Author Archives: admin


Innovative Biosensor Technology for Stem Cells Leads Way to Treatment of Alzheimers, Parkinsons Diseases – SciTechDaily

This unique biosensing platform consists of an array of ultrathin graphene layers and gold nanostructures. The platform, combined with high-tech imaging (Raman spectroscopy), detects genetic material (RNA) and characterizes different kinds of stem cells with greater reliability, selectivity and sensitivity than todays biosensors. Credit: Letao Yang, KiBum Lee, Jin-Ho Lee and Sy-Tsong (Dean) Chueng

A Rutgers-led team has created better biosensor technology that may help lead to safe stem cell therapies for treating Alzheimers and Parkinsons diseases and other neurological disorders.

The technology, which features a unique graphene and gold-based platform and high-tech imaging, monitors the fate of stem cells by detecting genetic material (RNA) involved in turning such cells into brain cells (neurons), according to a study in the journal Nano Letters.

Stem cells can become many different types of cells. As a result, stem cell therapy shows promise for regenerative treatment of neurological disorders such as Alzheimers, Parkinsons, stroke and spinal cord injury, with diseased cells needing replacement or repair. But characterizing stem cells and controlling their fate must be resolved before they could be used in treatments. The formation of tumors and uncontrolled transformation of stem cells remain key barriers.

A critical challenge is ensuring high sensitivity and accuracy in detecting biomarkers indicators such as modified genes or proteins within the complex stem cell microenvironment, said senior author KiBum Lee, a professor in the Department of Chemistry and Chemical Biology in the School of Arts and Sciences at Rutgers University-New Brunswick. Our technology, which took four years to develop, has demonstrated great potential for analyzing a variety of interactions in stem cells.

The teams unique biosensing platform consists of an array of ultrathin graphene layers and gold nanostructures. The platform, combined with high-tech imaging (Raman spectroscopy), detects genes and characterizes different kinds of stem cells with greater reliability, selectivity, and sensitivity than todays biosensors.

The team believes the technology can benefit a range of applications. By developing simple, rapid and accurate sensing platforms, Lees group aims to facilitate treatment of neurological disorders through stem cell therapy.

Stem cells may become a renewable source of replacement cells and tissues to treat diseases including macular degeneration, spinal cord injury, stroke, burns, heart disease, diabetes, osteoarthritis, and rheumatoid arthritis, according to the National Institutes of Health.

###

Reference: Dual-Enhanced Raman Scattering-Based Characterization of Stem Cell Differentiation Using Graphene-Plasmonic Hybrid Nanoarray by Letao Yang, Jin-Ho Lee, Christopher Rathnam, Yannan Hou, Jeong-Woo Choi and Ki-Bum Lee, 30 October 2019, Nano Letters.DOI: 10.1021/acs.nanolett.9b03402

The studys co-lead authors are Letao Yang and Jin-Ho Lee, postdoctoral researchers in Lees group. Rutgers co-authors include doctoral students Christopher Rathnam and Yannan Hou. A scientist at Sogang University in South Korea contributed to the study.

Read this article:
Innovative Biosensor Technology for Stem Cells Leads Way to Treatment of Alzheimers, Parkinsons Diseases - SciTechDaily

Shark Tank Season 11 Episode 8 Everything About Gallant Stem Cell Bank For Dogs As Seen on Shark Tank! Unknown Facts – TheNewsCrunch

Gallant Stem Cell Therapy For Dogs is one of the product companies to be featured on Shark Tank Season 11 Episode 8. The story behind the birth of Gallant Stem Cell Therapy For Dogs is pretty interesting. Here are some of the unknown facts about Gallant and its founders, Aaron Hirschhorn.

Aaron Hirschhorn is the founder and former-CEO of the popular dog-sitting marketplace DogVacay. Aaron is a noted entrepreneur with more than 20 years of experience in building companies and investing in them. DogVacay app was launched in 2013 and Aaron managed to raise $47 million from his erstwhile investors.

Aaron was the finalist in the Ernst & Young Entrepreneur of the Year Award 2016. In April 2017, Aarons DogVacay app merged with Rover.com and eventually went on to become a $1 billion pet services marketplace.

Trouble struck Aarons life when he suffered a massive back injury and was forced to undergo stem cell treatment which yielded amazing results to his surprise. Aaron, being an ardent dog lover wondered why this cutting-edge medical technology of stem cell transplants cannot be applied to dogs.

As a result, Gallant was born in the middle of 2018. According to Gallant, Your pups stem cells haveincredible healing power. Extract and store these powerful cells during your pets spay/neuter, so that you can unleash their potential when your best friend needs it most.

Ever since its inception, the mission of Gallant stem cell therapy is to help pets live a healthier life and make use of the epic technology of stem cell therapy in saving the lives of tons of dogs.

Dogs enter their senior years around 7 and begin feeling the effects of aging as early as 4! Traditional methods of treatment for injury and age-related conditions are expensive and can have harmful side effects. Stem cells are incredible natural healers. However, up to 99% of stem cells are lost over time due to aging. This forms the bottomline of Gallants business problem.

Gallant raised $7 million investment in August 2019.

https://gallant.com/

From the moment you entrust Gallant with your dogs stem cells, were actively invested in their long-term health and well-being. Working in tandem with you and your veterinarian, we will collect and store these powerful cells now, so down the road we can help to treat the most common health problems your dog may face. We will also update you on new and potentially life-changing treatments as they become available.

Pick your pups stem cell storage plan you dont have to have a spay/neuter procedure scheduled yet! You can always add that in later. Our proprietary process requires no additional training, so any veterinarian you trust to alter your dog is qualified. Ahead of your dogs spay/neuter, we will connect with your vet and send our collection kit directly to their office.

2. Collect

On the big day, we align with your vet before the procedure and arrange for a courier. During your dogs spay/neuter procedure, your veterinarian will take out the stem cell-rich reproductive tissue they would normally discard into the collection kit.

3. Preserve

Once the tissue is received by our scientists, we send confirmation to both you and your veterinarian. Your dogs tissue is first inspected for quality before isolating the stem cells. The stem cells are then counted and frozen in liquid nitrogen to preserve their potency in our secure, state-of-the-art laboratory. Once this process is complete, you and your veterinarian will be notified that your pets stem cells are safely stored. The cells are then monitored by our team to ensure they stay perfectly preserved.

4. Treat

Your pets stem cells are at the ready to be sent to your veterinarian if/when treatment is needed. Treatments are out-patient procedures and cost about $300. A stem cell procedure is not painful to your pet and does not require anesthesia to administer.

Gallants stem cell therapy is receiving a lot of exciting reviews online. The therapy has been successful in saving scores of dogs with conditions like osteoarthritis, skin conditions, chronic dry eye.

Gallant is offering a $395 off discount for using the code SHARKTANK

How did Gallant fare in Shark Tank Season 11? What did the Sharks have to tell about it? Did Gallant Get a Deal on Shark Tank? More information to be updated soon in this post.

Read more:
Shark Tank Season 11 Episode 8 Everything About Gallant Stem Cell Bank For Dogs As Seen on Shark Tank! Unknown Facts - TheNewsCrunch

These Israeli Companies Are Finding Innovative Ways To Improve Diabetes Care, Treatment | Health News – NoCamels – Israeli Innovation News

Diabetes is a major public health crisis that is approaching epidemic proportions around the globe and growing at an alarming rate. According to the International Diabetes Federation (IDF), over 425 million adults are currently living with diabetes. That number is expected to rise to 629 million by 2045.

The disorder, which occurs when the pancreas does not produce enough insulin (the hormone that regulates blood sugar) or when the body cannot use its produced insulin, has become so deadly, that the International Diabetes Federation said it was responsible for four million deaths in 2017 alone. The World Health Organization estimated diabetes to be the seventh leading cause of death globally in 2016.

Over 350 million people are at risk of developing Type 2 diabetes, when the body becomes to resistant to insulin due to lifestyle facts such as excess weight gain, while more than 1.1 million children are living with Type 1 diabetes, the disorder that occurs when the bodys immune system attacks cells of the pancreas that produce insulin, according to the International Diabetes Federation.

World Diabetes Day, marked annually on November 14 to honor the co-discoverer of insulin Canadian Dr. Frederick Banting, born on that day in 1891, aims to raise awareness of the impact of this disease while promoting its management, care, and prevention. For the past two years (including in 2019,) the theme of World Diabetes Day has been The Family and Diabetes promoting the familys role in awareness and education of the disorder.

To mark the day, NoCamels is taking a closer look at Israels role in advancing diabetes research and treatment as well as some of the companies with cutting-edge technology that stand out in the field.

Dr. Irit Yaniv, a general manager at Accelmed Ventures II, a new $100 million venture early-stage health tech fund for medical device and digital health startups and co-founder and chairperson of Type 2 diabetes medical device startup Digma Medical, calls diabetes the most dangerous global epidemic. Israel is no exception, she says, citing half a million people living with the disease in the country.

Additionally, about 300,000 are prediabetic, a condition manifesting as borderline high blood sugar levels and an increased risk to progress to diabetes Type 2 within a few years, she explains.

Dr. Yaniv says life science entrepreneurs address the challenges presented by the epidemic in a number of ways, including creating companies and projects aimed at reducing the risk of developing the diseases, development of novel drug delivery methods for diabetes drugs, and unique medical devices for managing the disorder.

SEE ALSO: 6 Israeli Companies At The Forefront Of Diabetes Care, Prevention, and Treatment

There are a few interesting examples such as oral insulin and nasal insulin delivery systems that were developed in Israel, Yaniv says. A recent success story is Nutrino, [an Israeli] software company for the management of diabetes that was acquired by Medtronic.

Treatment for Type 2 diabetes has been focused on lifestyle changes and pharmacologic solutions. Both have challenges including patient compliance and adverse effects such as weight gain, hypoglycemia, and other reactions, Yaniv says. More than 50 percent of the patients arent able to control the disease, even with combination therapeutics.

The medical device industry has made many efforts in recent years to address this need, Yaniv says, Companies such as GI Dynamics have paved the way for new therapeutic alternatives. Digma Medical has demonstrated initial positive clinical data with its unique duodenal ablation system.

Yaniv founded Digma Medical in 2013 with Ilan Ben Oren. Backed by leading venture capital firms such as Arkin Holdings and Peregrine Ventures, the company is dedicated to the development of its DiaGone device to treat insulin resistance. DiaGone is an endoscopic, disposable device, that uses innovative laser technology to treat the duodenum, a segment of the small intestine, without an implant. The Duodenal Glycemic Control procedure is a one-time 30 minute GI procedure, in which the gastroenterologist uses DiaGone to treat the duodenum for restoring the natural ability of the body to control glucose levels, said to provide long term remission from Type 2 diabetes and other metabolic syndrome-related diseases.

For Rami Epstein, who assumed the role of CEO at stem cell company Kadimastem in May 2019, a need exists to find a better solution for the management of diabetes in order to decrease the morbidity, mortality, and costs linked to it and its medical-related care, he tells NoCamels. This method is more than just controlling insulin levels in the body. It is controlling the dose of insulin administered to the body.

All Type 1 diabetes and 30 percent of Type 2 diabetes patients depend on the daily administration of insulin in order to control their glucose levels in the blood. This is not ideal since patients have to calculate insulin dosages and take into account meal times and portions, physical activity, and other parameters, he explains. Unfortunately, many patients do not manage to stabilize their blood glucose levels properly, thereby risking complications that arise from episodes of hypoglycemia or hyperglycemia,

Through Kadimastems groundbreaking stem-cell therapy technology, developed by the companys chief scientist Professor Michel Revel at the Weizmann Institute of Science and used as the basis for the companys founding in 2009, the Ness Ziona-based firm has developed and manufactured an off-the-shelf cell product for the treatment of insulin-dependent diabetes based on its proprietary tech platform. The tech platform has been used to treat multiple diseases, including ALS, through the expansion and differentiation of Human Embryonic Stem Cells (hESCs) into clinical-grade functional cells.

The product, called IsletRx, is currently in pre-clinical trials. Its goal is to free patients from continuous monitoring of blood sugar levels and repeated insulin injections. The drug contains an endless source of pancreatic functional islet cells, which produce and secrete insulin and glucagon in response to external glucose levels.

Meanwhile, Tel Aviv-based clinical-stage pharmaceutical company Oramed, which is focused on the development of oral drug delivery systems, announced this week that Phase IIb trial evaluating the efficacy and safety of its lead oral insulin candidate, ORMD-0801, has had positive results.

The study was a 90-day, double-blind, randomized, multi-center trial designed to evaluate the safety and efficacy of ORMD-0801 as a treatment for patients with type 2 diabetes, Oramed said in a statement. The primary efficacy endpoint was a reduction in Hemoglobin A1c (A1C, also known as HbA1c, is a key clinical measure of blood glucose control) at Week 12, with no weight gain.

Israeli scientists are taking diabetes management solutions one step further and adding machine learning and AI to the mix. DreaMed Diabetes, a medical tech startup founded in 2014 to develop these types of personalized solutions, announced in September that it had received clearance from the US Food and Drug Administration (FDA) as well as a CE Mark for its DreaMed Advisor Pro, an AI-based insulin dosing decision support software. The software is for patients with Type 1 diabetes using insulin pump therapy with continuous glucose sensors and blood glucose meters (BGMs)

The decision-support platform uses proprietary algorithms to process data from a range of connected devices, including insulin pumps and self-management glucometers. The data is then analyzed to provide an optimized insulin dosing treatment plan to maintain a balanced glucose level.

SEE ALSO: Israeli AI Startup Can Predict Which Diabetes Patients Will develop Kidney Disease

This clinical and technological advance leverages the power of artificial intelligence to optimize insulin administration in a streamlined and cost-effective manner, the company said in a statement.

This year I am more optimistic that a change will happen in how we manage diabetes. We see more technology adopted in all markets, more sharing of data between patients providers and industry all for the benefit of offering better care for patients, the companys CEO Eran Atlas tells NoCamels in an email. DreaMed is happy to be part of the leaders in this effort, by offering a unique artificial intelligence technology that can analyze data and recommend in only a few seconds how to optimize the technology. With such technology, the proliferation of expert care can be achieved even in emerging markets.

Another key player operating in artificial intelligence in the diabetes management market is Sweetch. Founded in 2013, Sweetch offers an AI-based platform that aims to identify those at high risk of developing Type 2 diabetes. The company calls itself the first AI-powered therapeutics solution to help people with the disorder and comes with a mobile app and a wireless Bluetooth-connected scale. The early prevention platform announced last year that it will partner with US-based integrated healthcare system WellSpan Health and provide its app to 15,000 employees, including 200 primary care and specialty physicians, as well as advanced practice clinicians in central Pennsylvania and northern Maryland.

In 2016, the startup raised $3.5 million in a Series A round led by equity crowdfunding platform OurCrowd and Philips.

Diabetes can cause circulation problems and related conditions such as peripheral arterial disease (PAD) which occurs when plaque builds up in the arteries and reduces blood flow to the limbs. For some patients, high levels of blood glucose can damage blood vessels and cause plaque build-up affecting healthy blood flow.

The northern Israel-based startupElastiMedhas developed a wearable medical device that doesnt treat diabetes patients directly but can help the patient improve his or her circulation.

It cant treat the disease directly, but it can treat some of its symptoms, says Elastimed CEO and founder Omer Zelka.

Compression socks improve circulation by squeezing the foot and calf muscles, which straightens out the vein walls to a better working state, says Advanced Tissue, the leading wound care supply provider. Compression therapy is particularly beneficial for diabetes patients because they improve circulation in a non-invasive manner, helping to maintain the right amount of pressure in feet and legs.

ElastiMeds sock uses battery-operated technology to activate a smart material that compresses and massage the legs to stimulate circulation. The pulses mimic contractions in the calf muscles that in turn increase blood flow.

The sock provides patients with a comfortable, easy-to-wear, highly effective, and cost-effective treatment option to prevent symptoms such as swelling, blood clots, leg ulcers and reduce athletes recovery time.

ElastiMed is currently finishing an ongoing clinical study to demonstrate the safety and the feasibility of this device and its ability to increase venous blood flow. The study is led by Dr. Vered Shuster Ben-Yosef, R&D Lab Manager of the company and is currently taking place at Hillel Yaffe Medical Center in Hadera. The company currently has a working prototype and aims to get the product on the market in early 2021.

Read more here:
These Israeli Companies Are Finding Innovative Ways To Improve Diabetes Care, Treatment | Health News - NoCamels - Israeli Innovation News

WCM-Q Explores Law and Ethics of Stem Cells and AI in Medicine – Al-Bawaba

The legal and ethical implications of using stem cells and artificial intelligence (AI) in medicine were discussed at the latest installment of Weill Cornell Medicine-Qatars (WCM-Q) Intersection of Law & Medicine series.

Expert speakers at the event discussed the impact of recent advances in stem cell science and AI on the practice of medicine in Qatar and explored how new legal frameworks could be developed to protect the rights and safety of patients in the MENA region. The day-long event was organized by WCM-Q in collaboration with Hamad Bin Khalifa University and the University of Malaya of Kuala Lumpur, Malaysia.

Stem cells are an exciting area for medical researchers because they have the potential to repair damaged or diseased tissues in people with conditions such as Parkinsons disease, type 1 diabetes, stroke, cancer, and Alzheimers disease, among many others. Stem cells can also be used by researchers to test new drugs for safety and effectiveness.

WCM-Qs Dr. Amal Robay, WCM-Q assistant professor in genetic medicine and director of research compliance, said: Stem cells have the capacity for unlimited or prolonged self-renewal, and they can differentiate themselves into many different cell types to become tissue- or organ-specific cells with special functions. The central ethical dilemma of stem cell science arises from the fact that embryonic stem cells are derived from human embryos or by cloning, she explained.

Visiting bioethics expert Dr. Jeremy Sugarman of Johns Hopkins University in Baltimore, US said that the public image of stem cell research had been damaged by a small number of high-profile cases in which scientists had behaved unethically. The field had also been hampered by different countries applying different laws to stem cell research, making international collaboration problematic, he said.

Meanwhile, the use of AI in healthcare has the potential to leverage analysis of large amounts of data to improve patient outcomes, but poses ethical concerns regarding privacy, the diversity of data sources, biases and relying on non-human entities for potentially life-changing decisions.

Dr. Barry Solaiman, assistant professor of law in the College of Law and Public Policy at HBKU said: Its very important that we bridge that gap between the professions of law and medicine, and that we understand the fundamental importance of ethicists to the advance of science. We need to consider how lawyers can help to develop laws to ensure that science advances and that it does so in ways that protect everyone involved.

The event, which was co-directed by Dr. Solaiman and Dr. Thurayya Arayssi, professor of clinical medicine and senior associate dean for medical education and continuing professional development at WCM-Q, also featured other expert speakers. Dr. Mohammad Firdaus Bin Abdul Aziz of the Faculty of Law at the University of Malaya, who spoke about stem cell regulations around the world, Dr. Faisal Farooq of Qatar Computing Research Institute, who spoke about AI in healthcare, Dr. Effy Vayena of the Swiss Institute of Technology on the ethical challenges of using machine learning in healthcare, Dr. Sharon Kaur of the Faculty of Law at the University of Malaya on global regulation of AI, and Dr. Mohammed Ghaly of Qatar Faculty of Islamic Studies on Islamic perspectives of bioethics in stem cell research. The visiting experts also engaged in two panel discussions, one examining the law and ethics of stem cell science, chaired by Dr. Adeeba Kamarulzaman, dean of medicine at the University of Malaya, and one on AI in healthcare chaired by Dr. Thurayya Arayssi, professor of clinical medicine and senior associate dean for medical education and continuing professional development at WCM-Q.

Dr. Arayssi said: I am very grateful that our expert speakers joined us to explore how legal frameworks can be developed to maximize the benefits of advances in stem cell research and AI for patients, while also respecting the rights, safety and cultural traditions of the everyone in the community.

The event was accredited locally by the Qatar Council for Healthcare Practitioners-Accreditation Department (QCHP-AD) and internationally by the Accreditation Council for Continuing Medical Education (ACCME).

Read this article:
WCM-Q Explores Law and Ethics of Stem Cells and AI in Medicine - Al-Bawaba

American Heart Association’s Research Achievement Award Presented to Harvard Scientist Peter Libby, MD, Who Discovered Role of Inflammation in CVD -…

PHILADELPHIA, Nov. 17, 2019 The American Heart Association, a global force for longer, healthier lives, has awarded its Research Achievement Award, recognizing a lifetime of extraordinary contributions to cardiovascular research, to Peter Libby, M.D., FAHA, Mallinckrodt Professor of Medicine at Harvard Medical School and a cardiovascular specialist at Brigham and Womens Hospital (BWH) in Boston.

Dr. Libbys pioneering work unraveling the role of inflammation in cardiovascular disease has been nothing short of paradigm changing. His career-long quest to understand how inflammation contributes to atherogenesis substantially deepened our understanding of heart disease, and his ability to translate his findings into the clinic has led to the development of novel new treatment strategies, said American Heart Association President Robert A. Harrington, M.D., FAHA, who presented the award.

Dr. Libbys independent research career included numerous first discoveries in the pathogenesis of atherosclerosis, including some of the mechanisms that lead to heart attack and stroke, said Dr. Harrington.

The award was presented today at the American Heart Associations Scientific Sessions 2019 in Philadelphia. The Associations Scientific Sessions is an annual, premier global exchange of the latest advances in cardiovascular science for researchers and clinicians.

Dr. Libby instigated and helped to lead the first large-scale, randomized clinical trial establishing inflammation as a therapeutic target in cardiovascular disease. His laboratory has focused on investigating the molecular and cellular mechanisms of atherosclerosis, and he continues to lead investigations that will add to our understanding of risk factors for atherosclerotic events and heart failure, among other important research questions, the award notes.

Inflammation was not considered a critically important contributor to atherogenesis prior to Dr. Libbys investigations. Indeed, the field focused largely on lipid metabolism and proliferation of smooth muscle cells when Dr. Libby began his independent research career, noted Jonathan D. Smith, professor of molecular medicine at the Cleveland Clinic, in a letter nominating Dr. Libby for the Research Achievement Award.

Over 30 years of research, Dr. Libbys discoveries included the finding that vascular wall cells can produce, as well as respond to, pro-inflammatory cytokines (especially Interleukin-1) small proteins that are important in cell signaling.

This discovery, initially met with considerable skepticism, laid the foundation for the recognition of novel paracrine and autocrine inflammatory cytokine signaling pathways in arterial disease, a mechanism now widely validated, Smith concluded.

Dr. Libby is a longtime American Heart Association volunteer. He is also a consulting physician at the Dana-Farber Cancer Institute. He served as Chief of Cardiovascular Medicine at BWH from 1998-2014 after heading its Vascular Medicine and Atherosclerosis Unit from 1990-1997. Prior to joining BWH, Dr. Libby was at Tufts New England Medical Center in Boston.

Dr. Libby earned his medical degree at the University of California, San Diego, and completed his training in internal medicine and cardiology at the Peter Bent Brigham Hospital (now Brigham and Womens Hospital). He also holds an honorary Master of Arts degree from Harvard University, and honorary doctorates from the Universit de Lille, France, and Universit Laval in Qubec. He has received numerous awards and recognitions for his research accomplishments, including the Basic Research Prize of the American Heart Association (2011), the Anitschkow Prize in Atherosclerosis Research of the European Atherosclerosis Society (2013), the Special Award of the Heart Failure Association of the European Society of Cardiology (2014) and the Ernst Jung Gold Medal for Medicine( 2016.) He has received a number of other awards including several lifetime achievement awards from various organizations.

Additional Resources:

The American Heart Associations Scientific Sessions is a premier global exchange of the latest advances in cardiovascular science for researchers and clinicians. Scientific Sessions 2019 is November 16-18 at the Pennsylvania Convention Center in Philadelphia. More than 12,000 leading physicians, scientists, cardiologists and allied health care professionals from around the world convene at the Scientific Sessions to participate in basic, clinical and population science presentations, discussions and curricula that can shape the future of cardiovascular science and medicine, including prevention and quality improvement. During the three-day meeting, attendees receive exclusive access to over 4,100 original research presentations and can earn Continuing Medical Education (CME), Continuing Education (CE) or Maintenance of Certification (MOC) credits for educational sessions. Engage in the Scientific Sessions conversation on social media via #AHA19.

About the American Heart Association

The American Heart Association is a relentless force for a world of longer, healthier lives. We are dedicated to ensuring equitable health in all communities. Through collaboration with numerous organizations, and powered by millions of volunteers, we fund innovative research, advocate for the publics health and share lifesaving resources. The Dallas-based organization has been a leading source of health information for nearly a century. Connect with us on heart.org, Facebook, Twitter or by calling 1-800-AHA-USA1.

View post:
American Heart Association's Research Achievement Award Presented to Harvard Scientist Peter Libby, MD, Who Discovered Role of Inflammation in CVD -...

Crizanlizumab for Sickle Cell Pain Reduction Approved by FDA – Drug Topics

The FDA today approved Novartis crizanlizumab, previously known as SEG101, indicated for the reduction in frequency of vaso-occlusive crises (VOCs) in adult and pediatric patients at least 16 years of age and older.

Crizanlizumab is currently the first and only approved biologic that works by binding to P-selectin, a cell adhesion protein that involved in multicellular interactions and can lead to vaso-occulsion in sickle cell disease, according to Novartis officialstatement. Novartis says that by binding to p-selectin on the surface of an activated endothelium and platelets, crizanlizumab blocks interactions between endothelial cells, platelets, RBCs, and leukocytes.

The approval of Adakveo marks a new era in the treatment of sickle cell disease, a genetic condition that places an extraordinary burden of unpredictable pain crises on patients and their families, saidSusanne Schaffert, PhD, president, Novartis Oncology says in astatement. The stories we have heard from patients about their sickle cell pain crises are devastating. We are pleased to help reimagine medicine together with the sickle cell community and offer new hope for fewer VOCs.

Trending:New HIV Vaccination Strategy Holds Promise

Todays approval is based upon the results of a SUSTAIN, a randomized, multicenter, placebo-controlled, double-blind study that included 196 patients with any genotype of sickle cell disease and a history of 2-10 VOCs in the previous 12 months.

The primary efficacy outcome for SUSTAIN, according to the release, was the annual rate of VOCs leading to a healthcare visit (i.e,. an acute episode of pain with no cause other than a vaso-occulsive event that required a medical facility visit and treatment with oral or parenteral opioids, or parenteral NSAIDs; acute chest syndrome; hepatic sequestration; splenic sequestration; and priapism requiring a visit to a medical facility).

Overall, the annual rate of VOCs in the crizanlizumab arm (1.63) experienced a 45% reduction compared to the placebo arm (2.98). Reductions in thecrizanlizumab arm were observed regardless of sickle cell genotype and/or hydroxyurea use.

Secondary and other efficacy outcomes included the annual rate of days hospitalized (crizanlizumab: 4 days; placebo: 6.87 days), the time to first VOC leading to a healthcare visit, and the number of patients that did not experience a VOC.

Read More:CRP Blood Test May Help Reduce Antibiotics Prescribed for COPD Flare-Ups

Warnings and precautions issued with crizanlizumab include infusion-related reactions and interference with automated platelet counts (i.e., platelet clumping).

Adverse reactions reported with the use of crizanlizumab include nausea, arthralgia, back pain, and pyrexia.

Novartis says that crizanlizumab should be available within the coming weeks.

Full Prescribing Information

See the article here:
Crizanlizumab for Sickle Cell Pain Reduction Approved by FDA - Drug Topics

Study: The secret of living to 110 – msnNOW

The secret to living past 100 could lie in your immune system, suggests a new study.

In a study recently publishedin Proceedings of the National Academy of Sciences (PNAS), scientists found that supercentenarians those who are 110 years of age or older have an overabundance of a certain type of disease-fighting cell within their immune systems, possibly explaining their longevity.

To come to this conclusion, researchers looked at the circulating immune cells from supercentenarians and controls aged 50 to 89. About 41,208 immune cell samples were taken from seven supercentenarians, while 19,993 cells were collected from the five controls.

The study found that while the supercentenarians and controls had roughly the same amount of T-cells overall, the former group had an excess amount of one particular subset of T-cells called cytotoxic CD4 T-cells. These cells, according to a news releaseon the findings, are aggressive and quickly destroy cancer and infection-causing cells.

In some cases, the cytotoxic CD4 T-cells accounted for 80 percent of the supercentenarians T-cells, while only 10 to 20 percent of the T-cells in the controls were cytotoxic CD4 T-cells, according to the research, which wasconducted by the RIKEN Center for Integrative Medical Science (IMS) and Keio University School of Medicine in Japan.

The super immune system cells are likely not a marker of youth, but rather a special characteristic of the supercentenarians, the researchers wrote. The cytotoxic CD4 T-cells are likely the offspring of a sole ancestor cell.

We believe that this type of cells, which are relatively uncommon in most individuals, even young, are useful for fighting against established tumors, and could be important for immunosurveillance, said Piero Carninci, the deputy director of RIKEN, in a statement. This is exciting as it has given us new insights into how people who live very long lives are able to protect themselves from conditions such as infections and cancer."

Gallery: 100 Ways to Live to 100 (Provided by Best Life)

Read the original here:
Study: The secret of living to 110 - msnNOW

Allogene allies with Notch to make CAR-T production more scalable – BioPharma-Reporter.com

Last year, Arie Belldegrun and David Chang, fresh from selling chimeric antigen receptor (CAR)-T pioneer Kite Pharma to Gilead Sciences, launched Allogene with $300m (271m) and a deal with Pfizer to access off-the-shelf cell therapies. The focus then, as now, was on taking CAR-T therapies mainstream by eliminating factors that could restrict them to niche status, such as the complex, costly production process.

Allogenes founding allogeneic technology moves it some way toward that goal, by enabling therapies to be made from donor cells rather than having to engineer cells taken from the patient themselves.

However, even if the allogeneic approach works as Allogene hopes, it will still require a steady supply of donor cells. When Allogene launched, it set its sights on making up to 100 doses from one donor sample.

The finite nature of donated T cells has spurred interest in induced pluripotent stem cells (iPSC), which could serve as a renewable source of materials for off-the-shelf CAR-T therapies. Notchs work to realize that potential caught the attention of Allogenes CEO, David Chang.

Chang said, We believe [it] to be a scalable and potentially more [good manufacturing practice] amenable manufacturing process. It might be amenable for large-scale manufacturing.

The early stage nature of the iPSC technology Notch is yet to enter the clinic means it is unclear whether the approach can live up to those expectations. An inability to show CAR-T doses are free from undifferentiated iPSCs and failure to generate functioning T cells from iPSCs are two potential stumbling blocks.

Allogene has seen enough potential to bet on Notch, though. The deal will see Allogene pay Notch $10m upfront, take a 25% stake in its new partner and commit to a package of milestones.

Notch will take iPSC AlloCAR T cells through preclinical development before Allogene steps in to test them in humans. Allogene will have global rights to any products resulting from the collaboration.

Other companies are also working to develop oncology cell therapies based on iPSCs. Fate Therapeutics is trialling an engineered natural killer cell therapy created from a clonal master iPSC line, while Bayer-backed startup Century Therapeutics recently raised $250m to take iPSC-derived treatments for blood cancers and solid tumors into the clinic. Takeda is also active in the space.

Continue reading here:
Allogene allies with Notch to make CAR-T production more scalable - BioPharma-Reporter.com

Stem Cell Media Market 2019| Recent Trends, In-depth Analysis, Market Size Research Report Forecast up to 2026 | Research Industry US – News Obtain

Global Stem Cell Media market report is the first of its kind research report that covers the overview, market dynamics, competitive analysis, and leading players numerous strategies to sustain in the global market. This report covers five top regions of the world and countries within, which shows the status of regional development, consisting of volume, size, market value, and price data.

The report takes a dashboard view of an entire Stem Cell Media market by comprehensively analyzing market circumstance and situation and the various activities of leading players in the market such as mergers, partnerships, and acquisitions. This unique report explains the present industry situations that give the crystal-clear picture of the global Stem Cell Media market to the clients.

Request For Sample PDF Report (Kindly Use Your Bussiness/Corporate Email Id to Get Priority): http://researchindustry.us/report/stem-cell-media-market-ric/697128/request-sample

Market Segmentation

Key players considered in the report include

Thermo FisherSTEMCELL TechnologiesMerck MilliporeLonzaGE HealthcareMiltenyi BiotecCorningCellGenixTakaraPromoCell

On the basis of types, the global Stem Cell Media market is primarily split into

Pluripotent Stem Cell CultureHematopoietic Stem Cell CultureMesenchymal Stem Cell CultureOther

Based on application, the global Stem Cell Media market is primarily split into

Scientific ResearchIndustrial Production

Some of the significant factors such as marketing strategy, factor analysis, cost analysis, industrial chain, distributors and sourcing strategy are included in this report which makes it an exclusive one. The report on the global Stem Cell Media market report is compiled by industry experts and properly examined which will highlight the key information required by the clients.

Regional Analysis

A unit of the report has given comprehensive information about regional analysis. It provides a market outlook and sets the forecast within the context of the overall global Stem Cell Media market. Research Industry US has segmented the global Stem Cell Media market into major geographical regions such as North America, Europe, Asia Pacific, South America, and the Middle East and Africa (MEA). Potential new entrants wishing to target only high growth areas are also included in this informative section of the global Stem Cell Media market.

Based on geography, the global Stem Cell Media market is divided into North America, Europe, Asia-Pacific, South America, and The Middle East & Africa. North America is further divided in the U.S., Canada, and Mexico, whereas Europe consists of the UK, Germany, France, Italy, and Rest of Europe. India, China, Japan, South Korea, and Rest of Asia-Pacific are the categorization of the Asia-Pacific region. The South America region includes Brazil, Argentina, and the Rest of South America, while The Middle East & Africa is categorized into GCC Countries, Egypt, South Africa, and the Rest of the Middle East & Africa.

Enquire Here For Queries Or Report Customization: http://researchindustry.us/report/stem-cell-media-market-ric/697128/request-customization

Following queries are answered in the Stem Cell Media report:-

Get In Touch!

Navale ICON IT Park,

Office No. 407, 4th Floor, Mumbai Banglore Highway, Narhe, Pune

Maharashtra 411041

phone +91-020-67320403

Email help@researchindustry.us

Read more here:
Stem Cell Media Market 2019| Recent Trends, In-depth Analysis, Market Size Research Report Forecast up to 2026 | Research Industry US - News Obtain

International Stem Cell Corporation Announces Financial Results for the Three and Nine-Months ended September 30, 2019 – Yahoo Finance

CARLSBAD, CA / ACCESSWIRE / November 15, 2019 / International Stem Cell Corporation (ISCO) (www.internationalstemcell.com) ("ISCO" or "the Company"), a California-based clinical stage biotechnology company developing novel stem cell-based therapies and biomedical products, today announced operating results for the three and nine months ended September 30, 2019.

"As we mentioned before we completed the enrollment of the Phase I Parkinson's disease clinical trial and currently involved in reorganizing our revenue-generating subsidiaries. We expect that we will see positive results of this reorganization next year." - commented Andrey Semechkin, PhD., CEO and Co-Chairman of ISCO.

Year-to-Date Financial Highlights

About International Stem Cell Corporation

International Stem Cell Corporation is focused on the therapeutic applications of human parthenogenetic stem cells (hpSCs) and the development and commercialization of cell-based research and cosmetic products. ISCO's core technology, parthenogenesis, results in the creation of pluripotent human stem cells from unfertilized oocytes (eggs). hpSCs avoid ethical issues associated with the use or destruction of viable human embryos. ISCO scientists have created the first parthenogenetic, homozygous stem cell line that can be a source of therapeutic cells for hundreds of millions of individuals of differing genders, ages and racial background with minimal immune rejection after transplantation. hpSCs offer the potential to create the first true stem cell bank, UniStemCell. ISCO also produces and markets specialized cells and growth media for therapeutic research worldwide through its subsidiary Lifeline Cell Technology (www.lifelinecelltech.com), and stem cell-based skin care products through its subsidiary Lifeline Skin Care (www.lifelineskincare.com). More information is available at http://www.internationalstemcell.com.

To subscribe to receive ongoing corporate communications, please click on the following link: http://www.b2i.us/irpass.asp?BzID=1468&to=ea&s=0

To like our Facebook page or follow us on Twitter for company updates and industry related news, visit: http://www.facebook.com/InternationalStemCellCorporation and http://www.twitter.com/intlstemcell

Safe Harbor Statement

Statements pertaining to anticipated developments, expected results of clinical studies, progress of research and development, and other opportunities for the company and its subsidiaries, along with other statements about the future expectations, beliefs, goals, plans, or prospects expressed by management constitute forward-looking statements. Any statements that are not historical fact (including, but not limited to statements that contain words such as "will," "believes," "plans," "anticipates," "expects," "estimates,") should also be considered to be forward-looking statements. Forward-looking statements involve risks and uncertainties, including, without limitation, risks inherent in the development and/or commercialization of potential products, regulatory approvals, need and ability to obtain future capital, application of capital resources among competing uses, and maintenance of intellectual property rights. Actual results may differ materially from the results anticipated in these forward-looking statements and as such should be evaluated together with the many uncertainties that affect the company's business, particularly those mentioned in the cautionary statements found in the company's Securities and Exchange Commission filings. The company disclaims any intent or obligation to update forward-looking statements.

Story continues

International Stem Cell Corporation and SubsidiariesCondensed Consolidated Balance Sheets(in thousands, except share data and par value)(Unaudited)

Assets

Cash

Accounts receivable, net

Inventory, net

Prepaid expenses and other current assets

Total current assets

Non-current inventory

Property and equipment, net

Intangible assets, net

Right-of-use assets

Deposits and other assets

Total assets

Liabilities, Redeemable Convertible Preferred Stock, and Stockholders' Equity (Deficit)

Accounts payable

Accrued liabilities

Operating lease liabilities, current

Related party payable

Advances

Warrant liability

Total current liabilities

Long-term deferred rent

Operating lease liabilities, net of current portion

Total liabilities

Commitments and Contingencies

Series D Redeemable Convertible Preferred stock, $0.001 par value, 50 shares authorized, 43 issued and

outstanding, with liquidation preference of $4,300 at September 30, 2019

Stockholders' Equity (Deficit)

Series B Convertible Preferred stock, $0.001 par value, 5,000,000 shares authorized, 250,000

issued and outstanding, with liquidation preferences of $423 and $411 at September 30, 2019 and

December 31, 2018

Series D Convertible Preferred stock, $0.001 par value, 50 shares authorized, 43 issued and

outstanding, with liquidation preference of $4,300 at December 31, 2018

Series G Convertible Preferred stock, $0.001 par value, 5,000,000 shares authorized, issued and

outstanding, with liquidation preference of $5,000 at September 30, 2019 and December 31, 2018

Series I-1 Convertible Preferred stock, $0.001 par value, 2,000 shares authorized, 814 issued and

outstanding, with liquidation preferences of $814 at September 30, 2019 and December 31, 2018

Series I-2 Convertible Preferred stock, $0.001 par value, 4,310 shares authorized,

issued and outstanding with liquidation preference of $4,310 at September 30, 2019 and December 31, 2018

Common stock, $0.001 par value, 120,000,000 shares authorized, 7,533,083 and 6,933,861 shares

issued and outstanding at September 30, 2019 and December 31, 2018

Additional paid-in capital

Accumulated deficit

Total stockholders' equity (deficit)

Total liabilities, redeemable convertible preferred stock and stockholders' equity (deficit)

International Stem Cell Corporation and SubsidiariesCondensed Consolidated Statements of Operations(in thousands, except per share data)(Unaudited)

Revenues

Product sales

Total revenues

Expenses

Cost of sales

Research and development

Selling and marketing

General and administrative

Total expenses

Loss from operations

Other income (expense)

Change in fair value of warrant liability

Interest expense

Miscellaneous income

Total other income (expense), net

Net income (loss)

Net income (loss) applicable to common stockholders

Net income (loss) per common share-basic

Net income (loss) per common share-diluted

Weighted average shares-basic

Weighted average shares-diluted

Contacts:

International Stem Cell CorporationRussell A. Kern, PhDPhone: 760-940-6383Email: ir@intlstemcell.com

SOURCE: International Stem Cell CORP

View source version on accesswire.com: https://www.accesswire.com/566897/International-Stem-Cell-Corporation-Announces-Financial-Results-for-the-Three-and-Nine-Months-ended-September-30-2019

More here:
International Stem Cell Corporation Announces Financial Results for the Three and Nine-Months ended September 30, 2019 - Yahoo Finance