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IMAC Holdings Receives FDA Authorization to Initiate Clinical Study of Its Umbilical Cord-Derived Allogenic Mesenchymal Stem Cells for the Treatment…

August 05, 2020 11:58 ET | Source: IMAC Holdings, Inc.

BRENTWOOD, Tenn., Aug. 05, 2020 (GLOBE NEWSWIRE) -- IMAC Holdings, Inc. (Nasdaq: IMAC) (the Company or IMAC), a provider of innovative medical advancements and care specializing in regenerative rehabilitation orthopedic treatments without the use of surgery or opioids, today announced the United States Food and Drug Administration (the FDA) approved its investigational new drug application, which IMAC submitted in May 2020, for the use of umbilical cord-derived allogenic mesenchymal stem cells for the treatment of bradykinesia, or the gradual loss and slowing down of spontaneous body movement, due to Parkinsons disease.

The Company will now initiate enrollment of 15 patients for its Phase 1 trial to evaluate the safety and tolerability of the stem cell product acquired from technology developed by a major research university to treat patients with Bradykinesia due to Parkinsons utilizing intravenous administration of Whartons jelly-derived mesenchymal stem cells. The Company believes that the causes of bradykinesia may be related to an inflammatory response in the body. The Companys new study is designed to confirm this belief and support the Companys long-term strategy for the use of regenerative medicine in combination with physical rehabilitation to reduce the effect of movement-restricting diseases.

Our regenerative rehabilitation centers have long focused on the importance of finding and applying non-opioid, non-surgical solutions to physical ailments in orthopedics. In 2017, our neurosurgeon researched opportunities to apply stem cells to treating Parkinsons, and we put a team together to design a treatment for our neurological patients that simply could not achieve maximum benefit from physical therapy alone, commented Jeffrey Ervin, IMACs Chief Executive Officer. Having received approval to proceed with our study, IMAC is extremely optimistic regarding the potential of this stem cell technology. This has the potential to not only expand proprietary service options for neurological patients, but also advance the way physically debilitating inflammatory conditions are managed as a whole. We would like to thank the FDA for the collaborative process and the partners who helped us achieve this milestone, including patient advocate, Doug Oliver and his team at Regenerative Outcomes.

The Phase 1 trial will consist of three treatment protocols: five patients with bradykinesia due to Parkinsons will receive a low dose intravenous infusion of stem cells, five patients will receive a medium dose intravenous infusion of stem cells and five patients will receive a high dose intravenous infusion of stem cells. The Phase 1 trial will be conducted over 12 months to determine the incidence and extent of adverse events, although the Company will also investigate the efficacy of its stem cell treatment. More information on the clinical trial, including patient criteria, can be found on clinicaltrials.gov.

IMAC will enroll participants from its existing clinics in Illinois, Tennessee, Kentucky and Missouri in its Phase 1 trial. Prospective enrollees may email fdatrial@imacregeneration.com to be considered for the trial. IMACs medical doctors and physical therapists have been trained to administer the treatment and manage the therapy for the clinical trial, which is anticipated to begin in 30 days.

About IMAC Holdings, Inc.

IMAC Holdings was created in March 2015 to expand on the footprint of the original IMAC Regeneration Center, which opened in Kentucky in August 2000. IMAC Regeneration Centers combine life science advancements with traditional medical care for movement restricting diseases and conditions. IMAC owns or manages 16 outpatient clinics that provide regenerative, orthopedic and minimally invasive procedures and therapies. It has partnered with several active and former professional athletes, opening six Ozzie Smith IMAC Regeneration Centers, two David Price IMAC Regeneration Centers, as well as Mike Ditka IMAC Regeneration Centers and a Tony Delk IMAC Regeneration Center. IMACs outpatient medical clinics emphasize its focus around treating sports and orthopedic injuries and movement-restricting diseases without surgery or opioids. More information about IMAC Holdings, Inc. is available at http://www.imacregeneration.com.

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Safe Harbor Statement

This press release contains forward-looking statements. These forward-looking statements, and terms such as anticipate, expect, believe, may, will, should or other comparable terms, are based largely on IMAC's expectations and are subject to a number of risks and uncertainties, certain of which are beyond IMAC's control. Actual results could differ materially from these forward-looking statements as a result of, among other factors, risks and uncertainties associated with its ability to raise additional funding, its ability to maintain and grow its business, variability of operating results, its ability to maintain and enhance its brand, its development and introduction of new products and services, the successful integration of acquired companies, technologies and assets, marketing and other business development initiatives, competition in the industry, general government regulation, economic conditions, dependence on key personnel, the ability to attract, hire and retain personnel who possess the skills and experience necessary to meet customers requirements, and its ability to protect its intellectual property. IMAC encourages you to review other factors that may affect its future results in its registration statement and in its other filings with the Securities and Exchange Commission. In light of these risks and uncertainties, there can be no assurance that the forward-looking information contained in this press release will in fact occur.

IMAC Press Contact: Laura Fristoe lfristoe@imacrc.com

IMAC Investor Contact: Bret Shapiro (516) 222-2560 brets@coreir.com

Source: IMAC Holdings, Inc.

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IMAC Holdings Receives FDA Authorization to Initiate Clinical Study of Its Umbilical Cord-Derived Allogenic Mesenchymal Stem Cells for the Treatment...

Hematopoietic Stem Cell Transplantation (HSCT) Market 2020: Regen Biopharma Inc, China Cord Blood Corp, CBR Systems Inc, Escape Therapeutics Inc,…

The latest report published by Regal Intelligence on Hematopoietic Stem Cell Transplantation (HSCT) market provides crucial market insights along with detailed segmentation analysis. The report examines key driving factors that are expected to drive the growth of the market.

Global Hematopoietic Stem Cell Transplantation (HSCT) Market Research Report gives knowledgeable information on various market situations, for example, potential development factors, factors controlling the development, market opportunities and dangers to the worldwide market. Also, the report broadly centers around competitive analysis of Hematopoietic Stem Cell Transplantation (HSCT) Market. The competitive analysis segment incorporates key manufacturers, fresh players, providers, market strategies, potential chances, operation landscape and analysis of the trends of the Hematopoietic Stem Cell Transplantation (HSCT) market. The market results are centered around current market scenario. To gauge and predict the degree of competition in this market. This report will likewise support all the manufacturers and speculators to have a superior comprehension of the investments to know where the market is heading.

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Leading players of Hematopoietic Stem Cell Transplantation (HSCT) including: Regen Biopharma Inc, China Cord Blood Corp, CBR Systems Inc, Escape Therapeutics Inc, Cryo-Save AG, Lonza Group Ltd, Pluristem Therapeutics Inc, ViaCord Inc

For Product type segment the report listed main product type:

Allogeneic Autologous

For Application segment the report listed main types:

Peripheral Blood Stem Cells Transplant (PBSCT) Bone Marrow Transplant (BMT) Cord Blood Transplant (CBT)

Key Highlights of the Hematopoietic Stem Cell Transplantation (HSCT) Market

Key Strategies adopted by major players Global driving factors of the market Developed and emerging markets Comprehensive description of the international players Market dynamic factors affecting the global market Evaluation of niche business areas Driving and restraining factors of the market growth Market share analysis

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Hematopoietic Stem Cell Transplantation (HSCT) Market 2020: Regen Biopharma Inc, China Cord Blood Corp, CBR Systems Inc, Escape Therapeutics Inc,...

In Depth Analysis and Survey of COVID-19 Pandemic Impact on Global Precision Cancer Therapies Market Report 2020 Key Players Abbott Laboratories,…

Report is a detailed study of the Precision Cancer Therapies market, which covers all the essential information required by a new market entrant as well as the existing players to gain a deeper understanding of the market.The primary objective of this research report named Precision Cancer Therapies market is to help making reliable strategic decisions regarding the opportunities in Precision Cancer Therapies market. It offers business accounts, industry investors, and industry segments with consequential insights enhancing decision making ability.nicolas.shaw@cognitivemarketresearch.com or call us on +1-312-376-8303.

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Global and Regional Precision Cancer Therapies Market Segmentation by Type: Hormone Therapy, Immunotherapies, Targeted Therapy, Monoclonal Antibody Therapy, Gene Therapy

Global Precision Cancer Therapies Market Segmentation by Applications: Hospitals, Diagnostic Centers, Oncology Clinics, Research Institutes

Major Market Players with an in-depth analysis: Abbott Laboratories, Bayer HealthCare, GlaxoSmithKline, OncoGenex Pharmaceuticals, Hospira, Boehringer Ingelheim, AstraZeneca, Aveo Pharmaceuticals

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The Precision Cancer Therapies market report offers the current state of the market around the world. The report starts with the market outline and key components of the Precision Cancer Therapies market which assumes a significant job for clients to settle on the business choice. It additionally offers the key focuses to upgrade the development in the Precision Cancer Therapies market. Some fundamental ideas are likewise secured by reports, for example, item definition, its application, industry esteem chain structure and division which help the client to break down the market without any problem. Also, the report covers different factors, for example, arrangements, efficient and innovative which are affecting the Precision Cancer Therapies business and market elements.

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The research comprises primary information about the products. Similarly, it includes supply-demand statistics, and segments that constrain the growth of an industry. It also includes raw materials used and manufacturing process of Precision Cancer Therapies market. Additionally, report provides market drivers and challenges & opportunities for overall market in the particular provincial sections.

Competitive Analysis has been done to understand overall market which will be helpful to take decisions. Major players involved in the manufacture of Precision Cancer Therapies product has been completely profiled along with their SWOT. Some of the key players include Abbott Laboratories, Bayer HealthCare, GlaxoSmithKline, OncoGenex Pharmaceuticals, Hospira, Boehringer Ingelheim, AstraZeneca, Aveo Pharmaceuticals. It helps in understanding their strategy and activities. Business strategy described for every company helps to get idea about the current trends of company. The industry intelligence study of the Precision Cancer Therapies market covers the estimation size of the market each in phrases of value (Mn/Bn USD) and volume (tons). Report involves detailed chapter on COVID 19 and its impact on this market. Additionally, it involves changing consumer behavior due to outbreak of COVID 19.

Further, report consists of Porters Five Forces and BCG matrix as well as product life cycle to help you in taking wise decisions. Additionally, this report covers the inside and out factual examination and the market elements and requests which give an entire situation of the business.

Regional Analysis for Precision Cancer Therapies North America (United States, Canada) Europe (Germany, Spain, France, UK, Russia, and Italy) Asia-Pacific (China, Japan, India, Australia, and South Korea) Latin America (Brazil, Mexico, etc.) The Middle East and Africa (GCC and South Africa)

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Chapters Define in TOC (Table of Content) of the Report: Chapter 1: Market Overview, Drivers, Restraints and Opportunities, Segmentation Overview Chapter 2: COVID Impact Chapter 3: Market Competition by Manufacturers Chapter 4: Production by Regions Chapter 5: Consumption by Regions Chapter 6: Production, By Types, Revenue and Market share by Types Chapter 7: Consumption, By Applications, Market share (%) and Growth Rate by Applications Chapter 8: Complete profiling and analysis of Manufacturers Chapter 9: Manufacturing cost analysis, Raw materials analysis, Region-wise Manufacturing expenses Chapter 10: Industrial Chain, Sourcing Strategy and Downstream Buyers Chapter 11: Marketing Strategy Analysis, Distributors/Traders Chapter 12: Market Effect Factors Analysis Chapter 13: Market Forecast Chapter 14: Precision Cancer Therapies Research Findings and Conclusion, Appendix, methodology and data source To check the complete Table of Content click here: @ https://cognitivemarketresearch.com/medical-devicesconsumables/precision-cancer-therapies-market-report#table_of_contents

The qualitative contents for geographical analysis will cover market trends in each region and country which includes highlights of the key players operating in the respective region/country, PEST analysis of each region which includes political, economic, social and technological factors influencing the growth of the market. The research report includes specific segments by Type and by Application. This study provides information about the sales and revenue during the historic and forecasted period of 2015 to 2027.

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In Depth Analysis and Survey of COVID-19 Pandemic Impact on Global Precision Cancer Therapies Market Report 2020 Key Players Abbott Laboratories,...

Celularity announces the activation of first California Clinical Trial Site following CIRM Grant Award to Advance Treatments for COVID-19 – PRNewswire

FLORHAM PARK, N.J., Aug. 5, 2020 /PRNewswire/ --Celularity today announced that it has been awarded a $750,000 COVID-19 Project grant by the California Institute for Regenerative Medicine (CIRM), one of the three clinical awards targeting the coronavirus. This grant will support California Institutions participating in the Phase I/II clinical trial of human placental hematopoietic stem cell derived natural killer (NK) cells (CYNK-001) for the treatment of adults with COVID-19.The University of California Irvine is the first CA site to open for patient enrollment.

CIRM's COVID-19 Project supports promising discovery, preclinical and clinical trial stage projects that could quickly advance treatments or vaccines that utilize stem and/or progenitor cells. Celularity will use the CIRM grant to support the evaluation of the anti-viral activities of its cryopreserved investigational product, CYNK-001, in underserved and disproportionately affected populations with COVID-19, an infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Celularity received clearance from the United States Food and Drug Administration to proceed with a Phase I/II study to evaluate the safety, tolerability, and efficacy of CYNK-001 in patients with COVID-19.

"Our investigational product CYNK-001 showed great promise in preclinical studies, and we are optimistic that it will prove effective against corona virus diseases, including COVID-19. As part of our rapidly-scalable placental-derived cellular medicine platform, CYNK-001 could play an important role in the public health response to outbreaks of COVID-19 or other coronaviruses," said Robert J. Hariri, MD, PhD, Founder, Chairman and CEO of Celularity. "We are very grateful to CIRM for supporting our effort to make novel cellular medicines available to medically underserved and disproportionately affected persons in California."

Xiaokui Zhang, PhD, Chief Scientific Officer and Principal Investigator under the CIRM grant says "CYNK-001 has a range of biological activities that not only recognize and destroy virus-infected cells, but also coordinate a robust immune response that may lead to an effective and durable defense against the viral infection."

The trial will evaluate the safety and the clinical efficacy of CYNK-001 in SARS-CoV-2 positive subjects as measured by clearance of the SARS-CoV-2 and improvement in clinical symptoms or improvement in radiological evaluation of disease related chest x-ray. The primary objective of the Phase I portion of the study is to evaluate the safety, tolerability, and efficacy of multiple CYNK-001 intravenous (IV) infusions in COVID-19 patients and will be administered to up to 14 patients in three doses over the course of seven days.

The Phase II portion of the study is a randomized, open-label, multi-site study measuring multiple doses of CYNK-001 against a control group experiencing a similar degree of infection with best supportive care, with two co-primary endpoints. The first co-primary endpoint is to determine the virologic efficacy of CYNK-001 in facilitating the clearance of SARS-CoV-2 from mucosal specimens and/or peripheral blood. The second co-primary endpoint is to assess the impact of treatment with CYNK-001 on clinical symptoms among patients with COVID-19 related lower respiratory tract infection.

Celularity has treated patients with severe COVID-19 and on ventilator support under compassionate use programs in U.S. CYNK-001 was well tolerated and may be associated with clinical benefit in selected cases.

About NK CellsNK cells are innate immune cells with an important role in early host response against various pathogens. Multiple NK cell receptors are involved in the recognition of infected cells. Studies in humans and mice have established that there is robust activation of NK cells during viral infection, regardless of the virus class, and that the depletion of NK cells aggravates viral pathogenesis.

About CYNK-001CYNK-001 is the only cryopreserved allogeneic, off-the-shelf NK cell therapy developed from placental hematopoietic stem cells. CYNK-001 is being investigated as a potential treatment option in adults with COVID-19, as well as for various hematologic cancers and solid tumors. NK cells are a unique class of immune cells, innately capable of targeting cancer cells and interacting with adaptive immunity. CYNK-001 cells derived from the placenta are currently being investigated as a treatment for acute myeloid leukemia (AML), multiple myeloma (MM), and glioblastoma multiforme (GBM). On 1 April, the U.S. Food and Drug Administration cleared the Company's Investigational New Drug (IND) application for the use of CYNK-001 in adults with COVID-19.

About COVID-19The virus causing COVID-19 is called severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and is a novel coronavirus that has not been previously identified. COVID-19 has become a global pandemic, with over 4.2 million confirmed cases in the USA and over 650,000 deaths reported to date worldwide.

About Celularity Celularity, headquartered in Florham Park, N.J., is a next-generation Biotechnology company leading the next evolution in cellular medicine by delivering off-the-shelf allogeneic cellular therapies, at unparalleled scale, quality, and economics. Celularity's innovative approach to cell therapy harnesses the unique therapeutic potential locked within the cells of the post partum placenta. Through nature's immunotherapy engine the placenta Celularity is leading the next evolution of cellular medicine with placental-derived T cells, NK cells, and pluripotent stem cells to target unmet and underserved clinical needs in cancer, infectious and degenerative diseases. To learn more visit celularity.com

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Celularity announces the activation of first California Clinical Trial Site following CIRM Grant Award to Advance Treatments for COVID-19 - PRNewswire

Progenitor Cell-Based Market 2020-2026 is Slated to Witness Tremendous Growth || Leading Players BAXTER INTERNATIONAL INC, Boehringer Ingelheim…

In Progenitor Cell-Based Market report, a systematic investment analysis has been performed which forecasts impending opportunities for the market players. The statistical and numerical data that has been included in this market report is represented with the tables, graphs and charts which eases the understanding of facts and figures. A proficient data and excellent forecasting techniques used in this report are synonymous with accurateness and correctness. Progenitor Cell-Based Market report is a painstaking analysis of existing scenario of the market which covers several market dynamics. The market study of this global Progenitor Cell-Based Market business report takes into consideration market attractiveness analysis where each segment is benchmarked based on its market size, growth rate & general attractiveness.

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Global progenitor cell-based marketis estimated to register a substantial CAGR in the forecast period of 2019 to 2026. The imminent market report contains data for historic year 2017, the base year of calculation is 2018 and the forecast period is 2019 to 2026. The growth of the market can be attributed to the rising geriatric population.

Some of the major companies functioning in globalprogenitor cell-based marketareF. Hoffmann-La Roche Ltd, Pfizer Inc., Merck & Co., Inc., Abbott, Vericel, Novartis AG, Alcon, GlaxoSmithKline plc, BAXTER INTERNATIONAL INC, Boehringer Ingelheim International GmbH, Amgen Inc., Bristol-Myers Squibb Company, Nuvasive, Inc., Organogenesis, Inc., Nu-Tech International, MiMedx, Stability Biologic., Takara Bio Inc., Caladrius, Biosciences, Inc., U.S. Stem Cell, Inc., Cesca Therapeutics and Osiris Therapeutics, Inc among others

Table of Contents is Available[emailprotected]https://www.databridgemarketresearch.com/toc?dbmr=global-progenitor-cell-based-market

Market Definition: Global Progenitor Cell-Based Market

Progenitor cellare the kind of stem cell which are located in bone marrow and also called as hematopoietic. These cells give rise to the different cell lines. The progenitor cells can divide and stem cells can replicate indefinitely. Progenitor cells are used in various neurological disorders such as Parkinson disease and Huntington disease.

Prevalence of Parkinsons disease (PD) increases with increasing age but an estimated four percent of people with Parkinsons disease are diagnosed before age 50, more than 10 million people worldwide are living with Parkinsons disease, and other neurological diseases.

Segmentation:Global Progenitor Cell-Based Market

Progenitor Cell-Based Market : By Type

Progenitor Cell-Based Market : By Therapeutic Application

Progenitor Cell-Based Market : By Cell Source

Progenitor Cell-Based Market : By End User

Progenitor Cell-Based Market : By Geography

Key Developments in the Progenitor Cell-Based Market:

Progenitor Cell-Based Market Drivers

Progenitor Cell-Based Market Restraints

Opportunities in the Progenitor Cell-Based Market Report :

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Progenitor Cell-Based Market 2020-2026 is Slated to Witness Tremendous Growth || Leading Players BAXTER INTERNATIONAL INC, Boehringer Ingelheim...

Global Myelofibrosis Treatment Market Overview By Growing Demands, Trends And Business Opportunities 2020 To 2029 – Owned

Trusted Business Insights answers what are the scenarios for growth and recovery and whether there will be any lasting structural impact from the unfolding crisis for the Myelofibrosis Treatment market.

Trusted Business Insights presents an updated and Latest Study on Myelofibrosis Treatment Market 2019-2029. The report contains market predictions related to market size, revenue, production, CAGR, Consumption, gross margin, price, and other substantial factors. While emphasizing the key driving and restraining forces for this market, the report also offers a complete study of the future trends and developments of the market.The report further elaborates on the micro and macroeconomic aspects including the socio-political landscape that is anticipated to shape the demand of the Myelofibrosis Treatment market during the forecast period (2019-2029). It also examines the role of the leading market players involved in the industry including their corporate overview, financial summary, and SWOT analysis.

Get Sample Copy of this Report @ Myelofibrosis Treatment Market by Diagnosis Type (Gene Mutation Analysis, Bone Marrow biopsy, Imaging Test, and Blood Tests), by Treatment Type (Chemotherapy, Blood Transfusions, Stem Cell Transplant, Splenectomy, Radiation Therapy, and Others), by Drug Type (Hydroxyurea, Immunomodulators, JAK Inhibitor, and Others), and by End-User (Hospitals, Clinics, and Bone Marrow Transplant Centers)-Global Industry Analytics, COVID-19 Business Impact, and Trends, 2020 2029

Abstract

The report covers forecast and analysis for the myelofibrosis treatment market on the global and regional level. The study provides historic data for 2016 and 2017 along with a forecast from 2018 to 2024 based on revenue (USD Million). The study includes drivers and restraints for the myelofibrosis treatment market along with the impact they have on the demand over the forecast period. Additionally, the report includes the study of opportunities available in the myelofibrosis treatment market on a global level.

In order to give the users of this report a comprehensive view of the myelofibrosis treatment market, we have included competitive landscape and analysis of Porters Five Forces Model for the market. The study encompasses a market attractiveness analysis, where diagnosis type, treatment type, drug type, and end users segments are benchmarked based on their market size, growth rate, and general attractiveness.

The report provides company market share analysis in order to give a broader overview of the key players in the market. In addition, the report also covers key strategic developments of the market including merger and acquisitions, new drug launch, drug pipeline, agreements, partnerships, collaborations & joint ventures, R&D, and regional expansion of major participants involved in the market on the global and regional basis. Moreover, the study covers price trends analysis, the product portfolio of various companies according to the region.

The study provides a decisive view of the myelofibrosis treatment market by segmenting the market into diagnosis type, treatment type, drug type, end users, and regions. All the segments have been analyzed based on present and the future trends and the market is estimated from 2018 to 2024. Based on diagnosis type, the market is segmented into gene mutation analysis, bone marrow biopsy, an imaging test, and blood tests. Based on treatment type, the market is segmented into chemotherapy, blood transfusions, stem cell transplant, splenectomy, radiation therapy, and others. Based on drug type, the market is segmented into hydroxyurea, immunomodulators, JAK inhibitor, and others. Based on end users, the market is segmented into hospitals, clinics, and bone marrow transplant centers. The regional segmentation includes the current and forecast demand for North America, Europe, Asia Pacific, Latin America, and the Middle East and Africa with its further categorization into major countries including the U.S., Canada, Germany, the UK, France, Spain, Italy, China, Japan, India, Brazil, and Mexico. This segmentation includes demand for myelofibrosis treatment based on individual diagnosis type, treatment type, drug type, and end users in all the regions and countries.

The report also includes detailed profiles of end players such as Eli Lilly and Company, Gilead Sciences Inc., F. Hoffmann-La Roche Ltd., Incyte Corporation, Merck & Co., Bristol-Myers Squibb Company, Novartis AG, Amgen Inc., and Celgene Corporation, among others.

The report segments the global myelofibrosis treatment market as follows:

Global Myelofibrosis Treatment Market: Diagnosis Type Segment Analysis

Gene Mutation Analysis Bone Marrow Biopsy Imaging Test Blood Test

Global Myelofibrosis Treatment Market: Treatment Type Segment Analysis

Chemotherapy Blood Transfusions Stem Cell Transplant Splenectomy Radiation Therapy Others

Global Myelofibrosis Treatment Market: Drug Type Segment Analysis

Hydroxyurea Immunomodulators JAK Inhibitors Others

Global Myelofibrosis Treatment Market: End-User Segment Analysis

Hospitals Clinics Bone Marrow Transplant Centers

Global Myelofibrosis Treatment Market: Regional Segment Analysis

North America

The U.S.

Europe

UK France Germany

Asia Pacific

China Japan India

Latin America

Brazil

Middle East and Africa

Quick Read Table of Contents of this Report @ Myelofibrosis Treatment Market by Diagnosis Type (Gene Mutation Analysis, Bone Marrow biopsy, Imaging Test, and Blood Tests), by Treatment Type (Chemotherapy, Blood Transfusions, Stem Cell Transplant, Splenectomy, Radiation Therapy, and Others), by Drug Type (Hydroxyurea, Immunomodulators, JAK Inhibitor, and Others), and by End-User (Hospitals, Clinics, and Bone Marrow Transplant Centers)-Global Industry Analytics, COVID-19 Business Impact, and Trends, 2020 2029

Trusted Business Insights Shelly Arnold Media & Marketing Executive Email Me For Any Clarifications Connect on LinkedIn Click to follow Trusted Business Insights LinkedIn for Market Data and Updates. US: +1 646 568 9797 UK: +44 330 808 0580

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Global Myelofibrosis Treatment Market Overview By Growing Demands, Trends And Business Opportunities 2020 To 2029 - Owned

Embryonic Stem Cell Research Without Limits | National Review

This is such a joke: As I posted a bit ago, the International Society for Stem Cell Research has published a set of ethical guidelines to govern ESCR. Well, I opineas I am wont to doon the matter in the Daily Standard. I note that the people selected to be the deciders were pretty much a stacked deck for a wide-open license: Unsurprisingly, many of the members of the ISSCR International Human Embryonic Research Guidelines Task Force, who wrote the Guidelines, are well known for advocating that scientists be given an open field.

University of Wisconsin bioethics professor R. Alta Charo, for example, has stated that a legal ban on all human cloning would violate scientists First Amendment right to conduct research. Another task force bioethicist, Northwestern Universitys Laurie Zoloth, previously advocated applying what she considers a Jewish understanding of the moral status of human embryos to guide the ethics of stem-cell researchwhich is to say, she would give embryos no moral status at all when outside the womb, and treat them as if they are simply water for the first 40 days of gestation.

Stanford University stem cell biologist Irving Weissman, another task force member, made headlines in 2005 when he reportedly announced plans to create a mouse with a human brain. Then there is Ian Wilmut, who supervised the cloning of Dolly the sheep, and who supports reproductive cloning at least for people who cant otherwise bear genetically related offspring. He also recently suggested tossing aside the usual rules that govern human medical experimentation in order to allow dying patients to be injected with embryonic stem cells, even though they are currently unsafe for human use.

And how far do the Guidelines suggest researchers be allowed to go? A lo-o-o-ong way. Remember when embryonic stem cell activists assured the nation that all they wanted to do was conduct experiments with leftover IVF embryos that were going to be destroyed anyway? Not anymore. The rigorous ISSCR research guidelines explicitly endorse the creation of new human embryosboth through IVF fertilization and somatic cell nuclear transfer cloningfor use and destruction in stem-cell research.

I note that these guidelines are strikingly similar to those published previously by the National Academy of Sciences. But we shouldnt be suprised: When it comes to biotechnology, the watchword of the century is anything goes.

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Embryonic Stem Cell Research Without Limits | National Review

BioTech Life Sciences Initiates New Study of Anti-Aging Formulas in Helping COVID-19 ‘Long-Haulers’ and Those Suffering With Chronic Fatigue Syndrome…

LONDON, Aug. 5, 2020 /PRNewswire/ --BioTech Life Sciences (BioTech https://btl.science) recently announced it was studying the effects of its proprietary formulas on long-term patient symptoms related to COVID-19 Post-Viral Fatigue (long-haulers) and chronic fatigue syndrome (C.F.S.).

The findings will be a part of a larger research study undertaken by the company, and is currently calling for voluntary participants; especially those who suffer from myalgic encephalomyelitis (M.E.), chronic fatigue syndrome, or Post-Viral Fatigue.

BioTech specializes in anti-aging, stem cell production and neuroscience, and has discovered a clear link between COVID-19 long-haulers, C.F.S., and the therapeutic benefits of certain anti-aging compounds.

The Link Between Post-Viral Fatigue and M.E./C.F.S.

According to the Cleveland Clinic and a recent Atlantic article, patients who survive COVID-19 typically recover in roughly two weeks' time. But there are a growing number of patients as many as 20% who inexplicably suffer with the disease for months, with longer lasting complications. These so called long-haulers report symptoms including fevers, chest pain, shortness of breath and debilitating fatigue.

Researchers are not sure why these patients experience COVID-19 for prolonged periods. Theories range from reinfection, to viral reactivation (similar to herpes), to a whole new syndrome initiated by COVID-19 infection. Patients are increasingly describing symptoms that are similar to the conditions of M.E./C.F.S, but more research is needed.

"What we're all seeing is a large, unexplained increase in people who are not making a full recovery from COVID-19," said Nicole Wong, lead researcher for BioTech. "We have already found several links between these long-haulers and M.E./C.F.S. patients. First, both groups seem to suffer from their cellular batteries mitochondria not producing enough energy. SARS-CoV-2 hijacks and destroys mitochondria, essentially eating their contents to replicate, and inflammatory cytokines such as TNF-alpha and IL-6, also reduce ATP-energy production."

Coronavirus blocking ACE2 causes a massive increase in free radicals and oxidative stress. These free radicals damage the lining of the blood vessels and can lead to blood clotting, thrombosis and the infamous cytokine-storm. It also increases enzyme CD38, which is known to greatly decrease ATP-energy production in multiple ways.

BioTech Life Sciences: Upcoming Clinical Trials Offer Hope

"While developing our anti-aging formulas, participants reported a profound increase in energy," said Romy Jardine, BioTech Chief Scientific Officer. "We discovered this was down to an increase in mitochondrial energy production, and this would likely help alleviate the crippling fatigue that many M.E./C.F.S. and long-haulers suffer with.

"The research is incredibly complex and will take time, as it involves the central nervous system, inflammatory cytokines, and multiple elements of the immune system. But now that we understand how to coax mitochondria into producing more energy, we're hopeful that this can be applied as a therapy for long-haulers and C.F.S. fatigue. Our upcoming clinical trials will begin to shed more light on those possibilities."

To learn more, or to take part in the upcoming BioTech clinical trial for C.F.S. or Post-Viral Fatigue sufferers, please visit: https://btlscience.typeform.com/to/XnVlAbmJ.

About BioTech Life Sciences

BioTech Life Sciences is a London-based company dedicated to research and development in anti-aging. Bringing the latest advances in stem cell production, DNA repair, epigenetics and neuroscience, BioTech optimizes health and promotes longevity. Currently involved in multiple research projects, BioTech is focusing on mitochondrial energy production (incl mitochondrial Biogenesis). BioTech is also studying Post-Viral Fatigue related to COVID-19, C.F.S. and M.E. Learn more about the latest BioTech developments at: http://www.BTL.science.

Disclaimer: These statements have not been evaluated by the FDA, MHRA, EMEA or any other regulatory or medical body. These products are not intended to diagnose, treat, cure, or prevent any disease. All information presented here is not a substitute for information from licensed healthcare practitioners. If you are on medication consult your healthcare professional about potential interactions or other complications.

Media Contact:

Freddy Keefe +44.7429.330606 [emailprotected]

SOURCE BioTech Life Sciences

http://btl.science

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BioTech Life Sciences Initiates New Study of Anti-Aging Formulas in Helping COVID-19 'Long-Haulers' and Those Suffering With Chronic Fatigue Syndrome...

COVID-19 Industry Impact On Autologous Stem Cell and Non-Stem Cell Based Therapies Market Revenue Develop Rapidly By 2019 2027 | Fibrocell Science,…

The report offers a systematic presentation of the existing trends, growth opportunities, market dynamics that are expected to shape the growth of the Autologous Stem Cell and Non-Stem Cell Based Therapies Market. The various research methods and tools were involved in the market analysis, to uncover crucial information about the market such as current & future trends, opportunities, business strategies and more, which in turn will aid the business decision-makers to make the right decision in future.

Whats keeping Caladrius Biosciences, Vericel Corporation, Fibrocell Science, Inc., Genzyme Corporation, BrainStorm Cell Therapeutics, Regeneus Ltd., and Dendreon Corporation. Ahead in the Market? Benchmark yourself with the strategic moves and findings recently released by CMI

Request a Sample Copy:https://www.coherentmarketinsights.com/insight/request-sample/523

List of Companies Mentioned:Caladrius Biosciences, Vericel Corporation, Fibrocell Science, Inc., Genzyme Corporation, BrainStorm Cell Therapeutics, Regeneus Ltd., and Dendreon Corporation.

1) Does Study provides Latest Impact on Market due to COVID & Slowdown?

Yes study have considered a chapter on Impact Analysis and this 2020 Edition of the report provides detailed analysis and its impact on growth trends and market sizing to better understand current scenario.

2) How companies are selected or profiled in the report?

List of some players that are profiled in the the report includes Caladrius Biosciences, Vericel Corporation, Fibrocell Science, Inc., Genzyme Corporation, BrainStorm Cell Therapeutics, Regeneus Ltd., and Dendreon Corporation.. list is sorted to come up with a sample size of atleast 50 to 100 companies having greater topline value to get their segment revenue for market estimation.

** List of companies mentioned may vary in the final report subject to Name Change / Merger etc.

3) Is it possible to narrow down business segments by Application of this study?

Yes, depending upon the data availability and feasibility check by our Research Analyst, further breakdown in business segments by end use application in relation to type can be provided (If applicable) by Revenue Size or Volume*.

4) What is the base year of the study? What time frame is covered in the report?

Furthermore, the years considered for the study are as follows:

Historical year 2014 2018

Base year 2018

Forecast period** 2019 to 2027 [** unless otherwise stated]

**Moreover, it will also include the opportunities available in micro markets for stakeholders to invest, detailed analysis of competitive landscape and product services of key players.

Detailed Segmentation:

On the basis of application, the global autologous stem cell and non-stem cell based therapies market is classified into:Neurodegenerative diseasesCardiovascular diseasesCancer and autoimmune diseasesSkin transplantationInfectious disease

Regions included:

o North America (United States, Canada, and Mexico)

o Europe (Germany, France, UK, Russia, and Italy)

o Asia-Pacific (China, Japan, Korea, India, and Southeast Asia)

o South America (Brazil, Argentina, Colombia)

o Middle East and Africa (Saudi Arabia, UAE, Egypt, Nigeria, and South Africa)

Global Autologous Stem Cell and Non-Stem Cell Based Therapies Market What to expect from this report:

Focused Study on Niche Strategy and Market Development & penetration Scenario

Analysis of M&As, Partnership & JVs in Global Autologous Stem Cell and Non-Stem Cell Based Therapies Industry in United States & Other Emerging Geographies

Top 10 Global Autologous Stem Cell and Non-Stem Cell Based Therapies Companies in Global Market Share Analysis: Leaders and Laggards in 2017, 2019

Gain strategic insights on competitor information to formulate effective R&D moves

Identify emerging players and create effective counter-strategies to outpace competitive edge

Identify important and diverse product types/services offering carried by major players for market development

And many more .

TABLE OF CONTENTS

Report Overview:It includes the Autologous Stem Cell and Non-Stem Cell Based Therapies market study scope, players covered, key market segments, market analysis by application, market analysis by type, and other chapters that give an overview of the research study.

Executive Summary:This section of the report gives information about Autologous Stem Cell and Non-Stem Cell Based Therapies market trends and shares, market size analysis by region and analysis of global market size. Under market size analysis by region, analysis of market share and growth rate by region is provided.

Profiles of International Players:Here, key players of the Autologous Stem Cell and Non-Stem Cell Based Therapies market are studied on the basis of gross margin, price, revenue, corporate sales, and production. This section gives a business overview of the players and shares their important company details.

Regional Study:All of the regions and countries analyzed in the Autologous Stem Cell and Non-Stem Cell Based Therapies market report is studied on the basis of market size by application, the market size by product, key players, and market forecast.

Download PDF Brochure @https://www.coherentmarketinsights.com/insight/request-pdf/523

Thanks for reading this article; you can also get individual chapter wise section or region wise report version like North America, Europe or Asia.

About Author:

Coherent Market Insights is a global market intelligence and consulting organization focused on assisting our plethora of clients achieve transformational growth by helping them make critical business decisions. We are headquartered in India, having office at global financial capital in the U.S. Our client base includes players from across all business verticals in over 150 countries worldwide. We are uniquely positioned to help businesses around the globe deliver practical and lasting results through various recommendations about operational improvements, technologies, emerging market trends and new working methods.

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COVID-19 Industry Impact On Autologous Stem Cell and Non-Stem Cell Based Therapies Market Revenue Develop Rapidly By 2019 2027 | Fibrocell Science,...

Orphan Drug Designation granted to tinostamustine in EU for very rare form of leukaemia – Pharmafield

Mundipharma has announced that the European Commission (EC) has now adopted the European Medicines Agency (EMA) Committee for Orphan Medicinal Products recommendation to grant Orphan Drug Designation to tinostamustine, an alkylating histone-deacetylase inhibiting molecule, for the treatment of T-cell prolymphocytic leukaemia (T-PLL).3

The EMA considers Orphan Drug Designation (ODD) status for medicines intended for the treatment, diagnosis or prevention of rare diseases or disorders that affect fewer than five per 10,000 people in the EU.4

T-PLL is an extremely rare and typically aggressive leukaemia.5,6 It affects approximately 2% of all patients with mature lymphocytic leukaemias1 and affects older adults with a median age at diagnosis of 61 years. It is more common in men than in women.2 T-PLL is characterised by the out-of-control growth of mature T-cells (T-lymphocytes). T-cells are a type of white blood cell that protects the body from infections.2 Due to its rarity, T-PLL can be misdiagnosed, resulting in poor patient outcomes.5 The condition is life-limiting and chronically debilitating, with fewer than 5% of patients surviving to five years from diagnosis.7 T-PLL generally progresses rapidly and does not respond well to standard multi-agent chemotherapy, with relapses being a common occurrence.5,6

Brian Sheehan, Chief Scientific Officer, Mundipharma Research added: Orphan drug designation is an important milestone in the development of tinostamustine, which is currently in early phase clinical trials. We are proud of our commitment to helping patients with rare and difficult-to-treat cancers, such as T-PLL, where therapeutic options are so limited and patients have a clear need for new therapies.

The EC decision adopting the EMA opinion follows that of the FDA, which granted tinostamustine ODD status for the treatment of T-PLL in March 2019.

Tinostamustine, is an alkylating histone-deacetylase inhibiting molecule in early phase clinical development for a range of rare and difficult-to-treat blood cancers and advanced solid tumours.Preclinical studies have shown that tinostamustine has the potential to improve access to the DNA strands within cancer cells, break them and counteract damage repair.8-11 The preclinical data also suggest that these complementary and simultaneous modes of action have the potential to overcome resistance towards some other cancer treatments.8-11

References

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Orphan Drug Designation granted to tinostamustine in EU for very rare form of leukaemia - Pharmafield