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Stem Cell Therapy Market Analysis 2021: Size, Share, Sales, Growth, Revenue, Type, Application & Forecast To 2027 SoccerNurds – SoccerNurds

Stem Cell TherapyMarket Size 2021 Industry Share, Strategies, Growth Analysis, Regional Demand, Revenue, Key Players and 2027 Forecast Research Report

The report envelops a few factors that have added to the development of the market lately. It features a couple of the main market drivers and investigations their effect available. Among all factors, the expanding number of organization consolidations and joint efforts decidedly affect market development. With this procurement, the organization will hope to beat its partners and in doing as such, set up a solid presence on the lookout. The report features a couple of the other organization consolidations that have graced the market as of late and measures their effect available.

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Top Key Players in this Market Research Report

Pharmicell Co., Ltd Holostem Terapie Avanzate S.r.l. Osiris Therapeutics, Inc. MEDIPOST Co., Ltd. Nuvasive, Inc. Celgene Corporation Anterogen Co., Ltd. Promethera Biosciences Fibrocell Science, Inc. RTI Surgical, Inc. RTI Surgical, Inc Cytori Therapeutics

By Types

Adult Stem Cells Human Embryonic Induced Pluripotent Stem Cells Very Small Embryonic Like Stem Cells

By Applications

Regenerative Medicine Drug Discovery and Development

Global Stem Cell Therapy Market is further classified on the basis of region as follows:

Some Point from Table of Content:

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Important Questions Answered

An Overview of the Impact of COVID-19 on Stem Cell Therapy Market:The emergence of COVID-19 has brought the world to a standstill. We understand that this health crisis has brought an unprecedented impact on businesses across industries. However, this too shall pass. Rising support from governments and several companies can help in the fight against this highly contagious disease. There are some industries that are struggling and some are thriving. Overall, almost every sector is anticipated to be impacted by the pandemic. We are taking continuous efforts to help your business sustain and grow during COVID-19 pandemics. Based on our experience and expertise, we will offer you an impact analysis of coronavirus outbreak across industries to help you prepare for the future.

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Stem Cell Therapy Market Analysis 2021: Size, Share, Sales, Growth, Revenue, Type, Application & Forecast To 2027 SoccerNurds - SoccerNurds

CAR T-Cell Therapy Enters the Arena in Multiple Myeloma With Ongoing Research Ahead – OncLive

The FDA approval of idecabtagene vicleucel (ide-cel; Abecma) has established a role for CAR T-cell therapy in heavily pretreated, relapsed/refractory multiple myeloma, with the product showing an unprecedented response rate and a generally favorable safety profile, said Saad Z. Usmani, MD, FACP.

However, with additional BCMA-directed constructs, allogeneic CAR T-cell products, and bispecific antibodies in the pipeline, ide-cel could become just 1 of many novel options the field.

BCMA-directed CAR T-cell therapy has good activity in heavily pretreated patients with multiple myeloma, including patients with triple-class refractory disease, said Usmani. Cytokine release syndrome [CRS], neurotoxicity, and low blood counts are [common], but patients [typically] recover from these adverse effects [AEs]. The timing of CRS and neurotoxicity could be different [between products], but we are seeing good activity [overall].

On March 26, 2021, the FDA approved ide-cel as the first BCMA-directed CAR T-cell therapy for patients with relapsed/refractory multiple myeloma after 4 or more prior lines of therapy, including an immunomodulatory agent (IMiD), a proteasome inhibitor (PI), and an anti-CD38 monoclonal antibody.1

The regulatory decision was based on data from the phase 2 KarMMA trial, in which ide-cel elicited an overall response rate (ORR) of 72% and a stringent complete response (sCR) rate of 28% in patients with relapsed/refractory myeloma who had received at least 4 prior treatments.2

Another CAR T-cell product, ciltacabtagene autoleucel (cilta-cel) is currently in the myeloma pipeline, having demonstrated an ORR of 96.9% and an sCR rate of 67.0% in the phase 1b/2 CARTITUDE-1 trial.3 Notably, the median time to onset of CRS was 1 day with ide-cel compared with 7 days with cilta-cel.2,3 In April 2021, Legend Biotech, the developer of cilta-cel, announced that a rolling submission of a biologics license application to support the approval of the drug for the treatment of patients with relapsed/refractory multiple myeloma has been completed.4

In an interview with OncLive during an Institutional Perspectives in Cancer webinar on CAR T-cell therapy, Usmani, chief of Plasma Cell Disorders and director of Clinical Research in Hematologic Malignancies at the Levine Cancer Institute of Atrium Health, discussed the rapidly changing cellular therapy paradigm in relapsed/refractory multiple myeloma.

Usmani: Ide-cel is a BCMA-directed CAR T-cell therapy that is the furthest along in terms of clinical development; we have the most follow-up with that particular construct. The key takeaway from the data [from the KarMMA trial], which were shared during the 2020 ASH Annual Meeting and Exposition, was that the initial signal of efficacy in the dose-escalation study did play out in the subsequent dose-expansion cohort. Longer-term follow-up [data have shown that] patients are getting minimal residual diseasenegative complete responses; some patients who have been off of treatment are showing sustained remissions at 2 years and beyond.

There doesnt appear to be any long-term safety concerns so far with [ide-cel]. The CRS and neurotoxicity that is seen is short term [and occurs] during the early parts of treatment, usually within the first month or so.

Importantly, an analysis [showed that]patients with high-risk cytogenetics [or] extramedullary multiple myeloma tended to have the same disease response with ORRs around 70% or higher.

KarMMA-2 [NCT03601078] has several different cohorts, including patients who are receiving ide-cel in earlier lines of treatment, patients who are receiving ide-cel with prior exposure to BCMA-directed therapy, and patients [who are receiving ide-cel] with high-risk disease, which will serve as a safety signalgenerating cohort.

[The KarMMA-2 trial] led to the development of the KarMMA-4 trial [NCT04196491], which is a frontline study for high-risk patients post induction.

The KarMMA-3 trial [NCT03651128] is another ongoing trial comparing ide-cel with standard triplet regimens in relapsed/refractory multiple myeloma. Some ide-cel studies [within] the Cooperative Group Setting were in the [Blood and Marrow Transplant Clinical Trials Network] looking at ide-cel after autologous stem cell transplant in high-risk patients [with multiple myeloma].

The next endeavor that we are going to have as we are thinking about CARrelated products is how quickly we can give these therapies. Currently, it takes between 4 to 6 weeks from the time that we think about giving a patient CAR T-cell therapy to getting them on a trial, to [them undergoing] apheresis, and finally, getting the product back. Logistically, this can take up to 2 months on clinical trials. It would be ideal to have an off-the-shelf option, which is where the ALLO-715 concept is very important.

If we have an allogeneic product from a single donor, we can make 100 off-the-shelf products ready to go. If I need to give such a product to a patient, I can start lymphodepleting chemotherapy and give them CAR T-cell therapy [shortly thereafter].

ALLO-715 tried to do that and is being evaluated in a dose-escalation, early-phase study. The important thing [about ALLO-715] is that about 90% of patients were treated within 5 days of enrolling, which is a much shorter timeframe [compared with autologous CAR T-cell therapy]. Moreover, there appears to be clinical activity [with ALLO-715] at the highest [dose] of 320 million [cells]. Six out of 10 patients had a response with 4 out of 10 having a very good partial response or better. [The trial has] short follow-up in a small cohort of patients, but the data are encouraging.

The early approvals will come in the relapsed/refractory setting for patients who have had exposure or refractoriness to PIs, IMIDs, and [monoclonal] antibodies. Most of our early usage once [CAR T-cell therapies] come to the clinic will be for those patients, and part of their usage will be dependent on how much capacity each transplant and cellular therapy center has. Having said that, we are probably going to have a little bit more flexibility in how we can bridge patients to CAR T-cell therapy. Getting patients to CAR T-cell therapy would be ideal, so we will try to do that for most patients. However, bispecific antibodies are also coming down the pike, so those will be good backup options too.

The second most mature dataset we have is with cilta-cel from the CARTITUDE-1 trial, [showing] a very impressive 97% ORR. With [cilta-cel], the time to CRS onset and neurotoxicity events is a bit delayed compared with ide-cel. As we think operationally, if both products [become] available to us, maybe one [product could be] given in the outpatient setting vs monitoring patients in the inpatient setting early on. Every center will look at things in a little bit of a different way based on their resources, but it is a good problem to have more than 2 options for patients.

We also have the bb21217 construct, which has the same construct as ide-cel. However, a PI3K inhibitor is utilized during the CAR T-cell expansion to push it toward more of a memory T-cell phenotype, [which could translate] to long-term remission for patients.

Then we have the LUMMICAR constructs, which are somewhat similar in terms of data and safety to ide-cel with lower-grade CRS. [With the investigational] PRIME-BCMA-101 [product], the CAR T cells do their job and then are out of the system quickly. There too, we are seeing low rates of CRS overall, as well as low [rates of] grade 3 or 4 CRS.

The efficacy and safety, as well as the vein-to-vein time, appear to be the keys [to getting CAR T-cell therapy into the clinic], but it is early. Im curious to see how all of this evolves, especially with ide-cel and cilta-cel as frontrunners.

The advantages in favor of CAR T-cell therapies are that although its more labor intensive early on, they dont require maintenance. Patients do enjoy that quality of life after having recovered from CAR T-cell therapy.

The disadvantages [include] production time and capacity of transplant centers, which play a role in discussing what may be the best option for patients. With the bispecific antibodies coming along, it is highly likely that we could see usage of antibody-drug conjugates and bispecific antibodies in the community setting even before patients come to see us for a CAR T-cell therapy consultation. There are a lot of nuances [to utilizing these products] that we will have to figure out once we have the therapies [available].

[Ultimately], the one-and-done approach that CAR T-cell therapy [provides] is quite unique and many patients will favor that.

Editors Note: This interview took place prior to the March 26, 2021, FDA approval of idecabtagene vicleucel in relapsed/refractory multiple myeloma.

Continued here:
CAR T-Cell Therapy Enters the Arena in Multiple Myeloma With Ongoing Research Ahead - OncLive

Leukemia Cutis: Symptoms and Treatment – Healthline

Leukemia cutis can happen when leukemia cells enter your skin. This rare condition causes patches of discolored skin to appear on the body.

In some cases, the appearance of leukemia cutis lesions on the skin is the first sign of leukemia a cancer of the blood and bone marrow.

Along with standard leukemia therapies, this complication can usually be addressed with topical treatments to help heal the damaged skin. If you have leukemia cutis, your outlook will usually depend on your age and the type of leukemia you have.

Leukemia cutis is an uncommon complication, affecting only about 3 percent of people with leukemia. However, it is often a sign that the cancer is at an advanced stage.

With leukemia, malignant leukocytes (white blood cells) are usually only present in the bloodstream. In the case of leukemia cutis, the leukocytes have entered the skin tissue, causing lesions to appear on the outer layer of your skin. The word cutis refers to the skin, or dermis.

Generally, leukemia cutis results in one or more lesions or patches forming on the outer layer of skin. This condition can mean that the leukemia is more advanced and may have spread to your bone marrow and other organs.

Because there are fewer healthy white cells to combat infections caused by other diseases, rashes and sores may be more common among people with leukemia. Low blood platelets from leukemia can cause damage to blood vessels that appear as red spots or lesions on the skin.

These may include:

However, these skin changes are different than those brought on by leukemia cutis.

While the legs are the most common area for leukemia cutis lesions to appear, they can also form on the arms, face, trunk, and scalp. These skin changes can include:

The lesions usually dont hurt. However, with certain types of leukemia particularly acute myeloid leukemia (AML) the lesions may bleed.

A dermatologist may initially diagnose leukemia cutis based on a physical examination of the skin and a review of your medical history. A skin biopsy is needed to confirm the diagnosis.

Leukemia cutis is a sign of leukemia. It wont develop if the body isnt already dealing with this type of blood cancer.

But leukemia isnt just one disease. There are multiple types of leukemia, each one classified by the kind of cell affected by the disease.

You can also have an acute or a chronic form of leukemia. Acute means it comes on suddenly and usually with more severe symptoms. Chronic leukemia develops more slowly and often with milder symptoms.

The types of leukemia that most commonly trigger leukemia cutis are AML and chronic lymphocytic leukemia (CLL).

Scientists arent sure why cancerous leukocytes migrate to skin tissue in some people with leukemia. It may be that the skin is an optimal environment for healthy leukocytes to transform into cancerous cells.

One possible risk factor that has emerged is an abnormality in chromosome 8, which has been found more often in individuals with leukemia cutis than in those without it.

Treating leukemia cutis usually includes treatment for leukemia as the underlying condition.

The standard leukemia treatment is chemotherapy, but other options may be considered depending on your overall health, your age, and the type of leukemia you have.

Other leukemia treatment options include:

For blood cancers, external beam radiation is a typical form of treatment. With this therapy, a focused beam of radiation is delivered outside the body from various angles. The goal is to injure the DNA in cancer cells to stop them from reproducing.

Immunotherapy, a type of biological therapy, uses the bodys own immune system to fight cancer. It is typically given by an injection that either stimulates immune system cells activity or blocks the signals cancer cells send to suppress the immune response.

Immunotherapy may also be given orally, topically, or intravesically (into the bladder).

Stem cell transplantation is more commonly known as a bone marrow transplant. Bone marrow is where blood stem cells develop. Stem cells can become any type of cell.

Through stem cell transplantation, healthy blood stem cells replace stem cells damaged by the cancer or by chemotherapy or radiation therapy. However, not everyone is a good candidate for this treatment.

Only treating the leukemia cutis lesions will not address the underlying disease of leukemia. That means treatments designed to remove or reduce lesions should be done in combination with systemic treatment for leukemia itself.

Treatments for leukemia cutis symptoms can include:

Again, these treatments will only treat the leukemia cutis lesions, but systemic treatment of the leukemia itself will be needed as well.

The length of time leukemia cutis lesions may last depends on many factors, including how well the leukemia itself is responding to treatment. If the leukemia goes into remission, its unlikely more lesions will appear.

With effective treatment, existing lesions could fade. However, other factors, including your age and overall health, can affect how widespread the lesions are and how long they may last.

There are encouraging trends in the treatment of leukemia, but it remains a challenging disease to treat and live with.

For people with AML who dont have leukemia cutis, research suggests that the survival rate at 2 years is about 30 percent. However, the survival rate drops to 6 percent among people with the skin lesions.

A separate study of 1,683 people with AML found that leukemia cutis was associated with a poor prognosis, and that those with AML and leukemia cutis may benefit from more aggressive treatment.

The outlook for people with CLL is better, with about an 83 percent survival rate at 5 years. The presence of leukemia cutis doesnt seem to change that outlook very much, according to a 2019 study.

Leukemia cutis is a rare complication of leukemia. It happens when malignant leukocytes invade the skin and cause lesions on the skins outer surface.

AML and CLL are more often associated with leukemia cutis than other types of leukemia.

While leukemia cutis usually means the leukemia is in an advanced stage, there are treatments for both the cancer and this uncommon side effect that may help extend life and improve its quality.

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Leukemia Cutis: Symptoms and Treatment - Healthline

Stem Cell Therapy Market is Set to Witness Impressive Growth | Top Players Osiris Therapeutics, Inc. (US), MEDIPOST Co., Ltd. KSU | The Sentinel…

The Stem Cell Therapy Market is expected to grow at a CAGR of 6.6% and is poised to reach US$XX Billion by 2027 as compared to US$XX Billion in 2020. The factors leading to this extraordinary growth is attributed to various market dynamics discussed in the report Our experts have examined the market from a 360 degree perspective thereby producing a report which is definitely going to impact your business decisions.

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The Stem Cell Therapy Market report at DECISIVE MARKETS INSIGHTS provides a comprehensive study that shows the technological advancements and innovations which are driving the growth of the industry. The report provides a detailed insight on the product pricing trends, market drivers, and potential opportunities which can propel the market performance over the forecasted period 2020-2027.The report also provides a detailed study on the challenges and threats faced by the companies due to the competition in the market.

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Stem Cell Therapy Breakdown Data by Type Allogeneic, Autologous

Stem Cell Therapy Breakdown Data by Application Musculoskeletal Disorders Wounds and Injuries Cardiovascular Diseases Surgeries Gastrointestinal Diseases Other Applications

Stem Cell Therapy Breakdown Data by Companies Osiris Therapeutics, Inc. (US), MEDIPOST Co., Ltd. (South Korea), Anterogen Co., Ltd. (South Korea), Pharmicell Co., Ltd. (South Korea), Holostem Terapie Avanzate Srl (Italy), JCR Pharmaceuticals Co., Ltd. (Japan), NuVasive, Inc. (US), RTI Surgical, Inc. (US), and AlloSource (US)

The Stem Cell Therapy Market report provides knowledge regarding the product in terms of volume and value,technological changes, and innovations that had changed in the recent past and can drive the growth of the industry in the upcoming times. The report is conducted after conducting several interviews with the key executives of the top key companies and experts in the market. The report endures a number of data that helps businesses to make investment decisions. The report also consists of a detailed study on the impact of the ongoing global crisis of the COVID-19 pandemic and how the pandemic had changed the markets cenario globally. The report also provides historical data before the pandemic and current data after the pandemic which helps to know the market share and the behavior of the businesses. The report also includes different strategies implemented by the top key players in the market to face the challenges of the pandemic.

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The report offers the type of products available in the market and their application with their end-uses. The report has segmented the market into different sub-segments which help the businesses to know the opportunities and act accordingly. The report provides a detailed analysis of the growth progression globally. The report also provides a detailed synopsis of the technological developments and innovations which can change the market scenario. The report also provides an analysis of the market dynamics such as drivers, restraints, constraints, and opportunities which will enhance the performance of the industry. The report explains in a detailed manner SWOT ANALYSIS, PESTEL ANALYSIS, CAGR ANALYSIS, COMPETITOR ANALYSIS, and many more which helps the businesses to know the prevailing opportunities and loopholes which are backing their business in the market. The report also provides detailed insight into the recent product launches and technological upgrades done by the top key players of the market and the strategies implemented by them. The report also helps businesses to know the opportunities available indifferent segments of the market. The report also provides a graphical presentation in the form of BAR DIAGRAMS, PIE CHARTS, and HISTOGRAMS which help the businesses to get a clear understanding of the market performance over the forecasted period 2020-2027.

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In depth analysis by industry experts Use of data triangulation method for examining the various aspects of the market Detailed profiling of the major competitors in the market A complete overview of the market landscape Computed Annual Growth Rate is calculated for period, 2020 2027

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Decisive Markets Insights Sunil Kumar Sales Head Email sales@decisivemarketsinsights.com US +18317045538 UK +441256636046

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Stem Cell Therapy Market is Set to Witness Impressive Growth | Top Players Osiris Therapeutics, Inc. (US), MEDIPOST Co., Ltd. KSU | The Sentinel...

Global Stem Cell Therapy Market 2020 SWOT Analysis, Growth Rate, and Market Share By Type, Application and Global Forecast 2027 – Los Hijos de la…

Regional Stem Cell Therapy Market Segment Analysis:

North America South America Asia Pacific Europe Middle East and Africa

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Table of Contents

Segment 1 Stem Cell Therapy Introduction and Market Overview by region, Product Overview, Market Segmentation, Market Dynamic(Opportunities, Drivers, Limitations)

Segment2 Upstream Raw Material, Manufacturing Cost Structure Analysis, Market Channel Analysis, Major Downstream Buyers of Stem Cell Therapy Analysis

Segment3 Global Stem Cell Therapy Capacity, Revenue (Value) by Region)

Segment4 Global Stem Cell Therapy Market value ($), production, growth rate, and market share by type

Segment5 Global Stem Cell Therapy Market Consumption, growth rate, and market share by application

Segment6 Stem Cell Therapy Production, Value ($), Price and Gross Margin by region

Segment7 Stem Cell Therapy Production, Consumption, Export, Import by Regions (2015-2020)

Segment8 Global Stem Cell Therapy Company Profiles

Segment9 Stem Cell Therapy Market Forecast Analysis

Segment10 Stem Cell Therapy Industry Barriers and New Entrants SWOT Analysis

Segment11 Research Findings and Conclusion

Segment 12 Appendix

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Global Induced Pluripotent Stem Cell (iPS Cell) Market Report 2021: In Total, At Least 68 Distinct Market Competitors Now Offer Various Types of iPSC…

DUBLIN, April 15, 2021 /PRNewswire/ -- The "Global Induced Pluripotent Stem Cell (iPS Cell) Industry Report 2021" report has been added to ResearchAndMarkets.com's offering.

The main objectives of this report are to describe the current status of iPSC research, patents, funding events, industry partnerships, biomedical applications, technologies, and clinical trials for the development of iPSC-based therapeutics.

Since the discovery of induced pluripotent stem cells (iPSCs) a large and thriving research product market has grown into existence, largely because the cells are non-controversial and can be generated directly from adult cells. It is clear that iPSCs represent a lucrative market segment because methods for commercializing this cell type are expanding every year and clinical studies investigating iPSCs are swelling in number.

Therapeutic applications of iPSCs have surged in recent years. 2013 was a landmark year in Japan because it saw the first cellular therapy involving the transplant of iPSCs into humans initiated at the RIKEN Center in Kobe, Japan. Led by Masayo Takahashi of the RIKEN Center for Developmental Biology (CDB), it investigated the safety of iPSC-derived cell sheets in patients with macular degeneration.

In another world-first, Cynata Therapeutics received approval in 2016 to launch the world's first formal clinical trial of an allogeneic iPSC-derived cell product (CYP-001) for the treatment of GvHD.

Riding the momentum within the CAR-T field, Fate Therapeutics is developing FT819, its "off-the-shelf" iPSC-derived CAR-T cell product candidate. Numerous physician-led studies using iPSCs are also underway in Japan, a leading country for basic and applied iPSC applications.

iPS Cell Market Competitors

Today, FUJIFILM CDI has emerged as one of the largest commercial players within the iPSC sector. FUJIFILM CDI was founded in 2004 by Dr. James Thomson at the University of Wisconsin-Madison, who in 2007 derived iPSC lines from human somatic cells for the first time ever. The feat was accomplished simultaneously by Dr. Shinya Yamanaka's lab in Japan.

In 2009, ReproCELL, a company established as a venture company originating from the University of Tokyo and Kyoto University, made iPSC products commercially available for the first time with the launch of its human iPSC-derived cardiomyocytes, which it called ReproCario.

A European leader within the iPSC market is Ncardia, formed through the merger of Axiogenesis and Pluriomics. Founded in 2001, Axiogenesis initially focused on generating mouse embryonic stem cell-derived cells and assays, but after Yamanaka's iPSC technology became available, it became the first European company to license it in 2010. Ncardia's focus is on preclinical drug discovery and drug safety through the development of functional assays using human neuronal and cardiac cells.

In total, at least 68 distinct market competitors now offer various types of iPSC products, services, technologies and therapies.

iPS Cell Commercialization

Methods of commercializing induced pluripotent stem cells (iPSCs) are diverse and continue to expand. iPSC cell applications include, but are not limited to:

Since the discovery of iPSC technology in 2006, significant progress has been made in stem cell biology and regenerative medicine. New pathological mechanisms have been identified and explained, new drugs identified by iPSC screens are in the pipeline, and the first clinical trials employing human iPSC-derived cell types have been initiated.

Key Topics Covered:

1. REPORT OVERVIEW 1.1 Statement of the Report 1.2 Executive Summary

2. INTRODUCTION 2.1 Discovery of iPSCs 2.2 Barriers in iPSC Application 2.3 Timeline and Cost of iPSC Development 2.4 Current Status of iPSCs Industry 2.4.1 Share of iPSC-based Research within the Overall Stem Cell Industry 2.4.2 Major Focuses of iPSC Companies 2.4.3 Commercially Available iPSC-Derived Cell Types 2.4.4 Relative Use of iPSC-Derived Cell Types in Toxicology Testing Assays 2.4.5 Toxicology/Safety Testing Assays using iPSC-Derived Cell Types 2.5 Currently Available iPSC Technologies 2.6 Advantages and Limitations of iPSCs Technology

3. HISTORY OF INDUCED PLURIPOTENT STEM CELLS (IPSCS) 3.1 First iPSC generation from Mouse Fibroblasts, 2006 3.2 First Human iPSC Generation, 2007 3.3 Creation of CiRA, 2010 3.4 First High-Throughput screening using iPSCs, 2012 3.5 First iPSCs Clinical Trial Approved in Japan, 2013 3.6 The First iPSC-RPE Cell Sheet Transplantation for AMD, 2014 3.7 EBiSC Founded, 2014 3.8 First Clinical Trial using Allogeneic iPSCs for AMD, 2017 3.9 Clinical Trials for Parkinson's disease using Allogeneic iPSCs, 2018 3.10 Commercial iPSC Plant SMaRT Established, 2018 3.11 First iPSC Therapy Center in Japan, 2019

4. RESEARCH PUBLICATIONS ON iPSCS 4.1 Categories of Research Publications 4.2 Percent Share of Published Articles by Disease Type 4.3 Number of Articles by Country

5. IPSCS: PATENT LANDSCAPE 5.1 Timeline and Status of Patents 5.2 Patent Filing Destinations 5.2.1 Patent Applicant's Origin 5.2.2 Top Ten Global Patent Applicants 5.2.3 Collaborating Applicants of Patents 5.3 Patent Application Trends iPSC Preparation Technologies 5.4 Patent Application Trends in iPSC Differentiation Technologies 5.5 Patent Application Trends in Disease-Specific Cell Technologies

6. CLINICAL TRIALS INVOLVING iPSCS 6.1 Current Clinical Trials Landscape 6.1.1 Clinical Trials Involving iPSCs by Major Diseases 6.1.2 Clinical Trials Involving iPSCs by Country

7. FUNDING FOR iPSCs 7.1 Value of NIH Funding for iPSCs 7.1.1 NHI's Intended Funding Through its Component Organizations in 2020 7.1.2 NIH Funding for Select Universities for iPSC Studies 7.2 CIRM Funding for iPSCs

8. GENERATION OF INDUCED PLURIPOTENT STEM CELLS: AN OVERVIEW 8.1 Reprogramming Factors 8.2 Overview of Four Key Methods of Gene Delivery 8.3 Comparative Effectiveness of Different Vector Types 8.4 Genome Editing Technologies in iPSCs Generation

9. HUMAN iPSC BANKING 9.1 Cell Sources for iPSCs Banking 9.2 Reprogramming methods used in iPSC Banking 9.3 Workflow in iPSC Banks 9.4 Existing iPSC Banks

10. BIOMEDICAL APPLICATIONS OF iPSCS 10.1 iPSCs in Basic Research 10.2 iPSCs in Drug Discovery 10.3 iPSCs in Toxicology Studies 10.4 iPSCs in Disease Modeling 10.5 iPSCs within Cell-Based Therapies

11. OTHER NOVEL APPLICATIONS OF iPSCS 11.1 iPSCs in Tissue Engineering 11.2 iPSCs in Animal Conservation 11.3 iPSCs and Cultured Meat

12. DEAL-MAKING WITHIN THE iPSC SECTOR 12.1 License Agreement between FUJIFILM Cellular Dynamics and Sana 12.2 Century Therapeutics Closes $160 Million Series C Financing 12.3 Bluerock Gains Access to Ncardia's iPSCs-derived Cardiomyocytes 12.4 Fate Therapeutics' Deal with Janssen Biotech 12.5 Century Therapeutics Acquires Empirica Therapeutics 12.6 $250 Million Raised by Century Theraputics 12.7 BlueRock Therapeutics Launched with $225 Million 12.8 Collaboration between Allogene Therapeutics and Notch Therapeutics 12.9 Acquisition of Semma Therapeutics by Vertex Therapeutics 12.10 Evotec's Extended Collaboration with BMS 12.11 Licensing Agreement between Allele Biotechnology and Astellas 12.12 Codevelopment Agreement between Allele & SCM Lifesciences 12.13 Fate Therapeutics Signs $100 Million Deal with Janssen 12.14 Allele's Deal with Alpine Biotherapeutics 12.15 Editas and BlueRock's Development Agreement

13. MARKET OVERVIEW 13.1 Global Market for iPSCs by Geography 13.2 Global Market for iPSCs by Technology 13.3 Global Market for iPSCs by Biomedical Application 13.4 Global Market for iPSCs by Cell Types 3.5 Market Drivers 13.6 Market Restraints

14. COMPANY PROFILES

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Global Induced Pluripotent Stem Cell (iPS Cell) Market Report 2021: In Total, At Least 68 Distinct Market Competitors Now Offer Various Types of iPSC...

Emergent drift of Dental Regenerative Products Market By the World in Upcoming Year 2021-2027 with Leading Key Players: Provia Laboratories, LLC,…

Stem cell-based regenerative medicine procedure replaces lost or damaged teeth in tissue engineering and stem cell biology by redrawing from autologous stem cells called tooth regeneration. Somatic stem cells are collected and reprogrammed into induced pluripotent stem cells as a source of new bioengineered teeth, placed in a reabsorbable biopolymer in the shape of a new tooth or directly in the dental plate.

The Global Dental Regenerative Products market elaborate report, offers a summary study on regional forecast, business size, and associated revenue estimations. The Dental Regenerative Products report more emphasizes primary challenges and growth trends adopted by leading makers of the market.

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Top Companies of Dental Regenerative Products Market:

Dental Regenerative Products Market Is Divided Into:

Based on end user, the dental regenerative products market can be segmented as:

The report provides a detailed breakdown of the Dental Regenerative Products Market region-wise and categorizes it at various levels. Regional segment analysis displaying regional production volume, consumption volume, revenue, and growth rate from 2019-2027 covers: Americas (United States, Canada, Mexico, Brazil), APAC (China, Japan, Korea, Southeast Asia, India, Australia), Europe (Germany, France, UK, Italy, Russia, Spain), Middle East & Africa (Egypt, South Africa, Israel, Turkey, GCC Countries)

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This Dental Regenerative Products Market research report also presents some significant practical oriented case studies which help to understand the subject matter clearly. This research report has been prepared through industry analysis techniques and presented in a professional manner by including effective info-graphics whenever necessary. It helps to gain stability in the businesses as well as to make the rapid developments to achieve a notable remark in the Global market space.

In This Study, The Years Considered To Estimate The Size Of Dental Regenerative Products Market Are As Follows:

History Year: 2015-2020

Base Year: 2020

Estimated Year: 2021

Forecast Year 2021 to 2027

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Emergent drift of Dental Regenerative Products Market By the World in Upcoming Year 2021-2027 with Leading Key Players: Provia Laboratories, LLC,...

Johnson & Johnson’s COVID-19 vaccine has been paused in Colorado. Here’s what you need to know. – The Denver Channel

DENVER -- Colorado on Tuesday paused its use of the Johnson & Johnson vaccine following guidance from the Centers for Disease Control Prevention (CDC), which reported six cases of rare blood clots tied to the vaccine.

None of the blood-clot cases were reported in Colorado as of Tuesday. But providers, out of an abundance of caution, put the J&J vaccine on hold as health officials investigate the vaccine's side effects.

Still, the Johnson & Johnson vaccine has made up only a small portion of the vaccines administered in Colorado.

Here's an overview of the J&J vaccine and its distribution in Colorado:

Through Monday, 122,280 J&J doses have been administered in Colorado. That's compared to 1,645,357 Pfizer vaccines and 1,529,767 Moderna vaccines.

On Monday, 358 people were vaccinated with the J&J in Colorado, compared to 4,497 with the Moderna vaccine and 9,477 with the Pfizer vaccine. bl Officials have expected for weeks to scale up usage of the one-dose J&J vaccine in Colorado, but those operations were limited even before Tuesday's news.

The J&J vaccine was put on hold at the Dick's Sporting Goods Park vaccination site on Wednesday after 11 people experienced adverse reactions to the shot. Two people were taken to the hospital.

The vaccine provider, Centura Health, later in the week said it was stopping J&J distribution at all of its drive-thru clinics in Colorado due to a national shortage and the adverse reactions. Those reactions ranged from nausea to dizziness after receiving the J&J vaccine.

How does the Johnson & Johnson vaccine differ from the others?

Johnson & Johnsons Janssen COVID-19 vaccine is a viral vector vaccine, which means it uses a modified version of a different virus (the vector) to deliver instructions to cells to produce the COVID-19 spike protein, according to the Center For Disease Control and Prevention.

The bodys immune system will then produce antibodies as it attacks the harmless spiked protein cells, building an immunity to the actual COVID-19 virus.

Viral vector vaccines were created in the 1970s, and have been studied for gene therapy, to treat cancer, and for molecular biology research, according to the CDC.

The Moderna and Pfizer vaccines are mRNA vaccines, which are a new type of vaccines. These type of vaccines give instructions to cells to make a harmless piece of the spike protein that is found on the surface of the COVID-19 virus, according to the CDC.

None of the three vaccines use the live virus that causes COVID-19.

Federal, state health officials react to pause of Johnson & Johnson vaccine in the US

During a news conference Tuesday after the CDC and the FDA recommended pausing the use of the vaccine, Jeff Zients, the White House COVID-19 response coordinator on the Johnson & Johnson vaccine, as well as Dr. Anthony Fauci, the director of the National Institute of Allergy and Infectious Diseases, said that despite the pause, the announcement would have no significant impact on the nations vaccination program, as the J&J vaccine makes up less than 5% of the more than 190 million recorded shots in arms in the United States to date.

Fauci, speaking to reporters from the White House, said the pause will give health officials time to study how to treat these rare cases of cerebral venous sinus thrombosis (CVST), which is normally treated with heparin, a blood thinner that prevents the formation of blood clots.

That would be a mistake in this situation because it could be dangerous and make the situation much worse. So, there's a clinically relevant reason why you want to make this known to people, Fauci said during the briefing. The pause not only allows us to take a look at the cases and learn more, but it is also a signal out there to help the physicians.

Fauci also said pausing the J&J vaccine would help health officials determine if there are any common denominators among the six women who suffered these adverse reactions, which could help health officials determine whether to rule out giving the vaccine to a certain group of people based on certain criteria.

Still, Fauci reiterated the six adverse reactions reported by the FDA and the CDC from the J&J vaccine are very rare, saying the Moderna and Pfizer vaccines which use a different technology than the J&J vaccine have shown no red flags that would cause federal health officials to stop their use.

The FDA acting the way they did today shows that they are indeed the gold standard, and I think that should reassure the American public that they will be very diligent and conservative in how they approach the vaccines, Zients said during the news conference. The fact that a pause was done, I think, just serves as a testimony to how seriously we take safety.

Zients said toward the end of the news conference he hoped to have the pause of the J&J vaccine resolved pretty soon, within days, two weeks, but that will largely be determined by what health officials learn about those six severe cases, according to acting FDA commissioner Dr. Janet Woodcock, who said the review could extend longer depending on "what we learn."

In Tuesdays announcement of the pause of the J&J vaccine, Dr. Anne Schuchat, the principal director of CDC, added that anyone who received the J&J vaccine over a month ago likely won't experience the clotting issues moving forward.

She also said that anyone who has taken the J&J vaccine within the last month and experienced "severe headaches, abdominal pain or leg pain" should contact their doctor, noting that the pain would be different than the typical aches and pains associated with the flu.

Fauci further recommended that people who recently got the J&J vaccine and who may be concerned to not get anxiety reaction.

Remember, its less than one in a million. However, having said that, pay attention, he said, noting that the main warning sign for potential clotting issues is headaches. Additionally, he said people should pay attention to anything that resembles a neurological symptom within three weeks after vaccination.

RELATED: Colorado pauses Johnson & Johnson COVID-19 vaccines following FDA, CDC recommendation

In Colorado, Dr. Eric France, the chief medical officer for the Colorado Department of Public Health and Environment (CDPHE), said during a news conference Tuesday afternoon that the pause on the J&J vaccine "is a strong reflection of the national oversight of vaccine safety, and added that he expects other severe cases to pop up over the next day or two across our state.

Hospitals across the nation may have cases today theyll report to CDC as well, France said. That should give us better sense and ability to determine is this just coincidence or something more associated with the vaccine.

Dr. Michelle Barron, the senior medical director of infection prevention at UCHealth, told Denver7 reiterated what Fauci said earlier Tuesday, that CVST is extremely rare, even for people who haven't been vaccinated.

"This occurs on average, about five out of a million people," Barron said. "And there's probably some genetic predisposition in the blood where you are more likely to clot."

Barron said the severe symptoms experienced by six women between 18 and 48 years old, and which were reported to the CDC and the FDA, appeared a week to 10 days after they got the vaccine. If you were inoculated more than 10 days ago, Barron said you shouldn't worry.

"I'd be more worried about potentially contracting COVID, actually," she said. "It's going to be much more common."

Denver Health's Chief Medical Officer, Dr. Connie Savor Price, echoed Barron's words, saying, "its unusual, but we do see it occur in cases outside of the vaccine."

"Well know more this afternoon from the CDC and we may expect guidance from the CDC as well," Price said, adding she hopes Tuesdays news does not create more vaccine hesitancy.

In terms of preventing that vaccine hesitancy, its incredibly important that we be transparent and investigate these issues if we do hear about them.

Still, it's possible Colorado could see more of these severe cases. On Tuesday, the CEO Centura Health, Peter Banko, confirmed with Denver7 its hospital system is treating at least one patient who is under investigation for "blood clotting issues" after receiving the J&J vaccine.

Banko could not share how recently the patient sought treatment or whether the patient is located in Colorado or Kansas (Centura Health operates in both states), but Centura's chief clinic officer said the patient did not receive the vaccine from Centura Health's drive-up clinics.

Gov. Polis, from his part, hailed the decision from the FDA and the CDC to pause the use of the J&J vaccine as a move designed to increase confidence in public health officials, while at the same time, urging Coloradans who were scheduled to receive the J&J vaccine to reschedule with their provider to receive a different shot. When asked about how the announcement from the FDA and the CDC would hurt vaccination efforts, Polis responded with some perspective.

We have 2.1 million Coloradans whove gotten at least one vaccine, thats roughly of state. There will be people with blood clots because we have a third of the population that has been vaccinated. The key question here is: Is there any statistical difference between the people who have been vaccinated and the people who havent been vaccinated with regard to any of these side effects? Polis said. We know that one thing is sure: COVID-19 is several orders of magnitude more dangerous than any reported incidences of side effects of these vaccines.

The FDA and CDC said Advisory Committee on Immunization Practices (ACIP) will meet Wednesday to review all data available from the U.S. as well as other countries to review the rates of these rare adverse reactions and assess their potential significance.

Denver7's Pattrik Perez contributed to this report.

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Johnson & Johnson's COVID-19 vaccine has been paused in Colorado. Here's what you need to know. - The Denver Channel

Global Alpha Thalassemia Market 2021 Industry Insights, Drivers, Top Trends, Global Analysis And Forecast to 2027 NeighborWebSJ – NeighborWebSJ

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Global Alpha Thalassemia Market 2021 Industry Insights, Drivers, Top Trends, Global Analysis And Forecast to 2027 NeighborWebSJ - NeighborWebSJ

Canavan Disease Treatment Market Growing Demand with Innovative Ideas Adopted by Key Players Johnson & Johnson Services, Inc., GlaxoSmithKline…

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Key Companies Operating in this Market Johnson & Johnson Services, Inc., GlaxoSmithKline plc, Novartis AG, Pfizer, Inc., Sanofi, F. Hoffmann-La Roche Ltd., and Amgen, Inc.

Market by Type Gene Therapy, Drug Therapy, Others

Market by Application Hospitals, Specialty Clinics, Ambulatory Surgical Centers, Others

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Canavan Disease Treatment Market Growing Demand with Innovative Ideas Adopted by Key Players Johnson & Johnson Services, Inc., GlaxoSmithKline...