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StemSpine to Launch in the United States Following Successful Treatments Overseas with 12+ Months Data Showing Safety and Efficacy (CELZ) – Stock Day…

PHOENIX, Oct. 17, 2019 /PRNewswire/ Creative Medical Technology Holdings, Inc. (OTC: CELZ), a leading commercial stage biotechnology company focused on Urology, Neurology and Orthopedics using stem cell treatments, today announced the successful clinical commercialization of StemSpine.

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StemSpine, a patented procedure for the treatment of chronic lower back pain (CLBP) utilizing a patients own stem cells, has successfully been implemented with the treatment of the first patients with over 12+ months of data showing safety and efficacy. The company plans to submit the results for publication in a peer reviewed journal imminently.

The company will begin commercializing StemSpine in the US with the launch of a new website and physician recruitment in the weeks ahead. As weve previously announced it was our goal to commercialize StemSpine in 2019, so were pleased with the progress of this technology and the value it brings to our company as domestic commercialization begins, said Timothy Warbington, President and CEO of Creative Medical Technology Holdings, Inc.

StemSpine will surely be welcomed by the over 50 million Americans suffering from CLBP in the United States as a drug free alternative. Currently, there are minimal treatment options for patients that suffer from this debilitating pain, with roughly 50% of patients progressing to opioids and surgery,1 said Thomas Ichim PhD, Chief Scientific Officer of Creative Medical Technology Holdings, Inc. and patent inventor.

About Chronic Lower Back Pain:

Chronic lower back pain represents a leading cause of disability worldwide and is the most common non-cancer reason for opioid prescription in the U.S. It affects up to 30% of U.S. adults and is estimated to cost the U.S. healthcare system over $100 billion each year.

Forward-Looking Statements

OTC Markets has not reviewed and does not accept responsibility for the adequacy or accuracy of this release. This news release may contain forward-looking statements including but not limited to comments regarding the timing and content of upcoming clinical trials and laboratory results, marketing efforts, funding, etc. Forward-looking statements address future events and conditions and, therefore, involve inherent risks and uncertainties. Actual results may differ materially from those currently anticipated in such statements. See the periodic and other reports filed by Creative Medical Technology Holdings, Inc. with the Securities and Exchange Commission and available on the Commissions website at http://www.sec.gov.

1 https://healthcare.utah.edu/publicaffairs/news/2019/10/heal-initiative.php

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SOURCE Creative Medical Technology Holdings, Inc.

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StemSpine to Launch in the United States Following Successful Treatments Overseas with 12+ Months Data Showing Safety and Efficacy (CELZ) - Stock Day...

Stem cells treatment gives hope in fighting Autism, blood disorders – OrissaPOST

Bhubaneswar: The advanced treatment of using stem cells for treating Autism and other neurological ailments have come as a ray of hope for the people living with some of these ailments. Medical experts working in the sector claim that the use of the technology improved the lives of many.

According to experts who practice stem cell therapy, the results have been overwhelming. Many of the patients have either been able to fight a deadly disease with the help of stem cells while many have been able to improve their quality of lives by using it. However, the technology is still not used widely in state hospitals.

Medical experts claim that stem cells could be used to treat neurological disorders like Autism, cerebral palsy, mental retardation, brain stroke, muscular dystrophy, spinal cord injury, head injury, cerebellar ataxia, dementia, motor neurone disease, multiple sclerosis while it has also been used to treat cancers like blood cancer with the help of bone marrow transplant when assisted by stem cell therapy.

However, treatment of Autism with stem cells is a new developing sector where visible changes are said to have been reported among children treated with this technology. However, the advanced technology which is now confined to only private sector is a bit expensive.

Autistic kids are usually treated with drugs for symptomatic relief, special education, occupational speech and behavioural therapies. In Autism, despite the best available medical and rehabilitative treatments satisfactory relief is still a far cry, said Dr Nandini Gokulchandran, Head Medical Services, NeuroGen Brain and Spine Institute, Mumbai.

Dr Gokulchandran claims that she has treated many cases of Autism in kids with stem cells which helped in overcoming their limited abilities. Under the treatment regime, an insertion procedure is undertaken followed by training to improve the skills and abilities of autistic kids.

Another neurologist, Dr Richa Bansod said that in India it has been reported that 1 in every 250 children have Autism and this number in increasing with better recognition and awareness of the condition. On the other hand, stem cells are now been used to fight deadly diseases.

Dr Joydeep Chakaborty, an oncologist and stem cell expert from HCG Cancer Hospital, Kolkata said, Stem cells and bone marrow transplants are now being used to cure blood cancer in many cases. It is also widely used to treat blood disorders like Thalassemia, Sickle Cell Anaemia and others.

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The ‘Magic’ Behind Every Successful Blockbuster Drug – DailyWealth

The Weekend Edition is pulled from the daily Stansberry Digest.

Twenty years ago, Stansberry Research founder Porter Stansberry hired me...

He wanted me to write about the economics of medicine for the everyday investor.

The goal was to track revolutions, not evolutions. That meant finding actionable information on new, world-changing drugs, not new hospital beds.

The first great drug we came across was a cancer drug called Gleevec. It worked miracles... but only for a vanishingly small number of cancer patients.

In fact, you needed a specific tragedy in your genetic code to get the defect that Gleevec could hit. If two clusters of your DNA split and rejoined in a special way, your body built a gene that didn't exist before, and it led to leukemia...

This was one of the first cancer genes ever discovered, and the pill landed right in its heart. Gleevec killed the cancer cells that made the target.

In the U.S. Food and Drug Administration's ("FDA") Phase II trials, the results were astonishing: 98% of people's cancers disappeared, meaning they had a "complete response" to the pill.

The FDA approved Gleevec based on the astonishing results.

But we passed on it. We never recommended subscribers invest in it. You see, despite the drug's promise, there was no buying opportunity back then...

The global pharmaceutical company Novartis (NVS) developed Gleevec.

Novartis was a $100 billion firm two decades ago, so investors had to balance the upside on a $1 billion (or more) blockbuster drug against the revenue of its other products.

This brings up an important point...

The world's largest drug firms are marketing machines as much as factories for innovation...

They must keep selling new drugs.

It typically takes about 10 years to develop a drug, and "patent protection" is 20 years... after which the drug then becomes a cheaper generic. So a drug company has roughly just 10 to 12 years to make back its return on investment.

That means if a Big Pharma company has two dozen drugs like Novartis did at the time then two or more will likely be coming off patent protection every year. That could mean a sudden 75% drop in revenue on that product line.

It's a complicated picture.

So instead, Porter and I focused on smaller pharmaceutical firms the ones that were pure inventors.

That's because big firms need to buy up the smaller firms' new drugs... so they can always be selling branded products.

In short, there's an economy in new medicines...

In the U.S., all medicine everything from hospital stays to ACE bandages is a segment of the economy that accounts for $3.5 trillion per year. But globally, medicines alone are worth $1.3 trillion in annual sales. And the latest inventions are valuable.

You should know, I'm not a doctor. And of course, neither is Porter...

So when we started to look for innovative medicines, we looked at it from a different perspective, like we were patients.

We didn't think we'd get all these dreaded diseases. But we knew some folks did or their families did so we respected that.

It's a medical spin on one of Porter's pillars of Stansberry Research: What would we want from you if our positions were reversed?

As we looked for new medicines to invest in, we looked at what was best for patients...

And that led us to a truth about side effects that at the time was alien to most doctors and Wall Street... People don't like side effects.

Sounds trivial, right? But here's the economic impact... When you realize that patients are customers, you realize they make choices. And they will always choose the safer course.

Imagine a drug that's 25% effective, with minimal side effects. Then compare it with a drug that's 50% effective that comes with severe side effects. You'd try the safer drug first.

There's no reason not to at least try it, because there's no downside. That's how a 25% effective drug can win 100% of the market... and disrupt "traditional" medicine.

Keep in mind, companies still need to prove the effectiveness of their medicines in controlled clinical trials. We didn't like herbal medicines, or success by anecdote, or outright falsehoods (like stem-cell treatments).

With our early subscribers, we entered the ground floor of a new way of looking at medicine...

We looked for biotechnology drugs that could be vastly more effective and safer than any drug or treatment before...

For example, we picked Intuitive Surgical (ISRG) in March 2004 when it was an $18 stock. A little more than a year later, in April 2005, we booked a 124% return. Today, ISRG shares trade for roughly $566.

The big idea here was robotic-assisted surgery plus, patents from the lone inventor who first imagined this concept. But these patents were more of a sketch than a device. The magic was in the engineering...

You see, engineering is what really drives biotech developments...

A core demand in our economy is reproducibility, or the ability to scale. You have a smartphone only because a billion people have smartphones. Otherwise, you'd be holding a Faberg egg. Let me explain...

More than a hundred years ago, Russian Tsar Alexander III purchased the first of these fancy eggs from Faberg, a jewelry firm founded in Saint Petersburg. It's said only as many as 69 eggs were created, and Alexander bought one each year.

They're now the ultimate luxury bauble. I'm not sure if one will hit the auction stand... But I figure they'd go for $20 million each today.

Meanwhile, for $1,000, you can buy the recently released iPhone 11 Pro Max from Apple (AAPL). It has front and rear cameras that capture hours of high-resolution video and can transmit pictures and video globally in real time.

Both a Faberg egg and the smartphone are hand-held objects. They're colorful, even glistening. But one is ultimately static and unmoving. The other is all about movement, up to and including moving images.

Another way to put this is that the Faberg egg is about what Faberg, the company's founder, wants you to see...

The smartphone is about giving you choices, which you can change at will.

Overall, the annual market for Faberg eggs is worth, well, nothing, because they're all in private hands. More than $500 billion worth of smartphones were sold around the world last year.

This is the value of craftsmanship versus engineering.

Twenty-first century medicine is like this, too...

Not a single advance in biotech is cut off from science and engineering. New chips, new software, and even new micro-fluidics shape what we can learn.

One of the trends we follow in my Stansberry Venture Technology financial advisory is artificial intelligence ("AI"), which has amazing potential in health care.

Consider cancer detection... Radiologists don't scan for brain tumors if you get an MRI for a stomachache. AI can.

This is a screening function by the machine itself a radiologist will confirm what the AI finds. But this means early detection to stop a cancer before it becomes life-threatening. It's a fail-safe.

What to do when the worst happens...

The American Cancer Society foresees 600,000 deaths from cancer in the U.S. in 2019. But for almost all types of cancer, the age-adjusted death rates are slowly decreasing.

Overall, that's tremendous news. It reflects, in large part, more refined radiation therapy machines, better surgical techniques, and safer, more effective medicines. (We cover all these advances in Venture Technology.)

But some exceptions exist... The death rates for liver, pancreatic, and uterine cancers are still increasing. For liver cancer, it's driven by hepatitis, alcohol, and obesity. For uterine cancer, it's obesity and lack of screening.

Fortunately, Big Pharma companies Gilead Sciences (GILD) and Merck (MRK) now offer cures for hepatitis (at steep prices, mind you). And better screening for uterine cancer will follow, as MRIs with AI move from the research stage into general practice.

So the real outlier is pancreatic cancer. But there's light at the end of the tunnel... Earlier this month, in the leading science journal Nature, we learned that pancreatic cancer might be caused by an infection from a common fungus the same one that causes dandruff and eczema.

So maybe anti-fungal medications can help with that.

As it happens, we're already tracking the first new class of anti-fungal drugs in Venture Technology. This is a developmental drug that completed its FDA Phase II mid-stage trials. And for fungal infections, it has a very high cure rate...

That's because it's new...

Fungi can evolve around the threat of an anti-fungal drug... just like bacteria can evolve around antibiotics, and fast-growing cancers evolve around targeted therapies like Gleevec.

Yes, that's right... The first drug that Porter and I thought was a revolution in cancer care Novartis' Gleevec turned out to be a temporary fix.

Research has since found that up to one-third of patients will not achieve "optimal response." In all these patients, their cancers surge back. We noted this recently while recommending another biotech company to Venture Technology subscribers in April 2018...

Novartis went on to make $12 billion globally on Gleevec. It's only recently run out of patent. The dark secret was that the target that Gleevec hit could mutate so the effect did not last.

In order to cure cancer, you need to do one of two things...

The first method is well-known...

It takes good diagnostics and good surgical techniques. Ideally, this is minimally invasive surgery, not open surgery. That's the goal.

But a problem occurs if there are two, three, five, or seven sites of cancer. Or if it's a spread-out tumor. Or if it's around a critical organ... like your spinal cord.

Many advanced cancers simply can't be treated with surgery.

Finally, let me tell you about the second method...

It's brand-new. We only confirmed it last month, when a therapy we've been tracking for three years won a gold medal at a major medical society.

We've been tracking this all over the world in San Diego... San Antonio... Washington... London... Milan... Turin... and Chicago. Plus, we'll keep tracking it in the years to come.

It's that powerful.

Indeed, it's already here it's at the turning point, which is the best time for investors to get involved.

More than a quarter of all U.S. cancer patients will get this treatment in 2020. But no one else is reporting on this.

Seriously. We scoured the popular press... and literally nothing came up. Thousands of medical articles describe it, but no major or minor news outlet has picked it up yet.

That's why we think this research, in addition to being life-changing or life-saving for those with cancer, is so valuable to investors. You can learn more about it right here.

Regards,

Dave Lashmet

Editor's note: Dave believes the study of cancer has crossed an important threshold... For the first time in his career, he says it's reasonable to start talking about a cure. It still may be a few years away, but that's why now is the time to invest in the trend... Dave and his team just put together an urgent video presentation with all the details. Watch it right here.

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The 'Magic' Behind Every Successful Blockbuster Drug - DailyWealth

Chick-fil-A has a new sit-down dining option to win over millennial parents – Business Insider India

Chick-fil-A is now a sit-down restaurant - if you want it to be.

This week, the chicken chain announced that it is launching Dine-In Mobile Ordering across the US. The service will allow customers to order their food via the chain's mobile app, picking the option to have the food delivered directly to their tables instead of picking it up at the counter.

Read more: Chick-fil-A's mobile sales are skyrocketing as execs say the chicken chain is entering a new tech-obsessed era

Chick-fil-A has been testing the service in certain markets for a few months. Khalilah Cooper, director of service and hospitality at the chain, and Kevin Purcer, Chick-fil-A's director of customer digital experience, told Business Insider earlier this year that the service was aimed, in part, at parents with young children.

"You just want to be able to get your kids squared away and sit down and not have to deal with kids standing in line and things like that," Purcer said.

Cooper said that the dine-in option is also popular with big groups in test markets. Additionally, it allows people to order add-ons, such as dessert, after they're sitting at their table with their entres.

"I think it's more seamless. It's easier. It gives them another way to engage with Chick-fil-A," Cooper said.

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Chick-fil-A has a new sit-down dining option to win over millennial parents - Business Insider India

Study finds suppressing particular mutation could limit the effects of Huntington’s – Daily Bruin

A UCLA study has potentially identified a method to halt the progression of Huntingtons disease and alleviate some of the damage it causes, according to a university press release.

The study, which was published in the journal Science Translational Medicine on Wednesday, found that suppressing a mutation in a particular nerve cell could limit the effects of Huntingtons disease.

According to the Mayo Clinics website, Huntingtons is caused by an inherited mutation in the Huntington gene. This disease leads to the progressive deterioration of nerve cells in the brain and can have a vast impact on a persons function, often resulting in movement, cognitive and psychiatric disorders, the website stated.

Huntingtons disease damages astrocytes, which are star-shaped brain cells that perform a number of important tasks. Damage takes place in the early stages of the disease and contributes to the neuropsychiatric symptoms, such as fatigue and feelings of irritability, that occur as the disease advances.

In the study, researchers observed the advancement of Huntingtons disease in samples taken from the brains of deceased humans as well as in living mice carrying the disease.

According to the press release, it was found that suppressing the mutation found in astrocytes enabled researchers to halt the diseases progression and repair some of the damage caused. Additionally, the study has established a database that can be used to study the role of astrocytes in other neurodegenerative diseases.

The studys lead investigator Baljit S. Khakh, a professor of physiology and neurobiology at the David Geffen School of Medicine at UCLA, previously led a team that developed a method to examine the brains of mice and observe the influence of astrocytes in real time, according to the press release.

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Study finds suppressing particular mutation could limit the effects of Huntington's - Daily Bruin

ArsenalBio joins next-gen cell therapy field with $85M A round – FierceBiotech

ArsenalBio has exited stealth with $85 million to discover and develop cell therapies. The biotech aims to differentiate itself from the ever-growing pack of cell therapy startups with technology that enables the insertion of large DNA sequences without the use of viral vectors.

The design and production of first-generation T-cell therapies entails using a viral vector to insert one cell-targeting transgene. ArsenalBio wants to use CRISPR-based genome engineering to rewrite far larger sections of DNA, potentially leading to better treatments that are faster and simpler to design and manufacture.

Some big names have bought into ArsenalBios idea. Beth Seidenbergs Westlake Village BioPartners, the Parker Institute for Cancer Immunotherapy (PICI) and Kleiner Perkins participated in the round.

Industry Insight Survey: Direct-to-Patient Distribution of Clinical Supplies

This industry survey seeks to gain insight on trial sponsors' perspective on offering a DTP option and their current level of awareness and understanding of any factors that may influence their ability to do so. The first 50 qualified respondents will receive a $5 Amazon gift card.

Responsibility for overseeing the use of the $85 million will fall on Ken Drazan, the former president of Grail. Drazen, CEO of ArsenalBio, is joined on the management team by Jane Grogan, Michael Kalos and Tarjei Mikkelsen. Grogan, Kalos and Mikkelsen used to work at Genentech, Johnson & Johnson and 10x Genomics, respectively.

The management team will build on the work of ArsenalBios scientific founders, who were brought into each others orbits through Sean Parkers PICI. Broad Institutes Bradley Bernstein, Kole Roybal from the University of California, San Fransisco (UCSF), the University of Pennsylvania's John Wherry and Nicholas Haining, formerly of Dana-Farber Cancer Institute, are among the scientific founders.

Alexander Marson and Theodore Roth, both of UCSF, are the other two scientific founders. Marson and Roth were part of a large group that authored a Nature paper last year on the reprogramming of human T-cell function and specificity with nonviral genome targeting.

The paper describes the use of an approach in line with that sketched out by ArsenalBio. Marson, Roth and their collaborators used a CRISPR-Cas9 targeting system to insert a 1.5-kb DNA cassette encoding for a TCR beta chain into a specific part of the T-cell genome. The researchers, who also used the approach to correct a pathogenic autoimmune mutation, see multiple benefits.

In approximately one week, novel gRNAs and DNA repair templates can be designed, synthesized, and the DNA integrated into primary human T cells that remain viable, expandable, and functional. The whole process and all required materials can be easily adapted to good manufacturing practices for clinical use. Avoiding the use of viral vectors will accelerate research and clinical applications, reduce the cost of genome targeting, and potentially improve safety, the researchers wrote.

ArsenalBio will initially focus on applying its CRISPR-based genome engineering technology to cancer indications, but its longer-term vision is to develop immune cell therapies more broadly.

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ArsenalBio joins next-gen cell therapy field with $85M A round - FierceBiotech

IND Application Submission To FDA For Phase 1 Trial Of Genetically Modified Autologous Cell Therapy For HIV Announced by American Gene Technologies -…

ROCKVILLE, Md., Oct. 18, 2019 /PRNewswire/ --American Gene Technologies (AGT) announced today the submission of an Investigational New Drug (IND)application to the U.S. Food and Drug Administration (FDA) for AGT's lead HIV program, AGT103-T, which is potentially a single-dose, lentiviral vector-based gene therapy developed for the purpose of eliminating HIV from people infected with the disease.

"Our aim is to treat HIV disease with an innovative cell and gene therapy that reconstitutes immunity to HIV and will control virus growth in the absence of antiretroviral drugs" said Chief Science Officer C. David Pauza, PhD. "Development of this complex product (AGT103-T) required our deep knowledge of both HIV disease and lentivirus vector technology; it is the first cell and gene immunotherapy addressing the most critical feature of HIV infection, which is the chronic absence of virus-specific CD4 T cells."

"We are excited to have reached this milestone of submitting our first IND application to the FDA for an HIV gene/cell therapy. This event brings us closer to reaching our mission to transform lives with genetic medicines. Based on our successful commercial-scale product manufacturing runs and features of the product observed in our laboratories, this therapy has a high potential to be effective. I feel confident that AGT103-Twill make an important difference in the lives of HIV infected persons," said Jeff Galvin, Founder and Chief Executive Officer of AGT."HIV is the first drug candidate to result from AGT's proprietary platform and model for creating gene and cell therapeutics more efficiently, predictably and reliably for clinical development. Our platform is also supporting robust efforts to cure the inherited disease phenylketonuria (PKU) and to introduce new therapies for cancer based on our proprietary methods for modifying tumor cells to activate the natural killing mechanisms of gamma delta T cells. Additionally, product development efforts behind this IND submission are supporting investigations into other chronic viral diseases that may be targeted in future human clinical trials.Success in HIV would allow AGT to accelerate these projects as well as quickly broaden our pipeline to dozens of infectious diseases, monogenic disorders, and cancers."

Upon acceptance by the FDA, this IND allows AGT to initiate a Phase 1 clinical trial that will investigate the safety of AGT103-T in humans, measure key biomarkers, and explore surrogate markers of efficacy. AGT expects to begin recruiting patients for the Phase 1 study in January.

About HIV

Today, approximately 37.9 people worldwide and 1.1 million people in the United States are living with HIV/AIDS. The U.S. Government has estimated that 38,700 Americans were newly infected with HIV in 2016 and 1.7 million individuals globally were newly infected with HIV in 2018 (HIV.gov).

Since the late 1980s, antiretroviral drugs have restored quality of life to persons living with HIV and, in some cases, have even been used to prevent new infections. However, no approved treatments can cure HIV. This is an unmet medical need that AGT seeks to address.

About AGT 103-T

AGT103-Tis a genetically-modified cell product made from a person's own cells. AGT's approach is unique in that it focuses on repairing the key immune system damage caused by HIV. When HIV infection causes this specific damage, killing of T helper cells required for immunity to HIV, the infected person becomes unable to eliminate the virus and thus, becomes chronically infected. AGT's approach is designed to repair the T helper cell defect and provide durable virus control that is not compromised by HIV strains that vary in sequence or use alternate ways to enter and infect T cells. AGT's AGT103-T HIV therapeutic drug should work to remove infected cells from the body and decrease or eliminate the need for lifelong antiretroviral treatment.

"Previous cell and gene therapies for HIV provided very low doses of critical virus-specific CD4 T cells that are needed to repair the immune defect caused by HIV. AGT103-T becomes highly enriched in these specific cells during our proprietary 12-day manufacturing process. By providing high doses of virus-specific helper T cells, which are protected from HIV damage by a safe genetic modification, AGT's goal is to rebuild the capacity for normal, unhindered immune responses against HIV that may control the infection and protect against future virus exposures. We believe this product will be suitable for persons in different disease stages and with multiple types of HIV infection" explains Chief Science Officer C. David Pauza, PhD.

AGT has entered into a Research Collaboration Agreement with the National Institute of Allergy and Infectious Diseases (NIAID) and was able to demonstrate AGT103-T's mechanism of action. Read about AGT's NIAID Research Collaboration Agreement here.

About American Gene Technologies (AGT)

American Gene Technologies (AGT)is a gene and cell therapy company with a proprietary gene-delivery platform for rapid development of cell and gene therapies to cure infectious diseases, cancers, and inherited disorders. The Company's mission is to transform people's lives through genetic medicines that rid the body of disease. The Company expects to take its patented lead candidate for an HIV cure into the clinic in 2019. AGT has received seven patents for its unique immuno-oncology approach to stimulate gamma-delta () T cells to destroy a variety of solid tumors. The Company has developed a synthetic gene for treatingPhenylketonuria (PKU), a debilitating inherited disease. AGT's treatment for PKU has been granted Orphan Drug Designation by the Food and Drug Administration (FDA), and it is expected to reach the clinic in 2020.

AGT Contacts

C. Neil Lyons, Chief Financial OfficerPhone: (301) 337-2269Email: info@americangene.com

Sasha Whitaker, Digital Marketing and CommunicationsPhone: (301) 337-2100Email: swhitaker@americangene.com

SOURCE American Gene Technologies

http://www.americangene.com

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IND Application Submission To FDA For Phase 1 Trial Of Genetically Modified Autologous Cell Therapy For HIV Announced by American Gene Technologies -...

Sean Parker helps create a CRISPRed cell therapy 2.0 play and he’s got a high-profile set of leaders on the team – Endpoints News

Medical animation has in recent years become an increasingly important tool for conveying niche information to a varied audience, particularly to those audiences without expertise in the specialist area. Science programmes today, for example, have moved from the piece-to-camera of the university professor explaining how a complex disease mechanism works, to actually showing the viewer first-hand what it might look like to shrink ourselves down to the size of an ants foot, and travel inside the human body to witness these processes in action. Effectively communicating a complex disease pathophysiology, or the novel mechanism of action of a new drug, can be complex. This is especially difficult when the audience domain knowledge is limited or non-existent. Medical animation can help with this communication challenge in several ways.Improved accessibility to visualisationVisualisation is a core component of our ability to understand a concept. Ask 10 people to visualise an apple, and each will come up with a slightly different image, some apples smaller than others, some more round, some with bites taken. Acceptable, you say, we can move on to the next part of the story. Now ask 10 people to visualise how HIVs capsid protein gets arranged into the hexamers and pentamers that form the viral capsid that holds HIVs genetic material. This request may pose a challenge even to someone with some virology knowledge, and it is that inability to effectively visualise what is going on that holds us back from fully understanding the rest of the story. So how does medical animation help us to overcome this visualisation challenge?

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Sean Parker helps create a CRISPRed cell therapy 2.0 play and he's got a high-profile set of leaders on the team - Endpoints News

REGENXBIO Announces Presentations at the European Society of Gene & Cell Therapy 27th Annual Congress – BioSpace

ROCKVILLE, Md., Oct. 17, 2019 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX), a leading clinical-stage biotechnology company seeking to improve lives through the curative potential of gene therapy based on its proprietary NAV Technology Platform, today announced the presentation of two posters at the European Society of Gene & Cell Therapy (ESGCT) 27th Annual Congress in Barcelona, Spain, taking place from October 22 to 25, 2019.

The data will be presented as follows:

Abstract Title: Characterization of a Novel AAV Capsid with Enhanced Brain Transduction Following Systemic Delivery (poster #P011)Presenter: Subha Karumuthil-Melethil, Ph.D., Senior Scientist, Target Discovery, REGENXBIOSession Title: Poster Session IDate/Time: Wednesday, October 23, 2019, 1:00 p.m. to 3:00 p.m. CESTLocation: Multipurpose Hall P011

Abstract Title: AAV9.hCLN2 (RGX-181) Improves Survival and Neuropathology in TPP1m1J Mice, a Model for CLN2 Batten Disease (poster #P018)Presenter: Nicholas Buss, Ph.D., Director, Preclinical Development, REGENXBIOSession Title: Poster Session IIDate/Time: Thursday, October 24, 2019, 1:15 p.m. to 2:45 p.m. CESTLocation: Multipurpose Hall P018

About REGENXBIO Inc.

REGENXBIO is a leading clinical-stage biotechnology company seeking to improve lives through the curative potential of gene therapy. REGENXBIO's NAV Technology Platform, a proprietary adeno-associated virus (AAV) gene delivery platform, consists of exclusive rights to more than 100 novel AAV vectors, including AAV7, AAV8, AAV9 and AAVrh10. REGENXBIO and its third-party NAV Technology Platform Licensees are applying the NAV Technology Platform in the development of a broad pipeline of candidates in multiple therapeutic areas. For more information, visit http://www.regenxbio.com.

Contacts:Tricia TruehartInvestor Relations and Corporate Communications347-926-7709ttruehart@regenxbio.com

Investors:Heather Savelle, 212-600-1902heather@argotpartners.com

Media:David Rosen, 212-600-1902david.rosen@argotpartners.com

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SOURCE REGENXBIO Inc.

Company Codes: NASDAQ-NMS:RGNX

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REGENXBIO Announces Presentations at the European Society of Gene & Cell Therapy 27th Annual Congress - BioSpace

Stem cell therapy hope for autism patients – The New Indian Express

By Express News Service

PURI:Stem cell therapy has offered hope to parents of children suffering from serious neurological disorders, said Dr Richa Bansod of Mumbai-based NeuroGen Brain and Spine Institute (BSI), here on Thursday.

She said latest advances in therapy hold great promise for autism in children. But they are suffering due to lack of awareness among parents.

Early treatment can significantly improve the condition and also effect recovery from the disorder, Dr Bansod said at a media conference here.

Citing one such example, she presented 16-year-old Anurag Champi of Bhubaneswar who has shown significant improvement after stem cell therapy. At present, the boy is being imparted speech therapy and necessary exercise to enable him for voice interface, said his mother Sangita.

In order to create awareness on the therapy among parents, a free autism treatment camp will be organised at Bhubaneswar on November 16. We are also providing free treatment to poor families at our Mumbai facility, said Dr Bansod.

Through neuro regenerative rehabilitation and stem cell therapy, brain stroke, brain and spine injuries caused by accident could be effectively treated, she added. Deputy Director of the institute Dr Nandini Gokulchandran was present.

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Stem cell therapy hope for autism patients - The New Indian Express