Biobanking Market to Witness an Outstanding Growth During 2019-2030 :Thermo Fisher Scientific Inc., PHC Holdings Corporation, QIAGEN NV – Media…

Media releases are provided as is by companies and have not been edited or checked for accuracy. Any queries should be directed to the company itself.

Market Industry Reports (MIR) has published a new report titled Biobanking Market - Industry Analysis, Size, Share, Growth, Trends, and Forecast, 20192030. According to the report, the biobanking market is estimated to be over US$ 1,900 Mn in 2018. It is anticipated to grow at a CAGR of 7.2% from 2019 to 2030.

Biobanking market plays a significant role in the development of biomedical and translational science due to the easy availability of biological samples to discover disease-specific biomarkers. A rising number of research activities used for diagnosis, prognosis and foreseeing drug reactions is expected to support the growth of this market. Increase in public and private funding for the creation of more biobanks is likely to positively contribute to the growth of the global biobanking market.

Get Access To Sample Pages: http://bit.ly/2Obbi4f

Major key Players:

Thermo Fisher Scientific Inc., PHC Holdings Corporation, QIAGEN N.V., Becton, Dickinson and Company, Merck KGaA, Hamilton Company, Avantor, Inc., Tecan Group Ltd., BioCision, Promega Corporation among others.

Biobanking market Segmentation:

Product & Services:

Equipment

Consumables

Services

Softwares

Sample Type:

Blood Products & Services

Biological Fluids

Cell Lines

Human Tissues

Nucleic Acids

Get Access to Data pack:http://bit.ly/37LgALU

Storage Type:

Automated

Manual

Application:

Clinical Research

Life Science Research

Regenerative Medicine

The preservation of cord blood stem cells is an emerging practice that promises a cure for more than 60 different types of diseases. Owing to increasing awareness about stem cell therapies, the large numbers of parents are choosing umbilical cord banks for their children. Moreover, many embryonic disorders can be investigated and treated through stem cell research. For instance, the transformation of early stem cells into different cell types helps to identify if there is any genetic error and can be resolved before the symptoms begin to manifest in the infant.

The main consideration limiting the development of the worldwide biobanking market is the significant expense of mechanization. In addition, the issues related with the obtainment of biospecimen test can hamper the development of biobanking market. For example, when the examples are moved starting with one area then onto the next area for preparing, the time interim among assortment and adjustment may prompt loss of some shaky markers. Also, there are sure moral issues for putting away the organic examples of human mishaps the general market development.

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Biobanking Market to Witness an Outstanding Growth During 2019-2030 :Thermo Fisher Scientific Inc., PHC Holdings Corporation, QIAGEN NV - Media...

Stem cell clinics much-hyped treatments lack scientific support – Science News

Joanna had just turned 62when she noticed that she couldnt stand very long before her right leg wouldhurt. She thought it was from an old injury, when her dog had slammed into herthigh. When the ache moved to her wrist, she went to a doctor who said shemight be getting arthritis.

Thepain quickly intensified. It just happened so rapidly, and I couldnt figureout why, says Joanna, who lives in a Houston suburb. Her doctors chalked it upto wear and tear. Youre getting older, she remembers them telling her.This was in early 2018.

Then she got an e-mail with a link to a video about stem cells and the conditions they could cure, including arthritis. I started watching it and then I just turned it off for a while because I thought, Im afraid Im going to get my hopes up too high, says Joanna, who asked that her last name not be used to protect her medical privacy.

Shestarted seeing full-page ads for stem cell seminars in the newspaper. Sheattended one at a local hotel, and the presenter announced that thousands ofpatients had benefited from stem cell injections. It was natural, the womansaid. No one had ever been harmed. The idea that the treatment wasnt a drugreassured Joanna.

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Shemade an appointment for the next day. It sounded too good to be true, but Iwas desperate, she says. She received injections into her back, neck andshoulder of stem cells from donated umbilical cord blood followed by an IV ofthe product the next day. The cost was $30,000, siphoned from her husbandspension. She knew she was taking a risk, but she felt hopeful.

Twodays later, her face began to burn and itch. Then her feet. She had pain inplaces that had never hurt before, like the joints of her fingers. Her hairstarted falling out, and she descended into a deep depression. Im totallymiserable, she says, months later. Im just agonizing in pain. Now I dontsee any hope.

Stem cells sold at clinics are driving whats thought to be a $2 billion global industry. Facebook pages announce seminars. Local newspapers are wrapped in ads vowing relief without surgery. Stem cells are billed as treatments for everything from autism to multiple sclerosis to baldness. Most commonly, the ads focus on orthopedic issues, especially aching knees.

Animportant point gets left out of the cheery ads: Theres not enough science tojustify using stem cells for any of the advertised conditions, including jointpain. None of the treatments advertised have been approved by the U.S. Food andDrug Administration. (The only approved stem cell treatments are for certaincancers and blood disorders.) Very few of the orthopedic studies in humans havebeen scientifically rigorous, and none have shown stem cells regrowingcartilage.

Itsnot even clear whether treatments being touted as stem cells contain viablestem cells or whether the contents should be defined as stem cells at all. Asthe stem cell industry grows rapidly, many researchers who are studying stemcells for their potential to regenerate tissues worry that the boomingmarketplace, which conflates hype with reality, might ultimately damageresearch progress.

The scientific and medical community ishaving to play defense, says Shane Shapiro of the Mayo Clinic Jacksonville inFlorida, who has conducted one of the very few published trials that comparedstem cells with a placebo for people with osteoarthritis. Misinformation andmisunderstanding about how cells are used to treat disease is proliferating.

The explosion of advertising reflects a dramatic turnaround from the controversy over stem cells that occupied the public in the early 2000s. At the time, scientists had learned how to generate lines of cells from embryos that were left over from in vitro fertilization and donated for research. In theory, the embryonic cells had the potential to treat disease by becoming a slew of different tissues, but their use became entangled with the politics of abortion. Then in 2001, President George W. Bush banned federal funding for research on embryonic stem cell lines not already in labs. Embryonic stem cell research has ridden the political tides since then: Restrictions were eased under Barack Obamas presidency, then Donald Trumps administration added restrictions on fetal tissue use.

Scientists tried to persuade the public to support the research by focusing on the great promise. They argued that stem cells might one day cure diseases by naturally repairing lost or damaged tissue. Actor Michael J. Fox, the most famous Parkinsons patient of his generation, testified to Congress in 1999 that stem cells could one day cure degenerative brain diseases. Joanna remembers Foxs passion. Thats what kind of made us aware of what stem cells were at the time, she says.

Broadly speaking, stem cells are cells capable of renewing themselves and taking on the identity of the tissue around them (SN: 3/19/16, p. 22). The early controversy about using embryonic cells has largely quieted down. The stem cells being marketed today are not embryonic; they come from bone marrow, fat tissue or birth products such as umbilical cord blood or amniotic fluid, all advertised as being able to regenerate cartilage. Clinic websites usually feature earnest testimonials with no hint of any possible negative side effects.

For the first part of the 2000s, stem cell treatments were largely sought through medical tourism. U.S. patients would travel to other countries for experimental treatments to cure diseases such as multiple sclerosis or spinal cord injury.

BioethicistLeigh Turner of the University of Minnesota in Minneapolis noticed a shiftaround 2012. One of the businesses that was part of that marketplace, acompany in South Korea, ended up popping up in the United States, he says. Thecompany, operating under the name Celltex, offered to remove stem cells from apatients own fat tissue, grow the cells in a lab and then reinject them.

Whenthe FDA sent a warning letter to the company in September 2012 stating that itsproducts must be approved before use in patients, the company moved itstreatments to Mexico. Regulations there are less stringent, though the businessremains headquartered in Houston.

Today, many clinics have learned how to operate just inside the margins of federal regulations, or simply ignore them. Turner and Paul Knoepfler of the University of California, Davis mapped the rise in U.S. stem cell clinics that market unapproved therapies, reporting in 2016 in Cell Stem Cell. The first few clinics emerged about 10 years ago, Turner says. By 2014, 2015, companies are pouring into the marketplace at a very rapid rate.

Knoepfler estimates that today more than 1,000 clinics across the country offer stem cells, though there are probably more because many doctors and chiropractors have simply added stem cells as a sideline to their main services. For some, stem cells are lucrative enough to support a business on its own. One in 4 stem cell providers in the Southwest offers the treatment exclusively, researchers at Arizona State University reported in August in Stem Cell Reports.

Thebusiness is extremely profitable, and the treatments are rarely covered byinsurance. Patients pay cash sometimes draining their life savings, takingout loans or drawing down retirement funds like Joanna did.

Often,when you go to business websites, theres not this kind of sober, frank,judicious accounting of risks and benefits or the possibility that theremight be no benefit, that someone could be harmed, Turner says. The websitestend to frame risks and benefits in a very misleading kind of way.

Andbecause each year tens of thousands of U.S. patients by Knoepflers estimate are getting cells in clinics outside of clinical trials, its difficult to knowexactly what the risks of the direct-to-consumer marketplace are. No one iskeeping track.

In 2018, researchers writing in Stem Cells Translational Medicine resorted to searching Google and the scientific literature, where they found 35 reports of serious consequences. Some patients in Florida lost their sight after getting stem cell injections into their eyes. In December, the FDA warned of serious illnesses in Nebraska linked to treatments with exosomes, products taken from placentas that are offered by some stem cell clinics.

A recent survey of neurologists, presented in March 2019 in Dallas at a meeting of the Americas Committee for Treatment and Research in Multiple Sclerosis, asked doctors how their patients had fared after receiving unapproved stem cell treatments. About 25 percent of the 204 neurologists who responded said patients had suffered serious consequences such as strokes and seizures. Three doctors reported that patients had died. Without study, its impossible to know why.

It makes sense that treatments for knee pain appear to dominate the industry the potential customer base is large and growing. More than 600,000 people in the United States had knee replacement operations in 2014, according to data released in 2018 by the American Academy of Orthopaedic Surgeons. That number is expected to rise as baby boomers age and obesity rates climb. As the body ages, shock-absorbing cartilage in the joints wears away, which can lead to painful bone-on-bone rubbing. Stem cells are advertised as an easy way to avoid surgery.

Sofar, though, its not clear thats true. Recently, Maarten Moen, a sports medicinephysician at Bergman Clinics in Naarden, Netherlands, and his colleaguesreviewed every clinical trial he could find that examined using stem cells forknee osteoarthritis. Stem cells are prohibited for use in Holland, says Moen,a member of the medical staff of the Dutch Olympic Committee. Thats why wewere conducting this: to see if we could convince people in our country topossibly start using this therapy. But only if we answer these two questions:Is it helpful? And also, is it safe?

The groups results appeared in 2017 in the British Journal of Sports Medicine. The team found only six human studies testing stem cells for knees, and none were large trials that included a placebo comparison. While the treatment appeared safe, effectiveness couldnt be determined. Every study had methodological problems. As a result, the authors didnt recommend stem cells for knee osteoarthritis. Moen has recently updated his review, but those results have not yet been published. He offers a preview: The evidence didnt get any stronger. He found only two clinical reports that had compared the treatment with a placebo.

Bothwere from Shapiro, of the Mayo Clinic. Its been nearly three years since wefirst published our early results, Shapiro says. With his trial as the firstpiece of the puzzle, he expected that, like anything else in science, wewould be followed by a bunch of other trials. So far, other published resultshave not been pouring in.

Shapiroand colleagues from the Mayo Clinic and Yale University School of Medicine hadtested 25 patients with mild knee osteoarthritis in both legs. The researcherstook about 50 milliliters of cells from each patients bone marrow,concentrated the cells in the laboratory and then injected them back into oneknee of each patient. The other knee got an injection of saline as a placebo.The patients did not know which knee got the experimental treatment.

Both the stem cell knee and the placebo knee improved by about an equal degree about 50 to 75 percent on a pain scale, the team reported in 2017 in the American Journal of Sports Medicine. We werent able to conclude that the stem cell product was any superior in pain relief to anything else, he says. Additionally, we did not see any cartilage regrowth. A 12-month follow-up published in October in Cartilage found similar results.

The fact that the saline alone helped patients feel better was not surprising. A meta-analysis published in 2017 in the American Journal of Sports Medicine examined whether simple saline injections helped knee pain. That review, by researchers at Rush University Medical Center in Chicago and the University of Toronto, found that saltwater alone provided relief on the level of some drugs. But why the knees that got the bone marrow cells in Shapiros study improved to an equal degree is still unclear, he says. So hes not yet ready to say the stem cells dont work.

WhatI think actually happened is that we injected a therapeutic substance in one oftheir knees, and we injected a nonharmful substance, which is the saline, inthe other knee, and the patients were able to get back to their life for aperiod of time that overall made them feel better, he says.

The Mayo study tested stem cells from the patients own bone marrow. But clinics also offer cells from the bodys fat tissue, extracted by liposuction. Doctors can use enzymes to strip away extraneous cells from the fat, leaving only the regenerative cells. But that therapy is also unproven. One study, conducted by researchers in Australia and published in February 2019 in Regenerative Medicine, involved 30 patients with knee osteoarthritis. Patients who received stem cells from fat reported a 69 percent improvement in their pain, compared with no change in a comparison group that did not receive the treatment. But that study offered no placebo injection for comparison.

A second study, by a South Korean team, had a placebo, but a small number of patients. Twelve patients who received stem cells from their own fat had a 55 percent improvement in pain (based on their responses to a questionnaire) compared with no substantial improvement among 12 patients who got a placebo shot, the researchers reported in March 2019 in Stem Cells Translational Medicine. Cartilage didnt regrow with stem cells, but it didnt shrink, which it did in the placebo group.

Butthe treatments in those studies differ from what is actually offered at stemcell clinics. In both of those studies, the researchers expanded orconcentrated the cells in the laboratory before injecting them into patients apractice that is allowed in the United States only in a scientific study. UnderFDA rules, U.S. stem cell centers are only allowed to move a patients owntissue from one place to another, with little manipulation of the cells,otherwise the treatment may be considered an unapproved drug.

Sports medicine physician Kenneth Mautner and colleagues at Emory University in Atlanta compared outcomes for 76 patients with arthritis who received a treatment that was closer to what doctors can do in their offices. Each patient received either cells taken from their own bone marrow or from fat tissue. In both cases, the cells were simply moved to another place within the patients own body. After six months, both groups showed pain reductions and neither treatment was better than the other, the researchers reported in the November 2019 Stem Cells Translational Medicine. There was about 70 to 75 percent improvement for those who actually did improve, Mautner says. About one-quarter of the patients did not get better. Patients with more advanced arthritis were less likely to benefit.

Buthis study had that common shortcoming: no placebo comparison. When yourepaying a lot of money, theres obviously a placebo effect, Mautner says. Itsnot just your mind convincing you that you feel better. The placebo effect canactually be chemicals and cytokines that then produce anti-inflammatory effectsin your joints.

Inaddition to bone marrow and fat tissue, a growing number of clinics areoffering products made from donated umbilical cord blood or other birthproducts, Knoepfler says. Those cells are easy to administer and dont requirethe expertise to extract cells from the body.

Butif there is little evidence for the effectiveness of stem cells from fat andbone marrow, Shapiro says, there is zero support for umbilical products inhuman studies. Im not even studying them yet, he says.

Hardly any evidencesupports the idea that treatments marketed as stem cells can regenerate worntissue, which is what many patients think they are buying. Theres very littleevidence that it will regrow your cartilage, says orthopedic surgeon JasonDragoo of the University of Colorado Denver.

Hisresearch team is conducting a study to see whether there are treatments thatmight increase cartilage thickness. One study pairs the cellular treatment withsurgery. The existing tissue may be more receptive to regrowth, he says, ifyou clear away the debris and all the other things, get it as cleaned up aspossible, then give the cells. Hes also conducting a study comparing theability of cells from fat to repair tiny tears in cartilage that is otherwisemostly healthy, a process he compares with filling potholes.

Buteven if cartilage wont regrow, he and others say, the procedure may stillreduce inflammation, which could quiet a painful knee. Theres also earlyevidence from animal studies that cells from bone marrow or fat might sendchemical signals that jump-start a persons own healing.

Biomaterials scientist Sowmya Viswanathan of the University of Toronto and colleagues reported a study of 12 patients receiving bone marrow cells in August in Stem Cells Translational Medicine. The study had no control group. We saw improvement in symptoms, in pain, in quality of life and in joint stiffness for all the patients. These are the things that the patients care about. The fact that it doesnt regenerate cartilage doesnt disprove its ability to still be a functional, useful cell therapy, she says. It might work, but maybe not in the way that patients expect.

Viswanathan worries thatthe current stem cell market is exploiting the work of scientists, piggybackingoff of the legitimate but early studies for immediate commercial gain, shesays.

Everythinggets called stem cells. Nomenclature is still very important because if youcant name it properly, then you dont even know that youre talking about twodifferent or three or four different things, she adds.

Many clinics call the cells in their products mesenchymal stem cells, a term taken from a 1991 paper by biologist Arnold Caplan of Case Western Reserve University in Cleveland. Yet in 2017 in Stem Cells Translational Medicine, Caplan advocated for a name change: Stem cell misconceptions have led some practitioners in the United States and worldwide to advertise the availability of stem cell treatments (i.e., MSCs can cure the blind, make the lame walk and make old tissue young again).

Viswanathan and other members of the International Society for Cellular Therapy published a position statement in October in Cytotherapy that cells commonly identified as mesenchymal stem cells should more precisely be called mesenchymal stromal cells in the scientific literature to reflect the lack of evidence that, when used as a medical treatment, those cells can renew themselves and form different tissues. (Stromal cells form the bodys connective tissue.) As long as everything is called stem cells, she says, clinics focused on profits will be able to exploit legitimate research for marketing purposes.

Andthere are so many questions left to answer. She worries about what happens whenpeople have bad reactions, like Joanna did. We dont fully understand repeatinjections. We dont know the dosing. If there is an adverse event, then what?she says. Then it sets back the kind of legitimate work thats being donebecause the difference isnt apparent to the funders and to the lay publicbecause everyones calling it exactly the same thing.

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Stem cell clinics much-hyped treatments lack scientific support - Science News

Scientists finally find link between stress and grey hair – nation.co.ke

Study shows stress accelerates hair greyingBy NASIBO KABALE More by this Author21hoursago

There is an infamous photo of former US president Barack Obama showing his appearance before and after he took office.

From the photo, it is clear that almost all of Obamas hair had greyed and he looked a lot older than his actual age. It was assumed that his line of work had a lot to do with his greying hair, something scientist have now confirmed.

Although the natural ageing process and genes play a huge role in the greying of hair, scientists have confirmed that stress is, indeed, a factor as well. A new study published in the journal Nature, associated stress with accelerated hair greying.

Researchers found that the norepinephrine from sympathetic nerves caused the stem cells to activate excessively, sending them into overload and depleting the colour reservoir.

According to the Harvard teams research paper, the specific type of stress associated with the brains fight-or-flight response is the culprit behind greying.

It revealed that when an individual had stress it caused a sympathetic nerve response that activated the stem cells responsible for colouring hair. Our study demonstrates that neuronal activity that is induced by acute stress can drive a rapid and permanent loss of somatic stem cells, and illustrates an example in which the maintenance of somatic stem cells is directly influenced by the overall physiological state of the organism, the team said.

The team made their discovery through a series of experiments that measured the effect of stress on the hair colour of mice. They exposed the animals to three different stressors such as pain, restraint and a model of psychological stress. The animals were stressed over several days by being restrained for four hours a day, Monday to Friday, or through combinations of damp bedding, rapid changes to lighting and tilting their cages.

The study gives hope now that scientists know the protein involved in causing damage to stem cells from stress and they can find out how to possibly delay the greying of hair. For example, the found out that when this protein cyclin-dependent kinase was suppressed, the treatment also prevented a change in the colour of mice fur.

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Scientists finally find link between stress and grey hair - nation.co.ke

Cancer Biological Therapy Market Size, Share, Technology, Included Features, Cost, Revenue, Manufacturers, Region, Applications and Forecast to 2025 -…

A new business intelligence Report Global Cancer Biological Therapy Marketis made covering in-depth analysis by manufacturers and key business segments. The report probes into the current trends, market drivers, growth opportunities, and restraints that are likely to impact the dynamics of the Cancer Biological Therapy Market over the forecast period 2020 2025. Cancer Biological Therapy Market Report presents a professional and deep analysis on the present state of Cancer Biological Therapy Market that Includes major types, major applications, Data type include capacity, production, market share, price, revenue, cost, gross, gross margin, growth rate, consumption, import, export and etc. Industry chain, manufacturing process, cost structure, marketing channel are also analysed in this report.

Introduction:, Cancer is the leading and second largest cause of death across the globe. The disease is characterized by disordered and deregulated cellular and stromal explosion along with reduced cell death and growth factor deprivation, and such other factors. There are many biological therapies that have been approved and being used by various cancer specialists across the globe. While there are many other therapies also which are under the research and development phase and are yet to be available for commercial use., , , Biological therapy treatment is treatment process which is performed with the help of living organisms, parts of living organisms or laboratory manufactured version of such content. Most of the biological therapies uses bacteria or vaccines to mimic the bodys immune system to act against cancer developing cells. These various types of biological therapies, which are most of the times stated to biological response modifier therapy or immunotherapy, but these types of therapies do not always target cancer cells directly. Further there are other biological therapies like sections of genetic material or antibodies which are commonly known as DNA or RNA, do aim at targeting cancer cells directly. There are some other types of biological therapies that inhibit specific molecules involved in development and growth of cancer tumor. Such therapies known as cancer targeted therapies. , The Europe, Middle East and Africa Cancer Biological Therapy market is expected to reach US$ 29,776.3 million by 2023 at a CAGR of 5.0% during the forecast period., , , EMEA Cancer Biological Therapy Market is further segmented into type of therapy which include Monoclonal Antibodies, Conjugated Monoclonal Antibodies, Cancer Growth Blockers, Interferons, Interleukins, Gene Therapy, Targeted Drug Delivery, Colony Stimulating Factor, Cancer Vaccines and other therapies. The Monoclonal Antibodies segment includes sub segment namely Naked Monoclonal Antibodies. Interferon segment is further sub segmented into Alpha Interferon, Beta Interferon and Gamma Interferon., , , On the basis on end users cancer biological therapy market is segmented into Hospitals & Clinics, Laboratories, Cancer Research Centers and other end users. Hospitals & Clinics accounted for the largest market share of EMEA cancer biological therapy market. Hospitals & Clinics commands maximum share of EMEA cancer biological therapy market in 2015. , On the basis of region, Europe accounted for the largest market share in biological therapy market. While Middle East and Africa region is expected to grow with a steady pace during forecast period.

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Objective of Studies:

Cancer Biological Therapy Market Statistics by Types:

Cancer Biological Therapy Market Outlook by Applications:

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Key Question Answered in Report.

Reasons to Buy the Report:

Market Size Forecasts:The authors of the report have provided accurate estimation of the global Cancer Biological Therapy market size based on value and volumeMarket Trend Analysis:This section of the report throws light on the approaching trends and developments in the global Cancer Biological Therapy marketFuture Prospects:The report here offers crucial information on the rewarding opportunities in the global Cancer Biological Therapy marketRegional Analysis:Inclusive analysis of the potential regions and their countries in the global Cancer Biological Therapy market is provided in this part of the reportSegmental Analysis:Here, key segments comprising product type, application, and end user and their contribution to the overall market size are discussed in detailCompetitive Landscape:Market participants will get an overview of the business strategies considered by their competitors to stay ahead of the curve. This analysis will help the players to make informed business decisions in future.

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Table of Contents:1 INTRODUCTION1.1 Definition1.2 Scope of Study1.2.1 RESEARCH OBJECTIVE1.2.2 ASSUMPTIONS & LIMITATIONS1.2.2.1 ASSUMPTIONS1.2.2.2 LIMITATIONS1.3 MARKET STRUCTURE:2 RESEARCH METHODOLOGY2.1 RESEARCH PROCESS:2.2 Primary Research2.3 SECONDARY RESEARCH:3 MARKET DYNAMICS3.1 DRIVERS3.1.1 GROWING Demand for newly developed Cancer Biological Therapy3.1.2 Growing trend of Outsourcing3.1.3 Growing Cancer Biological Therapy Industry in developing nations3.2 RESTRAINTS3.3 OPPORTUNITIES3.4 MACROECONOMIC INDICATORS4 MARKET FACTOR ANALYSIS4.1 Porters Five forces Model4.2 Bargaining power of suppliers4.3 BARGAINING POWER OF BUYERS4.4 THREAT OF NEW ENTRANTS4.5 Threat of Substitutes4.6 Intensity of Rivalry5 global Cancer Biological Therapy market, by Type6 global Cancer Biological Therapy market, By Application7 global Cancer Biological Therapy market, By Manufacturing Methods7.1 In-House Manufacturing7.2 Contract Manufacturing7.2.1 introduction8 Global Cancer Biological Therapy market, by region8.1 North America8.1.1 Introduction8.2 Europe8.2.1 Introduction8.3 Asia-Pacific8.3.1 introduction8.4 Middle East & Africa8.4.1 Introduction9 Competitive landscape9.1 Major Strategies adopted by market players9.1.1 STRATEGIC PARTNERSHIP9.1.2 Merger & Acquisition10 company profile

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Global Age Related Macular Degeneration (AMD) Market: Industry Analysis and Forecast (2019-2026) – Expedition 99

Global Age Related Macular Degeneration (AMD) Marketwas valued US$ XX Bn in 2018 and is expected to reach XX Bn by 2026, at a CAGR of XX % during a forecast period.

Age-related macular degeneration is the prominent cause of severe, irreversible vision loss in people over age 60. It occurs when the small central portion of the retina deteriorates.

Growing population across the globe and the demography reflecting the predominance of the older population, the global affliction of AMD continues to increase at an unprecedented rate. The development of gene therapy for AMD, the growth in the geriatric population, and awareness concerning the AMD are some major factors behind the growth of the global age-related macular degeneration (AMD) market. Additionally, High prevalence of AMD is one of the key drivers in the global age-related macular degeneration (AMD) market. Factors like aging, smoking, high cholesterol, and high blood pressure are causing the prevalence of AMD.

On the other hand, high cost of the treatment, off label usage and strict regulatory policies are some of the factors, which are expected to limit the growth in the global age-related macular degeneration (AMD) market.

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The risk of the occurring the AMD is directly proportional to the age. With the number of people aged above 60 years, the prevalence of AMD is also growing. In 2017, there were, about XX Mn people in the age group 60 years over across the globe, and the number is projected to grow XX Bn during the forecast period. So, the geriatric population is growing faster than younger age groups.

Wet Age-related Macular Degeneration (WAMD) treatment is expected to contribute significant share in the Global Age-Related Macular Degeneration (AMD), market. For wet AMD treatment, the anti-vascular endothelial growth factor is commonly used, which helps to pause or delay the progression of visual loss. By delaying the action of VEGF chemical, it aids to prevent the condition from progressing and partially reverse it. Anti-VEGF medicines include Eylea, Lucentis and Avastin.

Region-wise, The Asia Pacific region is projected to be leading region in the Global age-related macular degeneration (AMD) market. The market in the Asia Pacific region is set to experience favourable growth, which is driven by factors like the elderly population & rising health care expenditure. An increase in the obese population and economic development are also expected to boost the growth in the age-related macular degeneration (AMD) market.

A rise in the number of pipeline drugs for age-related macular degeneration is facilitating the industry key players to sustain in the global age-related macular degeneration market. Additionally, fast track drug designations and regulator government policies like tax benefits are some of the prominent factors aiding the new key players to enter in the age-related macular degeneration market. For instance, Fovista, which is a product of Ophthotech received fast track designation by U.S. FDA and launched in 2018.

The objective of the report is to present comprehensive analysis of global age related macular degeneration (AMD) 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 the all the aspects of industry with dedicated study of key players that includes market leaders, followers and new entrants by region. PORTER, SVOR, PESTEL analysis with the potential impact of micro-economic factors by region on the market have 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 clear futuristic view of the industry to the decision makers.The report also helps in understanding global age related macular degeneration (AMD) market dynamics, structure by analysing the market segments, and project the global age related macular degeneration (AMD) market size. Clear representation of competitive analysis of key players by Type, price, financial position, product portfolio, growth strategies, and regional presence in the global age related macular degeneration (AMD) market make the report investors guide.

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The Scope of the Report for Global Age Related Macular Degeneration (AMD) Market

Global Age Related Macular Degeneration (AMD) Market, By Type

Dry Age-related Macular Degeneration (DAMD) Wet Age-related Macular Degeneration (WAMD)

Global Age Related Macular Degeneration (AMD) Market, By Drug

Lucentis Eylea Avastin Others

Global Age Related Macular Degeneration (AMD) Market, By Stages

Intermediate Stage Age Related Macular Degeneration Early-Stage Age Related Macular Degeneration Late Stage Age Related Macular Degeneration

Global Age Related Macular Degeneration (AMD) Market, By Route ofAdministration

Intravenous Intravitreal

Global Age Related Macular Degeneration (AMD) Market, By Age Group

Above 75 Year Above 60 Year Above 40 Year

Global Age Related Macular Degeneration (AMD) Market, By End User

Hospitals & Clinics Dignostic Centers Academic Research Institutes

Global Age Related Macular Degeneration (AMD) Market, By Region

North America Europe Asia Pacific Middle East & Africa South America

Key players operating in Global Age Related Macular Degeneration (AMD) Market

Kubota Pharmaceutical Holdings Co. Ltd. Alimera Sciences Inc. Adverum Biotechnologies Inc. Gilead Sciences Inc. Apellis Pharmeceuticals Inc. F. Hoffmann-La Roche Ltd. Allergan plc. Bausch Health Companies Inc. Regeneron Pharmaceuticals Inc. Neurotech Pharmaceuticals Inc. Ophthotech Corporation Novartis AG Pfizer Inc. GlaxoSmithKline plc. Bayer AG

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MAJOR TOC OF THE REPORT

Chapter One: Age Related Macular Degeneration Market Overview

Chapter Two: Manufacturers Profiles

Chapter Three: Global Age Related Macular Degeneration Market Competition, by Players

Chapter Four: Global Age Related Macular Degeneration Market Size by Regions

Chapter Five: North America Age Related Macular Degeneration Revenue by Countries

Chapter Six: Europe Age Related Macular Degeneration Revenue by Countries

Chapter Seven: Asia-Pacific Age Related Macular Degeneration Revenue by Countries

Chapter Eight: South America Age Related Macular Degeneration Revenue by Countries

Chapter Nine: Middle East and Africa Revenue Age Related Macular Degeneration by Countries

Chapter Ten: Global Age Related Macular Degeneration Market Segment by Type

Chapter Eleven: Global Age Related Macular Degeneration Market Segment by Application

Chapter Twelve: Global Age Related Macular Degeneration Market Size Forecast (2019-2026)

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Global Age Related Macular Degeneration (AMD) Market: Industry Analysis and Forecast (2019-2026) - Expedition 99

UAB: 50 years of Improving Birmingham, Alabama and the World – Birmingham Times

UAB Magazine

Written by Charles Buchanan, Brett Bralley and Jay Taylor with editorial contributions from Matt Windsor and UAB Public Relations. Images from UAB Archives, Rachel Hendrix, Andrea Mabry, Sarah Parcak, Steve Wood and Getty Images. Web design by Tyler Bryant. Reprinted by permission of UAB Magazine.

UABs birth was like a ray of sunlight punching through the smog.

In 1969 the newly independent university, uniting a pioneering academic medical center and a growing extension center, brought the promise of a brighter future to a city eager for change.

Birmingham is better because of UAB. So are Alabama, America, and the world. In the following pages, discover some of the many ways that UAB has fulfilled its promiseby saving lives, solving problems, expanding knowledge, and opening doorsover 50 years.

1

Best of the best

UABs accolades shine a global spotlight on Birmingham and Alabama:

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A way to retrain the brain

Most scientists once believed that neuroplasticitythe brains ability to grow or repair itselfended in childhood. But research by UAB neuroscientist Edward Taub, Ph.D., contributed to a shift in thinking, and in the 1990s he developed constraint-induced (CI) therapy for stroke patients with poorly functioning limbs. As the intensive training helps patients learn to accomplish tasks with their affected limbs, the brain adapts by strengthening communication with those parts of the body. And the results have been remarkable: Most patients see a clinically significant level of improvement in their ability to use their affected limbs, and brain scans have shown an increase in gray matter. Taub and UAB clinical psychologist Gitendra Uswatte, Ph.D., have used CI therapy to help thousands of stroke patientsand adapted it for patients impacted by cerebral palsy, traumatic brain injury, multiple sclerosis, and spinal cord injury. Today CI therapy is in use worldwide.

3

Discoveries on ice

UAB scientists conduct a lot of research in the fieldbut none may go as far afield as James McClintock, Ph.D.; Charles Amsler, Ph.D.; and Maggie Amsler. Their investigations take place at Palmer Station, Antarctica6,898 miles from their campus offices. For two decades, the biologists have led teams that dive into the frigid waters surrounding the icy continent to study the chemical ecology of the unique marine algae and invertebrates living there. What theyve discovered could aid the search for new drugs to help humans. The group also chronicles the dramatic impact of climate change, such as ocean acidification, on Antarctic marine life. You can see climate change happening there like no other place on earth, says McClintock.

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A pinch of prevention

UAB endocrinologist Constance Pittman, M.D., turned her research passioniodines impact on thyroid functioninto a global mission. In the 1990s and 2000s, she teamed up with Kiwanis International and UNICEF to help eradicate iodine deficiency disorders (IDD), a prevalent cause of cognitive disabilities. Pittman traveled the world to convince companies to add iodine to table saltthe simplest solution for preventing IDD. And her work helped make a lasting impact.

5

Target: Diabetes

In 1973, UAB opened the nations first public diabetes hospitaland the first linked with an academic medical center. Today physicians on the front lines of the diabetes epidemic have an exciting new option to help their patients, thanks to breakthrough research from UABs Comprehensive Diabetes Center.

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Sharing stories that matter

WBHM 90.3 FM radio went on the air in 1976 as the 200th National Public Radio (NPR)-affiliated station. A member-supported service of UAB, WBHM provides global news and award-winning local coverage to Birmingham and the surrounding region. The station also recently welcomed StoryCorps, an NPR-affiliated initiative, to collect stories from the Birmingham community that will be housed at the Library of Congress in Washington, D.C.

7

Book of Life

Its tough to find a physician anywhere in the world who hasnt learned a few things from Tinsley Harrison, M.D. The legendary School of Medicine cardiologist and dean created and edited Harrisons Principles of Internal Medicine, which has been reprinted 20 times, translated into 14 languages, and become arguably the most recognized book in all of medicine, according to the Journal of the American Medical Association.

8

Foresight

The School of Optometry has been a pioneer since it opened in 1969 as the nations first optometry school associated with an academic medical center. Three years later, it became the first optometry teaching program affiliated with a Veterans Administration (VA) hospital, establishing a national model. Today more than 2,500 optometry staff and students from various schools work in the VA system nationwide.

9

Helping our hometown

Living and working in the heart of the city, UAB students, faculty, and staff cant help but feel a connection to Birmingham. Here are just a few ways Blazers have volunteered to support their neighbors:

10

A whole new ball game

Gene Bartow Mens basketball coach1977-1996

UAB started a winning tradition in 1977 when it hired coach Gene Bartow away from powerhouse UCLA to start a mens basketball program. He created a legendary team able to topple top rivals and reach the NCAA Tournament in just its third seasonthe first of 15 NCAA Tournament and 12 National Invitational Tournament appearances on its record. As UABs first athletic director, Bartow also helped UAB compete in other arenas. Today student-athletes in 18 sports give Birmingham reasons to cheer. Take a spin through some of the Blazers most memorable moments:

11

New views of history

Its as if Indiana Jones and Google Earth had a love child. Thats how UAB anthropology faculty member and National Geographic fellow Sarah Parcak, Ph.D., described space archaeology to Stephen Colbert on The Late Show in 2016. She has pioneered the use of high-resolution satellite imagery to search for the buried remains of lost civilizations. And her discoveries have thrilled people worldwide, including Colbert. She was even mentioned in a Jeopardy! answer earlier this year.

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Defense team

UAB immunologists have been among the first to shed light on the mechanisms powering our bodys defenses:

13

Game changers

Future football helmets may better protect athletes thanks to mechanical engineering professor Dean Sicking, Ph.D. (Before coming to UAB, he developed the lifesaving SAFER barriers used on NASCAR and IndyCar courses.) Analyzing data from thousands of helmet-to-helmet impacts in football, Sicking has developed designs for a new helmet that could address concussionsabsorbing as much energy of the impact as possible so that the athlete has less risk of brain injury.

14

The dividends of discovery

In 2018-2019, UAB received $602 million in research grants and awardsjust one year after surpassing the $500-million milestone for the first time. We are aiming high and exceeding our goals, and it is a testament to the UAB research communitys great ideas, hard work, and will to succeed, says Christopher Brown, Ph.D., vice president for research. A rise in research funding means more opportunities to explore the frontiers of knowledgebut it also enables UAB to attract top minds from around the country in health care, engineering, the sciences, and more, plus create new jobs that boost the local economy. Want to ensure that UAB continues its upward trajectory? Philanthropic support helps position the university to attain competitive research grants.

15

Giant leaps

Space is the place for UAB people and technology:

Researcher Larry DeLucas, O.D., Ph.D., became the first optometrist in orbit with a 1992 mission aboard the shuttle Columbia. There he conducted experiments to grow protein crystals, which give scientists a 3D view of protein structuresand a greater understanding of the roles they play in disease. DeLucas also served as chief scientist for the International Space Station in 1994-1995.

Astrophysicist Thomas Wdowiak, Ph.D., passed away in 2013, but his name lives onon Mars. The Red Planets Wdowiak Ridge honors the physics faculty members role in NASAs Mars Exploration Project. Wdowiak was in charge of operating the Mossbauer spectrometers onboard the Spirit and Opportunity rovers that helped uncover firm evidence that water once existed on Mars.

16

Focus on finances

Would you like to get better at saving, budgeting, or investing? Or do you dream of launching a business? The Regions Institute for Financial Education in the Collat School of Business has been helping people throughout the community develop practical, lifelong financial management skills since 2015. Some of its programs include a Money Math Camp for middle schoolers, a College Bridge Camp to prepare high schoolers for life after graduation, and for adults, a Do-It-Yourself Credit Repair Workshop.

17

Going green

Campus expansions have reshaped Birminghams Southside, and UAB works hard to be a good steward of that spaceand set a sustainable example. In 2008, UAB brought open green space into the heart of Birmingham by converting a city street into the Campus Green. Now UAB is aiming to reduce its greenhouse gas emissions by 20 percent and establish a clean energy standard of 20-percent renewable energy by 2025.

18

Ingenuity vs. Infection

Virus vanguards

Antiviral therapies are essential for treating everything from influenza to HIV. In 1977, UAB pediatrics experts Richard Whitley, M.D., and Charles Alford, M.D., helped spark the antiviral revolution by developing vidarabine, the first drug to treat encephalitis caused by the herpes simplex virus. In the 1990s, Whitley and his team transformed the herpes virus into a genetically engineered weapon against tumors.

Vaccines for everyone

The laboratory of Moon Nahm, M.D., is a national treasure, notes the National Institutes of Health. But its discoveries could help protect millions of children worldwide threatened by S. pneumoniae infections, the leading cause of pneumonia. (Nahms lab also is designated a World Health Organization Pneumococcal Reference Laboratory.) His mission is to make pneumonia vaccines more affordable for use in developing countries.

Global guardian

GeoSentinel is a worldwide network of clinics watching for potential pandemics in an increasingly interconnected world, ready to relay information quickly about new disease outbreaks and effective treatments. And it has Alabama roots. UAB travel medicine expert David Freedman, M.D., cofounded GeoSentinel, a collaboration between the International Society for Travel Medicine and the Centers for Disease Control and Prevention, in the 1990s. He also directed the network for 20 years.

19

Staying safe on the road

In 2002, UAB public health researchers unveiled the Digital Childa pioneering computer model evaluating the physical consequences of car crashes on young passengers at various stages of developmentto generate data that could lead to improved child safety devices. Shift gears to today, and researchers in UABs TRIP (Translational Research for Injury Prevention) Lab use virtual realitya first-of-its-kind SUV simulator built with Honda Manufacturing of Alabamato study distracted driving in an effort to save lives. The TRIP Lab also has a portable simulator for schools and community events to help educate students and others on the dangers of distracted driving.

20

A home for Birmingham history

Odessa WoolfolkEducator and civic leader

When Birmingham first dreamed of developing a civil rights museum and research center, UABs Odessa Woolfolk, then special assistant to the president and director of community relations, and Horace Huntley, Ph.D., a historian and first director of the African American studies program, helped lead efforts to turn that idea into a reality. The Birmingham Civil Rights Institute opened in 1992, with Woolfolk as president of its board of directors. Huntley also directed the institutes Oral History Project, which preserves the accounts of foot soldiers and other witnesses to the Birmingham campaign. Today the BCRI attracts visitors from around the world and is a key component of the Birmingham Civil Rights National Monument.

21

Invention in action

Faculty, staff, and students are designing the future for the rest of us. Preview some of their ingenious solutions:

Each year, biomedical engineering and business students develop technologies to help people overcome physical limitations. Examples include a joystick-controlled wheelchair for toddlerswhich won an international awardbuilt for the Bell Center for Early Intervention Programs, and a special scale to help wheelchair users monitor their weight, used by the Lakeshore Foundation. Another design, a mechanical umbrella to protect power wheelchair users from rainy weather, scored second place at the 2018 World Congress on Biomechanics.

Graphic design students in UABs Bloom Studio unleash their talents to support local nonprofits and underserved communities. You can spot their work on license plates and signs that promote and protect the Cahaba Riverpart of a collaboration with the Cahaba River Society.

Solution Studios pairs Honors College, engineering, and nursing students with UAB health professionals to tackle everyday problems affecting patient care. One team has designed a device prototype that could improve quality of life for patients wearing ostomy bags to expel waste. Another has focused on new, more comfortable methods of applying wires to the skin in settings such as intensive care units.

22

Spreading the word

Low literacy levels translate into increased high school dropout rates, a lower-performing workforce, and higher rates of social problems, say UAB School of Education experts. For years UABs Maryann Manning, Ed.D., led the charge to improve literacy across Alabama, launching programs such as a conference that attracted thousands of local schoolchildren to share their writing with authors and illustrators. Today the Maryann Manning Family Literacy Center continues her legacy, providing enrichment activities in reading, writing, math, arts, and science for children and helping teachers across Alabama learn innovative strategies to foster literacy skills in their classrooms.

23

The heart of innovation

John Kirklin, M.D.Surgery superstar

John Kirklin, M.D., helped put Birmingham on the medical map when he was recruited in 1966 to chair the Department of Surgery. He already was a superstar at the Mayo Clinic, where he had revolutionized cardiovascular surgery by improving the heart-lung machine and performing the first operations for a variety of congenital heart malformations. At UAB he continued to pursue new methods and techniques, such as the development of a computerized intensive care unit with continuous monitoring of vital functions, which became a model for ICUs worldwide.

When Kirklin passed away in 2004, colleagues estimated his medical innovations had saved millions of lives. And his legacy thrives in other ways: UAB is a world-class medical center in part because of Kirklins work behind the scenes, where he championed the combination of public and private investments to foster growth. His textbook, Cardiac Surgery, remains a must-read for anyone in the field. His name lives on in The Kirklin Clinic of UAB Hospital, which opened in 1992. And his son, cardiothoracic surgeon James Kirklin, M.D., directs UABs James and John Kirklin Institute for Research in Surgical Outcomes.

24

Birthplace of new businesses

UABs ideas and energy are an engine for entrepreneurship. The university was a founder of Birminghams Innovation Depot, where start-up companiessome born from UAB research breakthroughsfind the resources they need to grow. Today Innovation Depot is the Southeasts largest high-tech business incubator, home to more than 100 companies.

25

University of opportunity

In the fall of 2019, underrepresented students made up nearly 42 percent of UABs enrollment, and 20.5 percent of undergraduates were first-generation students. UAB has a long history of widening access to higher educationand potential careers in science and health careamong diverse students. Back in 1978, the Minority High School Research Apprentice Program began matching local students with faculty members for summer research experiences. Today, initiatives such as the Department of Surgerys Pre-College Internship for Students from Minority Backgrounds and the Neuroscience Roadmap Scholars program offer similar opportunities for students along their educational journeys.

26

Successful careers begin here

More than 135,000 alumni call UAB their alma mater. Today youll find them across the United States and around the world, working as leaders in health care, science, business, art, engineering, government, education, and other fields. Many stay connected with UAB through the National Alumni Society, which was established in 1979 and has 63 chapters in locations ranging from Washington, D.C., to Taiwan.

27

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UAB: 50 years of Improving Birmingham, Alabama and the World - Birmingham Times

Parkinsons Disease Treatment Market 2020 Global Industry Analysis, by Key Players, Segmentation, Application, Demand and Forecast by 2025 – Science…

Global Parkinsons Disease Treatment Market 2020-2025 Overview

The Parkinsons disease treatment market growth was driven because of increase in the geriatric population and the rise in the occurrence of the Parkinsons disease and the funding for research.

Global Parkinsons disease treatment market is anticipated to experience the substantial growth during the forecast period. Growth in the occurrence of the Parkinsons diseases is projected to supplement the growth of global Parkinsons disease treatment market in the coming future. In addition, the combined treatments supporting in the long action of constant dopaminergic stimulation medicines, neural transplantation and gene therapy is expected to fuel the Parkinsons disease treatment market growth.

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Parkinsons disorder is a neurological disorder affecting the movements of body. There are five stages of this disease and can hamper the individuals leg & hand movements, facial expressions getting worse with the growing age. Increase in the elderly population related to the rise in the investments in the activities of research & development, growth in the awareness for healthcare and the neurological disorders are the factors driving the global Parkinsons disease treatment market growth over the forecast period. On the other hand, due to the presence of the other treatments is hampering the Parkinsons disease treatment market growth.

Current developments in the Parkinsons disease treatment, for example, combined treatment to continue the effect of constant dopaminergic stimulation medicines, gene therapy, neural transplantation, neuroprotective treatment to reduce the disease prediction and support for the neurostimulation tools are estimated to provide large development in the global Parkinsons disease treatment market growth during the forecast period. Moreover, major characteristics that are fueling the requirement and demand for the global parkinsons disease treatment market are prevalence of parkinsons disease and growth in the geriatric population. Two important characteristics that are responsible to boost the Parkinsons disease treatment market development are prevalence of the neurodegenerative syndrome and rise in the elderly population. Although, increase in the medicines in the pipeline and growth in the R&D activities are anticipated to surge the Parkinsons disease treatment market size. In addition, lack of skills for the early diagnosis and large spending on treatment is projected to bolster the development of global Parkinsons disease treatment market.

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Key factor driving the growth of Parkinsons disease treatment market is the growth in the acceptance of the treatment for Parkinson disease in healthcare sector. For treating and detecting the dysfunctioning of the human beings central nervous system and the neurological damage because of lack of cells and nerves are the main function of Parkinsons disease treatment market.

Global Parkinsons disease treatment market is segmented into end-use, distribution channel, drug class and region. Based on end-use, market is divided into clinics and hospitals. On the basis of distribution channel, market is divided into retail pharmacies, online pharmacies and hospital. On considering the drug class, market is divided into MAO inhibitors, Levopoda/ Carbidopa and Dopamine Receptor Agonists.

Geographically, regions involved in the development of Parkinsons disease treatment market growth are Europe, North America and Asia Pacific. Asia Pacific is anticipated to show the rapid growth because of the increase in the trend of medical tourism and medical infrastructure. North America holds the largest

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Parkinsons disease treatment market share. Europe is dominating the Parkinsons disease treatment market because of the maximum market revenue in the coming years.

Key players involved in the Parkinsons disease treatment market analysis are Teva Pharmaceutical Industries, Novartis AG, Impax Laboratories and GlaxoSmithKline.

Key Segments in the Global Parkinsons Disease Treatment Market are-

By End-Use, market is segmented into:

By Distribution Channel, market is segmented into:

By Drug Class, market is segmented into:

By Regions market is segmented into:

What to expect from the Global Parkinsons Disease Treatment Market report?

Predictions of future made for this market during the forecast period.

Information on the current technologies, trends, devices, procedures, and products in the industry.

Detailed analysis of the market segmentation, depending on the types, devices, and products.

Government regulations and economic factors affecting the growth of the market.

An insight into the leading manufacturers.

Regional demographics of the market.

Who should buy this report?

Venture capitalists, Investors, financial institutions, Analysts, Government organizations, regulatory authorities, policymakers ,researchers, strategy managers, and academic institutions looking for insights into the market to determine future strategies

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Parkinsons Disease Treatment Market 2020 Global Industry Analysis, by Key Players, Segmentation, Application, Demand and Forecast by 2025 - Science...

What can hold back the hands of time? Scientists have looked at these five treatments – Ottawa Citizen

Scientists have been researching ways to increase a humans healthspan and possible lifespan for decades. Here are things they have considered, and what they have learned.

The intervention:Rapamycin

What is it? First identified in the 1970s in a soil sample from Easter Island, this FDA-approved drug is used to suppress the immune system in transplant patients. Counterintuitively, it also appears to boost immune function in healthy animals. Rapamycin may reduce inflammation, which increases with age. One study found that rapamycin rejuvenated the hearts of old mice. After treatment, there were significant improvements to cardiac function. Research with mice has also found that even when they where administered rapamycin late in life, the mice still had improvements to lifespan and their healthspan.

The verdict: Geroscientist Matt Kaeberlein said rapamycin shows the most promise of any drug that targets aging, in his opinion, although he doesnt necessarily think rapamycin will increase lifespan by 20 to 30 years on average in people. Although it might at the right dose. I do think theres reason to believe that rapamycin could improve several age-related health problems, including boosting immune function and protecting against dementia, cancers, and heart disease.

But critics say it is unclear what the downstream effects could be. If you take a compound like that for a few decades, there may be downstream effect a small epidemic of lymphoma, perhaps, said geriatrician Dr. Peter Boling. While it is approved to prevent rejection in organ transplant patients, it is not approved to treat aging.

There are also questions about side effects, which may include susceptibility to infection and the possibility of developing lymphoma.

We still dont know about all of the hidden dangers. As hopeful as we might be, we have to be aware of the limitations, said Boling.

The intervention: Metformin

What is it? This drug has been prescribed to millions of people to treat diabetes. Among other effects, it decreases insulin levels. It also appears to target biological mechanisms related to aging. Its anti-aging effects may be linked to its influences on metabolic and cellular processes associated with inflammation. It has been linked to lifespan extension and protection against age-related diseases in animal models.

The verdict: The speculation in scientific circles has been that many of the drugs used to treat early-stage chronic disease may be effective, at least in part, because they target aging itself.

Metformin is an interesting case, said Kaeberlein. It clearly increases survival in people with diabetes and likely would do the same for pre-diabetics and others with significant metabolic disease, which represents a growing percentage of adults, he said. However, its less clear whether metformin will be beneficial in people who are metabolically healthy and exercise regularly.

The studies in mice suggest that metformin is different from rapamycin, in the sense that metformin only increases lifespan by a very small amount and in some cases has been reported to have no effect or even shortens lifespan in mice.

The FDA has accepted a clinical trial, Targeting Aging with Metformin, known as TAME, which will test whether metformin can delay the onset of age-related diseases and conditions including cancer, cardiovascular disease and Alzheimers disease. The goal of the trial, which is estimated to cost $55 million, is not to help people live to be 120 years old but to add health to our years, said the American Federation for Aging Research.

Like metformin, several promising drugs show great potential and await trials. If successful, the TAME trial would give the pharmaceutical industry impetus to advance these drugs and transform aging from a period of sickness to a time of extended vitality.

The intervention: Caloric restriction

What is it? A dietary regimen that reduces calories while maintaining nutrients. Research in lab animals, which started almost a century ago, has shown that it is possible to delay age-related diseases in mice and rats through dietary and caloric restriction, but results have varied.

A parallel study of two groups of rhesus monkeys, one at the University of Wisconsin and the other at the U.S. National Institute on Aging, looked at the life-prolonging and health effects of a calorie-restricted diet. The researchers found that the Wisconsin monkeys on a diet with 30 per cent fewer calories than the control group survived to about 28 years for males and about 30 years for females a couple of years above average for monkeys in captivity. Calorie-restricted monkeys in both groups showed fewer age-related health conditions compared to the control monkeys.

Some biohackers people who use biological interventions to optimize health have embarked on caloric restriction diets, with the goal of living longer. Entrepreneur Dave Asprey, author of Bulletproof Diet, has said he plans to live to be 180 and is hacking his own biology with a number of interventions, including supplements and a strict diet.

The verdict so far: The rhesus monkey study also produced some contradictory findings. The National Institute on Agings study found that while the dieting monkeys showed improved health, they didnt necessarily live longer than the control monkeys. Its not clear why there was a difference between the two groups of monkeys, although they were fed different diets and had different feeding times and access to food. The ages at which they dieted may also have come into play.

There is no compelling evidence caloric restriction will work with people, said Doug Gray, a molecular biologist with an interest in the role of protein homeostasis in aging and diseases of aging at the Ottawa Hospital Research Institute.

If this sounds like a depressing route to extreme longevity, even scientists agree. Noted one researcher: Life might seem longer, but it wouldnt necessarily be longer.

The intervention: Gene editing

What is it? Genome editing, or gene editing, is a type of genetic engineering in which DNA is inserted, deleted, modified or replaced.

Last February, for example, the journal Nature Medicine reported on a therapy using CRISPR-Cas9 genome editing technology aimed at suppressing rapid aging in mice with the rare genetic disorder progeria, which causes accelerated aging. According to the report, two months after the therapy, the progeria mice were stronger and more active and had better heart health. Their lifespan also increased by about 25 per cent.

The verdict so far: Not ready for prime time, said Boling. Even though we have successfully mapped the human genome, and its technically possible to remove a gene sequence and replace it, we have yet to successfully edit genes in a complex organism. Many people dont want to eat food containing genetically-modified organisms, let alone become one, he said.

I dont think we have a clear handle on a special gene sequence that would essentially change the aging process. I would want to see if we could do it in a limited and focused way without undue downstream consequences.

In 2017, researchers at Stanford University medical school reported that injections of blood plasma from donors between the ages of 18 and 30 showed promise for helping human Alzheimers patients with mild to moderate symptoms regain some ability to perform basic daily tasks.Colleen De Neve Colleen De Neve / Calgary Herald

The intervention: Young blood

What is it? There have been a number of studies that looked at whether giving old mice blood from young mice could reverse some signs of aging. Even the researchers admitted it sounded creepy, but the results were intriguing. One study at the University of California, Berkeley, published in 2018, found that old mice showed benefits, including better muscle repair, from receiving blood from young mice. But young mice who received old blood had negative effects, including performing poorly on a strength test.

In 2017, researchers at Stanford University medical school reported that injections of blood plasma from donors between the ages of 18 and 30 showed promise for helping human Alzheimers patients with mild to moderate symptoms regain some ability to perform basic daily tasks, such as remembering to take their medications or preparing meals. The results were based on reports from the patients and their caregivers. The researchers cautioned that more research is needed, since the trial involved only nine patients who had received plasma infusions and nine who had received a placebo saline infusion.

The verdict so far: Dont try it. In a statement last February, the FDA said it had significant public health concerns about establishments that offer infusions of plasma from young donors to treat conditions ranging from normal aging and memory loss to Parkinsons disease, multiple sclerosis, Alzheimers disease, and PTSD.

Simply put, were concerned that some patients are being preyed upon by unscrupulous actors touting treatments of plasma from young donors as cures and remedies. Such treatments have no proven clinical benefits for the uses for which these clinics are advertising them and are potentially harmful, warned the FDA. There are reports of bad actors charging thousands of dollars for infusions that are unproven and not guided by evidence from adequate and well-controlled trials.

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What can hold back the hands of time? Scientists have looked at these five treatments - Ottawa Citizen

Snake venom can now be made in a lab and that could save many lives – KTVZ

If youre unlucky enough to have a poisonous snake sink its fangs into you, your best hope is an antivenom, which has been made in the same way since Victorian times.

It involves milking snake venom by hand and injecting it into horses or other animals in small doses to evoke an immune response. The animals blood is drawn and purified to obtain antibodies that act against the venom.

Producing antivenom in this way can get messy, not to mention dangerous. The process is error prone, laborious and the finished serum can result in serious side effects.

Experts have long called for better ways to treat snake bites, which kill some 200 people a day.

Now finally scientists are applying stem cell research and genome mapping to this long-ignored field of research. They hope it will bring antivenom production into the 21st Century and ultimately save thousands, if not hundreds of thousands, of lives each year.

Researchers in the Netherlands have created venom-producing glands from the Cape Coral Snake and eight other snake species in the lab, using stem cells. The toxins produced by the miniature 3-D replicas of snake glands are all but identical to the snakes venom, the team announced Thursday.

In a parallel breakthrough, scientists in India have sequenced the genome of the Indian cobra, one of the countrys big four snakes that are responsible for most of the 50,000 snakebite deaths India sees a year.

Theyve really moved the game on, said Nick Cammack, head of the snakebite team at UK medical research charity Wellcome. These are massive developments because its bringing 2020 science into a field thats been neglected.

Hans Clevers, the principal investigator at the Hubrecht Institute for Developmental Biology and Stem Cell Research in Utrecht, never expected to be using his lab to make snake venom.

A decade ago, he invented the technique to make human organoids miniature organs made from the stem cells of individual patients. Theyve allowed doctors to test the specific effects of drugs safely outside the body, something that has revolutionized and personalized areas such as cancer treatment.

So why did he decide to culture a snake venom gland?

Clevers said it was essentially a whim of three PhD students working in his lab whod grown bored of reproducing mouse and human kidneys, livers and guts. I think they sat down and asked themselves what is the most iconic animal we can culture? Not human or mouse. They said its got to be the snake. The snake venom gland.

They assumed that snakes would have stem cells the same way mice and humans have stems cells but nobody had ever investigated this, said Clevers.

After sourcing some fertilized snake eggs from a dealer, the researchers found they were able to take a tiny chunk of snake tissue, containing stem cells, and nurture it in a dish with the same growth factor they used for human organoids albeit at a lower temperature to create the venom glands. And they found that these snake organoids tiny balls just one millimeter wide produced the same toxins as the snake venom.

Open them up and you have a lot of venom. As far as we can tell, its identical. Weve compared it directly to the venom from the same species of snake and we find the exact same components, said Clevers, who was an author of the paper that published in the journal Cell last week.

The team compared their lab-made venom with the real thing at the genetic level and in terms of function, finding that muscle cells stopped firing when exposed to their synthetic venom.

The current antivenoms available to us, produced in horses not humans, trigger relatively high rates of adverse reactions, which can be mild, like rash and itch, or more serious, like anaphylaxis. Its also expensive stuff. Wellcome estimate that one vial of antivenom costs $160, and a full course usually requires multiple vials.

Even if the people who need it can afford it most snakebite victims live in rural Asia and Africa the world has less than half of the antivenom stock it needs, according to Wellcome. Plus antivenoms have been developed for only around 60% of the worlds venomous snakes.

In this context, the new research could have far-reaching consequences, allowing scientists to create a biobank of snake gland organoids from the 600 or so venomous snake species that could be used to produce limitless amounts of snake venom in a lab, said Clevers.

The next step is to take all that knowledge and start investigating new antivenoms that take a more molecular approach, said Clevers.

To create an antivenom, genetic information and organoid technology could be used to make the specific venom components that cause the most harm and from them produce monoclonal antibodies, which mimic the bodys immune system, to fight the venom, a method already used in immunotherapy treatments for cancer and other diseases.

Its a great new way to work with venom in terms of developing new treatments and developing antivenom. Snakes are very difficult to look after, Cammack said, who was not involved with the research.

Clevers said his lab now plans to make venom gland organoids from the worlds 50 most venomous animals and they will share this biobank with researchers worldwide. At the moment, Clevers said they are able to produce the organoids at a rate of one a week.

But producing antivenom is not an area that pharmaceutical companies have traditionally been keen to invest in, Clevers said

Campaigners often describe snakebites as a hidden health crisis, with snakebites killing more people than prostrate cancer and cholera worldwide, Cammack said.

Theres no money in the countries that suffer. Dont underestimate how many people die. Sharks kill about 20 per year. Snakes kill 100,000 or 150,000, said Clevers.

Im a cancer researcher essentially and I am appalled by the difference in investment in cancer research and this research.

One challenge to making synthetic antivenom is the sheer complexity of how a snake disables its prey. Its venom contains several different components that have different effects.

Researchers in India have sequenced the genome of the Indian Cobra, in an attempt to decode the venom.

Published in the journal Nature Genetics earlier this month, its the most complete snake genome assembled and contains the genetic recipe for the snake venom, establishing the link between the snakes toxins and the genes that encode them. Its not a straightforward cocktail the team identified 19 genes out of 139 toxin genes as the ones responsible for causing harm in humans.

Its the first time a very medically important snake has been mapped in such detail, said Somasekar Seshagiri, president of SciGenom Research Foundation, a nonprofit research center in India.

It creates the blueprint of the snake and helps us get the information from the venom glands. Next, his team will map the genomes of the saw-scaled viper, the common krait and the Russells viper the rest of Indias big four. This could help make antivenom from the glands as it will be easier to identify the right proteins.

In tandem, both breakthroughs will also make it easier to discover whether some of the potent molecules contained in snake venom are themselves worth prospecting as drugs allowing snakes to make their mark on human health in a different way to how nature intended by saving lives.

Snake venom has been used to make drugs that treat hypertension (abnormally high blood pressure) and heart conditions such as angina.

As well as being scary, venom is amazingly useful, Seshagari said.

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Snake venom can now be made in a lab and that could save many lives - KTVZ

Stem Cell Therapy Market Predicted to Accelerate the Growth by 2017-2025 – Jewish Life News

Stem Cell Therapy Market: Snapshot

Of late, there has been an increasing awareness regarding the therapeutic potential of stem cells for management of diseases which is boosting the growth of the stem cell therapy market. The development of advanced genome based cell analysis techniques, identification of new stem cell lines, increasing investments in research and development as well as infrastructure development for the processing and banking of stem cell are encouraging the growth of the global stem cell therapy market.

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One of the key factors boosting the growth of this market is the limitations of traditional organ transplantation such as the risk of infection, rejection, and immunosuppression risk. Another drawback of conventional organ transplantation is that doctors have to depend on organ donors completely. All these issues can be eliminated, by the application of stem cell therapy. Another factor which is helping the growth in this market is the growing pipeline and development of drugs for emerging applications. Increased research studies aiming to widen the scope of stem cell will also fuel the growth of the market. Scientists are constantly engaged in trying to find out novel methods for creating human stem cells in response to the growing demand for stem cell production to be used for disease management.

It is estimated that the dermatology application will contribute significantly the growth of the global stem cell therapy market. This is because stem cell therapy can help decrease the after effects of general treatments for burns such as infections, scars, and adhesion. The increasing number of patients suffering from diabetes and growing cases of trauma surgery will fuel the adoption of stem cell therapy in the dermatology segment.

Global Stem Cell Therapy Market: Overview

Also called regenerative medicine, stem cell therapy encourages the reparative response of damaged, diseased, or dysfunctional tissue via the use of stem cells and their derivatives. Replacing the practice of organ transplantations, stem cell therapies have eliminated the dependence on availability of donors. Bone marrow transplant is perhaps the most commonly employed stem cell therapy.

Osteoarthritis, cerebral palsy, heart failure, multiple sclerosis and even hearing loss could be treated using stem cell therapies. Doctors have successfully performed stem cell transplants that significantly aid patients fight cancers such as leukemia and other blood-related diseases.

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Global Stem Cell Therapy Market: Key Trends

The key factors influencing the growth of the global stem cell therapy market are increasing funds in the development of new stem lines, the advent of advanced genomic procedures used in stem cell analysis, and greater emphasis on human embryonic stem cells. As the traditional organ transplantations are associated with limitations such as infection, rejection, and immunosuppression along with high reliance on organ donors, the demand for stem cell therapy is likely to soar. The growing deployment of stem cells in the treatment of wounds and damaged skin, scarring, and grafts is another prominent catalyst of the market.

On the contrary, inadequate infrastructural facilities coupled with ethical issues related to embryonic stem cells might impede the growth of the market. However, the ongoing research for the manipulation of stem cells from cord blood cells, bone marrow, and skin for the treatment of ailments including cardiovascular and diabetes will open up new doors for the advancement of the market.

Global Stem Cell Therapy Market: Market Potential

A number of new studies, research projects, and development of novel therapies have come forth in the global market for stem cell therapy. Several of these treatments are in the pipeline, while many others have received approvals by regulatory bodies.

In March 2017, Belgian biotech company TiGenix announced that its cardiac stem cell therapy, AlloCSC-01 has successfully reached its phase I/II with positive results. Subsequently, it has been approved by the U.S. FDA. If this therapy is well- received by the market, nearly 1.9 million AMI patients could be treated through this stem cell therapy.

Another significant development is the granting of a patent to Israel-based Kadimastem Ltd. for its novel stem-cell based technology to be used in the treatment of multiple sclerosis (MS) and other similar conditions of the nervous system. The companys technology used for producing supporting cells in the central nervous system, taken from human stem cells such as myelin-producing cells is also covered in the patent.

Global Stem Cell Therapy Market: Regional Outlook

The global market for stem cell therapy can be segmented into Asia Pacific, North America, Latin America, Europe, and the Middle East and Africa. North America emerged as the leading regional market, triggered by the rising incidence of chronic health conditions and government support. Europe also displays significant growth potential, as the benefits of this therapy are increasingly acknowledged.

Asia Pacific is slated for maximum growth, thanks to the massive patient pool, bulk of investments in stem cell therapy projects, and the increasing recognition of growth opportunities in countries such as China, Japan, and India by the leading market players.

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Global Stem Cell Therapy Market: Competitive Analysis

Several firms are adopting strategies such as mergers and acquisitions, collaborations, and partnerships, apart from product development with a view to attain a strong foothold in the global market for stem cell therapy.

Some of the major companies operating in the global market for stem cell therapy are RTI Surgical, Inc., MEDIPOST Co., Ltd., Osiris Therapeutics, Inc., NuVasive, Inc., Pharmicell Co., Ltd., Anterogen Co., Ltd., JCR Pharmaceuticals Co., Ltd., and Holostem Terapie Avanzate S.r.l.

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Stem Cell Therapy Market Predicted to Accelerate the Growth by 2017-2025 - Jewish Life News