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US FDA tells Cellectis to halt cell therapy trials after patient death – In-PharmaTechnologist.com

Posted: September 5, 2017 at 9:52 am

The US FDA has ordered Cellectis SA to halt studies of its cell therapy UCART123 after the death of a patient.

Cellectis announced the clinical hold yesterday, explaining it applied to both Phase I studies known as ABC123 and AML123 - in which the therapy is being examined.

The deceased man - a 78 year old in the ABC study who was suffering with relapsed blastic plasmacytoid dendritic cell neoplasm (BPDCN) died nine days after receiving the first dose of UCART123.

According to Cellectis, after a preconditioning regimen involving fludarabine and cyclophosphamide, the patient was treated with UCART123 on August 16.

Five days later he experienced a grade 2 Cytokine Release Syndrome (CRS) and a grade 3 lung infection which improved after treatment with tocilizumab and antibiotics.

However, at day eight the patient experienced a grade 5 CRS event and grade 4 Capillary Leak Syndrome that did not respond to corticosteroids and tociluzumab. He died the following day.

Cellectis also revealed the first patient treated in the AML study, a 58-year old woman suffering acute myeloid leukemia who received the same preconditioning regimen and the same dose of UCART123, had recoveered after experiencing similar complications.

According to the firm She experienced an initial grade 2 CRS at Day 8, worsening to a grade 3 at Day 9 and resolving at Day 11 with treatment management in intensive care unit. She also experienced a grade 4 Capillary Leak Syndrome at Day 9, resolved at Day 12.

Cellectis said it is working closely with the investigators and the FDA in order to resume the trials with an amended protocol including a lowered dosing of UCART123.

Background

UCART123 consists of T-cells modified to target the CD123 antigen on the surface of cancerous cells.

The therapy which is made on Cellectis behalf by the LFB Group subsidiary CELLforCURE- is produced using Talen gene editing to insert genes that encode a chimeric antigen receptor (CAR) that targets the CD123 antigen.

Unlike autologous cell therapies made from the specific patients own cells, UCART123 is composed of lymphocytes harvested from an unrelated, so called universal donor.

According to Cellectis, Talen gene editing prevents the T-cells from interacting with non-target proteins, thereby reducing side-effects

The US Food and Drug Administration (FDA) cleared Cellectis to start trialling UCART123 in February.

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Zika kills brain cancer cells, may find use as therapy – The San Diego Union-Tribune

Posted: September 5, 2017 at 9:52 am

Zika, notorious for ravaging the brains of babies, could be useful in treating a particularly deadly brain cancer.

The virus kills glioblastoma stem cells, say researchers at UC San Diego and Washington University in St. Louis. They tested in human cell cultures and a mouse model of the disease

Moreover, Zika largely spared mature brain cells, the researchers say in a study published Tuesday in the Journal of Experimental Medicine.

People with glioblastoma rarely survive more than two years, although survival rates vary according to age and how aggressive the tumor is.

Study authors suggest a tamed version of the virus could be used along with other treatment to improve survival rates.

U.S. Senator John McCain was recently diagnosed with glioblastoma. The disease killed U.S. Senator Ted Kennedy, singer-actress Ethel Merman and retired baseball player Gary Carter.

Glioblastomas are treated with surgery, followed by radiation and chemotherapy. However, it is impossible to remove all the cancer without also removing healthy tissue and risking brain damage. So the cancer nearly always comes back.

Cancer stem cells cause the recurring tumors. These cells bear strong genetic resemblances to normal stem cells, and can proliferate greatly. Just one cell can regrow an entire tumor.

Glioblastoma stem cells also resist chemotherapy and radiation. But because they are stem cells, they are vulnerable to Zika. The virus causes an abnormally small head, or microcephaly, by destroying immature neural cells.

The study authors say a modified Zika virus could be applied after surgery, penetrating to the remaining cancer cells and killing them. One author, Jeremy Rich, M.D., is a renowned brain cancer specialist who recently joined UC San Diego from Cleveland Clinic. The first author, Zhe Zhu, also researches at UCSD.

Brain cancer specialists not involved with the study said by email it is scientifically sound, but there is a long way to go before it could be used in patients.

The science in this study is good considering the limitations of test tube and mice models, said Keith Black, M.D., chair of neurosurgery at Cedars-Sinai Medical Center in Los Angeles. What we don't know is how these results will translate to humans, given how different the complex human tumors are compared to simplistic mice models.

Before a Zika-based therapy can be tested in people, toxicity studies need to be completed in animals, along with regulatory approvals from the U.S. Food and Drug Administration and the institutes where the trial is to be conducted, Black said.

The approach has precedent in viral therapy by San Diegos Tocagen to treat glioblastoma, said Faith Barnett, M.D., a neurosurgeon with Scripps Green Hospital in La Jolla. Tocagens therapy is already being tested on glioblastoma patients. It uses poliovirus and retroviruses, a class of virus that includes HIV.

Whether Zika virus is a better vector needs to be determined, Barnett said. Clearly, we need creative approaches to improve current cancer therapies.

Unlike Zika, Tocagens viruses dont directly attack the brain cancer cells. Instead, they deliver a gene to the cancer that primes it for destruction when exposed to a drug precursor or prodrug.

The prodrug is converted into a toxic drug inside the cancer cells through an enzyme the gene codes for. Normal cells dont get the gene, and so are unaffected by the prodrug.

Go online to http://tocagen.com/patients for more information on Tocagens clinical trials.

For further reading

McCain completes round of radiation, chemo for brain cancer

UC San Diego hires renowned brain cancer expert Jeremy Rich

Blocking a tumor suppressor gene actually slows down one kind of glioblastoma

Survival time increases for those with deadly brain cancer: Study

Cancer genes hide outside chromosomes

Mom delays cancer care to protect baby she says saved her

Gary Carter to treat brain tumor with chemotherapy

Glioblastoma Anti-Angiogenesis Resistance Mechanism Found by Salk Researchers

bradley.fikes@sduniontribune.com

(619) 293-1020

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What is hyperemesis gravidarum? Pregnant Kate Middleton again suffering rare severe morning sickness condition – Mirror.co.uk

Posted: September 5, 2017 at 9:51 am

The Duchess of Cambridge is expecting her third child - and is once again suffering from the severe morning sickness which blighted her previous pregnancies.

Kate was in the early stages of her pregnancy with Prince George when she was admitted to hospital in December 2012 with hyperemesis gravidarum, a rare condition which causes severe vomiting during pregnancy.

Awareness of her tendency to the condition meant her second pregnancy was announced relatively early, rather than waiting for the 12 week milestone, as she cancelled public duties due to sickness.

For women suffering hyperemesis gravidarum, the severity of the vomiting can cause dehydration, weight loss and a build-up of toxins in the blood or urine called ketosis.

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It affects 3.5 per 1,000 pregnant women and can cause women to vomit blood.

Symptoms also include severe nausea, low blood pressure and fast heart rate, headaches, lethargy or confusion.

It is treated by giving women fluids intravenously and by anti-sickness tablets.

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The cause of HG is unknown. The leading theories state that it is an adverse reaction to the hormonal changes of pregnancy.

It is more common in multiple pregnancies and is commonly experienced during the first 8 to 12 weeks of pregnancy.

A scientific study has given preliminary evidence there may be a genetic component.

Symptoms can be aggravated by hunger, fatigue, prenatal vitamins (especially those containing iron), odours, and diet.

"In very simple terms hyperemesis means vomiting a lot and gravidarum means in pregnancy," said consultant obstetrician Daghni Rajasingam, spokeswoman for the Royal College of Obstetricians and Gynaecologists in 2014.

"The diagnosis is given when women cannot keep food or fluid down because she has severe vomiting.

"The women who are vomiting pretty much constantly, that cannot keep any nutrients down, they need to be admitted to hospital."

She said the length of stay in hospital depends on each patient but many women are discharged in a matter of days.

"It depends on how well the woman is keeping fluids down," Ms Rajasingam added.

She said the condition is thought to be caused by elevated levels of the "pregnancy hormone" hCG.

The body begins to produce human chorionic gonadotrophin (hCG) after conception.

While cases of very severe, protracted and prolonged periods of vomiting are rare, nausea and vomiting in pregnancy is very common, affecting 60% to 80% of women.

About 5% of mothers-to-be will be admitted to hospital during their pregnancy with some degree of the condition, Ms Rajasingam said.

Once admitted, doctors will monitor women and let them go home once they can keep fluids down.

Some alternative therapies are used to help reduce the symptoms and duration of the nausea and vomiting, including acupuncture, travel sickness bands, eating ginger and other herbal remedies.

The condition is most common in the first 12 weeks of pregnancy, Ms Rajasingam added.

Caitlin Dean, trustee of the charity Pregnancy Sickness Support, also suffered from the condition.

"Imagine having a stomach bug that lasts for days and days, months and months - it is just relentless," she said.

"Any movement, any sound, any smell just makes you vomit.

"I vomited 20 to 30 times a day for the first few months, in the latter part it was just once or twice a day but it's still unpleasant.

"One of the big issues with it is isolation because is causes many women to be bed-bound.

"There is a real lack of understanding about the condition."

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Testosterone replacement therapy associated with improved urinary, sexual function – ProHealth

Posted: September 5, 2017 at 9:51 am

Reprinted with the kind permission of Life Extension.

August 23 2017.An article appearing on July 18, 2017 in theJournal of Urologydocuments improvements in sexual function, urinary function and quality of life among men who receivedtestosterone replacement therapy.

The prospective registry study involved 656 men with low testosterone levels and symptoms of testosterone deficiency, among whom 360 were regularly treated with parenteral testosterone undecanoate for up to 10 years. The remainder of the subjects, who chose not to be treated with testosterone, received biannual routine clinic visits.

The researchers, from Boston University School of Medicine and School of Public Health in collaboration with German urologists, found that men who received testosterone therapy experienced significant decreases in their International Prostate Symptom Score, post-voiding bladder volume and Aging Males Symptoms scale, which assesses health-related quality of life. The percentage of patients without erectile dysfunction significantly improved in the testosterone treated group, from 17.1% at the beginning of the study, to 74.4% of the study at the last visit. In contrast, subjects who did not receive the hormone experienced deterioration in erectile function as well as in voiding functions. Prostate specific antigen (PSA), a marker which, when elevated, is associated with an increased risk of prostate cancer, remained unchanged in both groups over the course of the study.

While there were five deaths, 8 nonfatal strokes and 8 nonfatal heart attacks over the 8-month median follow-up period in the untreated group, none of these events occurred among those who received testosterone.

Long-term testosterone therapy, in men with testosterone deficiency, was well tolerated with excellent adherence suggesting a high level of patient satisfaction, authors Karim Sultan Haider and colleagues conclude. A progressive and sustained improvement in urinary and sexual function was recorded in men receiving long-term testosterone therapy, contributing to overall improvement in quality of life.

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Testosterone Replacement Therapy Market Global Insights and … – E News Access (press release)

Posted: September 5, 2017 at 9:51 am

Global Testosterone Replacement Therapy Market Research Report 2017 to 2022 provides a unique tool for evaluating the market, highlighting opportunities, and supporting strategic and tactical decision-making. This report recognizes that in this rapidly-evolving and competitive environment, up-to-date marketing information is essential to monitor performance and make critical decisions for growth and profitability. It provides information on trends and developments, and focuses on markets and materials, capacities and technologies, and on the changing structure of the Testosterone Replacement Therapy Market.

Companies Mentioned are AbbVie, Pfizer, Eli Lilly, Teva Pharmaceuticals, Mylan, Bayer HealthCare Pharmaceuticals, Antares Pharma, Ferring Pharmaceuticals, Allergan, Antares Pharma, Sandoz, Clarus Therapeutics, Juniper Pharmaceuticals, Endo International, Acerus Pharmaceuticals, Forendo Pharma, MetP Pharma, Repros Therapeutics

The Global Testosterone Replacement Therapy market consists of different international, regional, and local vendors. The market competition is foreseen to grow higher with the rise in technological innovation and M&A activities in the future. Moreover, many local and regional vendors are offering specific application products for varied end-users. The new vendor entrants in the market are finding it hard to compete with the international vendors based on quality, reliability, and innovations in technology.

This report segments the Global Testosterone Replacement Therapy market on the basis of types, Gels, Injectables, Patches, Other On the basis of application, the Global Testosterone Replacement Therapy market is segmented into Hospitals, Clinics, Other

Browse full report at: https://www.marketinsightsreports.com/reports/090117112/global-testosterone-replacement-therapy-market-professional-survey-report-2017

This independent 112 page report guarantees you will remain better informed than your competition. With over 165 tables and figures examining the Testosterone Replacement Therapy market, the report gives you a visual, one-stop breakdown of the leading products, submarkets and market leaders market revenue forecasts as well as analysis to 2022.

Geographically, this report is segmented into several key Regions, with production, consumption, revenue (million USD), and market share and growth rate of Testosterone Replacement Therapy in these regions, from 2012 to 2022 (forecast), covering Global, Europe, Japan, China, India , Southeast Asia, Other.

The report provides a basic overview of the Testosterone Replacement Therapy industry including definitions, classifications, applications and industry chain structure. And development policies and plans are discussed as well as manufacturing processes and cost structures.

Then, the report focuses on Global major leading industry players with information such as company profiles, product picture and specifications, sales, market share and contact information. Whats more, the Testosterone Replacement Therapy industry development trends and marketing channels are analyzed.

The research includes historic data from 2012 to 2016 and forecasts until 2022 which makes the reports an invaluable resource for industry executives, marketing, sales and product managers, consultants, analysts, and other people looking for key industry data in readily accessible documents with clearly presented tables and graphs. The report will make detailed analysis mainly on above questions and in-depth research on the development environment, market size, development trend, operation situation and future development trend of Testosterone Replacement Therapy on the basis of stating current situation of the industry in 2017 so as to make comprehensive organization and judgment on the competition situation and development trend of Testosterone Replacement Therapy Market and assist manufacturers and investment organization to better grasp the development course of Testosterone Replacement Therapy Market.

Inquire for sample copy at: https://www.marketinsightsreports.com/reports/090117112/global-testosterone-replacement-therapy-market-professional-survey-report-2017/inquiry

The study was conducted using an objective combination of primary and secondary information including inputs from key participants in the industry. The report contains a comprehensive market and vendor landscape in addition to a SWOT analysis of the key vendors.

There are 15 Chapters to deeply display the Global Testosterone Replacement Therapy market.

Chapter 1, to describe Testosterone Replacement Therapy Introduction, product scope, market overview, market opportunities, market risk, market driving force;

Chapter 2, to analyze the top manufacturers of Testosterone Replacement Therapy, with sales, revenue, and price of Testosterone Replacement Therapy, in 2016 and 2017;

Chapter 3, to display the competitive situation among the top manufacturers, with sales, revenue and market share in 2016and 2017;

Chapter 4, to show the Global market by regions, with sales, revenue and market share of Testosterone Replacement Therapy, for each region, from 2012to 2017;

Chapter 5, 6, 7, 8 and 9, to analyze the key regions, with sales, revenue and market share by key countries in these regions;

Chapter 10 and 11, to show the market by type and application, with sales market share and growth rate by type, application, from 2012 to 2017;

Chapter 12, Testosterone Replacement Therapy market forecast, by regions, type and application, with sales and revenue, from 2017to 2022;

Chapter 13, 14 and 15, to describe Testosterone Replacement Therapy sales channel, distributors, traders, dealers, Research Findings and Conclusion, appendix and data source.

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MarketInsightsReports provides syndicated market research reports to industries, organizations or even individuals with an aim of helping them in their decision making process. These reports include in-depth market research studies i.e. market share analysis, industry analysis, information on products, countries, market size, trends, business research details and much more. MarketInsightsReports provides global and regional market intelligence coverage, a 360-degree market view which includes statistical forecasts, competitive landscape, detailed segmentation, key trends, and strategic recommendations.

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Zika virus kills brain cancer stem cells – Washington University School of Medicine in St. Louis

Posted: September 5, 2017 at 9:49 am

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Virus potentially could be used to treat deadly disease

Brain cancer stem cells (left) are killed by Zika virus infection (image at right shows cells after Zika treatment). A new study shows that the virus, known for killing cells in the brains of developing fetuses, could be redirected to destroy the kind of brain cancer cells that are most likely to be resistant to treatment.

While Zika virus causes devastating damage to the brains of developing fetuses, it one day may be an effective treatment for glioblastoma, a deadly form of brain cancer. New research from Washington University School of Medicine in St. Louis and the University of California San Diego School of Medicine shows that the virus kills brain cancer stem cells, the kind of cells most resistant to standard treatments.

The findings suggest that the lethal power of the virus known for infecting and killing cells in the brains of fetuses, causing babies to be born with tiny, misshapen heads could be directed at malignant cells in the brain. Doing so potentially could improve peoples chances against a brain cancer glioblastoma that is most often fatal within a year of diagnosis.

We showed that Zika virus can kill the kind of glioblastoma cells that tend to be resistant to current treatments and lead to death, said Michael S. Diamond, MD, PhD, the Herbert S. Gasser Professor of Medicine at Washington University School of Medicine and the studys co-senior author.

The findings are published Sept. 5 in The Journal of Experimental Medicine.

Each year in the United States, about 12,000 people are diagnosed with glioblastoma, the most common form of brain cancer. Among them is U.S. Sen. John McCain, who announced his diagnosis in July.

The standard treatment is aggressive surgery, followed by chemotherapy and radiation yet most tumors recur within six months. A small population of cells, known as glioblastoma stem cells, often survives the onslaught and continues to divide, producing new tumor cells to replace the ones killed by the cancer drugs.

In their neurological origins and near-limitless ability to create new cells, glioblastoma stem cells reminded postdoctoral researcher Zhe Zhu, PhD, of neuroprogenitor cells, which generate cells for the growing brain. Zika virus specifically targets and kills neuroprogenitor cells.

In collaboration with co-senior authors Diamond and Milan G. Chheda, MD, of Washington University School of Medicine, and Jeremy N. Rich, MD, of UC San Diego, Zhu tested whether the virus could kill stem cells in glioblastomas removed from patients at diagnosis. They infected tumors with one of two strains of Zika virus. Both strains spread through the tumors, infecting and killing the cancer stem cells while largely avoiding other tumor cells.

The findings suggest that Zika infection and chemotherapy-radiation treatment have complementary effects. The standard treatment kills the bulk of the tumor cells but often leaves the stem cells intact to regenerate the tumor. Zika virus attacks the stem cells but bypasses the greater part of the tumor.

We see Zika one day being used in combination with current therapies to eradicate the whole tumor, said Chheda, an assistant professor of medicine and of neurology.

To find out whether the virus could help treat cancer in a living animal, the researchers injected either Zika virus or saltwater (a placebo) directly into the brain tumors of 18 and 15 mice, respectively. Tumors were significantly smaller in the Zika-treated mice two weeks after injection, and those mice survived significantly longer than the ones given saltwater.

If Zika were used in people, it would have to be injected into the brain, most likely during surgery to remove the primary tumor. If introduced through another part of the body, the persons immune system would sweep it away before it could reach the brain.

The idea of injecting a virus notorious for causing brain damage into peoples brains seems alarming, but Zika may be safer for use in adults because its primary targets neuroprogenitor cells are rare in the adult brain. The fetal brain, on the other hand, is loaded with such cells, which is part of the reason why Zika infection before birth produces widespread and severe brain damage, while natural infection in adulthood causes mild symptoms.

The researchers conducted additional studies of the virus using brain tissue from epilepsy patients and showed that the virus does not infect noncancerous brain cells.

As an additional safety feature, the researchers introduced two mutations that weakened the viruss ability to combat the cells defenses against infection, reasoning that the mutated virus still would be able to grow in tumor cells which have a poor antiviral defense system but would be eliminated quickly in healthy cells with a robust antiviral response.

When they tested the mutant viral strain and the original parental strain in glioblastoma stem cells, they found that the original strain was more potent, but that the mutant strain also succeeded in killing the cancerous cells.

Were going to introduce additional mutations to sensitize the virus even more to the innate immune response and prevent the infection from spreading, said Diamond, who also is a professor of molecular microbiology, and of pathology and immunology. Once we add a few more changes, I think its going to be impossible for the virus to overcome them and cause disease.

Zhu Z, Gorman MJ, McKenzie LD, Chai JN, Hubert CG, Prager BC, Fernandez E, Richner JM, Zhang R, Shan C, Wang X, Shi P-Y, Diamond MS, Rich JN, Chheda MG. Zika Virus Has Oncolytic Activity against Glioblastoma Stem Cells. The Journal of Experimental Medicine. Sept. 5, 2017.

This study was funded by the National Institutes of Health (NIH), grant numbers R01 AI073755, R01 AI104972, CA197718, CA154130, CA169117, CA171652, NS087913 and NS089272; the Pardee Foundation; the Concern Foundation; the Cancer Research Foundation and the McDonnell Center for Cellular and Molecular Neurobiology of Washington University.

Washington University School of Medicines 2,100 employed and volunteer faculty physicians also are the medical staff of Barnes-Jewish and St. Louis Childrens hospitals. The School of Medicine is one of the leading medical research, teaching and patient-care institutions in the nation, currently ranked seventh in the nation by U.S. News & World Report. Through its affiliations with Barnes-Jewish and St. Louis Childrens hospitals, the School of Medicine is linked to BJC HealthCare.

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Revolutionary cancer treatment comes with hefty price tag – Washington Examiner

Posted: September 5, 2017 at 9:49 am

A new cancer treatment will be sold for nearly half a million dollars, sparking criticism from some patient advocates.

On Wednesday, the Food and Drug Administration approved the first gene therapy in the U.S. called Kymriah, which customize a patient's own immune cells to fight a type of leukemia through a therapy called CAR-T.

The drug's maker, Novartis, plans to sell the treatment for $475,000 for the one-time dose.

The company said the price is actually below some independent estimates, including an appraisal from the United Kingdom's National Institute for Cost Effectiveness that pegged a cost-effective price between $600,000 and $750,000.

"We looked at the current standards of care, such as the cost of allogenic stem cell transplants, which is between $540,000-$800,000 for the first year in the U.S.," Novartis said in a statement to the Washington Examiner. "These external assessments as well as our own health economic analysis of the value of Kymriah, all indicated that a cost effective price would be $600,000 to $750,000."

Novartis said that by setting the price below that figure it could help to "support sustainability of the healthcare system and patient access while allowing a return for Novartis on our investment."

It added that it is working with the Centers for Medicare and Medicaid Services for a value-based approach to the drug. That would mean that CMS payments for medicine would be based on how well it works on patients.

But some advocates are upset at the high price tag.

"Kymriah's price tag is simply a continuation of the pattern of sky-high launch prices that spins further out of control each year," according to the Campaign for Sustainable Rx Pricing, an advocacy group that includes insurers, nurses, hospitals and doctors. "While we are very excited about the potential for CAR-T therapies to save lives, Novartis' pricing decision disappointingly pushes an unsustainable trend even closer to the breaking point."

Other groups are more heartened by Novartis' value-based purchasing agreement with CMS.

"While we await more specific details of the agreement reached between Novartis and CMS, we believe this arrangement will be a win for patients, as it recognizes the need to reward outcomes and ensure the cost of treatment is a reflection of its clinical success," said Joel White, president of the Council for Affordable Health Coverage, a coalition of employers, insurers and patient groups.

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Why are Bill Gates and Richard Branson investing in meat that costs $18000 a pound?, by Gene Marks – The Keene Sentinel

Posted: September 5, 2017 at 9:49 am

The world loves meat. So much so that demand for meat products is projected to grow by nearly 70 percent by 2050. But meat production places a significant strain on the planets resources. Research shows that todays meat-producing efforts use one-third of the Earths fresh water and land surface, and generate nearly one-fifth of all greenhouse gas emissions.

But thats not going to stop most of us from eating it because its too darn delicious. The founders behind San Francisco-based Memphis Meats know this, and theyre responding with what could be a disruptive change to the trillion-dollar meat production industry. Memphis Meats is making clean meat. Its also delicious. But theres one problem: It costs about $18,000 a pound.

Well, thats what it costs right now. The hope is that itll cost a lot less in the future. To get the price down to a more palatable level for consumers, the company just raised $17 million (to add to a previous $5 million invested) from the likes of Bill Gates, Richard Branson, and other tech and venture superstars, including food industry giants like Cargill. All of them are super-jazzed by the idea of clean meat.

So what is this stuff?

Its meat thats grown from stem cells in a lab. It uses about 1 percent of the land and 10 percent of the water needed to raise traditional animals and will mostly eliminate the need to feed, breed and slaughter livestock. Plus, the technology works-the company has already produced beef, chicken and duck from stem cells. But, of course, theres a lot more work to do. So the company will be using its newly raised cash to scale up operations and reduce production costs while staffing up-hiring chefs, scientists, creative and business people.

Meat demand is growing rapidly around the world. However, the way conventional meat is produced today creates challenges for the environment, animal welfare and human health, Uma Valeti, the companys chief executive said in a press release. Were going to bring meat to the plate in a more sustainable, affordable and delicious way.

Memphis Meats isnt the only company racing to produce meats in the lab. Competitors like Mosa Foods, Beyond Meats and Impossible Foods (recently featured in a Washington Post piece by Caitlin Dewey) are also working on lab-grown meat products for mass public commercialization. Theres still a long way to go, but the infant industry looks like a great opportunity for both future entrepreneurs and investors. In the meantime, just pass the A-1 sauce, please?

Gene Marks owns the Marks Group, a Bala Cynwyd, Pa.-based consulting firm and writes regularly for The Washington Posts On Small Business blog.

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Eric Brown, BANK VI Hero of the Week – Salina Post

Posted: September 5, 2017 at 9:49 am

It is not everyday that a person gets the opportunity to save someones life. But a forgotten cheek swab over five years ago gave Eric Brown that opportunity. Eric is the BANK VI Hero of the Week.

Eric has worked the Salina Copy Co. for 22 years. Five years ago, while at a Kansas State University football game, he was approached by volunteers who were doing cheek swabs for DKMS, a national bone marrow donor program that works to match donors with cancer patients.

Hesitant at first, Eric finally gave into peer pressure as his friends began filling out the short form and getting their cheeks swabbed.

Eric said he had never even given blood before and was hesitant to even add organ donor to his drivers license but decided to participate anyway.

Five years after being added to the registry, Eric got the call; a 30-year-old Canadian woman with cancer needed a bone marrow transplant and Eric was her only match.

I questioned whether it was even real when I first got the call because they called the office while I was away, Eric said. So I did some research and the timelines matched up. It was all pretty strange at first.

For Eric, there wasnt much of a decision to make. He was flown to Washington, D.C. where he spent six hours in a chair as they collected stem cells from his blood. The stem cells saved the womans life. He later found out that the recipient wouldnt have lived through the end of the month without the transplant.

Eric said the whole experience had a profound affect on him. He has since started working with DKMS, collecting DNA samples through cheek swabs to add people to the registry.

There are about 14,000 people who require this transplant each year and half of them go wanting. Eric said that everyone has a match out there, it is just a matter of finding them and adding them to the registry.

We all have people we are matches with and it is just a matter of time before one of them needs. We were a match all along and it just came to the forefront when she was diagnosed.

Eric said he will continue to put on drives and if anyone is wanting to be added to the registry, they can visit Copy Co. at 2346 Planet Ave for more information.

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Continuing the debate about right-to-die issues in Appleton – Idaho Statesman

Posted: September 4, 2017 at 9:47 am

Nearly one year after Jerika Bolen, the Appleton teenager with an incurable genetic disease, announced her intention to go without a life-sustaining ventilator, experts say her case has had surprisingly minimal impact on the right-to-die debate.

"I fully expected it to continue in the dialogue," said Paul J. Ford, director of the NeuroEthics Program at Cleveland Clinic, about Jerika's story.

Bolen died last September after a lifelong battle with spinal muscular atrophy type 2, which destroys nerves cells in the brain stem and spinal cord that control voluntary muscle activity. She died at Sharon S. Richardson Hospice in Sheboygan Falls, after a final summer that included a prom in her honor in July.

"When I decided, I felt extremely happy and sad at the same time," Jerika told USA TODAY NETWORK-Wisconsin in July 2016. "There were a lot of tears, but then I realized I'm going to be in a better place, and I'm not going to be in this terrible pain."

Jerika's decision drew national attention, including an overwhelming amount of support from well-wishers worldwide. But her story also drew the ire of disability rights groups who attempted to intervene in Jerika's decision to stop treatment.

"It was an exceedingly complicated case," said Arthur Caplan, head of the division of bioethics at New York University's School of Medicine. "(Jerika) was 14, so not quite old enough to be legally able to make her decisions, but old enough that many (medical experts) would say she was old enough to help determine her care."

Jerika was mostly immobile and in chronic pain from SMA. She ranked her pain as a seven on a scale of one to 10 on her best days.

Medications had damaged her body. She had more than 30 visits to operating rooms. She had her spine fused in 2013 and the heads of her femurs removed in 2015.

The day of Jerika's death, Jen Bolen, who declined to be interviewed for this story, told USA TODAY NETWORK-Wisconsin that "no one in their right mind would let someone suffer like she was."

"Suffering is a pretty strong, compelling reason to back away," Caplan said.

Not Dead Yet, a national disability rights group, was one of five disability rights groups that asked authorities to conduct an investigation into Jerika's care.

Diane Coleman, Not Dead Yet's president and CEO, said the groups questioned Jerika's decision to die, as well as the public's response.

"We were trying to be gentle and respectful, but also to say that Jerika had a lot to live for, even if she couldn't yet see that herself," Coleman said.

A letter Not Dead Yet and other disability rights groups wrote in early August 2016 raised questions about Jerika's care and said the teenager was "clearly suicidal." Disability Rights Wisconsin also wrote a letter to Outagamie County child protection authorities.

"For Jerika's case, it really pushes the boundaries between the right to refuse treatment and assisted suicide," Coleman said. "If she had continued using her (ventilator)...things would be different, and she didn't get to get there.

"Almost all of the coverage supported her death. That's what's wrong."

Ford said it's difficult from the outside to understand a person's life and level of suffering.

"(Jerika) went through a lot," Caplan said. "She knows more about that than many people weighing in on what should happen."

Caplan said Jerika's story didn't take on the dimension of Terry Schiavo, a Florida woman who remained in a "persistent" vegetative state for 15 years, or Brittany Maynard, a 29-year-old with brain cancer who relocated to Oregon so she could legally kill herself with medication.

"(Jerika) was saying, 'I've been through so much. I don't want to do this anymore,'" Caplan said. "Which is an important question, but it isn't quite analogous to what happens either when someone requests help in dying or says, 'I don't want to be maintained because I'm so old and so frail that there's no point.' She was in a different situation."

Caplan said Americans are "completely and utterly confused" about right-to-die issues, including how to deal with mental impairment in dying, whether to honor a child's request and even what constitutes death.

"Where views diverge is saying how much suffering is too much to ask someone to bear, and whose responsibility is it to partake in ending a life if it's more suffering than anyone ought to bear," Ford, the Cleveland Clinic ethicist, said.

One of those issues is physician-assisted suicide. Public opinion about the practice remains divided: a 2013 Pew Research Center survey found that 47 percent of Americans approve of laws to allow the practice for the terminally ill, while 49 percent disapprove.

Five states California, Colorado, Oregon, Vermont and Washington and Washington, D.C., have legalized the practice, and Montana recognized it following a state Supreme Court ruling.

Ford said there was "a great energy among states" to continue the legislation for terminally ill adults a year ago.

"Those have sort of taken a backseat, recently," he said.

Earlier this year, Wisconsin State Rep. Sondy Pope introduced legislation, modeled closely after other physician-assisted suicide laws, that would allow terminally ill Wisconsin adults to receive medication to end their lives.

"It's about as restrictive as it could be. ... There are so many safeguards that it's almost impossible to use," Pope said.

Pope, who conceded that the legislation has no immediate chance of becoming law, said she would support legislation to allow a minor who isn't terminal to die with "very, very thoughtful safeguards that include input from loved ones."

"That's way down the road in a case-by-case individual basis ... It doesn't seem right, morally, to say, 'I'm sorry. You're not 18. You have to suffer.'"

___

Information from: Post-Crescent Media, http://www.postcrescent.com

An AP Member Exchange shared by the Post-Crescent.

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Continuing the debate about right-to-die issues in Appleton - Idaho Statesman

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