Page 1,258«..1020..1,2571,2581,2591,260..1,2701,280..»

Leading geneticist George Church says reversing the aging process in humans could be 20 years away – 60 Minutes – CBS News

Posted: December 7, 2019 at 10:41 am

The geneticist whose work helped map the human genome, the first step in the quest to manipulate what is essentially the software of human life, says reversing the aging process in humans may be less than 20 years away. George Church takes Scott Pelley into his Harvard Medical School lab to see his latest work for a 60 Minutes report to be broadcast Sunday, December 8, at 7:30 p.m. ET and 7 p.m. PT on CBS.Thanks to Church and others whose work decoded DNA, called the building blocks of life, the day when humans will no longer be prone to viruses or genetic diseases is coming. But one of the next breakthroughs could be reversing the basic process of age itself. "Age reversal is something that's been proven about eight different ways on animals," says Church. He tells Pelley that in mice, tissue damage has been repaired, reaction times sped up and cognition improved.

Knowing the specific functions of genes in a creature's DNA allows scientists to edit or add genes to the sequence and change outcomes. A paper just published by Church and several other scientists shows how added multiple genes in mice improved heart and kidney function and levels of blood sugar. "The gene function is going down [with age] and so we're boosting it back up by putting in extra copies of the gene," he explains, saying that this is gene therapy.The next step toward replicating this science in humans is to achieve the same results in a clinical trial using dogs that he is conducting now. The process could be perfected in humans in less than 20 years says Church. "That veterinary product might be a couple years away. And then that takes another 10 years to get through the human clinical trials."Church's lab at Harvard is working on about a hundred cutting-edge projects. They are currently experimenting with growing mini-organs from patients' own cells, to help test the effectiveness of medicine. And they are also aiming to turn these organoids, as they are called, into organs available for transplant. Another project is a start-up to make full-scale pig organs safe for human transplant. Church and his team also want to program human DNA to prevent people from hosting viruses, which could offer the cure for the common cold. Church's lab has also received much attention for its project to create a modern version of the extinct woolly mammoth, a process known as de-extinction.Church acknowledges the controversial nature of such experimenting, but says it's already being done. He understands the world may not be ready for some of the implications of this technology. "The more powerful or the more rapidly moving the technology, the more cautious we need to be, the bigger the conversation involving lots of different disciplines, religion, ethics, government, art to see what its unintended consequences might be."

2019 CBS Interactive Inc. All Rights Reserved.

More here:
Leading geneticist George Church says reversing the aging process in humans could be 20 years away - 60 Minutes - CBS News

Posted in Gene therapy | Comments Off on Leading geneticist George Church says reversing the aging process in humans could be 20 years away – 60 Minutes – CBS News

Rett Among Disorders Targetted for Gene Therapies in Partnership Deal – Rett Syndrome News

Posted: December 7, 2019 at 10:41 am

Sarepeta Therapeutics and StrideBio will collaborate to advance novel gene therapies for four genetic neurological disorders, including Rett syndrome, the companies have announced.

Under the agreement, StrideBio, which specializes in viral-based delivery systems for gene therapy, will conduct initial research, development, and manufacturing for the first four gene targets in these neurological disorders: MECP2 (Rett syndrome), SCN1A (Dravet syndrome), UBE3A (Angelman syndrome), and NPC1 (Niemann-Pick).

The main goal of the early development stage is to obtain investigational new drug approvals from the U.S. Food and Drug Administration, which are mandatory to start clinical trials.

In turn, Sarepta, a company focusing on precision genetic medicine, expands its gene therapy pipeline by gaining exclusive licenses on the selected targets. It also gains the possibility to extend licensing to four additional targets (for a total of eight) in neuromuscular and central nervous system diseases.

StrideBio owns aplatform to create adeno-associated viral (AAV) vectors, a class of modified viruses that are used to deliver gene therapy. They are engineered to be harmless (non-infectious) and work to deliver functioning genes directly into specific cells and tissues.

One of the current challenges in gene therapy is that some people carry a natural immunity against AAVs, in the form of neutralizing antibodies that react against these vectors and prevent gene therapies from working. In addition, immune reactions against AAVs can also become toxic for patients. This limits the number of patients who can benefit from AAV-based gene therapies, as carriers of neutralizing antibodies are excluded from gene therapy trials and treatments.

StrideBios platform addresses this problem by creating novel AAV capsids, or protein shells, that enclose the genetic material to be delivered and are able to escape pre-existing neutralizing antibodies.

As such, the platform holds promise for gene therapies to be used in a greater number of patients, the company says.

These new capsids can also be engineered to improve specific delivery of gene therapy to tissues of interest in a particular condition.

Sarepta and StrideBio plan to address re-dosing challenges as well in patients who have received some sort of AAV-based gene therapy.

With our partnership with StrideBio, Sarepta continues to build on its leadership position in gene therapies to treat rare diseases. We are excited to work with StrideBio and access its innovative AAV platform for next-generation capsids, Doug Ingram, Sareptas president and CEO, said in a press release.

Our partnership with StrideBio expands our research portfolio by up to eight new targets and ensures that we gain access to new technology and targets while not distracting Sarepta from its near-term priorities, he added.

Sapan Shah, PhD, StrideBios CEO, said: This partnership will provide significant resources and expertise to enable StrideBios continued rapid expansion of our research and manufacturing platform, as well as accelerate the development of AAV gene therapies for multiple rare disease targets.

We are looking forward to working together with Sarepta to bring novel treatments to patients as quickly as possible, he added.

Sarepta will pay StrideBio $48 million as upfront payment, in addition to future payments for development, regulatory, and commercial milestones for the four programs. StrideBio will also receive royalties on potential worldwide sales.

If the collaboration is expanded to the four additional targets, Sarepta will pay up to $42.5 million along with future milestone payments.

Ana is a molecular biologist with a passion for discovery and communication. As a science writer she looks for connecting the public, in particular patient and healthcare communities, with clear and quality information about the latest medical advances. Ana holds a PhD in Biomedical Sciences from the University of Lisbon, Portugal, where she specialized in genetics, molecular biology, and infectious diseases.

Total Posts: 2

Jos is a science news writer with a PhD in Neuroscience from Universidade of Porto, in Portugal. He has also studied Biochemistry at Universidade do Porto and was a postdoctoral associate at Weill Cornell Medicine, in New York, and at The University of Western Ontario in London, Ontario, Canada. His work has ranged from the association of central cardiovascular and pain control to the neurobiological basis of hypertension, and the molecular pathways driving Alzheimers disease.

Originally posted here:
Rett Among Disorders Targetted for Gene Therapies in Partnership Deal - Rett Syndrome News

Posted in Gene therapy | Comments Off on Rett Among Disorders Targetted for Gene Therapies in Partnership Deal – Rett Syndrome News

Sangamo and Pfizer Announce Updated Phase 1/2 Results Showing Sustained Increased Factor VIII Activity Through 44 Weeks Following SB-525 Gene Therapy…

Posted: December 7, 2019 at 10:41 am

BRISBANE, Calif. & NEW YORK--(BUSINESS WIRE)--Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a genomic medicine company, and Pfizer, Inc. (NYSE: PFE), today announced updated follow-up results from the Phase 1/2 Alta study evaluating investigational SB-525 gene therapy in patients with severe hemophilia A. The data showed that SB-525 was generally well tolerated and demonstrated sustained increased Factor VIII (FVIII) levels following treatment with SB-525 through to 44 weeks, the extent of follow-up for the longest treated patient in the 3e13 vg/kg dose cohort. Data from 11 patients treated with SB-525 will be featured in a poster presentation today, December 7, 2019, at the 61st Annual Meeting of the American Society of Hematology (ASH) in Orlando, FL. The SB-525 ASH poster, which includes the full set of data, is available on Sangamos website in the Investors and Media section under Events and Presentations.

I am pleased that all five patients in the high dose (3e13 vg/kg) cohort rapidly achieved normal levels of Factor VIII, and that Factor VIII levels have been stable and durable in the normal range for the first two patients up to 44 and 37 weeks following treatment respectively, with no bleeding events or factor usage up to a follow up of 44 weeks in the longest treated patient, said Barbara Konkle, M.D., Bloodworks Northwest, Professor of Medicine at University of Washington and a Principal Investigator of the Alta study. It is important to continue to follow these patients to determine whether these results are sustained in the longer term as the combination of a favorable safety profile coupled with sustained expression at a level that prevents bleeding and allows normal activity will be the hallmark of a successful gene therapy for hemophilia A.

Alta study data presented at ASH included 11 patients treated across four ascending dose cohorts: 9e11 vg/kg (2 patients), 2e12 vg/kg (2 patients), 1e13 vg/kg (2 patients) and 3e13 vg/kg (5 patients). The data cutoff date was October 17, 2019.

An analysis of plasma FVIII antigen was assessed by ELISA and demonstrated antigen concentrations consistent with the FVIII activity measured by the chromogenic assay. Dose dependent increases in FVIII activity over baseline were observed across the dose cohorts. The lower-dose cohorts indicate durable FVIII activity with up to 52 weeks of follow-up.

In the 3e13 vg/kg dose cohort, patients achieved normal range FVIII activity within 5-7 weeks of treatment with SB-525. The first two patients treated in this cohort (Patients 7 and 8) have achieved stable FVIII levels, demonstrating durability in the normal range through 44 and 37 weeks, respectively, as measured by the chromogenic assay. The two patients most recently treated in this cohort (Patients 10 and 11), with 22 and 12 weeks of follow-up, respectively, demonstrated a similar pattern of FVIII expression. The FVIII expression pattern observed in Patient 9 differed from that of other patients in the cohort. Seven weeks following treatment, Patient 9 achieved normal range FVIII levels. Beginning at week 13, FVIII levels in that patient fluctuated in a range below normal, but still well above the level needed to prevent spontaneous bleeding. At week 18, FVIII levels in Patient 9 began to increase, and as of the latest measurement at week 24, continued to rise. No patient in the 3e13 vg/kg dose cohort has experienced bleeding events up to 44 weeks of follow-up, and no patient in this dose cohort required factor replacement following initial use of prophylactic factor.

SB-525 was generally well tolerated across all dose cohorts. The treatment-related adverse events include: alanine aminotransferase (ALT) elevation (36.4%, n=4), pyrexia (27.3%, n=3), increased aspartate aminotransferase (18.2%, n=2), tachycardia (18.2% n=2), fatigue (9.1%, n=1), hypotension (9.1%, n=1) and myalgia (9.1%, n=1). Treatment-related serious adverse events (SAEs) of hypotension (grade 3) and fever (grade two) occurred in one patient in the 3e13 vg/kg cohort six hours following dosing with SB-525 that fully resolved within 24 hours. No similar events were reported in the other patients dosed in that cohort. No patients treated with SB-525 experienced an ALT elevation associated with loss of Factor VIII expression. In the 3e13 vg/kg dose cohort, four patients experienced transient low grade ALT elevations (>1.5 x baseline) that were managed with a tapering course of oral steroids. The study does not use corticosteroids prophylactically, initiating them only in the event of an ALT elevation that is greater than 1.5x baseline.

The updated results from the Alta study suggest that SB-525 may represent a differentiated gene therapy for patients with severe hemophilia A, said Bettina Cockroft, M.D., Chief Medical Officer of Sangamo. The results continue to suggest that if sustained over a longer duration, SB-525 has the potential to be a predictable, reliable, and safe treatment that may bring clinical benefits to patients with severe hemophilia A.

Sangamo has completed the manufacturing technology transfer and initiated the transfer of the Investigational New Drug (IND) Application to Pfizer, which is expected to be completed in the first quarter 2020. Pfizer is enrolling patients in the Phase 3 lead-in study, the data from which is expected to provide a baseline for patients who are subsequently enrolled into the Phase 3 study (ClinicalTrials.gov Identifier: NCT03587116).

We are pleased with the progress that we have made in progressing SB-525 gene therapy toward a Phase 3 registrational study, including enrolling the first patient in the 6-month lead-in study. We expect to dose the first patient in the Phase 3 registrational study in 2020, said Seng Cheng, Senior Vice President and Chief Scientific Officer of Pfizers Rare Diseases Research Unit. We continue to believe that if the observed safety and efficacy results are sustained, this gene therapy has the potential to transform the treatment paradigm of severe hemophilia A.

About the Alta study

The Phase 1/2 Alta study is an open-label, dose-ranging, multicenter clinical trial designed to assess the safety and tolerability of SB-525 in patients with severe hemophilia A. The mean age of the 11 patients assessed is 30 years (range 18-47 years). All 11 patients are male. The U.S. Food and Drug Administration has granted Orphan Drug, Fast Track, and regenerative medicine advanced therapy (RMAT) designations to SB-525, which also received Orphan Medicinal Product designation from the European Medicines Agency. SB-525 is being developed as part of a global collaboration between Sangamo and Pfizer.

About SB-525 Gene Therapy

SB-525 comprises a recombinant adeno-associated virus serotype 6 vector (AAV6) encoding the complementary deoxyribonucleic acid for B domain deleted human FVIII. The SB-525 vector cassette was designed to optimize both the vector manufacturing yield and liver-specific FVIII protein expression. The SB-525 transcriptional cassette incorporates multi-factorial modifications to the liver-specific promoter module, FVIII transgene, synthetic polyadenylation signal and vector backbone sequence.

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.

Pfizer Inc: Working together for a healthier world

At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products, including innovative medicines and vaccines. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world's premier innovative biopharmaceutical companies, we collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. For more than 150 years, we have worked to make a difference for all who rely on us. We routinely post information that may be important to investors on our website at http://www.pfizer.com. In addition, to learn more, please visit us on http://www.pfizer.com and follow us on Twitter at @Pfizer and @Pfizer_News, LinkedIn, YouTube and like us on Facebook at Facebook.com/Pfizer.

Sangamo Forward Looking Statements

This press release contains forward-looking statements regarding Sangamo's current expectations. These forward-looking statements include, without limitation, statements relating to the investigational hemophilia A gene therapy, SB-525, including its potential therapeutic benefits; the potential long-term durability of SB-525 gene therapy; SB-525 having the potential to be a predictable and reliable treatment that may bring clinical benefit to patients with hemophilia A and to potentially represent a transformative treatment paradigm; plans to advance SB-525 into a potential registrational study; the potential benefits of the RMAT and Orphan medicine designation for SB-525; and other statements that are not historical fact. These statements are not guarantees of future performance and are subject to risks and assumptions that are difficult to predict. Factors that could cause actual results to differ include, but are not limited to, risks and uncertainties related to: the research and development process; additional data, including the risk that the data reported from the Alta to date may not be indicative of the final results from the Alta study or that such final results may not validate and support the safety and efficacy of SB-525; the completion of the Alta study; the possibility of unfavorable new clinical data from the Alta study and further analyses of existing clinical data from the study that may material change clinical outcomes; the risk that clinical trial data are subject to differing interpretations and assessments by regulatory authorities; whether regulatory authorities will be satisfied with the design of and results from the clincal studies relating to SB-525, any potential registrational studies or any other clinical studies of SB-525; whether Sangamo will be able to maintain or receive the benefits associated with RMAT, Orphan Drug, Fast Track and Orphan Medicinal Product designations for SB-525; Sangamo's reliance on Pfizer and other third-parties to meet their clinical and manufacturing obligations; Sangamos ability to maintain strategic partnerships; and the potential for technological developments by Sangamo's competitors that will obviate Sangamo's gene therapy technology. Further, there can be no assurance that the necessary regulatory approvals will be obtained for SB-525 or that Sangamo and its partners will be able to develop commercially viable product candidates. 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 and Sangamo's most recent Quarterly Report on Form 10-Q. 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.

Pfizer Disclosure Notice: The information contained in this release is as of December 7, 2019. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments.

This release contains forward-looking information about an investigational hemophilia A agent, SB-525, including its potential benefits, that involves substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. Risks and uncertainties include, among other things, the uncertainties inherent in research and development, including the ability to meet anticipated clinical endpoints, commencement and/or completion dates for our clinical trials, regulatory submission dates, regulatory approval dates and/or launch dates, as well as the possibility of unfavorable new clinical data and further analyses of existing clinical data; risks associated with interim data; the risk that clinical trial data are subject to differing interpretations and assessments by regulatory authorities; whether regulatory authorities will be satisfied with the design of and results from our clinical studies; whether and when drug applications for any potential indications for SB-525 may be filed in any jurisdictions; whether and when regulatory authorities in any jurisdictions may approve any such applications, which will depend on myriad factors, including making a determination as to whether the product's benefits outweigh its known risks and determination of the product's efficacy and, if approved, whether SB-525 will be commercially successful; decisions by regulatory authorities impacting labeling, manufacturing processes, safety and/or other matters that could affect the availability or commercial potential of SB-525; and competitive developments.

A further description of risks and uncertainties can be found in Pfizer's Annual Report on Form 10-K for the fiscal year ended December 31, 2018 and in its subsequent reports on Form 10-Q, including in the sections thereof captioned "Risk Factors" and "Forward-Looking Information and Factors That May Affect Future Results", as well as in its subsequent reports on Form 8-K, all of which are filed with the U.S. Securities and Exchange Commission and available at http://www.sec.gov and http://www.pfizer.com.

Read more:
Sangamo and Pfizer Announce Updated Phase 1/2 Results Showing Sustained Increased Factor VIII Activity Through 44 Weeks Following SB-525 Gene Therapy...

Posted in Gene therapy | Comments Off on Sangamo and Pfizer Announce Updated Phase 1/2 Results Showing Sustained Increased Factor VIII Activity Through 44 Weeks Following SB-525 Gene Therapy…

UPDATED: Astellas snags a gene therapy upstart with $3B buyout bid inspiring forecasts of more M&A ahead – Endpoints News

Posted: December 7, 2019 at 10:41 am

Exhilarating. A major advance. A milestone achievement. If one had just tuned into the panel comments on Biogens presentation at CTAD, it would seem that the biotech had an impressive, disease-modifying Alzheimers drug in aducanumab.

But off the stage, reactions to their admittedly complicated dataset and the biotechs explanation for resurrecting a drug that failed its futility analysis were a lot more mixed, with analysts continuing to question whether the evidence is substantial enough to warrant an FDA approval and raising new doubts on the safety side.

In an investor call later in the day, execs noted that they are not planning another study and stood by their intention, publicized in October to much surprise, to submit regulatory filings based on what they have.

We dont file willy nilly, said Al Sandrock, head of R&D. We only go to filing when we believe that there is a benefit-risk argument based on science, based on data. And if you look at our history, we havent done filings right and left without good reason.

Biogen had a theory going into the Clinical Trials on Alzheimers Disease meeting.

Unlock this story instantly and join 67,000+ biopharma pros reading Endpoints daily and it's free.

SUBSCRIBE SIGN IN

Read the original here:
UPDATED: Astellas snags a gene therapy upstart with $3B buyout bid inspiring forecasts of more M&A ahead - Endpoints News

Posted in Gene therapy | Comments Off on UPDATED: Astellas snags a gene therapy upstart with $3B buyout bid inspiring forecasts of more M&A ahead – Endpoints News

FerGene Announces Pivotal Phase 3 Study of Nadofaragene Firadenovec Met Its Primary Endpoint With More Than Half of Patients With High-Grade…

Posted: December 7, 2019 at 10:41 am

WASHINGTON--(BUSINESS WIRE)--FerGene, a new gene therapy company formed by Ferring Pharmaceuticals and Blackstone Life Sciences, announced today positive results from the pivotal Phase 3 clinical trial evaluating nadofaragene firadenovec (rAd-IFN/Syn3), an investigational gene therapy, for the treatment of high-grade, Bacillus Calmette-Gurin (BCG) unresponsive non-muscle invasive bladder cancer (NMIBC). FKD Therapies Oy (FKD) has led the development and regulatory filing of nadofaragene firadenovec, which has been studied in 33 centers across the U.S. in collaboration with the Society of Urologic Oncology Clinical Trials Consortium (SUO-CTC). The results were presented during the bladder cancer session at the Society of Urologic Oncology 20th Annual Meeting in Washington D.C.

The Phase 3 study of 157 patients from the U.S. met its primary endpoint with 53% of CIS Ta/T1 patients (carcinoma in situ; bladder cancer that is confined to the superficial layer, with or without concomitant high-grade Ta or T1 papillary disease) achieving a CR at three months, and 24% continuing to show a CR at 12 months. Moreover, the study also demonstrated broad efficacy in this difficult to treat patient population with a 73% HGRF survival in patients with papillary disease at three months and 44% HGRF survival at 12 months. In the study, nadofaragene firadenovec was instilled directly into the patients bladder every three months. All responses at 12 months were confirmed by protocol-mandatory five-point biopsies.

Bladder cancer is one of the most frequently occurring cancers with an estimated 699,450 people living with bladder cancer and more than 80,000 new cases diagnosed each year in the U.S. alone.1 In high-grade NMIBC patients, BCG is the standard treatment, and, although effective, over 60% of these tumors eventually re-occur. 2,3

Currently, patients living with high-grade NMIBC who are unresponsive to BCG have few treatment options and often face bleak outcomes, including complete bladder removal, known as cystectomy, said Colin P. N. Dinney, MD, Professor and Chairman of the Department of Urology at The University of Texas M.D. Anderson Cancer Center. Cystectomy is a complex and life-altering surgical procedure for patients, so these positive results from the Phase 3 trial of nadofaragene firadenovec are highly promising for patients. It would be gratifying to provide an alternative that addresses the critical unmet need for effective second-line therapy for patients facing radical cystectomy.

Efficacy Analysis*

AssessmentPeriod

CIS Ta/T1 Disease (n=103) CR(% [n])

High-Grade Ta/T1 Papillary Disease (non CIS)

(n=48) HGRF Survival (% [n])

Month 3

53.4% (55)

72.9% (35)

Month 6

40.8% (42)

62.5% (30)

Month 9

35.0% (36)

58.3% (28)

Month 12

24.3% (25)

43.8% (21)

*151 patients

In the Phase 3 trial, the most common adverse events (AEs) included fatigue, bladder spasm and discharge around the catheter, micturition urgency, hematuria, chills, fever, headache, painful urination, urinary tract infection, and diarrhea. No grade 4 or 5 treatment-related AEs were reported in the study. Study drug-related AEs were transient and local in nature, with a median duration of less than two days, with the exception of fatigue, which had a median duration of 11 days and urinary frequency which had a median duration of 41 days. There was a 1.9% percent rate of discontinuations due to study drug-related AEs.

We are pleased with these Phase 3 data results, including the complete response rates and favorable safety profile seen with nadofaragene firadenovec, said Nigel R. Parker4, PhD, of FKD Therapies Oy. These data were part of our submission package to the FDA, and we look forward to continuing to work with the agency to potentially bring nadofaragene firadenovec to patients with BCG unresponsive disease.

As a practicing urologist and trial investigator, its encouraging to see these types of efficacy and safety results in patients with high-grade NMIBC, an area thats been in need of new innovative treatment options for more than 20 years, said Neal Shore, MD, FACS, Medical Director, Carolina Urologic Research Center. These robust clinical results further demonstrate the potential of nadofaragene firadenovec as a valuable treatment option for NMIBC patients.

The U.S. Food and Drug Administration (FDA) has validated FKDs Biologics License Application (BLA) and granted Priority Review for nadofaragene firadenovec, which previously received Fast Track and Breakthrough Therapy Designations.

About nadofaragene firadenovec

Nadofaragene firadenovec (rAd-IFN/Syn3) is an investigational gene therapy being developed as a treatment for patients with high-grade, BCG unresponsive, NMIBC. It is an adenovirus vector-based gene therapy containing the gene interferon alfa-2b, administered by catheter into the bladder every three months. The vector enters the cells of the bladder wall, where, it breaks down, releasing the active gene to do its work. The internal gene/DNA machinery of the cells picks up the gene and translates its DNA sequence, resulting in the cells secreting high quantities of interferon alfa-2b protein, a naturally occurring protein the body uses to fight cancer. This novel gene therapy approach thereby turns the patient's own bladder wall cells into multiple interferon microfactories, enhancing the body's natural defenses against the cancer.

About Non-Muscle Invasive Bladder Cancer (NMIBC)

NMIBC is an early form of bladder cancer which is present in the superficial layer of the bladder and has not invaded deeper into the bladder or spread to other parts of the body.5 It is estimated that there will be 80,000 new cases of bladder cancer in the U.S. in 2019; more than 70% of these cases present as NMIBC.2,6 In patients with high-grade NMIBC, intravesical BCG is the recommended treatment; however, between 30% and 50% cases with high-grade disease will recur.7 The outcome for BCG unresponsive patients is poor, with total cystectomy (complete removal of the bladder) often being the next treatment option.8

About FerGene

FerGene, a new gene therapy company and Ferring subsidiary, has been created to potentially commercialize nadofaragene firadenovec in the U.S. and to advance the global clinical development. FerGenes goal is to bring this promising therapy to a patient population which has seen little improvement in their standard of care over the past twenty years. Blackstone Life Sciences will invest $400 million USD and Ferring will invest up to $170 million USD in FerGene. Ferring will also potentially launch and commercialize nadofaragene firadenovec outside of the U.S.

About FKD Therapies Oy

FKD Therapies Oy is a specialist gene therapy company based in Kuopio, Finland originally conceived by scientific and medical founders, Dr Nigel R Parker and Professor Seppo Yla-Herttuala4, for the specific purpose of undertaking the development of adenovirus mediated interferon alfa-2b. FKD has led the overall development of nadofaragene firadenovec through manufacturing at FinVector Oy, late stage clinical trials and the current BLA filing. FinVector Oy and FKD Oy are part of the Trizell Group.

About Ferring Pharmaceuticals

Ferring Pharmaceuticals is a research-driven, specialty biopharmaceutical group committed to helping people around the world build families and live better lives. Headquartered in Saint-Prex, Switzerland, Ferring is a leader in reproductive medicine and maternal health, and in specialty areas within gastroenterology and urology. Founded in 1950, Ferring now employs approximately 6,500 people worldwide, has its own operating subsidiaries in nearly 60 countries and markets its products in 110 countries.

1 National Cancer Institute. Cancer Stat Facts: Bladder Cancer. Available at: https://seer.cancer.gov/statfacts/html/urinb.html. Last accessed: December 2019.

2 Maruf, M et al., Non invasive bladder cancer: a primer on immunotherapy. Cancer Biol Med. 2016;13(2):194-205.

3 Derr, L et al., Intravesical Bacillus Calmette Guerin Combined with a Cancer Vaccine Increases Local T-Cell Responses in Non-muscle-Invasive Bladder Cancer Patients. Clin Cancer Res. 2017;23(3):717-725.

4 AIV Institute for Molecular Sciences, Kuopio, Finland.

5 Anastasiadis A, de Reijke TM. Best practice in the Treatment of Nonmuscle Invasive Bladder Cancer. Ther Adv Urol. 2012;4(1):13-32

6 Ghatalia, Pooja et al. Approved checkpoint inhibitors in bladder cancer: which drug should be used when?. Therapeutic advances in medical oncology vol. 10 1758835918788310. 30 Jul. 2018, doi:10.1177/1758835918788310.

7 Cambier S et al. EORTC Nomograms and Risk Groups for Predicting Recurrence, Progression, and Disease-specific and Overall Survival in NonMuscle-invasive Stage TaT1 Urothelial Bladder Cancer Patients Treated with 13 Years of Maintenance Bacillus Calmette-Gurin. European Urolology. 2016, Vol. 69(1): 60-69.

8 Cookson, M et al.,Use of intravesical valrubicin in clinical practice for treatment of nonmuscle-invasive bladder cancer, including carcinoma in situ of the bladder. Therapeutic Advances in Urology. 2014, Vol. 5(5):181-191.

Follow this link:
FerGene Announces Pivotal Phase 3 Study of Nadofaragene Firadenovec Met Its Primary Endpoint With More Than Half of Patients With High-Grade...

Posted in Gene therapy | Comments Off on FerGene Announces Pivotal Phase 3 Study of Nadofaragene Firadenovec Met Its Primary Endpoint With More Than Half of Patients With High-Grade…

Synthetic Stem Cells Market Is Expecting Revolutionary Growth 2019 with Top Key Players: North Carolina State University (NCSU), Zhengzhou University…

Posted: December 6, 2019 at 8:50 am

The global synthetic stem cells market was valued at approximately USD +14 million in 2019 and is expected to generate around USD +42 million by 2027, at a CAGR of around +19% between 2019 and 2027.

Synthetic stem cells offer therapeutic benefits comparable to those from natural stem cells and could reduce some of the risks associated with stem cell therapies. Additionally, these cells have better preservation stability and the technology is generalizable to other types of stem cells.

Get a sample Report of this Market now! @ https://www.reportconsultant.com/request_sample.php?id=12250

Global Synthetic Stem Cells Market 2019 by Key Players, Regions, Type and Application, Forecast to 2027 Market report contains a forecast of the next 5 years, starting 2019 and ending 2027 with a host of metrics like supply-demand ratio, market frequency, dominant players of the market, driving factors, restraints, and challenges.

Synthetic Stem Cells Market Top Leading Vendors :-

The overviews, SWOT analysis and strategies of each vendor in the Synthetic Stem Cell market provide understanding about the market forces and how those can be exploited to create future opportunities.

Get up to 60% Discount on this report @: https://www.reportconsultant.com/ask_for_discount.php?id=12250

Synthetic Stem Cells Market Segment by Types

Synthetic Stem Cells Market Segment by Applications

Synthetic Stem Cells Market reports provides 5 year pre-historic and forecast for the sector and include data on socio-economic data of global. Key stakeholders can consider statistics, tables & figures mentioned in this report for strategic planning which lead to success of the organization. Synthetic Stem Cells Market reports provides a comprehensive overview of the global market size and share.

The report also contains market revenue; sales, Synthetic Stem Cells Market production and manufacturing cost that could help you get a better view on the market. The Report Focuses on the key global Synthetic Stem Cells manufacturers, to define, describe and analyse the sales volume, value, market share, market competition landscape, SWOT analysis and development plans in next few years.

See the complete table of contents and list of exhibits, as well as selected illustrations and example pages from this report @ https://www.reportconsultant.com/enquiry_before_buying.php?id=12250

The study objectives of this report are:

About us:

Report Consultant is a prime destination for your business aptitude and analytical solutions because we provide qualitative and quantitative sources of information that are proficient to give one-stop solutions. We skillfully syndicate qualitative and quantitative research in exact proportions to have the best report, which not only gives the most recent insights but also assists you to grow.

Contact us:

Rebecca Parker

(Report Consultant)

The United States,

sales@reportconsultant.com

http://www.reportconsultant.com

Read the original:
Synthetic Stem Cells Market Is Expecting Revolutionary Growth 2019 with Top Key Players: North Carolina State University (NCSU), Zhengzhou University...

Posted in North Carolina Stem Cells | Comments Off on Synthetic Stem Cells Market Is Expecting Revolutionary Growth 2019 with Top Key Players: North Carolina State University (NCSU), Zhengzhou University…

Clinic pitches unproven treatments to desperate patients, with tips on raising the cash – Seattle Times

Posted: December 6, 2019 at 8:50 am

By the time he called the Lung Health Institute, Ed Garbutt was desperate. The Dallas computer-parts salesman could barely walk the length of his house without gasping for breath. Unable to work, Garbutt, 64, was going broke paying for trips to the emergency room.

Lung Health Institute staffers were reassuring, Garbutt recalled, telling him that more than 80% of their patients with lung disease said they found relief through their stem-cell treatments which would cost him $5,500, thanks to a summer sale. He said they told him that if he didnt have the money, he could get it other ways, like fundraising on GoFundMe.

So Garbutt raised $1,500 in donations, tapped the last of his savings and charged the rest on his credit card. I spent every dime I had, he said, hoping it would make a difference.

Over the past decade, hundreds of clinics have sprouted across the United States selling stem-cell therapies for incurable conditions such as Garbutts lung disease, Parkinsons disease and macular degeneration. But often, patients say, the only thing affected is their finances.

Former patients of the Tampa-based Lung Health Institute said they were encouraged to take out bank loans or borrow money from family members. Some withdrew from their retirement accounts and took up church offerings. Others borrowed against their homes.

What theyre doing is taking a predatory approach to people with progressive, fatal diseases, said Gregory Cosgrove, chief medical officer for the Pulmonary Fibrosis Foundation. His foundation issued a warning this year against such stem-cell therapies, noting that desperate patients continue to succumb to an onslaught of marketing and branding.

Even in a booming industry long denounced by medical experts, the Lung Health Institute has been singled out for its aggressive marketing and unproven claims. In 2015, for example, pulmonologists at Johns Hopkins wrote to the Food and Drug Administration urging it to take action against the Lung Health Institute. We would ask that the FDA take necessary action to prevent the further advertising of this unproven treatment, their letter read.

Since 2013, the company has conducted a multimillion-dollar campaign to lure patients with targeted online ads, hyped claims and high-pressure seminars, according to internal documents and former staff members.

In interviews, former employees responsible for fielding patients calls said they were given monthly sales quotas. Former company doctors and nurses described working as closers, using their medical credentials to persuade wavering patients to put money down.

In two lengthy interviews, the companys chief operating officer, Ann Sells Miller, defended the company, saying its treatments have helped many patients who have no other options. Miller and other executives dismissed complaints about their marketing strategies and treatments, saying their critics are often people who dont understand their stem-cell procedures or lawyers looking to make money by filing lawsuits against them.

Our patients come to us. We dont call them. They come to us because their current standard of care is not working for them, Miller said. She said the companys marketing is intended to educate people with the disease.

The reason the company offers financial tips, Miller said, is to make sure that patients understand what their treatment options are and to discuss the associated finances with it.

FDA considers many stem-cell treatments illegal

The FDA has not approved most stem-cell treatments and has said it considers many of them illegal. Miller and other officials at Lung Health Institute said they believe their treatment doesnt require FDA approval. Nevertheless, the company now plans to apply to the FDA for approval, said Marc Scheineson, the companys lawyer, even though this is a long, expensive and arduous process This action distinguishes LHI from the bulk of the other providers of stem cell and related blood-based therapies.

This article is based on documents obtained by The Washington Post, including internal memos, telephone scripts, emails and financial records. The Post also interviewed 14 former employees of the Lung Health Institute, including marketers, doctors, nurses and patient coordinators, whose job is to talk to potential customers. All were approached separately and spoke on the condition of anonymity; most said they were required to sign nondisclosure agreements and feared that the company would sue them for speaking out.

Their assertions were corroborated by The Post using documents and accounts from patients such as Garbutt and in some cases confirmed by the company itself.

A year and half after receiving treatments at the Lung Health Institute, Garbutts health has gotten worse. He can no longer shop or cook. He uses his monthly Social Security disability check to pay someone to make his meals.

Meanwhile, he is still struggling to pay off a $3,000 credit card bill from the procedure.

I maxed out my credit card to pay for the stem cells. I dont know how Ill pay it back, he said. Im just trying to take it one day at a time.

The story of Laser Spine and its Lung Health Institute offspring

The Lung Health Institute which operates clinics in Florida, Arizona, Texas, Tennessee and Pennsylvania and has treated, by its own count, more than 5,800 people began in many ways as the offspring of another company: the Laser Spine Institute.

Laser Spine was co-founded in 2005 by James St. Louis, an osteopath and orthopedic surgeon who offered a minimally invasive alternative to traditional neck and back surgery. As Laser Spine grew into a nationwide chain, with ubiquitous cable TV ads, it claimed to have a 98% patient satisfaction rate.

But the company was also the subject of dozens of malpractice lawsuits. In 2011, nine surgeons interviewed by Bloomberg Businessweek said many surgeries by Laser Spine were unnecessary or inappropriate. In response, Laser Spine officials at the time cited in-house surveys showing patient satisfaction. In 2014, a competitor sued Laser Spine, accusing it of using illegal marketing practices such as offering free airfare and hotels to persuade Medicare patients to sign up for procedures. Laser Spine officials denied the allegations in court, and the case has not been resolved.

This year, Laser Spine abruptly shuttered its business after banks froze its assets amid multiple lawsuits.

Laser Spines chief operating officer for some years was St. Louiss son, Jimmy St. Louis III. In 2011, the son left his fathers company and founded what would become the Lung Health Institute, using capital raised from some of his fathers investors, according to an early email to investors. Jimmy St. Louis also enlisted his dad as the Lung Health Institutes chief medical officer.

In an interview last year at its Tampa, Florida, headquarters, the younger St. Louis said he started the Lung Health Institute not to make money, but because he lost grandparents to lung disease.

There hasnt been any movement in this space really in 30 years, he said. Its an area of medicine thats been largely neglected.

A former employee who worked at Laser Spine and followed St. Louis to the Lung Health Institute before leaving the company for another job said, He took the Laser Spine business and marketing and made an exact carbon copy. The only thing we did different was swap out the product stem cells instead of spine surgery.

Lung clinics typical customer: elderly people with incurable disease

The Lung Health Institute developed a marketing profile of its typical customer: elderly patients suffering from incurable lung diseases who need supplemental oxygen and are not able to leave home easily and therefore spend hours online, said former employees.

Early on, the companys marketers bought ads on search engines such as Google and Bing so its website would appear prominently whenever anyone searched for cure and treatment for illnesses such as chronic obstructive pulmonary disease, said three former marketing team members.

They bought ads on solitaire and blackjack sites popular among older patients, the former marketers said, and if a city was hit by a snowstorm, they would quickly buy more search ads in that location, knowing patients on oxygen tanks would be homebound. And they targeted cities with direct flights to their clinic locations, knowing that patients on oxygen often struggled to travel with their equipment, former marketers said.

Patients who attended seminars held by the company said they were offered discounts if they put down a deposit on the spot.

In a statement, the company said its marketing strategy focuses on patient education and advocacy through several platforms, such as our website, online seminars.

The ads generated hundreds of leads each month as patients called, emailed or clicked for more information, internal budget documents show. Those in charge of converting the leads into sales were called patient coordinators.

Former coordinators said they were given a minimum quota of 10 sales each month. And as recently as last year, coordinators got paid only if they made a sale, working purely on commission, according to Miller, the companys COO. In recent months, the company has returned to the practice of giving coordinators a base salary in addition to their commission, Miller said. She disputed former coordinators assertions that they were given firm quotas, saying that like any healthy organization, we have to have projections.

According to a 2013 marketing script, if patients asked whether the treatments were approved by the Food and Drug Administration, coordinators were taught to respond: While the treatments are not FDA approved all of the drugs and equipment we use are FDA-approved.

If patients asked why insurance wouldnt cover the procedure, the script told coordinators to answer: I am sure that one day it will, however right now we want to provide treatment to those who want it.

If patients asked whether the treatments would work on them, coordinators were taught to point to a handful of patient testimonials.

Several patient coordinators said they were troubled by these calls. Some people wouldnt have that much money, and youre doing everything you can to convince them to use it on something youre not sure even works, said a woman who worked at the Lung Health Institute two years and left for another company after she said she became uncomfortable with the job. People would call afterward and say, I trusted you, but I dont feel any better. Some would call just to yell: I spent all this money, and you guys said this and that. You sold me fake medicine. Often Id need a drink by the end of the day.

Patients urged to beg, borrow, and crowdfund their treatment

When patients couldnt afford the procedure, the company frequently urged them to find other sources of money, according to its own website.

A November 2017 company blog post explained that some patients have turned to relatives for a loan or a gift, while others have held bake sales, garage/yard sales, walkathons, potlucks and raffles. The blog also suggested obtaining a fixed-term loan with monthly payments.

Crowdfunding was a frequent suggestion. A 2018 study found that more than 13,000 people had made donations for stem-cell treatment campaigns listed on two crowdfunding platforms as of December 2017.

Almost a third of all those campaigns were related to the Lung Health Institute. No one goes as far as they do in actively and explicitly pushing their patients to crowdfund and fundraise, said Leigh Turner, the studys co-author and a bioethicist at the University of Minnesota, who is serving as a pro bono expert witness in a lawsuit against the company.

Lung Health Institute COO Miller said, We dont track information as far as how many patients use fundraising efforts or financing efforts in order to come here.

GoFundMe has policies that prohibit fundraising for therapies considered illegal by a regulatory body. But last year, GoFundMes company blog included an upbeat post touting stem-cell treatments offered by for-profit clinics.

Patients can find a number of clinics that promise to relieve pain or help regain declining motor skills, all with a single stem-cell injection, the blog said. Hundreds of conditions fall under this umbrella, with promises of curing blood disorders like sickle cell anemia, to autoimmune diseases like multiple sclerosis.

After The Post asked about the blog post, GoFundMe took it down. The company said it also launched an audit of content on its website. But months later, the site continues to host thousands of campaigns raising money for stem-cell treatments, including more than a hundred that mention the Lung Health Institute by name.

Former patient Tammy Rivero, who is 62 and lives on an $800 monthly disability check, said in court testimony that a patient coordinator persuaded her to borrow against her home at the end of a dirt road in Hildebran, North Carolina.

Since receiving the treatment in 2015, however, Riveros illness has gotten much worse. Doctors say she now needs a double lung transplant to survive, which would be covered by Medicare and Medicaid. But Rivero doesnt have the money to rent an apartment near the transplant center for months of mandatory pre- and post-surgery rehabilitation. That would cost about $7,000, Rivero said the same amount she paid the Lung Health Institute.

Im going to pass away for $7,000, she said.

Rivero and another former patient have filed a lawsuit accusing the Lung Health Institute of deceptive marketing practices, and more than 30 other former patients or their representatives are seeking to join them in a proposed class-action lawsuit, said their lawyer, Ben Vinson. Among them is Tom Johnston, a Michigan man who recalls the excitement of his wife, Judy, upon seeing one of the companys online ads.

Tom Johnston, a retired pipe welder, said clinic staffers told his wife she would no longer need her oxygen tank after the procedure.

His wife died a year later, Johnston said, still haunted by the cost. She kept apologizing to me for spending our money. I said, We spent it together.

In court filings, the Lung Health Institute has denied the allegations of deceptive and unfair practices. In a statement the company pointed out that all patients sign an informed- consent form, which warns that the treatment might not improve their conditions.

As with any medicine, there are no guarantees, the company said.

No longer touting stem cells, its now platelet-rich plasma platelet-concentrate

The companys descriptions of its procedure have evolved over the years, but the basic premise has remained the same: extract blood from patients, spin it in a centrifuge to isolate stem cells or platelet-rich plasma platelet-concentrate, then reintroduce those using an IV into the patients bloodstream, where they naturally find their way to damaged parts of the lung and heal them.

Lung disease experts say there is no evidence such treatments work.

National medical groups including the American Lung Association and COPD Foundation have warned against such stem-cell treatments.

Miller said the Lung Health Institute has never been contacted by the FDA. She noted that its clinics have never had to report a serious adverse event. And she said that out of the 5,800 patients the company has treated in total, very few have filed lawsuits.

In 2016, the company self-published a white paper on its website that said almost 85% of patients say they experienced improvements in quality of life. Since then, the company has presented similar data in academic conference presentations and articles.

But unlike many medical studies, the Lung Health Institutes do not include a control group of patients who received a placebo. And all of its data, except for a one-page conference presentation, relied on follow-up phone surveys with patients rather than physical measurements, such as pulmonary function tests. The companys own researchers acknowledged the limitations of the data, concluding in one report: There is a very real possibility that response may simply be a placebo effect.

A stem-cell researcher, Arnold Caplan hired by the Lung Health Institute to testify in court as its expert said he found the data convincing.

The truth is, I dont exactly know how [the treatments] work, said Caplan, a biologist at Case Western Reserve University. But after seeing the phone surveys conducted by the company, he said, The important point for me is, there are clearly statistically relevant and positive outcomes from these treatments.

But three leading pulmonologists with no connection to the company or to any legal action said they found the data unconvincing and flawed, given its lack of comparative groups and placebo controls and other methodological problems.

Its borderline propaganda to suggest this information is evidence of efficacy, said Cosgrove, a pulmonologist at National Jewish Health in Denver, which runs one of the worlds largest interstitial lung disease programs.

The companys claims are a nothing, a come on, said Michael Matthay, a pulmonologist and stem-cell researcher at the University of California at San Francisco. Those statements are not supported by any medical data or medical studies.

There has never been a randomized trial for this treatments effect on lung diseases, said Marilyn Glassberg Csete, an expert in lung diseases and stem-cell therapies at the University of Miami. Theres no data.

Some patients said they felt better after the cellular procedures.

During a reporters visit to the Lung Health Institutes Tampa offices, company executives arranged interviews with two patients Larry Wood, 71, and Marie Hilton, 74 who said the treatment improved their breathing.

Before the infusion, Hilton said, I couldnt go grocery shopping I couldnt clean my house or vacuum without oxygen. She said she was able to stop using an oxygen tank after her $12,000 treatment last year.

Wood said he paid $6,500 for the procedure in 2014 after being offered a discount at a company seminar. I found within about three weeks I had improved lung function, he said. But the improvements only lasted about 10 months, he said, and he now pays $1,500 every three to four months for booster treatments.

Researchers said anecdotes like that are what make clinical trials so important. You want to rule out things like placebo effects, Cosgrove said. If you as a patient paid $10,000 for treatment, youre going to want it to work. You may even start taking care of yourself better to try to make it work. There are all sorts of factors that you need to control for.

Google cracks down and sales leads drop

The FDA has made clear that selling unapproved stem-cell therapies is illegal and won a recent lawsuit barring a prominent clinic from offering a treatment based on fat cells. After the FDA started cracking down on fat-based stem-cell treatments, the Lung Health Institute stopped selling them and focused on selling its blood-based treatments.

Company executives said they made the change not to avoid regulation, but because they felt the blood-based treatment was less invasive.

In summer 2017, Google suddenly stopped permitting the Lung Health Institute to buy search engine ads, a crucial source of sales leads, according to five former employees.

When asked by The Post about its actions related to Lung Health Institutes ads, Google declined to comment. In a statement, the company said: If we find ads that violate our policies, we take immediate action, which can include taking down violating ads or suspending an account altogether.

Lung Health Institute officials denied that they did anything wrong and said Google began to update its internal policy and rules for advertising related to regenerative medicine. Company officials said, [We] hold ourselves to the highest standards and will continue to evolve to stay within guidelines.

The result was a sharp drop in sales leads. They told us to start calling back every one of our old leads, to hand out discounts and offer booster treatments to past patients, one former coordinator said. We didnt know if we were going to survive.

Around the same time, the company changed its name. For years, it had been called the Lung Institute, but in 2017, the company inserted the word Health and moved to a new main website thelunghealthinstitute.com. Former employees said the rebranding solved some of the search engine and ad problems. Company officials said it was done to reflect expanded services.

In September of this year, Google announced a policy barring ads for unproven or experimental medical techniques such as most stem cell therapy. Google said it was taking the step after seeing a rise in bad actors attempting to take advantage of individuals by offering untested, deceptive treatments.

Amid growing scrutiny and regulation of stem-cell clinics, the Lung Health Institute made another change last year, removing all mention of stem cells from its website. The company now calls its procedure cellular therapy and platelet-rich plasma platelet-concentrate, or PRP-PC. Company officials said that their procedure hasnt changed, and that they still believe their treatment contains stem cells. They said their language change reflects how regenerative medicine has evolved.

The move, however, came after the FDA issued tougher regulations making clear most stem-cell therapies being sold are illegal and promising to crack down on bad actors.

Attorney Scheineson, a former top FDA official who now represents the Lung Health Institute, said in an interview that because the companys sole treatment now is PRP-PC, it isnt subject to stem-cell regulations and instead is governed by rules for blood banks.

FDA officials declined to talk about Lung Institute, but have said in recent months that their agency has struggled to regulate an industry that is rapidly expanding and morphing.

FDA officials said in general that PRP isnt covered by the same regulations as stem cells. But they also said that using a device such as a centrifuge to manufacture PRP for an unproven medical use such as treating COPD may still require review by the FDA. The FDA has never approved the use of a centrifuge for COPD, they said.

In addition, generally if a product is described as something that can treat a disease, then it is subject to much tougher regulation, according to FDA experts.

When you start saying it will improve COPD, thats an intended use that, from FDAs perspective, would require a higher degree of regulation, said Mark Schwartz, an attorney who served as deputy director in FDAs Office of Compliance and Biologics Quality between 2012 and 2015.

The company said it plans to begin the application process with the FDA for conducting a clinical trial and getting FDA approval needed for its stem-cell treatment. At the same time, the company said, it will keep selling its treatment even as it makes its FDA application.

Meanwhile, Lung Health Institute executives have made plans to expand. Late last year, the Lung Health Institute was acquired by Medovex, a medical technology products company run by former Laser Spine executive Bill Horne. In April, the company raised $7.2 million in new capital, and in recent weeks it raised another $6 million. Horne has said he plans to open more Lung Health Institute clinics.

In July, Medovex announced that it was changing its name to H-CYTE and had entered into a business partnership with a startup called Rion run by two researchers from the prestigious Mayo Clinic to develop a new proprietary cellular platform to treat COPD.

In news releases, the company said the two researchers Atta Behfar and Andre Terzic, who research regenerative medicine at Mayo had joined its board of directors.

When reached by phone, Behfar said he was unaware that patients have accused the Lung Health Institute of deceptive marketing and sued the company he was partnering with. To be perfectly frank, I dont have much awareness in regards to what Lung Health Institute has done, he said.

Behfar said the goal of the partnership is to test a new cellular treatment for COPD different from the one the Lung Health Institute currently sells using FDA-sanctioned clinical trials. The new treatment will not be sold to patients until its proved effective by rigorous science, Behfar said.

Contrary to the news releases, however, the two Mayo researchers never agreed to serve on the board of directors, according to Behfar and Rions chief administrative officer, Mike Pfenning. Weve asked them to issue a retraction to correct that, Pfenning said. They just agreed to serve in an unpaid advisory role.

In an interview this fall, Miller chief operating officer for H-CYTE and the Lung Health Institute insisted that Terzic and Behfar were indeed members of her companys board of directors. But in a news release this month, the company said the two doctors had resigned from the board of directors and instead become scientific advisers.

Miller said the company hopes to sell the new treatment it is developing initially to COPD patients. But they plan to expand that business model and sell it eventually to many more patients suffering from a whole range intractable diseases.

Read this article:
Clinic pitches unproven treatments to desperate patients, with tips on raising the cash - Seattle Times

Posted in North Carolina Stem Cells | Comments Off on Clinic pitches unproven treatments to desperate patients, with tips on raising the cash – Seattle Times

Next level giving: A piece of your heart can literally save lives – NWAOnline

Posted: December 6, 2019 at 8:48 am

Many of us look for ways to give back during the holidays as a chance to demonstrate gratitude for what we have by helping others who might not be so fortunate. Northwest Arkansas is chock full of wonderful nonprofit organizations that can always use a helping hand, but if you're looking for a way to kick your giving up a notch, consider these three organizations for a chance to -- literally -- give a piece of yourself to save someone else's life.

Community Blood Center of the Ozarks

3503 S. Thompson, Springdale, (479) 927-1200

1400 SE Walton Blvd., Bentonville, (479) 464-2506

"There are 12 hospitals in Northwest Arkansas that use blood that comes from our center and nowhere else," says Community Blood Center of the Ozarks Marketing Manager Chris Pilgrim. "And over 40 hospitals from southwest Missouri and Northwest Arkansas, combined."

Donating blood is one of the easiest ways to save someone's life, says Pilgrim, but only a small percentage of the population actively participates. Out of the 37% of Americans who are eligible, only 10% actually give.

"You would think that a fear of needles would be the No. 1 reason people don't give blood -- and while that's pretty significant, it's not the biggest reason," he says. "The biggest is just that people have never been asked. It's kind of something that goes on in the background. It takes a conscious decision for 200 people a day to donate blood and keep things going here."

If aversion to needles is your issue, fear not, says Pilgrim.

"If you're scared of needles, it doesn't hurt very much -- it's a slight sting, and the needle is in your arm for maybe 10 minutes," he says. "When you're finished with your donation, you walk out. It's that easy. It doesn't take much time or any money, but it has a real impact on someone's life. That's the biggest gift you can give, when you save lives."

And each donation, says Pilgrim, saves multiple lives.

"We used to say that one donation could save three lives, because we divided it up into red blood cells, platelets and plasma, but your blood donation could get divided up and go with lots of people -- the more you give, the more you multiply."

While all blood donations are valued in order to keep the area hospitals fully stocked, Pilgrim says that some blood types are a lot more in demand than others.

"There are a couple of specific blood products that we look for," says Pilgrim. "First of all, when you're talking about red blood cells, O Negative is a universal type. Even though only 6% of the population is Type O Negative, it's used more than its fair share in trauma cases when you can't readily type a victim. The other universal is AB plasma -- it can be given to anybody."

You can give blood at any of the center's locations -- there are also two Missouri locations -- and it's suggested that you first make an appointment online to expedite your visit. Pilgrim says the bulk of the donations, however, are collected at blood drives.

"The vast majority of the blood we collect comes from places where we take our show on the road -- churches, schools, businesses," he explains. "If you have a business that wants to hold a blood drive, please give us a call. We can take you through the steps and help make it as painless and rewarding as possible."

Project Zero

theprojectzero.org

Tiphanie Gurwell, Northwest Arkansas outreach coordinator for the nonprofit organization Project Zero, says there are hundreds of children in Arkansas who are waiting to be adopted -- and it's her organization's goal to find each and every one of those children a home. Project Zero, according to its mission statement, will "diligently and enthusiastically promote adoption through the foster care system with the ultimate goal of finding a forever family for every child that is waiting."

Project Zero works specifically with a group of children who might be harder to place, says Gurwell.

"A lot of these kids are part of a sibling group, or they have special needs, or they're teenagers," she says. "So they're what we would consider the harder-to-place kids. When most people go into adoption, they want younger kids; that number doesn't take into consideration the kids that are having their parental rights terminated but are getting adopted quickly. We generally don't advocate for a child under the age of 5 unless they're in a sibling group or have a special need."

Gurwell says one of the ways the organization seeks to connect potential adoptive parents with children are its private events where children and adults mix and mingle and get to know each other, like the one coming up in Little Rock.

"Seventy-nine percent of the kids [in state care] will attend this event," says Gurwell. "They'll come and get Christmas presents and play fun games, all while interacting with families who are looking to adopt. They may connect in a way they don't just by looking at a photo on the internet. It's kind of a game changer, because you get that one opportunity, and it's no longer just a picture or a number -- you get to meet with and talk to the child."

Even one visit to the organization's website is enough to personalize its mission: It maintains a "Heart Gallery," a collection of pictures, biographies and, sometimes, videos of the children for whom they're advocating. The photos show smiling, hopeful faces, and the biographies are heartbreakingly forthright about the trauma the child might have endured and the special needs that resulted. But they also give insight into each child's particular personality and their hopes and dreams for their futures.

"I really didn't have a family in my past, and I would like to start over and build a new life in a new family that loves me, and I love them, and that cares about me and loves me and understands what I've been going through," says Andreka, a teenager, in a short video. Though the teenagers in the Heart Gallery may be aging out of the system soon, their need for a permanent placement is still great, says Gurwell.

"Typically, the kids that age out of foster care don't end up doing the best," explains Gurwell. "If you grew up your whole life, and no one ever taught you how to budget, how to pay a bill, how to apply for a loan, how to apply for college -- what ends up happening is that, at the age of 18 or 21, they age out with very little knowledge. [The Division of Children and Family Services] does the best they can do, given their resources, but when you get out in the real world, and you're working a minimum wage job, you're trying to go to college and there's no one to ask for help? The statistics show they're likely to end up in the same situation that they were removed from. A lot of them will end up in jail or homeless.

"I think it's important for people to get these kind of negative stereotypes out of their head -- like, they're going to come into my house angry, or they don't want to be adopted. There are a million different excuses people have when talking about teens, but I've had the opportunity to meet a lot of our teens, and they do want to be adopted. They want to be loved. Even if it's a short period -- let's say you adopt at 16 or 17 years old. Those two years can be a game changer. They've got someone to come home to. It may be a minimum time in your home, but it's a lifetime commitment to that child."

Gurwell says there's no one profile of a family that would make good adoptive parents.

"Every child has a different story," she says. "Some kids need a single mother because of their trauma. Some kids need a two-parent family or need to be the only child or youngest child in the home. Each case is so unique. I would say the only thing we wish for in our families is, obviously, that they be able to support the child financially without government assistance. From our organization's perspective, we want families who are open-minded, we want families who aren't going to come in and say, 'I want a kid 5 and under.' We want families who say, 'We are called to do this, but we don't know what it looks like, so let's just roll with it and see what happens.' I think sometimes when we put barriers up of what we don't want, it limits the connections you might make with someone you might not even think about looking at -- but then you meet a child, and it's a game changer."

For those interested in exploring the possibilities of adoption, the Project Zero website is a great place to start and can explain what the next steps in the process would be.

Be the Match

Bethematch.org

(800) MARROW-2

When Bill Brashear got the news that his son was diagnosed with acute lymphoblastic leukemia, it was a shock: His son was a healthy young man in the prime of his life who had never experienced previous health issues.

"It was gut wrenching," he says. "It was horrible. But the wonderful thing that came out of it was [our knowledge of] Be the Match."

Early on in his treatment, Brashear's son needed a blood stem cell transplant; fortunately, a match was found within his family. But when he needed another one later on, the family turned to the international donor database Be the Match.

"They did a search for [my son's] DNA makeup and didn't find a match in anyone in the United States but found a young man in Germany," says Brashear. "They harvested this person's blood cells in Germany, a courier was there, got the blood cells that he had donated, flew back to the United States, and the next day, they were infused in [my son]."

Clifford Ackerman now works with the organization as a patient and lead liaison, but his first introduction to Be the Match was as a patient when he was diagnosed with non-Hodgkin's lymphoma.

"I had two sisters and a fraternal twin, and nobody matched me," he says. "I found a match through Be the Match, and now I have a blood brother who saved my life by joining the registry eight years before to help someone in his community. We just celebrated Thanksgiving -- if you want to show how thankful you are for what you have, this is a wonderful way."

Be the Match collects donations in three areas: peripheral blood stem cells (PBSC), marrow and umbilical cord blood. These donations can be used to help treat 70 different blood diseases and cancers. Be the Match facilitated nearly 6,200 transplants in 2018. But with nearly 70 percent of patients requiring transplants outside their friends and family group, new donors are always needed.

"It's very similar to donating plasma platelets," Ackerman explains of the outpatient process, which is open to donors ages 18 to 44. "Nothing is completely painless -- there's always a small discomfort to save a life. With this process, it's either a bit of achiness before or after the process. It's not like what you see on Grey's Anatomy or ER or House -- you don't feel pain or discomfort during, but maybe some achiness afterward."

Most matches are found by people who match the patient's ethnic background, and the likelihood of a patient finding a match in the system ranges from 77% for white patients, 57% for American Indian and Alaska Native patients, 46% for Hispanic or Latino patients, 41% for Asian or Pacific Islander patients and 23% for African-American patients.

The entire process, from the initial medical exam to determine eligibility through the donation procedure, usually takes around 30 hours, says Ackerman, and is entirely free for the donor -- it's either paid for by the patient's insurance or by Be the Match.

"We pay for the travel, the meals and even for one companion," says Ackerman. "Even tolls, mileage, day care -- even pet care. If they come up to us and say, 'Hey, I started a new job or ran out of paid time off', we'll even cover their wages."

Ackerman says a young man named Blee, a 2014 graduate from Pulaski Academy in Little Rock, is currently looking for a matching donor to help treat his aplastic anemia. To start the process to see if you're a match for Belee -- or another patient currently waiting on a donor -- scan the QR code pictured with this story or text NWADG4aCure to 61474. Ackerman says the initial screening is simple and fast, and a swab kit can be mailed to your home address quickly.

"Be the Match is such a big deal," says Brashear. "It saved [my son's] life, and it's saved other people's lives, but we don't hear enough about it. That's why I'm shouting from the rooftops and ringing the bells and whatever else to get the word out -- because it might save somebody's life, for sure."

Courtesy Photo The Heart Gallery on the Project Zero website is a great place to find out more information about the children in the foster care system who are seeking permanent homes in Arkansas -- like Jawaun.

Courtesy Photo The Heart Gallery on the Project Zero website is a great place to find out more information about the children in the foster care system who are seeking permanent homes in Arkansas -- like Jawaun.

NWA Democrat-Gazette/CHARLIE KAIJO Community Blood Center of the Ozarks' Chris Pilgrim says the majority of the blood donations the organization collects come from community-organized blood drives like this one at Rogers High School in November. Contact the CBCO if or your organization would like to host a blood drive.

NAN Our Town on 12/05/2019

Read more:
Next level giving: A piece of your heart can literally save lives - NWAOnline

Posted in Alaska Stem Cells | Comments Off on Next level giving: A piece of your heart can literally save lives – NWAOnline

A premier meeting and a medical marvel; In-The-News for Dec. 2 – Alaska Highway News

Posted: December 6, 2019 at 8:48 am

In-The-News is a roundup of stories from The Canadian Press designed to kickstart your day. Here is what's on the radar of our editors for the morning of Dec. 2.

What we are watching in Canada ...

MISSISSAUGA, Ont. Canada's premiers are meeting today just outside Toronto for the first time as a group since the federal election.

The campaign laid bare some regional divisions, and the premiers of Saskatchewan and Alberta where the Liberals won no seats have been especially vocal about their asks from Ottawa.

Saskatchewan's Scott Moe and Alberta's Jason Kenney want Prime Minister Justin Trudeau to change the equalization formula, but there is unlikely to be consensus on that around the premiers' table.

Moe, who is chair of the Council of the Federation, says all of the premiers will come to the meeting with various priorities and differing opinions, but the goal is to find a few issues on which they have common ground.

Ontario Premier Doug Ford says health care is a concern for everyone, and that all premiers want a 5.2 per cent annual increase to the Canada Health Transfer.

Climate policy will be another tough area to get all parties on side. Ontario, Saskatchewan, Alberta and Manitoba have all launched legal challenges against the federal carbon price, while others have accepted it or launched their own programs.

---

Also this ...

A hockey player paralyzed in the Humboldt Broncos bus crash says he's thrilled with the progress he's made since receiving spinal surgery in Thailand a month ago.

Doctors implanted an epidural stimulator in Ryan Straschnitzki's spine and one week later injected stem cells above and below the injury to try to reverse some of the damage.

The 20-year-old has just a week to go before returning home to Airdrie, Alberta.

Straschnitzki, paralyzed from the chest down, says he's been able to straighten his legs and walk with the use of a wheeled machine.

He says the experience has left him at a loss for words, shocked and excited all at the same time.

Straschnitzki, who's hoping to make the Canadian sledge hockey team, took his sled with him to Thailand and has been sitting in it as part of his rehab.

He has finally been cleared by doctors and is to get some ice time in Bangkok later this week.

---

ICYMI (in case you missed it) ...

WHITEHORSE, Yukon Canada is getting its first Arctic university.

This past week, the Yukon legislature passed a bill to make Yukon College a university. It will be an institution with an Indigenous flavour that will make it as unique as the region it is to serve.

"Everybody knows we're moving toward something big and something special," said Tom Ullyett, chairman of the board of governors.

The idea of a northern university has been kicked around since at least 2007 when a survey in all three territories found residents wanted more influence over Arctic research. Northern First Nations have been asking for one for 50 years.

Nunavut and the Northwest Territories have colleges that teach courses toward degrees from southern institutions and have announced plans to broaden their post-secondary offerings.

Yukon College has done the same in science, education and social work and also offers courses towards bachelor's degrees in Indigenous governance and business administration.

Once the college is transformed, it will become the first institution in the territories to grant a degree under its own name. Diplomas the first graduates of the governance program get next spring will read "Yukon University."

The institution, which will also offer trades programs, will allow northerners to further their education closer to home.

---

What we are watching in the U.S. ...

NEW YORK A wave of new laws in 15 states that allow people to make claims of sexual abuse going back decades could bring a deluge of lawsuits against the Roman Catholic Church that could surpass anything seen so far in its clergy abuse crisis.

Associated Press interviews with attorneys and clergy abuse watchdog groups found it could result in at least 5,000 new cases against the church and more than $4 billion in payouts.

It's a financial reckoning playing out in such Catholic strongholds as New York, California and New Jersey, among eight states that go the furthest with "lookback windows" allowing sex abuse claims no matter how old.

Catholic leaders worry about the difficulty of defending such old cases, and more dioceses are considering bankruptcy and victim compensation funds.

---

What we are watching in the rest of the world ...

MADRID Delegates from almost 200 countries have begun a two-week international climate conference in Madrid that seeks to step up efforts to stop global warming.

U.N. Secretary-General Antonio Guterres is warning that the efforts so far are insufficient to overcome the "point of no return" in climate change.

"What is lacking is political will," Guterres told reporters on the eve of the COP25 meeting, which opened today.

The summit, which moved to the Spanish capital after Chile had to pull out amid anti-government protests, aims to put the finishing touches to the rules governing the 2015 Paris accord.

That involves creating a functioning international emissions-trading system and compensating poor countries for losses they suffer from rising sea levels and other consequences of climate change.

---

This report by The Canadian Press was first published on Dec. 2, 2019.

See the original post:
A premier meeting and a medical marvel; In-The-News for Dec. 2 - Alaska Highway News

Posted in Alaska Stem Cells | Comments Off on A premier meeting and a medical marvel; In-The-News for Dec. 2 – Alaska Highway News

Find the Best Stem Cell Clinics in Wyoming – Stem Cell …

Posted: December 6, 2019 at 8:47 am

Long Business Description:

Welcome to Wyoming Stem Cell Therapy!Dr. Todd Beckstead is a surgeon in Casper, Wyoming and is affiliated with Wyoming Medical Center. He received his medical degree from the University of Utah School of Medicine and has been a practicing surgeon for 15 years. Dr. Todd specializes in Stem Cell and PRP Injection Therapy. The Mesenchymal stem cells are isolated from your own fatty tissue. These cells have the potential to become: Bone, Cartilage, Tendon, Muscle, Blood Vessels & Nerve Tissue cells and can replace lost or damaged tissue. This treatment can be used to help:

Shoulder PainKnee PainHip PainAnkle PainNeck and Back PainOsteoarthritis

We also offer out-of-town phone consultations!About Dr. BecksteadDr. Beckstead grew up in Wyoming and attended Glenrock High School. He received his training as a paramedic at Weber State University and worked as a paramedic for 8 years. He graduated from the University of Utah with a degree in Biochemistry. Dr. Beckstead attended medical school at the University of Utah and then completed his General Surgery Residency at the Phoenix Integrated Residency Program in 1999. During his General Surgery Residency, he received extra training in vascular surgery. Dr. Beckstead, along with his wife, daughter and two sons moved to Casper, Wyoming in 1999. He states that his goal has always been to return to Wyoming to practice surgery and to raise his children. Dr. Beckstead is board certified in General Surgery and has been practicing with our group since 1999.

Read the original post:
Find the Best Stem Cell Clinics in Wyoming - Stem Cell ...

Posted in Wyoming Stem Cells | Comments Off on Find the Best Stem Cell Clinics in Wyoming – Stem Cell …

Page 1,258«..1020..1,2571,2581,2591,260..1,2701,280..»