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Global Precision Cancer Therapies Market 2020: Analysis, Industry Growth, Current Trends and Forecast till 2025 – The Daily Philadelphian

The recently updated and published report titled Global Precision Cancer Therapies Market 2020 by Company, Type and Application, Forecast to 2025, by MarketQuest.biz comprises an exhaustive study of the market that gathers important and crucial information of market size, growth rate, market possibilities, and market revenue forecast from 2020-2025. The report can assist the stakeholders to understand key trends and prospects in the global Precision Cancer Therapies market as well as identify the growth opportunities and competitive scenarios. Crucial aspects covered in the report include key market trends, key dominating players, chapter-wise segregation. Mainly, the report promotes an ambitious landscape of the market, business overview, their policies, and recent developments.

NOTE: Our analysts monitoring the situation across the globe explains that the market will generate remunerative prospects for producers post COVID-19 crisis. The report aims to provide an additional illustration of the latest scenario, economic slowdown, and COVID-19 impact on the overall industry.

Company Profiles:

Every market participant needs to be familiar with the competitive scenario in the global Precision Cancer Therapies industry. The industry research report layouts historical and forecast market data, demand, application details, price trends, and company shares of the leading player by geography. The industry analysts have examined the strategic activities of the competitors to help the key players increase their competitiveness. The report studies the progress of leading players based on crucial parameters, including market share, new developments, global reach, local competition, price, and production. Some of the major companies included in the report are: Abbott Laboratories, Aveo Pharmaceuticals, OncoGenex Pharmaceuticals, Bayer HealthCare, AstraZeneca, GlaxoSmithKline, Boehringer Ingelheim, Hospira

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The study provides an in-depth overview of country-level break-up classified as potentially high growth rate territory, countries with the highest market share in past and current scenario. Some of the regional break-up classified in the study are: North America (United States, Canada and Mexico), Europe (Germany, France, United Kingdom, Russia and Italy), Asia-Pacific (China, Japan, Korea, India, Southeast Asia and Australia), South America (Brazil, Argentina), Middle East & Africa (Saudi Arabia, UAE, Egypt and South Africa)

Market segmentation by product: Hormone Therapy, Immunotherapies, Targeted Therapy, Monoclonal Antibody Therapy, Gene Therapy

Market segmentation by application: Hospitals, Diagnostic Centers, Oncology Clinics, Research Institutes

In the regional analysis, the report highlights the prospective region, which is estimated to generate opportunities in the global Precision Cancer Therapies market in the forthcoming years. The report incorporates data regarding the supply and demand situation, the competitive scenario, and the challenges for market growth. Components such as market drivers, restraints, challenges, and opportunities for the market are explained in detail. The report additionally provides a complete assessment of the expected behavior about the future market and changing market scenario.

ACCESS FULL REPORT: https://www.marketquest.biz/report/4804/global-precision-cancer-therapies-market-2020-by-company-type-and-application-forecast-to-2025

Key Deliverables of The Report Are As Follows:

Customization of the Report:

This report can be customized to meet the clients requirements. Please connect with our sales team ([emailprotected]), who will ensure that you get a report that suits your needs. You can also get in touch with our executives on +1-201-465-4211 to share your research requirements.

About Us

MarketQuest.biz is a leading global Market Research agency providing expert research solutions, trusted by the best. We understand the importance of knowing what global consumers watch and buy, further using the same to document our distinguished research reports. MarketQuest.biz has worldwide presence to facilitate real market intelligence using latest methodology, best-in-class research techniques and cost-effective measures for worlds leading research professionals and agencies. We study consumers in more than 100 countries to give you the most complete view of trends and habits worldwide. MarketQuest.biz is a leading provider of Full-Service Research, Global Project Management, Market Research Operations and Online Panel Services.

Contact Us Mark Stone Head of Business Development Phone: +1-201-465-4211 Email: [emailprotected] Web: http://www.marketquest.biz

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Global Precision Cancer Therapies Market 2020: Analysis, Industry Growth, Current Trends and Forecast till 2025 - The Daily Philadelphian

Cutting-edge Treatment Offers Hope to Infant With Spinal Muscular Atrophy – Adventist Review

November 17, 2020

By Sheann Brandon, Loma Linda University Health

Loma Linda University Childrens Hospital in Loma Linda, California, United States, recently gave its first administration of a new gene replacement therapy to an infant who screened positive for spinal muscular atrophy(SMA). SMA is the top genetic killer of children under the age of two, and the treatment potentially provides a symptom-free life for the patient.

Childrens Hospital physicians said the new drug therapy Zolgensma is a revolution in neurological pediatric care.

This therapy represents a new opportunity for us to intervene and change childrens long-term prospects, and sometimes if we can treat the disease in time, we can restore them to full health, David Michelson, chief of the division of child neurologyand director of the pediatric muscular dystrophy association clinics at Childrens Hospital, said. This therapy is a chance to wipe a patients health slate clean.

The patient was diagnosed with SMA through the state of Californias newborn screening program. Even though the patient seemed perfectly healthy during the first weeks of life, the health-care team worked against the clock to treat the patient before the first onset of symptoms. Studies have shown that infants who receive the therapy as soon after diagnosis as possible have better outcomes than those who receive delayed treatment.

SMA is a rare genetic disease that causes a persons muscles to weaken and become smaller over time. In an infant, this affects development, including crawling, walking, sitting, and head control. Severe types of SMA affect the muscles used for swallowing and breathing and, untreated, lead to ventilator dependence and a high risk of mortality.

According to Michelson, the patients neurologist, there are four types of SMA. These types differ in their severity and at what age they will manifest in a persons body. SMA type I, the most common of the severe forms, can present in infants as early as three months and is often fatal by the age of two.

The new therapy involves one of only three approved drugs to treat SMA in children under two and is the only single-dose treatment option for SMA patients. Hospitals across the country are only beginning to provide this therapy to qualifying patients since the treatment received U.S. Food and Drug Administration (FDA) approval in May 2019.

Michelson said he and his team dont yet know exactly how the treatment will affect the patient.

We may not know how much we helped, since we were able to treat him before he developed symptoms, Michelson said. Best case scenario is he will never develop any symptoms of the disease.

The original version of this story was posted on the Loma Linda University Health news site.

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Cutting-edge Treatment Offers Hope to Infant With Spinal Muscular Atrophy - Adventist Review

Molecular Testing With Universal Method Comparable to Traditional Method in Hereditary Solid Tumors – Targeted Oncology

In multiple solid malignancies, including breast, ovarian, colorectal, and pancreatic cancers, there is a subset of patients with a hereditary predisposition for these diseases, but the current testing criteria do not mention this subset. In an effort to provide more information of genetic testing in this population, a study of Memorial Sloan Kettering Cancer Center (MSKCC) patients was conducted to test the traditional guideline-based method of testing versus universal testing of a broad cancer patient population over a 5-year period.

A total of 7235 patients were included in the analysis and tested for 76 to 88 cancers. Through this study, investigators uncovered pathogenic and likely pathogenic (P/LP) variants in 7.5% (95% CI 6.6%- 8.4%) of 3,341 patients with breast cancer, 17.4% (95% CI, 14%- 21.6%) of 384 those with ovarian cancer, 13.5% (95% CI, 9.8%- 18%) of 252 patients with colorectal, and 8.8% (95% CI, 5.1%-14.8%) of 136 patients with pancreatic cancer.

Overall, the study found that testing with universal method was comparable to the guideline-based method, implying that universal testing can expand genetic testing to patient populations who are in need but are currently underserved.

In an interview with Targeted Oncology during the 2020 Association for Molecular Pathology (AMP) Annual Meeting, Ozge Ceyhan-Birsoy, PhD, assistant directorof the Laboratoryfor Molecular Medicine, MSKCC, discussed genetic testing methods for patients with hereditary predisposition and the molecular research underway at MSKCC to improve testing in this patient population.

TARGTED ONCOLOGY: In recent years, what advances have we see in cancer genetics?

Ceyhan-Birsoy: There have been significant advances in the range of genetic testing options for cancer patients in recent years. More patients are now able to receive molecular testing on their tumors to identify optimal targeted therapies for their cancer and germline genetic testing to uncover hereditary cancer predisposition. A paired analysis of tumor and normal DNA is increasingly being adapted, which improves the interpretation of both somatic and germline mutations. Additionally, incorporation of RNA analysis has expanded the scope of mutations that can be detected and characterized. Finally, the use of cell-free DNA now allows us to profile a patients tumor using only their blood.

TARGETED ONCOLOGY: How can hereditary predisposition inform oncologist for care/treatment decisions?

Ceyhan-Birsoy: Identifying hereditary mutations that predispose patients to cancer has important implications for their treatment and management. There are established targeted therapies available now for certain germline defects. For instance, germline mutations in certain homologous recombination and mismatch repair genes can predict response to PARP inhibitor and immune-checkpoint inhibitor therapies, respectively. Some therapies may pose high risk for patients with particular gene mutations, such as radiation therapy risks for patients with germline TP53 mutations. In addition, identifying hereditary cancer predisposition is critical to allow timely surveillance and prophylactic interventions for future cancers that the patient may be at higher risk of developing. As germline mutations are heritable, this information provides the opportunity for early surveillance in the patients family members, as well.

TARGETED ONCOLOGY: Can you explain how this MSKCC study came about?

Ceyhan-Birsoy: Genetic testing for hereditary cancer predisposition is traditionally performed in a guideline-dependent and targeted manner. In current practice, only patients who meet established criteria from national and professional organizations receive genetic testing and typically get tested for a small number of genes selected based on their tumor type, age of onset, and family histories. MSKCC has been 1 of the first institutes to pilot a universal testing approach for cancer patients, providing comprehensive germline testing of all known cancer predisposition genes without pre-selection of patients based on traditional genetic testing criteria. We have been performing both targeted and universal testing for our patients since 2015.

In this study, we aimed to understand how the yields (positive rates) of these 2 testing approaches compare to each other in greater than 4000 patients who had traditional and more than 9,000 patients who had universal testing at MSKCC in the past 5 years. We also assessed whether universal testing identified additional findings that would have been missed in a targeted testing approach for any given patient.

TARGETED ONCOLOGY: What are the key results of this analysis?

Ceyhan-Birsoy: We saw that universal germline testing without preselection of patients based on current guidelines yielded comparable rates of positive results to traditional guideline-dependent testing approach, particularly in patients with breast, ovarian, and pancreatic cancers. In addition, universal testing uncovered mutations that predispose to other cancers in about 9% of patients in genes that are not routinely tested for their diagnosis. Approximately half of those conferred high to moderate risk to cancer and about 40% of them implicated early surveillance or prophylactic surgery recommendations to prevent other cancers.

TARGETED ONCOLOGY: What is a key takeaway from your AMP 2020 presentation and explain the implications of these findings?

Ceyhan-Birsoy: Our results suggest that the preselection of patients for genetic testing based on the current guidelines may not significantly increase the likelihood of identifying a germline mutation in certain patient populations. A universal and comprehensive testing approach further provides the benefit of identifying hereditary risk for other cancers, allowing early surveillance and prophylactic interventions.

TARGETED ONCOLOGY: How can this information be applied in oncology clinics?

Ceyhan-Birsoy: Our study underlies the advantages of universal and comprehensive testing for cancer patients. However, there are many challenges that may limit the application of this approach for all cancer patients, including the cost of testing, resources needed to provide pre-test and post-test genetic counseling to patients, and the potential to discover more variants of uncertain significance that may lead to higher number of inconclusive results. Future efforts should be dedicated to providing wider groups of cancer patients access to genetic testing, which can aid in their clinical care and in the care of their family members.

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Molecular Testing With Universal Method Comparable to Traditional Method in Hereditary Solid Tumors - Targeted Oncology

Alpha Thalassemia Market Research Provides an In-Depth Analysis on the Future Growth Prospects and Industry Trends Adopted By the Competitors |…

Global Alpha Thalassemia Market 2025 Report Provides Porters Five Forces Analysis Illustrates the Potency of Buyers & Suppliers Operating in the Industry & the Quantitative Analysis of The Global Market from 2019 to 2025 is Provided to Determine the Market Potential.

Alpha Thalassemia Market Data and Acquisition Research Study with Trends and Opportunities 2019-2025 The study of Alpha Thalassemia market is a compilation of the market of Alpha Thalassemia broken down into its entirety on the basis of types, application, trends and opportunities, mergers and acquisitions, drivers and restraints, and a global outreach. The detailed study also offers a board interpretation of the Alpha Thalassemia industry from a variety of data points that are collected through reputable and verified sources. Furthermore, the study sheds a lights on a market interpretations on a global scale which is further distributed through distribution channels, generated incomes sources and a marginalized market space where most trade occurs.

Along with a generalized market study, the report also consists of the risks that are often neglected when it comes to the Alpha Thalassemia industry in a comprehensive manner. The study is also divided in an analytical space where the forecast is predicted through a primary and secondary research methodologies along with an in-house model.

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The following manufacturers are covered: Bluebird Bio Novartis Kiadis Pharma Acceleron Pharma

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Segment by Regions North America Europe China Japan

Segment by Type Iron Chelating Drugs Gene Therapy

Segment by Application Hospitals Private clinics Other

For a global outreach, the Alpha Thalassemia study also classifies the market into a global distribution where key market demographics are established based on the majority of the market share. The following markets that are often considered for establishing a global outreach are North America, Europe, Asia, and the Rest of the World. Depending on the study, the following markets are often interchanged, added, or excluded as certain markets only adhere to certain products and needs.

Here is a short glance at what the study actually encompasses: Study includes strategic developments, latest product launches, regional growth markers and mergers & acquisitions Revenue, cost price, capacity & utilizations, import/export rates and market share Forecast predictions are generated from analytical data sources and calculated through a series of in-house processes.

However, based on requirements, this report could be customized for specific regions and countries.

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Major Point of TOC:

Chapter One: Alpha Thalassemia Market Overview

Chapter Two: Global Alpha Thalassemia Market Competition by Manufacturers

Chapter Three: Global Alpha Thalassemia Production Market Share by Regions

Chapter Four: Global Alpha Thalassemia Consumption by Regions

Chapter Five: Global Alpha Thalassemia Production, Revenue, Price Trend by Type

Chapter Six: Global Alpha Thalassemia Market Analysis by Applications

Chapter Seven: Company Profiles and Key Figures in Alpha Thalassemia Business

Chapter Eight: Alpha Thalassemia Manufacturing Cost Analysis

Chapter Nine: Marketing Channel, Distributors and Customers

Chapter Ten: Market Dynamics

Chapter Eleven: Global Alpha Thalassemia Market Forecast

Chapter Twelve: Research Findings and Conclusion

Chapter Thirteen: Methodology and Data Source 13.1 Methodology/Research Approach 13.1.1 Research Programs/Design 13.1.2 Market Size Estimation 13.1.3 Market Breakdown and Data Triangulation 13.2 Data Source 13.2.1 Secondary Sources 13.2.2 Primary Sources 13.3 Author List 13.4 Disclaimer

About HongChun Research: HongChun Research main aim is to assist our clients in order to give a detailed perspective on the current market trends and build long-lasting connections with our clientele. Our studies are designed to provide solid quantitative facts combined with strategic industrial insights that are acquired from proprietary sources and an in-house model.

Contact Details: Jennifer Gray Manager Global Sales + 852 8170 0792 [emailprotected]

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Alpha Thalassemia Market Research Provides an In-Depth Analysis on the Future Growth Prospects and Industry Trends Adopted By the Competitors |...

Intrathecal Pumps Market 2020 Industry Size and Share Evolution to 2026 by Growth Insight, Trends – The Daily Philadelphian

The Global Intrathecal Pumps Market to gain from rapid technological advancements taking place in the market. Recently Fortune Business Insights has published a report, titled Intrathecal Pumps Market Size, Share and Global Trend By Medication (Baclofen, Hydromorphone Morphine, Clonidine, Midazolam, Bupivacaine, Ziconotide), By Application (Pain Management, Spasticity Management), By End Users (Hospitals & Clinics, Ambulatory Surgery Centers, Others), and Geography Forecast till 2026

Market Segmentation:

By Medication

By End Users

Reasons to Purchase this Report:

Asthma Treatment Market

Legionella Testing Market

Anti-Fungal Drugs Market

Sleep Apnea Devices Market

Impact of COVID-19 on the Medical Devices Market

Cancer Cachexia Market

Gene Therapy Market

Human Insulin Market

Antithrombin Market

Dermatitis Drugs Market

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Intrathecal Pumps Market 2020 Industry Size and Share Evolution to 2026 by Growth Insight, Trends - The Daily Philadelphian

$30 billion to fight COVID-19 over next five years – Sydney Morning Herald

NSW will commit $29.6 billion to a COVID-19 health and economic package over the next five years following unprecedented emergency health spending to weather the pandemic.

Treasury forecasters are working on an assumption that a vaccine will be available by mid-next year, with an estimated 20 per cent of people vaccinated by October.

NSW will spend a total of $1.6 billion on COVID-19 programs in 2020-2021 including $500 million to support COVID clinics, quarantine programs, extra pathology testing and contact tracing.Credit:Getty/Lisa Maree Williams

Social distancing restrictions are likely to be maintained until a vaccine is widely available and most of the population immunised.

Up to $1.6 billion of the COVID-19 response budget will be used for 2020-2021 health programs, including $500 million to support clinics, quarantine programs, extra pathology testing and contact tracing.

More than $458 million will be used to fast track elective surgeries delayed by the pandemic and $20 million will accelerate COVID-specific research and clinical trials.

Some $385 million will be used to purchase additional personal protective equipment.

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Treasurer Dominic Perrottet described the mental health toll as one of the pandemics most insidious hidden costs.

More than $66 million will fund additional mental health clinicians and peer workers, expanding the Police, Ambulance and Clinical Early Response model, enhancing therapeutic activities in inpatient units, increasing capacity and responsiveness of the Mental Health line and expanding virtual mental health services

Overall health spending accounted for one third of the total NSW Budget, Health Minister Brad Hazzard said.

It included $66 million over three years beginning in 2021-22 to fund additional specialist mental health clinicians. Almost $56 million over four years will go to end of life and palliative care, including 5000 additional non-clinical End of Life Support, specialist allied health professionals, education and training, and bereavement and psychosocial support services.

Almost $50 million in 2020-2021 will fund access to lifesaving cell and gene therapies, including CAR T-cell therapy for children and young adults with acute lymphoblastic leukaemia, adults with diffuse large B-cell lymphoma, as well as gene therapy services for blinding eye disease and children with spinal muscular atrophy, and monoclonal antibody therapy for children with neuroblastoma.

A $17 million-pilot program will provide in-home care for pregnant women suffering from hyperemesis gravidarum (severe morning sickness), and Tresillian and Karitane will receive more than $10 million over four years to extend virtual residential parenting services.

There is $10 million over four years to plan and undertake a NSW stroke ambulance pilot project geared towards rapid diagnosis and treatment of strokes.

The governments hospital building boom over the past several years continues. Treasurer Dominic Perrottet said the 29 upgraded hospitals and health facilities announced before the 2019 election would be under way before March 2023.

The Australian Medical Association NSW said it was concerned by the state government's continued emphasis on funding health infrastructure over current funding for staffing and resourcing.

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"Hospitals and healthcare staff are struggling to meet patient demand," AMA NSW President Dr Danielle McMullen said.

The recent concerns raised about resourcing and services at Blacktown Hospital highlight the importance of funding all hospitals appropriately," she said.

Dr McMullen was also concerned funding to fast track elective surgeries wont move the needle enough to improve patient access.

We can see that access is deteriorating and wait times are getting worse," she said. "Patients are waiting more than a year for elective surgery in some cases and we know these figures only tell half the story.

Get our Coronavirus Update newsletter for the day's crucial developments and the numbers you need to know. Sign up toThe Sydney Morning Herald'snewsletterhereandThe Age'shere.

Kate Aubusson is Health Editor of The Sydney Morning Herald.

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$30 billion to fight COVID-19 over next five years - Sydney Morning Herald