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Sam Konduros named president and CEO of SC Biotechnology Industry Organization – Greenville News

Posted: March 16, 2017 at 4:42 am

Sam Konduros(Photo: Provided)

Sam Konduros, a former executive director of Greenville Health Systems Research Development Corporation, was named on Monday as the new president and CEO of the S.C. Biotechnology Industry Organization.

SCBIO is a statewide, non-for-profit that represents and organizes innovators in medicine, medical devices and biomaterials.

Konduros is a currently a member of the SCBIO Board of Directors.

I greatlyappreciate the SCBIO boardspassion forservingand advancing South Carolinas rapidly growing life sciences community and industry sector, and for their vote of confidence in my leadership capabilities for the organization going forward, Konduros said in a statement.

Architecture and design firm adds new hire to Greenville office

Verizon looks to fill 100 positions at new telesales center in Greenville

Konduros, a business leader and biomedical and economic development consultant, is the founder of SK Strategies LLC, launched in 2004, and has led a number of state economic development efforts.

He was the founding president and CEO of theUpstate S.C. Alliance, and is a former chairman for the Greenville Chamber of Commerce and a former committee member of the S.C. Chamber of Commerce.

Konduros has a law degree from the University of South Carolina and an undergraduate degree from Clemson University. He is alsoa graduate of the Economic Development Institute at the University of Oklahoma.

Sams strengths in knowing the biotech sector and his deep experience in business and economic development were compelling, Erin Ford, chair of SCBIO, said in a statement. The board was won over by his vision for the growth of SCBIO.

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Waiting to Reprogram Your Cells? Don’t Hold Your Breath – Scientific American

Posted: March 16, 2017 at 4:41 am

Guiding a recent tour of a Kyoto University lab, a staff member holds up a transparent container. Inside are tiny pale spheres, no bigger than peas, floating in a clear liquid. This is cartilage, explains the guide, Hiroyuki Wadahama. It was made here from human iPS cells.

A monitor attached to a nearby microscope shows a mass of pink and purple dots. This is the stuff from which the cartilage was grown: induced pluripotent stem cells, often called iPS cells. Scientists can create these seemingly magical cells from any cell in the body by introducing four genes, in essence turning back the cellular clock to an immature, nonspecialized state. The term pluripotent refers to the fact iPS cells can be reprogrammed to become any type of cell, from skin to liver to nerve cells. In this way they act like embryonic stem cells and share their revolutionary therapeutic potentialand as such, they could eliminate the need for using and then destroying human embryos. Also, iPS cells can proliferate infinitely.

They can also give rise, however, to potentially dangerous mutations, possibly including ones that lead to cancerous tumors. Thus, iPS cells are a double-edged swordtheir great promise is tempered by risk. Another problem is the high cost of treating a patient with his or her own newly reprogrammed cells. But now Japanese researchers are trying a different approach.

When Kyoto University researcher Shinya Yamanaka announced in 2006 that his lab had created iPS cells from mouse skin cells for the first time, biologists were stunned. In 2007, along with James Thomson of the University of WisconsinMadison, Yamanaka repeated the feat with human skin cells. Many hailed the opening of an entirely new field of personalized regenerative medicine. Need new liver cells? No problem. Patients could benefit from having their own cells reprogrammed into ones that could help treat disease, potentially eliminating the prospect of immune rejection. In 2012 Yamanaka shared the Nobel Prize in Physiology or Medicine with John Gurdon for discovering that mature cells can be converted to stem cells. By reprogramming human cells, scientists have created new opportunities to study diseases and develop methods for diagnosis and therapy, the Nobel judges wrote. To capitalize on the discovery, Kyoto University set up the $40-million Center for iPS Cell Research and Application (CiRA), which Yamanaka directs.

A decade after the Yamanaka teams groundbreaking discoveries, however, iPS cells have retreated from the headlines; to the layperson, progress seems scant. There has only been one clinical trial involving iPS cells, and it was halted after a transplant operation on just one patienta Japanese woman in her 70s with macular degeneration, a condition that can lead to blurry vision or partial blindness. Doctors at Kobe City Medical Center General Hospital used her skin cells to grow iPS cells, which were reprogrammed into retinal cells and implanted in her eye. The treatment stopped the degeneration but the trial was halted in 2015 because genetic mutations were detected in another batch of iPS cells intended for another patient. Regulatory changes, under which the Japanese government allowed the distribution of iPS cells for clinical use, also prompted researchers to switch the study to a more efficient process of using cells from third-party donors instead of using a patients own cells. The Japanese government has a lot of incentives to considerwere developing a new science, a new technology and also a new economic market, says CiRA spokesperson Peter Karagiannis. So theres the ethical issues, but theres also money to be made. How do we balance the two?

The Kobe clinical trial had a lot riding on it. And the setback followed a major stem cell scandal in which biologist Haruko Obokata of the Riken Center for Developmental Biology was found to have falsified data in studies, published in 2014, that claimed a new method of achieving pluripotency. Then, earlier this year, Yamanaka had to apologize at a news conference after it was discovered that a reagent used to create iPS cells at CiRA was mislabeled, which could mean the wrong reagent was used. Although the mix-up is being examined, the center has halted supplies of some of its iPS cells to researchers across Japan; the error also set back by a few years a CiRA project to produce clinical-grade platelets from iPS cells.

But Yamanaka says he remains focused on the bigger picture of iPS cells and is still optimistic they can not only help researchers but may be key to transformative clinical therapies. CiRA still has a bank of tens of millions of iPS cells that have already been reset and checked for safety, so they can be used in patient applications. In terms of regenerative medicine, things have gone quicker than I expected, Yamanaka says, adding, iPS cells have exceeded expectations because of their potential for disease modeling, which allows us to elucidate unknown disease mechanisms, and drug discovery.

Those hoping for quick clinical success should remember it takes time for revolutionary treatments to go from lab bench to bedside, says Andras Nagy, a stem cell researcher at Mount Sinai Hospitals LunenfeldTanenbaum Research Institute in Toronto, who has not been directly involved in Yamanakas work. If you fully appreciate the paradigm-shifting nature of iPS cells, tremendous progress has in fact been made over the past 10 years, says Nagy, who in 2009 established a method of creating stem cells without using viruses (which had initially been used to deliver reprogramming genes into targeted cells). By comparison, penicillin was discovered as an antibiotic in 1928, but it was not available in the clinic until the early 1940s.

Researchers in Japan are meanwhile using iPS cell technology to pave the way to better drugs. For instance, CiRAs Kohei Yamamizu recently reported developing a cellular model of the bloodbrain barrier made entirely from human iPS cells. It could become a useful tool for testing drugs for brain diseases.

All eyes, however, are back on Kobe City Medical Center General Hospital, which is resuming its retina trialthis time with iPS cells from donors instead of cells from patients themselves. Using CiRAs bank of iPS cells, there are significant time and cost savingsit could be one fifth the cost of cell preparation and patient transplant or less. The initial study, with its personalized approach, reportedly cost about $875,000 for just one patient. We plan to evaluate the efficacy of transplanting the [donor] cells and consider the feasibility of using this method as a routine treatment in the future, accessible to the wider society, study co-leader Masayo Takahashi of the RIKEN Center for Developmental Biology said at a February press conference in Kobe. Her husband Jun Takahashi, a researcher at CiRA, is also planning to use donor-derived iPS cells for a clinical applicationto help treat patients with Parkinsons disease.

Nagy admits the promise of personalized cell regeneration is probably too costly for mainstream use, and he believes genomic editingin which DNA is inserted or deletedis key to safe iPS cell implants. For his part, Yamanaka is cautiously optimistic about iPS cells as a therapeutic tool.

Regenerative medicine and drug discovery are the two key applications for iPS cells, Yamanaka says. With the use of iPS cell stock, we are now able to work quicker and cheaper, so thats the challenge going forward.

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Antibody fights pediatric brain tumors in preclinical testing | News … – Stanford Medical Center Report

Posted: March 16, 2017 at 4:41 am

The most exciting aspect of our findings is that no matter what kind of brain tumor we tested it against, this treatment worked really well in the animal models, said Cheshier, who is also a pediatric neurosurgeon at Lucile Packard Childrens Hospital Stanford. In mice that had been implanted with both normal human brain cells and human brain cancer cells, there was no toxicity to normal human cells but very, very active tumor-killing in vivo, he said.

Given the encouraging results of the new study and the ongoing research on anti-CD47 antibodies in adults, the antibodies are expected to reach clinical trials in children with brain cancer in one to two years, he added.

The anti-CD47 antibodies help the immune system to detect an important difference between cancerous and healthy cells: Cancer cells make eat me signals that are displayed on their cell surfaces, while healthy cells do not. However, cancer cells hide these eat me signals by producing large quantities of CD47, a dont eat me protein that is found on the surface of both healthy and malignant cells. When CD47 is blocked by antibodies, immune cells called macrophages can detect the cancer cells eat me signals. Macrophages then selectively target, engulf and destroy the cancer cells without harming healthy cells, because normal cells lack the eat me signals.

The Stanford team conducted a long series of experiments using different combinations of tumor cells and healthy cells in culture, as well as in various mouse models in which human brain cancer cells had been implanted in mice. Highlights of their experiments included the following:

The anti-CD47 antibodies did not completely eliminate all tumors, suggesting that the antibodies may not be able to completely penetrate large tumors, the researchers noted.

To maximize their effects, the antibodies will likely need to be combined with other forms of cancer treatment, a concept the researchers plan to investigate further, Cheshier said. In the future, patients may receive combinations of immune therapies and lower doses of standard cancer treatments, he said, adding, The question is: Can we wisely combine immune therapies and other approaches to make cancer treatment more efficacious and less toxic?

Anti-CD47 antibodies also may have an advantage over other immunotherapies in that they activate macrophages, which completely engulf and eat cancer cells, Cheshier noted. In many forms of immunotherapy, the cells you target die and spill their contents, which can cause dysregulated immune responses, he said. Anti-CD47 antibodies may produce fewer such side effects, though the idea remains to be tested.

Other Stanford co-authors of the paper are medical students Abdullah Feroze, Rogelio Esparza and Michael Zhang; postdoctoral scholars Suzana Kahn, PhD, Anne Volkmer, MD and Stephen Willingham, PhD; research assistants Anitha Ponnuswami, Theresa Storm, Cyndhavi Narayanan and Pauline Chu; senior research associate Jie Liu, MD, PhD; undergraduate research associate Chase Richard; Aaron McCarthy, a former life sciences research professional and animal colony manager; Patricia Lovelace, research and development engineer; Simone Schubert, life science researcher; visiting scholar Gregor Hutter, MD, PhD; Griffith Harsh, MD, professor of neurosurgery; Michelle Monje, MD, PhD, assistant professor of neurology; Yoon-Jae Cho, MD, a former assistant professor of neurology and neurological sciences; Ravi Majeti, MD, PhD, associate professor of medicine; senior scientist Jens Volkmer, MD; Paul Fisher, MD, professor of pediatrics; Gerald Grant, MD, associate professor of neurosurgery; Gary Steinberg, MD, PhD, professor of neurosurgery; Hannes Vogel, MD, professor of pathology and of pediatrics; and Michael Edwards, MD, professor of neurosurgery.

Cheshier, Monje, Majeti, Fisher, Grant and Edwards are members of Stanfords Child Health Research Institute. Cheshier, Weissman, Harsh, Monje, Majeti, Fisher, Grant, Vogel and Edwards are members of the Stanford Cancer Institute. Weissman is the director of the Stanford Institute for Stem Cell Biology and Regenerative Medicine and of the Ludwig Center for Cancer Stem Cell Research and Medicineat Stanford.

Scientists from SickKids, the Hospital for Sick Children in Toronto; University Hospital, Dusseldorf; and Johns Hopkins University also contributed to the study.

The study was funded by National Institute of Neurological Disorders and Stroke (grant NINDSK08NS070926); the National Cancer Institute (grant P30CA006973); the California Institute for Regenerative Medicine; the Price Family Charitable Fund; the Center for Childrens Brain Tumors at Stanford; St. Baldricks Foundation; the American Brain Tumor Foundation; the Seibel Stem Cell Institute; the Pew Charitable Trusts; the Dr. Mildred-Scheel Foundation/German Cancer Aid; the German Research Foundation; the McKenna Claire Foundation; the Matthew Larson Foundation; Alexs Lemonade Stand Foundation; The Cure Starts Now; the Lyla Nsouli Foundation; the Dylan Jewett, Connor Johnson, Zoey Ganesh, Dylan Frick, Abigail Jensen, Wayland Villars and Jennifer Kranz memorial funds; the Virginia and D. K. Ludwig Fund for Cancer Research; the Lucile Packard Foundation for Childrens Health; the National Institutes of Health (grant UL1TR001085); the Tashia and John Morgridge Endowed Pediatric Faculty Scholar and Fellowships Awards; and the Anne T. and Robert M. Bass Endowed Faculty Scholarship in Pediatric Cancer and Blood Diseases. The study was also funded by gifts from George Landegger; Rider and Victoria McDowell; Charles Comey and Judith Huang; and Colin and Jenna Fisher.

Stanfords Department of Neurology & Neurological Sciences also supported the work.

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At 6th Annual Clinical Trial Supply New England 2017 Conference in Boston Asymmetrex Introduces A First Specific … – Benzinga

Posted: March 16, 2017 at 4:41 am

On March 8-9 in Boston, stem cell medicine biotechnology start-up Asymmetrex led attendees at the 6th Annual Clinical Trials Supply New England 2017 conference in discussions about the need for quality controls for the supply of tissue stem cells used for treatments in either FDA-approved clinical trials or unregulated private stem cell clinics. Though these two stem cell treatment settings are often contrasted regarding their safety and effectiveness, Asymmetrex stressed that patient care and research progress is compromised in both because of the lack of essential quality control tests for the number and quality of transplanted tissue stem cells.

Boston, MA (PRWEB) March 14, 2017

At the 6th Annual Clinical Trials Supply New England 2017 conference, held in Boston from March 8-9, James Sherley, M.D., Ph.D., director of Asymmetrex, led discussions that evaluated the quality of U.S. supplies of stem cells used in clinical trials compared to private stem cell clinics. Private stem cell clinics have been criticized for not employing research standards that are necessary to establish the therapeutic effectiveness of treatments with statistical confidence. In part because of this difference in practice, they are also often accused of making unproven claims about the effectiveness of their therapies.

Sherley presented comparisons of key operational elements to argue that, given good intent in both settings, the two different settings of stem cell treatments had both distinct and shared shortcomings. He noted, however, that the most significant shortcoming, which stem cell clinical trials and private stem cell clinics share, was perennially overlooked.

Based on the number of reported stem cell clinical trials and private stem cell clinics, Sherley estimated that close to a quarter-million patients in the U.S. now receive stem cell treatments each year. Though many of these occur within FDA-approved clinical trials, their number is dwarfed nearly 10 times by the number of treatments that occur in private stem cell clinics. It shocked the audience of clinical trial suppliers to learn that there was no stem cell quality control test performed for any of these many treatments.

Even for approved stem cell medicine treatments like bone marrow transplantation and umbilical cord blood transplant, there is no stem cell-specific quality control test available. Counts of total cells are made, but these do not adequately predict stem cell number or function. Biomarkers designated for tissue stem cells are also expressed by stem cells' more abundant non-stem cell products. So, the biomarkers lack sufficient specificity to be used to count and monitor tissue stem cell function.

Without a quality control test for tissue stem cell number, stem cell treatments in all settings proceed without knowing the dose of treating tissue stem cells. This previously unavoidable therapeutic blind spot creates an instant treatment risk. It also precludes effective analyses to optimize treatment procedures, to compare different treatments, or to relate treatment outcomes to tissue stem cell dose. Without knowing stem cell dose, the interpretation of any stem cell treatment in terms of stem cells as the responsible agents is compromised.

In this context, Sherley announced briefly to attendees that Asymmetrex's new AlphaSTEM Test for counting adult tissue stem cells and providing data on their viability and tissue cell renewal function represented the needed first quality control test for tissue stem cell treatments, whether in clinical trials, in private stem cell clinics, or approved therapies. In particular, he indicated that both stem cell treatment patients and progress in stem cell medicine would benefit from existing clinical trial supply companies developing into future private stem cell clinic supply companies to insure the quality of stem cell treatment preparations. Sherley said that, of course, their partnership with Asymmetrex to implement its new stem cell-specific quality control test was an all around best solution for accelerating progress in stem cell transplantation medicine.

About Asymmetrex

Asymmetrex, LLC is a Massachusetts life sciences company with a focus on developing technologies to advance stem cell medicine. Asymmetrex's founder and director, James L. Sherley, M.D., Ph.D. is an internationally recognized expert on the unique properties of adult tissue stem cells. The company's patent portfolio contains biotechnologies that solve the two main technical problems production and quantification that have stood in the way of successful commercialization of human adult tissue stem cells for regenerative medicine and drug development. In addition, the portfolio includes novel technologies for isolating cancer stem cells and producing induced pluripotent stem cells for disease research purposes. Currently, Asymmetrex's focus is employing its technological advantages to develop and market facile methods for monitoring adult stem cell number and function in stem cell transplantation treatments and in pre-clinical assays for drug safety.

For the original version on PRWeb visit: http://www.prweb.com/releases/2017/03/prweb14146903.htm

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3 Women Blinded By Unproven Stem Cell Treatments – NPR

Posted: March 16, 2017 at 4:41 am

Scientists have long hoped that stem cells might have the power to treat diseases. But it's always been clear that they could be dangerous too, especially if they're not used carefully.

Now a pair of papers published Wednesday in the New England Journal of Medicine is underscoring both the promise and the peril of using stem cells for therapy.

In one report, researchers document the cases of three elderly women who were blinded after getting stem cells derived from fat tissue at a for-profit clinic in Florida. The treatment was marketed as a treatment for macular degeneration, the most common cause of blindness among the elderly. Each woman got cells injected into both eyes.

In a second report, a patient suffering from the same condition had a halt in the inexorable loss of vision patients usually experience, which may or may not have been related to the treatment. That patient got a different kind of stem cell derived from skin cells as part of a carefully designed Japanese study.

The Japanese case marks the first time anyone has given induced pluripotent stem (iPS) cells to a patient to treat any condition.

"These two reports are about as stark a contrast as it gets," says George Q. Daley, Harvard Medical School's dean and a leading stem cell researcher. He wrote an editorial accompanying the two papers. "It's really striking."

The report about the three women in their 70s and 80s who were blinded in Florida is renewing calls for the Food and Drug Administration to crack down on the hundreds of clinics that are selling unproven stem cell treatments for a wide variety of medical conditions, including arthritis, autism and stroke.

"One of the big mysteries about this particular case and the mushrooming stem cell clinic industry more generally is why the FDA has chosen to effectively sit itself out on the sidelines even as this situation overall grows increasingly risky to patients," says Paul Knoepfler, a University of California, Davis, stem cell researcher who has studied the proliferation of stem cell clinics.

"The inaction by the FDA not only puts many patients at serious risk from unproven stem cell offerings, but also it undermines the agency's credibility," Knoepfler wrote in an email.

In response to a query from Shots, an FDA spokeswoman wrote in an email that the agency is in the process of finalizing four new guidelines aimed at clarifying how clinics could use stem cells as treatments. The agency also noted that it had previously issued a warning to patients.

In the meantime, "consumers are encouraged to contact FDA and the appropriate state authorities in their jurisdictions to report any potentially illegal or harmful activity related to stem cell based products," the FDA email says.

Other researchers say the cases should stand as a warning to patients considering unproved stem cell treatments, especially those tried outside carefully designed research studies.

"Patients have to be wary and tell the difference between the snake oil salesmen who are going to exploit them and the kind of slow, painstaking legitimate clinical trials that are also going on," Daley says.

The New England Journal of Medicine report did not name the Florida clinic, but noted that the treatment was listed on a government website that serves as a clearinghouse for research studies. The sponsor is listed as Bioheart, Inc., which is part of U.S. Stem Cell Inc. in Sunrise, Fla.

Kristen Comella, the scientific director of U.S. Stem Cell, would not discuss the cases. "There were legal cases associated with eye patients that were settled under confidentiality, so I am not permitted to speak on any details of those cases due to the confidentiality clause," Comella said by phone.

She acknowledged, however, that the clinic had been performing the stem cell procedures. They were discontinued after at least two patients suffered detached retinas, she says.

But Comella defended the use of stem cells from fat tissue to treat a wide variety of other health problems.

"We have treated more than 7,000 patients and we've have had very few adverse events reported. So the safety track record is very strong," Comella says. "We feel very confident about the procedures that we do, and we've had great success in many different indications."

According to the New England Journal of Medicine report, The Florida clinic was using adult stem cells, which circulate in various parts of the body, including in fat tissue. While those cells may someday be turn out to be useful for treating disease, none have been proven to work.

The body produces a variety of stem cells. The kind that have generated the most excitement and controversy are human embryonic stem cells, which are derived from early human embryos and can be coaxed to become any kind of cell in the body.

Scientists are also excited about iPS cells, which can be made in the laboratory by turning any cell in the body, such as skin cells, into cells that resemble embryonic stem cells.

Those are the cells that were tested by the Japanese scientists. The stem cells were converted into retinal pigment epithelium (RPE) cells, which are the cells that are destroyed by macular degeneration.

"This represents a landmark," says Daley. "It's the first time any patient has been treated with cellular derivatives of iPS cells. So it's definitely a world first."

Daley noted that the scientists only treated one of the patient's eyes in case something went wrong, to ensure remaining vision would not be threatened in the other eye.

After at least a year, no complications had occurred and the patient had not experienced any further deterioration of vision in the treated eye. While that is promising, more patients would have to be treated and followed for much longer to know whether that approach is successful, Daley says.

"Given that macular degeneration is the most frequent cause of vision loss and blindness in the elderly and our population is aging, the prevalence of macular degeneration is going up dramatically," Daley says. "So to be able to preserve or even restore sight would be a really remarkable medical advance."

Despite the potentially encouraging results with the first patient, Daley noted that the Japanese scientists decided not to treat a second patient and suspended the study. That's because they discovered worrisome genetic variations in the RPE cells they had produced for the second patient.

"They weren't certain these would cause problems for the patient, but they were restrained enough and cautious enough that they decided not to go forward," Daley says. "That's what contrasts so markedly with the approach of the second group, who treated the three patients with an unproven stem cell therapy that ended up have devastating effects on their vision."

In this case, the New England Journal of Medicine report says, patients paid $5,000 each to receive injections of solutions that supposedly contained stem cells that were obtained from fat removed from their abdomens through liposuction.

Even though the safety and effectiveness of this procedure is unknown, all three patients received injections in both eyes.

"That's what led to these horrible results," says Thomas Albini, a retina specialist at the University of Florida's Bascom Palmer Eye Institute, who helped write the report.

Before the procedure, all three women still had at least some vision. Afterwards, one woman was left completely blind while the other two were effectively blind, Albini and his colleagues reported.

The cases show that patients need to be warned that something that "sounds too good to be true may indeed be too good to be true and may even be horrible," Albini says.

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Mesoblast’s (MESO) Regenerative Cell Therapy Proves Itself in Back Pain Trial – Economic Calendar

Posted: March 16, 2017 at 4:41 am

This morning, Australian biotech company Mesoblast Ltd (NASDAQ:MESO) announced encouraging phase 2 trial data regarding its regenerative therapy for chronic lower back pain (CLBP). Mesoblasts proprietary allogeneic Mesenchymal Precursor Cells (MPCs) are given to patients via a single injection and, in the clinical trial, have proved to spark significant improvement in both lower back pain and function that lasted for at least 36 months.

The sustained benefits on pain and function over three years seen with a single injection of Mesoblasts cell therapy have the potential to transform the treatment paradigm for chronic low back pain due to disc degeneration, said Dr. Hyun Bae, the trial investigator and Director of the Spine Institute.

According to Bae, there is growing evidence that disc degeneration can be healed instead of needing to be replaced or fused. Researchers are quickly arriving at this inflection point in the treatment of lower back pain, which is especially critical given the ongoing opioid abuse epidemic sweeping the nation.

Researchers believe that MPCs are turned on by signals in damaged tissues that spark factors to block damaging inflammation and begin repairing the afflicted area.

The phase 2 trial in question involved 100 patients, who were treated with either six million or 18 million MPCs via one intra-discal injection or a placebo of either saline or hyaluronic aid. The primary endpoints were a 50 percent drop in Visual Analog Scale (CAS), which is a pain metric, and a 15-point reduction in Oswestry disability index (ODI) at both the one and two year marks.

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The primary endpoint composite at the two-year mark was met by 41 percent of patients in the 6 million MPC arm, 35 percent in the 18 million arm, with just 18 percent and 13 percent in the placebo groups. The phase 2 results support the companys criteria for its ongoing phase 3 program.

Mesoblast is confident that the durable treatment outcomes in lower back pain are part of an overarching mechanism that might also have a positive effect in other types of chronic conditions where a single injection of MPCs can lead to sustained benefits. Two of these potential indications, according to Mesoblast, are chronic heart failure and biological-resistant rheumatoid arthritis.

Following the trial data being released, Maxim Groups Jason Kolbert reaffirmed a Buy rating on Mesoblasts stock and maintained a price target at $14.00. The upside indicated is 81 percent.

The market opportunity is significant and the treatment fits ideally within the existing paradigm the analyst told investors this morning. Injecting cells versus steroids with a better AE profile and now a better long-term result.

Earlier this month, Mesoblast announced that its MSC-100-IV therapy had been given Fast Track designation by the Food and Drug Administration (FDA) for its use in children with steroid refractory acute Graft Versus Host Disease (aGVHD). This type of designation shortens the FDA review path from ten months to six months, and certain portions of the Biologics License Application (BLA) can be sent in on a rolling basis rather than when everything is finished.

The author of this article holds no position in any of the stocks mentioned above.

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Free diabetes self-management workshops offered in Pleasantville – Shore News Today

Posted: March 16, 2017 at 4:40 am

PLEASANTVILLE Quality Insights Quality Innovation Network, supported locally by Healthcare Quality Strategies Inc., is partnering with Pleasantville to provide free diabetes workshops as part of the Everyone with Diabetes Counts program.

The EDC program is a national initiative of the Centers for Medicare and Medicaid Services.

The program offers free self-management workshops for people with Medicare who have diabetes, their family members and caregivers.

The free workshops follow the Stanford University Diabetes Self-Management Program.

The workshops are designed to help individuals learn how to manage their diabetes and take control of their health through behavior modification and coping techniques. Participants will learn about diabetes and its risks, preventing complications, the importance of healthy eating, the role of exercise, how to deal with stress and difficult emotions, managing medications, effective communication with healthcare providers, and much more.

This free six-week workshop will be offered at the Pleasantville Branch Library, 33 Martin Luther King Jr. Ave.

Workshops are 10 a.m. to 12:30 p.m. Tuesdays from April 11 to May 16.

Everyone must register by the second workshop session.

Each participant, one per household, will receive a free book, Living a Healthy Life with Chronic Conditions at the second workshop session.

For information or to register, call Jarmaine Williams at 732-955-8168. Visit http://www.qualityinsights-qin.org to learn more about Quality Insights Quality Innovation Network, or to read real success stories about people with diabetes in New Jersey who have completed this program and made motivational improvements to their health and lives.

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Intensive Type 2 Diabetes Treatment Promising – WebMD

Posted: March 16, 2017 at 4:40 am

By Karen Pallarito

HealthDay Reporter

WEDNESDAY, March 15, 2017 (HealthDay News) -- Instead of managing type 2 diabetes as a chronic condition, what if people could beat the disease?

That was the thinking behind a small pilot study, which suggested that intensive treatment with oral medicine, insulin, diet and exercise might knock out the disease, at least for several months, in certain patients.

Up to 40 percent of patients who were treated experienced complete or partial remission for three months, the study found.

"We are now able to possibly reverse diabetes, and that really motivates patients to do their best in terms of losing weight and making sure their sugars are normalized," said lead author Dr. Natalia McInnes.

She's an assistant professor of endocrinology and metabolism at McMaster University in Ontario, Canada.

However, relatively few participants remained in remission a year later, diabetes experts noted.

"Rates of diabetes remission did not appear to differ significantly at 52 weeks between 'control' and 'intervention' groups, so the effects do not appear to be sustained," said Dr. Christine Lee of the U.S. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).

And, Dr. Philip Kern, professor of endocrinology at the University of Kentucky in Lexington, added, "If you don't sustain the lifestyle intervention, then the disease is going to come back."

The bodies of people with type 2 diabetes don't use insulin properly. Insulin is a hormone that helps move sugar into cells to be used as fuel. At first, the body responds by making more insulin, but eventually, your body cannot make enough insulin to keep up with the demand. This leads to increasing blood sugar levels. Over time, uncontrolled blood sugar levels can damage the nerves, eyes, kidneys or heart, according to the American Diabetes Association.

Adults newly diagnosed with type 2 diabetes were invited to participate in the trial. Each was randomly assigned to receive either two months or four months of treatment, or "usual diabetes care" (the control group).

The trial included 83 people, aged 30 to 80 years. The participants had had type 2 diabetes for up to three years, and managed their diabetes with diet alone or with one or two drugs. People already taking insulin were excluded from the study.

Senior investigator Dr. Hertzel Gerstein of McMaster University devised the drug combo used in the trial, McInnes said.

Patients received two oral diabetes medicines -- metformin (Glucophage, Glumetza, Fortamet) and acarbose (Precose) -- plus a long-acting type of injectable insulin called insulin glargine (Lantus), based on evidence that these drugs can slow or prevent diabetes, Gerstein explained in a news release from the Endocrine Society.

Once the experiment began, the two intervention groups stopped other diabetes medicines and started the new regimen, according to the report.

A dietician provided a suggested meal plan, encouraging patients to cut 500 to 750 calories a day.

A kinesiologist (body movement expert) prescribed individual fitness programs with a goal of 150 minutes of moderate-intensity exercise per week, by week 16 of the trial. Patients were also given pedometers and instructed to work toward 10,000 steps per day.

Control group members received standard blood-sugar management advice, the study authors noted.

Hemoglobin A1c tests, which measure average blood sugar levels over the past two to three months, were administered at four points during the study. An A1c level below 5.7 percent is considered normal, according to the American Diabetes Association.

In the study, complete remission was defined as an A1c under 6.0 percent and no need for diabetes medication. Partial remission was an A1c of less than 6.5 percent and no need for diabetes medication.

Three months after the intervention, 11 out of 27 people in the 16-week study group experienced complete or partial diabetes remission, versus six out of 28 in the eight-week study group, and four out of 28 in the control group, the researchers found.

It isn't clear whether the diabetes remission was due to medical therapy with drugs or weight loss with intensive lifestyle therapy, said NIDDK's Lee, who is program director in the diabetes, endocrinology and metabolic diseases division.

The study authors didn't evaluate the cost of the intervention versus potential cost savings. McInnes suspects it would save money in the long term if it reversed the disease and prevented expenses related to ongoing diabetes care and complications.

She said additional studies are needed to assess whether it's possible to achieve higher, and prolonged, rates of remission with similar combinations of therapies.

Kern said the study serves as a reminder that lifestyle interventions in diabetes "really do work."

The study was published online March 15 in the Journal of Clinical Endocrinology & Metabolism.

WebMD News from HealthDay

SOURCES: Natalia McInnes, M.D., assistant professor, endocrinology and metabolism, department of medicine, McMaster University, Ontario, Canada; Christine Lee, M.D., program director, division of diabetes, endocrinology and metabolic diseases, U.S. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Md.; Philip Kern, professor of endocrinology, University of Kentucky, Lexington; March 15, 2017, Journal of Clinical Endocrinology & Metabolism, online

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Intensive Type 2 Diabetes Treatment Promising - WebMD

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Scientists Reverse Type 2 Diabetes with Intensive Medical Treatment – Voice of America

Posted: March 16, 2017 at 4:40 am

Scientists have reversed Type 2 diabetes in a study of patients who underwent intensive medical treatment to control their blood sugar levels.

By following a regimen of strict diet, exercise and medications, up to 40 percent of the participants managed to stay in remission for three months after stopping their medication.

The research was conducted by investigators at McMaster University in Ontario, Canada.

Researchers divided 83 individuals with Type 2 diabetes into three groups. Two of the groups received intensive metabolic intervention that included a personalized meal plan that cut their daily caloric intake by 500 to 750 calories per day. They were also given an individualized exercise plan, met with a dietitian regularly and took medication and insulin at bedtime to help control blood glucose.

The only difference is one group was intensively treated for 16 weeks while the other group received the same intervention for just eight weeks.

They were compared to a third group of participants that was given standard diabetic management information from a health care provider, including lifestyle advice.

All of the participants had their blood glucose measured at 20, 28 and 52 weeks to see how well their blood sugar was controlled.

After eight and 16 weeks of the intensive intervention, medication was stopped in both groups.

In the 16-week group, 11 of 27 participants met the criteria for complete or partial remission of their diabetes for a period of three months after the trial.

In the eight-week intensive therapy group, six out of 28 individuals were in remission for three months after the intervention was completed. Only four out of 28 patients in the control group showed remission.

The results of the study were published in the Journal of Clinical Endocrinology and Metabolism.

Could change diabetes treatment

Lead researcher Natalia McInness thinks the finding may shift the way adults with diabetes are treated from simply managing their blood sugar levels to a program of intensive therapy to put the disease into remission. Under that strategy, patients would be watched for signs of relapse and treated accordingly.

In Type 2 diabetes, the body either doesnt make enough of the hormone insulin, in severe cases, to ferry nutrients into cells or the cells become resistant to insulin.

Either way, McInness believes the intensive therapy intervention gives the pancreas a rest, decreasing fat stores in the body that in turn improve insulin production and sensitivity. The pancreas is the organ that produces insulin.

She said the findings support the notion that Type 2 diabetes can be reversed, at least in the short term, through strict medical management. The idea of putting diabetic patients into remission, said McInness, could be very appealing, motivating them to make significant lifestyle changes.

Diabetes is a growing epidemic worldwide and patients struggle to maintain blood sugar levels in the normal range to avoid severe complications like heart disease, blindness and kidney failure.

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Scientists Reverse Type 2 Diabetes with Intensive Medical Treatment - Voice of America

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Whole-body Vibration May Improve Diabetes Control, Study Finds – Voice of America

Posted: March 16, 2017 at 4:40 am

Researchers have found that a less strenuous form of exercise known as whole-body vibration may work just as well as regular exercise in helping to control diabetes. WBV, as it's called, could also benefit people who find it difficult to exercise.

Scientists say WBV transmits energy through the body when someone is standing, sitting or lying on a gently vibrating device, causing muscles to contract and relax many times each second.

The effect may be to strengthen and increase muscle mass, improving blood sugar control along with other problems seen in diabetes. At least, that's what studies in mice suggest.

Bearing in mind that exercise is good for everyone, including people with diabetes, researchers at Augusta University in Augusta, Georgia, studied five-week-old male rodents, comparing the effects of whole-body vibration to that of running on a treadmill.

Vibrating platform

A cage containing both normal and specially bred obese, diabetic mice was placed on a gently vibrating platform for 20 minutes per day for 12 weeks.

Another group of rodents both diabetic and healthy mice was trained to run on a treadmill for 45 minutes a day for the same period of time.

A third group of diabetic and healthy mice remained sedentary and were used for comparison.

Investigators saw similar health benefits in the diabetic mice that ran on the treadmill and those exposed to whole-body vibration.

Meghan McGee-Lawrence, an assistant professor in the Department of Cellular Biology and Anatomy at the Medical College of Georgia, said the results of the study showed that "vibration may be just as effective as exercise at combating some of the negative consequences of obesity and diabetes."

Biomarker improvements

McGee-Lawrence said mice subjected to whole-body vibration and those that ran on the treadmill were both able to decrease fat in the liver, improve insulin sensitivity and increase muscle fiber.

While there was improvement in the biomarkers of diabetic WBV mice and treadmill mice, they never became as healthy as the normal animals.

During the study, the mice were weighed weekly. Researchers found that the diabetic mice subjected to vibration and the treadmill gained less weight after the study was over than the sedentary rodents.

There was also evidence that whole-body vibration might improve the bone strength of diabetics.

The study was published in the journal Endocrinology.

McGee-Lawrence said researchers are now trying to determine the mechanisms that underlie improved diabetes control in both exercise and whole-body vibration mice.

More study urged

There are vibrating chairs and beds available on the market, but McGee-Lawrence cautioned people against starting a routine of whole-body vibration and thinking they are controlling their diabetes.

"We know that some whole-body vibration ... seems to be good for the body, but too much can be a bad thing," she said. "And in terms of finding ways to apply that [to humans] ... I think we need some more studies to guide us on that so that when folks start doing this, we get the best beneficial effects we can without running the risk of having any potential side effects."

One potential harm of too much vibration, often seen heavy-machine operators, is tissue inflammation.

If researchers are able to repeat the results in humans, McGee-Lawrence said, whole-body vibration could be a useful add-on to the treatment of diabetes.

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Whole-body Vibration May Improve Diabetes Control, Study Finds - Voice of America

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