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Gates Foundation, NIH Bet on Gene Therapy To Bring Cheap HIV and Sickle Cell Cures to Sub-Saharan Africa – Newsweek

The National Institutes of Health (NIH) announced a partnership with the Bill and Melinda Gates Foundation on Wednesday to fund the development of targeted cures for HIV and sickle cell disease with a view to helping people in developing countries using gene therapy. With most of the populations affected by each disease residing in sub-Saharan Africa, treatments are being sought with regional conditions in mind.

The NIH and the Gates Foundation are investing $100 million in the initiative to develop low-cost gene therapies. The announcement follows President Donald Trump's pledge in his 2019 State of the Union address that the United States would eradicate HIV within the next decade. The Trump administration has also tried to draw more attention to sickle cell disease (SCD) in the past few years, according to a press release from NIH.

Sickle cell disease is a blood disorder that can cause anything from mild pain to heart failure. Human immunodeficiency virus (HIV) is a communicable disease that, if left untreated, wipes out the immune system. People with SCD inherit the disease from their parents, whereas HIV is acquired through blood contamination with certain bodily fluids of an infected person. While the mechanisms of transmission are different, both diseases are carried in the genome of infected individuals. Globally, both diseases also disproportionately impact individuals in lower-income communitiesand scientists believe that both could be combatted with gene-based treatments.

The past few years have seen unprecedented strides toward cures for these two diseases using gene therapy, which the NIH defines as experimental technique wherein doctors insert genes into a patient's cells so their body can more effectively resist a disease. It can include inserting a healthy variant of a gene to replace the unhealthy copy that causes a disease, or placing an entirely new gene in the body to fight the disease.

"Dramatic advances in genetics over the last decade have made effective gene-based treatments a reality... Yet these breakthroughs are largely inaccessible to most of the world by virtue of the complexity and cost of treatment requirements, which currently limit their administration to hospitals in wealthy countries," the press release states. The new initiative will focus on developing treatments that can be delivered in "low-resource settings."

Speaking on the initiative's viability, Dr. Ronald Mitsuyasu, a professor of medicine in hematology-oncology at the University of California, Los Angeles with more than 25 years of experience in HIV clinical trials research, told Newsweek that this sort of solution has been attempted in the past, but gene therapy hasn't yet proved successful in treating HIV.

"There have been several attempts to use gene therapy for HIV by either incorporating genes that suppress HIV genes, producing decoys for various viruses required processes needed for viral replication, or substituting inactive genes for functional genes of HIV," he said.

But those living in developing countries have not had as many chances to benefit from these solutions as those living in places like the U.S., according to the press release.

"SCD and HIV are major burdens on health in low-resource communities around the world," the press release read. "Approximately 95% of the 38 million people living with HIV globally are in the developing world, with 67% in sub-Saharan Africa, half of whom are living untreated. Fifteen million babies will be born with SCD globally over the next 30 years, with about 75% of those births occurring in sub-Saharan Africa."

Further, the prediction indicates that three-quarters of those infants will be born into low-income countries and communities. Between 50 and 90 percent of babies born with the disease in sub-Saharan African countries will die before the age of five, according to the release.

So, the NIH and the Gates Foundation's initiative aims to identify potential cures for both diseases as well as partner with groups in Africa to identify candidates on whom these new cures can be tested.

We are losing too much of Africa's future to sickle cell disease and HIV. Beating these diseases will take new thinking and long-term commitment. I'm very pleased to see the innovative collaboration announced today, which has a chance to help tackle two of Africa's greatest public health challenges." Matshidiso Rebecca Moeti, M.B.B.S., the World Health Organization's regional director for Africa said of the initiative.

Mitsuyasu said he agreed that continued investigation into gene-based cures would eventually yield worthwhile results. "I personally believe that it should be possible to ultimately develop a gene therapy approach to overcome ... HIV," Mitsuyasu said. "Continued scientific developments in the field of gene therapy will eventually allow for the conquest of most genetic and viral gene integrated diseases."

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Gates Foundation, NIH Bet on Gene Therapy To Bring Cheap HIV and Sickle Cell Cures to Sub-Saharan Africa - Newsweek

EXCLUSIVE: Brian Cage Talks His Back Injury From Rebellion and How Stem-Cell Therapy Greatly Helped – LordsofPain.net

During yesterdays IMPACT media call, I had the pleasure of speaking with heavyweight champion Brian Cage, where I asked the former Lucha Underground star about the trip he took to Columbia for Stem-Cell therapy to rehab his back from an injury sustained at the Rebellion pay per view last April. Cage recalled the incident as one of the most painful in his career, but explains that the treatment was greatly beneficial, and highly recommends it to those in the industry. He also reveals how the guy who got him involved is a huge fan of the business, which has led to a wave of wrestlers traveling to Columbia to heal their bodies.

The injury was awful. One of the most painful moments of my career. I literally thought my career might be over. It kept me off TV and being able to defend my title for quite some time. I was doing everything under the sun to try and recover from that, including going to Columbia and getting the stem-cells, and I do believe it did have a substantial benefit to it. The guy that got me involved in that is a huge fan of wrestling. Thats why if you havent noticed theres been a handful of wrestlers going down there lately. Ive already been semi-educated and into stem-cells as well. Just the healing nature and what the benefits are and its a shame that you cant get the actual umbilical stem-cells here in the states.

The champ would then state that he will most-likely be going back for future injuries and maintenance.

YesIt helped me get past this. Its beneficial, and more likely be doing it again in the future. For maintenance or any other injury that may occur.

(Visited 12 times, 12 visits today)

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EXCLUSIVE: Brian Cage Talks His Back Injury From Rebellion and How Stem-Cell Therapy Greatly Helped - LordsofPain.net

Pharmacquired: Eylea could be in trouble, but that doesn’t make Regeneron a buyer – BioPharma Dive

Regeneron will lose out on hundreds of millions of dollars if a rival to its top-selling drug performs the way Wall Street expects. Even more would be at risk if recently proposed changes to government insurance become a reality.

In these situations, when a drugmaker's biggest product is under fire, acquisitions can look like an attractive way to put out the flames. AbbVie's $63 billion bid to acquire Allergan stems almost entirely from the buyer trying to find new revenue streams before generics start eating away at its mega-blockbuster drug, Humira.

But Regeneron isn't like other drugmakers. In the 30 years since its founding, it has never acquired another company. Though Regeneron isn't completely shut off to the idea of doing M&A, there's little to indicate the biotech is actively trying to change its deal track record.

Regeneron maintains that it doesn't need to buy drugs because of its R&D skills. Under the direction of CEO Len Schleifer and Chief Scientific Officer George Yancopoulos, the biotech has brought seven new medicines to market, including five from a long-standing partnership with Sanofi.

"When I look at Gilead, for example, or even Biogen [there is] a lot of investor pressure to buy something," Evan Seigerman, a Credit Suisse analyst, told BioPharma Dive. "Regeneron is still good at telling the narrative that 'we can develop our own assets and we have the best capabilities, so we're not going to buy anything.'"

The biggest of those assets is Eylea, a drug for multiple eye diseases that hit $6.75 billion in global sales last year.

For 2019, the average Wall Street estimate has Eylea reaching $7.43 billion in sales. For 2020 and beyond, however, analysts are torn about how it will fare in light of a new competitor.

*Selection of four investment bank forecasts for global Eylea sales

Earlier this month, Novartis began selling in the U.S. a drug for wet AMD, an age-related vision loss disease for which Eylea is also approved. Novartis on its third quarter earnings call touted how the drug, Beovu, is off to a strong launch, though the company didn't provide sales numbers.

While some analysts initially viewed Beovu's label as weaker than expected Christopher Raymond of Piper Jaffray called the drug "little more than an also-ran" it is still poised to steal market share from Eylea. Just how much share is the big question facing Regeneron.

RBC Capital Markets' research team said it recently spoke with an eye specialist who plans on switching one-third of her Eylea-treated wet AMD patients to Beovu. On a broader scale, the American Society of Retina Specialists found in a recent survey of 1,009 people from ophthalmology organizations that 50% plan on prescribing Beovu for wet AMD patients who don't adequately respond to drugs like Eylea or Roche's Lucentis.

Beovu may not be the only challenge to Eylea, either. President Donald Trump and Democrats in the House of Representatives have pitched different plans that would affect how Medicare pays for certain drugs. Medicare Part B spends more on Eylea than any other drug, leaving it particularly exposed if changes to government insurance take shape.

Amid these uncertainties, Regeneron's share price has fallen 16% since the beginning of the year. By contrast, the Nasdaq Biotechnology Index, which includes Regeneron, rose 13% over the period.

"They really do have quite a successful R&D engine," Kennen MacKay of RBC said. "But with the stock trading where it is, maybe there's a feeling that's no longer enough."

Jacob Bell / BioPharma Dive, market data

Regeneron's success is tied to its prowess in developing monoclonal antibodies a type of drug that, while a novelty in the past, is now a mainstay of many drugmakers' pipelines.

Some on Wall Street fret that Regeneron's competitive edge may have weakened as more companies entered this space. Last month, Geoffrey Porges of SVB Leerink went so far as to pose the provocative question: "Is Regeneron becoming the TiVo of biopharma?"

Whether or not those worries are valid, analysts can't envision Regeneron buying anything because that would be so out of character.

"These companies really do have a certain genetic makeup of what they're about, especially Regeneron," Cowen & Co.'s Yaron Werber told BioPharma Dive. "Doing M&A is not something that's in their DNA."

The threats to Eylea are therefore unlikely big enough or realized enough to push Regeneron toward acquisitions. According to consensus figures provided by Credit Suisse, analysts envision sales of the eye drug growing over the next year in spite of Beovu, as it takes greater market share in areas like diabetic macular edema.

Investors also have other bright spots to keep their attention off M&A. Dupixent, a treatment for eczema and asthma, achieved triple-digit growth over the last year and could help offset future hits to Eylea.

Regeneron's pipeline drugs, meanwhile, face significant competition.Roche and Amgen are working on rival cancer agents, while Merck & Co., Bristol-Myers Squibb and Alexion Pharmaceuticals already market blockbuster drugs for diseases that Regeneron is targeting.

"There's a deep pipeline, but it's lacking that one disruptive product that investors always want to see," Werber said. "It's a pipeline that still is getting defined."

Regeneron could find that disruptive product through bets on newer technologies. The company entered a gene editing deal with Intellia Therapeutics in 2016, a cell therapy deal with Bluebird bio in 2018, and an RNA-focused deal with Alnylam Pharmaceuticals this April.

"There's nothing inherently good about doing M&A."

Nouhad Husseini

Head of Business Development, Regeneron

While Regeneron has favored partnerships to acquisitions, it could do the latter if it wanted. By the end of June, the company held just over $1 billion in cash and cash equivalents and another $4.5 billion in marketable securities.

"The deal we did with Alnylam, or Intellia, or any of our partners where we're accessing external innovation, we could have just as easily decided to acquire one of those companies," Nouhad Husseini, Regeneron's head of business development, said in an interview.

Husseini holds reservations about outright acquisitions, though he said he could see Regeneron buying something in the short- or medium-term. Collaborations have worked out well, he notes, because both sides can stay focused on the science without getting distracted by the upheaval that often comes from M&A.

"The way I look at it is: M&A and doing a partnering deal, it's shades of gray and there are pros and cons. It's a way of structuring the deal, nothing more than that," Husseini said. "We really value these companies who have this independent entrepreneurial spirit, and I've seen firsthand what happens when big companies come in and acquire these little companies."

Scientific independence is a value shared by other biotech dealmakers as well.

Gilead and Galapagos structured their $5.1 billion research deal so the smaller company would remain a motivated partner, according to Gilead CEO Daniel O'Day. Gilead also announced in May that it will keep separate its cell therapy subsidiary, Kite Pharma, which O'Day reasoned would improve efficiency.

Jeffrey Leiden, the CEO of Boston-based Vertex, told BioPharma Dive earlier this year that he planned on letting Semma Therapeutics, which Vertex had just acquired for $1 billion, operate with more autonomy because of the target company's leadership team and expertise in stem cell-derived therapies.

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Pharmacquired: Eylea could be in trouble, but that doesn't make Regeneron a buyer - BioPharma Dive

NK Cell Therapy Market 2019, Analysis by Industry Trends, Size, Share, Company Overview, Growth, Development and Forecast by 2025 – Health News Office

Global Blood Gas and Electrolyte Analyzer Market Report 2019 Market Size, Share, Price, Trend and Forecast is a professional and in-depth study on the current state of the global Blood Gas and Electrolyte Analyzer industry.

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Chapter 4, the Blood Gas and Electrolyte Analyzer breakdown data are shown at the regional level, to show the sales, revenue and growth by regions, from 2019 to 2025.

Chapter 5, 6, 7, 8 and 9, to break the sales data at the country level, with sales, revenue and market share for key countries in the world, from 2019 to 2025.

Chapter 10 and 11, to segment the sales by type and application, with sales market share and growth rate by type, application, from 2019 to 2025.

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NK Cell Therapy Market 2019, Analysis by Industry Trends, Size, Share, Company Overview, Growth, Development and Forecast by 2025 - Health News Office

Global 3D Cell Culture Markets, 2019-2025: Cancer & Stem Cell Research Displays the Potential to Grow at Over 21.9% – ResearchAndMarkets.com -…

DUBLIN--(BUSINESS WIRE)--The "3D Cell Culture - Market Analysis, Trends, and Forecasts" report has been added to ResearchAndMarkets.com's offering.

The 3D Cell Culture market worldwide is projected to grow by US$2.2 Billion, driven by a compounded growth of 21%.

Cancer & Stem Cell Research, one of the segments analyzed and sized in this study, displays the potential to grow at over 21.9%. The shifting dynamics supporting this growth makes it critical for businesses in this space to keep abreast of the changing pulse of the market. Poised to reach over US$1.9 Billion by the year 2025, Cancer & Stem Cell Research will bring in healthy gains adding significant momentum to global growth.

Representing the developed world, the United States will maintain a 22.6% growth momentum. Within Europe, which continues to remain an important element in the world economy, Germany will add over US$82.5 Million to the region's size and clout in the next 5 to 6 years. Over US$106.9 Million worth of projected demand in the region will come from the rest of the European markets.

In Japan, Cancer & Stem Cell Research will reach a market size of US$135.6 Million by the close of the analysis period. As the world's second largest economy and the new game changer in global markets, China exhibits the potential to grow at 20.5% over the next couple of years and add approximately US$386.3 Million in terms of addressable opportunity for the picking by aspiring businesses and their astute leaders.

Presented in visually rich graphics are these and many more need-to-know quantitative data important in ensuring quality of strategy decisions, be it entry into new markets or allocation of resources within a portfolio. Several macroeconomic factors and internal market forces will shape growth and development of demand patterns in emerging countries in Asia-Pacific.

All research viewpoints presented are based on validated engagements from influencers in the market, whose opinions supersede all other research methodologies.

Competitors identified in this market include:

For more information about this report visit https://www.researchandmarkets.com/r/8wpjwb

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Global 3D Cell Culture Markets, 2019-2025: Cancer & Stem Cell Research Displays the Potential to Grow at Over 21.9% - ResearchAndMarkets.com -...

UCI IN THE NEWS OCT. 25, 2019 – UCI News

Orange County Register, Oct. 25, 2019Hyundai to test self-driving vehicles as shuttle service in IrvineBotRide is being marketed to UC Irvine students, who may not have cars or if they do, struggle to find parking, [Daniel] Han said. The company also is collaborating with researchers in the universitys business and engineering schools. Nick Schaffer, director of external relations for the UCI Paul Merage School of Business, called the collaboration an opportunity for our school and students to be on the forefront of digital transformation. As we prepare our students to be leaders in the digitally driven world, this immersive experience allows them to gain first-hand insight into how technology is disrupting the business landscape. [Subscription required, you can request an electronic copy of the article by sending an email to communications@uci.edu.]

The Stem Cellar, Oct. 25, 2019 (Video)A bridge to the future: training the next generation of stem cell scientistsOne of our recent Bridges graduates is Zach Wagoner. Zach was a biology student and wondering what to do next to help him get some experience for a job when someone told him about the Bridges program. That set him on a course that is changing his life. So how did the random conversation impact Zach? The team at the UC Irvine Sue and Bill Gross Stem Cell Research Center shot this video to answer that question.

The New York Times, Oct. 24, 2019Opinion: The United States Has Never Truly Been a DemocracyIts telling that many of the arguments about the end of democracy suggest its because weve given too much power to the masses, that weve become too democratic. Apaper byShawn Rosenberg, professor of political science and psychological science at the University of California, Irvine,claims that the problem is social media and that other technologies have disrupted the role of elites in guiding the masses through the intricacies of policy and economics. [Subscription required, campus-wide access provided by UCI Libraries. Sign-up here: AccessNYT.com]

Voice of OC, Oct. 25, 2019Cooperative Garden Promotes Food Self-Determination for Santa AnaThey are also setting up an aquaponics system, which UC Irvine donated. Giant plastic tanks sit empty, waiting to hold plants that will grow in water. A separate tank will hold fish, probably tilapia, and the fish waste will be filtered to provide nutrients for the plants. Volunteers from UC Irvine are coming on Nov. 16 to finish setting up the system and the public is invited to come and help.

Daily Pilot, Oct. 24, 2019Double, double toil and trouble a new exhibit on witchcraft opens at UC IrvineA new exhibit on witchcraft and its rise as a feminist identity is opening to the public Friday at the Langson Library at UC Irvine. We Are the Witches You Couldnt Burn tracks the history and evolution of witchcraft between the 16th and 21st centuries. Derek Quezada, outreach and public services librarian for UCI, said inspiration for the exhibit came out of work he was doing with a group of art history students to practice curation based on avant-garde Russian art. [Subscription required, you can request an electronic copy of the article by sending an email to communications@uci.edu.]

Previously In the News

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UCI IN THE NEWS OCT. 25, 2019 - UCI News

Mini-brains may already be sentient and suffering, scientists warn – Big Think

Neuroscientists are "perilously close" to crossing serious ethical lines by experimenting with mini-brains that might be complex enough to feel pain. In fact, experiments with mini-brains (also called organoids) might have already crossed those lines.

"If there's even a possibility of the organoid being sentient, we could be crossing that line," Elan Ohayon, the director of the Green Neuroscience Laboratory in San Diego, California, told The Guardian. "We don't want people doing research where there is potential for something to suffer."

On Monday, Ohayon and his colleagues presented a computational study at Neuroscience 2019, the world's largest annual meeting of neuroscientists. The study aimed to establish guidelines for scientists to determine when exactly a mini-brain develops consciousness.

"Assessment informed by the models and associated dynamics suggests that current organoid research is perilously close to crossing this ethical Rubicon and may have already done so," the paper states. "Despite the field's perception that the complexity and diversity of cellular elements in vivo remains unmatched by today's organoids, current cultures are already isomorphic to sentient brain structure and activity in critical domains and so may be capable of supporting sentient activity and behavior."

Mini-brains are tiny lumps of tissue made from stem cells that are capable of generating rudimentary neural activity, and researchers use them in neuroscience experiments. The main benefit of mini-brains is that scientists can conduct important research that sheds light on the human brain all without having to use actual human or animal brains.

As Big Think's Robby Berman noted in March, mini-brains are relatively rudimentary. The most advanced organoid possesses a couple million neurons twice that of a cockroach, but far fewer than an adult zebrafish. The human brain, meanwhile, has some 100 billion neurons. But mini-brains are becoming more complex.

A 2018 study showed that organoids implanted in mouse brains are capable of attaching to the animal's blood supply and sprouting new connections. In another recent study, researchers created a mini-brain with retinal cells, which are the neurons that process visual information. In August, a paper published in Cell Stem Cell described how researchers developed an organoid that is capable of producing brain waves similar to those of premature human babies.

"We never had a brain organoid that can function like the human brain," biologist and researcher Alysson Muotri told Discover Magazine. "The electrical activity of these brain organoids are emitting something we see during normal human development. So, it's a strong indication that what we have should work and function like the human brain."

Some scientists think that mini-brains are still too rudimentary to experience anything like what humans would call pain, and therefore the community doesn't need to worry about creating a nightmarish torture scenario for mini-brains. But others argue that scientists should establish clear guidelines for consciousness so can stop experiments before they effectively create new way for beings to suffer.

"We don't really know actually where this is all going," Patricia Churchland, a Salk Institute professor emerita who studies the linkage between philosophy and neuroscience, told the San Diego Union-Tribune. "It's very, very difficult to predict the future in science, as in baseball."

In the computational study presented on Monday, the researchers discussed five domains through which consciousness might be defined: [1] compositional (e.g., atomic, molecular), [2] causal (e.g., genetic, evolutionary), [3] anatomical (e.g., cellular, network geometry, brain regions), [4] physiological (e.g., cellular, network, whole brain activity), and [5] behavioral (e.g., embodied, virtual). But they also noted a strange and alarming possibility:

"It is important to note that the observations in this computational study point at minimal guidelines and undoubtedly would fail to identify alternate forms of sentience."

Related Articles Around the Web

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Mini-brains may already be sentient and suffering, scientists warn - Big Think

UK and China scientists developing new drugs to fight Tuberculosis – University of Birmingham

Micky Tortorella (GIBH) speaking at Guangzhou Municipal Government

University of Birmingham scientists have worked with partners in Guangzhou to develop new drugs that can tackle global health epidemics, which have an impact on Chinas rural communities.

Researchers at the University of Birmingham joined forces with their counterparts at the Guangzhou Institutes of Biomedicine and Health (GIBH) to develop a promising hit for anti-Tuberculosis therapy and initiate a drug discovery effort.

In order further to develop the drug and make it available to TB patients, particularly those with drug-resistant strains of the disease, Birmingham and GIBH are working to progress future development of the compounds through the independent spin-out company Legion.

University of Birmingham Vice-Chancellor Professor Sir David Eastwood heard more about the research project from the collaborative team during his recent visit to Guangzhou.

Professor Sir David Eastwood commented: The University of Birmingham is a world leader in molecular chemistry and biosciences, and our partnership with experts at GIBH is making promising progress in the fight against global health epidemics.

We are a global university with a civic outlook and I am delighted that our work with colleagues at GIBH is progressing development on compounds that could help to improve health outcomes for millions of people, particularly in communities across rural China.

The drug discovery effort has been led by Professor John Fossey and Dr Luke Alderwick, Director of the Birmingham Drug Discovery Facility - from the Universitys Schools of Chemistry and Biosciences. At GIBH, the efforts have been headed by Dr Cleopatra Neagoie, chemistry team leader and Micky Tortorella, Director of the Drug Discovery Pipeline.

Professor John S. Fossey commented: We designed and synthesised the first generation of molecules in Birmingham and a team of expert GIBH researchers synthesised and optimised the molecules. Thanks to a wider team involving our postgraduate students, we developed a number of compounds, which have great promise as therapeutic treatments.

Working online has been essential for us - allowing us smoothly to share project data across borders contributing greatly to the success and sustainability of our partnership. We look forward to a new chapter in drug development as GIBHs spinout company progresses our discoveries in China.

Teams based in Britain and China used innovative data sharing technology developed by the University of Birmingham to help them to work faster and more effectively whilst separated by thousands of kilometres.

One of the most important online tools they used is the University of Birminghams BEAR DataShare facility. This allows the team to share project-related data securely across the world even by mobile phone, using a specially developed app.

Resistant TB is an unmet medical need in China and this joint project is very important to the citizens of China. Great things are on the way and we are delighted that our research is now at the point where we can take it to the next level of development, commented Micky Tortorella.

GIBH is a high-profile research institute, run by the Chinese Academy of Sciences, the Peoples Government of Guangdong Province, and the Peoples Government of Guangzhou Municipality. Research areas include stem cell and regenerative medicine, chemical biology, public health, immunology and infectious diseases.

The University of Birmingham has a long-standing relationship with the city of Guangzhou, which is also the sister city of Birmingham itself. The University opened its Guangzhou Centre in 2011 and its China Institute has forged close links with partners in the city and beyond.

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UK and China scientists developing new drugs to fight Tuberculosis - University of Birmingham

Repairing the brain through stem cell therapy – Monash Lens

Theres a new frontier in medicine that seeks to cure not just treat symptoms by regenerating healthy tissue destroyed by disease.

In the firing line are currently incurable diseases that impose enormous suffering, debilitation and costs. This includes the muscle wasting inflicted by muscular dystrophy, for example, or the loss of brain neural cells in the case of Parkinsons disease.

Its the latter that the startup Convalesce Inc is primarily targeting, based on the development of a self-assembling and self-repairing material called AmGel. It contains nanofibres capable of nurturing stem cells to replace damaged nerves a function that can make or break the use of stem cells therapeutically.

To get all the interacting factors right meant drawing on nanotechnology, bioengineering, cell biology, developmental biology and material science super-advanced stuff.

AmGels development and commercialisation, however, owes a great deal to a new model for producing the next generation of innovators in this case, Convalesces co-founder, Dr Subhadeep Das.

He graduated with a PhD in 2017 from an academy specifically established to use advanced multidisciplinary research techniques to address critical global challenges, including in energy, infrastructure and manufacturing. Called the IITB-Monash Research Academy, its a joint venture between the Indian Institute of Technology Bombay (IITB) and Monash University.

Speaking from the prestigious IndieBio accelerator program in San Francisco, Das explains that stem cell technology perfectly fits the academys mission. These are cells that are potentially game-changing for medicine, yet their use is held back by the cells complex relationship to its molecular, cellular and extra-cellular environment.

You cant just inject stem cells into inflamed and damaged tissue. They dont survive in that micro environment, Das says. The solution requires drawing on multiple disciplines like having smaller pieces for a jigsaw puzzle.

For Parkinsons disease, that involves understanding the biophysicality of the brain and the dimensions and topography of its subcellular structures. This has led to the designing of nanofibres that form a scaffold for stem cells to attach and grow into. This matrix also cues stem cell growth and development into functioning nerve cells.

To get all the interacting factors right meant drawing on nanotechnology, bioengineering, cell biology, developmental biology and material science super-advanced stuff, Das says.

The science, however, is just the first step towards a cure. Convalesce constitutes the second phase meeting the testing, regulatory and commercialisation hurdles needed to get a viable therapy to patients.

Das admits the learning curve has been steep in the segue from research to commercialisation. Working alone, he might not have succeeded.

Instead, he took advantage of ongoing support provided by the IITB-Monash Research Academy, including the provision of exclusive rights to the intellectual property for AmGel, and mentoring from across both universities, especially from the academys CEO, Professor Murali Sastry.

He discovered that while starting a company is tough, there are people who are willing to help if you reach out. Its making the connections in the first place that matters.

On that score, the Monash alumni office do a great job. They provided us with introductions to alumni that included highly successful entrepreneurs and heads of venture firms. These are people who are willing to help because of the connection with Monash University.

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Repairing the brain through stem cell therapy - Monash Lens

Richard Young, Ph.D., Founder of CAMP4 Therapeutics, Elected to National Academy of Medicine – Business Wire

CAMBRIDGE, Mass.--(BUSINESS WIRE)--CAMP4 Therapeutics, a biotechnology company unraveling transcriptional machinery and the network of signaling pathways to accelerate drug discovery and development across therapeutic areas, announced that Richard Young, Ph.D., one of the companys founders, has been elected to the National Academy of Medicine (NAM). Dr. Young, a Member of the Whitehead Institute and Professor of Biology at the Massachusetts Institute of Technology (MIT), was one of 90 regular members and 10 international members elected to NAM earlier this week. Election to NAM is considered one of the highest honors in the fields of health and medicine, recognizing individuals who have made major contributions to the advancement of the medical sciences, health care and public health. Dr. Young was elected to the National Academy of Sciences in 2012 as well.

Dr. Youngs research focuses on mapping the regulatory circuitry that controls cell state and differentiationusing experimental and computational technologies to determine how signaling pathways, transcription factors, chromatin regulators, and small RNAs control gene expression.

CAMP4 was founded based on the seminal discoveries made by Dr. Young, along with Leonard Zon, M.D., Grousbeck Professor of Pediatric Medicine at Harvard Medical School, Investigator at Howard Hughes Medical Institute, and Director of the Stem Cell Program at Boston Childrens Hospital.

Based on Drs. Young and Zons discoveries, CAMP4 has built its proprietary Gene Circuitry Platform, with which it is pioneering a systematic and scalable approach to discover new, druggable targets to control gene expression to treat diseases across all therapeutic areas.

On behalf of the entire CAMP4 team, I want to congratulate Rick on this tremendous and well-deserved honor, said Josh Mandel-Brehm, President and Chief Executive Officer of CAMP4. In addition to all of his remarkable scientific accomplishments that have the potential to impact peoples lives around the world, and the numerous resulting accolades bestowed on him, I am continually struck by Ricks incredible humility and humanity. We are grateful to have the opportunity to work with and advance Ricks science and vision.

Dr. Young received his Ph.D. in Molecular Biophysics and Biochemistry at Yale University, conducted postdoctoral research at Stanford University and joined Whitehead Institute and MIT in 1984. He has served as an advisor to the National Institutes of Health, the World Health Organization, the Vatican and numerous scientific societies and journals. Dr. Young has founded and advised companies in the biotechnology and pharmaceutical industry and is currently a member of the Board of Directors of CAMP4, Syros Pharmaceuticals and Omega Therapeutics. His honors include Membership in the National Academy of Sciences, the Chiron Corporation Biotechnology Research Award, Yales Wilbur Cross Medal, and in 2006 Scientific American recognized him as one of the top 50 leaders in science, technology and business.

The National Academy of Medicine, established in 1970 as the Institute of Medicine, is an independent organization of eminent professionals from diverse fields including health and medicine; the natural, social, and behavioral sciences; and beyond. It serves alongside the National Academy of Sciences and the National Academy of Engineering as an adviser to the nation and the international community. Through its domestic and global initiatives, the NAM works to address critical issues in health, medicine, and related policy and inspire positive action across sectors. The NAM collaborates closely with its peer academies and other divisions within the National Academies of Sciences, Engineering, and Medicine.

View the Whitehead Institutes statement on Dr. Youngs election to NAM.

About CAMP4 Therapeutics

At CAMP4 Therapeutics, we are revolutionizing drug discovery and development to be faster, smarter and better. With our Gene Circuitry Platform, we have discovered how to dial up or dial down the expression of any gene. Using the foundational insights enabled by our platform, we are pioneering a systematic and scalable approach to discover new, druggable targets to control gene expression to treat diseases across all therapeutic areas. This approach involves creating tissue-specific Gene Circuitry Maps that comprehensively reveal the transcriptional machinery and its connected network of signaling pathways governing gene expression. Each map serves as its own therapeutic area discovery engine, revealing dozens, sometimes even hundreds of disease-solving opportunities. Our goal is to decipher the transcriptional machinery and signaling networks controlling gene expression for all cell types central to disease, ultimately delivering druggable targets for a multitude of undruggable diseases. Our vision is to create a world where a treatment for every disease is possible. Learn more about us at http://www.camp4tx.com.

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Richard Young, Ph.D., Founder of CAMP4 Therapeutics, Elected to National Academy of Medicine - Business Wire