Yearly Archives: 2019


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

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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

Weekly pick of Neuroscience news from around the world – Brain Tumour Research

The big news story for the cancer community this week has been the setting up of a new transatlantic research alliance with the ambition to develop new strategies and technologies to detect cancer at its earliest stage.

Those involved in this initiative, including Cancer Research UK (CRUK) believe thatearly detection is essential to help more people beat cancer a patients chance of surviving their disease improves dramatically when cancer is found and treated earlier.

Early diagnosis is, of course, a wish of the brain tumour community. All too often we hear of patients who have had to wait many months, with many visits to the GP before establishing the cause of their symptoms. However, we must not forget that earlier diagnosis may bring relief but there remains a lack of treatments. There is still no cure for many brain tumour patients

In the Report of the Task and Finish Working Group on Brain Tumour Research released February 2018 this was summed up perfectly by brain tumour activist Peter Realf who said While I endorse the need to improve earlier diagnosis, this alone without a cure will simply mean that patients face a longer walk to the grave.

In Texas there is work on in vitro blood brain barrier (BBB) models to equate their strengths and weaknesses. In-vitro means in the glass so these models are constructed with microorganisms, cells, or biological molecules outside their normal biological context e.g. in the petri dish or test tube. Work in this arena has previously been under taken at our University of Portsmouth centre. A combinatorial approach of in vitro BBB models and in-vivo (within the living) methods is thought to be key to the development of CNS therapeutics (medicines) with improved pharmacokinetic (the movement refers to the movement of drug into, though, and out of the body) properties and better BBB penetrability.

Most cancers kill because tumour cells spread, or metastasise, beyond the primary site, for example breast, to invade other organs, brain being one. Now, a University of Southern California (USC), study has found that circulating tumour cells in the blood target a particular organ and this knowledge may enable the development of treatments to prevent the spread of these metastatic cancers.

Analysis of these cells identified regulator genes and proteins within the cells that apparently directed the cancers spread to the brain. The team were therefore able to predict that a patients breast cancer cells would eventually migrate to the brain.

Assistant professor of stem cell and regenerative medicine at the Keck School of Medicine at USC, Min Yu, also discovered that a protein on the surface of these brain-targeting tumour cells helps them to breech the blood brain barrier and lodge in brain tissue, while another protein inside the cells shield them from the brains immune response, enabling them to grow there.

We can imagine someday using the information carried by circulating tumour cells to improve the detection, monitoring and treatment of the spreading cancers, Yu said.

A compound effective in killing chemotherapy-resistant glioblastoma-initiating cells (GICs) has been identified, raising hopes of producing drugs capable of eradicating refractory tumours (tumours that dont respond to treatment) with low toxicity.

As we are all too aware, despite longstanding and earnest endeavours to develop new remedies, the prognosis of most glioblastoma patients undergoing chemotherapies and radiotherapies remains poor with a median survival period of approximately 15 months.

One of the reasons for this is the lack of methods to eradicate its cancer stem cells, or glioblastoma-initiating cells (GICs), that demonstrate tumourigenicity (ability to form tumours) and resistance to chemotherapies and radiotherapies.

This study successfully cultured human GICs resistant to temozolomide (TMZ), the gold standard chemotherapy drug used for treating glioblastoma.

Then a high-throughput drug screening was conducted to identify a compound that could specifically kill or inflict damage to GICs, but not normal cells such as neural stem cells and astrocytes.

Compound 10580 was successfully identified as being capable of killing or inflicting damages to GICs whilst at the same time exhibiting no visible toxicity

"Compound 10580 is a promising candidate for developing drugs against glioblastoma and other recurring cancerssaid Toru Kondo of Hokkaido University's Institute for Genetic Medicine who led the study.

What is also interesting here is the collaborative nature of the study group with Hokkaido University, working alongside FUJIFILM Corporation and the National Institute of Advanced Industrial Science and Technology (AIST).

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Cesca Therapeutics Forms Joint Venture with Healthbanks Biotech (USA) to Provide Immune Cell Banking and Cell Processing Services – PRNewswire

RANCHO CORDOVA, Calif., Oct. 22, 2019 /PRNewswire/ -- Cesca Therapeutics Inc.(Nasdaq: KOOL), a market leader in automated cell processing and autologous cell therapies for regenerative medicine, and ThermoGenesis, its wholly owned device subsidiary, today announced that the company has entered into a definitive joint venture agreement with HealthBanks Biotech (USA) Inc., one of the world's leading stem cell bank networks, to commercialize its proprietary cell processing platform, CAR-TXpress, for use in immune cell banking as well as for cell-basedcontract development and manufacturing services (CMO/CDMO). The joint venture will be named ImmuneCyte Life Sciences Inc. ("ImmuneCyte") and is expected to officially launch during the fourth quarter of 2019.

Under terms of the agreement, ImmuneCyte will initially be owned 80% by HealthBanks Biotech and 20% by Cesca. Cesca will contribute to ImmuneCyte exclusive rights to use ThermoGenesis' proprietary cell processing technology for the immune cell banking business and non-exclusive rights for other cell-based contract development and manufacturing services. Cesca will also contribute its clinical development assets to the joint venture, as the company has decided to discontinue these activities in order to focus exclusively on the device business.

Once operational, ImmuneCyte will be among the first immune cell banks in the U.S. to provide clients with the opportunity to bank their own healthy immune cells for future use as a resource for cell-based immunotherapies, such as dendritic cell and chimeric antigen receptor (CAR) T-cell therapies. ImmuneCyte will utilize ThermoGenesis' proprietary CAR-TXpress platform which allows for the isolation of different components from 200 ml of blood in cGMP compliant, closed system. Given that the CAR-TXpress platform can increase cell processing efficiency by up to 16-fold as compared with the traditional, labor-intensive ficoll gradient centrifugation-based cell processing method, ImmuneCyte is expected to offer customers an unparalleled competitive advantage, including an ability to store their own immune cells at a tangibly lower cost.

"The ImmuneCyte joint venture will be paramount to the execution of our strategy to become a preferred cell processing and manufacturing solution provider in the cell and gene therapy field," said Dr. Chris Xu, Chairman and Chief Executive Officer of Cesca Therapeutics. "CAR-T therapeutic research is advancing rapidly. Partnering with HealthBanks Biotech, one of the foremost stem cell bank networks, with an experienced team and an established global infrastructure, will offer customers the ability to preserve younger, healthier and uncontaminated immune cells for potential future use. By applying our proprietary CAR-TXpress technology to immune cell banking and other CDMO cellular manufacturing services, we will allow for the manufacture and production of more effective and less costly immunotherapies."

In 2017, the U.S. Food and Drug Administration (FDA) approved two CAR-T cell therapies, under breakthrough designation, for the treatment of advanced B cell leukemia and lymphomas. Both use autologous (a patient's own) immune T cells to fight cancer and have reported an over 80% response rate in the "no-option" patient group, for those who have failed both chemo- and radiation therapies. This has helped to spur massive global interest for the development of additional CAR-T immunotherapies1. By the end of September 2019, there were over 800 CAR-T cell clinical trials registered on the http://www.clinicaltrials.gov website, targeting a wide variety of blood cancers and solid tumors.

Although highly effective, several recent studies on the eligibility of patients to enroll in CAR-T clinical trials showed that as many as 30-50% of cancer patients may not be eligible to enroll or to get sufficient CAR-T cells manufactured for the therapy. Reasons may include: (1) the function of the immune system declines with age and can be negatively affected by other medical conditions, (2) most standard cancer therapies, such as chemotherapy and radiation, destroy the immune system, and (3) in many cases of advanced cancer, cancer cells will enter circulation, invade and interfere with the body's natural production of immune cells. According to a recently reported JULIE trial, a CAR-T clinical trial in relapsed or refractory diffuse large B-cell lymphoma (DLBCL), one-third of the 238 screened patients failed to be enrolled, and more than half of the 238 failed to receive the intended CAR-T therapy2,3. ImmuneCyte will offer customers the ability to preserve younger, healthier and uncontaminated immune cells, for potential future use in advanced cancer immunotherapy.

About HealthBanks Biotech (USA) Inc.HealthBanks Biotech, headquartered in Irvine, CA, is one of the leading stem cell bank networks in the world and offers services globally through its sister companies located in the United States and other regions and nations. HealthBanks Biotech is accredited by the FDA, AABB, and CAP. The HealthBanks Biotech group was originally founded in 2001 with a vision that stem cells and cell and gene therapies could transform modern medicine. HealthBanks Biotech is a subsidiary of Boyalife Group, Inc. (USA), an affiliate of Boyalife (Hong Kong) Limited, the largest stockholder of Cesca. For more information about HealthBanks Biotech (USA) Inc., pleasevisit:www.healthbanks.us.

About ImmuneCyte Life Sciences Inc.ImmuneCyte will provide clients with the opportunity to bank their own immune cells when the cells are "healthy and unaffected" as a future resource for cellular immunotherapies, such as CAR-T. ImmuneCyte utilizes a proprietary CAR-TXpress platform, a GMP compliant close-system capable of automated separating and cryopreserving different components from blood.For more information about ImmuneCyte Life Sciences Inc., pleasevisit:www.immunecyte.com.

About Cesca Therapeutics Inc.Cesca Therapeuticsdevelops, commercializes and markets a range of automated technologies for CAR-T and other cell-based therapies. Its device division, ThermoGenesis develops, commercializes and markets a full suite of solutions for automated clinical biobanking, point-of-care applications, and automation for immuno-oncology. The Company has developed a semi- automated, functionally closed CAR-TXpressplatform to streamline the manufacturing process for the emerging CAR-T immunotherapy market. For more information about Cesca and ThermoGenesis, pleasevisit: http://www.cescatherapeutics.com.

Company Contact:Wendy Samford916-858-5191ir@thermogenesis.com

Investor Contact:Paula Schwartz,Rx Communications917-322-2216pschwartz@rxir.com

References:

1. Facts About Chimeric Antigen Receptor (CAR) T-Cell Therapy, Leukemia and Lymphoma Society (2018). https://www.lls.org

2. Updated Analysis of JULIET Trial: Tisagenlecleucel in Relapsed or Refractory DLBCL (2018).

3. Eligibility Criteria for CAR-T Trials and Survival Rates in Chemorefractory DLBCL. Journal of Clinical Pathways (2018).

SOURCE Cesca Therapeutics Inc.

http://www.cescatherapeutics.com

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Cesca Therapeutics Forms Joint Venture with Healthbanks Biotech (USA) to Provide Immune Cell Banking and Cell Processing Services - PRNewswire