Novo backs ‘breakthrough’ antifungal player’s $60M round with a focus on rare mold infections – Endpoints News

The plight of antibiotics developers has been well documented: chronically underfunded research, daunting scientific challenges, and little commercial upside even for the ones that make it to the market. But in an adjacent corner of the antimicrobial space, an antifungal player is out to paint a very different picture.

F2G, a UK-Austria hybrid, has raised $60.8 million for its final push toward the clinic. Clearing the test could pave the way for its drug to be the first new antifungal agent in 20 years.

Thats how sparse the landscape has been, CEO Ian Nicholson told Endpoints News.

Its not for the lack of need, Nicholson noted. Much like in the antibacterial space, antifungal resistance is common occurring in 30% of patients taking the mainstay triazoles. Left untreated, the mortality rates for some of these rare mold infections targeted by F2G can be between 90% and 100%. Because fungi are eukaryotes just like humans, it has been difficult to discover new targets and corresponding new chemical entities.

The biotech began as a spinout of the University of Manchester, tapping into technologies that enabled them to manipulate and analyze fungal genes. F2G scientists eventually zeroed in on DHODH or dihydroorotate dehydrogenase, a key enzyme that helps fungi create the building blocks it needs to grow.

As it turned out, this blockade also kills the fungus. Out of this new class of antifungals dubbed orotomides, the lead candidate olorofim has been designated a breakthrough therapy (a first for antifungals, according to Nicholson), an orphan drug as well as a qualified infectious disease product. The ongoing open label Phase IIb study is testing it in a variety of rare mold infections, including invasive aspergillosis, scedosporiosis, lomentosporiosis, fusariosis, scopulariopsosis and coccidioidomycosis (valley fever).

For the upcoming Phase III, though, F2G plans to focus solely on invasive aspergillosis where a single study involving a couple hundred patients is expected to cement approval.

Valley fever is also a top priority in the US, where CMO John Rex, the former head of infection at AstraZeneca, leading a clinical team.

Compared to bacterial infections, fungal infections typically need to be treated for much longer, a matter of months rather than days. Theres no abundance of cheaply priced generics, and payers that F2G has talked to agreed that any new entrants should be priced relatively high.

Its a similar therapeutic area, but in many respects commercially it is much more like a rare disease drug than conventional anti-infective drug, CFO Ralf Schmid said.

Citing Gileads AmBisome as an example and an entrenched rival, Schmid pointed out the drug can cost $1,400 per day despite the availability of generics.

Just to set the context, added Naveed Siddiqi, a partner at Novo Ventures, the big drugs in the states are voriconazole and propiconazole, and they both at peak sold somewhere between $700 million and over $800 million.

Novo came on board for the first $60 million round back in 2016. Morningside Ventures, another existing investor, stepped up for the new funding alongside Brace Pharma Capital, Advent Life Sciences and new backer Cowen.

In addition to funding the clinical trial, the financing is also expected to scale up the current 20-person team in preparation for launch. Nicholson said the growth will be substantial but dont expect it to match the pharma rivals.

Because these infections occur in the context of transplants or cancer, when theyre immunosuppressed, a small company with a relatively limited salesforce and commercial organization can actually address this, Siddiqi said.

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Novo backs 'breakthrough' antifungal player's $60M round with a focus on rare mold infections - Endpoints News

CanSino reaps $748M windfall from Shanghai IPO as it warns Covid-19 vaccine won’t be a huge money maker – Endpoints News

CanSino began the year with a clear goal to secure a secondary listing on Shanghais STAR market. Then something more urgent came along: As a rising vaccine developer on a mission to bring global standard immunizations to China, it heeded the call to make a vaccine to protect against a virus that would paralyze the whole world.

Xuefeng Yu and his team managed to keep doing both.

More than a month after CanSinos Covid-19 vaccine candidate is authorized for military use in China, the Hong Kong-listed company has made a roaring debut in Shanghai. It fetched $748 million (RMB$5.2 billion) by floating 24.8 million shares, and soared 88% on its first trading day.

At RMB$209.71 apiece, its the second most expensive IPO ever on the nascent tech board, according to the South China Morning Post.

In opening the STAR market last year, Shanghais stock exchange followed its Hong Kong counterparts footsteps. By lowering the listing requirements to accommodate pre-revenue tech and biotech companies, both bourses are looking to lure domestic upstarts back from Nasdaq.

Its not uncommon for STAR stocks to jump dramatically or even double upon their debuts. In fact, CanSino closed at a lower price than expected.

The first-day gain turned out to be smaller than traders expected because of worries about frothy valuations on the overall A-share market, Ivan Li, a money manager at Shanghai-based Loyal Wealth Management, told SCMP. But investors still have confidence in the stock and its vaccines in the pipeline.

Covid-19 has delayed clinical plans for its earlier-stage vaccines, CanSino reported in its prospectus, which are candidates designed to protect against pneumococcal diseases as well as diphtheria, tetanus and pertussis.

Meanwhile, logistical troubles are still stalling the plan to test the coronavirus vaccine, Ad5-nCoV, in Canada. With political tension and speculation running high, CanSino has turned to Saudi Arabia to kick off its first Phase III test like all the other Chinese vaccine makers, its opting to do late-stage studies in places where infections are still widespread.

Even if the Phase III results are positive, though, dont expect it to be a money maker. CanSino noted that the Chinese government might be taking control of pricing and supply as well as exports, leading to a lower profit margin than other products.

An Ebola vaccine developed with a scientist from Chinas army whos also a collaborator on the Covid-19 program remains the only approved product in CanSinos portfolio. Two meningococcal vaccines are now under regulatory review.

The company wrote that its building a sales and marketing team, with the goal being to expand from the current 20-plus to 100 by the end of 2020.

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CanSino reaps $748M windfall from Shanghai IPO as it warns Covid-19 vaccine won't be a huge money maker - Endpoints News

Roche pulls a tumor micro-environment drug out of the freezer, hands it to a UK upstart – Endpoints News

Two years after pulling it from clinical development, Roche has handed control of a solid tumor cancer drug to a tiny Oxford University spinout.

For an undisclosed fee, Celleron Therapeutics acquired the drug, an anti-CSF1R antibody thats designed to modulate the tumor micro-environment an increasingly popular approach among cancer drug developers. Celleron says it will now put the drug into trials for patients with tenosynovial giant cell tumors, a rare disease where series of benign tumors begin to grow around the joints and tendons. Its caused by cells over-producing CSF1R.

The deal appears to be a straight biotech-repurposing-off-the-Pharma-shelf deal. Although Roche launched 4 different trials for the drug one of which is still technically on-going the Swiss pharma retired the drug as part of a broad pipeline sweep back in October of 2018. It was a business decision, the company wrote on one withdrawn studys page on clinicaltrials.gov, stipulating there were no safety or efficacy concerns.

In fact, the antibody had looked promising in the only efficacy results that ever surfaced. In a Phase I study published in The Lancet Oncology, 24 out of 28 patients responded to the drug, and two of them had a complete response.

Celleron will now have a chance to test whether those results can bear out in larger trials. The company says its built a proprietary platform around epigenetic control and immune modulation, but most of their clinical efforts so far have focused on an in-licensed drug from AstraZeneca that inhibits histone deacetylase, a class of enzymes that change one of the types of epigenetic markers on DNA. Theyve put it into Phase I and Phase II trials in the UK and in China in different combinations and different cancers, including T-cell lymphomas and HCC.

Still, Celleron has its own assets, including a series of preclinical assets that target histones. They also have CXD201, a molecule that inhibits topoisomerase, one of the enzymes that winds and unwinds DNA. And they say they use biomarker data to match the best drugs to the best patients.

The company has never announced how much capital theyve raised, but they said in 2017 they raised funding from a South Korean consortium.

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Roche pulls a tumor micro-environment drug out of the freezer, hands it to a UK upstart - Endpoints News

Stem Cell And Regenerative Therapy Market Industry Outlook, Growth Prospects and Key Opportunities – Kentucky Journal 24

The global stem cell and regenerative medicines market should grow from $21.8 billion in 2019 to reach $55.0 billion by 2024 at a compound annual growth rate (CAGR) of 20.4% for the period of 2019-2024.

Report Scope:

The scope of this report is broad and covers various type of product available in the stem cell and regenerative medicines market and potential application sectors across various industries. The current report offers a detailed analysis of the stem cell and regenerative medicines market.

The report highlights the current and future market potential of stem cell and regenerative medicines and provides a detailed analysis of the competitive environment, recent development, merger and acquisition, drivers, restraints, and technology background in the market. The report also covers market projections through 2024.

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The report details market shares of stem cell and regenerative medicines based on products, application, and geography. Based on product the market is segmented into therapeutic products, cell banking, tools and reagents. The therapeutics products segments include cell therapy, tissue engineering and gene therapy. By application, the market is segmented into oncology, cardiovascular disorders, dermatology, orthopedic applications, central nervous system disorders, diabetes, others

The market is segmented by geography into the following regions: North America, Europe, Asia-Pacific, South America, and the Middle East and Africa. The report presents detailed analyses of major countries such as the U.S., Canada, Mexico, Germany, the U.K. France, Japan, China and India. For market estimates, data is provided for 2018 as the base year, with forecasts for 2019 through 2024. Estimated values are based on product manufacturers total revenues. Projected and forecasted revenue values are in constant U.S. dollars, unadjusted for inflation.

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Report Includes:

28 data tables An overview of global markets for stem cell and regenerative medicines Analyses of global market trends, with data from 2018, estimates for 2019, and projections of compound annual growth rates (CAGRs) through 2024 Details of historic background and description of embryonic and adult stem cells Information on stem cell banking and stem cell research A look at the growing research & development activities in regenerative medicine Coverage of ethical issues in stem cell research & regulatory constraints on biopharmaceuticals Comprehensive company profiles of key players in the market, including Aldagen Inc., Caladrius Biosciences Inc., Daiichi Sankyo Co. Ltd., Gamida Cell Ltd. and Novartis AG

Summary

The global market for stem cell and regenerative medicines was valued at REDACTED billion in 2018. The market is expected to grow at a compound annual growth rate (CAGR) of REDACTED to reach approximately REDACTED billion by 2024. Growth of the global market is attributed to the factors such as growingprevalence of cancer, technological advancement in product, growing adoption of novel therapeuticssuch as cell therapy, gene therapy in treatment of chronic diseases and increasing investment fromprivate players in cell-based therapies.

In the global market, North America held the highest market share in 2018. The Asia-Pacific region is anticipated to grow at the highest CAGR during the forecast period. The growing government funding for regenerative medicines in research institutes along with the growing number of clinical trials based on cell-based therapy and investment in R&D activities is expected to supplement the growth of the stem cell and regenerative market in Asia-Pacific region during the forecast period.

Reasons for Doing This Study

Global stem cell and regenerative medicines market comprises of various products for novel therapeutics that are adopted across various applications. New advancement and product launches have influenced the stem cell and regenerative medicines market and it is expected to grow in the near future. The biopharmaceutical companies are investing significantly in cell-based therapeutics. The government organizations are funding research and development activities related to stem cell research. These factors are impacting the stem cell and regenerative medicines market positively and augmenting the demand of stem cell and regenerative therapy among different application segments. The market is impacted through adoption of stem cell therapy. The key players in the market are investing in development of innovative products. The stem cell therapy market is likely to grow during the forecast period owing to growing investment from private companies, increasing in regulatory approval of stem cell-based therapeutics for treatment of chronic diseases and growth in commercial applications of regenerative medicine.

Products based on stem cells do not yet form an established market, but unlike some other potential applications of bioscience, stem cell technology has already produced many significant products in important therapeutic areas. The potential scope of the stem cell market is now becoming clear, and it is appropriate to review the technology, see its current practical applications, evaluate the participating companies and look to its future.

The report provides the reader with a background on stem cell and regenerative therapy, analyzes the current factors influencing the market, provides decision-makers the tools that inform decisions about expansion and penetration in this market.

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Stem Cell And Regenerative Therapy Market Industry Outlook, Growth Prospects and Key Opportunities - Kentucky Journal 24

Radiation to treat pediatric cancers may have lasting impact on heart and metabolic health – Science Codex

Bottom Line: Adult survivors of childhood abdominal and pelvic cancers who had been treated with radiation therapy experienced abnormalities in body composition and had worse cardiometabolic health compared with the general population.

Journal in Which the Study was Published: Cancer Epidemiology, Biomarkers & Prevention, a journal of the American Association for Cancer Research

Author: Carmen Wilson, PhD, assistant member in the Epidemiology and Cancer Control department at St. Jude Children's Research Hospital

Background: "Body composition abnormalities and cardiometabolic impairments are of concern among survivors given that in the general population, these conditions increase the risk of developing life-threatening diseases including cardiovascular disease and type 2 diabetes," said Wilson. The impacts of radiation therapy on metabolic health have been previously reported for survivors of pediatric leukemia, brain tumors, and hematopoietic stem cell transplants, but the impacts on survivors of pediatric abdominal and pelvic tumors remained unclear, she said.

How the Study was Conducted: In this study, Wilson and colleagues assessed 431 adult survivors of pediatric abdominal or pelvic solid tumors who had been previously treated at St. Jude Children's Research Hospital. The median age of participants during the study was 29.9 years. The most frequent childhood diagnoses were neuroblastoma, Wilms tumor, and germ cell tumor, and the median age of participants at diagnosis was 3.6 years. Approximately 37 and 36 percent of participants had received abdominal and pelvic radiation therapy, respectively, as part of their treatment.

To assess the impacts of radiation therapy, the authors compared the participants' body composition, metabolic abnormalities, and physical function to those of the general population, using age-, sex-, and ethnicity-matched data from the 2013 to 2014 National Health and Nutrition Examination Survey (NHANES).

Results: Wilson and colleagues found that compared with data from NHANES, the survivors in their study were significantly more likely to have insulin resistance (33.8 percent vs. 40.6 percent), high triglycerides (10.02 percent vs. 18.4 percent), and low levels of high-density lipoproteins, commonly referred to as "good cholesterol" (28.9 percent vs. 33.5 percent). There were no significant differences in the levels of low-density lipoproteins ("bad cholesterol") between survivors and the general population.

The analyses also demonstrated that survivors of abdominal and pelvic solid tumors had lower relative lean body mass than the general population and that the lower relative lean body mass was associated with the dose of prior abdominal or pelvic radiation. Lean body mass, which measures the non-fat content of the body, is related to basal metabolic rate; therefore, an individual with lower lean body mass burns fewer calories while resting than someone with higher lean body mass, Wilson explained.

There was no significant difference in relative fat body mass between survivors and the general population; however, survivors who had high relative fat mass had reduced quadricep strength and poor physical performance (as measured by a sit-and-reach test and distance covered during a six-minute walk) compared with survivors who had low relative fat mass.

Author's Comments: "It is possible that abdominal and pelvic-directed radiation therapy damages postural muscles or subtly impairs sex hormone production, ultimately affecting muscle mass," said Wilson. She explained that radiation therapy has been shown to cause muscle injury, resulting in muscle fiber loss and loss of muscle regenerative cells, in animal studies. Wilson added that lifestyle choices may also impact relative lean mass and cardiometabolic health among survivors.

Wilson suggested that future research could examine the impact of radiation therapy and other cancer treatments on fat distribution across the body since increased abdominal obesity has been shown to be a better predictor of adverse health effects than measures of overall obesity.

In addition, Wilson is interested in exploring how interventions directed at lifestyle behaviors could improve lean mass and decrease fat mass among survivors of pediatric cancers. "While it may not be possible to avoid radiation therapy as a key treatment for many solid tumors, early research suggests that resistance training interventions in survivors increase lean mass," said Wilson. "Further work is needed to see if training would also impact cardiometabolic impairments in this population."

Study Limitations: A limitation of the study is that cardiometabolic outcomes may have been measured differently in the study cohort compared with those surveyed by NHANES.

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Radiation to treat pediatric cancers may have lasting impact on heart and metabolic health - Science Codex

Scientists hope to bring Malaysian rhinoceros back from extinction with stem cell technology – The Province

The last Sumatran rhinoceros individual of Malaysia Iman, photographed at her sanctuary on the island of Borneo in October 2019. KAISA SIREN / LEHTIKUVA

Some skin, eggs and tissue samples are all that remain of Malaysias last rhino, Iman, who died last November after years of failed breeding attempts.

Now scientists are pinning their hopes on experimental stem cell technology to bring back the Malaysian variant of the Sumatran rhinoceros, making use of cells from Iman and two other dead rhinos.

Im very confident, molecular biologist Muhammad Lokman Md Isa told Reuters in his laboratory at the International Islamic University of Malaysia.

If everything is functioning, works well and everybody supports us, its not impossible.

The smallest among the worlds rhinos, the Sumatran species was declared extinct in the wild in Malaysia in 2015. Once it had roamed across Asia, but hunting and forest clearance reduced its numbers to just 80 in neighboring Indonesia.

Iman, 25, died in a nature reserve on Borneo island, following massive blood loss caused by uterine tumors, within six months of the death of Malaysias last male rhino, Tam.

Efforts to get the two to breed had not worked.

He was the equivalent of a 70-year-old man, so of course you dont expect the sperm to be all that good, said John Payne of the Borneo Rhino Alliance (BORA), who has campaigned for about four decades to save Malaysias rhinos.

It was obvious that, to increase the chances of success, one should get sperm and eggs from the rhinos in Indonesia. But right till today, Indonesia is still not keen on this.

ACROSS THE BORDER

Indonesias environment ministry disputed accusations of cross-border rivalry as a reason why Malaysias rhinos died out, saying talks continue on ways to work with conservationists in the neighboring southeast Asian nation.

Because this is part of diplomatic relations, the implementation must be in accordance with the regulation of each country, said Indra Exploitasia, the ministrys director for biodiversity conservation.

The Malaysian scientists plan to use cells from the dead rhinos to produce sperm and eggs that will yield test-tube babies to be implanted into a living animal or a closely related species, such as the horse.

The plan is similar to one for the African northern white rhinoceros, which number just two. Researchers in that effort reported some success in 2018 in producing embyronic stem cells for the southern white rhino.

But the process is still far from producing a whole new animal, say Thomas Hildebrandt and Cesare Galli, the scientists leading the research.

And even if it worked, the animals lack of genetic diversity could pose a threat to long-term survival, Galli told Reuters.

Indonesian scientist Arief Boediono is among those helping in Malaysia, hoping success will provide lessons to help his countrys rhinos.

It may take five, 10, 20 years, I dont know, Arief added. But there has already been some success involving lab rats in Japan, so that means there is a chance.

Japanese researchers have grown teeth and organs such as pancreas and kidneys using embryonic stem cells from rats and mice in efforts to grow replacement human organs.

For now, however, Imans hide will be stuffed and put on display alongside Tam in a Borneo museum.

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Scientists hope to bring Malaysian rhinoceros back from extinction with stem cell technology - The Province

Cell Isolation/Cell Separation Market Research Report by Product, by Cell Type, by Cell Source, by Technique, by Application, by End User – Global…

August 13, 2020 05:16 ET | Source: ReportLinker

New York, Aug. 13, 2020 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "Cell Isolation/Cell Separation Market Research Report by Product, by Cell Type, by Cell Source, by Technique, by Application, by End User - Global Forecast to 2025 - Cumulative Impact of COVID-19" - https://www.reportlinker.com/p05913776/?utm_source=GNW

The Global Cell Isolation/Cell Separation Market is expected to grow from USD 6,356.88 Million in 2019 to USD 14,485.68 Million by the end of 2025 at a Compound Annual Growth Rate (CAGR) of 14.71%.

Market Segmentation & Coverage: This research report categorizes the Cell Isolation/Cell Separation to forecast the revenues and analyze the trends in each of the following sub-markets:

Based on Product, the Cell Isolation/Cell Separation Market studied across Consumables and Instruments. The Consumables further studied across Beads, Disposables, and Reagents, Kits, Media, and Sera. The Instruments further studied across Centrifuges, Filtration Systems, Flow Cytometers, and Magnetic-Activated Cell Separator Systems.

Based on Cell Type, the Cell Isolation/Cell Separation Market studied across Animal Cells and Human Cells. The Human Cells further studied across Differentiated Cells and Stem Cells.

Based on Cell Source, the Cell Isolation/Cell Separation Market studied across Adipose Tissue, Bone Marrow, and Cord Blood/Embryonic Stem Cells.

Based on Technique, the Cell Isolation/Cell Separation Market studied across Centrifugation-Based Cell Isolation, Filtration-Based Cell Isolation, and Surface Marker-Based Cell Isolation.

Based on Application, the Cell Isolation/Cell Separation Market studied across Biomolecule Isolation, Cancer Research, In Vitro Diagnostics, Stem Cell Research, and Tissue Regeneration & Regenerative Medicine.

Based on End User, the Cell Isolation/Cell Separation Market studied across Biotechnology & Biopharmaceutical Companies, Hospitals & Diagnostic Laboratories, and Research Laboratories & Institutes.

Based on Geography, the Cell Isolation/Cell Separation Market studied across Americas, Asia-Pacific, and Europe, Middle East & Africa. The Americas region surveyed across Argentina, Brazil, Canada, Mexico, and United States. The Asia-Pacific region surveyed across Australia, China, India, Indonesia, Japan, Malaysia, Philippines, South Korea, and Thailand. The Europe, Middle East & Africa region surveyed across France, Germany, Italy, Netherlands, Qatar, Russia, Saudi Arabia, South Africa, Spain, United Arab Emirates, and United Kingdom.

Company Usability Profiles: The report deeply explores the recent significant developments by the leading vendors and innovation profiles in the Global Cell Isolation/Cell Separation Market including Beckman Coulter Inc. (Subsidiary of Danaher Corporation), Becton, Dickinson and Company, Bio-Rad Laboratories, Inc., GE Healthcare, Merck KGaA, Miltenyi Biotec, Pluriselect Life Science Ug (Haftungsbeschrnkt) & Co. Kg, Stemcell Technologies, Inc., Terumo Bct, and Thermo Fisher Scientific, Inc..

FPNV Positioning Matrix: The FPNV Positioning Matrix evaluates and categorizes the vendors in the Cell Isolation/Cell Separation Market on the basis of Business Strategy (Business Growth, Industry Coverage, Financial Viability, and Channel Support) and Product Satisfaction (Value for Money, Ease of Use, Product Features, and Customer Support) that aids businesses in better decision making and understanding the competitive landscape.

Competitive Strategic Window: The Competitive Strategic Window analyses the competitive landscape in terms of markets, applications, and geographies. The Competitive Strategic Window helps the vendor define an alignment or fit between their capabilities and opportunities for future growth prospects. During a forecast period, it defines the optimal or favorable fit for the vendors to adopt successive merger and acquisition strategies, geography expansion, research & development, and new product introduction strategies to execute further business expansion and growth.

Cumulative Impact of COVID-19: COVID-19 is an incomparable global public health emergency that has affected almost every industry, so for and, the long-term effects projected to impact the industry growth during the forecast period. Our ongoing research amplifies our research framework to ensure the inclusion of underlaying COVID-19 issues and potential paths forward. The report is delivering insights on COVID-19 considering the changes in consumer behavior and demand, purchasing patterns, re-routing of the supply chain, dynamics of current market forces, and the significant interventions of governments. The updated study provides insights, analysis, estimations, and forecast, considering the COVID-19 impact on the market.

The report provides insights on the following pointers: 1. Market Penetration: Provides comprehensive information on the market offered by the key players 2. Market Development: Provides in-depth information about lucrative emerging markets and analyzes the markets 3. Market Diversification: Provides detailed information about new product launches, untapped geographies, recent developments, and investments 4. Competitive Assessment & Intelligence: Provides an exhaustive assessment of market shares, strategies, products, and manufacturing capabilities of the leading players 5. Product Development & Innovation: Provides intelligent insights on future technologies, R&D activities, and new product developments

The report answers questions such as: 1. What is the market size and forecast of the Global Cell Isolation/Cell Separation Market? 2. What are the inhibiting factors and impact of COVID-19 shaping the Global Cell Isolation/Cell Separation Market during the forecast period? 3. Which are the products/segments/applications/areas to invest in over the forecast period in the Global Cell Isolation/Cell Separation Market? 4. What is the competitive strategic window for opportunities in the Global Cell Isolation/Cell Separation Market? 5. What are the technology trends and regulatory frameworks in the Global Cell Isolation/Cell Separation Market? 6. What are the modes and strategic moves considered suitable for entering the Global Cell Isolation/Cell Separation Market? Read the full report: https://www.reportlinker.com/p05913776/?utm_source=GNW

About Reportlinker ReportLinker is an award-winning market research solution. Reportlinker finds and organizes the latest industry data so you get all the market research you need - instantly, in one place.

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Cell Isolation/Cell Separation Market Research Report by Product, by Cell Type, by Cell Source, by Technique, by Application, by End User - Global...

Stem Cell Therapy Market Size by Top Companies, Regions, Types and Application, End Users and Forecast to 2027 – Bulletin Line

Allosource

Competitive Landscape of the Stem Cell Therapy Market:

The market for the Stem Cell Therapy industry is extremely competitive, with several major players and small scale industries. Adoption of advanced technology and development in production are expected to play a vital role in the growth of the industry. The report also covers their mergers and acquisitions, collaborations, joint ventures, partnerships, product launches, and agreements undertaken in order to gain a substantial market size and a global position.

1.Stem Cell Therapy Market, By Cell Source:

Adipose Tissue-Derived Mesenchymal Stem Cells Bone Marrow-Derived Mesenchymal Stem Cells Cord Blood/Embryonic Stem Cells Other Cell Sources

2.Stem Cell Therapy Market, By Therapeutic Application:

Musculoskeletal Disorders Wounds and Injuries Cardiovascular Diseases Surgeries Gastrointestinal Diseases Other Applications

3.Stem Cell Therapy Market, By Type:

Allogeneic Stem Cell Therapy Market, By Application Musculoskeletal Disorders Wounds and Injuries Surgeries Acute Graft-Versus-Host Disease (AGVHD) Other Applications Autologous Stem Cell Therapy Market, By Application Cardiovascular Diseases Wounds and Injuries Gastrointestinal Diseases Other Applications

Regional Analysis of Stem Cell Therapy Market:

A brief overview of the regional landscape:

From a geographical perspective, the Stem Cell Therapy Market is partitioned into

North America o U.S. o Canada o Mexico Europe o Germany o UK o France o Rest of Europe Asia Pacific o China o Japan o India o Rest of Asia Pacific Rest of the World

Key coverage of the report:

Other important inclusions in Stem Cell Therapy Market:

About us:

Verified Market Research is a leading Global Research and Consulting firm servicing over 5000+ customers. Verified Market Research provides advanced analytical research solutions while offering information enriched research studies. We offer insight into strategic and growth analyses, Data necessary to achieve corporate goals, and critical revenue decisions.

Our 250 Analysts and SMEs offer a high level of expertise in data collection and governance use industrial techniques to collect and analyze data on more than 15,000 high impact and niche markets. Our analysts are trained to combine modern data collection techniques, superior research methodology, expertise, and years of collective experience to produce informative and accurate research.

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Stem Cell Therapy Market Size by Top Companies, Regions, Types and Application, End Users and Forecast to 2027 - Bulletin Line

Scientists distinguish new method that causes leukemia – Laboratory Equipment Magazine,Microbiology and Healthcare News,Scientific Equipment News -…

Every year, 1.1 million new cases of blood cancers are diagnosed globally. Currently, chemotherapy remains the most common and efficient plan of treatment. On the other hand, the development of aggressive types of leukemia in adults stimulates a need for early detection and new therapeutic approaches to achieve better clinical outcomes.

In a novel step ahead, researchers from the Cancer Science Institute of Singapore (CSI Singapore) at the National University of Singapore (NUS) have identified covalently closed circular RNAs (circRNAs) from key genes involved in embryonic growth and provided greater understanding of their functions in haematological malignancies.

This work has provided insights into a new mechanism for the regulation of H2AK119ub levels in hematopoietic progenitors via interaction of circASXL1-1 and BAP1,-Sudhakar Jha, Assistant Professor, Cancer Science Institute of Singapore, National University of Singapore

Mutations in additional sex combs-like 1 (ASXL1) receptor, an epigenetics remodeler, are found in acute myeloid leukemia (AML), chronic myelomonocytic leukemia (CMML) and myelodysplastic syndrome (MDS), and are associated with poor overall survival. Lately, the ASXL1 gene locus was shown to undergo alternative splicing to produce circRNAs.

While previous studies on circRNAs have mostly been concentrated on understanding the roots of the non-coding RNAs, the CSI Singapore research team headed by Assistant Professor Sudhakar Jha investigated the function of circRNAs in modulating the epigenetics landscape as well as the effects on differentiation in hematopoietic development and leukemogenesis.

The findings of this study were published in the prestigious scientific journal Haematologica in July 2020.

New mechanism accountable for leukemia development CircRNAs have been shown to have higher equilibrium, are plentiful, and highly conserved compared to linear RNAs.

In addition, they can be detected in extracellular vesicles, exosomes and blood plasma thus highlighting their possible as non invasive biomarkers. During RNA sequencing, the research team discovered circRNA isoforms in the ASXL1 gene locus.

The teams analysis made inroads into understanding the use of circASXL1-1 in leukemia. Their statistics show that depletion of circASXL1-1 led to decreased H2AK119 ubiquitination (H2AK119ub) and this had been through BRCA-1 related protein (BAP1) action, a deubiquitinating enzyme and a significant epigenetic regulator at leukemia. Tapping on the newly established comprehension, the research team aims to identify genes involved in myeloid differentiation program of haematopoietic stem cells (HSCs).

These enzymes can in turn be targeted to restore the normal path of differentiation in leukemia or to assist induce apoptosis of abnormally differentiated cells. The epigenetic signature recognized may thus pave the way for future therapeutic improvements ofepi-drugs.

Moving forward, the research team intends to create data supporting the use of circASXL1-1 in antisense therapy for malignant and non-malignant blood disorders using the recently obtained knowledge. More to the point, findings from this study will lay the foundation for the development of new RNA-based therapeutics for leukemia.

Source:

Journal reference:

Jadhav, S. P., circASXL1-1 regulates BAP1 deubiquitinase activity in leukemia. Haematologica.doi.org/10.3324/haematol.2019.225961.

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Scientists distinguish new method that causes leukemia - Laboratory Equipment Magazine,Microbiology and Healthcare News,Scientific Equipment News -...

CurePSP Partners With Rainwater to Support Pioneering Neurodegeneration Research – Yahoo Finance

Study will use miniature brains cultivated from stem cells to study protein mutations

CurePSP has awarded a $100,000 grant for a potentially breakthrough study that will employ 3D organoid models that have been shown to produce structures similar to those seen in the human brain to understand the effects of protein mutations that are associated with neurodegeneration.

The grant will assist the Tau Consortium Stem Cell Group, created and supported by the Rainwater Charitable Foundation, in helping to extend the scope of this multidisciplinary and multiyear study. The funding has been provided through generous donations from Frank Semcer, Sr., in honor of his wife Mary Jane Semcer; and from F. Jackson Phillips, in honor of his wife, Linda A. Phillips. Both women have received diagnoses of progressive supranuclear palsy (PSP), a rare form of neurodegeneration that involves pathological accumulation of the tau protein, a type of naturally occurring protein in the brain. CurePSPs grant was made under the auspices of the Prime of Life Brain Initiative, a collaborative venture with Rainwater to advance research into neurodegeneration.

The CurePSP grant will support research conducted by investigators of the Tau Consortium Stem Cell Group including Dr. Sally Temple of the Neural Stem Cell Institute, Dr. Alison Goate of the Ichan School of Medicine at Mount Sinai, Dr. Justin Ichida of the University of Southern California, Dr. Celeste Karch of Washington University, and Dr. Martin Kampmann of the University of California San Francisco.

Sometimes called "disease in a dish," 3D organoids are grown from skin-derived stem cells of patients and healthy individuals. Studies using these patient derived cell cultures aim to avoid some of the challenges and limitations of using animal models in research, including lack of construct validity of data (the degree to which data measures what it claims to be measuring) collected from animal studies when projected to humans. Since the first development of 3D neuronal cell cultures (organoids) less than 10 years ago, efforts have focused on the standardization and reproducibility of organoids protocols. Even more recently, genetic engineering techniques (CRISPR) and sequencing methods such as single-cell RNA sequencing have enabled greater robustness and a deeper understanding of these personalized human-derived disease models.

Dr. Kristophe J. Diaz, Vice President Scientific Affairs for CurePSP, said, "The use of human-derived disease models as opposed to reliance solely on animal models is a crucial step in the study of complex neurodegenerative disorders. We are thrilled to participate in this landmark study with the Tau Consortium and thank the Semcers and Phillips for their support."

Patrick Brannelly, Managing Director of the Tau Consortium, added, "PSP has become a key focus in the study of neurodegeneration for several of the worlds best academic institutions. CurePSPs collaboration in this study is greatly valued. We look forward to our continued partnership through the Prime of Life Brain Initiative."

CurePSP was an early supporter of the work of the Neural Stem Cell Institute with grants to Dr. David Butler for his work in developing therapeutic agents to prevent tau protein accumulation with novel antibody-based reagents called intrabodies and to Dr. Mo Liu for her pioneering work in developing PSP organoids.

About CurePSP

CurePSP is the nonprofit advocacy organization focused on progressive supranuclear palsy, corticobasal degeneration, and other prime of life neurodegenerative diseases, a spectrum of fatal brain disorders that often strike during a persons most productive and rewarding years. Currently, there is no effective treatment or cure for these diseases, which affect more than 150,000 people in the U.S. alone. Since it was founded in 1990, CurePSP has funded nearly 200 research studies and is the leading source of information and support for patients and their families, other caregivers, researchers and doctors, and allied healthcare professionals. CurePSP is based in New York City. Please visit http://www.curepsp.org for more information.

About the Rainwater Charitable Foundation

The Rainwater Charitable Foundation was created in the early 1990s by renowned investor and philanthropist Richard E. Rainwater. The foundation supports a range of different programs in K-12 education, medical research, and other worthy causes. In order to deliver on its mission to accelerate the development of new diagnostics and treatments for tau-related neurodegenerative disorders, the Rainwater Charitable Foundation Medical Research team manages the Tau Consortium and the Rainwater Prize Program for advances in neurodegenerative disease research. With more than $100 million invested to date, Rainwater support has helped to advance eight treatments into human trials. For more information, please visit http://www.tauconsortium.org.

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Contacts

David Kemp kemp@curepsp.org 802-734-1185

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