in the last three months, it pivoted to build this platform specifically to fight the coronavirus pandemic.

Now, it is ready to partner with other labs and companies to grow SARS-CoV-2 virus in these lung cells and start testing these drugs.

He claims that the startup has already collaborated with two players, and is also expecting to start working with facilities in the US soon.

How has the coronavirus outbreak disrupted your life? And how are you dealing with it? Write to us or send us a video with subject line 'Coronavirus Disruption' to editorial@yourstory.com

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This startup aims to treat coronavirus using stem cell research - YourStory

Cellular Biomedicine Group to Report First Quarter 2020 Results on May 6, 2020 – Olean Times Herald

NEW YORK and SHANGHAI, May 1, 2020 /PRNewswire/ --Cellular Biomedicine Group Inc. (NASDAQ: CBMG) ("CBMG" or the "Company"), a biopharmaceutical firm engaged in the drug development of immunotherapies for cancer and stem cell therapies for degenerative diseases, today announced that it will release its financial results for the first quarter ended March 31, 2020 after the market closes on Wednesday, May 6, 2020.

The Company will host a conference call and webcast with the investment community on Wednesday, May 6th at 5:00 p.m. Eastern Time, featuring remarks by Tony Liu, CEO, CFO and Executive Director of CBMG.

What:

Cellular Biomedicine Group First Quarter 2020 Results Conference Call

Date:

Wednesday, May 6, 2020

Time:

5:00 p.m. Eastern Time

Live Call:

Toll-Free: +1-833-423-0438

International: +1-918-922-6623

China: +86 800-870-0169 or +86 400-682-8609

Conference ID: 7690079

Webcast:

https://edge.media-server.com/mmc/p/wwg78hh5

Replay:

Toll-Free: (855) 859-2056

International: (404) 537-3406

Conference ID: 7690079

(Available approximately two hours after the completion of the live call until 8:00 p.m. ET on May 20, 2020)

About Cellular Biomedicine Group, Inc.Cellular Biomedicine Group, Inc. (NASDAQ: CBMG) develops proprietary cell therapies for the treatment of cancer and degenerative diseases. It conducts immuno-oncology and stem cell clinical trials in China using products from its integrated GMP laboratory. The Company's GMP facilities in China, consisting of twelve independent cell production lines, are designed and managed according to both China and U.S. GMP standards. Its Shanghai facility includes a "Joint Laboratory of Cell Therapy" with GE Healthcare and a "Joint Cell Therapy Technology Innovation and Application Center" with Thermo Fisher Scientific, which partnerships focus on improving manufacturing processes for cell therapies. CBMG currently has ongoing CAR-T Phase I clinical trials in China. The China NMPA (formerly CFDA) approved the Company's IND application for a Phase II trial for AlloJoin, CBMG's "Off-the-Shelf" allogenic haMPC therapy for the treatment of Knee Osteoarthritis (KOA), and has accepted the Company's IND application for a Phase II trial for ReJoin autologous haMPC therapy for the treatment of KOA. CBMG is included in the broad-market Russell 3000 Index and the small-cap Russell 2000 Index, and the Loncar China BioPharma index. To learn more about CBMG, please visit http://www.cellbiomedgroup.com.

Company Contact:Derrick C. LiHead of Strategy and Investor Relations, CBMGPhone: 917-717-0994Email: derrick.li@cellbiomedgroup.com

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Cellular Biomedicine Group to Report First Quarter 2020 Results on May 6, 2020 - Olean Times Herald

Dr. David C. Karli’s Opinion on Regenerative Medicine and Age Prevention | – SpaceCoastDaily.com

Aging is an inevitable process. We cannot escape or prevent getting older but what if theres a fascinating field of medicine that can manage the aging process and prolong our health and vitality and longevity as we age?

Aging is an inevitable process. We cannot escape or prevent getting older but what if theres a fascinating field of medicine that can manage the aging process and prolong our health and vitality and longevity as we age?

Keeping in mind that there may never be an approach to totally stop or reverse aging, there have been some surprising disclosures to how Regenerative Medicine can naturally heal our body without the use of any surgical procedure.

Rejuvenating Old Cells to Healthy ones

The paces, stresses, and complexities in life drive us to age prematurely thereby breaking down our cells. Cell breakdown may lead to several health conditions like cancer, heart disease, Alzheimers and others.

Driving our bodies to age quickly, cell-breakdown is host to many age-related diseases, causing more than 100,000 deaths per day.

Dr David C Karli is an Ivy-trained physician, specialized in treating athletic injuries by inducing regenerative medicine and stem cell therapy in treatments.

He accepts the fact that patients can increase an additional 30 years of life by using Regenerative Medicine. One such innovation uses stem cells, however, there are issues with these cells.

They may not replace the original, diseased cells rapidly enough, or they may start to replicate uncontrollably, bringing about malignant growth.

Yet, Regenerative Medicine definitely guarantees the complete curing of a wide range of diseases, and ideally, slowing down the aging process too.

Stem Cell Therapy Programs with Promising Results

With solid funding and rapid advancements, one stem cell therapy that promises great outcomes is transfusions. In this therapy, stem cells are extracted from the patient and grown in cell culture to increase the number of cells. Following this, those cells are injected back into the patients body.

Dr. Karlis keen interest in Transfusions led him to create biologic products that can cause an age-related decline in a persons strength, endurance, and various other physical abilities.

At his biotech firm, Greyledge Technologies, biologic products are prepared by processing materials (blood or bone marrow) and implanting them into the human body to replicate the diseased tissues.

With an FDA-registered laboratory environment, the outcomes are promising and are an anti-aging protocol.

Telomeres may be the next-gen solution for Anti Aging

Telomeres are essential parts of our DNA that are connected to the premature aging cells. Situated at the end caps of our DNA strands, the information within Telomeres is lost while DNA replicates to the extent that they stop replicating.

If DNA replicates without losing information, scientists believe that Telomeres can significantly help to slow down the aging process.

Similar is the case with Metformin, a pharmaceutical reagent that improves wound healing. Proven to counteract aging, Metformin is now being tested for its unique ability to mimic calorie restriction.

Anti-Aging Through Regeneration

Utilizing induced tissue regeneration, this technology is a new approach to anti-aging treatment. Combining telomerase therapy and induced tissue regeneration, anti-aging through regeneration includes the study of the impact on age-related diseases like diabetes, metabolic disorders, cardiovascular disease, and others.

This technique focuses on the cells that are generated in our body during youth. As we age, these cells are lost and lead to a metabolic imbalance.

Scientists and Researchers are trying to find a way in which these cells can be restored to reverse the signs of aging and create a balance.

Humans have the ability to regenerate damaged and diseased tissues. However, this only happens during the first few weeks of development. With the help of Artificial Intelligence, scientists are trying to unlock this potential ability in humans.

The Future of Anti-Aging

With several breakthroughs on the horizon, cure-all promises and best outcomes, these anti-aging protocols have a long way to go.

While the introduction of regenerative medicine and stem cell therapies to redefine orthopedic treatment sounds like a miracle, there are still unexplored paths that need to be taken.

With all the benefits regenerative medicine has to offer, there will always be an eye on the never-ending search for the fountain of youth.

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Dr. David C. Karli's Opinion on Regenerative Medicine and Age Prevention | - SpaceCoastDaily.com

Stem Cell Therapy Market Growth Opportunities, Challenges, Key Companies, Drivers and Forecast to 2026 Cole Reports – Cole of Duty

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Global Stem Cell Therapy Market: Competitive Landscape

This section of the report lists various major manufacturers in the market. The competitive analysis helps the reader understand the strategies and collaborations that players focus on in order to survive in the market. The reader can identify the players fingerprints by knowing the companys total sales, the companys total price, and its production by company over the 2020-2026 forecast period.

Global Stem Cell Therapy Market: Regional Analysis

The report provides a thorough assessment of the growth and other aspects of the Stem Cell Therapy market in key regions, including the United States, Canada, Italy, Russia, China, Japan, Germany, and the United Kingdom United Kingdom, South Korea, France, Taiwan, Southeast Asia, Mexico, India and Brazil, etc. The main regions covered by the report are North America, Europe, the Asia-Pacific region and Latin America.

The Stem Cell Therapy market report was prepared after various factors determining regional growth, such as the economic, environmental, technological, social and political status of the region concerned, were observed and examined. The analysts examined sales, production, and manufacturer data for each region. This section analyzes sales and volume by region for the forecast period from 2020 to 2026. These analyzes help the reader understand the potential value of investments in a particular country / region.

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The report provides an in-depth analysis of the size of the Stem Cell Therapy world market, as well as recent trends and future estimates, in order to clarify the upcoming investment pockets.

The report provides data on key growth drivers, constraints and opportunities, as well as their impact assessment on the size of the Stem Cell Therapy market.

Porters 5 Strength Rating shows how effective buyers and suppliers are in the industry.

The quantitative analysis of the Stem Cell Therapy world industry from 2020 to 2026 is provided to determine the potential of the Stem Cell Therapy market.

This Stem Cell Therapy Market Report Answers To Your Following Questions:

Who are the main global players in this Stem Cell Therapy market? What is the profile of your company, its product information, its contact details?

What was the status of the global market? What was the capacity, the production value, the cost and the profit of the market?

What are the forecasts of the global industry taking into account the capacity, the production and the value of production? How high is the cost and profit estimate? What will be the market share, supply, and consumption? What about imports and export?

What is market chain analysis by upstream raw materials and downstream industry?

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Tags: Stem Cell Therapy Market Size, Stem Cell Therapy Market Trends, Stem Cell Therapy Market Growth, Stem Cell Therapy Market Forecast, Stem Cell Therapy Market Analysis

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Stem Cell Therapy Market Growth Opportunities, Challenges, Key Companies, Drivers and Forecast to 2026 Cole Reports - Cole of Duty