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Global Multiple Myeloma Treatment Market-Industry Analysis and forecast 2019 2027: By Application, Type, and Region. – Good Night, Good Hockey

Global Multiple Myeloma Treatment Marketsize was valued US$ XX Mn. in 2019 and the total revenue is expected to grow at 11.34% from 2019 to 2027, reaching nearly US$ XX Mn.

The report study has analyzed the revenue impact of COVID -19 pandemic on the sales revenue of market leaders, market followers, and market disrupters in the report, and the same is reflected in our analysis.

Multiple myeloma, also known as Kahlers disease, is a type of blood cancer of plasma cells that are found in the bone marrow. Multiple myeloma causes cancer cells to accrue in the bone marrow, where they attack the strong blood cells.

Multiple myeloma treatments have developed significantly above the last decade. New multiple myeloma treatments have provided efficient survival rates between myeloma patients. It has been also observed that the future drug pipeline of multiple myeloma is promising, biological drugs and stem cell-based therapies are likely to fuel the multiple myeloma treatment market in the upcoming years. On the other hand, the costs of radiotherapeutic equipment implementation, a limited number of target patients population, strict legal regulations are expected to hamper the market growth. Likewise, the MMR report contains a detailed study of factors that will drive and restrain the growth of the multiple myeloma treatment market globally.

Multiple Myeloma accounts for approximately 2.5% of the cancer-related deaths globally and is the second most major type of blood cancer next to Hodgkins Lymphoma. According to the World Cancer Research Fund, in 2018, above 159500 cases of multiple myeloma were diagnosed with the condition, where the occurrence rate among women and men was found in the ratio 1.2:1. The onset of the disease occurs after the age of 60. In recent times, the age of onset is drastically decreasing. In the year 2001, only two medications were available for treating multiple myeloma but now in 2020, 18 medicines are available. Moreover, there are over 25 FDA-approved drugs for treating multiple myeloma with therapeutics such as pomalidomide, carfilzomib, panobinostat, and ixazomib. The availability of new medications has given new hope for better treatments and better results and thus affecting the growth of the market as well. However, the survival of patients with a limited response while receiving treatment with primary immunodeficiency therapy remains poor and is one of the major challenges.

The MMR report covers the segments in the multiple myeloma treatment market such as type and application. By application, the hospital is expected to continue to hold the largest XX.85% share in multiple myeloma treatments market thanks to growing specialist doctors providing the best chance of long term survival.

North Americas multiple myeloma treatments market was valued at US$ XX.26 Mn. in 2019 and is expected to reach a value of US$ XX.13 Mn. by 2027, with a CAGR of 9.3%. The number of patients in the U.S is growing YoY with nearly 14600 new cases diagnosed annually. In 2017 alone there were approximately 142000 patients diagnosed for multiple myeloma.

Europe and the South African population are prone to develop multiple myeloma when compared with Asian economies. Though, the population in the APAC region outwits Europe and Africa. Further, growing the adoption rate of novel therapies, coupled with the support from the government along with non-government organizations and improving the survival of multiple myeloma patients.

The research study includes the profiles of leading players operating in the global multiple myeloma treatment market. Eli Lilly Company acquired ARMO Biosciences to develop immunotherapies for the treatment of cancer, hypercholesterolemia, inflammatory, and fibrosis diseases.

The objective of the report is to present a comprehensive analysis of the Global Multiple Myeloma Treatment Market including all the stakeholders of the industry. The past and current status of the industry with forecasted market size and trends are presented in the report with the analysis of complicated data in simple language. The report covers all the aspects of the industry with a dedicated study of key players that includes market leaders, followers, and new entrants. PORTER, SVOR, PESTEL analysis with the potential impact of micro-economic factors of the market has been presented in the report. External as well as internal factors that are supposed to affect the business positively or negatively have been analyzed, which will give a clear futuristic view of the industry to the decision-makers. The report also helps in understanding Global Multiple Myeloma Treatment Market dynamics, structure by analyzing the market segments and projects the Global Multiple Myeloma Treatment Market size. Clear representation of competitive analysis of key players by Application, price, financial position, Product portfolio, growth strategies, and regional presence in the Global Multiple Myeloma Treatment Market make the report investors guide. Scope of the Global Multiple Myeloma Treatment Market

Global Multiple Myeloma Treatment Market, by Applications

Hospitals Clinics Cancer Treatment and Rehabilitation Centers Global Multiple Myeloma Treatment Market, by Type

Proteasome Inhibitors Immunomodulatory Agents (IMiDs) Histone Deacetylase (HDAC) Inhibitors Immunotherapy Cytotoxic Chemotherapy Global Multiple Myeloma Treatment Market, by Region

Asia Pacific North America Europe South America Middle East & Africa Key players operating in Global Multiple Myeloma Treatment Market

Celgene Corporation Janssen Biotech, Inc. Bristol-Myers Squibb Company Novartis AG Cellectar Biosciences Inc. Millennium Pharmaceuticals Amgen, Inc. bbVie Genzyme Corporation Juno Therapeutics Eli Lilly and Company Glenmark Pharma

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Global Multiple Myeloma Treatment Market-Industry Analysis and forecast 2019 2027: By Application, Type, and Region. - Good Night, Good Hockey

Vida Ventures co-leads Dyne’s $115M megaround for next-gen oligo therapies aimed squarely at muscles – Endpoints News

Dyne Therapeutics started out last April with a modest $50 million to mine targeted muscle disease therapies from its in-house conjugate technology. The biotech has now convinced more investors that its got gems on its hands, closing $115 million in fresh financing to push its next-gen oligonucleotide drugs into the clinic.

Vida Ventures and Surveyor Capital led the round, joined by a group of other new backers including Wellington Management Company, Logos Capital and Franklin Templeton.

Atlas where Dyne was incubated also returned alongside Forbion and MPM.

Stefan Vitorovic, who co-founded Vida with Arie Belldegrun and others, took the lead on this one. Dynes FORCE platform matches exactly their appetite for bold visions in the future of medicine, with the potential to deliver life-changing outcomes for patients with muscle diseases, he said.

This is how the biotech plans to do it: By linking an antibody to an oligonucleotide, Dynes therapies are engineered to hone in on muscle cells and degrade only disease-causing RNA, thereby avoiding systemic toxicity issues.

Romesh Subramanian, a co-founder of what is now Translate Bio, helped launch the operations as an entrepreneur-in-residence at Atlas. Hes since handed the CEO baton to Joshua Brumm and moved to the CSO post.

When you deliver a naked oligo, very little gets to the muscle, he told C&EN back in 2019.

That means a lack of specificity and potential safety problems for drugs like Sareptas controversial Exondys 51. While Dyne is aiming directly at that market with its Duchenne muscular dystrophy program, its initial focus is on myotonic dystrophy.

Trailing closely is a third therapy for facioscapulohumeral muscular dystrophy, followed by discovery work in the cardiac and metabolic arenas.

How would the approach compare to gene therapies, which are cropping up at Sarepta and other newer players focused on muscle diseases? We didnt get a chance to ask Dyne, which is shying away from interviews this morning perhaps a sign of upcoming plans in a booming biotech IPO market.

Under Braum, Dyne has been on a bit of a hiring spree recently, poaching Susanna High from bluebird to be COO, appointing ex-Celgene exec Daniel Wilson as VP of intellectual property, and scooping Debra Feldman from Sage Therapeutics as head of regulatory.

Continued here:
Vida Ventures co-leads Dyne's $115M megaround for next-gen oligo therapies aimed squarely at muscles - Endpoints News

Global Nerve Repair and Regeneration Market Outlook 2020: Company Profiles of Key Players Axogen, Baxter, Nevro, Nuvectra, Polyganics and Stryker -…

DUBLIN--(BUSINESS WIRE)--Aug 10, 2020--

The "Nerve Repair and Regeneration - Global Market Outlook (2018-2027)" report has been added to ResearchAndMarkets.com's offering.

The Global Nerve Repair and Regeneration market accounted for $6.46 billion in 2018 and is expected to reach $21.68 billion by 2027 growing at a CAGR of 14.4% during the forecast period. Some of the key factors propelling the market growth are technological developments for nerve repair and regeneration and an increase in healthcare expenses by government with sympathetic policies. However, elevated prices associated with devices is a restraining factor for the growth of the market.

By product, the neurostimulation and neuromodulation devices segment is expected to grow at a significant market share during the forecast period due to mounting incidence of peripheral nerve injuries, technological development in the field. Sympathetic reimbursement policies are expected to drive the growth of this market segment in the next five years. On the basis of geography, Asia Pacific is anticipated to hold considerable market share during the forecast period due to increasing numbers of patients suffering from chronic diseases, and an increase in government initiatives for the development of healthcare services in the region.

What the report offers:

Key Topics Covered:

1 Executive Summary

2 Preface

3 Market Trend Analysis

3.1 Introduction

3.2 Drivers

3.3 Restraints

3.4 Opportunities

3.5 Threats

3.6 Product Analysis

3.7 Application Analysis

3.8 End User Analysis

3.9 Emerging Markets

3.10 Impact of Covid-19

4 Porters Five Force Analysis

4.1 Bargaining power of suppliers

4.2 Bargaining power of buyers

4.3 Threat of substitutes

4.4 Threat of new entrants

4.5 Competitive rivalry

5 Global Nerve Repair and Regeneration Market, By Product

5.1 Introduction

5.2 Neurostimulation and Neuromodulation Devices

5.2.1 Internal Neurostimulation Devices

5.2.1.1 Deep Brain Stimulation

5.2.1.2 Gastric Electrical Stimulation

5.2.1.3 Sacral Nerve Stimulation

5.2.1.4 Spinal Cord Stimulation

5.2.1.5 Vagus Nerve Stimulation

5.2.2 External Neurostimulation Devices

5.2.2.1 Transcranial Magnetic Stimulation

5.2.2.2 Transcutaneous Electrical Nerve Stimulation

5.3 Biomaterials

5.3.1 Nerve Wraps

5.3.2 Nerve Connectors

5.3.3 Nerve Conduits

5.3.4 Nerve Protectors

6 Global Nerve Repair and Regeneration Market, By Application

6.1 Introduction

6.2 Nerve Grafting

6.2.1 Autografts

6.2.2 Allografts

6.2.3 Xenografts

6.3 Neurostimulation and Neuromodulation Surgeries

6.3.1 Internal Neurostimulation and Neuromodulation Surgeries

6.3.2 External Neurostimulation and Neuromodulation Surgeries

6.4 Direct Nerve Repair/Neurorrhaphy

6.4.1 Epineural Repair

6.4.2 Group Fascicular Repair

6.4.3 Perineural Repair

6.5 Stem Cell Therapy

7 Global Nerve Repair and Regeneration Market, By End User

7.1 Introduction

7.2 Ambulatory Surgery Centers

7.3 Clinics

7.4 Hospitals

8 Global Nerve Repair and Regeneration Market, By Geography

8.1 Introduction

8.2 North America

8.3 Europe

8.4 Asia Pacific

8.5 South America

8.6 Middle East & Africa

9 Key Developments

9.1 Agreements, Partnerships, Collaborations and Joint Ventures

9.2 Acquisitions & Mergers

9.3 New Product Launch

9.4 Expansions

9.5 Other Key Strategies

10 Company Profiling

10.1 Abbott Laboratories

10.2 Axogen

10.3 Baxter

10.4 Boston Scientific

10.5 Integra Lifesciences

10.6 Livanova

10.7 Medtronic

10.8 Neuropace

10.9 Nevro

10.10 Nuvectra

10.11 Orthomed

10.12 Polyganics

10.13 Stryker

For more information about this report visit https://www.researchandmarkets.com/r/f3k098

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Global Nerve Repair and Regeneration Market Outlook 2020: Company Profiles of Key Players Axogen, Baxter, Nevro, Nuvectra, Polyganics and Stryker -...

Regenerative Medicine & Stem Cell Practice in Medical Spas …

In todays video, we talk about how medical spas and medical practices handle some of the legal issues with regenerative medicine, and stem cell therapies.

Im Michael H. Cohen, founding attorney of the Cohen Healthcare Law Group. Weve advised hundreds of healthcare industry clients on healthcare and FDA legal issues. Our clients include medical spas and healthcare companies that work with stem cell therapies and regenerative medicine.

Weve also gotten a lot of client questions about use of stem cell therapies, whether by medical doctors, naturopathic physicians, or midlevel practitioners such as RNs. As healthcare and FDA attorneys working in regulatory territory, we receive many deep-in-the-weeds questions.

For example, what about injecting stem cells for beauty and cosmetic treatments?

Using stem cells in IV infusions?

Are stem cell therapies covered within state law on nonsurgical medical cosmetic procedures?

Do stem cell therapies require an initial, in-person exam by an MD or under MD supervision by a PA or in collaboration by an NP?

What about procedures such as micro-needling, do these require medical supervision and a good faith exam?

Let me give you three tips to help you keep you in mind when youre looking to get a healthcare lawyer to address these kinds of legal questions.

First, a lot of the law simply says no. It doesnt tell you what you can do, only in broad terms what you cant do. So, when youre looking for legal advice, youre really asking for a professional read by an attorney, between the yes and the no. Obviously, either extreme is unsatisfying and doesnt give you any real guidance.

What you want in a healthcare lawyer is knowledge, skill and experience. A good healthcare lawyer can tell you, this particular scenario is more likely to get you in regulatory trouble, that scenario is more likely not going to be the biggest enforcement priority.

This week, one of our clients, a medical doctor who also runs a medical spa, told me that his biggest competitors were marketing and advertising their services, using advertising copy that he considered deceptive and misleading. He was at wits end trying to compete with these industry players who just dont follow the rules. Its not fair.

We talked through some of the strategies they were using and the legal risks that they were undertaking. Finally, he listened, and concluded: dont poke the bear. In a way, the process of mapping out the regulatory landscape helped him clarify his own business decision.

Second, a lot of these questions come under state law and they have to do with what licensing statutes, regulations, and Board policy statements say.

The federal government doesnt regulate the practice of medicine, or the healthcare practice of other licensed professionals. Rather, the United States Constitution leaves the regulation of health, safety and welfare up to the States.

And so, each State will have different laws and rules about what medical spas can do; about who can do what kinds of therapies; about whether you need a doctor to perform therapy X or Y or whether this can be done by an RN under MDs supervision; or, whether some services can and cant be performed by a licensed esthetician, because for example, they might constitute the practice of medicine.

Depending on your legal budget, it often doesnt make sense to research the law in all states, or even a lot of states. If youre a medical spa in one location, then obviously, your state law matters; and if your business is multi-state, sometimes we focus on key states or we get a small sampling of the ones with the toughest rules.

My third tip is, dont rely on advice which you got from someone else, because it is often incorrect, and based on facts and circumstances that dont necessarily apply to your situation.

As an example, recently, one medical spa came to our Firm with all of these questions swirling around in their minds. They were worried, because a medical spa in the same neighborhood had been visited by a very, very, super friendly medical board investigator, who was asking too many questions, in too friendly a way; and across town, medical spas had been raided by enforcement officials in a very heavy-handed way.

Up till then, the medical spa had thought it was legally safe, because, after all, it had a HIPAA-compliant software platform, and had its doctor making remote Skype calls with patients, before the RN would initiate a whole host of regenerative medicine therapies.

This kind of scenario in fact created much regulatory jeopardy.

The medical spa client basically told us: we use stem cells we get here from Company X, we mix them up in the back of our office with formula Y, then we inject them here and there as the doctor emails us, were only doing it for beauty, we think its ok, we just want some clarification on the laws.

OK, so if the speed limit is 55 and Im going 90, but Im telling you its ok because Im driving an old Chevy, my seat belt if fastened, I have a radar detector, and Ive also surrounded myself with white light and asked the angels to protect me which by the way is not a bad idea, but dont rely on it when you go 90 because if I drive too fast and I have a long way to go and I want to get there quickly all I want to know is, i just want to know if am I legally ok I mean, my cousins lawyers half-sisters friend, who swears by this and also asked a lawyer, said it was ok, as long as I dont go over 90 miles an hour .

I know it sounds really silly, but its the sort of thing we hear, in one form or another all the time.

And thats why you cant take excuses, and your healthcare lawyers experience and professional lens can help you interpret the law.

Thanks for watching. Heres to the success of your healthcare venture, we look forward to speaking with you soon.

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Regenerative Medicine & Stem Cell Practice in Medical Spas ...

As it happened: Banks fuel 1.8% ASX surge to three-week high – The Sydney Morning Herald

Investors are getting their head around the fact that monetary policy is going to remain accommodating for a long, long, long time, he said.

The 104-page statement revealed downgraded estimates for Australia suggesting the economy will not be strong enough to withstand an interest rate rise until at least 2023.

Mr Miller now expects the RBA to do more easing, which would be good for domestic banks. The banks share prices increased significantly amid low trading volumes on Monday. Commonwealth Bank shares gained 3.4 per cent to $73.98, National Australia Bank shares gained 3 per cent to $17.46, taking the stock back to where it was on the last day in July. Similarly, Westpac gained 3.3 per cent to $17.36 on below-average trading volumes, and ANZ Bank gained 2.7 per cent to $18.17.

Portfolio manager at Tribeca Investment Partners Jun Bei Liu said there was some optimism in the market thanks to Victorias lower COVID-19 infection numbers. The state remains in Stage 4 lockdown but on Monday recorded 322 infections, the lowest in two weeks.

Banks were sold off on fears the recession may last longer than expected, she added. The financial sector dropped 2.7 per cent last week and has been stuck in a trading range since June.

Property trusts and travel names did very well on Monday, Ms Liu added, with Scentre Group up 3.4 per cent to $1.99 and Webjet up 4.2 per cent to $3.24.

Among the consumer staples cohort Blackmores, Woolworths, and Coles enjoyed the best gains. The vitamin-maker gained 3.1 per cent to $74.50, Woolies gained 2.8 per cent to $40.04 and Coles was up 2.6 per cent to $18.85.

News Corp gained 6.5 per cent to a nearly-six months high of $20.81 after a flurry of analyst upgrades following last weeks results.

Utilities also out-performed on Monday with APA Group up 3 per cent to $11.44, Spark Infrastructure up 3.6 per cent to $2.31, and AusNet Services up 2 per cent to $1.83.

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As it happened: Banks fuel 1.8% ASX surge to three-week high - The Sydney Morning Herald

‘Help us save our little superhero’ -parents of boy (6) with rare cancer – Independent.ie

The parents of a six-year-old boy who is battling a rare form of cancer say they want to give their superhero son "a normal childhood".

ittle Auryn Phelan, from Malahide, Co Dublin - a massive fan of the Avengers superheroes - has endured 13 rounds of chemotherapy, two major surgeries, stem cell transplants and 14 rounds of radiotherapy.

As he nears the end of his treatment in Crumlin Children's Hospital, there is little disease left.

However, stage four neuroblastoma has an extremely high relapse rate and there are few treatment options if it returns. Tragically, survival rates are low.

His parents are now fundraising to get him a place on a clinical trial in the US.

"He has been surrounded by sadness, unspeakable horrors in hospital and endured medical procedure after procedure. We just want to give Auryn back a normal, healthy childhood," said his mum Trisha Gibbons.

"Aside from all the horrible procedures, he has missed out on so much of his childhood in the last year - the simple things that people take for granted have been denied to him.

LOVABLE

"Auryn is a gorgeous, energetic, funny, lovable boy who just wants to be a child and do what children do.

"This cancer journey has impacted Auryn and our family so much and has taken such a toll on both Auryn's physical and mental wellbeing," she added.

While the country endured lockdown, Auryn has had to face his own lockdown since he was diagnosed at just four-years-old.

That means no playdates with his friends and being unable to do simple, every-day things liking going to the shop.

"Due to his compromised immune system and constant risk of infection, we were required to keep him indoors, out of school and away from other children," said Trisha.

She and her husband Barry Phelan have set themselves the task of raising 375,000 by next January to enable Auryn to take part in a vaccine trial at the Slone Kettering Memorial Hospital in New York. All funds raised will go towards his treatment.

A GoFundMe appeal online has already raised more than 60,000.

"This vaccine is not available in Ireland, so our only option is to travel overseas.

"It has had very promising phase one results and we will do everything in our power to save our wonderful boy and get Auryn this treatment."

The family have set up the Auryn's Heroes fundraising campaign and are planning a series of events in Trisha's native Co Mayo and Barry's native Co Sligo as well as in Dublin.

They are also encouraging people to sign up for the virtual Vhi Virtual Women's Mini Marathon in October and run it in aid of Auryn's Heroes.

GENEROSITY

A separate 2km virtual Children's Superhero Walk, which will see children don their favourite superhero costumes and raise money, is also planned by Auryn's Heroes in October.

"We just want to give Auryn back a normal healthy childhood and put this journey behind both him and us for good. We are incredibly grateful to the people of our home counties of Mayo and Sligo, as well as our adopted home of Dublin, and indeed the country for the support and generosity you have shown to us," said Trisha.

Full details of how to donate and fundraise can be found at aurynsheroes.ie.

Irish Independent

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'Help us save our little superhero' -parents of boy (6) with rare cancer - Independent.ie

Stem Cell And Regenerative Therapy Market: Global Forecast over COVID-19 2024 – eRealty Express

globalstem cell and regenerative medicines marketshould 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.

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.

Request for Report Sample:https://www.trendsmarketresearch.com/report/sample/11723

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 futur

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.

More Info of Impact[emailprotected]https://www.trendsmarketresearch.com/report/covid-19-analysis/11723

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Stem Cell And Regenerative Therapy Market: Global Forecast over COVID-19 2024 - eRealty Express

Stem Cell Cartilage Regeneration Market 2020 Size by Product Analysis, Application, End-Users, Regional Outlook, Competitive Strategies and Forecast…

New Jersey, United States,- The most recent Stem Cell Cartilage Regeneration Market Research study includes some significant activities of the current market size for the worldwide Stem Cell Cartilage Regeneration market. It presents a point by point analysis dependent on the exhaustive research of the market elements like market size, development situation, potential opportunities, and operation landscape and trend analysis. This report centers around the Stem Cell Cartilage Regeneration business status, presents volume and worth, key market, product type, consumers, regions, and key players.

The COVID-19 pandemic has disrupted lives and is challenging the business landscape globally. Pre and Post COVID-19 market outlook is covered in this report. This is the most recent report, covering the current economic situation after the COVID-19 outbreak.

Key highlights from COVID-19 impact analysis:

Unveiling a brief about the Stem Cell Cartilage Regeneration market competitive scope:

The report includes pivotal details about the manufactured products, and in-depth company profile, remuneration, and other production patterns.

The research study encompasses information pertaining to the market share that every company holds, in tandem with the price pattern graph and the gross margins.

Stem Cell Cartilage Regeneration Market, By Type

Stem Cell Cartilage Regeneration Market, By Application

Other important inclusions in the Stem Cell Cartilage Regeneration market report:

A brief overview of the regional landscape:

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Market Research Intellect provides syndicated and customized research reports to clients from various industries and organizations with the aim of delivering functional expertise. We provide reports for all industries including Energy, Technology, Manufacturing and Construction, Chemicals and Materials, Food and Beverage, and more. These reports deliver an in-depth study of the market with industry analysis, the market value for regions and countries, and trends that are pertinent to the industry.

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Stem Cell Cartilage Regeneration Market 2020 Size by Product Analysis, Application, End-Users, Regional Outlook, Competitive Strategies and Forecast...

Re-Stem-Funded Study Targeting Mitochondrial Dysfunction in Aging and Age-Related Diseases Published in Science Advances Journal – Press Release -…

Aug. 9, 2020 / PRZen / SUZHOU, China -- Re-Stem Biotech (Re-Stem or the Company), a biotechnology firm engaged in the research and development of cell therapies targeting osteoarthritis, spinal cord injury and various cancers recently funded in part a study titled "Solid-phase inclusion as a mechanism for regulating unfolded proteins in the mitochondrial matrix". Researchers at The Johns Hopkins University School of Medicine, led by Rong Li, Ph.D., published their findings in the journal "Science Advances" (view full article here: https://advances.sciencemag.org/content/6/32/eabc7288) The study may provide mechanistic insights for mitochondrial dysfunction observed in aging and age-related diseases.

About Mitochondrial Dysfunction Mitochondrial dysfunction is a hallmark of age-related diseases, such as cardiovascular diseases and neurodegenerative diseases. During aging, damaged/unfolded proteins in mitochondria that are failed to be degraded gradually accumulate. In addition, recent evidence suggests that non-mitochondrial proteins constituting pathological aggregates in neurodegenerative diseases also accumulate in mitochondria and cause mitochondrial dysfunction. However, it remains unclear how excessive damaged proteins are managed within mitochondria when known quality control mechanisms become inadequate, and how they contribute to mitochondrial dysfunction during the aging process.

About the Study The researchers discovered that excessive unfolded proteins in the mitochondrial matrix are consolidated into novel structures, which they named Deposits of Unfolded Mitochondrial Proteins (DUMP). DUMP formation is an age-dependent process, while accelerated DUMP formation causes mitochondrial dysfunction and premature aging. They found that DUMP formation was not random, but specific in mitochondria near endoplasmic reticulum (ER), another organelle in cells. The contact sites between mitochondria and ER regulate DUMP formation via transferring lipids between two organelles. Via a series of genetic and live-cell imaging studies, researchers identified key enzymes of mitochondrial lipid metabolism that control DUMP formation. Manipulation of these enzymes modulates DUMP formation, therefore, potentially they could be targets for anti-aging or treating age-related diseases.

About Re-Stem Biotech Re-Stem Biotech (Re-Stem) is a biotechnology firm engaged in the research and development of cell-based therapies and products. Backed by state of the art GMP facilities and an international team of world-leading scientists, doctors and management team, Re-Stem currently has a robust technology platform including four profitable therapies on the market and eight other therapies and products in the pipeline. Incorporated and headquartered in 2012 in Suzhou, China, Re-Stem is focused on the large and aging population of China. It also operates clinics and research and development laboratories in Shenzhen, Beijing, Kunming and Ganzhou. For more information visit Re-Stem Biotech website: https://www.restembio.com/

Forward-Looking Statements Statements in this press release relating to plans, strategies, trends, specific activities or investments, and other statements that are not descriptions of historical facts and may be forward-looking statements are inherently subject to risks and uncertainties, and actual results could differ materially from those currently anticipated due to a number of factors, which include those regarding our ability to implement objective, plans and strategies for future operations. Forward-looking information may be identified by terms such as "will," "may," "expects," "plans," "intends," "estimates," "potential," or "continue," or similar terms or the negative of these terms. Although Re-Stem believes the expectations reflected in the forward-looking statements are reasonable, it cannot guarantee that future results, performance or achievements will be obtained. Re-Stem does not have any obligation to update these forward-looking statements other than as required by law.

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Re-Stem-Funded Study Targeting Mitochondrial Dysfunction in Aging and Age-Related Diseases Published in Science Advances Journal - Press Release -...

ASX Biotechs Surfing The Covid Story – FN Arena News

By Tim Boreham, Editor, The New Criterion

The ASX biotechs surfing the COVID-19 story

Normally investors shun speculative plays in times of market uncertainties, but thats not been the case with ASX-listed life sciences stocks across the drug, diagnostics and device sectors.

Naturally, the biotechs drawing a connection with fighting or detecting the virus spurious or otherwise have seen their valuations soar. Not that investor interest is limited to the Covid cluster, with capital raisings in the sector supported across the board.

A notable winner valuation-wise is Genetic Signatures ((GSS)), which markets molecular diagnostics tests for bacterial and viral conditions including superbugs, sexually transmitted diseases and norovirus (the number one plague of cruise ships before the coronavirus hopped on board).

Sold under the Easyscreen brand, the kits allow for rapid and accurate detection in large volumes. The tests take the genetic information of the targeted organism and change the genetic sequence to reduce the number of variables.

And, yes, the company is a COVID-19 story as well. Before the plague descended, the companys Easyscreen tests had not been able to distinguish Sars-cov-2 from say, Severe Acute Respiratory Syndrome (SARS), but the company has devised a variant to do just that.

Reporting a 278% revenue surge to $4.7m for the June quarter, management called out demand for the COVID-19 tests as a growth driver.

Broker Bell Potter notes the global molecular diagnostics market was worth more than $US6bn in 2018 and is expected to grow to $US10bn by 2026.

The sectors also been a hotbed of acquisitions, such as Thermo Fishers recently-lobbed $US11.5bn offer for Dutch diagnostic group Qiagen and Danaher Corps $US4bn acquisition of US counterpart Cepheid in 2018.

We expect merger and acquisition activity to continue in the space and Genetic Signatures is strategically well positioned to attract interest as it further expands into key US and European markets and grows is product suite, Bell Potter says.

While Genetic Signatures is a case of building incremental revenues, stem cell developer Mesoblast ((MSB)) is on the cusp of company-moving announcements pertaining to several late-stage clinical trials and expected US approval of its therapy for graft versus host disease (a common affliction for transplant patients).

Naturally, most investors are focused on the COVID-19 trial which involves treating critical-care patients with its off the shelf therapy remestemcel-L (branded Ryoncil).

Most coronavirus victims die from acute respiratory distress syndrome (ARDS), an inflammatory condition caused by the immune systems response to the virus.

Mesoblast aimed to enrol 300 patients across 30 US hospitals a moving target given the disease epicentre is moving from region to region.

Nonetheless, the first patients were dosed in May, with an interim analysis is due when at least 30% of the patients have been treated for 30 days.

In other words, investors should soon know whether the company is on the cusp of a major treatment breakthrough.

And if thats not enough excitement, Mesoblast expects to announce results from two phase III studies: a 566-patient effort for chronic heart failure and a 404-patient trial for chronic lower back pain caused by disc degeneration.

Also in the stem-cell space, Cynata Therapeutics ((CYP)) is planning to carry out its own COVID-19 clinical trials not just in relation to ARDS, but sepsis and cytokine release syndrome (all causes of COVID-19 deaths).

The company is encouraged by pre-clinical modelling and has regulatory approval to carry out a trial.

The company planned to enrol 24 intensive care patients in NSW but perhaps it should refocus efforts south of the Murray.

It was fairly clear that Australias prevention measures effectively flattened the curve and we quickly ran out of available patients, Cynata chief Ross Macdonald said before the Victorian resurgence.

Tackling the cause of COVID-19 mortalities is one thing, but what if the risk of contracting the diseases could be more accurately predicted beyond the clinical factors of age and co-morbidities such as heart disease and diabetes?

That way, the denizens of locked down geographies such as Victoria could discard their masks and emerge from isolation.

Meanwhile, shares in kidney disease house Dimerix ((DXB)) last week soared on positive clinical results pertaining to a rare condition called focal segmental glomerusclerosis (FSGS).

But the drug candidate in question, DMX-200 has also been selected for appraisal in a global trial to treat ARDS, the common element between ARDS and FSGS being fibrosis.

Known in shorthand as REMAP-CAP, the World Health Organisation endorsed trial aims to enrol 7000 patients across more than 200 sites. DMX-200 is one of many potential therapies being looked at, but the beauty for Dimerix is the trial costs are paid the governments that are funding REMAP-CAP.

Changing tack, molecular diagnostics house Genetic Technologies ((GTG)) has filed a provisional patent for a genetics-based assessment of the risk of developing COVID-19.

Based on third-party genomic data from 1500 COVID-19 patients, the company intends to develop a prototype model to identify patients most likely to require hospitalisation should they contract the disease.

If and when a vaccine materialises, the genetic profiling could help to prioritise who gets jabbed first.

Hitherto known for its predictive breast cancer kits, Genetic Technologies has never matched its performance to its promises.

But US investors have been willing to support the stock, with the company raising $US5.1m in a placement via its Nasdaq listing.

Disclaimer: Under no circumstances have there been any inducements or like made by the company mentioned to either IIR or the author. The views here are independent and have no nexus to IIRs core research offering. The views here are not recommendations and should not be considered as general advice in terms of stock recommendations in the ordinary sense.

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ASX Biotechs Surfing The Covid Story - FN Arena News