New test for Alzheimers to begin trial – SouthCoastToday.com

SOUTH KINGSTOWN, RHODE ISLAND A comparatively simple eye exam that could detect Alzheimers disease many years before severe clinical symptoms appear is about to undergo a clinical trial sponsored by University of Rhode Island, Butler Hospital in Providence and BayCare Health System, a system of 15 hospitals and other centers in central Florida.

The so-called retinal screening tests someday could be administered by optometrists and ophthalmologists at considerably less cost than todays PET scans, which can detect the buildup of amyloid plaque in the brain, associated with Alzheimers, before symptoms appear. Such scans cost thousands of dollars and are not typically covered by most insurance plans.

When our study is completed, we want to make the technology available so that optometrists and ophthalmologists could screen for the retinal biomarkers we believe are associated with Alzheimers disease and watch them over time, said Peter Snyder, URIs vice president for research and economic development and professor of biomedical and pharmaceutical sciences, and a principal investigator in the $5-million study.

If clinicians see changes, they could refer their patients to specialists early on, Snyder said. We believe this could significantly lower the cost of testing. We may then identify more people in the very earliest stage of the disease, and our drug therapies are likely to be more effective at that point and before decades of slow disease progression.

Dr. Stephen P. Salloway, director of Butlers Memory and Aging Program, affiliated with Brown University, said the study closely aligns with the mission of Butler Hospital and Brown University to develop new approaches to detect Alzheimers risk early and keep the brain healthy so memory loss never occurs. Also key to the research in Rhode Island will be Jessica Alber, Ryan Research Assistant Professor of Neuroscience at URIs Ryan Institute for Neuroscience, who will lead the Butler team.

According to Mondays announcement of the study, researchers are seeking to enroll 330 people between the ages of 55 and 80 ranging from very healthy and low-risk adults, to persons with concerns about their memory, as well as patients with mild Alzheimers disease.

Participants will be examined at four different times over three years, according to the announcement, and each study visit includes an eye exam, a medical history discussion, some tests of how people think and how well they remember new information, the retinal imaging that is very much like the kind done at the eye doctors office, and measures of mood, walking and balancing, sleep habits and other types of medical information.

Eligible individuals in the Rhode Island area interested in participating in the study should contact Butlers Alzheimers Prevention Registry, butler.org/alzregistry, or call 401-455-6402. Those living near Tampa, St. Petersburg or Clearwater, Florida, should call Catrina Montgomery at (727) 298-6077. Dr. Stuart Sinoff, medical director of Neurosciences for BayCare Health Systems West Region in Pinellas County, is the studys principal investigator in Florida.

The retinal-screening study is the latest indication that Rhode Island has emerged as a leader in Alzheimers research, with numerous studies at centers including URI, Rhode Island Hospital, Butler Hospital and Brown University, home to the Carney Institute for Brain Science. Sciences may not always be collaborative, but ongoing cooperation in the Ocean State is providing promise in the invariably fatal disease.

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Monmouth President appointed to Illinois Board of Higher Ed – WGIL Radio News

Monmouth College President Clarence Wyatt is getting a new title, member of the Illinois Board of Higher Education.

Gov. J.B. Pritzker announced Wyatts appointment on Friday to the panel that oversees institutions of higher education in Illinois.

The Governor has the authority to appoint 10 of the boards 16 members.

Wyatt has been Monmouths president since 2014.

The Pritzker administration writes about Wyatt that under his leadership Monmouth has attracted a more geographically diverse and academically gifted student body. Pritzker also says that under his leadership Monmouth has risen in national rankings, attracted a more academically gifted student body and new STEM majors like data science, neuroscience, and engineering.

They also credit him for his leadership in developing new academic programs, including majors in data science, engineering, and neuroscience.

He holds a Bachelors degree in English and History, as well as a Masters degree and Ph.D. in American History.

Wyatts more than 40-year career in higher education began at Centre, where he played a key role in helping that college rise to a prominent place among national liberal arts colleges.

He is also a founding member of Presidents United to Solve Hunger or PUSH, a coalition of more than 60 colleges and universities worldwide working to fight hunger and malnutrition.

Wyatts appointment is technically pending until hes confirmed by the State Senate.

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Monmouth President appointed to Illinois Board of Higher Ed - WGIL Radio News

Stress-recovery wearable helps the body bounce back with Covestro polycarbonate blend – Yahoo Finance

What's next in wearables

PITTSBURGH, Jan. 7, 2020 /PRNewswire/ -- Wearables are seemingly everywhere, monitoring our sleep, tracking our heart rate variability (HRV)a key metric of health and recoveryand more. But what if they could do more? Imagine a device that empowers you to get better sleep, feel more relaxed and have more energy by actively enhancing the body's resilience to stress. Sound impossible? Meet Apollo!

Makroblend M525 PC+polyester blend from Covestro lends toughness and chemical resistance to the Apollo wearable. (Photo: Apollo Neuroscience)

Click to Tweet: At #CES2020, see how @apollohrv helps the body bounce back from stress with @CovestroUS polycarbonate blend: http://bit.ly/2Fmslfb

According to Kathryn Fantauzzi, CEO and co-founder of Apollo Neuroscience, Inc., Apollo is the first wearable that helps the body beat stress by rapidly restoring its natural equilibrium for better sleep, energy and more. She explains that, unlike other wearables, Apollo doesn't just track your bodyit uses vibration to improve your recovery from stress. Originally developed by physicians and neuroscientists at the University of Pittsburgh, Apollo's gentle vibration waves signal safety to the body and improve HRVall through the sense of touch.

Since Apollo is worn on the wrist or ankle, the wearable required a material that withstands everyday productssuch as lotions, perfumes and detergentsas well as drops and daily wear and tear. Makroblend M525 PC+polyester blend from Covestro delivers the toughness and chemical resistance needed to create this durable yet lightweight device.

"Wearables have a long checklist of needs to meet, and it all starts with the right materials," said Doug Hamilton, global healthcare marketing leader, Covestro LLC.

Zachary Williams, market development, Healthcare Polycarbonates, Covestro LLC, added, "Makroblend M525 PC+polyester blend meets two important requirementstoughness and chemical resistanceto help Apollo users find balance with a strong and lightweight device that remains unchanged when exposed to a variety of personal care products."

"Apollo is about empowering people to take control of their healththat's why we chose Covestro as a partner," said John Maholtz, chief operating officer at Apollo Neuroscience. "Covestro's premier materials ensure that Apollo users experience a clean, comfortable and long-lasting product that is just as resilient as they are."

The device works in tandem with an intuitive app which, according to Apollo, features a variety of programs that help users:

Attendees at the following shows will be able to experience first-hand how the Apollo device helps their body adapt to stress:

Learn about what else Covestro has in store for CES: http://www.solutions.covestro.com/en/highlights/campaigns/ces-2020.

About Covestro LLC:Covestro LLC is one of the leading producers of high-performance polymers in North America and is part of the global Covestro business, which is among the world's largest polymer companies with 2018 sales of EUR 14.6 billion. Business activities are focused on the manufacture of high-tech polymer materials and the development of innovative solutions for products used in many areas of daily life. The main segments served are the automotive, construction, wood processing and furniture, electrical and electronics, and healthcare industries. Other sectors include sports and leisure, cosmetics and the chemical industry itself. Covestro has 30 production sites worldwide and employed approximately 16,800 people at the end of 2018.

Story continues

About Apollo Neuroscience:Apollo is the first wearable that actively helps your body adapt to stress, for better sleep, focus, energy, and more. While other wearables track your body, Apollo empowers you to change it, harnessing the power of neuroscience to deliver gentle waves of vibration shown to rapidly restore your body's natural equilibrium. Apollo works by signaling safety to the body and has been scientifically-validated to improve heart rate variability (HRV), a key metric of health and recovery. Apollo has been evaluated in university-led trials and has been tested by over 2,000 users. For more information, visit http://www.apolloneuro.com.

Find more information at http://www.covestro.usorwww.solutions.covestro.com/en/materials/plastics.

Forward-Looking StatementsThis news release may contain forward-looking statements based on current assumptions and forecasts made by Covestro AG. Various known and unknown risks, uncertainties and other factors could lead to material differences between the actual future results, financial situation, development or performance of the company and the estimates given here. These factors include those discussed in Covestro's public reports which are available at http://www.covestro.com. The company assumes no liability whatsoever to update these forward-looking statements or to conform them to future events or developments.

Makroblend is a registered trademark of the Covestro Group.

This press release is available for download from our website. Click here to view all our press releases.

Editor's Note: Follow news from Covestro on Twitter: https://twitter.com/CovestroUS

Contact John Skabardonis Telephone +1 412 413 5444 Email John.Skabardonis@covestro.com

View original content to download multimedia:http://www.prnewswire.com/news-releases/stress-recovery-wearable-helps-the-body-bounce-back-with-covestro-polycarbonate-blend-300982115.html

SOURCE Covestro LLC

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Stress-recovery wearable helps the body bounce back with Covestro polycarbonate blend - Yahoo Finance

Childhood Deprivation May Have Long-term Impact on Adult Brain Size – Technology Networks

Researchers from King's College London have shown that the brains of young adult Romanian adoptees who were institutionalised as children are around 8.6% smaller than the brains of English adoptees who have not suffered this form of deprivation.

According to the research, the longer the time the Romanian adoptees spent in the institutions, the smaller the total brain volume, with each additional month of deprivation associated with a 0.27% reduction in total brain volume. Deprivation related changes in brain volume were associated with lower IQ and more symptoms of attention deficit hyperactivity disorder (ADHD).

Published in Proceedings of the National Academy of Sciences (PNAS), the study analysed the MRI brain scans of 67 young adults, aged 23-28 years, who were exposed to severely depriving conditions in Romanian institutions under the Communist regime and subsequently adopted into nurturing families in the UK. They were compared to the MRI brain scans of 21 English adoptees aged 23-26 years who had not suffered this institutional deprivation.

MRI scans were conducted at the Centre for Neuroimaging Sciences at King's College London, as part of the Medical Research Council (MRC) funded English and Romanian Adoptees Brain Imaging Study (ERABIS). This is part of the larger ERA project that has collected information from Romanian and English adoptees over time including measures of mental health and cognitive performance.

This is the first time research has examined the impacts of severe early childhood deprivation on the brain structure of young adults.

Statistical analysis showed that, in this group of young Romanian adults, those changes in brain volume that were related to deprivation were also associated with lower IQ and more ADHD symptoms. This implies that changes in brain structure could play a mediating role between the experience of deprivation and levels of cognitive performance and mental health.

The research investigated other possible factors that could have influenced the results but found the results were unaffected by level of nutrition, physical growth and genetic predisposition for smaller brains.

The principle investigator of the study, Professor Edmund Sonuga-Barke from the Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London said: 'The English and Romanian Adoptees (ERA) study addresses one of the most fundamental questions in developmental psychology and psychiatry - how does early experience shape individual development? It's essential to recognise that these young people have nearly always received great care in loving adoptive families since they left the institutions. However, despite a lot of positive experiences and achievements there remain some deep-seated effects of deprivation on these young adults.'

First author, Dr Nuria Mackes from the IoPPN said: 'Previous research on the English and Romanian Adoptees (ERA) study has suggested that the emergence and persistence of low IQ and a high level of ADHD symptoms involves structural changes in the brain but, until now, we have not been able to provide direct evidence of this. Showing these very profound effects of early deprivation on brain size and then showing that this difference is associated with low IQ and greater ADHD symptoms provides some of the most compelling evidence of the neuro-biological basis of these problems following deprivation.'

The study also investigated where these changes were occurring in the brain and what localised features contributed to the differences. In comparison to the UK adoptees, the young Romanian adults who had suffered deprivation as children had markedly smaller right inferior frontal regions of the brain both in terms of volume and surface area.

In contrast the right inferior temporal lobe was larger in volume and surface area and thickness for the Romanian young adults and this was associated with lower levels of ADHD symptoms. This implies that this increase in volume and surface area in this region may play a compensatory role in preventing development of ADHD symptoms. In the right medial prefrontal region, the longer the duration of deprivation, the larger the volume and surface area.

The neuroimaging lead for the study, Professor Mitul Mehta from the IoPPN said: 'We found structural differences between the two groups in three regions of the brain. These regions are linked to functions such as organisation, motivation, integration of information and memory. It's interesting to see the right inferior temporal lobe is in fact larger in the Romanian young adults and that this was related to fewer ADHD symptoms, suggesting that the brain can adapt to reduce the negative effects of deprivation. This may explain why some individuals appear less affected than others by deprivation. We believe this is the first time that research has shown such compelling evidence of compensatory effects around deprivation.'

The Romanian young adults in the study had entered into institutions in the first few weeks of life, where they were often malnourished with minimal social contact and little stimulation. The time spent in institutions before adoption into families in the UK varied between 3 and 41 months.

Reflecting on the implications of the study Professor Sonuga-Barke said: 'By investigating the long term impact of deprivation our research highlights the need for a life-span perspective on the provision of any help and support, especially during the transition to adulthood. More speculatively the evidence of neural compensation in the inferior temporal lobe provides encouragement to look for ways that might help the brain adjust to deprivation and to improve outcomes. For example, it would be interesting to see if targeting this area directly through cognitive training might reduce ADHD symptoms.'

Reference: Mackes, N. K., Golm, D., Sarkar, S., Kumsta, R., Rutter, M., Fairchild, G., Mehta, M. A., Sonuga-Barke, E. J. S., & Team, on behalf of the E. Y. A. F. (2020). Early childhood deprivation is associated with alterations in adult brain structure despite subsequent environmental enrichment. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.1911264116

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.

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Global NEUROSCIENCE ANTIBODIES AND ASSAYS Market, Trends, Analysis, Opportunities, Share and Forecast 2019-2025 – Digits N Markets News

Global NEUROSCIENCE ANTIBODIES AND ASSAYS Market to reach USD 5.1 billion by 2025. The increasing automation of high-throughput screening and the availability of robust data management software tools, which enable researchers to develop systemic and process-oriented approaches toward neuroscience antibodies and assays techniques are some of the factors contributing to the growth of this segment.

Global NEUROSCIENCE ANTIBODIES AND ASSAYS Market valued approximately USD 2.1 billion in 2016 is anticipated to grow with a healthy growth rate of more than 10.3% over the forecast period 2017-2025

To request a sample copy or view summary of this report, click the link below: http://digitsnmarkets.com/sample/5594-global-neuroscience-antibodies-and-assays-market

The objective of the study is to define market sizes of different segments & countries in recent years and to forecast the values to the coming eight years. The report is designed to incorporate both qualitative and quantitative aspects of the industry within each of the regions and countries involved in the study. Furthermore, the report also caters the detailed information about the crucial aspects such as driving factors & challenges which will define the future growth of the market.

Additionally, the report shall also incorporate available opportunities in micro markets for stakeholders to invest along with the detailed analysis of competitive landscape and product offerings of key players. The detailed segments and sub-segment of the market are explained below:

By Product

By Technology

By End-User

Some of the key manufacturers involved in the market are. Thermo Fisher Scientific, Abcam, Bio-Rad, Merck KGAA, Cell Signaling Technology, Genscript, Rockland Immunochemicals. Bio Legend, Santa Cruz Biotechnology, Tecan, F. Hoffmann-La Roche, Siemens. Acquisitions and effective mergers are some of the strategies adopted by the key manufacturers. New product launches and continuous technological innovations are the key strategies adopted by the major players.

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Digits N Markets has a vast repository of latest market research reports on trending topics, niche company profiles, market size and other relevant data released by renowned publishers. We have access to the database related to niche markets and trending topics in various industries. We also update the data regularly to provide recent statistics to the client. Recent data and reports will be featured on our websites and clients will be able to access the same. Our clients will be able to benefit from qualitative & quantitative insights in the report which will support them in taking concrete business decisions.

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Global NEUROSCIENCE ANTIBODIES AND ASSAYS Market, Trends, Analysis, Opportunities, Share and Forecast 2019-2025 - Digits N Markets News

Neuroscience Antibodies & Assays Market 2020 : Global Analysis On Key Companies Like Roche Ltd, Thermo Fisher Scientific And Industry Forecast By…

Neuroscience antibodies & assays market is anticipated to grow with a significant rate in the coming years, owing to the increasing incidence of neurological disorders, growing pharmaceutical & biotechnology industries and increasing investments in neuroscience research. On the other hand, increasing research & development activities are projected to offer novel growth opportunities for the players operating in the neuroscience antibodies & assays market, in the coming years

Neuroscience involves the study of nervous system, where the research is completely relies on assays and antibodies. These antibodies and assays are specific that helps to identify and examine reactions on the cellular, biochemical and molecular level. Antibody-based approaches are used for the localization, isolation and characterization of targeted proteins that majorly used in the cellular and molecular neuroscience. On the other hand, the use of assays provide an efficient, valuable solution for determination of critical targets that are involved in synaptic signaling, neural development and neurodegeneration.

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Global Neuroscience Antibodies & Assays Market Analysis to 2027 is a specialized and in-depth study with a special focus on the global medical device market trend analysis. The report aims to provide an overview of neuroscience antibodies & assays market with detailed market segmentation by product, technology, application, end user and geography. The global neuroscience antibodies & assays market is expected to witness high growth during the forecast period. The report provides key statistics on the market status of the leading neuroscience antibodies & assays market players and offers key trends and opportunities in the market.

Below mentioned is the list of few companies engaged in the neuroscience antibodies & assays market:-

As, The report also includes the profiles of key neuroscience antibodies & assays market companies along with their SWOT analysis and market strategies. In addition, the report focuses on leading industry players with information such as company profiles, components and services offered, financial information of last 3 years, key development in past five years.

Key developments in the neuroscience antibodies & assays market as organic and inorganic growth strategies. Various companies are focusing on organic growth strategies such as product launches, product approvals and others such as patents and events. Inorganic growth strategies activities witnessed in the market were acquisitions and partnership & collaborations. These activities have paved way for expansion of business and customer base of market players. The market players from neuroscience antibodies & assays market are anticipated to lucrative growth opportunities in the future with the rising demand for neuroscience antibodies & assays in the global market.

The global neuroscience antibodies & assays market is segmented:-on the basis of product, technology, application and end user. Based on product, the market is segmented as consumables and instruments. On the basis of technology, the global neuroscience antibodies & assays market is segmented into molecular diagnostics, clinical chemistry, immunoassays/immunochemistry and others. Based on application, the market is segmented as in vitro diagnostics, research and drug discovery. Based on end user, the market is segmented as hospitals & diagnostics centers, academic & research institutes and pharmaceutical & biotechnology companies.

e report provides a detailed overview of the industry including both qualitative and quantitative information. It provides overview and forecast of the global neuroscience antibodies & assays market based on various segments. It also provides market size and forecast estimates from year 2017 to 2027 with respect to five major regions, namely; North America, Europe, Asia-Pacific (APAC), Middle East and Africa (MEA) and South & Central America. The neuroscience antibodies & assays market by each region is later sub-segmented by respective countries and segments. The report covers analysis and forecast of 18 countries globally along with current trend and opportunities prevailing in the region.

The report analyzes factors affecting neuroscience antibodies & assays market from both demand and supply side and further evaluates market dynamics effecting the market during the forecast period i.e., drivers, restraints, opportunities and future trend. The report also provides exhaustive PEST analysis for all five regions namely; North America, Europe, APAC, MEA and South & Central America after evaluating political, economic, social and technological factors effecting the neuroscience antibodies & assays market in these regions.

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Alzheon Announces Appointment of Peter N. Laivins as Head of Commercial Strategy and Planning – Business Wire

FRAMINGHAM, Mass.--(BUSINESS WIRE)--Alzheon, Inc., a clinical-stage biopharmaceutical company focused on developing new medicines for patients suffering from Alzheimers disease (AD) and other neurodegenerative disorders, announced today that Peter N. Laivins, MBA, has been appointed Head of Commercial Strategy and Planning. Mr. Laivins brings more than 20 years of leadership in the biopharmaceutical industry, with broad expertise in business strategy and commercialization for Alzheimers therapies, including his experience at Pfizer launching ARICEPT for symptomatic treatment for AD and at Elan Biopharmaceuticals leading commercial strategy for bapineuzumab as an anti-amyloid immunotherapy for AD.

Peter brings unparalleled depth of business and commercial expertise to Alzheon, with a unique track record of shaping the Alzheimers commercial landscape and a career-long passion to fight this debilitating disease, said Martin Tolar, MD, PhD, Founder, President and Chief Executive Officer of Alzheon. Peters skills will be invaluable as we move our lead drug ALZ-801 into Phase3 trials and prepare for future commercialization of potentially the first oral and well tolerated disease-modifying treatment for millions of Alzheimers patients and their families.

Most recently, Mr. Laivins was the Senior Vice President of Strategic Development Program Leadership at Tesaro, Inc., with oversight of five development teams, portfolio management and competitive intelligence. Previously, at Merrimack Pharmaceuticals, he served as Senior Vice President and Head of Late Stage Development, where he led the successful clinical development, NDA submission and FDA approval of Onyvide the first new therapy for pancreatic cancer in two decades. Mr. Laivins career in neuroscience drug development includes his role as Vice President of Strategic Brand Management for Elan Biopharmaceuticals, with responsibility for the Alzheimers portfolio, including bapineuzumab, and the multiple sclerosis portfolio, including TYSABRI. At Pfizer, Mr. Laivins held positions of increasing responsibility, including the Global Team Leader in Neuroscience, leading the launch of Aricept which achieved peak sales exceeding $3 billion. Beyond neuroscience, he also served as Group Leader for US Oncology Marketing at Pfizer. Mr. Laivins is a graduate of McGill University with a Bachelor of Science in microbiology and immunology and Master of Business Administration.

Im excited to join the team at Alzheon at this important juncture in Alzheimers drug development. Last year we saw convincing clinical validation of anti-amyloid therapy, which confirmed that targeting amyloid toxicity can slow disease progression and provide clinical improvement in patients, said Mr. Laivins. We believe ALZ-801 could be transformative as the first oral disease modifying treatment for Alzheimers and provide an important advance for patients and their families.

About ALZ-801

Alzheons lead product candidate, ALZ-801, an oral anti-amyloid drug candidate that is an optimized prodrug of tramiprosate, has shown promising results in analyses of clinical data1,2 and a novel therapeutic mechanism of action.3 ALZ-801 has received Fast Track designation from the U.S. Food and Drug Administration. The clinical data for ALZ-8014 and its active agent, tramiprosate, suggest long-term clinical efficacy in AD patients with the apolipoprotein E4 (APOE4) genotype and a favorable safety profile.1,2 ALZ-801 acts through a novel enveloping molecular mechanism of action blocking the formation of toxic amyloid oligomers3 associated with the development and progression of AD.6 The cognitive improvements observed in AD patients in the tramiprosate Phase 3 studies may be attributed, in part, to the therapeutic anti-oligomer action of 3-sulfopropanoic acid (3-SPA), an endogenous substance in the human brain, discovered by Alzheon scientists, that inhibits the formation of neurotoxic beta amyloid oligomers.5 3-SPA is the primary metabolite of ALZ-801 in humans and its discovery elucidates the beneficial pharmaceutical attributes of ALZ-801, including a favorable safety profile, selectivity against beta amyloid oligomers, and excellent brain penetration. ALZ-801 increases levels of 3-SPA in the brain and augments the bodys natural mechanism for blocking the formation of toxic amyloid oligomers.5 The initial Phase 3 program for ALZ-801 will focus on patients with the homozygous APOE4/4 genotype at the Early stage of AD, with the potential for future expansion to additional Alzheimers populations.6

About Alzheon

Alzheon, Inc. is committed to developing innovative medicines by directly addressing the underlying pathology of devastating neurodegenerative disorders. Our lead Alzheimers clinical candidate, ALZ-801, is a Phase 3-ready, first-in-class, small molecule oral inhibitor of beta amyloid aggregation and neurotoxicity hallmarks of Alzheimers disease. ALZ-801 is a novel prodrug that builds on the safety and efficacy profile of the active compound tramiprosate, which has been evaluated in clinical trials involving over 2,000 Alzheimers patients. Our clinical expertise and technology platform are focused on developing drug candidates using a precision medicine approach based on individual genetic and biological information to advance therapies with the greatest impact for patients.

Alzheon Publications1Abushakra et al. Journal of Prevention of Alzheimers Disease, 20162Abushakra et al. Journal of Prevention of Alzheimers Disease, 20173Kocis et al. CNS Drugs, 20174Hey et al. Clinical Pharmacokinetics, 20185Hey et al. CNS Drugs, 20186Tolar et al. Alzheimers & Dementia, 2019

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Alzheon Announces Appointment of Peter N. Laivins as Head of Commercial Strategy and Planning - Business Wire

The 13 Universal Emotions Evoked by Music – Technology Networks

The Star-Spangled Banner stirs pride. Ed Sheerans The Shape of You sparks joy. And ooh l l! best sums up the seductive power of George Michaels Careless Whisper.

UC Berkeley scientists have surveyed more than 2,500 people in the United States and China about their emotional responses to these and thousands of other songs from genres including rock, folk, jazz, classical, marching band, experimental and heavy metal.

The upshot? The subjective experience of music across cultures can be mapped within at least 13 overarching feelings: Amusement, joy, eroticism, beauty, relaxation, sadness, dreaminess, triumph, anxiety, scariness, annoyance, defiance, and feeling pumped up.

Imagine organizing a massively eclectic music library by emotion and capturing the combination of feelings associated with each track. Thats essentially what our study has done, said study lead author Alan Cowen, a UC Berkeley doctoral student in neuroscience.

We have rigorously documented the largest array of emotions that are universally felt through the language of music, said study senior author Dacher Keltner, a UC Berkeley professor of psychology.

Cowen and fellow researchers have translated the data into an interactive audio map where visitors can move their cursors to listen to any of thousands of music snippets to find out, among other things, if their emotional reactions match how people from different cultures respond to the music.

Potential applications for these research findings range from informing psychological and psychiatric therapies designed to evoke certain feelings to helping music streaming services like Spotify adjust their algorithms to satisfy their customers audio cravings or set the mood.

While both U.S. and Chinese study participants identified similar emotions such as feeling fear when hearing the Jaws movie score they differed on whether those emotions made them feel good or bad.

People from different cultures can agree that a song is angry but can differ on whether that feeling is positive or negative, said Cowen, noting that positive and negative values, known in psychology parlance as valence, are more culture-specific.

Across cultures, study participants mostly agreed on general emotional characterizations of musical sounds, such as anger, joy and annoyance. But their opinions varied on the level of arousal, which refers in the study to the degree of calmness or stimulation evoked by a piece of music.

How they conducted the study

For the study, more than 2,500 people in the United States and China were recruited via Amazon Mechanical Turks crowdsourcing platform.

First, volunteers scanned thousands of videos on YouTube for music evoking a variety of emotions. From those, the researchers built a collection of audio clips to use in their experiments.

Next, nearly 2,000 study participants in the United States and China each rated some 40 music samples based on 28 different categories of emotion, as well as on a scale of positivity and negativity, and for levels of arousal.

Using statistical analyses, the researchers arrived at 13 overall categories of experience that were preserved across cultures and found to correspond to specific feelings, such as depressing or dreamy.

To ensure the accuracy of these findings in a second experiment, nearly 1,000 people from the United States and China rated over 300 additional Western and traditional Chinese music samples that were specifically intended to evoke variations in valence and arousal. Their responses validated the 13 categories.

Vivaldis Four Seasons made people feel energized. The Clashs Rock the Casbah pumped them up. Al Greens Lets Stay Together evoked sensuality and Israel (Iz) Kamakawiwooles Somewhere over the Rainbow elicited joy.

Meanwhile, heavy metal was widely viewed as defiant and, just as its composer intended, the shower scene score from the movie Psycho triggered fear.

Researchers acknowledge that some of these associations may be based on the context in which the study participants had previously heard a certain piece of music, such as in a movie or YouTube video. But this is less likely the case with traditional Chinese music, with which the findings were validated.

Cowen and Keltner previously conducted a study in which they identified 27 emotions in response to visually evocative YouTube video clips. For Cowen, who comes from a family of musicians, studying the emotional effects of music seemed like the next logical step.

Music is a universal language, but we dont always pay enough attention to what its saying and how its being understood, Cowen said. We wanted to take an important first step toward solving the mystery of how music can evoke so many nuanced emotions.

Reference

Cowen et al. (2020) What music makes us feel: At least 13 dimensions organize subjective experiences associated with music across different cultures. PNAS. DOI: https://doi.org/10.1073/pnas.1910704117

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VoxNeuro Announces Research Project With St. Joseph’s Healthcare Hamilton – Business Wire

HAMILTON, Ontario--(BUSINESS WIRE)--At the close of 2019, VoxNeuro joined a pilot study conducted by the Womens Health Concerns Clinic & Mood Disorders Program at St. Josephs Healthcare Hamilton. The study is led by Dr. Benicio Frey and Dr. Flavio Kapczinski, and has been designed to identify biomarkers of bipolar disorder.

Dr. Frey, the studys Principal Investigator, is the Academic Head of the Mood Disorders Program, and is the Medical Director of the Womens Health Concerns Clinic at St. Joseph's Healthcare. He also holds the position of Associate Professor at the Department of Psychiatry and Behavioural Neurosciences at McMaster University. Specializing in psychiatry, biochemistry and brain imaging in bipolar disorder, Dr. Frey has more than 150 articles published in peer-reviewed journals.

Dr. Kapczinski, Psychiatrist at St. Josephs Healthcare Hamilton, professor and Director of the Neuroscience Graduate Program at McMaster University, is a leading author in the area of mood disorders and has published over 430 peer-reviewed articles (over 22,000 citations). Dr. Kapczinski and colleagues helped to develop the concepts of neuroprogression and staging in bipolar disorder, published in 2009. This current study intends to add objective details to Dr. Kapczinskis staging model by assessing whether the brains connectivity alterations are associated with illness progression in bipolar disorder.

Dr. Kapczinski was an early supporter of VoxNeuros work, founded on the lifetime research of Dr. John F. Connolly, a colleague of Dr. Kapczinski at McMaster University and VoxNeuros Chief Science Officer. In an interview in the fall of 2017, Dr. Kapczinski spoke to the potential of VoxNeuros Cognitive Health Assessments and the impact they will have on both brain injuries and mood disorders, If someone is having depressive symptoms but then we think the origin is actually repeated brain injuries, having a tool that can confirm that can put us on the right trackHaving an objective measurement related to the brain function of people who have suffered traumatic brain injuries is enormous, clinically.

For this project, the teams are collaborating on the assessments application to mood disorders, specifically bipolar. The current classifications of psychiatric diagnoses are based purely on behavioural observation and self-report, and lack of substantial biological validation. This contrasts sharply with the rest of medicine where diagnosis and treatment are routinely aided by biological tests that are based on validated biomarkers. Biological markers, or biomarkers, are quantitative measurements that provide information about biological processes, a disease state, or about response to treatment (FDAs Biomarkers Research Group definition). The objective of the study is to create a biological bank of potential biomarkers to investigate etiology, prognosis, and/or treatment response in individuals with bipolar disorder.

VoxNeuros Cognitive Health Assessments are being used alongside blood tests and various behavioural and clinical assessments to identify the most effective tools to accurately predict onset, diagnose, inform prognoses and track treatment responses for bipolar disorder. Specifically, in addition to the objective reports provided by VoxNeuros Cognitive Health Assessments, the EEG data is being used to investigate functional connectivity patterns as a potential biomarker for bipolar disorder. A recent review showed that abnormal fronto-cortical connectivity may be involved in bipolar disorder across mood states. These connectivity disturbances possibly contribute to emotional dysregulation, and cognitive impairments in bipolar disorder.

If the pilot study results support the hypothesis, a follow-on multi-year longitudinal study will be pursued to widen the data, track participants throughout diagnoses & treatment, and assess the accuracy of prognoses. This is one of VoxNeuros first examples of being integrated into a clinical study to provide objective measures to guide the examination of researchers hypotheses.

Were looking forward to working closely with St. Josephs Healthcare and St. Joes Research Institute on this project. Its a perfect example of the strong opportunities that exist between VoxNeuro, other innovative healthcare startups being built in this region, and the industry leading healthcare teams right here in our own backyard. Spinning our technology out of McMaster University, were extremely fortunate to be headquartered in Hamilton Canadas leading health sciences research cluster, says Kimberly Elliott, COO of VoxNeuro.

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VoxNeuro Announces Research Project With St. Joseph's Healthcare Hamilton - Business Wire

BioXcel Therapeutics Announces First Patient Enrolled in Phase 1b/2 Study of BXCL501 for Acute Treatment of Agitation Associated with Dementia -…

Foundational study with plans to address multiple types of agitation associated with dementia

Expands the potential therapeutic use of BXCL501 beyond neuropsychiatric disorders

Topline results expected in mid-2020

NEW HAVEN, Conn., Jan. 07, 2020 (GLOBE NEWSWIRE) -- BioXcel Therapeutics (BTI or Company) (Nasdaq: BTAI), a clinical-stage biopharmaceutical company utilizing artificial intelligence approaches to identify and advance the next wave of medicines in neuroscience and immuno-oncology, today announced that the first patient has been enrolled in a Phase 1b/2 study of BXCL501, the Companys proprietary sublingual thin-film formulation of dexmedetomidine (Dex), for the acute treatment of agitation in patients with dementia.

We are excited to advance the clinical development of BXCL501 in agitation associated with dementia, a third potential indication for our lead product candidate, commented Robert Risinger, M.D., Vice President, Clinical Development of BTAI. With no approved treatments, there is a significant need for better treatment options for the 6 million patients in the U.S. with dementia, many of whom will experience agitation during the course of their disease. We believe our candidate, BXCL501, with its unique mechanism and convenient oral dosing, has the potential to rapidly reduce agitation associated with dementia without excessive sedation or other undesired side effects. This study builds upon the foundation for a broad BXCL501 program in dementia, including the treatment of chronic agitation and the prevention of agitation using a wearable device in combination with BXCL501.

The multicenter, randomized, double-blind, placebo-controlled, ascending dose Phase 1b/2 study is designed to evaluate the efficacy, pharmacokinetics, safety and tolerability of BXCL501 in adults 65 years and older who exhibit acute agitation associated with all forms of dementia, including Alzheimer's disease. The dementia program expands on the Phase 1b study performed with BXCL501 in 135 patients with agitation associated with schizophrenia, and also builds on the positive results observed in reducing agitation with intravenous Dex in Alzheimers disease patients. This is an adaptive design and is expected to assess multiple dose cohorts of BXCL501 or matching placebos. Following the completion of each dose cohort, a safety and tolerability review is expected to be performed to determine the next tested dose. The study is designed to assess agitation as measured by the Pittsburgh Agitation Scale, a validated clinical instrument, as well as improvement in the modified Cohen Mansfield Agitation Inventory and Positive and Negative Syndrome Scale, Excitatory Component (PEC).

About BXCL501

BXCL501 is a potential first-in-class, proprietary sublingual thin film of dexmedetomidine, a selective alpha-2a receptor agonist for the treatment of acute agitation. BTI believes that BXCL501 directly targets a causal agitation mechanism and the Company has observed anti-agitation effects in multiple clinical studies across multiple neuropsychiatric indications. BXCL501 has also been granted Fast Track Designation by the U.S. Food and Drug Administration for the acute treatment of agitation.

A Phase 1b safety and efficacy study of BXCL501 yielded positive dose-response data. BXCL501 is being evaluated in the SERENITY program, consisting of two Phase 3 studies for the acute treatment of agitation in patients with schizophrenia (SERENITY I) and bipolar disorder (SERENITY II). BXCL501 is also being evaluated in a Phase 1b/2 trial for the treatment of agitation associated with dementia.

About Agitation Associated with DementiaDementia is a neurocognitive condition caused by damage to brain cells that leads to a decline in cognitive abilities and independent function. It affects approximately 6 million individuals in the United States, with Alzheimers disease accounting for 60-70% of these cases. During the course of the disease, patients with dementia often suffer from psychological and behavioral symptoms, such as agitation, which has been reported in up to 70% of patients. Agitation associated with dementia can negatively affect both the patient and caregivers quality of life. Caregiver burden can contribute significantly to burnout, which can result in premature institutionalization of the patient. Treating agitation associated with dementia has been a challenge for providers and current standards of care often have a slow onset of action and/or cause excessive sedation. There are currently no FDA-approved therapies for the treatment of dementia-related agitation, and off-label therapies have black box warnings associated with their use.

About BioXcel Therapeutics, Inc.BioXcel Therapeutics, Inc. is a clinical stage biopharmaceutical company utilizing artificial intelligence to identify improved therapies in neuroscience and immuno-oncology. BTI's drug re-innovation approach leverages existing approved drugs and/or clinically validated product candidates together with big data and proprietary machine learning algorithms to identify new therapeutic indices. BTI's two most advanced clinical development programs are BXCL501, a sublingual thin film formulation designed for acute treatment of agitation resulting from neuropsychiatric disorders, and BXCL701, an orally administered systemic innate immunity activator designed for treatment of a rare form of prostate cancer, pancreatic cancer and advanced solid cancers in combination with other immuno-oncology agents. For more information, please visit http://www.bioxceltherapeutics.com/.

Forward-Looking StatementsThis press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements in this press release include but are not limited to the timing and data from clinical development initiatives and trials for BXCL501. When used herein, words including anticipate, being, will, plan, may, continue, and similar expressions are intended to identify forward-looking statements. In addition, any statements or information that refer to expectations, beliefs, plans, projections, objectives, performance or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking. All forward-looking statements are based upon BTI's current expectations and various assumptions. BTI believes there is a reasonable basis for its expectations and beliefs, but they are inherently uncertain. BTI may not realize its expectations, and its beliefs may not prove correct. Actual results could differ materially from those described or implied by such forward-looking statements as a result of various important factors, including, without limitation, its limited operating history; its incurrence of significant losses; its need for substantial additional funding and ability to raise capital when needed; its limited experience in drug discovery and drug development; its dependence on the success and commercialization of BXCL501 and BXCL701 and other product candidates; the failure of preliminary data from its clinical studies to predict final study results; failure of its early clinical studies or preclinical studies to predict future clinical studies; its ability to receive regulatory approval for its product candidates; its ability to enroll patients in its clinical trials; its approach to the discovery and development of product candidates based on EvolverAI is novel and unproven; its exposure to patent infringement lawsuits; its ability to comply with the extensive regulations applicable to it; its ability to commercialize its product candidates; and the other important factors discussed under the caption Risk Factors in its Quarterly Report on Form 10-Q for the quarterly period ended September 30, 2019, as such factors may be updated from time to time in its other filings with the SEC, which are accessible on the SECs website at http://www.sec.gov.

These and other important factors could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent managements estimates as of the date of this press release. While BTI may elect to update such forward-looking statements at some point in the future, except as required by law, it disclaims any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing BTIs views as of any date subsequent to the date of this press release.

BioXcel Therapeutics, Inc.www.bioxceltherapeutics.com

Investor Relations:John Grazianojgraziano@troutgroup.com1.646.378.2942

Media:Julia Deutschjdeutsch@troutgroup.com1.646.378.2967

Source: BioXcel Therapeutics, Inc.

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BioXcel Therapeutics Announces First Patient Enrolled in Phase 1b/2 Study of BXCL501 for Acute Treatment of Agitation Associated with Dementia -...