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Breaking News: Cardiol Therapeutics Announces Clinical Steering Committee for Phase 2 International Trial in Acute Myocarditis Using CardiolRx(TM) 100…

Cardiol Therapeutics Inc. (TSX: CRDL) (OTCQX: CRTPF), a leader in the production of pharmaceutical cannabidiol (CBD) products and in the development of innovative cannabidiol medicines for heart disease, is pleased to announce the formation of the Clinical Steering Committee (CSC) for a Phase 2 international trial in acute myocarditis using the Companys CardiolRx100 cannabidiol formulation.

The CSC, which comprises key opinion leaders in acute myocarditis from North America and Europe, recently met during the American Heart Associations Scientific Sessions in Philadelphia held November 16th to 18th. The role of the CSC is to advise on the trial design, provide overall supervision of the trial, and ensure that it is being conducted in accordance with the principles of Good Clinical Practice. The CSC has oversight of the protocol, any protocol amendments, and provides advice to the investigators on all aspects of the trial.

Acute myocarditis is characterized by inflammation of the heart muscle (myocardium). The most common cause is viral infection of the heart tissue which is initially responsible for the inflammation. In a significant number of cases, perhaps due to an autoimmune process, the inflammation persists with ongoing myocardial damage and depressed heart function. Although the symptoms are often mild, myocarditis remains an important cause of acute and fulminant heart failure and is the most common cause of sudden cardiac death in people less than 35 years old. In addition, some patients proceed to develop chronic dilated cardiomyopathy which continues to be the leading indication for cardiac transplantation. Symptoms include chest pain, fatigue, shortness of breath, and arrhythmias. Because of the progressive damage to heart cells, heart failure develops (defined as the inability of the heart to pump sufficient blood to meet the needs of the body). The study will use left ventricular ejection fraction (LVEF) as one measure of heart function.

CardiolRx100 is Cardiol Therapeutics pure pharmaceutically (cGMP) produced high concentration cannabidiol formulation that is THC free (<10ppm). Based on the large body of experimental evidence of the anti-inflammatory and cardioprotective properties of cannabidiol in models of cardiovascular disease, Cardiol believes there is an opportunity to develop a potential breakthrough therapy for acute myocarditis that would be eligible for designation as an orphan drug. In the United States, an orphan drug designation is granted for pharmaceuticals being developed to treat medical conditions affecting fewer than 200,000 people. These conditions are referred to as orphan diseases. In the U.S. and the European Union, orphan drugs are eligible for accelerated marketing approvals and companies developing orphan drugs typically receive other incentives, including a prolonged period of market exclusivity that can extend over seven years, during which the drug developer has sole rights to market the drug.

Cardiol has assembled eight highly distinguished thought leaders in cardiology from North America and Europe to oversee and guide our acute myocarditis trial that is being planned at world leading heart institutes, including the Cleveland Clinic, the Mayo Clinic, the Houston Methodist DeBakey Heart and Vascular Center, the University of Ottawa Heart Institute, and Charit University Medicine Berlin, stated David Elsley, President and CEO of Cardiol Therapeutics. The U.S. orphan drug program was successfully utilized to accelerate the first FDA approval of cannabidiol for the treatment of two pediatric epilepsy orphan diseases. We see a similar opportunity with our international trial in acute myocarditis to fast track the development of our CardiolRx formulation for a serious cardiovascular orphan disease for which there is currently no accepted standard of care.

Members of Cardiols Acute Myocarditis CSC include:

Dennis M. McNamara, MD (Chair)

Dr. Dennis McNamara is a Professor of Medicine at the University of Pittsburgh. He is also the Director of the Heart Failure/Transplantation Program at the University of Pittsburgh Medical Center. Dr. McNamara received his undergraduate/graduate education at Yale University, New Haven, Connecticut, and Harvard Medical School, Boston, Massachusetts, respectively. He completed his internship, residency, and cardiology fellowship at Massachusetts General Hospital in Boston. McNamaras current research interests include etiology and pathogenesis of dilated cardiomyopathies; inflammatory syndromes of cardiovascular disease; myocardial recovery in recent onset non-ischemic primary cardiomyopathy; etiology and management of peripartum cardiomyopathy; and genetic modulation of outcomes in cardiovascular disease.

Leslie T. Cooper, Jr., MD (Co-Chair)

Dr. Leslie T. Cooper, Jr., is a general cardiologist and the chair of the Mayo Clinic Enterprise Department of Cardiovascular Medicine, as well as chair of the Department of Cardiovascular Medicine at the Mayo Clinic in Florida. Dr. Coopers clinical interests and research focus on clinical and translational studies of rare and undiagnosed cardiomyopathies, myocarditis, and inflammatory cardiac and vascular diseases, such as giant cell myocarditis, cardiac sarcoidosis, eosinophilic myocarditis, and Takayasus arteritis. He has published over 130 original peer-reviewed papers, as well as contributing to and editing books on myocarditis. In addition to his clinical and research work, Dr. Cooper is a fellow of the American College of Cardiology, the American Heart Association, the European Society of Cardiology Heart Failure Association, the International Society for Heart and Lung Transplantation, and the Society for Vascular Medicine and Biology. He is also the founder and former president of the Myocarditis Foundation and continues to serve on its Board of Directors.

Arvind Bhimaraj, MD

Dr. Arvind Bhimaraj is a specialist in Heart Failure and Transplantation Cardiology and is Assistant Professor of Cardiology, Institute for Academic Medicine, at Houston Methodist and at Weill Cornell Medical College, NYC. He has been Co-Director of the Heart Failure Research Laboratory at Houston Methodist since 2016. His area of focus is anti-fibrotic mechanisms and how to promote recovery of a damaged heart. Dr. Bhimaraj was a Heart Failure Fellow at the Cleveland Clinic from July 2010 to September 2011. Dr. Bhimaraj also specializes in Interventional Cardiology, is board certified in Cardiovascular Disease, and the author of numerous cardiovascular publications.

Matthias Friedrich, MD

Dr. Matthias Friedrich is Full Professor with the Departments of Medicine and Diagnostic Radiology at the McGill University in Montreal and Chief, Cardiovascular Imaging at the McGill University Health Centre. He is also Professor of Medicine at Heidelberg University in Germany. Dr. Friedrich earned his MD at the Friedrich-Alexander-University Erlangen-Nrnberg, Germany. He completed his training as an internist and cardiologist at the Charit University Medicine Center, Humboldt University in Berlin. Dr. Friedrich founded one of the first large Cardiovascular Magnetic Resonance centres in Germany at the Charit University Hospital in Berlin. After his move to Canada, from 2004 to 2011, he was Director of the Stephenson Cardiovascular MR Centre at the Libin Cardiovascular Institute of Alberta and Professor of Medicine within the Departments of Cardiac Sciences and Radiology at the University of Calgary, Canada. From 2011 to 2015, he directed the Philippa and Marvin Carsley Cardiovascular MR Centre at the Montreal Heart Institute and was Michel and Renata Hornstein Chair in Cardiac Imaging at the Universit de Montral.

Peter Liu, MD

Dr. Peter Liu is the Chief Scientific Officer and Vice President, Research, of the University of Ottawa Heart Institute, and Professor of Medicine and Physiology at the University of Toronto and University of Ottawa. He was the former Scientific Director of the Institute of Circulatory and Respiratory Health at the Canadian Institutes of Health Research, the major federal funding agency for health research in Canada. Prior to that role, he was the inaugural Director of the Heart & Stroke/Lewar Centre of Excellence in Cardiovascular Research at University of Toronto. Dr. Liu received his MD from the University of Toronto, and postgraduate training at Harvard University. His laboratory investigates the causes and treatments of heart failure, the role of inflammation, and the identification of novel biomarkers and interventions in cardiovascular disease. Dr. Liu has published over 300 peer-reviewed articles in high impact journals and received numerous awards in recognition of his research and scientific accomplishments.

Wai Hong Wilson Tang, MD

Dr. Wai Hong Wilson Tang is the Advanced Heart Failure and Transplant Cardiology specialist at the Cleveland Clinic in Cleveland, Ohio. Dr. Tang is also the Director of the Cleveland Clinics Center for Clinical Genomics; Research Director, and staff cardiologist in the Section of Heart Failure and Cardiac Transplantation Medicine in the Sydell and Arnold Miller Family Heart & Vascular Institute at the Cleveland Clinic. He attended and graduated from Harvard Medical School in 1996, having over 23 years of diverse experience, especially in Advanced Heart Failure and Transplant Cardiology. Dr. Tang is affiliated with many hospitals including the Cleveland Clinic and cooperates with other doctors and physicians in medical groups including The Cleveland Clinic Foundation.

Barry Trachtenberg, MD

Dr. Barry H. Trachtenberg is a cardiologist specializing in heart failure and cardiac transplantation. He is also the director of the Michael DeBakey Cardiology Associates Cardio-Oncology program, an evolving field devoted to prevention and management of cardiovascular complications of cancer therapies such as chemotherapy and radiation. His clinical experience includes heart failure and heart transplantation, mechanical support pumps, and cardio-oncology. He has contributed to multiple publications related to advanced heart failure, cardiac transplantation, regenerative therapies, and ventricular assist devices. Dr. Trachtenberg is a member of the American Heart Association, the International Society for Heart and Lung Transplantation, the Heart Failure Society of America, and the International CardiOncology Society of North America.

Carsten Tschpe, MD

Dr. Carsten Tschpe is Professor of Medicine and Cardiology and Vice Director of the Department of Internal Medicine and Cardiology, Charit University Medicine Berlin. He received his doctorate in medicine in 1993 and has over 140 peer-reviewed publications, including overview and book articles, and 120 international original articles. His research interests include inflammatory cardiomyopathy, diabetic cardiopathy, and ischemic cardiopathy. He also includes diastolic dysfunction, endothelial dysfunction, peptide systems, and experimental and clinical studies in cardiology and stem cells in his research studies. For his outstanding research work, Dr. Tschpe was awarded the prestigious Arthur Weber Prize by the German Cardiac Society Cardiovascular Research.

About Cardiol Therapeutics

Cardiol Therapeutics Inc. (TSX: CRDL)(OTCQX: CRTPF) is focused on producing pharmaceutical cannabidiol (CBD) products and developing innovative therapies for heart disease, including acute myocarditis and other causes of heart failure. The Companys lead product, CardiolRx, is designed to be one of the safest and most consistent CBD formulations on the market. CardiolRx is pharmaceutically produced, cGMP certified, and is THC free. The Company plans to commercialize CardiolRx in the billion-dollar market for medicinal cannabinoids in Canada and is also pursuing distribution opportunities in Europe and Latin America.

In heart failure, Cardiol is planning an international clinical study of CardiolRx in acute myocarditis, a condition caused by inflammation in heart tissue, which remains the most common cause of sudden cardiac death in people less than 35 years of age. The Company is also developing proprietary nanotechnology to uniquely deliver pharmaceutical CBD and other anti-inflammatory drugs directly to sites of inflammation in the heart that are associated with heart failure. Heart failure is the leading cause of death and hospitalization in North America with associated healthcare costs in the U.S. alone exceeding $30 billion. For further information about Cardiol Therapeutics, please visitwww.cardiolrx.com.

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Breaking News: Cardiol Therapeutics Announces Clinical Steering Committee for Phase 2 International Trial in Acute Myocarditis Using CardiolRx(TM) 100...

Redruth woman travels over 3,500 miles to meet the stranger who saved her life – Cornwall Live

Ashop assistantfrom Redruthisappealing for people to become bone marrow donors after meeting the stranger who saved her life.

Carol Timmins was diagnosed with aplastic anaemia in January 2014.

The 58-year-old said: "Being told that I had bone marrow failure came as a great shock. I had no idea what it actually meant but soon realised that I was very, very sick.

"Id previously been diagnosed with Chronic Fatigue Syndrome, so feeling tired and lacking energy had been a way of life for several years. The initial treatment that I received was regular blood transfusions until May when I started an Antilymphocyte Globulin treatment.

"By September it was apparent that the treatment was not working and a bone marrow transplant was my best chance of survival."

Carolhad a bone marrow transplant inDecember 2014from a stranger. Patients and donors must remain anonymous for two years after a transplant takes place.

After this period has passed, if both the patient and donor would like to meet, they can contact blood cancer charity Anthony Nolan, who are then able to put them in contact with each other.

In September 2019, Carol and her husband Paul, travelled from Cornwall to Detroit, USA, to meet her lifesaver.

She added: "Ninety days after my transplant I had decided that it was time to thank my donor so I sent an anonymous letter through Anthony Nolan. Within a few weeks I received a reply. We were both overjoyed at receiving such an important piece of mail and he was very pleased that I was making a good recovery."

From that moment she set her sights on thanking her donor in person.

"I knew that it would be a few years before I could travel but I made it my goal. I had to thank the man who had saved my life," Carol said.

As time passed by, the medication reduced and their correspondence increased. There was a turning point in her life when she was told that she had the option to release her personal information, and to request her donors details.

Carol continued: "I decided not to rush into it, as I needed time to comprehend exactly what that would mean. I had come so far, and to be able to correspond with my donor directly would be quite surreal."

Through letter writing, they contemplated at how their paths had crossed and shared stories about their families. In May 2018 she exchanged personal details with her donor.

She said: "It was a truly amazing day learning the name of the man I had written to for four years - Darin."

Through emails they exchanged family photos and started to make plans for her trip. Their friendship blossomed and finally, in September 2019 they met for the first time.

"The welcome that I received at the airport was something that only dreams are made of. After hugs and tears of joy with Darin and his wife Valerie, I was introduced to a local news channel who were delighted to witness and report on such an emotional and inspiring story," added Carol.

Carol and Paul stayed at Darin and Valeries home in Detroit for eight days. During that time they shared their experiences as a donor and recipient, reminiscing about a very surreal time in their lives.

Carol added: "Darin said that if he was asked to donate again he would do it in a heartbeat.

"I consider myself truly blessed to have found a donor who was a perfect match, but to have the opportunity to thank the man who gave me his bone marrow has meant the world to me.

"Please dont wait until it happens to you or yours, people are dying waiting for their perfect match and you can help them by joining the register. Without Darin I probably wouldnt be here today, so if youre a healthy 16-30 year old (or you know someone who is), Anthony Nolan needs you.

"My heartfelt thanks go to Anthony Nolan and to all of the potential donors on the register, as well as the wonderful team of doctors and nurses who treated me."

Anthony Nolan is the charity that finds matching donors for people with blood cancer and gives them a second chance of life.

It also carries out ground-breaking research to save more lives and provide information and support to patients after a stem cell transplant, through its clinical nurse specialists and psychologists, who help guide patients through their recovery.

Henny Braund, chief executive of Anthony Nolan said "Its fantastic to see Carol,living her life to the fullest andDarinshould be incredibly proud of the difference he has made to Carol and her family.

"Our amazing stem cell donors are lifesavers and they continue to give patients with blood cancer a second chance of life. Anyone wanting to find out more can visit our website to join the stem cell register or support our work by making a donation, which will help give someone likeCarola second chance of life in the future. Without you there is no cure."

For more information, visit the Anthony Nolan website here.

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Redruth woman travels over 3,500 miles to meet the stranger who saved her life - Cornwall Live

Chemotherapy and constant pills but DWP tells Hull man Kye Eastwood ‘you’re fit for work’ – Hull Daily Mail

A young Hull man whose life was saved by the generous people of Hull after being diagnosed with terminal cancer says he is looking forward to the future.

In 2014, Kye Eastwood, now 28, faced an unimaginable battle after being told there was nothing more UK doctors could do for him in his battle against Hodgkins Lymphoma - but there was hope.

The people of Hull heroically clubbed together and raised 46,000 within a month, paying for ground breaking - and life-saving - stem cell - treatment in Maryland, US.

Now, five years on, Kye and his fianc Chanelle Urquhart, 24, of Kingswood, are looking forward to their lives together - after what Kye has described as one of the most difficult years of his life.

Although the pioneering treatment cleared Kye of cancer, Kye has ongoing health issues. He is still undergoing chemotherapy and he is unable to work.

Despite this, he was told he was not allowed his PIP (Personal Independence Payment) benefits from the Department for Work and Pensions (DWP) after he underwent an eligibility assessment.

He said the report was "all wrong", stating he could do a number of things he could not do, which meant he was deemed fit for work.

He said: The report said I had a healthy complexion - that is completely wrong in the first place because of the vitiligo (pigmentation of the skin) I have.

Chanelle said he also split open a sore on his back trying to lift his arms further above his head during the assessment and it still needs treatment months later.

Although he has since had his benefits reinstated after the report was proved to be wrong, the trauma of living without any income and the strain it put on him for months has taken its toll.

He said: Someone came around in March theyd decided I was poorly enough for them to come to me rather than me go to them. I was on my cycle of chemo at the time and having massive allergic reactions.

Everything in the report was wrong and the woman who came didnt even look at any of the medical evidence and made out that I could move more.

"What the report said was not reflective of what happened in the meeting. We got a letter saying I wasnt entitled and why, and the report shed sent off.

Kye appealed and received another assessment and a complaint was put into the DWP by Chanelle, who sent pictures of Kyes skin and statements from every one of his doctors and specialists who see him in Rotherham.

Three months later, Kyes benefits were reinstated.

Chanelle said: He was three months without them, which help with his mobility. He was struggling to get to Rotherham, the treatment which ultimately keeps him alive.

She added the complaint has been escalated and is being looked at by an independent case examiner.

A DWP spokesman said: "We have apologised to Mr Eastwood for the confusion over his reapplication for PIP. It was resolved promptly and he is in receipt of all the benefits he is entitled to."

Chanelle said Kye would love nothing more than to go back to work but he needs something flexible that could work around treatment and hospital appointments.

She said: He was always working before the cancer and would love to go back to work and do things but its trying to find something he would be able to do safely, and something that would work around his health problems.

Kye added: I dont know an employer that would want me to be off at least a week every month while I go to my appointments.

During Kye's treatment the couple flew back and forth to Washington for a period of seven months and were able to stay at the amazing centre along with other families of people having treatment there.

During the time between treatments, they were able to explore the country and while staying in San Antonio in 2015 when they had been together for just six months, Kye proposed.

Chanelle said: At the time it happened, we hadnt been together for very long but we didnt know if he was going to survive. We instantly clicked and it was obvious it was going to work out.

Kye said: I knew I was going to do it. Wed known each other for years.

Five years later and they are still going strong - Chanelle even got to be the one to tell Kye he was cancer-free.

She said: He was in America and Id had to stay at home because I couldnt get the time off work.

"Theyd done a scan and the doctor had emailed me and told me he was completely clear. I was in Morrisons and was crying. I was trying to call him but he didnt have any signal.

I got through to him and just said, your cancer has completely gone'. Then he went to the car and told his mum.

Despite the relief at being given the all clear, Kye has faced difficulty during his recovery and still suffers side effects from all of his treatments.

Not long after he was told he was in remission, he started to suffer with a condition called Graft Versus Host Disease (GvHD).

The disease is classed as a medical complication of receiving of transplanted tissue from a different person such as Kyes stem cell treatment.

The white blood cells left in the donated tissue only recognise the receiver as foreign and begin to attack the receivers cells.

This has left Key with patches of dry skin on his body. His skin is thinner and he has vitiligo, which changes the pigment and colour.

Kye said: It started with a bit of itchy skin and I had a dry patch that wouldnt go away and we went for blood tests and they kept coming back really abnormal, my liver levels were through the roof.

Chanelle said: That was quite worrying as its quite dangerous and they were trying all sorts of things.

He now goes to Rotherham every week for treatment for the GvHD, and is on daily chemotherapy tablets.

He says he has tried a lot of different treatments but at the moment, this combination is working - although doctors are looking at other methods.

The GvHD in itself keeps the cancer at bay so doctors want to try and find a healthy balance.

Chanelle said: Hes hooked up to a machine that removes a certain volume of blood cells, which they separate. They give him his red blood cells back and treat the white blood cells with a UV light before putting them back in his body."

As well as GvHD Kye suffers with fatigue, breathlessness, bad sinuses and says he is now going deaf.

He has tried to get back to his fitness level before the cancer, even trying out BMXing, but he tires easily and becomes weak.

Despite all of the stress and heartache throughout this year, the pair are now looking forward to the future.

Kye said: Chanelle wants to finish her degree and get a job and a nice house. Were quite different to a lot of people who get engaged and start planning a wedding straight away. Weve got all the time in the world.

Ill have to be five years in remission before no more check ups, but the scares are always there.

They always will be, Chanelle added.

Kye and Chanelle say a few years down the line, they are still hugely grateful to the people of Hull for helping them to save his life.

Chanelle said: We would like to say thank you to everyone who contributed any money, or shared the story, or got involved in any of the fundraisers.

"They are what made this possible and have given Kye this second chance at life and they are why he is still here.

He was on palliative care and was going to die he probably wouldnt have made it to Christmas.

Kye said: It feels like such a long time ago. Im definitely looking forward to 2020."

Sophie Corcoran is a reporter for Hull Live and the Hull Daily Mail. Her interests include positive news, news about homelessness, court news and breaking news.

You can follow all the latest stories on her Facebook page here , her Twitter page here or on the Hull Live website here.

You can also call her on 01482 315174 or email sophie.corcoran@reachplc.com

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Chemotherapy and constant pills but DWP tells Hull man Kye Eastwood 'you're fit for work' - Hull Daily Mail

Innovative cell therapy research boosted by state funds – AroundtheO

An innovative new research project from UOs Robert Guldberg has captured the attention of Oregons economic development agency Business Oregon and the UOs Office of the Vice President for Research and Innovation.

Guldbergs $1.2 million project, which zeroes in on one of the central challenges of the fast-growing cell therapy industry, is the first to tap into the University Innovation Research Fund. The new state fund is designed to support research at Oregon universities that drives innovation and economic development.

The manufacturing sector around cell therapy repair or replacement of tissues such as bone, cartilage, blood vessels and skin is a rapidly growing biomedical market. Guldbergs project, which is co-funded by the Department of Defense, could help make Oregon a player in a sector that is projected to be worth $8 billion to $10 billion within the next decade.

Cell therapy has potential applications for everything from treating cancers to repairing spinal cord injuries to improving weakened immune systems. But one of the limitations of current methods of manufacturing is the high cost and variability of using animal-based culture media, Guldberg says.

The standardized media that Guldberg and his collaborators are seeking to develop could help accelerate the development and manufacturing of regenerative medicine products.

The impact of this project will be to develop and validate chemically defined and animal-free culture media that cost-effectively meets cell manufacturing industry standards and needs, said Guldberg, vice president and Robert and Leona DeArmond Executive Director of the Phil and Penny Knight Campus for Accelerating Scientific Impact. This project could help enable greater availability of new cell therapies to more patients and for a broader range of clinical applications.

Department of Defense funding for the project comes through the Medical Technology Enterprise Consortium supported by the U.S. Army Medical Research and Material Command program and in partnership with RegenMed Development Organization.

Not only does this research promise to lead to novel therapeutic treatments for patients but it will also open new doors for engagement with industry partners and the Department of Defense for UO researchers but also for other state research universities and biotechnology enterprises, said David Conover, vice president for research and innovation.

Conover stressed the collaborative elements that gave rise to the University Innovation Research Fund, which represents a unique partnership between Oregon universities and Business Oregon. Working with the states business development agency, he and other senior research officers from Oregons public universities successfully advocated for a state fund that would help attract more federal funds to support economic development.

We made the case before the state Legislature and they came through with the funding, Conover said. Its a real triumph and proof that our public universities can work together to achieve benefits for the state of Oregon.

State Rep. Dan Rayfield, a Corvallis Democrat and co-chair of the Joint Committee on Ways and Means, said he was proud to support the passage of the fund.

We know that Oregons research universities are frequently competing for federal grants that could contribute to the states well-being, but often they require nonfederal funding as a match, Rayfield said. This fund is a way for the state to show our commitment to innovation and economic development, and Im excited about this first project and many more to come. Its going to have a big return on investment for Oregon.

Projects supported by the innovation fund not only must fuel innovation and commercialization of technology from Oregons public universities but must also align with priority industries, such as advanced manufacturing, high technology, outdoor gear and apparel, health care innovation, food and beverage, and forestry and wood products. Guldbergs project checked several of these boxes, said Chris Harder, director of Business Oregon.

The state of Oregon strongly supports innovation at our states universities and we see great potential in Dr. Guldbergs groundbreaking research in the rapidly growing field of cell therapy manufacturing, Harder said. This award and the collaborative project behind it shows the potential we have to grow biotechnology industries in Oregon.

An internationally renowned researcher and entrepreneur in the regenerative medicine field, Guldberg is well-positioned to lead the states efforts to expand its cell manufacturing sector. He has co-founded five companies and is the past president of the Tissue Engineering and Regenerative Medicine International Society Americas Chapter.

Before arriving at the UO from Georgia Tech to lead the Knight Campus, Guldberg helped lead a successful application to the National Science Foundation to establish a Center for Cell Manufacturing Technologies and participated in the development of a national roadmap for cell manufacturing in partnership with federal agencies, several universities and numerous biotech companies, including several companies with a presence in Oregon.

The project has already amassed a long list of industry collaborators and is expected to attract more interest moving forward as new partnerships are established through the Medical Technology Enterprise Consortium.

Through participating in these consortia, Oregon has the opportunity to tap into investment from these industry partners as well as create new technologies with the potential to lead to new start-up companies, Guldberg said.

Another benefit of participation, Guldberg says, is the training of Oregon students in a rapidly growing field and therefore job creation. Cost share on the project will fund three undergraduate scholars to help fulfill the scope of work but also provide them with experiential training and mentorship from senior staff scientists.

Kate Petcosky-Kulkarni, UOs director of strategic research initiatives, is hopeful other researchers will follow Guldbergs lead and apply for matching funding through the University Innovation Research Fund.

The program creates a new research opportunity that wasnt there a year ago, Petcosky-Kulkarni said. It effectively ups the ante and allows faculty to apply for funds that they might not otherwise pursue due to high match requirements.

UO researchers interested in applying for matching funds through the University Innovation Research Fund can find more information online. Potential applicants are required to contact Research Development Services at rds@uoregon.edu to discuss the project before preparing the application materials to confirm alignment with project goals.

By Lewis Taylor, University Communications

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Innovative cell therapy research boosted by state funds - AroundtheO

Luca Biavati, MD, on Bone Marrow T-Cells for Adoptive Cell Therapy – Cancer Network

Luca Biavati, MD, from Johns Hopkins Medicine, discussed bone marrow T-cells and bone marrow infiltrating lymphocytes as a source for adoptive cell therapy at the 34th Annual Meeting & Pre-Conference Programs of the Society for Immunotherapy of Cancer (SITC 2019).

Transcript:

So, the conference is about cancer immunotherapy. And what makes me excited about it is, I study bone marrow T-cells and bone marrow infiltrating lymphocytes as a source for adoptive cell therapy. So, the whole conference is about the use of either monoclonal antibodies or vaccines or adoptive cell therapy to at least improve treatment of cancer.

Ive seen several posters and presentations about how to study the tumor micro-environment and T-cells, and also several ways on how to improve adoptive cell therapy and immunotherapy in several different solid tumors and hematological cancers.

And there have been several improvements on the applicability of these techniques. Theyre still a lot expansive, but I see that maybe theyre going to be more available and definitely more efficient and effective in the foreseeable future.

Well in 5 years probably like well have a whole new set of problems we are not actually seeing right now, as it happened like 5 years ago when we were thinking about now. So yeah, probably like well have new issues with cancer therapies that now we dont see because were not close enough to see that kind of problems yet. Probably like better progression-free survival, better treatments, and then obviously new problems.

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Luca Biavati, MD, on Bone Marrow T-Cells for Adoptive Cell Therapy - Cancer Network

Sangamo Announces UK Authorization of a Phase 1/2 Clinical Trial Evaluating the CAR-Treg Cell Therapy TX200 for Kidney Transplantation – BioSpace

Being the first company to test a CAR-Treg candidate in humans is an important milestone for Sangamo and this exciting new frontier of cellular therapy. We believe that the TX200 program will be invaluable in expanding our understanding of the safety and mechanism of action of CAR-Treg cells and their relevance in the clinic, said Adrian Woolfson, BM, BCh, PhD, Head of Research and Development at Sangamo. This innovative and personalized cellular therapy approach for HLA-A2 mismatched kidney transplantation is designed to help regulate the bodys immune system specifically and locally to promote acceptance of an immunologically mismatched donor organ. Beyond transplantation, we plan to explore the potential of CAR-Tregs in a range of autoimmune and inflammatory diseases.

TX200 is an autologous (cells collected from the patient) HLA-A2-targeted CAR-Treg cell therapy. The patients regulatory T cells (Tregs), a type of white blood cell which plays a key role in regulating the immune response and inflammation, are collected and genetically engineered with a Chimeric Antigen Receptor (CAR) designed to bind to HLA-A2. HLA-A2 is a protein belonging to the human leukocyte antigen (HLA) system. Donor/recipient mismatch in HLA molecules is a primary contributor to organ transplant incompatibility and may ultimately lead to immune-mediated rejection of the transplanted organ. The recipients immune system can recognize this HLA-A2 mismatch and may attack the new kidney carrying the HLA-A2 protein, potentially leading to graft rejection.

TX200 HLA-A2 CAR-Treg cells are designed to accumulate and localize within the new kidney where the HLAA2 protein is present, thereby utilizing the ability of Tregs to suppress immune responses against the transplanted kidney. This approach aims to help the recipients immune system accept the new kidney and induce immunological tolerance, potentially allowing tapering and eventual elimination of accompanying standard-of-care immune suppressive treatments.

Kidney transplantation is the treatment of choice for patients with ESRD who must otherwise remain on long-term dialysis. To prevent graft rejection, transplanted patients are treated with lifelong immune suppressive therapy, which impacts the bodys immune system broadly and is associated with multiple side effects, including an increased risk of infectious complications, cancer, and other drug-related toxicities.

TX200, which has been developed in collaboration with Professor Megan Levings of the University of British Columbia1, entered Sangamos pipeline in 2018 as part of the acquisition of TxCell. Beyond kidney transplantation, Sangamo intends to use its zinc finger nuclease (ZFN) gene editing technology to develop next-generation autologous and allogeneic CAR-Treg cell therapies for use in treating autoimmune and inflammatory diseases.

About the STEADFAST study

The STEADFAST study is a multicenter, open-label, single ascending dose, dose-ranging Phase 1/2 study. Sangamo plans to run this study in five different countries in Europe: United Kingdom, France, Netherlands, Germany, and Belgium.

About Sangamo Therapeutics

Sangamo Therapeutics is committed to translating ground-breaking science into genomic medicines with the potential to transform patients lives using gene therapy, ex vivo gene-edited cell therapy, and in vivo genome editing and gene regulation. For more information about Sangamo, visit http://www.sangamo.com.

Forward Looking Statements

This press release contains forward-looking statements regarding Sangamo's current expectations. These forward-looking statements include, without limitation, statements regarding the potential benefits of cell therapy, including but not limited to Treg therapy, the Company's ability to develop and commercialize product candidates to address genetic diseases with the Company's proprietary technologies and the timing of commencement or next stages of such programs and the anticipated benefits therefrom. These statements are not guarantees of future performance and are subject to certain risks, uncertainties and assumptions that are difficult to predict. Factors that could cause actual results to differ include, but are not limited to, the outcomes of clinical trials, the uncertain regulatory approval process, uncertainties related to the execution of clinical trials and uncertainties that research outcomes will support clinical programs. Actual results may differ from those projected in forward-looking statements due to risks and uncertainties that exist in Sangamo's operations and business environments. These risks and uncertainties are described more fully in Sangamo's Annual Report on Form 10-K for the year ended December 31, 2018 as filed with the Securities and Exchange Commission on March 1, 2019 and Sangamo's Quarterly Report on Form 10-Q for the quarter ended September 30, 2019 that it filed on November 6, 2019. TX200 is an investigational product and has not been determined to be safe or efficacious by regulatory authorities. Forward-looking statements contained in this announcement are made as of this date, and Sangamo undertakes no duty to update such information except as required under applicable law.

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Sangamo Announces UK Authorization of a Phase 1/2 Clinical Trial Evaluating the CAR-Treg Cell Therapy TX200 for Kidney Transplantation - BioSpace

Kiadis sheds half its staff as lead cell therapy bombs – – pharmaphorum

Dutch biotech Kiadis Pharma has abandoned its lead cell therapy and axed half its workforce after a failed phase 3 trial forced a complete rethink of its strategy.

The decision to drop ATIR101 for graft-versus-host disease (GVHD) a complication of transplants comes after an interim analysis of data from its phase 3 trial which suggested the T-cell immunotherapy was unlikely to show an improvement over cyclophosphamide, a standard therapy for GVHD.

Amsterdam-based Kiadis says that survival was better in the cyclophosphamide group than had been expected when the trial was designed. Also, there were fewer than expected cases of severe GVHD in the control arm so a much larger study would be required to show an effect of ATIR01.

Despite spending several years developing ATIR01, Kiadis has decided to cut its losses and refocus on its natural killer (NK) cell therapies, which are at an earlier stage of clinical development.

The announcement caught investors by surprise, despite earlier warnings by the biotech that all was not well with the programme and chances of an approval in 2020 were looking increasingly shaky.

Those concerns proved well-founded after the EMA rejected its regulatory filing for the therapy last month, having previously also turned it down in 2017. The phase 3 trial was designed to put ATIR-1 back on track, however, and in the meantime Kiadis had been building production capacity as it geared up for a possible commercial launch.

Shares in the biotech lost a third of their value after the announcement yesterday, and continued to slide today as investors who backed the company with a 28 million private placement in May to help fund the phase 3 programme digested the news that Kiadis remains several years away from having a therapy on the market.

Shareholders are also having to adjust to the pivot towards the NK cell therapy pipeline, which includes therapies based on cells harvested from patients as well as off-the-shelf treatments.

Staff involved in the commercial scale-up of ATIR01 are bearing the brunt of the layoffs as Kiadis cuts its costs and redirects its cash reserves at around 47 million (around $52 million) as of the end of the third quarter to the NK programmes.

Its most advanced candidate now is K-NK002, that aims to reduce blood cancer relapse after bone marrow transplants that will once again be compared with cyclophosphamide standard therapy. A phase 1/2 trial is due to start next year.

Also heading for a phase 1/2 trial in 2020 is K-NK003 for patients with relapse and refractory acute myeloid leukaemia, according to the biotech.

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Kiadis sheds half its staff as lead cell therapy bombs - - pharmaphorum

The Conference Forum Announces the Launch of Cell & Gene Therapy Day in NYC – PR Web

We are witnessing significant innovation in cell and gene therapies, and we are at a turning point of advancing these technologies for solid tumors.

NEW YORK (PRWEB) November 19, 2019

The inaugural Cell & Gene Therapy Day takes place February 27, 2020 at the Crowne Plaza Times Square in New York City. The one-day event will be chaired by Dr Aiman Shalabi, VP R&D, Cell and Gene Therapies for GSK, with a diverse group of leaders in the space.

We are witnessing significant innovation in cell and gene therapies, and we are at a turning point of advancing these technologies for solid tumors, said Dr Shalabi. This conference will engage global leaders on a series of scientific, investment landscape, regulatory and manufacturing topics with the ambition of accelerating these treatments to patients with solid cancers.

Cell & Gene Therapy Day will focus primarily on the promising data and progress for solid tumors. IO and cell therapy expert Dr Arie Belldegrun, Allogene, is the opening keynote and will kick off the day by addressing advancements in CAR-T cell therapy.

Immunotherapy expert, Dr Crystal Mackall, Director of the Stanford Center for Cancer Cell Therapy at Stanford University School of Medicine, will deliver a cornerstone presentation on new scientific frontiers in cell therapies for solid tumors. Dr Mackall has been a leader in treating hematologic tumors, with extensive work using CAR to target CD19 and CD22 in childhood leukemia.

The day will touch upon several different areas of cell and gene therapy. Dr Peter Marks, Director of the Center for Biologics Evaluation and Research at the Food and Drug Administration, will lead a panel on the evolution of regulatory policy for cell and gene therapy.

IO360 veteran Dr Ramy Ibrahim, Parker Institute for Cancer Immunotherapy, will address master protocols in cell and gene therapy, and his companys own innovations in the field. Dr Ibrahim will also lead a discussion on the latest in collaborative development paradigms for cell therapies with Dr Elad Sharon, National Cancer Institute, and Dr Mitch Finer, ElevateBio.

Leaders from Loncor Investments, Cancer Research Institute, IQVIA and the Alliance for Regenerative Medicine will trace through the landscape and evolution of the cell and gene therapy marketplace.

One portion of the day will focus on pivotal developments in solid tumor treatment. The National Institutes of Healths Dr Stephanie Goff will address tumor-infiltrating lymphocytes as a way of treating cancer. Dr Maria Fardis, Iovance, will speak on TILs as a way targeting individual tumor mutations. Dr Shalabi will return for an update on NY-ESO-1. Dr John Connolly, Tessa Therapeutics, will highlight the prognostic values of antiviral responses and using virus-specific T cells as a solid tumor immunotherapy platform. The day will conclude with debates on combinations with checkpoints, and bedside versus centralized manufacturing.

About Cell & Gene Therapy Day: Cell & Gene Therapy Day convenes stakeholders spanning the science and business communities to report on the latest cell and gene therapy progress to fight a wider range of cancers beyond hematologic malignancies. Cell & Gene Therapy Day is available an independent one-day program with a luncheon and networking reception, or attendees can register for the three day IO360 program, which includes the Cell & Gene Therapy Day. For more information on IO360, please click here.

About the Conference Forum:The Conference Forum is a life science industry research firm that develops conferences primarily around how to get therapeutics to patients faster. They examine and challenge the complex ecosystem of drug development and delivery, bringing ideas together from a variety of sources to help advance clinical research with common goals that are patient-focused. They are committed to creating the best content, exchange of ideas and solutions among peers, as well as providing high-quality networking.

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BioCardia Reports 2019 Third Quarter Financial Results and Business Highlights – GlobeNewswire

SAN CARLOS, Calif., Nov. 19, 2019 (GLOBE NEWSWIRE) -- BioCardia, Inc.[Nasdaq: BCDA], a leader in the development of comprehensive solutions for cardiovascular regenerative therapies, today reported financial results and business highlights for the third quarter 2019 and filed its quarterly report on Form 10-Q for the three and nine months ended September 30, 2019 with the Securities and Exchange Commission.

Update on Ongoing CardiAMP Autologous Cell Therapy Pivotal Heart Failure Trial:The company recently received FDA approval for an IDE supplement for the Phase III pivotal CardiAMP Heart Failure Trial of its lead therapeutic candidate. This will enable patients in the control group to cross over to CardiAMP treatment once their follow-up for the CardiAMP Trial has been completed. The IDE supplement also enables BioCardia to cover all out-of-pocket insurance co-pays for patients with Medicare coverage, so their participation in the trial will now be free. These two areas were previously barriers to participation for patients, who were eager to receive the therapy and less interested in being in the control arm, and were also responsible for their own co-pays. The company expects these changes, coupled with site-specific action plans, to further accelerate trial enrollment, which currently stands at 58 patients enrolled to date at 24 world class U.S. centers.

Third Quarter 2019 Business Highlights:

Third Quarter 2019Financial Results:

Achievements around our investigational CardiAMP cell therapy were the highlights of the last quarter, with a positive DSMB review, FDA approval of our IDE supplement, and a new European patent recognizing the innovation inherent in our pre-treatment assay designed to optimize patient outcomes and lower costs, said BioCardia CEO Peter Altman, PhD. At the same time, we made great progress with our other innovations: the first commercial use of the new AVANCE steerable introducer sheath in September, which can leverage the growing market for transseptal procedures, and extension of our AstraZeneca relationship, which enables our Helix delivery system to be used with new therapies being developed outside of the company.

Anticipated Upcoming Milestones:

About BioCardiaBioCardia, Inc., headquartered in San Carlos, California, is developing regenerative biologic therapies to treat cardiovascular disease. CardiAMP and CardiALLO cell therapies are the Companys biotherapeutic product candidates in clinical development. The Company's current products include the Helix transendocardial delivery system, the Morph steerable guide and sheath catheter portfolio, and the new AVANCE steerable introducer family. BioCardia also partners with other biotherapeutic companies to provide its Helix systems and clinical support to their programs studying therapies for the treatment of heart failure, chronic myocardial ischemia and acute myocardial infarction.

Forward Looking Statements This press release contains forward-looking statements that are subject to many risks and uncertainties. Forward-looking statements include, among other things, references to the enrollment of our clinical trials, the availability of data from our clinical trials, filings with the FDA, FDA product clearances, the efficacy and safety of our products and therapies, statements regarding our intentions, beliefs, projections, outlook, analyses or current expectations. Such risks and uncertainties include, among others, the inherent uncertainties associated with developing new products or technologies, regulatory approvals, unexpected expenditures, the ability to raise the additional funding needed to continue to pursue BioCardias business and product development plans and overall market conditions. We may find it difficult to enroll patients in our clinical trials due to many factors, some of which are outside of our control. Slower than targeted enrollment could delay completion of our clinical trials and delay or prevent development of our therapeutic candidates. These forward-looking statements are made as of the date of this press release, and BioCardia assumes no obligation to update the forward-looking statements.

We may use terms such as believes, estimates, anticipates, expects, plans, intends, may, could, might, will, should, approximately or other words that convey the uncertainty of future events or outcomes to identify these forward-looking statements. Although we believe that we have a reasonable basis for each forward-looking statement contained herein, we caution you that forward-looking statements are not guarantees of future performance and that our actual results may differ materially from the forward-looking statements contained in this press release. As a result of these factors, we cannot assure you that the forward-looking statements in this press release will prove to be accurate. Additional factors that could materially affect actual results can be found in BioCardias Form 10-Q filed with the Securities and Exchange Commission on August 9, 2019, including under the caption titled Risk Factors. BioCardia expressly disclaims any intent or obligation to update these forward-looking statements, except as required by law.

Media Contact: Michelle McAdam, Chronic Communications, Inc.Email:michelle@chronic-comm.comPhone: 310-902-1274

Investor Contact: David McClung, Chief Financial OfficerEmail:investors@BioCardia.comPhone: 650-226-0120

BIOCARDIA, INC.Condensed Statements of Operations

(Unaudited In thousands, except share and per share amounts)

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BioCardia Reports 2019 Third Quarter Financial Results and Business Highlights - GlobeNewswire

The global cell and gene therapy market is growing at a CAGR of over 24% during the forecast period 2018-2024 – P&T Community

NEW YORK, Nov. 18, 2019 /PRNewswire/ --

The global cell and gene therapy market is growing at a CAGR of over 24% during the forecast period 20182024.

Read the full report: https://www.reportlinker.com/p05827567/?utm_source=PRN

The major drivers contributing to the growth of the global cell and gene therapy market are the growing incidence of several chronic and terminal diseases, including cancer, the launch of new products, the increasing availability in clinical evidences of these products in terms of safety and efficacy, the rapid adoption of CAR T-cell therapy, favorable regulatory support in the development of these treatment, and improved manufacturing expertise in these products.

The following factors are likely to contribute to the growth of the cell and gene therapy market during the forecast period: Increased Pool of Patient Population with Several Ailments Favorable Regulatory Support and Increasing Special Designations for Cell and Gene Therapy Products Growing Demand for CAR T-cell Therapy Products Increasing Strategic Acquisition Activities

The study considers the present scenario of the cell and gene therapy market and its market dynamics for the period 2018?2024. It covers a detailed overview of several market growth enablers, restraints, and trends. The study covers both the demand and supply aspects of the market. The report profiles and examines leading companies and other prominent companies operating in the market.

Cell and Gene Therapy Market: Segmentation

This research report includes detailed market segmentation by product, application, end-user, and geography. The global cell therapy market is growing at a steady rate, and this trend is expected to continue during the forecast period due to the increased patient base with a wide range of diseases/ailments. The segment is likely to witness upward growth on account of expanded expertise in the manufacturing of stem cell-based products.

The gene therapy segment is expected to witness faster growth as the penetration of these products is increasing at a significant rate, especially in developed economies. The market is expected to grow during the forecast period due to the increased patient base for the existing gene remedy products, expected the launch of other gene therapy-based products for several indications, and expanded indication approvals for existing commercially available products.

The oncology segment accounts for the highest share of the global market. The growth of the oncology segment is increasing at a fast rate on account of the growing prevalence of several types of cancers. Currently, the available products not only modify the disease but also improve the quality of the patient's life, thereby decreasing the mortality rate. The market in the dermatology segment is increasing at a steady rate. This segment owns its growth to the increasing incidence and prevalence rate of several types of wounds, which are difficult to treat under normal conditions and the launch of innovative products. The dermatology segment is likely to showcase growth due to the high product availability of wound care products in the market.Hospitals are the leading end-user segment. The segment is growing mainly due to the increasing incidence/prevalence of chronic diseases such as cancer, cardiovascular diseases, diabetes, and chronic wound on account of diabetes feet, pressure ulcers, and other injuries.

Market Segmentation by Products Cell Therapy Gene TherapyMarket Segmentation by Distribution Channel Type Oncology Dermatology Musculoskeletal OthersMarket Segmentation by End-users Hospitals Wound Care Centers Cancer Care Centers Ambulatory Surgical Centers Others

Geographical Insights

The US market dominates the cell and gene therapy market in North America due to the high prevalence of chronic diseases and other conditions, which require these treatment methods. There is also comparably high utilization and wide accessibility of these therapies. The oncology segment is likely to witness significant growth in North America.The market in Europe is expected to witness upward growth in the near future on account of the growing prevalence of chronic diseases and rising elderly population. In Europe, cell and gene therapy products are considered to be part of the Advanced Therapy Medicinal Products (ATMPs), which are commonly known as regenerative medicine globally.

Market Segmentation by Geography North Americao USo Canada APACo Japano Chinao South Koreao Australia Europeo Germanyo Franceo UKo Spaino Italy Latin Americao Brazilo Mexico MEAo Turkeyo Saudi Arabiao UAE

Key Vendor AnalysisThe global market is characterized by the presence of a few global, large-scale companies and several small to medium-scale companies offering one or two cell and gene therapy products. Global players are majorly offering innovative products with the potential of disease-modifying characteristics that are generating significant revenues, especially in Europe and US regions. Most innovative and breakthrough products are approved in the European countries and the US. Vendors are targeting mostly developed economies such as the US, Germany, France, the UK, Spain, and Japan as the uptake of these products is higher in these countries than low and middle-income countries. However, the market in these regions is at the nascent stage.

Key Vendors Gilead Sciences Spark Therapeutics Novartis AG Organogenesis Amgen Osiris Therapeutics Dendreon Vericel

Other Prominent Vendors Anterogen Tego Sciences Japan Tissue Engineering JCR Pharmaceuticals Medipost MolMed AVITA Medical CollPlant Corestem Biosolution Stempeutics Research Orchard Therapeutics Takeda Pharmaceutical Company CHIESI Farmaceutici CO.DON AnGes GC Pharma JW CreaGene APAC Biotech Nipro Corp. Terumo Orthocell bluebird bio

Key Market InsightsThe report provides the following insights into the market for the forecast period 20192024. Offers sizing and growth prospects of the market for the forecast period 20192024. Provides comprehensive insights on the latest industry trends, forecast, and growth drivers in the market. Includes a detailed analysis of growth drivers, challenges, and investment opportunities. Delivers a complete overview of segments and the regional outlook of the market. Offers an exhaustive summary of the vendor landscape, competitive analysis, and key strategies to gain a competitive advantage.

Read the full report: https://www.reportlinker.com/p05827567/?utm_source=PRN

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The global cell and gene therapy market is growing at a CAGR of over 24% during the forecast period 2018-2024 - P&T Community