Category Archives: Embryonic Stem Cells

Human Embryonic Stem Cells, Germ Cells, and Cell-Derived …

NOTE: THIS GUIDANCE REPLACES OHRPS NOVEMBER 16, 2001, GUIDANCE ENTITLED, GUIDANCE FOR INVESTIGATORS AND INSTITUTIONAL REVIEW BOARDS REGARDING RESEARCH INVOLVING HUMAN EMBRYONIC STEM CELLS, GERM CELLS, AND CELL-DERIVED TEST ARTICLES. CLICK HERE FOR THE NOVEMBER 16, 2001 GUIDANCE.

Office for Human Research Protections Department of Health and Human Services

Guidance for Investigators and Institutional Review Boards Regarding Research Involving Human Embryonic Stem Cells, Germ Cells and Stem Cell-Derived Test Articles

Date:March 19, 2002

Scope: This document describes when research activities involving human embryonic stem cells (hESCs), human embryonic germ cells derived from fetal tissue, or hESC- or germ cell-derived test articles are considered human subjects research and what regulatory controls apply to that research.

Target Audience: Investigators who conduct research with these cells and test articles, sponsors of such research, institutions where the research is conducted, and Institutional Review Boards (IRBs) that review human subject research involving these cells or test articles.

APPLICABLE REGULATIONS AND LAWS

CONDITIONS REGARDING FEDERAL FUNDING OF RESEARCH ON HUMAN EMBRYONIC STEM CELLS

GUIDANCE

Under HHS regulations at 45 CFR Part 46, human subject means a living individual about whom an investigator (whether professional or student) conducting research obtains (1) data through intervention or interaction with the individual, or (2) identifiable private information.

HHS-conducted or supported research that involves neither interactions nor interventions with living individuals or obtaining identifiable private information is not considered human subjects research. Accordingly, in vitro research and research in animals using already derived and established human cell lines, from which the identity of the donor(s) cannot readily be ascertained by the investigator, are not considered human subject research and are not governed by the HHS or FDA human subject protection regulations appearing at 45 CFR Part 46 and 21 CFR Parts 50 and 56. IRB review is not required for such research.

Use of Identifiable Private Information

HHS-conducted or supported research that uses human cell lines where the donor(s) may be identified, including cells that retain links (such as a code) to identifying information is generally considered human subject research that is governed by 45 CFR Part 46 because the donors are human subjects. IRB review and approval is required for such research.

In vitro research or research in animals using a human cell line that retains a link to identifying information ordinarily would not be considered human subjects research if: (1) the investigator and research institution do not have access to identifiable private information related to the cell line; and (2) a written agreement is obtained from the holder of the identifiable private information related to the cell line providing that such information will not be released to the investigator under any circumstances. In this case, the research may be considered to not involve human subjects because the identity of the donor(s) could not be readily ascertained by the investigator or associated with the cell line. Under such circumstances, an institution or an IRB could determine that IRB review of the research using the cell line was not needed.

Intervention or Interactions with the Individual

All HHS-conducted or supported clinical research that involves interactions with living individuals, including the transplantation of human cells or test articles, such as differentiated cells derived from human embryos or human fetal tissue, into human recipients is human subjects research subject to HHS regulations at 45 CFR Part 46 because recipients are human subjects. IRB review and approval is required for such research.

Furthermore, all clinical research involving use of cells or test articles regulated by FDA as drugs, devices, and biological products is subject to regulation and oversight by FDA. This clinical research must be conducted in compliance with FDAs regulations governing INDs or IDEs regardless of source of funding. All human studies conducted under INDs and IDEs are subject to FDAs IRB and informed consent regulations.

Public Law 103-43, Research on Transplantation of Fetal Tissue, also applies to clinical research involving the transplantation of cells or test articles derived from human fetal tissue into human recipients.

In addition, other Federal, State or local laws may also apply to transplantation or other research involving these cells or test articles.

RELATED GUIDANCE

For further information regarding this guidance, please contact OHRP at ohrp@hhs.gov or 240-453-6900).

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Inside the twisted world of ‘rapist’ designer Peter Nygard: book – The Loppy

Peter Nygard, the flamboyant Canadian fashion mogul, built a nearly billion-dollar fortune hawking slacks and blouses at Sears, Walmart and his own store in Times Square. Known as a hard-partying Peter Pan, the man Forbes dubbed The Polyester Phenom was often surrounded by young women and threw legendary parties at his homes in the Bahamas and Los Angeles.

But it all came to a halt in February when the FBI raided Nygards Manhattan office. The bust came just a week after 10 unidentified women filed a federal lawsuit accusing the 78-year-old of a decades-long sex-trafficking scheme in which he recruited, lured, and enticed young, impressionable and often impoverished children and women, with cash payments and false promises of lucrative modeling opportunities only to, allegedly, sexually assault and rape them. On April 22, 36 more women joined a class-action complaint against Nygard.

The new book Predator King: Peter Nygards Dark Life of Rape, Drugs and Blackmail (Hot Books) by Melissa Cronin tells this dark story. (Nygards lawyer, who has sent a cease-and-desist letter to the books publisher, told The Post: Predator King recklessly presents a one-sided, unreliable, and wholly misleading portrayal of the allegations against Mr. Nygard.) Here, an adapted excerpt chronicles how Nygard allegedly used his power and privilege to take advantage of people.

Much of the alleged illegal activity is said to have taken place in and around Nygards 150,000-square-foot estate in Lyford Cay, Bahamas, which featured fake volcanos spouting dry ice, a gym on the beach, statues of nudes supposedly modeled on Nygards exes, a disco hut with cameras under the floors, an underground Mayan-themed cave housing 30 cars and an indoor swimming pool with glass through the middle, which allegedly had dolphins on one side and sharks on the other.

Massive cauldrons come to life, blazing with flames. The eyes of concrete Mayan-style gargoyles and snakes glow like embers. Angry organ chords in a minor key shoot out across the ocean, the beach and the surrounding properties: the foreboding first notes of the theme to Andrew Lloyd Webbers Phantom of the Opera.

When Peter Nygard was in residence at Nygard Cay, neighbors say, that was the nightly soundtrack. In the booming early 2000s, Nygard Cay was a playground for lingerie and bikini models flown in from Las Vegas and other major US cities.

According to Nygards [house manager], Richette Ross, his staffers used Facebook posts and messages to promote upcoming parties, which offered free dinners, massages, pedicures, and boat rides to guestsmainly females, said Ross. Mr. Nygard didnt like the competition.

Once the party began, though, Nygard would kick off a twisted competition of his own, she claimed. As guests arrived, they would be photographed and entered into Nygards personal database. He even rated them upon entry, Ross claimed: A, B, C or D, with A being the most beautiful. Ross claimed [those] women had to have what Nygard called a nice toilet a nice ass. It had to be big and round.

Ross claimed, Throughout the day, hed ask a particular girl if shed like to stay the night. If she said no? Ross alleged, Then theres always drugging.

Ross said that she personally witnessed one of Nygards bartenders drop a pill into a girls drink.

Around 10:00, we were almost ready to shut down, Ross claimed, when she spotted the girl again. She was crying naked in the office. Disorientated.

Tragically, according to Ross, this wasnt an unusual occurrence. She claimed, It happened often. She even said that at least once, she saw a girl escape from the property, only to be brought back by Bahamian police, apparently against her will.

When the New York Times covered the sexual assault accusations against Nygard earlier this year, it revealed that two accusers interviewed had then recanted and said they had been paid to lie by Ross. (Nygard has also claimed that his billionaire neighbor, Louis Bacon, with whom hes feuded for years, has paid people to make false statements about him.) However, Ross denied having paid anyone to lie and passed a polygraph test supporting her denial. In the book, Ross alleges that she herself even fell prey to her boss wicked scheme

Nygards girlfriend offered [Ross] a glass of wine. It seemed unusual, and she declined the offer to focus on her work. Still, Ross said, She stopped me and insisted I have that glass of wine. As I was going up the stairs I felt a warmness coming over my body. I turned to tell [Nygard] I wasnt feeling good. I remember going down.

When I came to, Ross alleged, he was penetrating me. I could see from the mirror (on the ceiling). I knew he was on top of me. I remember trying to ease my way to the edge of the bed He raped me.

Ross finally quit working for Nygard in 2014. She found support in a local nonprofit organization founded to help sexual violence victims. Ross even became a sort of leader in the community, introducing other alleged victims to the organization in the hopes of getting them therapy and the community support theyd never had.

She even has alleged that Nygard went so far as to kill her family dog. The New York Times found that Nygard actually wired her $10,000 at one point, emailing Ross: I sent you money to buy a new dog. (He blamed the dogs death on a political rival.)Before long, though, Ross had made herself a target. At one point, I was basically in hiding, she alleged, describing threats that were issued all the time.

According to the book, Nygard had almost unlimited power to do what he wanted in the Bahamas after bribing officials from the governments Progressive Liberal Party.

Former Nygard employee Richette Ross said she was personally tasked with putting together payoffs for high-ranking [Progressive Liberal Party] members.

[She claimed to have seen] stacks of $10,000 bundles from the bank stuffed into bags for delivery. For some, Ross said even that method of handoff was too risky. She claimed that Nygard got creative in his efforts to pay off politicos.

Mr. Nygard had required that I order some very large fish, she said. He had about $100,000 in $10,000 bundles. He told me he wanted me to break them up, roll them, and put them in this fish.

According to records obtained by the Bahamas Tribune, Shane Gibson [a member of the PLP] received $94,131.10 deposited into his Miami bank account from the Nygard Companies in 2012 and 2013. The donations were usually $5,000 or more, and were deposited on a semi-regular basis, marked services or travel.

When confronted with the records, Gibson, the Minister of Immigration and Labor at the time, told the Tribune that they were campaign donations, as well as financial contributions to community programs he was spearheading, like scholarships for local students. Gibson would later be photographed at one of Nygards pamper parties in 2014. (Gibson did not respond to The Posts requests for comment.) With Nygards support, the PLP rolled to victory in 2012 and the designer was quick to claim credit.

According to court documents obtained by the Tribune newspaper shortly [after the election] the government determined that appropriate acreage should be leased to Mr. Peter Nygard so he could develop a stem cell facility as a part of what was termed a touristic development.

Nygard admitted to having [met with government officials], but his attorneys later claimed that the minutes of that meeting had been fabricated, and that he had no desire to curry preferential treatment by the Bahamian government. The campaign to get his stem cell mecca built, though, would consume him for the next several years.

Nygard, obsessed with staying young, ended up establishing his stem cell research company in nearby St. Kitts. The alleged purpose: to use aborted fetuses from his pregnant girlfriends to provide him with fresh stem cells.

Nygard seemed to suggest that something like that could be afoot when he talked about the technology behind his treatments publicly. I may be the only person in the world, he bragged, who has my own embryos growing in a petri dish.

When I came to he was on top of me. I remember trying to ease my way to the edge of the bed.

Peter Nygards former house manager Richette Ross, claiming in Predator King that he drugged and raped her

One of his girlfriends, Suelyn Medeiros, wrote in her 2014 memoir about a trip she took with Nygard to Ukraine, where he was having stem cell research done.

He asked, Suelyn, do you know what the best stem cells are? she writes.

She did: Embryos.

Correct! she says Nygard responded. If you got pregnant and had an abortion, we could use those embryonic cells and have a lifes supply for all of us: you, your mother and me. A lot of people are doing it.

Medeiros says she was beyond stunned.

This was the sickest thing Id ever heard Peter say, she writes. I couldnt speak for a moment Finally, catching my breath, I said, Peter, I do not believe in abortion.

On Feb. 13, 2020, a class-action complaint on behalf of several Jane Does was filed in the US District Court for the Southern District of New York and revealed Nygards depravation.

On so many nights, it was alleged, the same story would unfold: Nygard lures the victims to his bedroom or has them ushered there by groomers, under the false pretense of discussing a potential modeling contract in private, where he uses physical force or coercion or knowing the victim has not attained the age of 18 years, to engage in commercial sex acts and coerce and force them to engage in unwanted sexual acts

The amounts of money provided to the victims is more than most of [them] have seen at one time in their entire lifetimes He promises many victims that he will contact them about future modeling contracts. However, in the vast majority of cases, Nygard never intends to follow through with the modeling contracts and tells his victims this for the sole purpose of maintaining control over them.

[He] also threatens the victims with implied or express threats of retribution if they tell anyone about what happened, often implying or expressly threatening to have his victims killed if they do not cooperate.

Today, Nygards Lyford Cay estate is quiet no more Phantom of the Opera melodies after it was seized by local authorities in 2018 because of illegal dredging, according to Canadas National Post. The moguls company filed for Chapter 15 bankruptcy in New York last week, and Nygard is reportedly in Winnipeg, Manitoba, awaiting the outcome of the FBI investigation.

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Inside the twisted world of 'rapist' designer Peter Nygard: book - The Loppy

Lack of investment is the biggest challenge in stem cell research – Express Healthcare

India with its huge population can become an ideal place for medical research in stem cell, but due to lack of awareness and investment, its progress is slowing down. Vipul Jain, CEO, Advancells talks about the companys vision for stem cell research and progress in India, to Usha Sharma

Give us a brief about your companys inception?

I have been a part of healthcare marketing for over 12 years now and somewhere in 2009-10, a few patients started talking about stem cell therapies if I could help them find a centre, where they could opt for these therapies. Unfortunately, none such centre operated in India and there were very few across the world. Once I studied the subject in-depth it occurred to me that this would be the future of medicine and it was the right time to enter this field. The hope of changing medicine as we know it today inspired me to get into this practice and I established Advancells in 2013.

In the past seven years of our operations, we have grown strength to strength and are today one of the largest providers of stem cell therapies in India.

When we started Advancells, we aimed at becoming a pioneer in the research and development of regenerative medicine. We wanted to have India at the forefront of protocols and technologies in the industry and so we decided to venture into a wide array of services. In order to become a centre of medical advancement, we had to ensure we offered services to all sorts of patients, irrespective of their condition. We believe in treating our patients in a progressive manner.

Tell us about the challenges you faced while setting up your business?

Lack of investment is the biggest challenge. Most new investments in healthcare sector still come from Trusts and charities who enter the segment for charity and with a no-profit no-loss mindset. This restrains their capacity to invest in research and new technologies and hence it is not easy to get cutting edge technologies in the country. India with its huge population base can be a perfect place for strong medical research but the lack of awareness and investment are the major reasons for India to lag behind in research. It is not easy for healthcare researchers to attract private money as private investors are worried about the long gestation period for their investment.

The other major challenge is the acceptance of doctors of a new branch of medicine. It is very difficult to convince doctors of a new way to treat patients and understandably they want long term follow-up data. This data will take time to come and hence growth can not be as fast as you expect it to be. Government regulations are another challenge as agencies are always a little slow to react to innovation.

The expense of research and clinical preliminaries is high in the case of regenerative medicine, in this way confining the research objectives. Aside from cost/enormous speculations, other challenges are administrative difficulties with changing rules across nations, on account of contrasts in the suppositions and social perspectives. Setting up a solitary/regular arrangement or rule worldwide to administer stem cell research could be helpful. Human embryos for research, somatic cell, nuclear move, IPSCs have raised concerns due to their long hatching periods.

So how does your model work?

Advancells works in four different verticals. Firstly, we produce basic human stem cells that are used by partner hospitals and doctors in providing regenerative therapies to the patients. Advancells also writes protocols for therapies and provide training to doctors on various facets of regenerative medicine. In the second vertical, we produce organ, species and disease-specific primary cells, which are used by research institutes, academic institutes and pharma companies around the world to further their research in the field of biology and drugs.

In the third vertical, we produce our patented range of bioscaffolds which once seeded with our cells, are used in the regeneration of bones, organs and healing of wounds. Fourthly, we print 3D human organs and finally seed our scaffolds with our primary cells and paste them on the 3D printed organ models and try to create working modal of a human organ that can be used by pharma companies for drug discovery models. Our moonshot is to be able to produce a transplantable human artificial organ that can one day put an end to mortality rate due to non-availability of transplantable human organs.

We are essentially a B2B business where doctors and hospitals, research institutes, pharma companies etc., are our clients, but we regularly get approached by a number of patients both from India and abroad who want our protocols for treatment. We do provide B2C services to such patients also.

We are currently operating out of our centralised lab in Noida, Delhi/NCR and are able to ship cells to various hospitals not just across India but also in various countries around the world.

Does India have well-defined stem cell treatment regulations?

Surprisingly very well. India has been always been a follower especially when it comes to medical research. There has hardly been any major medical innovation that has come out of India but things seem to be changing this time. It looks like there will be a good case study where India might just take the lead in stem cell technology and be a world leader in it. We have all the required resources and brainpower to make it happen, all we need is a supportive legislature, progressive regulators, understanding investors and gritty innovators and you will see things rolling.

The Government of India has started promoting Stem Cell Research with the help of its agencies. The focus is on identifying diseases and conditions that can be cured. Programmes to support embryonic and adult stem cell research are in place. Some of the developments include setting up human embryonic stem cell lines, using limbal stem cells to repair corneal surface disorder; classification of haematopoietic, mesenchymal and liver stem cells; as well as segregation of stem cells into neural, cardiac and cell lineages, etc.

For the rest of the world, there are many researchers who are creating pathbreaking records. Scientists from the University of California, for instance, have created an approach via stem cells to deal with cancerous tissue while anticipating some dangerous reactions of chemotherapy by treating the disease in a progressive manner.

So whats the scope for stem cell research/ therapy?

Stem cells present a unique opportunity to treat the disease that currently is termed as untreatable. They also help us in treating the diseases from the core and not just managing the symptoms. These properties give regenerative medicine a unique status.

You conduct 15-20 treatment in a month despite the unclear regulations in India? Do you see this as a challenge and deal with it?

We deal only with hospitals and doctors who have taken permission from the government and hence the reach is very low.

How do you differentiate your therapies from other existing players? What all guideline you follow and what is the success ratio?

There is no real credible competition for us. The big players in the market are primarily into cord blood banking and for the therapy is a side product on which they dont concentrate. There are few doctors who practice regenerative medicine on their own but could never match up with the product catalogue or research backing that we have.

There is an exhaustive consent form and clear inclusion and exclusion criterion and the patients are council-led at multiple points before the procedure.

Which are the therapeutic areas Advancells provides stem cell solutions and how safe are they? What is your future plan?

Advancells provide stem cell solutions for orthopaedics, neurology, diabetes etc. It is completely safe. We are targeting to venture into Cosmetics, Ophthalmology.

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Lack of investment is the biggest challenge in stem cell research - Express Healthcare

AgeX Therapeutics: Revolutionary Potential But Extremely Early – Seeking Alpha

AgeX Therapeutics (AGE) is an interesting company in the up-and-coming longevity space. This article will take a look at the science behind their current development programs as well as the leading figures and stakeholders in the company. AgeX is certainly a very risky bet, both because of the low probability of any preclinical asset eventually gaining approval and because it is unclear whether the company has the financial resources to develop their current pipeline assets. Despite that, I do believe the potential reward of success could be tremendous for investors, and the continued vote of confidence from a major longevity investment company is meaningful in my opinion. At this time, my model does justify potentially taking a small, speculative position in the company while it is trading under $1/share, but nothing more than that until AgeXs outlook becomes clearer.

AgeX was founded in 2017 as a subsidiary of BioTime, Inc., a cell therapy biotech now known as Lineage Cell Therapeutics (LCTX). In 2018, AgeX was spun out from BioTime in connection with a public offering for AgeX, with BioTime shareholders receiving 1 share of AgeX for every 10 shares of BioTime they owned. Since that time, AgeX has operated as an independent, publicly-traded company.

AgeXs focus as a company is to develop therapies that target biological aging. AgeX intends to do this primarily through 2 major technologiesPureStem and inducible tissue regeneration ((iTR)). PureStem is a technology platform used to generate young pluripotent stem cell-derived cellular therapies for use in treating the degenerative diseases of aging. iTR is literally intended to reverse the age of human cells back to the very beginning of life by restoring the capacity of tissues to regenerate following injury, a process which is lost with aging.

Although AgeX is less than 3 years old, several members of its management have been involved in research related to AgeXs developmental technology for decades. For example, the companys CEO, Michael D. West, Ph.D., invented the PureStem and iTR technologies which are based on over 25 years of his research. Dr. West has written multiple books and scientific papers on stem cells and aging in general and is widely considered a pioneer in the field.

In addition to Dr. West, noted longevity researcher Aubrey de Grey, Ph.D., is also involved as the VP for New Technology Development. Dr. de Grey is the Chief Scientific Officer for the SENS Research Foundation which has spun out numerous anti-aging companies over the years, and he commonly appears in mainstream media outlets discussing longevity research. Dr. de Grey is perhaps most widely known for his ideas about the longevity escape velocity, the idea that at some point in the future, technology may reach a point where for each year you are alive, longevity research is able to add more than one additional year to your lifespan, essentially rendering humans immortal aside from accidents, homicides, etc.

AgeXs 3 current assets in the pipelineeach of which utilizes PureStem or iTRare all still in preclinical workup. This means a tremendous amount of cash will be required before any of these therapies even have the potential of bringing in revenue.

Figure 1: AgeXs Pipeline (source: AgeX website)

Even if successful, each of these preclinical assets could still be a decade and $100+ million away from FDA approval (source: The Pharmagellan Guide to Biotech Forecasting & Valuation). Given that at year-end 2019 the company only had $2.35 million in cash and equivalents, AgeX has a lot of capital raising to do to have any shot at realizing their technologys potential.

AgeX has several possible ways to get this much-needed capital. AgeX could certainly raise capital by selling additional shares on the open market, diluting current shareholders. Im sure some of this will take place but given the companys current market cap is barely over $32 million, it might be difficult for the company to get even close to the necessary amount through this method alone. That being said, anyone considering an investment in AgeX needs to be soberly aware of the likelihood of substantial dilution over the coming years.

For its part, AgeX is clearly aware of its current capital constraints and has made several moves aimed towards alleviating at least some of their near-term liquidity problems. In late 2019, AgeX incorporated a subsidiary specifically for the development of iTR, Reverse Bioengineering, Inc. This structural change is interesting, primarily because AgeX explicitly says in their corporate presentation regarding the creation of Reverse Bioengineering that the new company may take on third-party equity investment. If Reverse Bioengineering does take on early-stage venture funding, it could help AgeX to afford the development of iTR, but its again another obvious potential way that an investor in AgeX may have their interest in future iTR profits diluted.

A possible source of ongoing financial support for AgeX is its relationship with Juvenescence Limited, a holding company for biotechs involved in the longevity space. Juvenescence bought a 45.8% stake in AgeX shortly before the company was spun out from BioTime. This transaction was for 14.4 million shares at $3 each its certainly not a bad sign that a company with as much experience in longevity as Juvenescence thought AgeX shares were worth more than 3x the level at which they are currently trading. Thus, Juvenescence has a clear and significant interest in the success of AgeX. In 2019, Juvenescence agreed to provide AgeX with a $2 million unsecured loan. With a 2019 full year loss of over $12.5 million though, AgeX was still in need of money.

Accordingly on March 30, 2020, AgeX entered into another loan agreement with Juvenescence, with an immediate $500 thousand being disbursed to AgeX. There are 2 big differences with this loan facility though. First, the loan could be for as much as $8 million. Second, however, any amount loaned in excess of the first $500 thousand will this time be secured by AgeXs assets as well as the fact that Juvenescence can force AgeX to implement a cost reduction plan that could entail significant reductions in staffing and research and development activities. Further loans could even cause AgeX to have to issue additional shares to Juvenescence.

This sort of loan would cause me substantial concern if Juvenescence didnt have a large equity interest in AgeX. As it is though, Juvenescence stands to benefit too much from AgeXs potential success to use the terms of such a loan facility for its short-term benefit and AgeXs detriment. Its also worth noting that the CEO of Juvenescence is on AgeXs board. While AgeXs cash situation is certainly something to watch closely, my fears are assuaged somewhat that a well-funded company like Juvenescence is incentivized to help AgeX develop and commercialize its technology.

One early way AgeX could potentially monetize its technology is through licensing and partnerships. In fact, this is listed as item number 1 in the business strategy section of the companys recent 10-K, where AgeX says they hope to bring in early revenue streams this way. There is already some limited evidence of this strategy bearing fruit.

First, AgeX has partnered with ImStem Biotechnology, Inc. for the use of its pluripotent stem cell lines in developing an investigational therapy for multiple sclerosis. Imstem recently announced that an FDA clinical hold had been lifted and their IND was accepted. This should lead to the initiation of a Phase 1 trial for the therapy this year.

Also, involvement by Juvenescence may help to cross-pollinate AgeX technology with that of its other portfolio companies. One such example of this already taking place is with Lygenesis, a company focused on organ regeneration. Lygenesis is apparently exploring the use of AgeX technology to eliminate the need for immunosuppression in recipients of Lygenesis organ therapies. This is exactly the type of use that will hopefully increase demand for AgeXs UniverCyte technology.

AgeX will also realize some near-term income from its LifeMap Sciences subsidiary. This subsidiary sells the rights on a subscription basis to the GeneCards Database Suite, which is an integrated biomedical knowledgebase of human genes, variants, proteins, cells, biological pathways, diseases, and the relationships between them. The service currently has over 3.5 million users including users from more than 45 major biopharma companies. This income, however, will likely never offset more than a fraction of the companys total expenses, as it only brought in $1.3 million and $1.2 million in subscription revenue in 2019 and 2018 respectively.

Garnering a substantial amount of partnerships and accompanying revenue is certainly something that could de-risk the value proposition for AgeX. While nothing you can really hang your hat on, its worth noting that management said in their November letter to shareholders that they hope to announce several collaborations in the coming months.

AgeX has a number of cell-based technologies that, from the outside looking in, appear to be a little further along in the development process than iTR. As discussed immediately above, AgeXs stem cell technology looks ripe for partnerships, and each such partnership would provide critical additional data and experience to help move along AgeXs own proprietary assets.

The first of their cell-based technologies is PureStem, AgeXs allogeneic cell therapy platform that is based on human embryonic progenitors, cells in state of development between stem cells and adult cells. The company says these PureStem cells are distinct from competitors stem cell products because they would be commercialized as off-the-shelf products, be pure and industrially scalable, have lower cost of goods per unit, be amenable to traditional pharma supply chain logistics, and have the potential for acceptable reimbursement prices.

Figure 2: Diagram Depicting PureStem Clinical Use (source: corporate presentation)

AgeX says PureStem could have higher clinical adoption because of these expected cost savings and more simplified processes than with autologous stem cell technologies, where an individual is treated only with their own stem cells.

A second AgeX technology, UniverCyte, is what would allow for universal, off-the-shelf stem cell products. Based on the mechanism by which a fetus is protected from its hosts immune system, UniverCyte is a proprietary method for making cell that are off-the-shelf compatible with basically any recipient. The licensing possibilities for such a technology seem virtually endless, and I will certainly be watching for any such developments in the coming months.

AgeX is developing 2 proprietary assets utilizing their stem cell technology. Their lead pipeline asset, AGEX-BAT1, looks to brown fat to help with type 2 diabetes. Brown fat or brown adipose tissue (BAT) is thought to be prevalent in young people but slowly goes away as they age. BAT is far more metabolically active than the typical white fat that has negative consequences for the body, and experimental evidence in mice has shown that increased levels of BAT in older mice led to weight loss and increased insulin sensitivity.

AgeX intends to create BAT with its PureStem technology and use it as a therapy in diabetic patients. The metabolic activity of brown fat is a popular idea and research topic currently, so this idea has some support outside of just AgeX. It certainly would be a big deal to AgeX if successful because the overall diabetes therapy market is huge projected to be about $59 billion by 2025.

The second stem cell therapy currently in the pipeline is AGEX-VASC1, a program to develop vascular progenitors for use in treating ischemic heart disease. The idea is to deliver vascular progenitors made from AgeX pluripotent stem cells into ischemic heart tissue to regenerate collateral circulation in patients with coronary artery disease. AgeX is hoping to begin preclinical animal testing soon. Again this is a huge potential market, but as with most of AgeXs potential, it is years away from being realized if ever.

iTR would be revolutionary as this seems to be the first attempt at getting a true cellular regeneration or reprogramming technology into the clinic and then eventually onto market if all goes well. iTR would truly turn back the clock for treated cells to a non-diseased, younger state rather than just treating symptoms.

iTR utilizes small molecules to turn on regeneration of cells. The human body can only naturally regenerate certain cells and even then, only in a limited capacity. The novel approach taken by iTR may trigger complete regeneration of cells, and potentially organs and limbs. The premise behind iTR is that embryonic cells have a capacity for regeneration that is lost at the embryonic to fetal transition. With this loss, humans can no longer generate new cells or repair damaged cells to maintain a peak physical condition. The aim of iTR is to return an aged cell back to a youthful state, without crossing over to pluripotency, the point where stem cells have yet to differentiate or become a particular type of cell.

Company researchers and collaborators recently published that they reverted cells from a 114-year old back to pluripotent stems cells via iTR technology. Despite how promising it looks, iTR remains in the preclinical phase though. Its extremely hard to quantify the potential value of such a technology, but the one certain thing is that the road to a marketed iTR product will be a long and expensive one.

Even though any such value is incredibly speculative given that AgeX having an approved drug is likely a decade or more away, I attempted to assign a present value to the potential future cash flows AgeX could receive from their 3 current pipeline assets. All of the markets for these potential therapies are extremely competitive ones with numerous current therapies and doubtless many others that will come out long before AgeXs do.

Accordingly, I modeled a fairly low 10% peak market share despite how transformative AgeXs therapies could ultimately be. Also, I only gave AgeXs therapies a 5% overall chance of reaching the market given their extremely early and novel nature and especially the fact that none of them have reached the clinic yet. Below are charts showing my models for each of these pipeline therapies:

Figure 3: My Present Value Estimates for AGEX-BAT1, AGEX-VASC1, and AGEX-iTR1547 (source: data from AgeXs 10-K and my calculations based on them)

As you can see in Figure 3, even though any cash flow from the pipeline is many years away, there is still a good bit of present value to each of these assets because of how large potential market size is likely to be. I then subtracted out my estimates of expenses, which were $117 million each for R&D for the 3 main therapies and SG&A expenses scaled up from the current level to eventually being 35% of revenue once these therapies hit the market.

Figure 4: My Fair Value Estimate for AgeX (source: data from AgeXs 10-K and my calculations based on them)

My best attempt at a fair value estimate for AgeX at present is about $1.31 per share. Although this is now 50% above current levels, as you can see from Figure 5 AgeX was trading at roughly my fair value estimate before the recent broader market sell-off.

Figure 5: AgeX Stock Chart (source: finviz)

In theory, this suggests the company is presently undervalued and could even have meaningful short-term upside. Its worth noting though the far higher risk of loss of capital though when trading a company with no assets in the clinic and as little cash as AgeX versus the later stage biopharma stocks I more commonly invest in and write about. Although I have a great deal of respect for many of those involved in the company and personally find this area of development fascinating and compelling, I'm holding off on it as an investment at this time while I continue to watch the company with great interest.

AgeX has an extremely long road ahead of it. While my model does suggest some potential upside, I consider the company to be in the ballpark of fair value even at these low levels because of the high amount of uncertainty in their pipeline and their cash-strapped balance sheet. The only reason in my mind that justifies holding any position here is that AgeX seems to have novel and potentially lucrative technology that could result in partnerships which might quickly change the companys outlook. Any substantial rise in the share price though without a partnership, improvement to the balance sheet, or major pipeline progress would be a reason to sell in my opinion.

Disclosure: I/we have no positions in any stocks mentioned, and no plans to initiate any positions within the next 72 hours. I wrote this article myself, and it expresses my own opinions. I am not receiving compensation for it (other than from Seeking Alpha). I have no business relationship with any company whose stock is mentioned in this article.

Additional disclosure: Im not a registered investment advisor. Despite that I strive to provide the most accurate information, I neither guarantee the accuracy nor the timeliness. Past performance does NOT guarantee future results. I reserve the right to make any investment decision for myself without notification. The thesis that I presented may change anytime due to the changing nature of information itself. Investment in stocks and options can result in a loss of capital. The information presented should NOT be construed as a recommendation to buy or sell any form of security. My articles are best utilized as educational and informational materials to assist investors in your own due diligence process. You are expected to perform your own due diligence and take responsibility for your actions. You should also consult with your own financial advisor for specific guidance as financial circumstances are individualized.

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AgeX Therapeutics: Revolutionary Potential But Extremely Early - Seeking Alpha

Human Embryonic Stem Cells (HESC) Market Overview, Top Companies, Region, Application and Global Forecast by 2026 – Latest Herald

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Global Human Embryonic Stem Cells (HESC) Market Segmentation

This market was divided into types, applications and regions. The growth of each segment provides an accurate calculation and forecast of sales by type and application in terms of volume and value for the period between 2020 and 2026. This analysis can help you develop your business by targeting niche markets. Market share data are available at global and regional levels. The regions covered by the report are North America, Europe, the Asia-Pacific region, the Middle East, and Africa and Latin America. Research analysts understand the competitive forces and provide competitive analysis for each competitor separately.

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Human Embryonic Stem Cells (HESC) Market Region Coverage (Regional Production, Demand & Forecast by Countries etc.):

North America (U.S., Canada, Mexico)

Europe (Germany, U.K., France, Italy, Russia, Spain etc.)

Asia-Pacific (China, India, Japan, Southeast Asia etc.)

South America (Brazil, Argentina etc.)

Middle East & Africa (Saudi Arabia, South Africa etc.)

Some Notable Report Offerings:

-> We will give you an assessment of the extent to which the market acquire commercial characteristics along with examples or instances of information that helps your assessment.

-> We will also support to identify standard/customary terms and conditions such as discounts, warranties, inspection, buyer financing, and acceptance for the Human Embryonic Stem Cells (HESC) industry.

-> We will further help you in finding any price ranges, pricing issues, and determination of price fluctuation of products in Human Embryonic Stem Cells (HESC) industry.

-> Furthermore, we will help you to identify any crucial trends to predict Human Embryonic Stem Cells (HESC) market growth rate up to 2026.

-> Lastly, the analyzed report will predict the general tendency for supply and demand in the Human Embryonic Stem Cells (HESC) market.

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Table of Contents:

Study Coverage: It includes study objectives, years considered for the research study, growth rate and Human Embryonic Stem Cells (HESC) market size of type and application segments, key manufacturers covered, product scope, and highlights of segmental analysis.

Executive Summary: In this section, the report focuses on analysis of macroscopic indicators, market issues, drivers, and trends, competitive landscape, CAGR of the global Human Embryonic Stem Cells (HESC) market, and global production. Under the global production chapter, the authors of the report have included market pricing and trends, global capacity, global production, and global revenue forecasts.

Human Embryonic Stem Cells (HESC) Market Size by Manufacturer: Here, the report concentrates on revenue and production shares of manufacturers for all the years of the forecast period. It also focuses on price by manufacturer and expansion plans and mergers and acquisitions of companies.

Production by Region: It shows how the revenue and production in the global market are distributed among different regions. Each regional market is extensively studied here on the basis of import and export, key players, revenue, and production.

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Tags: Human Embryonic Stem Cells (HESC) Market Size, Human Embryonic Stem Cells (HESC) Market Growth, Human Embryonic Stem Cells (HESC) Market Forecast, Human Embryonic Stem Cells (HESC) Market Analysis

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Human Embryonic Stem Cells (HESC) Market Overview, Top Companies, Region, Application and Global Forecast by 2026 - Latest Herald

Role of MyHC-embryonic protein in muscle development and disease – Tech Explorist

Dr. Sam J. Mathew, Assistant Professor at DBTs Regional Centre for Biotechnology (RCB), Faridabad, found out that loss of MyHC-embryonic protein leads to muscle abnormalities, including alterations in muscle fiber type, fiber number, and fiber size.

Secondly, the MyHC-embryonic protein is required to regulate the rate of differentiation of the muscle stem cells during development, and this effect is mediated by fibroblast growth factor (FGF) signaling. Although MyHC-embryonic is expressed in all muscles, they find that loss of MyHC-embryonic has differential effects on distinct muscles, and the adult mice lacking MyHC-embryonic displayed abnormal curved spine (scoliosis), an abnormality seen in individuals with Freeman-Sheldon Syndrome (FSS).

Targeted mouse models, they have characterized the function of MyHC-embryonic and developmental myosins in general, during embryonic stages of development. Loss of function of MyHC-embryonic leads to scoliosis in adult mice, a defect seen in FSS patients, and this mouse model could thus be a valuable tool in understanding the defects underlying this congenital disorder.

Myosins are proteins that are present in all cell types, meant for fundamental cellular functions such as cell movement, cell division, and transport of cargoes within cells. A specialized set of myosin proteins known as muscle myosins are expressed by the skeletal muscle, which are required for muscle contraction. While most muscle myosin proteins are expressed in the adult muscle, two are expressed only during embryonic development.

Very little is known about these developmentally expressed muscle myosins except that mutations in the gene encoding one of the myosins, MYH3, leads to Freeman-Sheldon Syndrome (FSS) in humans, a genetic disease causing severe musculoskeletal abnormalities including joint deformities, bent fingers, club feet, curved spine and facial anomalies. FSS patients have compromised movement, respiratory, speech and feeding problems, and delayed growth and development.

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Role of MyHC-embryonic protein in muscle development and disease - Tech Explorist

The Republicans who were once so pro-life they fought over one woman on life support now want to sacrifice grandma for the economy – The Independent

Years after the United States elected a president with the motto America First, we just pulled ahead in a race no one wants to win: the most deaths from the novel coronavirus. In order to limit casualties from a catastrophic second wave, states have enacted measures of differing severity, from shutting down some businesses to move severe shelter in place orders mandating citizens stay in their homes.

However, months into this disruption, some restless Americans are looking for a way out and there are Republican politicians eager to placate them. Senator Rand Paul of Kentucky bemoaned the lack of commerce on Twitter and threw his support behind re-opening the economy. Georgia Governor Brian Kemp is way ahead of him, announcing plans to lift restrictions on businesses from bowling alleys to hair salons amidst widespread pushback in his own state. Lt. Governor Dan Patrick of Texas skipped the subtext and went straight to the point with the breathtaking assertion that there are more important things than living, a statement that presumably doesnt include himself or his loved ones.

Its puzzling how these politicians think re-opening will lead to business as usual with an unpredictable contagion floating around. Commerce relies on consumers, and if a majority of those consumers are rightfully afraid for themselves and their families, how exactly is the government supposed to put things back to pre-pandemic levels without forcing us to go to the mall on pain of arrest?

Sharing the full story, not just the headlines

Even if they just intend to let those who dont care about the risks shop, go to work and pretend everything is normal, theres a very real danger that way more Americans will die as a result. But according to Lt. Gov. Patrick, its a justifiable sacrifice for the good of the nations GDP.

This is fascinating coming from a party that has long labeled itself as pro-life over the years when it suits them. Lets look at one of the most extreme examples: Terri Schiavo, a woman whose private medical battle became a tool for the Republican party during the early 2000s. After a Florida trial court concluded that Schiavo was in a persistent vegetative state and would have wanted the feeding tube keeping her alive to be removed, Republicans at all levels became involved. Governor Jeb Bush pulled in everyone from his brother in the White House to the United States Congress to unsuccessfully fight the trial courts order for years. It would seem to a casual observer that this was a political party that would stop at nothing to save a life.

This wasnt the first time Republicans (or the Bushes) were performatively pro-life. During his first year in office President George W. Bush severely limited federal funding for research involving embryonic stem cells, giving evangelical conservatives an important win. Bush continued to oppose bills to loosen these restrictions, citing concerns that taxpayers would be funding the destruction of potential life. Again, if you didnt know anything else about the GOP you would think that their concerns were so pure as to encompass cells that could become a human being someday.

This stated concern for life didnt stop with the Bush brothers. Republicans took a stand during debates surrounding President Obamas signature legislation, the Affordable Care Act. This proposed legislation aimed to increase the amount of people with health insurance (which is positively correlated with life preservation). However, former GOP vice presidential candidate Sarah Palin asserted repeatedly that the law would lead to death panels that would decide whether elderly Americans would live or die. Inspired by Palin, the right painted a dystopian picture of a future where liberal judges would decide grandmas fate. A decade later and pearl-clutching at treatment of older Americans has taken a turn since they are inconveniently deemed to be more at risk of dying of Covid-19. Now the elderly, it seems, are at best inessential to public life and, at worst, expendable sacrifices to the gods of capitalism.

Here is whats revealing in each of those episodes: championing the life of Terri Schiavo, or the potential life of stem cells, or the imaginary life of a condemned grandma didnt cost Republicans a nickel. But the people who would potentially die if re-opening measures are scaled back are expensive. Theyre also inconvenient for the partys narratives. They include the medical workers who counter-protest the Confederate flag-wavers who want to be able to get a haircut. They are immigrants who risk their lives to provide you with food. They are, disproportionately, black, indicative of the virulent racism in our country.

Championing their lives means economic sacrifice with no legislative gain. That is, apparently, a bridge too far.

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The Republicans who were once so pro-life they fought over one woman on life support now want to sacrifice grandma for the economy - The Independent

Sustainably Yours: The importance of understanding and trusting in Science – The Phuket News

In his book 21 Lessons for The 21st Century, historian Yuval Noah Harari begins by writing, In a world deluged by irrelevant information, clarity is power. Before the Internet, access to information was relatively limited, and media was concentrated in the hands of a few corporations, which had its problems.

When it comes to supposed facts about COVID-19 posted on the internet, its best to check first with those doing the real checking: scientists. Photo: AFP

Today, with YouTubers, bloggers, and social media at our fingertips, the world is filled with more information than ever. The problem is that much of it is fake news and rumours. Too many voices are clamouring for our attention, but few are fact-checked for accuracy.

Since the spread of COVID-19 began, weve seen snake oil salesmen hawking cures and prophylaxis, and the spread of conspiracy theories about the viruss origins.

In a world where breathing the same air as someone else can kill you, misinformation can be as deadly as the virus. Now more than ever we need to be mindful of what we say, what we post, and how we behave. So, we need to understand and trust in science.

Why Should We Believe in Science?

According to Harvard Professor Naomi Oreskes, author of Why Trust Science?, for several decades there has been an organised campaign to undermine the publics trust in science funded mainly by industries whose financial interests are threatened by its findings.

At its core, science is the study of how the natural world works.

It has a long history of success, and when done correctly it is the single best method of inquiry we have for the pursuit of truth. Because of science, we have aeroplanes, cars, GPS, the Internet, smartphones and modern medicine. The only reason we know that COVID-19 exists is because of science. More importantly, science is a self-policing system of checks and balances that exists to reveal problems and correct inaccuracies.

It begins with the scientific method, something we all learned in school:

Once a scientist has drawn a conclusion, it undergoes rigorous scrutiny by colleagues who are working in the same discipline. This process of scrutiny can lead to rejecting or accepting the hypothesis, redesigning the experiment or finding additional data to support the conclusion. If the claim is valid, the scientist then publishes their work in a reputable scientific journal such as Nature or Science.

Submission of a paper begins the rigorous peer-review process where experts in the same field deliberately challenge the scientists arguments, inspect their data and look for errors in their methodology. So, before a claim is made and the general media gets a hold of it, a study is peer-reviewed and subjected to scrutiny by dozens, if not hundreds of other experts in the same field.

In areas where there is a scientific consensus, such as the relative safety and efficacy of vaccines, or that climate change is anthropogenic, thousands of studies on these topics have been published over decades and reviewed by thousands of scientists in dozens of countries.

Professor Oreskes notes that a critical aspect of scientific judgment is that it is done collectively and not individually. This weeds out personal biases or someone who might have a specific agenda.

Scientific claims are put through a process much like a trial. Questions are posed, data is analysed, and facts are debated before the community comes to a consensus. This process can take years, even decades. So, when your beliefs are founded on scientific consensus, you are relying on the knowledge of dozens if not hundreds, or thousands of experts in their fields.

Because COVID-19 is still so new, there are lots of unknowns. It will take time to review the data and draw definitive conclusions. There remains speculation about how the virus transmits, whether recovered patients acquire sustained immunity, the effect of heat and humidity have on infection rates and the viability of various treatments, among other things. Nevertheless, our reaction to COVID-19 should be grounded in facts, evidence and empirical data rather than, unfounded opinions, suppositions and fears.

Science Makes Mistakes

Like any other human discipline, science has its failures. For example, in 2014, Japanese biologist Haruko Obokata knowingly falsified data regarding the creation of stimulus acquired pluripotent (STAP) cells in mice. If her claim had been valid, it would have revolutionised the production of embryonic stem cells, which are blank cells that can be programmed to become any of 200 different cell types in the human body, including bone, hair, skin or muscle.

However, due to the self-policing nature of science, within days, other biologists in her field refuted her claims after failing to replicate her experiments. Within months, her paper was retracted, and her career ended in disgrace.

Knowing that science sometimes makes mistakes and admits and corrects for them shouldnt make us trust it any less if anything it should make us believe in it more. Especially when compared to other methods of inquiry, which have no process of scrutiny.

The Problem with Intuition

In his book Thinking Fast Thinking Slow, Nobel Prize-winning behavioural economist Daniel Kahneman defined intuition as, Thinking that you know something without knowing why you do. As an example, he poses this problem:

A bat and ball cost $1.10.

The bat costs one dollar more than the ball.

How much does the ball cost?

If you answered 10 cents, you are incorrect. This question confounds 50% of students from some of the best universities in the world.

The correct answer is 5 cents.

Kahneman identifies two methods for problem-solving. System 1 is quick, intuitive, spontaneous and effortless. It instantly helps us to recognise faces, to act when confronted with dangers and to solve simple questions. System 2 is slow, rational, reflective and effortful. It gets into the drivers seat when you focus and concentrate on a complicated problem.

The problems occur when we try to use System 1 to make complex decisions that require System 2. People will often make judgements based on intuition when a given situation is easy to imagine. For example, when asked what the most dangerous method of generating energy is, public opinion is usually most negative toward nuclear. However, on a per terawatt-hour basis, atomic energy has killed far fewer people than oil, coal and even solar. But because most people conflate nuclear power with war, they tend to answer incorrectly.

When our perception of reality is based on stories that people tell us, rather than science, facts and evidence, it leads to poor decisions. In the modern world, we need to learn to think in terms of data as it is a far too complicated a place to always reason by intuition.

Linear Vs. Exponential Thinking

Part of the reason many governments didnt foresee the problems COVID-19 would create is that their leaders are linear thinkers.

As an example, if you take 30 linear steps, you move 30 standard paces from where you started, or about 30 metres. However, if you take 30 exponential steps, one, two, four, eight, sixteen by the time you get to the last step, you end up a billion metres from where your started thats about 26 times around the planet!

Its the reason why at the beginning of March the United States only had 65 infections and by April 14 it had over 500,000.

We are In This Together

Whether we like it or not, we are in this together. The virus doesnt distinguish between race, social class, tourist, expat or Thai.

We must be careful about what we say or post in social media. The virus kills quickly, but misinformation can also kill by influencing people to do foolish things.

For sources of science that have been peer-reviewed or vetted by experts, you can go to the following websites:

PubMed

The Lancet

Nature Medicine

The New England Journal Of Medicine

The British Medical Journal

WebMD

Healthline

When we depend on intuition, gossip, fake news and conspiracy theories to make decisions, we get leaders who make demonstrably poor decisions that lead to disastrous consequences. In this regard many people think of Donald Trump.

To quote John F. Kennedy, We are not here to curse the darkness, but to light the candle that can guide us through that darkness to a safe and sane future.

Science, both literally and figuratively, is that light; to disregard it is to remain in the dark.

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Sustainably Yours: The importance of understanding and trusting in Science - The Phuket News

Mogrify and Sangamo announce collaboration and exclusive license agreement for Mogrify’s iPSC- and ESC-derived regulatory T cells – SelectScience

Mogrify Ltd (Mogrify), a UK company aiming to transform the development of cell therapies by the systematic discovery of novel cell conversions, and Sangamo Therapeutics (Sangamo), a genomic medicine company, have announced that they have executed a collaboration and exclusive license agreement for Sangamo to develop allogeneic cell therapies from Mogrifys proprietary induced pluripotent stem cells (iPSCs) and embryonic stem cells (ESCs) and Sangamos zinc finger protein (ZFP) gene-engineered chimeric antigen receptor regulatory T cell (CAR-Treg) technology.

Mogrify is delighted to announce its second commercial deal with a US biopharma and the first in the exciting field of T cell immunotherapy, said Dr. Darrin M. Disley OBE, CEO, Mogrify. The combination of Mogrifys proprietary systematic cell conversion technology and Sangamos regulatory T cell platform and proprietary ZFP platform is a natural fit. Sangamo is at the forefront of the development of a world-class engineered ZFP genome editing platform and we are very happy to be partnering with such an innovative company.

This license agreement provides Sangamo with access to Mogrifys cell conversion technology, which will diversify our options as we develop off-the-shelf allogeneic CAR-Treg cell therapies, said Jason Fontenot, SVP, Head of Cell Therapy at Sangamo. We expect this collaboration to accelerate our development of scalable and accessible CAR-Treg cell therapies, so that we can potentially deliver treatments to patients with inflammatory and autoimmune diseases more rapidly.

Mogrifys technology enables the transformation of any human cell type into any other human cell type. This transformation is achieved using transcription factors or small molecules identified using proprietary big data technologies. iPSCs and ESCs provide an evergreen starting material for the generation of Tregs, and facilitate more complex engineering and greater manufacturing scalability, potentially enabling the resulting therapies to be more cost-effective and thus more accessible to larger patient populations.

Under the terms of the agreement, Mogrify will be responsible for the discovery and optimization of the cell conversion technology from iPSCs or ESCs to regulatory T cells, and Sangamo will be granted exclusive rights to use Mogrifys technology to create Tregs from iPSCs or ESCs. Sangamo expects to then use its ZFP gene-engineering technology and therapeutic development capabilities to transform these Tregs into novel off-the-shelf allogeneic CAR-Treg cell therapy candidates and hopes to take them through clinical development through to registration for the treatment of inflammatory and autoimmune diseases.

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Mogrify and Sangamo announce collaboration and exclusive license agreement for Mogrify's iPSC- and ESC-derived regulatory T cells - SelectScience

Stem Cell Therapy Market Research Outlook, Recent Trends and Growth Forecast 2020-2025 – Cole of Duty

The Stem Cell Therapy report provides independent information about the Stem Cell Therapy industry supported by extensive research on factors such as industry segments size & trends, inhibitors, dynamics, drivers, opportunities & challenges, environment & policy, cost overview, porters five force analysis, and key companies profiles including business overview and recent development.

Stem Cell Therapy MarketLatest Research Report 2020:

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In this report, our team offers a thorough investigation of Stem Cell Therapy Market, SWOT examination of the most prominent players right now. Alongside an industrial chain, market measurements regarding revenue, sales, value, capacity, regional market examination, section insightful information, and market forecast are offered in the full investigation, and so forth.

Scope of Stem Cell Therapy Market: Products in the Stem Cell Therapy classification furnish clients with assets to get ready for tests, tests, and evaluations.

Major Company Profiles Covered in This Report

Gilead,Novartis,Organogenesis,Vericel

Stem Cell Therapy Market Report Covers the Following Segments:

Product Type: Adult Stem Cells, Human Embryonic Stem Cells (hESC), Induced Pluripotent Stem Cells, Very Small Embryonic Like Stem Cells

Application: Regenerative Medicine, Drug Discovery and Development

North America

Europe

Asia-Pacific

South America

Center East and Africa

United States, Canada and Mexico

Germany, France, UK, Russia and Italy

China, Japan, Korea, India and Southeast Asia

Brazil, Argentina, Colombia

Saudi Arabia, UAE, Egypt, Nigeria and South Africa

Market Overview:The report begins with this section where product overview and highlights of product and application segments of the global Stem Cell Therapy Market are provided. Highlights of the segmentation study include price, revenue, sales, sales growth rate, and market share by product.

Competition by Company:Here, the competition in the Worldwide Stem Cell Therapy Market is analyzed, By price, revenue, sales, and market share by company, market rate, competitive situations Landscape, and latest trends, merger, expansion, acquisition, and market shares of top companies.

Company Profiles and Sales Data:As the name suggests, this section gives the sales data of key players of the global Stem Cell Therapy Market as well as some useful information on their business. It talks about the gross margin, price, revenue, products, and their specifications, type, applications, competitors, manufacturing base, and the main business of key players operating in the global Stem Cell Therapy Market.

Market Status and Outlook by Region:In this section, the report discusses about gross margin, sales, revenue, production, market share, CAGR, and market size by region. Here, the global Stem Cell Therapy Market is deeply analyzed on the basis of regions and countries such as North America, Europe, China, India, Japan, and the MEA.

Application or End User:This section of the research study shows how different end-user/application segments contribute to the global Stem Cell Therapy Market.

Market Forecast:Here, the report offers a complete forecast of the global Stem Cell Therapy Market by product, application, and region. It also offers global sales and revenue forecast for all years of the forecast period.

Research Findings and Conclusion:This is one of the last sections of the report where the findings of the analysts and the conclusion of the research study are provided.

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We publish market research reports & business insights produced by highly qualified and experienced industry analysts. Our research reports are available in a wide range of industry verticals including aviation, food & beverage, healthcare, ICT, Construction, Chemicals and lot more. Brand Essence Market Research report will be best fit for senior executives, business development managers, marketing managers, consultants, CEOs, CIOs, COOs, and Directors, governments, agencies, organizations and Ph.D. Students.

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Stem Cell Therapy Market Research Outlook, Recent Trends and Growth Forecast 2020-2025 - Cole of Duty