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Restorative Medicine: IV Therapy in NYC Announces Partnership with Better Health Chiropractic, PC – Press Release – Digital Journal

November 21st, 2019 2:41 pm

Restorative Medicine: IV Therapy, based in New York, NY, has announced a trusted partnership with Better Health Chiropractic, PC. Restorative Medicine: IV Therapy is a provider of IV therapy nutrition New York NY services and was founded by Dr. Vladimir Alexeyenko, M.D. The practice is geared towards serving the needs of those who want a way to counteract the damage that stress and modern living have been causing. Dr. Alexeyenko wants to emphasize that people often work long hours at a desk, eat on the run, have disrupted sleep, and are exposed to environmental toxins. All of that stress can weaken the bodys immune system and make it more difficult to fight off disease.

Dr. Vladimir Alexeyenko says, We offer vitamin infusions, hydration IV therapy treatments, and other IV therapy solutions that will energize you and restore your body and mind. Our bodies need fuel, not just any fuel, but the right mix of vitamins, minerals, water, and hormones. The human form is a complex system that relies on many compounds to get up and go. There is a perfect balance that helps us feel great but, modern life, especially in urban areas, robs us of that balance.

Dr. Vladimir Alexeyenko is a licensed physician who has developed IV infusion therapy using his in-depth knowledge regarding the human body and what it requires to be able to perform at peak efficiency. He wants to point out that he established Restorative Medicine: IV Therapy based on the philosophy that preventing disease is better than cure.

He says, We can prescribe and administer any infusion that can restore your energy, increase your metabolism, rebalance levels of vitamins and minerals, and strengthen your immune system. You will see and feel the results immediately. At Restorative Medicine, your body will regain the ability to heal itself thanks to IV vitamin therapy and other IV drips that will revive your energy, restore cell function as you go back to your vibrant and busy life.

With nutrients, vitamins, minerals, and fluids being essential in helping the body function well and in flushing out toxins, these are provided in IV drips and booster form for preventative medicine. The treatments supervised by Dr. Alexeyenko can help in fighting disease, boosting energy levels, and strengthening the immune system. This allows patients to have more control over their health journey. However, this requires the guidance of an experienced physician like Dr. Alexeyenko.

Dr. Vladimir Alexeyenko also provides IV ozone therapy New York NY services. This is designed to get rid of viruses, toxins and infections from the body. Its purpose is to oxygenate the blood to create an aerobic environment, which is hostile to microbes that thrive on anaerobic metabolism. It should be noted that while ozone can be dangerous when inhaled, it is not harmful in the bloodstream. Ozone therapy may be used by people who frequently travel and breath recycled air. It may also help during the flu season as it may be able to boost the bodys immune system.

According to Dr. Alexeyenko, IV therapy may be able to provide long lasting vitality and bring back systemic balance to the human body. IV therapy has an advantage over supplements or pills because the latter are taken orally and are diluted during digestion. On the other hand, IV therapy allows the nutrients, vitamins and minerals to their work at the cellular level.

Dr. Vladimir Alexeyenko has been practicing medicine for more than 25 years. He has always sought to be up-to-date regarding the study and use of restorative, holistic treatments. He also prescribes modern medical treatments but his long term goal is to guide his patients into the use of conventional and integrative practices and treatments designed to prevent ill health.

Those interested in IV therapy NYC services can visit the Restorative Medicine: IV Therapy website or contact them on the phone or through email. They are open from Monday to Friday, 9:00 am to 6:00 pm. Saturdays and Sundays are by appointment only.

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For more information about Restorative Medicine: IV Therapy, contact the company here:

Restorative Medicine: IV TherapyDr. Vladimir Alexeyenko(917) 994-9390doctor@vladimiralexeyenkomd.comRestorative Medicine: IV Therapy2 W 46th St Ste 806, Rm2New York, NY 10036

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A guide to CBD topicals, balms, and lotions – Leafly

November 21st, 2019 2:41 pm

Rae LlandNovember 18, 2019

(Irina_Strelnikova/iStock)

CBD, or cannabidiol, is a compound produced by cannabis and hemp plants. Unlike THC, CBD doesnt produce a feeling of being high.

CBD topicals such as lotions, balms, gels, or creams are infused with CBD to produce skin-friendly products that contain the medicinal properties of CBD. In topical form, CBD is most popularly used for managing pain and inflammation.

CBD topicals penetrate the skin to provide targeted relief, without entering the bloodstream. This makes them a fantastic choice for anyone who wants to focus the healing properties in specific problem areas rather than feel the effects throughout their body. CBD topicals can potentially provide relief for a variety of pain, headache, and skin issues such as:

Lo Friesen, lead chemist for cannabis wellness company Heylo, believes CBD topicals are also a fantastic preventative medicine. She says using these topicals every day, multiple times a day allows the body to not only uptake CBD quicker, but also build a CBD level in those areas and prevent worsening inflammation.

Its just preventative maintenance, says Friesen. For example, people who have arthritis in their hands who use [CBD topicals] on their hands every day are going to have less pain, less inflammation. Theyre going to have less pain in their hands over time than people who use it to treat [the pain as it happens].

Some CBD topicals may have bases such as shea butter, or oils like coconut, avocado, jojoba, or vitamin E. These nourishing ingredients are great for the skin, providing added benefit to the medicinal properties of CBD. Its also possible to find more traditional lotions with CBD or products with an Aquaphor base.

While lotions will be water based, creams usually have a fat or oil base, and balms a thicker base such as beeswax. Water-based lotions absorb more quickly into the skin, but oil based CBD topicals are more easily absorbed and get into the skin deeper. Meanwhile, gels can be useful for easier thicker application, making them possibly preferable for those with reduced hand dexterity, such as arthritis patients.

At the end of the day however, Friesen says, Just take your favorite skin care product and find something with similar ingredients, add CBD, and youve already made it better.

Unfortunately, due to an oversaturated market and lack of regulation, not all CBD topicals will produce the desired results. CBD can be sourced from either hemp or traditional cannabis, but their resulting extracts typically have quite a few differences in terms of the diversity of compounds found within them.

CBD extracts from cannabis tend to include a wide diversity of helpful compounds whereas hemps chemical diversity is more limited. Youll also want to make sure that a hemp-derived product actually contains CBDhemp seeds or stalk dont produce CBD, so its important to understand which part of the hemp plant was used in the extraction process.

Whats more, some products claim to have an abundance of CBD in them, but the reality doesnt always match the label. So how can consumers make sure they are getting a quality product?

Dr. Jeremy Riggle, chief scientist with cannabis wellness company Marys Medicinals weighed in:

Not all CBD products are created equal, and consumers should do their research. Ask questionswhat type of CBD extract does it contain: full spectrum, broad spectrum, or isolate? Where is the raw material sourced from? Does the producer use organic and sustainable agricultural practices? Does the supplier have a Certificate of Analysis showing test results for pesticides, heavy metals, residual solvents, microbials, cannabinoid potency, and terpene profile?

Finally, its worth noting that milligram content can make a difference, and with CBD, higher is generally better. Friesen says you get what you pay for, but that this is also why some make the switch over to CBD:THC topical products. Friesen believes these 1:1 or 1:3 ratio products are more effective than CBD on its own, due to the cannabinoids tendency to amplify each others effects. As such, patients may be able to use less to achieve similar effects, than they would with a CBD only product, and save money in the process.

All in all, there are plenty of great topical CBD products on the market for those who want to try a targeted method of delivering these helpful cannabinoids to problem areas and add CBD to their wellness routine.

Rae Lland is a freelance writer, journalist, and former editor for Weedist and The Leaf Online. With a focus on culture, music, health, and wellness, in addition to her work for Leafly, she has also been featured in numerous online cannabis publications as well as print editions of Cannabis Now Magazine. Follow her on Instagram @rae.lland

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Beefing Up the East End’s Substance Abuse Treatment – East End Beacon

November 21st, 2019 2:41 pm

When Quannacut Outpatient Services substance abuse treatment center was preparing to move into its new facility across Riverhead in July, a rumor quickly spread through patients that it may be closing. But that rumor was quickly replaced with the real news, which is quite good: Not only has the facility tripled in size in its new location, but it is now better able to accommodate its mission to treat not only substance abuse, but also mental and physical health needs that are often unavailable to people in substance abuse treatment.

Stony Brook Eastern Long Island Hospital and Quannacut held a ribbon-cutting celebrating the opening of the new 1,400-square-foot offices at 905 East Main Street in Riverhead on Nov. 20, and theyre planning to open another satellite outpatient center at 291 Hampton Road in Southampton this month, which will fill a gap in outpatient substance abuse treatment on the South Fork.

The expansion was made possible by a $1.6 million grant received in 2017 from the New York State Department of Healths Statewide Health Care Facility Transformation Program. A goal of this program is to make it easier for people, especially those with Medicaid, to receive preventative medical services, in an effort to reduce emergency room visits for non-emergencies.

The new Quannacut outpatient center in Riverhead has three medical examination rooms, and is in the process of hiring medical staff under the guidance of Medical Director Dr. Jarid Pachter, said Quannacut Outpatient Services Director David Cohen on a mid-November tour of the facility. He said some of the top medical needs among patients there are infectious diseases, often related to substance use, and basic primary care needs, often longstanding chronic conditions that have gone untreated.

Theres a general rule of thumb, he said, that about 1/3 of people who visit the emergency room also have an untreated behavioral health need, while 1/3 of the people in Quannacuts program also come in with untreated medical needs.

Stony Brook Eastern Long Island Hospital, which is in Greenport, opened Quannacut as an inpatient rehabilitation program in 1989, expanding with an outpatient program that moved from Mattituck to Harrison Avenue in Riverhead in 2001. Quannacut is a Native American word that means hope.

Mr. Cohen said that, when he arrived shortly after that, the outpatient program was seeing around 70 patients at a given time. Now, he said, they have about 300 active patients, and accept walk-in patients on Mondays and Fridays from 9 a.m. to noon.

This new integration of medical and psychiatric services builds on strengths already existing within ELIH and Stony Brook University Hospital.

ELIH has long had the only inpatient psychiatric facility on the East End, and the hospitals recent affiliation with Stony Brook University Hospital, which has a psychiatric emergency room, is designed to integrate mental health and substance abuse treatment throughout the continuum of care.

This is a sea change for health care, where traditionally medical, psychiatric and substance abuse professionals had worked in separate silos. Mr. Cohen said some medical and substance abuse practices dont want to deal with people with certain mental health issues or medications, he said, in part become some psychiatric medications are addictive.

Were experts here on co-occurring conditions, he said. Our staff is heavily trained. Not one thing works best for each individual.

Dr. Richard Rosenthal, director of the Division of Addiction Psychiatry at Stony Brook University, said the addition of Quannacuts services to the Stony Brook network is part of a larger endeavor integrating addiction, mental health and primary care.

Substance use disorders are classified as psychiatric disorders, but they are overseen by different regulatory agencies, said Dr. Rosenthal. The truth is a continuum is the rule rather than the exclusion.

Dr. Rosenthal added that, as part of this integration of care, the Stony Brook University Hospital network is training doctors to administer buprenorphine shots in the emergency rooms in Southampton and Greenport.

Buprenorphine has not gotten as much public attention as naloxone, better known as Narcan, an immediate opioid antidote carried by first responders to revive people from opioid overdoses. But once they survive an overdose, opioid users who want to quit will need a way to manage their withdrawal symptoms. Thats where buprenorphine, a medically administered opioid used to treat withdrawal, comes in.

Dr. Rosenthal said Dr. Kenneth Kaushansky, the dean of the Universitys Renaissance School of Medicine, has fully backed training Stony Brook doctors to administer buprenorphine, which has historically had a difficult time gaining traction with medical doctors.

To prescribe buprenorphine, you need to be trained, and its substantive training, said Dr. Rosenthal. Patients come in and agree to go into treatment, theyre given a couple doses, which they complete at home, and they get a referral and connection to outpatient treatment. They may need to stay overnight.

Its very safe, and its really no big deal, he said, adding that 130 Stony Brook doctors have been trained to administer buprenorphine. The patient feels better. It protects them from the nods and it medically stabilizes them. Its a lifesaver.

Dr. Rosenthal added that the way doctors are trained also plays a role in alleviating the opioid crisis.

Were training doctors differently regarding pain, he said. Thats a big, big shift in terms of what we were doing even five years ago.

Even primary care doctors operating in practices affiliated with Stony Brook are now giving patients screening questionnaires for substance abuse and mental health issues as soon as they walk in for routine medical appointments.

Doctors are practical people. They believe the same thing regular people do, said Dr. Rosenthal. Theres a culture change. We want to know if people are thinking of self-harm. We need to do a better job helping people when they feel desperate and hopeless.

Despite the major leap the new facility is bringing to Quannacut, the staff there arent resting on their laurels. They are currently working on an adolescent program, and they run two sober houses within 15 minutes of the Riverhead center.

But those houses, which have just 18 beds, all for male residents, are just a drop in the bucket compared with the need. Quannacut would ultimately like to add a female sober house as well.

Housing is the number one thing that undermines treatment, said Mr. Cohen. A lot of people we see are one step away from homelessness. Our houses are always filled, and theres always a waiting list.

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ViiV Healthcare announces exclusive licensing agreement with the National Institutes of Health for investigational bNAb with potential for long-acting…

November 21st, 2019 2:41 pm

LONDON--(BUSINESS WIRE)--ViiV Healthcare, the global specialist HIV company majority owned by GSK, with Pfizer Inc. and Shionogi Limited as shareholders, today announced that the company will be developing the investigational broadly neutralising antibody (bNAb) N6LS for the treatment and prevention of HIV-1, as part of an exclusive licensing agreement between GSK and the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health (NIH).

Broadly neutralising antibodies are antibodies that can recognise and block the entry of different strains of HIV into healthy cells. N6LS is an antiviral bNAb that works by binding to a specific site (gp120) on the surface of HIV that prevents its entry into uninfected immune system cells (CD4+ T-cells). By blocking HIVs entry into human CD4+ cells, HIV replication is halted, and the HIV transmission process may be prevented.1

Kimberly Smith, M.D., Head of Research & Development at ViiV Healthcare, said: We are excited to advance N6LS from its current proof of concept stage to the next step in its development by studying this bNAb as a long-acting medicine that could potentially be used for both treatment and prevention of HIV. By continuing to research new ways that people living with HIV can reach undetectable viral loads, we build on our ten-year history of furthering innovative science in HIV and take another important step forward in ending the epidemic.

ViiV Healthcare looks forward to initiating a phase IIa study with material manufactured by the NIAID Vaccine Research Center that will evaluate the efficacy, safety, tolerability, and pharmacokinetic profile of N6LS in adults living with HIV.

Additional details about N6LSN6LS was originally discovered and developed by scientists at NIAIDs Laboratory of Immunoregulation and VRC. NIH and GSK entered into a Cooperative Research and Development Agreement (CRADA) to jointly identify and further develop new bNAbs such as N6LS that could serve as the next generation of treatment regimens for people living with HIV and preventative options for HIV transmission. This exclusive license outlines a programme for ViiV Healthcares development of N6LS as well as milestone payments and royalties to the NIAID.

About ViiV HealthcareViiV Healthcare is a global specialist HIV company established in November 2009 by GlaxoSmithKline (LSE: GSK) and Pfizer (NYSE: PFE) dedicated to delivering advances in treatment and care for people living with HIV and for people who are at risk of becoming infected with HIV. Shionogi joined in October 2012. The companys aim is to take a deeper and broader interest in HIV/AIDS than any company has done before and take a new approach to deliver effective and innovative medicines for HIV treatment and prevention, as well as support communities affected by HIV.

For more information on the company, its management, portfolio, pipeline and commitment, please visit http://www.viivhealthcare.com.

About GSKGSK is a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. For further information please visit http://www.gsk.com.

_____________________1 Kumar R, Qureshi H, Deshpande S, Bhattacharya J. Broadly neutralizing antibodies in HIV-1 treatment and prevention. Ther Adv Vaccines Immunother. 2018;6(4):6168.

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Regenerative Medicine: Overcoming The Supply Chain Challenges – Contract Pharma

November 21st, 2019 2:41 pm

Regenerative medicine is one of modern sciences most exciting developments. Defined by the Medical Research Council, regenerative medicine is an interdisciplinary field that seeks to develop the science and tools that can help repair or replace damaged or diseased human cells or tissues to restore normal function.

In the human body, the liver is the only organ capable of regenerating itself spontaneouslyeven after serious injurybut in the future, any part of the human body may be capable of doing so. Our own cells will also be able to treat and cure diseases and conditions of the blood and immune system, as well as restore the blood system after treatments for specific cancers.

Once only imaginable in science fiction, the latest applications include engineered skin tissue to treat burn victims, custom-grown bones for implants and joint replacements, personalized dietary treatments using gut bacteria and just recently, the worlds first 3D vascularized engineered heart was created using a patients own cells and biological materials.

As scientists understanding and the tools at their disposal become more advanced, the closer to the widespread commercialization of regenerative medicine the pharmaceutical industry finds itself.However, offering regenerative medicine therapies at scale requires one of the biggest shake-ups to the global pharmaceutical supply chain ever seen. Without it, the world risks missing out on the curative promises of this next-generation medical technology.

Regenerative medicine is one of, if not the most, exciting advancements in modern science which has far-reaching benefits for big pharma, healthcare systems and patient outcomes.

Regenerative medicine is a growth industry in more than one sense of the word; as a sector, its growing from strength to strength. In fact, last year the global regenerative medicine market was worth $28 billion and its expected to grow to $81 billion by 2023.

As a more efficient and less invasive alternative to transplanting cells or organs to replace damaged or lost tissue, established pharma companies alongside small biotech start-ups are racing to discover and bring to market medicine-based approaches that stimulate the bodys natural ability to repair itself.The cutting-edge innovations of regenerative medicine generally fall into three distinct categories:

Replenish Replace Rejuvenate

Stem cells can generate vital growth factors to naturally reduce inflammation, increase muscle mass, repair joints, grow hair and boost the immune system, replenishing the body. Organ regeneration and 3D printing are replacing the reliance on the failing donor system and overcoming the issue of organ rejection. The root causes of aging are being better understood and delayed by using stem cells to rejuvenate the body.

Marking a new era in healthcare and one which has the promise of addressing the needs of an aging population challenged by escalating chronic diseases, regenerative medicine is certainly a game-changer. Beyond more effective medical treatments that can be applied routinely despite age, comorbidities, or disease severity, it also has the potential to cure many of todays incurable diseases and support healthcare systems to move towards a preventative model.

Today, regenerative medicine is largely confined to a research environment. In fact, according to a recent report, there were 1,028 clinical trials for regenerative therapies taking place globally at the end of 2018.

Regenerative medicine is poised to transform healthcare as we know it, offering potential cures for deadly diseases which before would require long-term treatment to manage. However, while billions are being spent on regenerative medicine research and clinical studies, little resource has, so far, been allocated to the management and delivery of innovative medical therapies at scale.

Currently, the race appears to be on between smaller Medtech companies and large multi-national pharmaceutical companies to see who wins first-mover advantage in the regenerative medicine market. Today, many established pharmaceutical companies prefer to partner with Medtech startups to in-license products in early clinical development stages as opposed to conducting early development on their own which comes at a huge cost. This is a risk-reduction tactic, but it could mean big pharma misses the boat.

The question remains unanswered as to whether a peer-to-peer collaborative model will prosper where Medtech companieswho are in some instances one step ahead of big pharma in terms of drug developmentare happy to be a third-party provider to big pharma who have the budgets and networks to truly deliver the regenerative medicine revolution.

Regulation is, and will continue to, play a hugely important role in delivering regenerative medicines from a lab setting to a clinical setting. Only recently, the FDA announced a new policy framework for the development of regenerative medicine products, taking into account the dynamic and fast-moving nature of the field.

Ultimately, the governments aim is to protect patients from products that pose potential significant risks, while accelerating access to safe and effective new therapies according to Former FDA Commissioner Dr. Scott Gottlieb. The FDA plans to achieve this over the coming years by driving stakeholder engagement with the developing regulatory framework in order to efficiently advance access to safe and effective regenerative medicine advanced therapies.

However, so far, progress by the pharma industry in coming into compliance with FDAs regulations for regenerative medicines has been slow, despite the grace period set by the FDA before it fully exercises enforcement fast approaching (ending in November 2020).

In order to speed up the process of bringing novel medicines to market, the FDA is toying with the idea of fast-tracking products that are deemed low risk to patients if sponsors have engaged with the regulatory process and demonstrated responsibility by filing Investigational New Drug Applications (INDs).

The FDA has also promised to strengthen its enforcement action against drug developers who are marketing unapproved products, prioritizing cases where the threat to patient health and safety is largest.For example, last November the FDA stepped in where a Californian business was selling stem cell products using umbilical cord blood for the treatment of arthritis and other conditions, despite this form of treatment not having FDA approval for that particular use. Several patients (at least 12) undergoing this treatment were hospitalized after developing infections of the bloodstream and joints, as well as abscesses along the spine and skull.

In summary, one of the FDAs central aims over the coming years is to drive stakeholder engagement with the developing regulatory framework for regenerative medicine advanced therapies in order to efficiently advance access to safe and effective new products.

The promise of regenerative medicine requires an innovative look at the complete product lifecycle, including the development of an efficient distribution network.

Once these novel drugs become mainstream, the entire healthcare ecosystem will have to adapt. Regulatory approval for any drug relies on it safely and successfully fulfilling its medical intent. As such, information about supply chain management needs to be submitted to the regulator after the completion of phase three clinical trials, including packaging, labeling, storage and distribution.

The clinical supply chains required to deliver these therapies are arguably the most complex the industry has seen so far, even more so than for biologic medicine. Thats because, unlike many mass-market drugs, regenerative medicine is either personalized or matched to a unique donor-recipient.

The distribution of regenerative medicine therapies is further complicated by the fact they are also extremely sensitive to exogenous factors like time and temperature. Therefore, there are strict conditions under which these therapies must be transported and received.

Advanced IT solutions and monitoring systems are being developed and employed to ensure end-to-end traceability across the pharma supply chain. These are giving clinicians access to view the progress of therapies and their distribution in real-time and allow users to automatically schedule or amend material collections in line with manufacturing capacity, helping to keep the supply chain as agile as possible and avoid costly wastage.

The live tissues and cells which form the basis of regenerative medicine products are highly sensitive and some have a shelf life of no more than a few hours, making distribution a complex task. Therefore, materials need to be transported from the site of harvest to manufacturing facilities, and from manufacturing facilities to medical institutions under strictly controlled conditions, within certain time periods and temperatures, according to different cell and tissue requirements which can vary from product to product.

Temperature-controlled logistics solutions are vital to ensure a safe, effective and financially viable supply chain network for these high-value shipments. Cryopreservation is one technique increasingly being used to deliver medicines at optimum temperature using vapor phase nitrogen, however, many clinical settings remain ill-equipped to handle such equipment.

Onsite production is an alternative manufacturing arrangement, particularly for autologous products which are derived from a patients own cells. However, this throws up a number of compliance and infrastructure challenges, as the hospital would need to comply with a host of regulations including installing a licensed clean room which may not be possible given budget restrictions and limited space onsite.As a first-generation technology, stakeholders will have a greater tolerance for higher pricing, but only for a limited time period. By streamlining the currently very expensive manufacturing process and improving supply chain management, yields will automatically get larger and costs will slowly come down.

While there are many challenges in the road ahead, 2019 certainly appears to be the start of regenerative medicines move to the big time. Just like big data and artificial intelligence is transforming the practice of medicine, regenerative medicine holds the promise of extending the bodys natural ability to replenish, replace and rejuvenate itself.

If the global health industry can work collaboratively on overcoming the challenges presented by delivering safe and effective advanced therapies, a dramatic extension of the human healthspan is possible. We may even reach the point where no disease is considered incurable, transforming healthcare as we know it.

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The Opioid Epidemic: Past and Future – Psychology Today

November 21st, 2019 2:41 pm

When I said goodbye to Dylan on November 21st, 2013, I did not think itwould bethe last time I would see him. He left me smiling, on his way to visit a friend in Long Beachfor the night.That evening, at the young age of 26, Dylan was found deceased. His cause of death was an accidental overdose on Oxycodone.

Dylan was one of over 16,000 Americans who died in prescription painkiller related deaths in 2013 (in 2017 it was 47,600).The current opioid epidemic is unprecedented. Reports state that more than 130 people die from opioid-related drug overdoses each day, with the economic cost of the opioid crisis estimated to be $504 billion.

While effective analgesics, opioids are highly addictive, and adult patients undergoing surgery who receive an opioid prescription are at an increased risk of misusing and persistently using opioids. Time and time again, America witnesses thesame story:a patient visits a doctorcomplaining about a sudden moderate pain or perhaps a chronic issue; the doctor provides the quickest solution on the market, prescription narcotic painkillers; the patient leaves satisfied and often on their way to a nasty addiction.

But whyis this story becoming more common rather than less, despite increasing awareness of the prevalence of addiction in mainstream American culture? Why havephysicians dishedoutmore of these medications in recent years,rather than refusing to provide them to patients?How and why did opioids transition from being a treatment for end of life illness and postoperative pain relief to a commonly doled out solution to headaches and back pains? Theory suggests, and research confirms, that doctors were influenced by pressure from two angles: that of the manufacturers and of the patients.

The irony is that prescription narcotics do not fit their new purpose. According to Dr. Andrew Kolodny, president of the Physicians for Responsible Opioid Prescribing, controlled narcotics such as Hydrocodone and Oxycodone are actually ineffective in treating long-term pain.However, in a culture of fast food, instant messaging, and quick results, Americans seeking pain relief are not as concerned with the long-term solution.

A lot of societys trust goes into the capabilities of modern medicine, and while the rise of prescription opioids was strongly driven by manufacturers and pharmaceutical companies, patients welcomed it.And when the patients have a demand, the pressure to fulfill these needs falls on the doctors. As Celine Gounder, physician, public-health specialist, and medical journalist wrote in the New Yorker, The promise of a set of medicines that could cure pain was appealing to many patientsand, with a customer-is-always-right mentality having pervaded the doctors office, patients were able to pressure physicians to satisfy their requests for the pain pills theyd begun hearing about. Gounder explains the difficulties for a doctor to deny the requests of their patients and send them out of their visit dissatisfied. Doctors have a hard time saying no, whether a patient is asking for a narcotic to relieve pain or an antibiotic for the common cold. We are predisposed to say yes, even if we know it isnt right.

Whats worse is the consistent consumption of drugs like Hydrocodone and Oxycodone leads to increased tolerance and a condition called hyperalgesia, which is the increased sensitivity to pain after long term intake of pain medication.These consequences, in turn, require more pain medication for the patient and dependency develops before the drugs were ever technically abused.

With such a gradual progression to reliance on drugslabeled as legal and supplied in unnecessarily high quantities by an authority figure in a lab coat, patients and drug seekers do not fear the consequences of addiction or overdose. It is difficult to believe that the doctors we trust and depend on would put us at risk with the frequency and justification of prescription, the amount of opioids per prescription, and the number of refills on each prescription. The reality is that pain medication is not meant for long term use and the amount of pain after an operation should only last up to one weekHowever, theres not enough awareness about how serious this crisis is, Kolodny said. I dont think enough doctors know that these painkiller medicines dont work for chronic pain.

The pharmaceutical companies, from the start of this painkiller epidemic,capitalized on their ability to keep doctors misinformed. Big drug manufacturers recruited attractive marketers to convince physicians that their drug was the best painkiller on the market. We had cheerleaders from Big Ten schools, with no medical background or knowledge, put into a boot camp to learn the workings of the pharmaceutical industry, the doctor they will be selling to, and the benefits of their drug. It is these businessmen and women that are going into our doctors offices and selling our health care providers on what will be best for us, our family, our friends, and our loved ones.And doctors have been temporarily pleased when their patients reportless pain, considering their job well done.

Unfortunately, once a doctor has begun prescribing these medications to the patients, it is difficult for them and their successors to cease providing these drugs. Taking that stand would lead to unhappy and dissatisfied patients, and the potential accusations against the doctors of malpractice. There are also the doctors who just dont want to take the extra time during a busy day to explain why that prescription for a narcotic isnt a good idea and those who use the promise of prescription narcotics to persuade patients to keep their medical appointments, or to take their other medications, writes Gounder.Dr. Sanjay Gupta expressed similar concerns in hisCNN article:It is easier for a doctor to write a prescription than to explore other effective options to combat pain, and it is easier for patients to take those prescription pills than to search for alternatives themselves. Both those things must absolutely change."

So how can the methodology of doctors treating pain be improved? Just as important, how can the patients understanding of a doctors decision to deny narcotics in certain circumstances be improved? The work must be done on multiple levels.Primarily, between the physicians and the FDA, there needs to be a relabeling of painkillers. Currently, the labeling on narcotics has no suggested maximum dose or duration of use by the FDA. Kolodny describes this as being very broad. He insists thatthe way to turn this epidemic around is for doctors to prescribe painkillers more cautiously." And according to Kolodny, the FDA must change the labeling requirements on prescription painkillers so that it is easier for medical schools and the larger medical community to prescribe these meds more cautiously."

The next step would be providing education to healthcare providers from sources other than the pharmaceutical companies. While doctors, for the most part, have good intentions when prescribing medication, they receive no more than a week's worth of education on pain and pain management. Education on addiction, predispositions to addiction, and abuse of medication could help doctors better identify at-risk patients and take preventative measures or connect those suffering to treatment.

As patients of our doctors and consumers of the pharmaceutical industrys products,we must also take some action. With the knowledge that these medications could lead to negative consequences, we have the choice to seek other forms of pain management. Further, there are DNA tests available to see if you are predisposed to addiction. As a society, it is important that we know our own bodies and takesteps to put an end to this pill epidemic.

Dylans death isjust one of the countless lives lost. When we receive a prescription, we never think it could change our lives or the lives of others. Dylan did not get his first pain killer prescription with the intention to abuse the medication. However, as the refills were readily available, so was the opportunity to develop what turned out to be adeadlydependency. In a society where we are addicted to relief, a small prescription needs a big warning.

This blog has been written by Dina Khoury and Dr. Zeev Kain. Khouryisa medical student who is planning a career in psychiatry,UC Irvine School of Medicine.

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The Opioid Epidemic: Past and Future - Psychology Today

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Smart toilets could turn your pee into research gold – Mashable

November 21st, 2019 2:41 pm

Pee could be a health goldmine. And to make the most of it, the world needs smart toilets.

That's what a new, small-scale study published in Nature this month seeks to establish: whether regular urine collection and analysis of the thousands of telling, changing indicators in our pee can reliably serve up information about a person's health.

The study's University of Wisconsin authors, Dr. Joshua Coon and Dr. Ian Miller, say more research is still needed as the 10-day experiment only had two subjects: Coon and Miller themselves. However, they also think that a non-invasive device that could collect and analyze a person's urine like, say, a smart toilet could work as a revolutionary tool for personalized, predictive health care.

Oh, and wouldn't you know it, they're making one such smart toilet themselves. But they're not the only ones.

How Coon and Miller envision the smart toilet of the future.

Image: Dasom (Somi) Hwang

Recently, health-tech companies and even big tech players like Apple and Google have gotten into the business of harvesting health data, mostly from AI assistants, fitness trackers, smartwatches and even the smartphone in your hand. The current drumbeat in healthcare is that big data will be able to help us monitor our health in real time, as well as predict disease and health trends at a societal level in the future. And in this coming era of data-driven medicine, the study's authors think that urine is an untapped resource.

Coon and Miller research metabolic systems at the University of Wisconsin and Morgridge Institute for Research (with work partially funded by the National Institute for General Medical Sciences). They analyze the molecules that reflect what our body has metabolized (called "metabolites"), whether that's something we ingest, or is the consequence of an internal bodily process.

Researchers have already established that there are thousands of metabolites in urine, with many of them linked to our own habits like smoking, drinking, sleep, exercise, and even disease. As our habits change, so do the levels of these metabolites.

"There aren't that many bodily fluids that you can get access to that have a window into health," Dr. Michael Snyder, a Stanford University professor who studies biomedical data for healthcare, and is not involved in the study, said. "Urine is just one of those that it makes sense to be monitoring."

The theory is that, on an individual level, regularly keeping track of your urine could give you information you can act on. For example, it could eventually tell if you have a urinary tract infection brewing before you even display symptoms, or if you're getting enough exercise, drinking too much alcohol, or are registering inflammation that could cause disease down the line.

It could also serve as a compliment to the sort of digital healthcare many people are already doing, such as monitoring heartbeats with Apple Watches. Coon says that analyzing urine for lifestyle information could give a person a fuller vision of the why behind having heart troubles something an Apple Watch alone can't do.

Your pee could turn out to be somewhat of a "fingerprint."

Even beyond what this data can tell about an individual, Coon says we don't yet know what a large batch of this data from many people could tell us about disease outbreak, or other types of medical predictions down the line.

To tap into this potential, Coon and Miller tried to see if they could measure how information in urine corresponds with lifestyle choices, such as sleep or alcohol consumption. By keeping track of their habits, they were able to establish that specific metabolites do fluctuate based on lifestyle.

Your pee could also turn out to be somewhat of a "fingerprint." The metabolic makeup of our urine varies from person to person it looked different even just between the study's two subjects! Knowing a person's "baseline" levels could make personalized healthcare more precise. For example, if a person's baseline changes, Miller says that that could serve as a warning sign, enabling "preventative treatment, instead of dealing with symptoms as they show up."

Regularly comparing that baseline to changes is what particularly intrigues Snyder.

"This frequent measurement lets you really follow changes in [a person's] health state, and that's rarely done in medicine," Snyder said. "Knowing your own personal health state is very, very important. And then finding shifts from that is the key to early detection of disease long before it's symptomatic."

The study presented a third finding: Collecting pee is not only time-consuming and resource-intensive it's annoying. Which is why they say the technology needs to catch up.

"It turns out its not convenient to collect every urine sample you make we found that out," Coon said. "But if you had a toilet that did that for you, that would make a difference."

Coon's research group is working on a smart toilet that does just that. They say they will have a prototype to demonstrate their ideas in Spring 2020, though they declined to share any preliminary images with Mashable. After that, it will be about getting funding, conducting clinical trials, and bringing it to market. It may sound like a long way off, but their vision is clear.

"The device that we are working toward is just the toilet," Coon said. "It looks like a toilet, and it samples [urine] without you having to do anything. That is a way I think to be able to acquire data that will be helpful to people."

Coons' device would sample urine every time an individual uses the toilet, and has a built-in lab tool (called a mass spectrometer) to measure samples. That reading would go to a patient's smartphone, where they could monitor their health in real time, or even send that info to doctors, or healthcare analysis companies.

An early model of Toto's discontinued smart toilet.

Image: YOSHIKAZU TSUNO / AFP via Getty Images

Another company, Toto, built a smart toilet in the early 2000s that would allegedly "analyze sugar levels in urine, check blood pressure, body weight and even measure body temperature and hormone balance." However, Toto discontinued it, owing to low demand.

Other companies including Panasonic and even Google have made moves to develop smart toilets. But they were all limited in function, collecting measurements like blood pressure, body fat, and blood in the urine. Coon sees his device as more far-reaching, with consequences for both the individual and society.

"The fascinating thing for me about this is that there are so many possibilities that one could imagine," Coon said. "It really comes down to if one could build this device, and make these measurements on a large population, it would really, we think, open the doors to changing how we think about tracking health and lifestyle."

Is Coon's vision for his smart toilet realistic?

While Snyder agrees with the theory that regularly monitoring metabolites in urine can deliver health insights, he is skeptical that Coon's 10-day, two-person study lays sufficient groundwork.

"I think we need larger studies to demonstrate utility," Snyder said. "I don't doubt in the long run they will be useful. The question is just how quickly, and I don't know the answer to that."

Other experts (and competitors) are even less gung-ho.

"I just dont think its very practical," Vik Kashyap, the founder of human waste analysis company Toi Labs, said. "They're exploring interesting things, but I dont know if theyre ever going to make their way into the real world."

At Toi Labs, Kashyap and his team have been studying the best way to bring health tech into the bathroom for years. His company is currently conducting clinical trials for their own smart toilet product, True Loo. It uses AI to analyze pictures of stool and urine for health insights (what your poo looks like can apparently tell you a lot about your health!). Kashyap said that the choice to use photography instead of the "mass spectrometer" lab tools like Coon was intentional because he says that the tools and science Coon is relying upon have some major flaws in a commercial setting.

"Weve been working on a smart toilet for more than a couple decades combined," Kashyap said. "For this kind of approach to reach the market, it would be a very slim chance."

Kashyap views mass spectrometers as large, expensive tools that work in the lab, "but don't necessarily work in an everyday toilet environment."

Kashyap is also not sold on Coon's science. He says that mass spectrometers are good at looking for specific things, like in drug testing. But does not believe they are proven as well as they need to be for a true at-home smart toilet.

Other competitors and experts share that skepticism. Raja Dhir, the co-founderand co-CEO of microbiome research company Seed Health, doesn't see the potential for urine testing without also testing blood and poop.

"The concept of continuous measurement of biological data is intriguing," Dhir told Mashable. However, he's not convinced that people will actually get much use of out of it in the real world.

Still, Coon, Miller, and even Snyder are optimistic that, with enough study, time, and investment they can prevent the future of healthcare from just being flushed down the drain.

"Ive been saying that someday, we need a smart toilet," Snyder said. "I think the day is here."

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Smart toilets could turn your pee into research gold - Mashable

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Breaking Down The Invitae Short (Podcast Transcript) – Seeking Alpha

November 21st, 2019 2:41 pm

Editors' Note: This is the transcript of the podcast we published last week on Invitae (NYSE:NVTA). We hope you enjoy.

Daniel Shvartsman: Welcome to the Razor's Edge. I'm Daniel Shvartsman. I'm joined by Seeking Alpha author Akram's Razor on this show. Each episode we take an investing idea or theme that Akram has been looking at for his personal investing as well as the Seeking Alpha marketplace service he runs, also called The Razor's Edge. We look at the ideas themselves, stress test them, try to figure out where they might go right or wrong, talk about what's been going on, and talk about the research and analysis that led to this take.

The idea to share some current investing ideas here into consideration, but also get the ins and outs of deep fundamental market research today. This week's topic has a lot behind it. The ticker symbol is NVTA. The stock is Invitae. Akram released a short case on the company on Seeking Alpha on October 11th, that went long in terms of breaking down why the genetic testing company was more like a WeWork than an Amazon. In other words, the company has had prodigious revenue growth, but it's come at a cost of increasingly negative cash flows and limited competitive advantage, in Akram's view. Was a thoroughly researched short case and as is often the case it's attracted a lot of attention, both positive and negative.

On today's Razor's Edge, we're going to talk about what brought Akram to this case, what investors are missing, and some of the reactions since he went public on Invitae. We're also joined by a colleague of Akram's, James who can add some insight on this topic based on research he's done on the stock as well.

Before we begin a quick disclaimer and disclosure; The Razor's Edge is a podcast on Seeking Alpha's The Investing Edge channel. The views discussed belong to either Akram, James in this case, or me respectively, and nothing on this podcast should be taken as investment advice. We'll disclose any positions in any stocks discussed at the end of the podcast, though upfront I can say I have no positions in any of the stocks we plan to discuss, Akram is short Invitae and long Myriad Genetics, and James is short, Invitae. We're recording this on the morning of November 4th.

Listen to or subscribe to The Investing Edge on these podcast platforms:

All right, guys. Good morning. Welcome.

Akram Razor: Good morning.

James: Good morning. Thanks.

DS: So let's just go really basic, why Invitae? What brought -- why does your radar get on this stock? Where did they come up?

AR: That's definitely an interesting part of the story. I guess the starting point was, there was people shorting Myriad. So I follow the Southern Investigative Reporter. And they've done a couple short pieces on that. And I kind of have taken a look at it briefly, which caused me to take a brief look at Invitae, and that was probably like, May or June. And then Ilumina missed big time on earnings, and I've traded Ilumina several times of the year. I've never traded any of these other stocks in terms of that. But it kind of got me interested in the space. And I guess what kind of, I mean, like, I think I had pinged James on it a couple times being like this is like this is worth looking into, but like neither of us had really gotten that excited about it.

And then there was a report that came out by a short seller, recommending the stock is an amazing long idea, which I read, because I know the short seller and his work. Once I read that, I was like, I need to look at this company a little closer. And then just the typical process, like pulling up their filings, seeing exactly what's going on financially, and I was just like, wow, this is just an incinerator. What are they doing? Why is -- like, what's the business model?

And that brought me to, there's an author on Seeking Alpha who had published a lot on this over the years, capital markets, laboratories and read their work, and they made these Amazon compares where, obviously, that's where you get a little bit of a heightened radar, when a laboratory diagnostic company is being compared to Amazon, which I mean, I don't know also if you know -- and I had like a brief experience with Theranos in 2000 it was say like, early 2014, like back when it was like -- I was picking on the Decacorns then, my favorite, like when I used to write my market commentary and I'd have a little bit of fun with it.

At the time, the two I was having fun with were Zenefits and Theranos. But I mean in Theranos' case, like I was just curious as far as what like -- I mean, it was a private company, $10 billion, obviously a lot of hype. I was like, wow, do I short Quest and LabCorp, right? I mean, I can't make -- I can't invest in Theranos. But if this company is so revolutionary like it, there's this pretty simple thesis out there in the public markets where I mean, if they're going to stick a lab in a box, I should go short Quest Diagnostics and LabCorp.

And I have, on the medical side, an extensive network of friends and family. So I ended up doing just one call with someone who'd been at Quest and in the laboratory diagnostic space, pretty senior for about 20 years. And like, I mean, it was like a 30 minute conversation. I felt stupid by the time it was over. It was just like, he's like, are you an idiot, you can't stick a Lab-in-a-Box. It was like -- it was literally like that, after like being very polite for a little while. So that type of stuff kind of intrigued me. And Theranos ended up being Theranos. I never really did much more with it after that. And then Wall Street Journal came after it, and it became this cautionary tale. I don't know if James -- did you follow Theranos very closely, I don't even know if we really discussed that?

J: No, I had heard from some VC friends who were very skeptical of it all the way through. But I wasn't that close to the name myself.

AR: Yeah, I mean, neither of us I would say, I would characterize myself as close to it. But I mean, I did take the time to literally be like, hey, do I short these stocks because of Theranos, right? It was like an investment idea at the time.

So yeah, I mean, I guess that's what started it, right. I mean, like Theranos had this -- and then the message was just kind of just like affordable blood testing for all, a social cause being compared more to, like technology differentiating companies and I mean, Elizabeth Holmes like to associate herself when she talked about things, when she compared herself to the Google Founders and Facebook and like, I mean, if you saw the documentaries like here we were at, in Brazil, and this is where we -- who was sitting there, and the Google guys, and the Amazon and Facebook, and we are the stars of the show, right?

And if you look at Invitae, I mean, like on the surface, it's like there's a social enterprise element to it, right? Where it's just like, we have a mission, and this mission is to make genetic testing affordable for all. I mean, like, they don't care, they don't describe themselves as like a laboratory diagnostics company, right?

DS: Well, they --

AR: That was a genetic information company. Go ahead.

DS: Yeah. I mean, if you look, I have got their 10-K open, their last one and it's -- our goal is to aggregate a majority of the world's genetic information into a comprehensive network that enables sharing of data among network participants to improve healthcare and clinical outcomes. So it's this.

AR: Yeah, so what does that mean?

DS: Right. You know, it is this very -- it is very big mission, right. It is very big.

AR: Yeah, I mean, James, obviously has some views on this. Like, I mean, what do you think of that part?

J: Well, I think that really comes down to the crux of the investment case here, which is, just because something sounds good as a sound bite doesn't mean that it actually makes sense in business. And so the idea of accumulating the world's genetic information, you would argue, seems like if you could do that would allow you to capture rents on that database. But there are very real issues with that. Namely the company has said that they won't do that. And then when they're pressed about how -- whether or not they will do that, they kind of seem to give non answers what I can tell.

So that's one of the questions right that that I think would be very helpful for the company to lay out there, very specifically, which is, if we gather all this data up, and specifically what data is being gathered? Are they -- is that data, they've also released to a common database, like they say they have been doing, is there additional data that they're not releasing?

AR: Well, I mean, the data that they're sharing with the common database is the variant of unknown significance data, right? So I mean, that's what they're contributing to Clinvar. We don't really know. But like, I mean, I'll be honest, like if I was to go in and have hereditary cancer test, I would have never thought once about, like, who the lab doing the test is or ask the oncologist anything, but like literally now knowing this business, I mean like, make sure you're not using Invitae, because I have no clue what they're going to do with that data.

Like my DNA is a product for them to figure out somewhere down the road just to do something with it, I mean, it's so -- like James just said, it's very bizarrely unclear, which is decidedly convenient when you're running a business model like this.

DS: So step back for a second. So the thesis -- the company's thesis is that they're providing genetic tests. And then they're aggregating that, they provide it at -- arguments are they providing it for below the cost that they actually have to pay to their providers to actually deliver the test but low cost testing that they can then -- if we're going to use the Silicon Valley jargon, that they get the flywheel of more genetic data and improve, they get a lot of volume, and eventually, that's both going to give them scale to lower the costs, but then also they're aggregating this huge genetic database, which as you kind of point out, Akram, they're going to have to do something with to make it reasonable, which raises concerns in of itself. But the idea is that eventually they'll get scale from offering at cost that will allow them to become a profitable business, I think. That's how I understood the company's take and the company's argument.

AR: I mean, like James just said the company hasn't explained that. So if you look at this company's history, this isn't like a startup, number one, right. So this company was founded in 2009. They've been at this for a decade, okay. Initially, they were kind of rare disease focused, right?

Like where they're deriving the revenue, if they were to actually describe themselves accurately, they would be like, we do hereditary cancer testing far cheaper than Myriad, right? And I mean, like, I think that's an important thing to look at this. I mean, there are sources of revenue, which is generally speaking what has attracted people to the stock, it's not science, right. It's not like you've developed a test or you're like Foundation Medicine and you've got this companion diagnostic clinical trials and you are about to do something where you're going to earn a high margin, because you've developed something nobody else has. That's typically, what people get excited about in science and biotechnology, right?

You get rewarded for R&D, okay. These guys have approached the market that Myriad discovered the BRCA mutation in 1994, okay. That's like what the indication of hereditary cancer right? I understand cancer, 90% of it is not hereditary. So you're looking -- when you talk hereditary, there's a less than 10% chance that it's something hereditary. That's helpful from a clinical standpoint, as far as your treatment for cancer diagnosis, whether it's early or late stage or whatnot.

So this company came into this space in the sense that Myriad had a monopoly on this gene, right? They started doing their first BRCA testing lab kit was like 1996. They had the patent on that gene till 2013 when the Supreme Court struck it down, right. So these guys entered this space, essentially, from that standpoint as a competitor against Myriad. And once that space kind of opened up in hereditary cancer testing, I mean like, well, you can't patent these genes, right? Which is great for competition, but what's the flip side of it?

If I make a major discovery on gene X correlates to disease Y, right? And I can't patent it and I'm running like a test that kind of identifies that historically, kind of tough to build a very profitable business around it. So when we go back to like what you were saying about like this whole genetic information and whatnot, the most interesting thing about this business is look at the rest of the landscape. Nobody's selling the story, like Myriad's still the revenue leader in hereditary cancer testing.

The other space the company is in deriving revenue from is reproductive health, carrier screening, non-invasive prenatal screens. And that's the most crowded market ever. It's got Ilumina and Sequenom, which is owned by LabCorp, like pretty much, they control the IP there. And then there's like a half a dozen other competitors owned by large companies.

So like, in hereditary cancer, you've got Myriad. And then you kind of have this like at a huge, huge, huge discount to Myriad prices, Invitae, right? I mean, like now they're running what, $99 tests, okay? So you look at it and you can sit here we can just, like figuring out what they want to do data wise and the fact that it's Vegas kind of important. It's also important in the context of -- well, there's a whole industry here, right? I mean, this is at least what -- we got some heat when we cautioned this like, some of this has attracted obviously a lot of retail investors by using the Amazon compare. And, in the initial thesis it was like a cautionary mention at the end, like that the laboratory diagnostic space doesn't need another Theranos.

And at least in Theranos' case, what they were selling to investors was we're building a better mousetrap essentially, right? Like we've got -- we've engineered something that's going to change the way we are able to do testing. And that's not the story here. The story here, I mean, if you go back to the founder in 2016, there's a couple of interviews with him. And he literally says like, we're providing the same test that everyone else is providing, we're just making them more affordable. That was that's their initial story, right.

So I mean, you do kind of run into something like that, which is where, like some people may think it like, you know, oh, it's very, self-serving or opportunistic to compare this to WeWork. It is, exactly like WeWork from a business standpoint. Like you can't get around that fact. And I think the Amazon like -- and this is not like some guy writing a really bullish Seeking Alpha article and using hyperbole, the management sticks to compares. I mean, they -- literally they have a slide in their investor deck, what we can learn from Amazon, and they make statements like our competitors -- what did they say, James, is like the competitors margin is our opportunity or

J: Yeah, something that effect. Yeah, you've heard a lot of ground there, Akram. I think the important aspect of what you've said and the commonality among all those points is that the management team has made some very high level statements about the promise of this industry and the promise of their company. And they could really answer a lot of these questions if they wanted to, right? They could say, okay, here is our revenue breakdown from cancer or nips [ph], kind of other panels, which don't have necessarily the clinical efficacy.

Or they could say, here's our -- here's what we're getting from the various cost cutting or network effects or economies of scale that we promised. And here's how this is going to develop, but they don't they just say, trust us, it's all going to work out. And the way that it's not [ph] going to work out is that it worked out for Amazon. So it's there's not much transparency, there's a lot of just kind of big picture verbiage I would say.

AR: Yeah. I mean, 100% and like, I mean, you get the Amazon story, Daniel, right. I mean, if you look at it, people like, if you look, well, come on, Amazon was losing money. No, Amazon was improving operating cash flow from literally from day one. I mean, people forget, like, you make money selling DVDs and books online, particularly if you don't pay your suppliers for 100 days, right? I mean, like, where was Amazon after a decade? It was already a behemoth, right?

So when you look at it, Amazon had someone else, i.e., their suppliers funding their growth. It's free, cheap capital. This company went and IPOed in 2015, at $16 a share, had like 25 million shares outstanding. They're at 100 now, four years later, right? I mean, it's like, they keep going back to the well. So if you're an investor and you're looking at it from a return on investment on money, you're giving them. I mean, you have a serious problem. And if you look at it, and you say, hey, I'm going to compare myself to Amazon. Well, Amazon had a cost structure that attacked this cost structure of brick and mortar, okay?

They benefited from so many things. We didn't have sales taxes, if you were paying on Amazon as a consumer. They benefited from the fact that they went into markets with huge existing volume already, books and DVDs. They didn't have to convince people to buy X, Y and Z. They were already huge volume markets. I mean, I'm sorry, but like hereditary cancer testing. It's not something people get excited about to go online or buy as a gift for a friend.

I mean, like, we get the DTC space, and even that has already slowed down drastically, and that's Ancestry. And if Ancestry slowed down at like 30 million tests, right, like, you really think people are going to be super excited as individual consumers to be like, I really need to figure out whether I have a history of cancer right now. I mean

J: Well, and more importantly, more importantly, I think there's a healthy amount of skepticism in the medical community whether or not these tests are useful, right? Like the issue with any test is, if you find something, an indicator of a disease. Does that help you catch the disease? Does it help you catch it earlier than existing testing or physical exams, or other ways of seeing the diseases there? And then can you do anything about it?

So, I think one of the issues here is even if you were to send your saliva [ph] sample out, and you came back with saying indication that you might have liver cancer potentially. A, you wouldn't know, if that were real, because it's really just a correlation at this point. There's not enough data. B, even if you knew, it was real, there's really not much to do except worry about it. And so you have a lot of additional burdens on the patient and the healthcare system in terms of emotional and financial burdens, without any clear benefit.

And so I think within -- as I'm saying, within breast cancer, that there is a clear benefit in terms of efficacy and outcomes. But for the rest of the space, it's really not clear. And that's why, if you look at the treatment protocols for most of the commercial payers, they don't pay for all these tests, because the research doesn't demonstrate that they should.

DS: So one of the things I'm -- as we're throwing around these comparisons. I'm thinking about the -- there's a notion in Silicon Valley and sort of abroad, the market, the idea of tech, tech as a category is becoming less and less meaningful, because companies are adopting online models or tech models to different verticals. And what I think about with Theranos and Invitae, specifically, healthcare is a very complicated sector, both in terms of the way payers work and we can get into Medicare in a little bit, but the way the payment system works.

And I'm not talking even about what might or might not happen in the future with changes to insurance. But just -- that's, I think, always been fairly -- you have to really work through it. And the articles for example, there's looking at the different reimbursement codes and that sort of thing. Like, it's more than you have to do to figure out, well, are they going to buy this software tool or not?

And then also, Theranos is a problem, because they were actually -- there were issues of fraud around people, things that were supposed to help people's health. And so I guess I'm just kind of, I guess, I wanted to hear a little bit more about like, because -- a lot of the response.

AR: Well, I mean, look -- let's, I mean, if you think about Theranos, where really was the fraud. The fraud like, I mean, if you read the indictment, what she's really on the hook for the biggest time is misleading investors, okay. I mean, that's the biggest part.

Yes, correct, like at the end, there was issues with the lab testing and they were getting inaccurate results because by the time she did that deal with Walgreens, and clearly they were at a point where they were desperate for showing meaningful revenue, because they need to raise more cash, right? Because they still haven't made the Edison work, right? They're trying to engineer a problem. They're working on it.

She didn't set out to commit fraud, right? She set out to build -- to stick a Lab-in-a-Box, right? But she had bigger aspirations. She wanted to take -- that she wanted to aggregate your data. She wanted to stick it in this cloud called Yoda, right? I mean, if you look today, you still have people who defend -- I mean, what's his name?

DS: Yeah.

AR: Tim Draper has really defended her. And what does he defend her on the point, and his point is that look, she had this vision to give you a movie of your health, i.e. like look, I get my blood work once a month, and that goes into a cloud, right? And my physician can track it. And I'm building a historical picture of a trend, by having more real time information on my blood work, cholesterol, everything right? So that creates preventative medicine in their view, right? Like your ability to have an earlier and more accurate versus a snapshot, right?

So he's like, look, she had that and was great and I genuinely have discussed this with James. I believe if she had IPOed this company and the company had started out as like, hey, she's got this Edison and this finger stick. It would have been just like binary tech play, right? She either makes it or she doesn't. And people would have debated that and thought that out there would been the believers. And then there would have been the skeptics, but she would have had plenty of time, as she gauged how that was working, okay?

To find something that generates revenue, which investors are willing to pay for, like with her inflated market cap on the Edison optimism, where she could just do regular lab testing like Quest and like LabCorp, but she would obviously do it at a lower price, right? But she would sell you the story that I'm going to stick this in the cloud, and you're going to pay a subscription fee, right? And that subscription fee to that cloud, Yoda, where all your information is and your general practitioner can access it and whatnot, that's the business. That's where I make money.

Of course, what's the problem with that business? And that business is -- well, I mean, that you're going to be like, well, you're losing a lot of money per test, doing your tests at a lower price than Quest and LabCorp or whatever to provide this back end service, why can't they do that, right? I mean, like, that becomes the same thing because you're going to need the same infrastructure. That's where she ran into issues. She's collecting data and she doesn't have the lab infrastructure to do it at the scale that these guys are doing.

If she'd been like these DTC companies, 23AndMe ancestry, she could have actually struck a deal, which is like, I'll be the cloud and I'll outsource the testing to them. And I will take a loss on the tests, because my investors are going to subsidize it, right? I mean, there was -- there would have been many Ways, but of course, she was also trying to kill their businesses. So it didn't work, right, with her engineering. but like, I mean, the bottom-line is, is if you look at it, like, it's something where you had a potential business model in that sense, where we would be asking the same questions that you'd ask about in detail, right? Like what are you doing that's different?

If you look at them today, Quest and LabCorp, they've entered into direct-to-consumer testing. I can go online and order my own tests and schedule the appointment and go pick them up, right? I'd like it's really, like, it's something where I don't even need to go through my medical practitioner if I want to get tested. And I don't know, to the degree I mean, I've discussed this with other people in the medical community on the testing side and I'm just, why isn't there a VIP service like, if I'm an extremely wealthy individual, where they come to my house, do the work, store in a cloud. And there's access to my blood work, on let's say -- but we don't have to do a monthly but let's say every three months, right?

These -- I mean like these are obviously options. So when you look at something like that and you see what went wrong with this company, her biggest mistake was being private. It's like -- because with her turtlenecks and Steve Jobs and Stanford dropout, I mean, the benefit of doubt, she would have gotten, if you look at the benefit of doubt, for example, that this company, Invitae has gotten. I mean, their CEO says one thing, and then he does the other three months later and nobody has cared like, at all. No one's asking questions. I mean, I don't know if you -- have you watched the CNBC, the Invitae interview with him on CNBC, Daniel?

DS: No. No, I haven't pulled that up.

AR: If you watch that, you would not understand what the company does. It's like we are the company the key opinion leaders turn to and this -- like, he does not say I'm a laboratory diagnostics genetic testing company, who derives primarily its revenue from doing these types of tests. And we're doing them at a significant discount to a competitor, who has had a monopoly in the space for ages. And we're using that to generate volume and we're hoping to parlay that into other sectors. And this is like -- this is our business model. Because to be -- to tell you the truth, if you look at this closely, I don't think they figured it out. They are trying to figure it out as they go along and that's part of the problem here.

DS: Isn't -- you said, if Theranos that they could have arguably sold tests below costs, but then put the -- like, isn't that essentially what the Invitae has? They haven't maybe laid out that vision but they're essentially selling below cost to get into -- like they could build that into the cloud sort of approach like?

AR: Okay. No, let's not make that mistake, okay? I'm saying that Theranos, if they wanted to, okay, and wanted to pivot for a story to sell, that sells well, when you're dressed like Steve Jobs, and you dropped out of Stanford, and you're a unique character and you're -- you've got a Board that has these people on it. And you've convinced Tim Draper and Larry Ellison to invest in you and whatnot, right? When you've dressed something like that, and you've ticked all those boxes, okay, you could just be like, hey, I'm going to do the same blood work everyone else is doing, I'm going to do it cheaper. So come to me. And how I'm going to make money off of it down the road, is I'm going to store that data, and it's going to give you a real time picture.

Now if you were to compare this on genetic information, my DNA isn't constantly changing, right? So if I'm doing -- if my focus is hereditary screening, i.e., what's been passed on to me, and what does that indicate?

What is the usefulness of that sitting there, right? Number one. And number two, in her case, it would be like, well, you still need to build the lab infrastructure to do the tests. You're going to have to do huge volume. So any business that -- like I mean, if you listen to the CEO, he literally sits on conference calls. And he's like, we hope to do half a million tests this year and reach a million people next year, and on our way to billions across the world. Well, what kind of infrastructure, you need Amazon infrastructure for that, right? I mean, how many geneticists do you need, genetic counselors? The industry doesn't even have the employees. I mean, we were discussing this, like, how big is that industry James.

J: It's well smaller than then I thought it was. I think it's in the thousands of genetic counselors. I forget it, 10,000 or 15,000.

AR: So you're going to need lab technicians, genetic counselors, you're going to need the physical footprint. You're going to need logistics. I mean have you looked -- like part of the thing that like -- we found kind of interesting is just look at Quest Diagnostics. I mean, there was a $100 price target slapped on this thing. That's the market cap of Quest, okay? They have 3,500 trucks like 26 planes, 6,000 patient access points, right? They have infrastructure to test everybody.

The internet bull on this stock, he's been close to management. He's done a lot of write ups on it. One of his write ups was just recently, and I read it and he's like, I visited the company and the CEO told me that they're actually paying for the trucks to go to FedEx, to pick up the samples and bring them back instead of waiting for FedEx to bring them to the lab. And he's like, I've never seen a company who cares about the customer so much. And I am like -- I mean, sorry, logistics are part of his business. Collecting the samples and the turnaround time and what the infrastructure you need to do it, right?

Like that's not something of like, hey, I really care about my customer. It's something you have to do and unfortunately, Quest and LabCorp are sitting there with huge economies of scale and scope and infrastructure and the same machines available to them, and the lab technicians and the geneticists and everything to flip this switch on, and they're not flipping it on. Why?

DS: Right.

AR: It doesn't make money, because the volume isn't significant enough and the cost isn't at that point. So when this company talks about driving down costs, no, they're not driving down costs. Everyone else has a lower cost per test already established, because they have higher volumes in the space, right? If you look at it Myriad's cost per sample is in the $140, $150 range. If you look across all these other labs, who are doing the stuff and the testing on the reproductive health they're all far lower, right?

So this is a last person in the space coming and trying to get to the volume, trying to get to the economies of scale and trying to drive it down, right? But they still are subject to the same cost infrastructure limits. It's not amazon.com. They haven't eliminated the blockbuster employees sitting, that when they're competing against in DVDs like a Netflix or an Amazon or whatnot, they haven't eliminated the huge physical retail footprint that a Barnes & Noble needed, right? Like, they still have the same limitations, from a cost standpoint. They're relying on Ilumina machines, consumables, Agilent, Read [ph] everybody -- like it's the vials from, what's the company that sells the vials?

J: OraSure

AR: OraSure, right, like you're buying the same stuff from the same people. So it's when you look at it from that standpoint, like if they were to sell you a story about data or whatever, it's like, well, everybody else can sell us a story about data. Why are they selling it to us?

J: It's an interesting dynamic here, because when there was the rebuttal by this bullish commentator/endorsed analyst of the company, there was a comment that, hey, it's not just the raw data, it's not just the genetic information that is useful, because genetic information in and of itself doesn't tell you enough about the disease. And I think that's a partial indictment of the whole process. But more importantly, what the analyst said is, what the company does is they take that information and they combine it with a patient's medical record. That includes all of their scans, their CTs, their MRIs, all their historical blood tests, all their physical exams, and then it takes that data. And if you get enough of that data, then you can start running effectively very large statistical relationships and figure out, okay, which genetic mutations might be associated with which diseases.

The problem with that is, as far as we know, that's not what's happening. And yet the company, again, they've kind of endorsed this, this guy is an analyst of record, the company hasn't come out and said that. But that's not what's happening. Because if it is what is happening, I think they're serious privacy concerns. So I think it's very different, if you as patients and [indiscernible] into 23AndMe, you might sign a paper, some paperwork somewhere, but if they're actually signing away the rights to all their medical records. Again, I don't believe they are, but again, this is what would need to happen in order for this data to be proprietary and useful. Then I would imagine the consumers are not aware of that.

And so you kind of have this catch 22, if you're getting the data, whatever, this guy refers to it as the golden data, whatever it is, if you're getting that data, such that it's useful, you're probably in violation of some privacy laws, whether or not you are in terms of you're covered legally, I think just patients don't understand that's what's happening. And if you're not getting that data, then there's a very real question as to what exactly is the use of just this genetic information without putting it into -- in context without kind of correlating it to these other disease markers?

And again, this is a question that could -- that's very answerable by the company as far as we know, has decided not to answer.

J: I mean, look, there's also two elements of that, right. If you remember also, in his rebuttal, he pointed out to a subscription model, right ,where he was even saying that this should be looked at from a dollar-based retention standpoint like a SaaS company. So I mean, again, if he's saying this, it's something that well was spoon fed to him, okay? And that's part of the element here, when you're dealing with something like this, and you look at that, it's like, all right, so like, I go in, I do a test for cancer, but you know, a BRCA screen. And you're saying -- are you essentially saying that, in year one, you generated revenue off of the actual testing, but then in year two, and year three, supposedly, my DNA is something that just sits there, and they can find ways to make money off of, by farming it for some sort of data that they can sell to pharma.

And it's tenuous at best to even understand how that model would work, because if you look at the rest of the industry, you just have to assume, they're all idiots. I mean, how many tests has Myriad done? I mean, look, when you go back to this thesis, Daniel, one of the most important things here is, when I put this on, this company was bigger than Myriad, literally in enterprise value, it was bigger than a company with $850 million in revenue, 20 years of testing. They've done 6 million tests through some -- to that effect I think it is at this point.

They have a database that they've made a trade secret since 2004, as far as variant data. They have four times the employees of Invitae. I mean, if you were to look at this company from there -- one notable institutional bull in the space, like this bull doesn't own any Myriad, okay. And they have a genetic spawn, and they did like kind of throw like a little bit of a shade at this thesis when it came out. And I mean, I can imagine they got a lot of questions because they own a lot of the stock and they were like, these are the companies leading in AI.

And then they like -- they listed Invitae like two other names. And then they put in their tweet, which was almost essentially directed, not my gen [ph], which I mean, for someone like me, I just -- I didn't even really spend much time getting into the AI nonsense. But if you look at Myriad how many people with machine learning backgrounds and data scientists do they employ, plenty.

You could just go on LinkedIn, look at it, and draw your conclusion. But they're not out running around saying, hey, we got AI, we're doing stuff. We're literally running machine learning models on your DNA. We're figuring out better ways, a secret sauce. Like who would advertise that? If you actually have made the data a trade secret, and you refuse to share it and they've gotten a lot of heat for it, literally the whole industry had to band together to contribute data freely to Clinvar, because Myriad won't share, because they're like, hey, fine, you took away our patent, but who cares about that. Our ability to interpret this is better than everybody else at this juncture.

So again, you look at it, at something like that, and you're just like, well, there's companies who've been doing this for decades. And you're just supposed to assume that like data science is completely irrelevant to them. But the company that acquired an AI startup in July, by September is a leader in this space. I mean what, you know.

DS: Solet me -- so there are a few directions to go here. But let's quickly touch on Myriad. It's -- you're using it as a payer here, as I think you mentioned, it's -- short sellers have kind of had their eyes on it. Somebody like Southern Investigative Reporting Foundation has reported about it. Why are you comfortable with that as the other side of this trade given the fact that they've also come under fire?

AR: I mean, I don't know James, you want to tackle this? I'm obviously a lot more bullish on Myriad then most people. I would say, like, I can't really get my head around the short thesis, and I can't get my head around the short thesis in a relative context. I mean, if you've looked at the space there are some companies with some pretty crazy valuations. Myriad is not a hard business to understand. They have a cash cow in hereditary cancer. They've used that to diversify into companion diagnostics, into carrier screening, now into these pharmaco-genetic tests, psychotropic like for depression, which is a very controversial area.

A lot of a lot of volatility around Myriad lately, let's say the last six months, has been tied to this gene site division, and the way the FDA wants to treat these tests, where I get a DNA test that like tells me, I'm more tolerant for Zoloft over Prozac. And no science has shown any clinical efficacy yet, and it's a controversial area, because there's obviously some doctors, and they've been doing -- they've been running clinical studies to try to get this approved. And they missed the primary endpoints on it. But there's also an argument that in depression, which is like opioids, a national crisis, essentially speaking, and it's not going to get better, that there's nothing, and something is better than nothing. I mean, two-thirds of antidepressants are prescribed by general practitioners. Not -- you're not talking about the psychiatry side here. These are not experts on these drugs or on mental health.

And the argument is that maybe you give them something that starts this out with a little bit more direction, however little incremental it is. Now when the stock got hammered in the summer, on its last earnings, was because they said the FDA is pushing back on them on the labeling. And then recently, there was another genetic psychotropic-related test company where the FDA allowed them to resume sending the test information, but to the doctors. So the patient just gets this, like here's what your genetics say, but nothing about the drugs. But the doctor actually gets the drug indications. And then that doctor can see that and that doctor can use that as part -- like as a helpful part of his treatment.

But again, you go back to -- they haven't been able to show scientifically and it's hotly debated. I mean, there was just recently something in -- two Harvard doctors had published something in one of the big journals on mental health, same thing with oncology, like outside of BRCA, like there was a recent paper basically like these other genes are like no better than a placebo.

So this is part of the problem in the space but I mean, I haven't -- I don't have the numbers in front of me. I mean, James do you remember off the top of your head, but I mean, I think it's like $850 million in revenue and like $150 million in EBITDA, something like that against a company with -- that did what, like $144 million in revenue last year and lost what $100 million.

J: Yeah, but larger now.

DS: Yeah, $850 million, trailing 12 months revenue, looks like EBITDA of over $100 million at least.

AR: Yeah. So like, you can look at that, I mean, and this is something when you look at stocks, I mean I was long, some Pinterest against the Snapchat short. And I thought about closing it before earnings. And the reason I thought about closing it is that you know, Snap is $16 billion and Pinterest is 15 billion and Twitter after its 35% decline is 18.2 billion AV. Yeah, Twitter's growing slower than the other two. But it's like three to four times the revenue base. And you got to kind of adjust for that, when you get to that point.

And you're like, this is a company that is in the advertising space, and it's doing -- it's going to do whatever issues its got, it's going to do 3.5 times what this is going to do and their enterprise values are a hair apart. So when you -- like this wasn't -- this is a case where if you would look at an Invitae, you'd be like, this has got to be like a quarter a fifth of the size of like, even if you are a believer and you're willing to buy into the speculation of a Myriad.

And then the other problem you have with it is that they're interrelated. All the revenue growth that is coming for Invitae is coming because Myriad hasn't come down in pricing. They've been fighting this price decline, because they've had the luxury to fight it as the leader in the space and they're extracting a premium for their testing, because they -- like there's a compelling argument, at least from their end, that based on the data we have in the history, our tests can more accurately predict what you have, as far as a likelihood of a hereditary cancer and indication reliably.

And it's ironic, and we were discussing this when we were working on this, like this company throw shade at who -- I mean, they throw shade at the DTC companies. Like they literally just gave a scientific presentation at this Houston Cancer Conference with Genetics or whatever, just like two weeks ago, where they were like, here's 23andMe's tests, okay, and this is what's wrong with it. Like 23AndMe gives you a BRCA test, that only is designed to detect three variants. Basically, if you're not an Ashkenazi Jew, it's useless.

But it's literally a report that is bundled in with the ancestry, with the health with the 50, 60, 70 reports, you get for $100 okay. It's not like you're going into buy this or you're going to your doctor and you're like, okay, I had breast cancer, I'm worried about a potential recurrence. Let's see family history. Do I need to get a mastectomy early because I have this mutation and that's a good preventative measure, et cetera, et cetera. They're not looking at 23AndMe. Like, it's -- you're competing in the clinical grade medical diagnostics market. But here's this company attacking the DTC companies who are not really their competitors.

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Sidestepping danger in the biotech sector – Investment Week

November 20th, 2019 4:46 am

Ailsa Craig of the International Biotechnology Trust

Passive equity products have become popular over the past decade as it has become easier and cheaper to track the performance of an index.

While this is a relatively low cost and straightforward way to access stocks and shares, active management remains the preferred choice for certain sectors.

We believe biotechnology is one such example. This industry often experiences high levels of binary risk.

Polar Capital: Healthcare headwinds short term in the US

The value of a biotechnology company can be significantly affected by the results of a single clinical trial or regulatory decision.

For example, in March 2019 Biogen announced it was halting the final phase of clinical trial for a drug known as aducanumab, which was designed to slow the progress of Alzheimer's disease. The share price fell 30% on the news.

If an investor buys a passive product that tracks a biotechnology index, there is no way to mitigate this type of individual stock risk.

An active manager can, however, sidestep this danger by selling out of the stock before the results of the trial are announced, therefore preserving capital.

The manager can then decide whether to reinvest or to allocate elsewhere once the results have been announced.

The biotechnology index is weighted by market capitalisation, giving it a significant exposure to the larger, well-established companies.

These firms are, however, often growing more slowly than smaller, more innovative companies.

Understanding the 'technological revolution in healthcare'

As an active manager does not have to mirror the reference benchmark, they can build a portfolio with a greater exposure to these faster growing firms.

It is also easier to implement an ethical investment strategy through an active manager.

For example, many investors want to avoid those companies that have profited from the opioid crisis.

Unless exchanged-traded fund providers exclude these firms from their benchmark index, this is impossible to do using a passive product.

Managing binary event risk and allocating a higher proportion of the portfolio to faster-growing biotechnology stocks has enabled active managers to outperform the benchmark.

Ailsa Craig is investment manager of the International Biotechnology Trust

Active management allows a manager to allocate a greater proportion of their portfolio to faster growing companies

It's easier for active managers to exclude stocks which do not match investors' ethical considerations.

Actively managed funds cost more than passively managed products, but the difference in price is not that significant

Actively managed funds come with manager risk

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Immunic, Inc. Expands Board of Directors with Appointment of Biotechnology Executive Barclay A. Phillips – P&T Community

November 20th, 2019 4:46 am

NEW YORK, Nov. 19, 2019 /PRNewswire/ --Immunic, Inc. (Nasdaq: IMUX),a clinical-stage biopharmaceutical company focused on developing best-in-class, oral therapies for the treatment of chronic inflammatory and autoimmune diseases, today announced the appointment of Barclay "Buck" A. Phillips, an established life sciences executive, investor and entrepreneur, to its Board of Directors, effective November 14, 2019. With this addition, Immunic's Board will total seven members.

"Buck's decades of relevant experience in the biotechnology sector, both as a Chief Financial Officer and investor, will add a unique perspective to our Board," stated Duane Nash, M.D., J.D., M.B.A., Chairman of the Board of Directors of Immunic. "We look forward to leveraging his significant expertise in the areas of financing strategy, capital markets, business development, and others, which he has garnered during his successful career as an executive and board member for multiple, Nasdaq-listed life science companies. Buck's addition to our team reflects our desire to build the Board during a time of continued clinical progress and we look forward to his contributions."

Until recently, Mr. Phillips was Chief Financial Officer and Senior Vice President of Corporate Development at G1 Therapeutics, Inc., where, among other achievements, he was instrumental in raising over USD 300 million in multiple equity financings. Before that, he served as Senior Vice President, Chief Financial Officer and Treasurer of vaccine company, Novavax, Inc., where he helped to raise more than USD 850 million in various financings to support the company's late-stage clinical programs. Prior, Mr. Phillips was Senior Vice President and Chief Financial Officer of Micromet, Inc., which, during his tenure, was acquired by Amgen Inc. for approximately USD 1.2 billion. Mr. Phillips's exposure to venture capital came earlier, while serving as a Managing Director at Vector Fund Management, focused on investments in late-stage life sciences companies, and during his time as Biotechnology Analyst and Director of Venture Investments at Invesco, where he held primary coverage responsibility for the universe of publicly traded biotechnology companies, while managing the firm's private equity investing, with a focus on life sciences.

Mr. Phillips has served on the boards of over a dozen public and private life sciences companies. He earned a Bachelor of Arts in economics from the University of Colorado at Boulder.

About Immunic, Inc.Immunic, Inc. (Nasdaq: IMUX) is a clinical-stage biopharmaceutical company developing a pipeline of selective oral immunology therapies aimed at treating chronic inflammatory and autoimmune diseases, including relapsing-remitting multiple sclerosis, ulcerative colitis, Crohn's disease, and psoriasis. The company is developing three small molecule products: IMU-838 is a selective immune modulator that inhibits the intracellular metabolism of activated immune cells by blocking the enzyme DHODH; IMU-935 is an inverse agonist of RORt; and IMU-856 targets the restoration of the intestinal barrier function. Immunic's lead development program, IMU-838, is in phase 2 clinical development for relapsing-remitting multiple sclerosis and ulcerative colitis, with an additional phase 2 trial planned in Crohn's disease. An investigator-sponsored proof-of-concept clinical trial for IMU-838 in primary sclerosing cholangitis is ongoing at the Mayo Clinic. For further information, please visit: http://www.immunic-therapeutics.com.

Cautionary Statement Regarding Forward-Looking Statements

This press release contains "forward-looking statements" that involve substantial risks and uncertainties for purposes of the safe harbor provided by the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical facts, included in this press release regarding strategy, future operations, future financial position, future revenue, projected expenses, prospects, plans and objectives of management are forward-looking statements. Examples of such statements include, but are not limited to, statements relating to Immunic's clinical and preclinical pipeline activities and the structure and composition of its board. Immunic may not actually achieve the plans, carry out the intentions or meet the expectations or projections disclosed in the forward-looking statements and you should not place undue reliance on these forward-looking statements. Such statements are based on management's current expectations and involve risks and uncertainties. Actual results and performance could differ materially from those projected in the forward-looking statements as a result of many factors, including, without limitation, risks and uncertainties associated with the ability to project future cash utilization and reserves needed for contingent future liabilities and business operations, the availability of sufficient resources to meet business objectives and operational requirements, the fact that the results of earlier studies and trials may not be predictive of future clinical trial results, the protection and market exclusivity provided by Immunic's intellectual property, risks related to the drug development and the regulatory approval process and the impact of competitive products and technological changes. A further list and descriptions of these risks, uncertainties and other factors can be found in the section captioned "Item 1A. Risk Factors," in the company's Current Report on Form 8-K filed on July 17, 2019, and in the company's subsequent filings with the Securities and Exchange Commission. Copies of these filings are available online at http://www.sec.gov or ir.immunic-therapeutics.com/sec-filings. Any forward-looking statement made in this release speaks only as of the date of this release. Immunic disclaims any intent or obligation to update these forward-looking statements to reflect events or circumstances that exist after the date on which they were made. Immunic expressly disclaims all liability in respect to actions taken or not taken based on any or all the contents of this press release.

Contact Information

Immunic, Inc.Jessica BreuManager IR and Communications+49 89 250 0794 69jessica.breu@immunic.de

Or

Rx Communications GroupMelody Carey+1-917-322-2571immunic@rxir.com

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Review of George Estreich, ‘Fables and Futures: Biotechnology, Disability, and the Stories We Tell Ourselves’ (opinion) – Inside Higher Ed

November 20th, 2019 4:46 am

A few months ago, I attended a forum on the politics and economics of disability. My impression was that the audience consisted mainly of people with disabilities -- an impression that has changed with time. Whatever the proportions may actually have been, my judgment was probably skewed by self-consciousness, and not just the usual awkwardness of finding a seat after the presentation was well underway. It had taken root long before I got to the room.

"Able-bodied" and "disabled" are categories that function in society at large as necessary and common-sensical, and they are weighted such that the first is posited as normal and predominant, and as such effectively invisible, while the other is an exceptional condition, making it, oddly, both conspicuous and ignorable as circumstances may dictate. With hindsight I am not at all sure more people at the talk had wheelchairs or canes than were present at other talks I attended at the conference. Besides, not every disability involves such a clear marker.

But since disability itself was the topic of the hour, the fact that I did not need any such assistance registered much more sharply than it ordinarily would. Eyeglasses didn't count. Experiential norms prevailing outside the room were not taken for granted, as became even more clear following the speaker's presentation. A number of people pointed out that no American Sign Language interpreter was present. Somehow I had not noticed. Not noticing certain things is a luxury you generally aren't even aware of enjoying.

As binary oppositions go, "able-bodied/disabled" proves much less stable than it appears. It's not just that the most gifted athlete or graceful dancer may be one bullet or automobile accident away from an irrevocable change in status. As mentioned, wearing glasses allows me to function as fully able, but they are a prosthesis for the lenses in my eyes, quite as much a wheelchair is for a paraplegic's legs. And the process of aging has a way of erasing the bright line between ability and its malfunctions. Time is not on the side of the able-bodied. With aging, the binary opposition runs right through the brain, so to speak. Jokes about "having a senior moment" acknowledge (and deflect) this reality. Our long-term command of the powers of attention and memory is contingent at best.

One of the things the reader can take away from George Estreich's Fables and Futures: Biotechnology, Disability, and the Stories We Tell Ourselves (MIT Press) is a heightened sense of how damaging it can be to think of "the disabled" in terms of a distinction between "us" and "them." An instructor in writing at Oregon State University, Estreich is also the author of The Shape of an Eye: A Memoir, about raising his daughter Laura, who has Down syndrome. I haven't read it, but she reappears throughout Fables and Futures without that making the book a memoir, exactly.

"Writing about Laura has its complications," Estreich notes. "For each sentence, I could add a page of narrative caveats, a fine print to govern the legal interpretation of anecdote: 'This positive description is not meant to inspire Though the author has strong opinions on a range of social issues, he declines to weaponize his daughter in their service. Laura is not an example in an argument She is a person, and by describing her the author intends to suggest what she is like and raise questions about the world she enters. This work is related to, yet different from, his work as a parent, which is to help her find, in every sense, her place.' Behind these caveats is the wish to control interpretation, and behind that vain hope is, in no particular order, a writer's ego, a father's protectiveness, and a deep familiarity with the average Internet comment section."

That is quite a few knives to juggle at the same time. And the list does not even include the issue on which Estreich concentrates here: the advancing biotechnology of prenatal testing and genetic editing. The book is a sort of intellectual travelogue, the author thinking his way across a landscape that is changing faster than it can be captured in concepts. When he attends an event in New Orleans that doubles as a professional conference for genetic counselors and a trade show for biotech companies, he notes, "The uneasy tension between old and new brought on by biotech: the more artifice the project requires, the more its advocates retail images of naturalness and purity." The quest to render the woolly mammoth "de-extinct" coexists with strong an implicit and largely unacknowledged strain of 21st-century eugenics.

Given the murderous consequences of one especially vehement form, we tend to think of eugenics as prone to goose-stepping. But a tangent from the memory of his daughter's participation in a county fair leads Estreich back to the era of Better Babies and Fitter Families contests at Midwestern state fairs, in which whole families underwent exams and answered questionnaires to determine which was freest from inherited defects. "If human improvement is on stage," he writes, "disability-based metaphors are usually skulking in the wings."

The author's worry -- which is also a father's worry -- concerns the possible cascade of effects of "our rapidly increasing, fine-grained knowledge of genetic variation." A culture that takes technological development as inevitable is dangerous enough, to itself and others, without having the option of decision making that "invoke[s] abnormality, a word capacious enough to hold everything and everyone considered different and undesirable." Estreich is uncommonly adept at presenting both experiences and ideas in layers, without the structure itself becoming either unmanageable or distracting. Anyone who reads it should expect the wheels in their head to keep spinning for a while afterward.

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Review of George Estreich, 'Fables and Futures: Biotechnology, Disability, and the Stories We Tell Ourselves' (opinion) - Inside Higher Ed

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Exclusive Research on Biotechnology-Based Chemical Market by CMFE Insights with Leading Players Sarnia-Lambton Research, UK and Norway business…

November 20th, 2019 4:46 am

Biotechnology-Based Chemical Market are items gotten from natural roots, for example, feedstock, plants, harvests, trees, and organic waste. This will benefit the reports users, that evaluates their position in the market as well as create effective strategies in the near future. They are a reasonable option in contrast to traditional synthetic concoctions and will assume a noteworthy job in decreasing the dependence on non-renewable energy sources. This can prompt diminished carbon discharge levels and keep up the biological parity. Lignocellulose is the most generally accessible crude material utilized for the creation of biofuels.

The report of CMFE Insights the Industrial substance application is foreseen to command the worldwide Biotechnology-Based Chemical Market growing CAGR of +16% during forecast period.

The report shields the development activities in the Biotechnology-Based Chemical which includes the status of marketing channels available, and an analysis of the regional export and import. The report ends with an inference for the global market as it was in industry. Researchers of this research report throw light on demand-supply chaining in the market. The forward-disapproved of people supporting the improvement of bio-based synthetic substances, specialists have been growing new sources and applications for Biotechnology-Based Chemical Market around the globe, delivering promising outcomes.

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The Report includes Several Company Profiles of who are market key players:

Biotechnology-Based Chemical Market by region:

The significant sorts of biotechnology are red, green, white, and blue biotechnology. Red biotechnology includes medicinal procedures, white biotechnology which is otherwise called dark biotechnology is primarily utilized in mechanical procedures, green biotechnology includes agrarian biotech procedures and blue biotechnology involves marine and amphibian procedures. Biotechnology-Based Chemical Market has wide applications crosswise over modern territories, for example, horticulture, prescription, sustenance generation, human services, and yield creation.

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Market by Type

Market by Application

The application, of worldwide Biotechnology-Based Chemical Market compounds is isolated into mechanical synthetic compounds, agribusiness, pharmaceuticals, and others. Leading key players have been profiled to get a clear insight into the businesses on the basis of successful strategies of the top level companies. Along with this, it also offers competitive significance among the several traders by presenting the facts and figures of market shares.

In this study, the years considered to estimate the market size of Biotechnology-Based Chemical Market are as follows:

About Us : CMFE Insights caters to clients needs by elucidating the power of innovation, thus thriving on business innovations. Our mission is to guide global businesses through our comprehensive market research reports. Through our infrastructural competence of digital transformations, we orchestrate escalated market efficiency for our clients by presenting them with capable growth opportunities in the global market scenario. Through the experienced eye of our research associates we help our clients to envision a flourishing future. CMFE Insights techniques is a perfect blend of both qualitative and quantitative modes, on basis of which we provide our clients with syndicated research reports to further enhance their strategic organizational decisions. CMFE Insights helps clients to build a pragmatic future in the innovative market industry.

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Women in Biotech: Katz Event Explores the Rewards and Challenges of a Career in Biotechnology – Yu News

November 20th, 2019 4:46 am

From the gene-editing powers of CRISPR-Cas9 to the creation of clean meat technologies, the biotechnology field continues to top one new development with another in rapid succession, and because of this innovative velocity, there is an increasing need for biotech leaders who understand both the science and the business of this ever-expanding field.

Where do women fit into this process? Do they face the same gender parity issues that they confront in other areas of science, technology, engineering and math, or STEM? What challenges should they prepare for as they launch a career in biotech?

A top-notch panel of scientists and entrepreneurs came together on Sept. 26, 2019, to answer these questions at the Katz School of Science and Healths first fall event for Women in Bio. Leading Biotech and Healthcare Organizations from Early to Late Stage, was co-organized by Dr. Rana Khan, director of the MS in Biotechnology Management and Entrepreneurship Program at the Katz School, and the New York Chapter of Women in Bio, the national organization for women in life sciences.

Panelists included Dr. Christina Brennan, vice president of clinical research, Northwell Health; Dr. Jeanne Magram, chief scientific officer, Quentis Therapeutics; Dr. Sandra Saldana, CEO and co-founder of Alva Health and adjunct professor at Yeshiva University; and Dr. Mani Mohindru, CFO and chief strategy officer at Cara Therapeutics.

The event was a resounding success with great speakers and engaged attendees, one of whom described it as a difference-making experience. It was empowering to sit in a roomful of professional women, in top roles, opening their hearts about the challenges they are going through. I came away with two new connections that are meaningful to my career. Thank you, YU, for hosting such a memorable event.

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Women in Biotech: Katz Event Explores the Rewards and Challenges of a Career in Biotechnology - Yu News

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Cellect Biotechnology Reports Third Quarter 2019 Financial and Operating Results – PRNewswire

November 20th, 2019 4:46 am

TEL AVIV, Israel, Nov. 19, 2019 /PRNewswire/ --Cellect Biotechnology Ltd. (NASDAQ: APOP), a developer of innovative technology which enables the functional selection of stem cells, today reported financial and operating results for the third quarter ended September 30, 2019 and provided a corporate update.

Recent Highlights

"Our clinical and regulatory teams remained focused during the third quarter and the more recent positive developments position us to achieve our goals, both in the U.S. and Israel," commented Dr. Shai Yarkoni, Chief Executive Officer. "In the U.S., the IND approval is a significant achievement and represents our first-ever FDA IND in the U.S., with Washington University School of Medicine. In Israel, our Phase 1/2 clinical study of ApoGraft is progressing slowly and we expect to complete the recruitment around the end of the year."

"With our prudent use of cash during the third quarter and the anticipated cash usage needs over the coming quarters, we continue to believe we have the resources to execute our clinical and regulatory plans for the foreseeable future," said Eyal Leibovitz, Chief Financial Officer.

ThirdQuarter 2019 Financial Results:

*For the convenience of the reader, the amounts above have been translated from NIS into U.S. dollars, at the representative rate of exchange on September 30, 2019 (U.S. $1 = NIS 3.482).

Strategic Review Progress Update

On May 16, 2019, the Company disclosed that it commenced plans to explore strategic alternatives to maximize shareholder value. Potential strategic alternatives that may be evaluated include, but are not limited to, an acquisition, merger, business combination, including in other business fields than the Company's in-licensing, or other strategic transaction involving the Company or its assets. The Company continues to evaluate business development opportunities and will keep investors informed as they mature or warrant investor disclosure.

About Cellect Biotechnology Ltd.

Cellect Biotechnology (APOP) has developed a breakthrough technology, for the selection of stem cells from any given tissue, that aims to improve a variety of stem cell-based therapies.

The Company's technology is expected to provide researchers, clinical community and pharma companies with the tools to rapidly isolate stem cells in quantity and quality allowing stem cell-based treatments and procedures in a wide variety of applications in regenerative medicine. The Company's current clinical trial is aimed at bone marrow transplantations in cancer treatment.

Forward Looking Statements

This press release contains forward-looking statements about the Company's expectations, beliefs and intentions. Forward-looking statements can be identified by the use of forward-looking words such as "believe", "expect", "intend", "plan", "may", "should", "could", "might", "seek", "target", "will", "project", "forecast", "continue" or "anticipate" or their negatives or variations of these words or other comparable words or by the fact that these statements do not relate strictly to historical matters. These forward-looking statements and their implications are based on the current expectations of the management of the Company only and are subject to a number of factors and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. In addition, historical results or conclusions from scientific research and clinical studies do not guarantee that future results would suggest similar conclusions or that historical results referred to herein would be interpreted similarly in light of additional research or otherwise. The following factors, among others, could cause actual results to differ materially from those described in the forward-looking statements: the Company's history of losses and needs for additional capital to fund its operations and its inability to obtain additional capital on acceptable terms, or at all; the Company's ability to continue as a going concern; or maintain its current operations; uncertainties involving any strategic transaction the Company may decide to enter into as the result of its current efforts to explore new strategic alternatives; uncertainties of cash flows and inability to meet working capital needs; the Company's ability to obtain regulatory approvals; the Company's ability to obtain favorable pre-clinical and clinical trial results; the Company's technology may not be validated and its methods may not be accepted by the scientific community; difficulties enrolling patients in the Company's clinical trials; the ability to timely source adequate supply of FasL; risks resulting from unforeseen side effects; the Company's ability to establish and maintain strategic partnerships and other corporate collaborations; the scope of protection the Company is able to establish and maintain for intellectual property rights and its ability to operate its business without infringing the intellectual property rights of others; competitive companies, technologies and the Company's industry; unforeseen scientific difficulties may develop with the Company's technology; and the Company's ability to retain or attract key employees whose knowledge is essential to the development of its products. Any forward-looking statement in this press release speaks only as of the date of this press release. The Company undertakes no obligation to publicly update or review any forward-looking statement, whether as a result of new information, future developments or otherwise, except as may be required by any applicable securities laws. More detailed information about the risks and uncertainties affecting the Company is contained under the heading "Risk Factors" in Cellect Biotechnology Ltd.'s Annual Report on Form 20-F for the fiscal year ended December 31, 2018 filed with the U.S. Securities and Exchange Commission, or SEC, which is available on the SEC's website, http://www.sec.gov, and in the Company's periodic filings with the SEC.

Cellect Biotechnology Ltd

Consolidated Statement of Operation

Convenience

translation

Nine months

ended

Nine months ended

Three months ended

September 30,

September 30,

September 30,

2019

2019

2018

2019

2018

Unaudited

Unaudited

U.S. dollars

NIS

(In thousands, except share and per

share data)

Research and development expenses

2,743

9,551

9,473

2,465

4,125

General and administrative expenses

2,249

7,832

11,001

2,768

3,929

Operating loss

4,992

17,383

20,474

5,233

8,054

Financial expenses (income) due to warrants exercisable into shares

(2,303)

(8,020)

(2,935)

(910)

(1,320)

Other financial expenses (income), net

393

1,369

(1,177)

489

64

Total comprehensive loss

3,082

10,732

16,362

4,812

6,798

Loss per share:

Basic and diluted loss per share

0.015

0.051

0.127

0.021

0.052

Basic and diluted loss per ADS

0.30

1.02

2.54

0.42

1.04

Weighted average number of shares outstanding used to compute basic and diluted loss per share

208,771,303

208,771,303

129,139,278

224,087,799

130,192,799

Cellect Biotechnology Ltd.

Consolidated Balance Sheet Data

ASSETS

Convenience

translation

September 30,

September 30,

December 31,

2019

2019

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Cellect Biotechnology Reports Third Quarter 2019 Financial and Operating Results - PRNewswire

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Food Biotechnology Market 2019| 2019 Applications, Types and Growing Trends, Share 2024 – Eastlake Times

November 20th, 2019 4:46 am

The global Food Biotechnology industry research report offers a detailed analysis of the current status of the market 2019. This extensive Global Food Biotechnology Market research report contains a brief on industry trends that can guide the business operators in the industry to get an idea of the market and strategize for their business development accordingly. The research report studies the market size, Food Biotechnology industry share, growth rate, key segments, CAGR (%) and key drivers. At the start, the report offers a basic introduction to the Food Biotechnology market including definitions, applications, classifications and industry chain analysis. The study serves as the international Food Biotechnology market consist of development past, competitive landscape study, and advancement states of Food Biotechnology in major geographical regions.

Get a sample of the report from https://www.orbisreports.com/global-food-biotechnology-market/?tab=reqform

Secondly, Food Biotechnology manufacturing processes and cost study are discussed as well as development policies and plans are also included. This Food Biotechnology market research report also gives the data on import/send out, supply-demand, and Food Biotechnology consumption values along with cost, revenue and gross margin by worldwide regions. This Food Biotechnology report will surely help you to understand and apply the ideas and guide you in making strong decisions. The world Food Biotechnology industry was valued in 2019 is XX Mn US$ and is evaluates to be XX Mn US$ forecasting to 2024, with a perspective CAGR of X.X %.

Food Biotechnology Market Major Manufacturers:

ABS GlobalArcadia BiosciencesAquaBounty TechnologiesBASF Plant ScienceBayer CropScience AGCamson Bio Technologies LtdDow AgroSciences LLCDuPont PioneerEvogene LtdHy-Line InternationalKWS GroupMonsantoOrigin Agritech LimitedSyngenta AG

The aim of Food Biotechnology report is to give an idea to the readers in making firm business decisions based on market latest trends and upcoming market improvement estimates in forecast years. The study contains Food Biotechnology market contributors including vendors/traders, buyers/distributors/, suppliers/sellers. Their Food Biotechnology marketing strategies are also provided. Global Food Biotechnology report analyses the historical data regarding the market growth, Food Biotechnology market scope and also offers the current and Food Biotechnology market upcoming information. The study of major growth opportunities and challenges to the Food Biotechnology market is included.

Food Biotechnology Market Types Are:

Transgenic CropsSynthetic Biology Derived Products

Food Biotechnology Market Applications Are:

AnimalsPlantsOther

For more Information or Any Query Visit: https://www.orbisreports.com/global-food-biotechnology-market/?tab=discount

The worldwide Food Biotechnology industry report offers a thorough study of the Food Biotechnology market. The report Food Biotechnology focuses industry vision from experts. An in-depth segmentation of the Food Biotechnology industry has been provided in the report. Moreover, the world Food Biotechnology industry report also includes the sub-segments. The key sector, the emerging and leading sectors, together with their growth stats have been cited in the Food Biotechnology market report.

After a brief outlook of the global Food Biotechnology market, the report studies the market dynamics. The major drivers helping Food Biotechnology market growth and the major constraints inhibiting Food Biotechnology market growth are provided in this report. In addition, the Food Biotechnology industry report also gives the threats and challenges that companies in the Food Biotechnology market need to focus on. The most influencing trends that will give the structure the Food Biotechnology market during the forecasting prospect are also provided in this report. Furthermore, the report expands on the regulatory scheme governing the Food Biotechnology market and its possible effects on the market in the foreseeable horizon.

The insight analysis on Food Biotechnology research report provides:

The evaluated Food Biotechnology growth rate together with size and market share over the forecast period 2019-2024. The primary factors estimated to drive the Food Biotechnology Market for the forecasting period 2019-2024. The major Global Food Biotechnology market regulatory bodies and what has been their business expanding strategy for leading so far. Influential trends shaping the growth probabilities of the Food Biotechnology Market.

In-depth and complete business outlook, Food Biotechnology market revenue study, business expansion strategies, and SWOT analysis of the major leading players have been served in the report. Vendors in the Worldwide Food Biotechnology market are focusing to explore their operations to developing regions. More, companies in the Food Biotechnology market are concentrating on innovation and standing their Food Biotechnology products at competitive prices. A detailed analysis of Food Biotechnology supply chain in the report will help readers to understand Food Biotechnology market clearly.

Click here to see full TOC https://www.orbisreports.com/global-food-biotechnology-market/?tab=toc

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Where Does JNCE Stock Rank in the Biotechnology Industry? – InvestorsObserver

November 20th, 2019 4:46 am

The 74 rating InvestorsObserver gives to Jounce Therapeutics Inc (JNCE) stock puts it near the top of the Biotechnology industry. In addition to scoring higher than 96 percent of stocks in the Biotechnology industry, JNCEs 74 overall rating means the stock scores better than 74 percent of all stocks.

Click Here to get the full Stock Score Report on Jounce Therapeutics Inc (JNCE) Stock.

Finding the best stocks can be tricky. It isnt easy to compare companies across industries. Even companies that have relatively similar businesses can be tricky to compare sometimes. InvestorsObservers tools allow a top-down approach that lets you pick a metric, find the top sector and industry and then find the top stocks in that sector.

These scores are not only easy to understand, but it is easy to compare stocks to each other. You can find the best stock in an industry, or look for the sector that has the highest average score. The overall score is a combination of technical and fundamental factors that serves as a good starting point when analyzing a stock. Traders and investors with different goals may have different goals and will want to consider other factors than just the headline number before making any investment decisions.

Jounce Therapeutics Inc (JNCE) stock is trading at $5.81 as of 10:05 AM on Thursday, Nov 14, a rise of $0.22, or 3.86% from the previous closing price of $5.59. The stock has traded between $5.62 and $6.19 so far today. Volume today is 195,167 compared to average volume of 163,071.

To see InvestorsObservers Sentiment Score for Jounce Therapeutics Inc click here.

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PDS Biotechnology (NASDAQ:PDSB) Will Have To Spend Its Cash Wisely – Yahoo Finance

November 20th, 2019 4:46 am

Even when a business is losing money, it's possible for shareholders to make money if they buy a good business at the right price. For example, biotech and mining exploration companies often lose money for years before finding success with a new treatment or mineral discovery. Nonetheless, only a fool would ignore the risk that a loss making company burns through its cash too quickly.

So should PDS Biotechnology (NASDAQ:PDSB) shareholders be worried about its cash burn? For the purpose of this article, we'll define cash burn as the amount of cash the company is spending each year to fund its growth (also called its negative free cash flow). The first step is to compare its cash burn with its cash reserves, to give us its 'cash runway'.

View our latest analysis for PDS Biotechnology

A company's cash runway is the amount of time it would take to burn through its cash reserves at its current cash burn rate. As at September 2019, PDS Biotechnology had cash of US$17m and such minimal debt that we can ignore it for the purposes of this analysis. Looking at the last year, the company burnt through US$12m. So it had a cash runway of approximately 17 months from September 2019. That's not too bad, but it's fair to say the end of the cash runway is in sight, unless cash burn reduces drastically. The image below shows how its cash balance has been changing over the last few years.

NasdaqCM:PDSB Historical Debt, November 12th 2019

Because PDS Biotechnology isn't currently generating revenue, we consider it an early-stage business. So while we can't look to sales to understand growth, we can look at how the cash burn is changing to understand how expenditure is trending over time. Remarkably, it actually increased its cash burn by 673% in the last year. With that kind of spending growth its cash runway will shorten quickly, as it simultaneously uses its cash while increasing the burn rate. Clearly, however, the crucial factor is whether the company will grow its business going forward. So you might want to take a peek at how much the company is expected to grow in the next few years.

While PDS Biotechnology does have a solid cash runway, its cash burn trajectory may have some shareholders thinking ahead to when the company may need to raise more cash. Generally speaking, a listed business can raise new cash through issuing shares or taking on debt. Commonly, a business will sell new shares in itself to raise cash to drive growth. We can compare a company's cash burn to its market capitalisation to get a sense for how many new shares a company would have to issue to fund one year's operations.

PDS Biotechnology has a market capitalisation of US$15m and burnt through US$12m last year, which is 85% of the company's market value. That suggests the company may have some funding difficulties, and we'd be very wary of the stock.

Even though its cash burn relative to its market cap makes us a little nervous, we are compelled to mention that we thought PDS Biotechnology's cash runway was relatively promising. Considering all the measures mentioned in this report, we reckon that its cash burn is fairly risky, and if we held shares we'd be watching like a hawk for any deterioration. For us, it's always important to consider risks around cash burn rates. But investors should look at a whole range of factors when researching a new stock. For example, it could be interesting to see how much the PDS Biotechnology CEO receives in total remuneration.

Story continues

Of course, you might find a fantastic investment by looking elsewhere. So take a peek at this free list of interesting companies, and this list of stocks growth stocks (according to analyst forecasts)

We aim to bring you long-term focused research analysis driven by fundamental data. Note that our analysis may not factor in the latest price-sensitive company announcements or qualitative material.

If you spot an error that warrants correction, please contact the editor at editorial-team@simplywallst.com. This article by Simply Wall St is general in nature. It does not constitute a recommendation to buy or sell any stock, and does not take account of your objectives, or your financial situation. Simply Wall St has no position in the stocks mentioned. Thank you for reading.

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Where Does FTSV Stock Rank in the Biotechnology Industry? – InvestorsObserver

November 20th, 2019 4:46 am

The 59 rating InvestorsObserver gives to Forty Seven Inc (FTSV) stock puts it near the top of the Biotechnology industry. In addition to scoring higher than 81 percent of stocks in the Biotechnology industry, FTSVs 59 overall rating means the stock scores better than 59 percent of all stocks.

Click Here to get the full Stock Score Report on Forty Seven Inc (FTSV) Stock.

Finding the best stocks can be tricky. It isnt easy to compare companies across industries. Even companies that have relatively similar businesses can be tricky to compare sometimes. InvestorsObservers tools allow a top-down approach that lets you pick a metric, find the top sector and industry and then find the top stocks in that sector.

Our proprietary scoring system captures technical factors, fundamental analysis and the opinions of analysts on Wall Street. This makes InvestorsObservers overall rating a great way to get started, regardless of your investing style. Percentile-ranked scores are also easy to understand. A score of 100 is the top and a 0 is the bottom. Theres no need to try to remember what is good for a bunch of complicated ratios, just pay attention to which numbers are the highest.

Forty Seven Inc (FTSV) stock is trading at $10.31 as of 10:05 AM on Thursday, Nov 14, a rise of $0.12, or 1.18% from the previous closing price of $10.19. The stock has traded between $10.28 and $10.57 so far today. Volume today is below average. So far 51,681 shares have traded compared to average volume of 211,996 shares.

To see InvestorsObservers Sentiment Score for Forty Seven Inc click here.

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Leading Alternative Healing Director of Total Health Institute Reviews and Receives 3rd Fellowship in Stem Cell Therapy – Yahoo Finance

November 20th, 2019 4:44 am

Total Health Institute Reviews

Chicago, IL, Nov. 14, 2019 (GLOBE NEWSWIRE) -- Dr. Keith Nemec the clinic director ofTotal Health Institute in Chicago has received yet another fellowship in his advanced research. Most recently Dr. Nemec received his fellowship in Stem Cell Therapy to add to his other fellowships in Regenerative Medicine and Integrative Cancer Therapies.

Dr. Nemec has overseen patient care for the last thirty-five years at Total Health Institute which is an alternative and integrative medical facility. Total Health Institute has seen over 10,000 patients who have traveled from around the world to seek Dr. Nemecs guidance in their healing journey.

Total Health Institute uses unique approach developed by Dr. Nemec called theSystems Sequence Approach to balance cellular communication between the cells, tissues, organs, glands and systems of the body. Dr. Nemec explains It is like knowing the combination to open the lock to complete healing. To open this lock, you must not only know the right systems to balance but also in the right sequence.

Dr. Keith Nemec is very excited about the research in stem cells and stem cell therapy that is why he focused his concentration in this area. According to Dr. Nemec All health and healing starts at the stem cell level. Whether a person has cancer, autoimmune disease or chronic diseases of aging they are all involving stem cells. In cancer, an inflammatory environment has mutated a normal stem cell into a cancer stem cell which is not killed with either chemotherapy nor radiation. This is why many times with conventional cancer treatment alone one tends to see improvements for a season but then return the cancer stem cell retaliates with a vengeance. Dr. Nemec also states Since all cells come from a base stem cell then the answer to all chronic disease can be found in activating the stem cells to produce an anti-inflammatory niche and continual healthy cell renewal.

Dr. Nemec is a member of the American Academy of Anti-Aging Medicine which is the largest and most prestigious group of Regenerative and Anti-Aging Medicine doctors in the world. He received his masters degree in Nutritional Medicine from Morsani College of Medicine. He has also published 5 books including: The Perfect Diet, The Environment of Health and Disease, Seven Basic Steps to Total Health and Total Health = Wholeness. Dr. Nemec has also published numerous health articles including: The Single Unifying Cause of All Disease and The answer to cancer is found in the stem cell and for 18 years he hosted the radio show Your Total Health in Chicago AM1160.

Total Health Institute boasts all 5 starreviews on RateMDs, an A+ rating onBBBand is top rated on Manta.

(630) 871-0000Keith@thi.co

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Researchers develop cell therapy to improve memory and stop seizures in mice following traumatic brain injury – Newswise

November 20th, 2019 4:44 am

MEDIA CONTACT

Available for logged-in reporters only

Newswise Irvine, Calif. November 15, 2019 Researchers from the University of California, Irvine developed a breakthrough cell therapy to improve memory and prevent seizures in mice following traumatic brain injury. The study, titled Transplanted interneurons improve memory precision after traumatic brain injury, was published today in Nature Communications.

Traumatic brain injuries affect 2 million Americans each year and cause cell death and inflammation in the brain. People who experience a head injury often suffer from lifelong memory loss and can develop epilepsy.

In the study, the UCI team transplanted embryonic progenitor cells capable of generating inhibitory interneurons, a specific type of nerve cell that controls the activity of brain circuits, into the brains of mice with traumatic brain injury. They targeted the hippocampus, a brain region responsible for learning and memory.

The researchers discovered that the transplanted neurons migrated into the injury where they formed new connections with the injured brain cells and thrived long term. Within a month after treatment, the mice showed signs of memory improvement, such as being able to tell the difference between a box where they had an unpleasant experience from one where they did not. They were able to do this just as well as mice that never had a brain injury. The cell transplants also prevented the mice from developing epilepsy, which affected more than half of the mice who were not treated with new interneurons.

Inhibitory neurons are critically involved in many aspects of memory, and they are extremely vulnerable to dying after a brain injury, said Robert Hunt, PhD, assistant professor of anatomy and neurobiology at UCI School of Medicine who led the study. While we cannot stop interneurons from dying, it was exciting to find that we can replace them and rebuild their circuits.

This is not the first time Hunt and his team has used interneuron transplantation therapy to restore memory in mice. In 2018, the UCI team used a similar approach, delivered the same way but to newborn mice, to improve memory of mice with a genetic disorder.

Still, this was an exciting advance for the researchers. The idea to regrow neurons that die off after a brain injury is something that neuroscientists have been trying to do for a long time, Hunt said. But often, the transplanted cells dont survive, or they arent able to migrate or develop into functional neurons.

To further test their observations, Hunt and his team silenced the transplanted neurons with a drug, which caused the memory problems to return.

"It was exciting to see the animals memory problems come back after we silenced the transplanted cells, because it showed that the new neurons really were the reason for the memory improvement, said Bingyao Zhu, a junior specialist and first author of the study.

Currently, there are no treatments for people who experience a head injury. If the results in mice can be replicated in humans, it could have a tremendous impact for patients. The next step is to create interneurons from human stem cells.

So far, nobody has been able to convincingly create the same types of interneurons from human pluripotent stem cells, Hunt said. But I think were close to being able to do this.

Jisu Eom, an undergraduate researcher, also contributed to this study. Funding was provided by the National Institutes of Health.

About the UCI School of Medicine: Each year, the UCI School of Medicine educates more than 400 medical students, as well as 200 doctoral and masters students. More than 600 residents and fellows are trained at UC Irvine Medical Center and affiliated institutions. The School of Medicine offers an MD; a dual MD/PhD medical scientist training program; and PhDs and masters degrees in anatomy and neurobiology, biomedical sciences, genetic counseling, epidemiology, environmental health sciences, pathology, pharmacology, physiology and biophysics, and translational sciences. Medical students also may pursue an MD/MBA, an MD/masters in public health, or an MD/masters degree through one of three mission-based programs: the Health Education to Advance Leaders in Integrative Medicine (HEAL-IM), the Leadership Education to Advance Diversity-African, Black and Caribbean (LEAD-ABC), and the Program in Medical Education for the Latino Community (PRIME-LC). The UCI School of Medicine is accredited by the Liaison Committee on Medical Accreditation and ranks among the top 50 nationwide for research. For more information, visit som.uci.edu.

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