Category Archives: Stem Cell Treatment


Tevogen Bio Announces Partnership With Preeminent Scientist Professor Neal Flomenberg, MD, to Investigate Proprietary T-Cell Therapy for Treatment of…

METUCHEN, N.J., Aug. 10, 2020 /PRNewswire/ --Tevogen Bio announces a joint partnership with renowned bone-marrow transplant expertNeal Flomenberg, M.D., Professor and Chair of the Department of Medical Oncology at Thomas Jefferson University, with the intent to evaluate Tevogen' s proprietary antigen-specific T cell technology as a potential treatment for COVID-19 and influenza-A patients.

This collaboration aims to harness Tevogen's proprietary immunotherapy platform and Dr. Flomenberg's expertise and research prowess to investigate potential treatments for viral infections.

Dr. Flomenberg has been at the forefront of immunogenetics and immunology for more than four decades. "Tevogen's technology resonated with me as there have been several groups who have used T cells to treat patients after bone-marrow transplants. The idea of utilizing T cell therapies to potentially treat COVID-19 and other viruses is truly remarkable," Flomenberg said. "I'm enthusiastic about moving forward with an investigation of Tevogen's technologies."

Tevogen CEO Ryan Saadi, M.D., M.P.H., is leading the new biotech's efforts. "Our work has been to pioneer T cell therapies that can be abundantly and efficiently reproduced to develop an affordable and scalable cellular treatment for the biggest global health threats, including COVID-19, influenza, and a variety of cancers. We are very excited about Dr. Flomenberg's contribution to our efforts and hope to initiate our investigational study soon."

In addition to developing its potential therapies, Tevogen is committed to organizational and manufacturing efficiency. This should allow it to engage in affordable innovation to the benefit of all patients.

About Tevogen Bio

Tevogen Bio was formed after decades of research by its contributors to concentrate and leverage their expertise, spanning multiple sectors of the health care industry, to help address some of the most common and deadly illnesses known today. The company's mission is to provide curative and preventative treatments that are affordable and scalablein order to positively impact global public health.

About Dr. Neal Flomenberg

Dr. Neal Flomenberg is the Chairman of Medical Oncology at Jefferson University in Philadelphia and also heads the Hematologic Malignancies, Blood and Marrow Transplantation (BMT) Program. Throughout his more than four decades of practice, he has maintained a longstanding interest in the immunogenetics and immunology of stem cell transplantation, with the goal of making transplantation safer and more widely available. Dr. Flomenberg developed an approach to bone-marrow transplants that uses half-matched relatives as donors, a breakthrough that assures that the majority of blood and bone-marrow cancer patients can benefit from this potentially curative treatment.

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SOURCE Tevogen Bio

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Tevogen Bio Announces Partnership With Preeminent Scientist Professor Neal Flomenberg, MD, to Investigate Proprietary T-Cell Therapy for Treatment of...

Stem Cell Alopecia Treatment Market 2020 by Manufacturers, Regions, Type and Application, Forecast to 2027 – Owned

Sanford Burnham Prebys Medical Discovery Institute

Stem Cell Alopecia Treatment Market: Competitive Landscape

This section of the report identifies various key manufacturers of the market. It helps the reader understand the strategies and collaborations that players are focusing on combat competition in the market. The comprehensive report provides a significant microscopic look at the market. The reader can identify the footprints of the manufacturers by knowing about the global revenue of manufacturers, the global price of manufacturers, and sales by manufacturers during the forecast period of 2015 to 2019.

Stem Cell Alopecia Treatment Market: Segment Analysis

The research report includes specific segments by region (country), by company, by Type and by Application. This study provides information about the sales and revenue during the historic and forecasted period of 2019 to 2027. Understanding the segments helps in identifying the importance of different factors that aid the market growth.

Global Stem Cell Alopecia Treatment Market, By Indication

Male Pattern Baldness Female Pattern Baldness Others

Stem Cell Alopecia Treatment Market: Regional Analysis

The research report includes a detailed study of regions of North America, Europe, Asia, and South America. The report has been curated after observing and studying various factors that determine regional growth such as economic, environmental, social, technological, and political status of the particular region. Analysts have studied the data of revenue, sales, and manufacturers of each region. This section analyses region-wise revenue and volume for the forecast period of 2015 to 2026. These analyses will help the reader to understand the potential worth of investment in a particular region.

North America(United States, Canada, and Mexico) Europe(Germany, France, UK, Russia, and Italy) Asia-Pacific(China, Japan, Korea, India, and Southeast Asia) South America(Brazil, Argentina, Colombia, etc.) The Middle East and Africa(Saudi Arabia, UAE, Egypt, Nigeria, and South Africa)

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Eli Lilly teams with Pieris on HER2+ tumors; Opdivo + Yervoy best chemo in mesothelioma – Endpoints News

Despite the FDA putting a partial clinical hold on its lead program only a few weeks ago, Boston-based Pieris Pharmaceuticals is plowing forward with a new collaboration.

Pieris will work with Eli Lilly to further advance studies on PRS-343, a 4-1BB/HER2 bispecific for HER2-positive tumors, in combination with the latters ramucirumab and paclitaxel for the second-line treatment of patients with HER2-positive gastric cancer in a single-arm, Phase II study.

At the time of the hold, regulators determined that the biotech could continue dosing patients already in the studies, but couldnt add patients until after it conducted an additional in-use and compatibility study of PRS-343 with various infusion materials under specific conditions to confirm suitability of PRS-343 for administration in clinical settings.

The FDA did not cite any adverse effects and the Phase II is still on track for later this year should the hold be lifted.

Under the terms of the new agreement, Eli Lilly will supply the additional compounds and collaborate on data while Pieris prepares to initiate Phase II. Max Gelman

A combination of Opdivo and Yervoy has proven more effective than chemotherapy as a first-line treatment for a form of mesothelioma in a Phase III study of 600 patients. In the study, one of numerous, Bristol Myers Squibb is running to test whether the two forms of checkpoint inhibitors can be complementary, 40.8% of patients with unresectable malignant pleural mesothelioma who received the immunotherapy cocktail survived for two years, compared with 27% of patients on the chemotherapy arm.

Just over 30% of patients in both arms of the trial experienced grade 3 or grade 4 adverse events, but patients were twice as likely to drop out as a result in the combination arm: 15%, compared with 7.4%.

Results were presented Saturday at the International Association for the Study of Lung Cancer Virtual Presidential Symposium. Jason Mast

In a Phase III trial announced Friday, patients given Hong Kong-based Xcoverys lead ALK inhibitor responded for twice as long as patients given Pfizers Xalkori. ALK-positive non-small cell lung cancer patients given Xcoverys ensartinib had a progression-free survival time of 25.8 months, compared to 12.7 months for the patients on Xalkori. The response rate was also higher for ensartinib, 75% compared to 67%.

The results are a positive sign for Xcovery but they are not necessarily surprising: Xalkori was the first ALK-inhibitor approved in 2011, but since then, other inhibitors have come out and proven far more durable. Late last year, Takedas Alunbrig showed a similar rate of progression-free survival. Jason Mast

Just a week and a half after signing a deal with Massachusetts-based Harbour BioMed to help incubate new startups, Viva Biotech has continued its march with a new acquisition.

The Chinese company a half-incubator, half-drug discovery business announced the purchase of 80% of Langhua Pharmaceutical for about $367 million. With the acquisition, Viva expects to expand its R&D capabilities and begin offering CDMO services.

We have steady confidence towards the business prospects and potential future growth of Langhua Pharmaceutical, Viva Biotech CEO Chen (Cheney) Mao said in a statement.

Viva offers both equity for service and cash for service models to US and Chinese biopharmas looking for outsourcing services. Max Gelman

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Eli Lilly teams with Pieris on HER2+ tumors; Opdivo + Yervoy best chemo in mesothelioma - Endpoints News

As it happened: Banks fuel 1.8% ASX surge to three-week high – The Sydney Morning Herald

Investors are getting their head around the fact that monetary policy is going to remain accommodating for a long, long, long time, he said.

The 104-page statement revealed downgraded estimates for Australia suggesting the economy will not be strong enough to withstand an interest rate rise until at least 2023.

Mr Miller now expects the RBA to do more easing, which would be good for domestic banks. The banks share prices increased significantly amid low trading volumes on Monday. Commonwealth Bank shares gained 3.4 per cent to $73.98, National Australia Bank shares gained 3 per cent to $17.46, taking the stock back to where it was on the last day in July. Similarly, Westpac gained 3.3 per cent to $17.36 on below-average trading volumes, and ANZ Bank gained 2.7 per cent to $18.17.

Portfolio manager at Tribeca Investment Partners Jun Bei Liu said there was some optimism in the market thanks to Victorias lower COVID-19 infection numbers. The state remains in Stage 4 lockdown but on Monday recorded 322 infections, the lowest in two weeks.

Banks were sold off on fears the recession may last longer than expected, she added. The financial sector dropped 2.7 per cent last week and has been stuck in a trading range since June.

Property trusts and travel names did very well on Monday, Ms Liu added, with Scentre Group up 3.4 per cent to $1.99 and Webjet up 4.2 per cent to $3.24.

Among the consumer staples cohort Blackmores, Woolworths, and Coles enjoyed the best gains. The vitamin-maker gained 3.1 per cent to $74.50, Woolies gained 2.8 per cent to $40.04 and Coles was up 2.6 per cent to $18.85.

News Corp gained 6.5 per cent to a nearly-six months high of $20.81 after a flurry of analyst upgrades following last weeks results.

Utilities also out-performed on Monday with APA Group up 3 per cent to $11.44, Spark Infrastructure up 3.6 per cent to $2.31, and AusNet Services up 2 per cent to $1.83.

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As it happened: Banks fuel 1.8% ASX surge to three-week high - The Sydney Morning Herald

‘Help us save our little superhero’ -parents of boy (6) with rare cancer – Independent.ie

The parents of a six-year-old boy who is battling a rare form of cancer say they want to give their superhero son "a normal childhood".

ittle Auryn Phelan, from Malahide, Co Dublin - a massive fan of the Avengers superheroes - has endured 13 rounds of chemotherapy, two major surgeries, stem cell transplants and 14 rounds of radiotherapy.

As he nears the end of his treatment in Crumlin Children's Hospital, there is little disease left.

However, stage four neuroblastoma has an extremely high relapse rate and there are few treatment options if it returns. Tragically, survival rates are low.

His parents are now fundraising to get him a place on a clinical trial in the US.

"He has been surrounded by sadness, unspeakable horrors in hospital and endured medical procedure after procedure. We just want to give Auryn back a normal, healthy childhood," said his mum Trisha Gibbons.

"Aside from all the horrible procedures, he has missed out on so much of his childhood in the last year - the simple things that people take for granted have been denied to him.

LOVABLE

"Auryn is a gorgeous, energetic, funny, lovable boy who just wants to be a child and do what children do.

"This cancer journey has impacted Auryn and our family so much and has taken such a toll on both Auryn's physical and mental wellbeing," she added.

While the country endured lockdown, Auryn has had to face his own lockdown since he was diagnosed at just four-years-old.

That means no playdates with his friends and being unable to do simple, every-day things liking going to the shop.

"Due to his compromised immune system and constant risk of infection, we were required to keep him indoors, out of school and away from other children," said Trisha.

She and her husband Barry Phelan have set themselves the task of raising 375,000 by next January to enable Auryn to take part in a vaccine trial at the Slone Kettering Memorial Hospital in New York. All funds raised will go towards his treatment.

A GoFundMe appeal online has already raised more than 60,000.

"This vaccine is not available in Ireland, so our only option is to travel overseas.

"It has had very promising phase one results and we will do everything in our power to save our wonderful boy and get Auryn this treatment."

The family have set up the Auryn's Heroes fundraising campaign and are planning a series of events in Trisha's native Co Mayo and Barry's native Co Sligo as well as in Dublin.

They are also encouraging people to sign up for the virtual Vhi Virtual Women's Mini Marathon in October and run it in aid of Auryn's Heroes.

GENEROSITY

A separate 2km virtual Children's Superhero Walk, which will see children don their favourite superhero costumes and raise money, is also planned by Auryn's Heroes in October.

"We just want to give Auryn back a normal healthy childhood and put this journey behind both him and us for good. We are incredibly grateful to the people of our home counties of Mayo and Sligo, as well as our adopted home of Dublin, and indeed the country for the support and generosity you have shown to us," said Trisha.

Full details of how to donate and fundraise can be found at aurynsheroes.ie.

Irish Independent

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'Help us save our little superhero' -parents of boy (6) with rare cancer - Independent.ie

ASX Biotechs Surfing The Covid Story – FN Arena News

By Tim Boreham, Editor, The New Criterion

The ASX biotechs surfing the COVID-19 story

Normally investors shun speculative plays in times of market uncertainties, but thats not been the case with ASX-listed life sciences stocks across the drug, diagnostics and device sectors.

Naturally, the biotechs drawing a connection with fighting or detecting the virus spurious or otherwise have seen their valuations soar. Not that investor interest is limited to the Covid cluster, with capital raisings in the sector supported across the board.

A notable winner valuation-wise is Genetic Signatures ((GSS)), which markets molecular diagnostics tests for bacterial and viral conditions including superbugs, sexually transmitted diseases and norovirus (the number one plague of cruise ships before the coronavirus hopped on board).

Sold under the Easyscreen brand, the kits allow for rapid and accurate detection in large volumes. The tests take the genetic information of the targeted organism and change the genetic sequence to reduce the number of variables.

And, yes, the company is a COVID-19 story as well. Before the plague descended, the companys Easyscreen tests had not been able to distinguish Sars-cov-2 from say, Severe Acute Respiratory Syndrome (SARS), but the company has devised a variant to do just that.

Reporting a 278% revenue surge to $4.7m for the June quarter, management called out demand for the COVID-19 tests as a growth driver.

Broker Bell Potter notes the global molecular diagnostics market was worth more than $US6bn in 2018 and is expected to grow to $US10bn by 2026.

The sectors also been a hotbed of acquisitions, such as Thermo Fishers recently-lobbed $US11.5bn offer for Dutch diagnostic group Qiagen and Danaher Corps $US4bn acquisition of US counterpart Cepheid in 2018.

We expect merger and acquisition activity to continue in the space and Genetic Signatures is strategically well positioned to attract interest as it further expands into key US and European markets and grows is product suite, Bell Potter says.

While Genetic Signatures is a case of building incremental revenues, stem cell developer Mesoblast ((MSB)) is on the cusp of company-moving announcements pertaining to several late-stage clinical trials and expected US approval of its therapy for graft versus host disease (a common affliction for transplant patients).

Naturally, most investors are focused on the COVID-19 trial which involves treating critical-care patients with its off the shelf therapy remestemcel-L (branded Ryoncil).

Most coronavirus victims die from acute respiratory distress syndrome (ARDS), an inflammatory condition caused by the immune systems response to the virus.

Mesoblast aimed to enrol 300 patients across 30 US hospitals a moving target given the disease epicentre is moving from region to region.

Nonetheless, the first patients were dosed in May, with an interim analysis is due when at least 30% of the patients have been treated for 30 days.

In other words, investors should soon know whether the company is on the cusp of a major treatment breakthrough.

And if thats not enough excitement, Mesoblast expects to announce results from two phase III studies: a 566-patient effort for chronic heart failure and a 404-patient trial for chronic lower back pain caused by disc degeneration.

Also in the stem-cell space, Cynata Therapeutics ((CYP)) is planning to carry out its own COVID-19 clinical trials not just in relation to ARDS, but sepsis and cytokine release syndrome (all causes of COVID-19 deaths).

The company is encouraged by pre-clinical modelling and has regulatory approval to carry out a trial.

The company planned to enrol 24 intensive care patients in NSW but perhaps it should refocus efforts south of the Murray.

It was fairly clear that Australias prevention measures effectively flattened the curve and we quickly ran out of available patients, Cynata chief Ross Macdonald said before the Victorian resurgence.

Tackling the cause of COVID-19 mortalities is one thing, but what if the risk of contracting the diseases could be more accurately predicted beyond the clinical factors of age and co-morbidities such as heart disease and diabetes?

That way, the denizens of locked down geographies such as Victoria could discard their masks and emerge from isolation.

Meanwhile, shares in kidney disease house Dimerix ((DXB)) last week soared on positive clinical results pertaining to a rare condition called focal segmental glomerusclerosis (FSGS).

But the drug candidate in question, DMX-200 has also been selected for appraisal in a global trial to treat ARDS, the common element between ARDS and FSGS being fibrosis.

Known in shorthand as REMAP-CAP, the World Health Organisation endorsed trial aims to enrol 7000 patients across more than 200 sites. DMX-200 is one of many potential therapies being looked at, but the beauty for Dimerix is the trial costs are paid the governments that are funding REMAP-CAP.

Changing tack, molecular diagnostics house Genetic Technologies ((GTG)) has filed a provisional patent for a genetics-based assessment of the risk of developing COVID-19.

Based on third-party genomic data from 1500 COVID-19 patients, the company intends to develop a prototype model to identify patients most likely to require hospitalisation should they contract the disease.

If and when a vaccine materialises, the genetic profiling could help to prioritise who gets jabbed first.

Hitherto known for its predictive breast cancer kits, Genetic Technologies has never matched its performance to its promises.

But US investors have been willing to support the stock, with the company raising $US5.1m in a placement via its Nasdaq listing.

Disclaimer: Under no circumstances have there been any inducements or like made by the company mentioned to either IIR or the author. The views here are independent and have no nexus to IIRs core research offering. The views here are not recommendations and should not be considered as general advice in terms of stock recommendations in the ordinary sense.

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In Depth Analysis and Survey of COVID-19 Pandemic Impact on Global Canine Stem Cell Therapy Coronavirus Impact Editon of Key Players VETSTEM…

Rising number of corona virus cases has impacted numerous lives and led to numerous fatalities, and has affected the overall economic structure globally. The Canine Stem Cell Therapy has analyzed and published the latest report on the global Canine Stem Cell Therapy market. Change in the market has affected the global platform. Along with the Canine Stem Cell Therapy market, numerous other markets are also facing similar situations. This has led to the downfall of numerous businesses, because of the widespread increase of the number of cases across the globe.href=mailto:nicolas.shaw@cognitivemarketresearch.com>nicolas.shaw@cognitivemarketresearch.com or call us on +1-312-376-8303.

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The major players in the Canine Stem Cell Therapy market are VETSTEM BIOPHARMA, Cell Therapy Sciences, Regeneus, Aratana Therapeutics, Medivet Biologics, Okyanos, Vetbiologics, VetMatrix, Magellan Stem Cells, ANIMAL CELL THERAPIES, Stemcellvet . Some of the players have adopted new strategies to sustain their position in the Canine Stem Cell Therapy market. A detailed research study is done on the each of the segments, and is provided in Canine Stem Cell Therapy market report. Based on the performance of the Canine Stem Cell Therapy market in various regions, a detailed study of the Canine Stem Cell Therapy market is also analyzed and covered in the study.

Report Scope: Some of the key types analyzed in this report are as follows: Allogeneic Stem Cells, Autologous Stem cells

Some of the key applications as follow: Veterinary Hospitals, Veterinary Clinics, Veterinary Research Institutes

Following are the major key players: VETSTEM BIOPHARMA, Cell Therapy Sciences, Regeneus, Aratana Therapeutics, Medivet Biologics, Okyanos, Vetbiologics, VetMatrix, Magellan Stem Cells, ANIMAL CELL THERAPIES, Stemcellvet

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In Depth Analysis and Survey of COVID-19 Pandemic Impact on Global Canine Stem Cell Therapy Coronavirus Impact Editon of Key Players VETSTEM...

Why Silicon Valley Execs Are Investing Billions to Stay Young – Robb Report

Entrepreneur Dave Aspreys end-of-life plans are quite simple, really, even if some of his ambitions sound laughably optimistic to most of us.I want to die at a time and by a method of my own choosing, and keep doing awesome things until that day, he tells me. I dont think its outrageous to believe Ill make it to 180 years old. And if I run out of energy, itll just be because I did too much cool shit for my own good.

Asprey is strolling across his lush property in British Columbia, holding up his phone and pointing out the specimens in this years garden as we chat over Zoom in the midst of the global pandemic. Hes protecting his skin from the sun with a goofy Outdoor Research hat and wearing a long string of beads that he says are each over a hundred years old, from cultures around the world.

Asprey, 48, is the founder of the Bulletproof wellness empire and a vocal champion of the movement to extend human life expectancy beyond 100 years. Hes made millions by experimenting on his own body and packaging his home-brewed discoveries into books, a podcast, consulting services and consumer products (you may have even tried his butter-laced coffee). Asprey, who was a web-security executive before he became the Bulletproof Executive, is just one of a cadre of tech elite who have begun directing their attentionand truckloads of moneytoward the problem of life extension. Jeff Bezos, Peter Thiel, Sergey Brin, Larry Ellisonname a Silicon Valley A-lister and he or she is likely funding longevity research, experimenting with anti-aging interventions or both. These are the masters of the universe who see no reason they cant take the tech industrys optimization obsession and apply it to the ultimate challenge: conquering death itself.

And their efforts appear to be paying off: Thanks to a recent explosion of advances in longevity medicine, Aspreys vision of living healthfully into his second century might not be so crazy. In fact, for people in middle age right now, a handful of therapies in clinical trials have the potential, for the first time in human history, to radically transform what old age looks like. If the life extensionists are right, a person whos 40 today might reasonably expect to still be downhill skiing, running a 10K or playing singles tennis at 100.

Dave Asprey Dave Asprey

If you do anti-aging right, Asprey insists, youll have a level of resilience and energy to fight what comes your way. If you get Covid-19, youre less likely to become very sick. The idea is that at a cellular level, youre making yourself very hard to kill.

The most extreme of the controversial interventions Asprey has undergone involved having stem cells extracted from his own bone marrow and fat and then injected into hundreds of locations on his body. Into every joint, between every vertebra and into my cerebrospinal fluid, face and sex organs, he tells me cheerfully. For what I spent on that, I could have bought a really nicely appointed Tesla.

He trots up a flight of stairs to his home office, which sits above a million-dollar lab filled with health gadgets, such as a cryochamber, a hypoxic trainer and an AI-enabled stationary bike. For a wealthy person, investing in your body should be a major part of your Im rich strategy, he explains. Personally, I think you should be spending at least 2 to 3 percent of your net worth on health and longevity. Get a personal chef who can cook you the right food. Its not that hard.

It might be an exaggeration to say BioViva CEO Liz Parrish believes death is optional, but for her, Aspreys goal of living to 180 shows a distinct lack of ambition. If you can reach homeostasis in the body, Parrish says, where its regenerating itself just a little bit faster than its degrading, then what do you die of? An accident or natural disaster, probably. Theres no expiration date at 90 or 100 years old.

Tall, blond and fit, Parrish cuts a strikingly youthful figure at 49one that might convince you to order whatever shes having. But, like Asprey, she has received criticism from the longevity research community for becoming patient zero in her own experimental drug trial, aimed at halting aging at the cellular level. In 2015, Parrish underwent telomerase and follistatin gene therapies in Bogota, Colombia. The procedures involved receiving around a hundred injections of a cocktail of genes and a virus modified to deliver those new genes into her bodys cells. The objective was to prevent age-related muscle loss and lengthen her telomeres: the caps at the end of our chromosomes. Scientists have identified their unraveling as not only a marker of aging but also a potential cause of age-related decline.

Liz Parrish Liz Parrish

Parrish told the media about her clandestine experiment and has published periodic updates on her condition in the five years since, and she reports that she has indeed increased her muscle mass and lengthened her telomeres. Parrishs punk-rock approach stems from her conviction that the medical-research communityboth the Food and Drug Administration (FDA) and researchers who arent business-mindedis moving too slowly, with too much red tape, when it comes to advancing aging therapeutics. But gene therapy is a relatively new area of medicine that brings with it a host of new risks, including cancer, severe immune reactions and infections caused by the viral vector used to deliver the drug.

Parrish downplays such worries. There may be risks, she tells Robb Report. But the known risk is that youre 100 percent likely to die. So you have to decide for yourself if the potential benefit outweighs that.

Humans have always aspired to find the fountain of youth, so people might be skeptical about the fact that anti-aging technologies are working now, says British investor and businessman Jim Mellon. But the fact is that this is finally happening, and we need to seize the moment. Mellon cofounded Juvenescence, a three-year-old pharmaceutical company thats investing in multiple technologies simultaneously to increase the odds of bringing winning products to market.

Mellon, 63, has made his fortune betting on well-timed investment opportunities, and he predicts that a new stock-market mania for life extension is just around the corner. This is like the internet dial-up phase of longevity biotech, he enthuses. If youd invested in the internet in the very early days, youd be one of the richest people on the planet. Were at that stage now, so the opportunity for investors is huge. According to a report by Bank of America Merrill Lynch, hes not wrong: The market for technologies to increase human life span is projected to grow sixfold to $610 billion in just the next five years.

When I talk to Mellon in the late spring, hes sequestered on the rugged coast of the Isle of Man, a tiny spit of land in the Irish Sea. Despite being what he describes as imprisoned there for 15 weeksand countingduring the Covid-19 shutdown, hes jovial and chatty and wants to make it clear that his interest in life extension is much more than financial. Working to extend life is an ethical cause, he says. If we can help people to live healthfully until the end of life, well transform the world completely. Well reduce a huge amount of pressure on failing health-care systems, and well have to reimagine pension and life insurance. This should be the number-one tick in anyones investment portfolio.

If youd like to get on board with this social-impact view of longevity, it helps to understand the trajectory of aging today. In Americas most affluent neighborhoods, the average life span is about 88 years. (Meanwhile, in this countrys poorest, it hovers around a meager 66 because of a raft of inequalities, such as diet, stress, smoking, pollution and health care.) For most people, health starts gradually diminishing in the last 15 years of life with the onset of chronic conditions, including arthritis, neurodegeneration and diabetes. If we could eliminate such diseases of aging, experts say, the US could save an estimated $7.1 trillion in health-care costs over the next 50 years. (Quite where all these sprightly centenarians might live on this already densely populated planet remains to be seen.)

Jim Mellon Eric Verdin

One of Mellons bets is on a class of drugs called senolytics, which destroy senescent cells: the so-called zombie cells that, for complex reasons, stop dividing as we age. Senescent cells harm the body by secreting compounds that cause inflammation in surrounding tissues. Many age-related conditionsarthritis, diabetes, Alzheimers, cancerhave an inflammatory component, and studies suggest that a buildup of senescent cells is a large part of the problem.

A number of biotech start-ups are devel- oping drugs that target cell senescence, but the furthest along is Unity Biotechnology, a company in South San Francisco that has three drugs in clinical trials to address aging conditions, starting with osteoar- thritis of the knee. Unity raised more than $200 million from such big names as Thiel and Bezos, who chipped in through their investment firms, before going public in 2018. Since then, Mellon has also bought a small stake.

The holy grail of senolytics will be the development of a preventive therapy to wipe out senescent cells in the body before they cause conditions of aging, theoretically extending life span. In June, a team from Sloan Kettering published new breakthrough research showing that CAR T cellstypically used for precision cancer therapycan also be used to target and kill senescent cells. Prescription senolytics for anti-aging therapy are still years away, but unsurprisingly, theres an audience of longevity enthusiasts who want to access such anti-aging miracles yesterdayand no shortage of FDA-unapproved ways to chase after them. For instance, after a few studies examined the senolytic effects of a chemotherapy drug called dasatinib, the website FightAging.org published a step-by-step guide to senolytic self-experimentation using chemotherapeutics.

It doesnt take a Ph.D. in biochemistry to guess that taking off-label chemo drugs might come with harmful side effects, but that hasnt stopped a zealous group of body-hackers from trying it themselves and chronicling their efforts online. The internet is littered with novice longevity adviceand sketchy anti-aging companies eager to separate the hopeful and desperate from their money, like the company that charges $8,000 for transfusions of plasma from the blood of teenagers and early-twentysomethings (yes, just like Gavin Belson on HBOs Silicon Valley). Many of these are at best ineffective and at worst deadly, since the same cellular systems that fuel growth in young people might cause cancer when tipped into overdrive. Imagine the tragic irony of paying tens of thousands for a therapy that promises to help you live longer but actually causes the cancer that kills you.

Adobe

Beyond the obvious red flags of repurposed chemo drugs and the bloodletting of teens, it can be difficult for a layperson to separate the world-changing longevity breakthroughs from the terrible ideas. Enter one of the worlds leading experts on longevity to help make sense of things.

Eric Verdin, 63, is president and CEO of the Buck Institute, a globally renowned center for aging research just outside San Francisco in Marin County. Verdin is bullish on the promise of living healthfully to at least 100. Today. But 180? Dont count on it. My prediction, based on everything we know today, is that getting to 120 is about the best we can do for the foreseeable future. Ill bet my house were not going to see anyone live to 180 for another 200 years, if ever, he says. But making everyone a healthy centenarian, this is something we can do today. And thats something to be excited about.

Verdins own lab at the Buck Institute studies the aging immune system and how its affected by lifestyle factors, such as nutrition and exercise. Informed by this research, Verdin follows a time-restricted diet in which he eats all of his meals in an eight-to-nine-hour window (similar to the Buchinger Wilhelmi process) and gets plenty of exercise mountain biking in Marins steep hills. The good news is that over 90 percent of what causes diseases of aging is environmental, and that means its within your control, he says.

But he emphasizes that responsible management of your health comes with limits, like avoiding experimental therapies. A group of people have decided to try some expensive and dangerous interventions, but there is zero evidence that any of these are going to help them live longer, he says. The problem, according to Verdin, is that the results of aging interventions in mouse trials can look very promising but rarely translate to success in humans. Theres a huge delta between the health of a stressed lab mouse and an optimally healthy mouse, Verdin says. So when you treat lab mice with longevity therapeutics, you see an outsized result that doesnt at all guarantee the same result in humans.

On the other hand, Verdin tells Robb Report, there are definitely new protocols worth getting excited about. Take, for instance, rapalogs, a class of drugs that interact with a protein called mTOR, which serves as a linchpin for multiple critical biological processes, including cell growth and metabolism. Rapalog drugs tamp down mTOR, possibly preventing age-related diseases such as diabetes, stroke and some cancers. The drug rapamycin, the most heavily studied formula, was approved in the US in 1999 to help prevent organ-transplant rejection. Last year the medical journal Aging published a rapturous opinion piece by oncologist Mikhail Blagosklonny in which he made the case that rapamycinin small or intermittent dosesis effective as a preventive treatment to ward off diseases of aging, and that, in the elderly, not taking rapamycin may be even more dangerous than smoking.

Eric Verdin Jim Hughes Photography

Later this year, a biotech firm called resTORbio, which was spun out of the Swiss-based Big Pharma company Novartis in 2017, is expected to seek FDA approval for its rapalog RTB101, which clinical trials have shown to slow age-related decline of the immune system and improve immune response in elderly people by more than 20 percent, a key factor in protecting vulnerable aging populations from disease. (It is currently in trials on elderly patients with Covid-19.) This is the furthest-along program of anything in the aging field, Joan Mannick, cofounder and chief medical officer of resTORbio, told MIT Technology Review last year. If health authorities approve this drug well have a product for people to prevent age-related diseases. Not just in our lifetime, but in, you know, a few years.

One of the many effects of rapamycin is that it mimics the mechanisms of calorie restriction. As Verdins lab and others have shown, fasting provides a number of anti-aging benefits, including insulin regulation, reduced inflammation and, to put it colloquially, clearing out the gunky by-products of metabolismpart of the reason Twitter CEO Jack Dorsey and other tech titans eat just a few meals per week. For lesser mortals, fasting is extremely hard to commit to and not much fun, hence the huge interest in calorie-restriction mimetics like rapamycin, which provide all the benefits without the downer not-eating part.

Of all the calorie-restriction mimetics, the one sparking the most excitement among longevity researchers is already on the market: metformin, a decades-old diabetes drug. Metformin became a part of the Silicon Valley health regimen several years ago after an epidemiological study showed that Type 2 diabetics who took the drug lived longer than non-diabetics who didnt. Just about everyone in the longevity industry takes metformin, Verdin tells me. He takes it himself, and nearly everybody I interviewed is taking or has taken it, too.

In April, Nir Barzilai, the renowned endocrinologist who spearheaded research on the anti-aging properties of metformin, announced in an opinion piece he co-authored in the journal Cell Metabolism that his lab is launching a large clinical trial to investigate the anti-aging effects of the drug on non-diabetic populations. Barzilais goal is to prove to the FDA that aging itselfrather than conditions associated with it, like Alzheimers and arthritiscan be targeted as a disease. If Barzilai is successful and the FDA approves aging as a treatment indication, the process of bringing longevity therapies to market would accelerate rapidly.

Just as the FDA was able to move faster to bring Covid-19 therapies to market this year, we will reach a tipping point when public opinion pushes the FDA to approve aging as an indication, and the longevity-research field will make leaps as a result, Mellon says. He has contributed funding to Barzilais metformin research, which he believes will be instrumental in proving that there are compounds that can extend human life across the board.

The fact of the matter is that the US has the best regulatory system for new drug development in the world, Mellon says. Were in the first era ever when humans can be bioengineered to live longer. And in 10 years, well have solutions that are even better than today. Just wait, its coming.

Liz Parrish

Jim Mellon

Diet: Vegetarian.Mindfulness practice: Nightly meditation.

Exercise regimen: 30 minutes of cardio and 10 minutes of weights, five days a week.

Anti-aging Rx: Regenerative gene therapies. Im certain most people will take them in the next couple decades.

180th-birthday wish: Solving another critical issue.

Sleep routine: 7.5 hours plus a 30-minute nap; in bed by 9 p.m.

Vitamins/supplements/ prescription meds: Vitamins D and B12, metformin.

Exercise regimen: Walk or run minimum 10,000 steps a day; weights three times week.

Anti-aging Rx: Green tea.

100th-birthday wish: Another 25 years.

Dave Asprey

Jim Hughes Photography

180th-birthday wish: Either a cruise to Mars or a 1970 Mustang Fastback, which by then will be 210 years old!

Sleep Routine: Avoid: coffee after 2 p.m., heavy workouts after 6 p.m., alcohol during the week and heavy eating in the evening.

Vitamins/supplements: Vitamin D, omega fatty acids, NMN, citrus bioflavonoid complex, fiber supplement, prebiotic supplement.

Diet: Fasting-mimicking diet once every four to six months; roughly 16:8 intermittent fasting at other times.

Mindfulness practice: Daily meditation.

Anti-aging Rx: I love cooking and eating, so I do not restrict food on the weekend. Happiness with friends and family is the surest path to longevity.

100th-birthday wish: A bike tour across the US, from coast to coast.

See more here:
Why Silicon Valley Execs Are Investing Billions to Stay Young - Robb Report

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Georgy is undergoing his last round of chemotherapy this week.

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

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

Hes got four more sessions after this and its finished.

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

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

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

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

Stem Cell Market Size, Share Analysis 2020 Business Strategies, Growth Opportunities, COVID 19 Outbreak, Emerging Technologies, Regional Trends and…

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