The UCB banking market to grace digital transformation curve at a … – Digital Journal

PRESS RELEASE

Published April 19, 2023

NEW YORK : UCB is collected from the umbilical cord of a newborn baby and also retrieved from the placenta after delivery. It is enriched with adult stem cells and these stem cells play a vital role in regulating all biological activities and in developing tissues in the human body.

The UCB banking marketreached USD 13,515.8 million in 2014 at a CAGR of 6.1%, to reach USD 19,335.6 million by 2020.

Globally, UCB banking market is growing rapidly due to increasing prevalence of chronic diseases coupled with the regenerative medicines. In addition, various government associations and initiatives are also supporting the growth of the market. North America has the largest market share, followed by Europe and Asia-Pacific, in the global UCB banking market. The global UCB banking market was valued at 10,900 million in 2010 and reached USD 12,774.8 million in 2013.

Umbilical cord blood banking is a process of collecting and storing umbilical cord blood for future medical use. Umbilical cord blood is a rich source of hematopoietic stem cells that can be used to treat various diseases such as leukemia, lymphoma, and other blood disorders. The umbilical cord blood banking market is growing at a rapid pace due to increasing awareness among parents about the potential benefits of storing their childs cord blood. This report aims to provide an overview of the umbilical cord blood banking market, its current trends, and future prospects.

Request For Free Sample Report of Umbilical Cord Blood Banking Market @https://www.persistencemarketresearch.com/samples/3043

Some of the major players operating in the UCB Banking Market:

However, strict license and accreditation procedures and high cord blood Banking Market fee in private banks hampers the growth of global UCB Banking Market. As a result, the global UCB Banking Market is expected to grow a CAGR of 6.1% during 2014-2020.

North America has the largest market for UCB Banking Market. Increasing prevalence of chronic diseases is key driver of UCB Banking Market in the region. In addition, various government associations have also led to the importance of cord blood donation and services for its future use in North America.

Similarly, the European UCB Banking Market is mainly driven by the increasing prevalence of diseases. In addition, increased awareness about therapeutic applications of cord blood and rising number of live births are also contributing in the growth of the UCB market in the region.

In Asia-Pacific, UCB Banking Market is growing due to rising aging population and increasing prevalence of chronic diseases. In addition, several government associations and increasing number of live births are also increasing the demand of cord blood Banking Market services in the region.

Get Premium Research Report @https://www.persistencemarketresearch.com/checkout/3043

Market Drivers

Globally, UCB Banking Market is growing rapidly due to increasing prevalence of chronic diseases coupled with the regenerative medicines. In addition, various government associations and initiatives are also supporting the growth of the market. North America has the largest market share, followed by Europe and Asia-Pacific, in the global UCB Banking Market. The global UCB Banking Market was valued at 10,900 million in 2010 and reached USD 12,774.8 million in 2013.

Globally, increasing prevalence of chronic diseases coupled with the emerging field of regenerative medicines is driving the UCB Banking Market. In addition, various government associations and initiatives are also supporting in the growth of the UCB Banking Market.

Market Restraints

Strict license and accreditation procedures impede the growth of UCB Banking Market. In addition, high Banking Market cost in private UCB banks is also hampering the growth of UCB Banking Market. Allogeneic hematopoietic stem cell transplantation and cord tissue storage are some of the major trends in UCB Banking Market.

Access full report @ https://www.persistencemarketresearch.com/market-research/umbilical-cord-blood-Banking Market-market.asp

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The UCB banking market to grace digital transformation curve at a ... - Digital Journal

How umbilical cords from babies are saving cancer patients’ lives – Daily Mail

Cancer patient Nilush Aponso knows he is only alive today thanks to a decision by two anonymous mothers to donate the umbilical cords of their newborn babies.

The blood the cords contained provided life-saving cells to cure his cancer.

Nilush, 42, from Barwell, Leicester, who owns a doggy day centre, had an aggressive type of blood cancer, acute myeloid leukaemia.

Initially, chemotherapy had seemed to clear the disease but three months after his treatment finished, the cancer returned.

He was told that the only treatment option left was a stem cell transplant donated cells that would make their way to his bone marrow, where they could grow and make healthy new blood cells.

Nilush, 42, from Barwell, Leicester, had an aggressive form of blood cancer. He said he encourages the customers at his doggy daycare to donate

Xin Tong with her husband Justas Budraitis and their baby daughter Luna Budraitis (pictured) from Manchester. The couple donated baby Luna's cord blood

'I'd spent eight months in and out of hospital, having three lots of chemotherapy and trying different types of drugs, more than I can remember,' says Nilush. 'But none of them worked and doctors told me my only option left was a transplant.'

Stem cells can be taken from a donor's blood or bone marrow, but the patient's tissue type needs to be matched.

'My younger brother was tested to see if he was a match, but sadly he wasn't,' says Nilush. 'And as I'm Sri Lankan, I was told the chance of finding a match was much lower than usual because there is a shortage of people from minority ethnic backgrounds on the bone marrow register.'

Those from a minority ethnic background have only a 37 per cent chance of finding a bone marrow match from an unrelated donor, whereas someone from a white Caucasian background has a 72 per cent chance because there are many more from this population signed up to the register.

A recruitment drive among the Sri Lankan community in London couldn't find a match for Nilush, so the only chance for him was a transplant of stem cells from cord blood, i.e. that which remains in the placenta and umbilical cord following the birth of a baby.

Stem cells from cord blood don't have to be as highly matched in terms of the donor tissue type as adult stem cells.

This blood is rich in blood stem cells similar to those found in bone marrow, and because these cells have the ability to transform themselves into different types of cells, they can be used to treat a range of blood cancers, genetic disorders and immune deficiencies.

The charity Anthony Nolan, which runs the oldest bone marrow register in the UK, is now campaigning to encourage more parents to donate their baby's cord blood.

Since starting its cord blood storage programme in 2008, 324 of its donations have been used for life-saving transplants: the charity aims to bank 800 cords a year, from as diverse a population as possible.

The major benefit of cord blood stem cell transplants is they're less likely to be rejected by the host than an adult donor's cells.

'The stem cells from cord blood are more nave as they haven't been exposed to the environment or pathogens that could cause disease to a patient,' explains Dr Roger Horton, lead cord specialist at Anthony Nolan.

'They don't react in a way that could negatively impact the patient's health as much long term, which is always a possibility with cells from adult donors. So we are able to have a higher degree of mismatch and the transplant can still be a success.'

If no suitable donor is found, the charity will scour international registers for a match, as happened with Nilush.

He knows the stem cells used in his transplant came either from the cord blood of a baby born in the U.S. or from one born in Australia, as both matched.

'I'm all over the place a Sri Lankan, living in England, with an immune system from an American or an Australian,' Nilush laughs.

As well as increasing the number of transplants possible, cord blood stem cells extend the age range of patients to those of retirement age.

'With adult donor cells, high doses of chemotherapy are needed to thoroughly clean out the patient's own immune system and the side effects of this can be too harsh for older patients or those with other complications,' explains Dr Horton.

'But when using cord blood, you can use much less intense chemo, so it's broadened the window for transplant to people who have recently retired or older.'

Cord blood transplants have also increased the survival rates of some blood cancers, particularly in young patients with high-risk blood cancers. The exact figures are due to be published later this year.

The drawback of using these cells is an umbilical cord only holds 70ml to 300ml of blood.

'It's a finite amount, so we can't go back for a top-up if a patient needs more, which of course we can do if an adult donor is a match,' Dr Horton adds. (And with some diseases 'only adult donor cells will work as it can be given in greater amounts'.)

The actual transplant is relatively simple, Dr Horton says.

'The bag of cord blood, which has been stored at minus 196c, is defrosted in a waterbath at the patient's bedside and is infused via a central line into the chest, in a process lasting less than 20 minutes,' he says.

'It then takes between seven and 28 days to repopulate the bone marrow and create a functioning immune system.'

After having the cord blood transplant in November 2013, Nilush had to stay in hospital for two months. Since then, he has remained cancer free.

Yet when he was diagnosed in June 2012, after losing weight and having no energy, he was told his cancer was so aggressive that he had to start treatment immediately. He wasn't even given the time to go home first.

'I just had to start the chemotherapy straight away,' he recalls.

Anthony Nolan collects cord blood from babies born at five hospitals: St Mary's Oxford Road and St Mary's Wythenshawe, both in Manchester; Leicester Royal Infirmary; Leicester General Hospital and King's College Hospital in London.

Separately, the NHS collects cord blood from University College London Hospital, St George's Hospital in London and Luton & Dunstable University Hospital.

'Immediately after the baby is born, and the placenta is delivered, one of our collectors takes away the placenta and umbilical cord,' says Dr Horton.

Once collected, the blood is processed and tested to ensure it is free of viruses and bacteria, and is used either for research or is frozen and banked to be used for patients in the UK or around the world. It's the same process for cord blood collected by the NHS.

Anthony Nolan works with the NHS in sharing the register and together they store about 35,000 cord blood donations in Nottingham and Bristol. Unlike blood donations, cord blood can be stored indefinitely.

Despite the amount already stored, more donations are needed, particularly to help patients from African, African-Caribbean, Asian, Chinese, Jewish, Eastern European and Mediterranean communities.

Xin Tong, 34, and Justas Budraitis, 29, donated their daughter's cord blood.

Xin was a blood donor in China and is pleased that her daughter Luna has followed suit, saying: 'She was born a life-saver'

The couple, from China and Lithuania respectively, met when they were studying at Manchester University. Now married and still living in the city, their daughter Luna was born on October 26, 2022, weighing 8lb 9oz.

'We wanted to welcome her into the world by doing something with significance,' says Xin, an e-commerce account manager.

We saw the posters up in the hospital about donating when we went for antenatal checks and decided to sign up,' Xin explains. 'It was a simple process and we were told that when we went to hospital for the birth I should tell the midwife, who would inform Anthony Nolan.

'I ended up going into hospital early as Luna had stopped growing and needed to be induced, but I was still able to donate the umbilical cord.'

Xin was a blood donor in China and is pleased that her daughter has followed suit.

'She was born a life saver she's really special,' says Justas, who is an IT consultant.

Understandably, Nilush and his wife Helen, 55, are also vocal about the importance of cord donation.

'I tell all my customers about its benefits and since then two of them have donated successfully,' Nilush says, proudly.

'I wish everyone would look into it. I don't know when the parents donated or who they are, but their decision to donate their babies' umbilical cords is why I am here today. And I want other people to have the same chance.'

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How umbilical cords from babies are saving cancer patients' lives - Daily Mail

Alzheimer’s study shows improved memory and mood with … – Drug Target Review

Using rodent models, the researchers emphasized the potential of newly generated neurons in adulthood to serve as therapy for addressing the functional deficits and pathology associated with Alzheimers disease.

In adult human brains, the hippocampus generates new neurons (adult-born neurons, or ABNs) throughout life, helping to maintain memories and regulate emotions. Scientists call this process adult hippocampus neurogenesis (AHN). In people with Alzheimers disease, this process is impaired, leading to reduced production of ABNs with poorer qualities. Given that Alzheimers patients often develop both cognitive symptoms (such as memory loss) and non-cognitive symptoms (such as anxiety and depression) for which AHN plays a critical role, one way to help Alzheimers patients achieve symptom relief could be to restore AHN.

Published in the journal Cell Stem Cell, scientists from University in Chapel Hill School of Medicine, US, demonstrated that stimulating a brain region called Supramammilary nucleus (SuM) located in the hypothalamus effectively enhanced adult-born neurons in the otherwise impaired Alzheimers brains of mice. After patterned stimulation of SuM, Alzheimers brains developed more ABNs with improved qualities. Importantly, activation of these SuM-modified ABNs restored both cognitive and affective deficits in Alzheimers mouse models.

It has been a longstanding question whether AHN can be sufficiently enhanced in impaired Alzheimers brains to improve brain function, said senior author Dr Juan Song. An important point to consider when addressing these questions is the low-level hippocampal neurogenesis, which becomes even lower in Alzheimers patients.

By manipulating a small number of ABNs in the Alzheimers brain, we demonstrate that ABNs can be enhanced even in the presence of Alzheimers pathology, and these enhanced ABNs are important for the restoration of behaviours and hippocampal function.

To enhance ABNs in Alzheimers brains, Song and colleagues adopted an elegant two-step ABN-enhancing strategy by first stimulating SuM using a patterned optogenetic paradigm with the goal of promoting the generation and developmental properties of ABNs, followed by stimulating the activity of SuM-enhanced ABNs using chemogenetics.

Optogenetics involves the use of light to alter the activity of brain cells expressing light-sensitive opsin genes. Chemogenetics involves the use of inert molecules to alter the activity of brain cells expressing designers receptors.

Interestingly, SuM stimulation alone or activation of ABNs without SuM stimulation failed to restore behavioural deficits in Alzheimers mice. Song said. These results suggest that multi-level enhancement of ABNs namely increasing their number, improving their developmental properties, and enhancing their activity is required to achieve their therapeutic benefits in Alzheimers brains.

When Song and colleagues further analysed the protein changes in the hippocampus of Alzheimers mice in response to activation of SuM-enhanced ABNs, the researchers found that several well-known protein pathways were activated inside cells. These pathways include the ones important for synaptic plasticity of neuronal cells that allow enhanced communication among them, as well as the ones important for phagocytosis of non-neuronal microglia that allow efficient plaque clearance.

It is striking that multi-level enhancement of ABNs through combined SuM and ABN stimulations allows such a small number of ABNs make profound functional contribution in diseased Alzheimers brains, Song said. We are eager to find out the mechanisms underlying these beneficial effects mediated by activation of SuM-enhanced ABNs on Alzheimers pathology and hippocampal function. Future efforts will be needed to develop drugs that mimic these beneficial effects mediated by activation of SuM-enhanced ABNs. Ultimately, the hope is to develop first-in-class, highly targeted therapies to treat Alzheimers and related dementia.

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Alzheimer's study shows improved memory and mood with ... - Drug Target Review

Biden Weaponized Health Care on Abortion, Transgender, COVID-19 – Daily Signal

FIRST ON THE DAILY SIGNALA coalition of conservative leaders and former federal government political appointees has compiled a game plan for the next conservative president to restore the Department of Health and Human Services to a focus on health care rather than forcing a leftist agenda down Americans throats.

From the COVID-19 pandemic to abortion funding and transgender mandates, HHS has twisted federal law and the pursuit of public health to marginalize people of faith and promote bureaucrats and leftist activism, warns a report edited by Roger Severino, former director of the HHS Office of Civil Rights under President Donald Trump. He argues that the next conservative president must reverse these abuses and return HHS to its proper role: the promotion of public health.

Few areas of life are more important, and more subject to abuse, than public health, Severino, vice president of Domestic Policy at The Heritage Foundation, told The Daily Signal in a statement Monday. Unfortunately, our public health agencies have replaced science and medicine with politics and ideology, and Americans now face shorter life spans as a result. Reform can only happen if entrenched special interests, from lawless bureaucratic leaders and Big Pharma, are reined in and rooted out. (The Daily Signal is The Heritage Foundations news outlet.)

Severino organized and edited a major report in the book Mandate for Leadership, compiled by the 2025 Presidential Transition Project, noting that after the COVID-19 pandemic was over, U.S. life expectancy continued to drop precipitously. A copy of the report on HHS was provided exclusively toThe Daily Signalfor this article.

The Heritage Foundation helped launch the 2025 Presidential Transition Project (also known as Project 2025) to equip a potential conservative president to govern effectively from Day One.

HHS has an outsized impact on the federal government, from its role in declaring public health emergencies to its management of Medicare and Medicaid to its $1.6 trillion annual budget. Under Presidents Joe Biden and Barack Obama, HHS has also used its power over health policy to promote abortion and transgender ideology.

Severinos team lays out five overarching goals for a conservative president intent on reshaping HHS: (1) protecting life from conception, protecting the rights of conscience of health care workers, and defending biological reality against gender identity ideology; (2) empowering patients to make their own health care choices, enabling providers to offer more options, and unleashing markets to drive down costs and improve quality; (3) promoting stable and flourishing married families instead of LGBT activism and single motherhood; (4) correcting the errors of the COVID-19 pandemic and preparing for the next health emergency; and (5) closing the revolving door between government and Big Pharma, where regulators leave government and work for companies they have regulated and pharmaceutical executives move from industry into regulatory agencies.

Severinos team breaks down the massive bureaucracy of HHS and presents specific recommendations for each branch of the behemoth agency. This article focuses on a few of the specific issues that motivate the major changes he recommends.

Many of the reports critiques and recommendations for a future HHS trace back to the departments abuses during the COVID-19 pandemic. It notes that while the HHS secretary declared a public health emergency, the threshold for what constitutes a public health emergencyhow many cases, hospitalizations, deaths, etc.was never defined.

Severinos team recommends that Congress restrict HHSs ability to declare indefinite public health emergencies, in part by establishing a set time frame for any emergency.

The report also recommends that the HHS secretary investigate, expose, and remediate any instances in which HHS violated peoples rights by colluding with Big Tech companies to silence dissent on COVID-19.

Severinos team says the Centers for Disease Control and Prevention should be broken up into two separate organizations: one dedicated to gathering scientific data and one responsible for making public health recommendationsan inescapably political function. The report notes that the CDC previously held back public health information on COVID-19 partially due to fear that the information might be misinterpreted.

CDC should report on the risks and effectiveness of all infectious disease-mitigation measures dispassionately and leave the should and must policy calls to politically accountable parties, the report suggests. Congress should ensure that CDCs legal authorities are clearly defined and limited to prevent an arbitrary and vacillating exercise of power, as the U.S. experienced during the pandemic.

Severinos report recommends that the Food and Drug Administration, not the CDC, should regulate vaccines, and calls for reforms to prevent the National Institutes of Healths inappropriate industry ties that create serious conflicts of interest.

The report notes that the National Institute of Allergy and Infectious DiseasesAnthony Faucis division of the NIHowns half of the patent for the Moderna COVID-19 vaccine, among thousands of other pharma patents. According to NIH documents, NIH Director Francis Collins, Fauci, and Faucis deputy director, Clifford Lane, all received royalty payments from pharmaceutical companies between 2009 and 2014.

The report faults NIH for funding gain-of-function viral research that may have been responsible for COVID-19.

Severinos team recommends HHS change many policies to protect unborn life and maternal health and to honor the religious convictions of Americans who object to the use of aborted baby body parts in medical research.

The CDC should fund studies into the risks and complications of abortion and require states to report abortion complications and babies born alive despite an attempted abortion, the team writes. It should prohibit research on aborted baby body parts, since such research can be easily replaced with research on adult stem cells. And it should avoid promoting abortion as health care.

The report condemns the CDCs current abortion and maternal mortality reporting systems as woefully inadequate, since states provide those statistics on a voluntary basis. Because liberal states have now become sanctuaries for abortion tourism, HHS should use every available tool, including the cutting of funds, to ensure that every state reports exactly how many abortions take place within its borders, at what gestational age of the child, for what reason, the mothers state of residence, and by what method.

Severinos team urges the FDA to reconsider its approval of chemical abortion drugs, an approval that currently faces a court challenge. The report notes that the complication rater for chemical abortion is four times higher than that of surgical abortion and that the chemical abortion drug mifepristone has been associated with 26 deaths of pregnant mothers, over 1,000 hospitalizations, and thousands more adverse events. It also calls the approval of this drug politicized and illegal from the start.

The report also calls for the FDA to loosen its restrictions on foreign-made vaccines that were not derived through or tested on aborted baby cells, reinstituting a Trump-era waiver for Japanese-made vaccines.

It urges the Centers for Medicare and Medicaid Services to block Planned Parenthood from receiving Medicaid funds and to redirect funds to health centers that provide real health care for women.

Severinos team urges HHS to audit the Centers for Medicare and Medicaid Services for compliance to the Hyde Amendment, which prevents federal funding of abortions, and to perform a full review of HHS efforts to promote abortion in the wake of the Supreme Courts overturning Roe v. Wade.

The report also urges various HHS departments to rescind ideologically motivated fearmongering guidance that the Biden administration released in the wake of the courts ruling, such as warnings about state governments targeting women for getting abortions.

Radical actors inside and outside government are promoting harmful identity politics that replaces biological sex with subjective notions of gender identity,' Severinos team warns. The report urges a potential conservative president to reverse this trend.

Bidens HHS has interpreted Section 1557 of the Affordable Care Act (also known as Obamacare), which prohibits discrimination on the basis of sex in health care, to forbid discrimination on the basis of gender identity and sexual orientation as well. Severinos team urges a future HHS secretary to explicitly revoke this guidance, as HHS did under Trump.

The report says that the Centers for Medicare and Medicaid Services should reissue and expand upon its 2016 decision that it cannot recommend gender reassignment surgery for Medicare beneficiaries, citing the growing body of evidence that such interventions are dangerous. (Many doctors recently testified in favor of a Florida rule blocking Medicaid coverage for experimental transgender interventions.)

The report also urges HHS to withdraw guidance allowing taxpayer funds to pay for cross-sex transitions.

It faults the NIH for having been at the forefront in pushing junk gender science, and encourages the agency to fund studies into the short-term and long-term negative effects of [cross-sex] interventions, including affirmation, puberty blockers, cross-sex hormones and surgeries, and the likelihood of desistence [abandoning the desire to change ones sex] if young people are given counseling that does not include medical or social interventions.

Severinos team notes that under liberal administrations, the office of HHS that he led, the Office for Civil Rights, has amassed a poor record of devoting resources to conscience and religious freedom enforcement and is often complicit in approving or looking the other way at the administrations own attacks on religious liberty.

The report encourages a prospective conservative president to direct the Office for Civil Rights to return to the Trump-era policies that initiated robust enforcement of these conscience laws. It urges HHS to reestablish waivers for state and child welfare agencies, especially for faith-based adoption and foster care agencies, which had previously been excluded from federal programs because they were unwilling to place children with same-sex couples.

Severinos team warns that Medicare and Medicaid operate runaway entitlements that stifle medical innovation, encourage fraud, and impede cost containment, in addition to which their fiscal future is in peril.

The report urges the Centers for Medicare and Medicaid Services to increase Medicare beneficiaries control over their own care; reduce regulatory burdens on doctors; ensure sustainability and value for both beneficiaries and taxpayers; and reduce fraud, waste, and abuse. It favors Medicare Advantage and urges Medicare to pay the same amount for outpatient procedures that it does for inpatient hospital services. It also encourages Medicare to reform payments along the lines of intensity and value of service, as opposed to a fee-for-service model.

Severinos team warns that Medicaid has a higher percentage of improper payments than any other federal program, and encourages the program to stop covering nonmedical services like air conditioning and housing. The report says the Centers for Medicare and Medicaid Services should give states more flexibility to strengthen program integrity and to incentivize personal responsibility through work requirements and private insurance.

Severinos team encourages HHS to decommission the CDC and NIH Foundations, nonprofit entities whose boards are populated with pharmaceutical company executives.

Private donations to these foundationsa majority of them from pharmaceutical companiesshouldnot be permitted to influence government decisions about research funding or public health policy, the report urges.

We must shut and lock the revolving door between government and Big Pharma, it adds. Regulators should have a long cooling off period on their contracts (15 years would not be too long) that prevents them from working for companies they have regulated. Similarly, pharmaceutical company executives should be restricted from moving from industry into positions within regulatory agencies.

Severinos team recommends more changes to HHS, including a prioritization of fatherhood in the many social programs HHS controls, and the elimination of the Head Start preschool program and the NIH Office of Equity, Diversity, and Inclusion.

Correction: This article has been corrected to reflect the authorship of the Project 2025 HHS report.

Have an opinion about this article? To sound off, please emailletters@DailySignal.comand well consider publishing your edited remarks in our regular We Hear You feature. Remember to include the url or headline of the article plus your name and town and/or state.

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Biden Weaponized Health Care on Abortion, Transgender, COVID-19 - Daily Signal

Enamine and Endogena Therapeutics a successful, multi-year … – StreetInsider.com

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KYIV, Ukraine--(BUSINESS WIRE)--Enamine Ltd., a provider of drug discovery services empowered with the worlds largest collections of building blocks, fragments, and screening compounds, gave an update of its long-standing research collaboration with Endogena Therapeutics AG, a clinical-stage biotech company focused on the development of endogenous regenerative medicines.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20230419005115/en/

Enamine provides Endogena with its integrated capability in medicinal chemistry to support Endogenas small molecule drug discovery programs in the fields of hit finding, hit-to-lead and lead optimization.

The companies have been collaborating under a Full Time Equivalent (FTE) model since 2019. The two discovery partners have been continuing their research collaboration to date, their research relationship not being impacted by the war in Ukraine. This collaboration extension, along with many others and new ones established by Enamine since February 24, 2022, already under the conflict, is a systematic positive trend experienced by the company, that demonstrates the support of its customers and the trust they have in receiving high-quality service backed up by the unparalleled number of diverse building blocks available at Enamine.

Sven Weiler, Vice President of Medicinal Chemistry at Endogena, commented: The interaction with colleagues from Enamine has been a smooth one from the start. In addition to the FTE model, it is great to have access to their huge compound collection and be able to flexibly use Enamines capacity to its full potential. We value the output and responsiveness of the Enamine team, helping us to achieve our demanding milestones. It is stunning to see how well Enamine has been able to keep pace after February 2022.

Michael Bossert, Head of Strategic Alliances at Enamine, added: After 13 months of the war in the country, we are especially pleased to announce our collaboration with Endogena, a long-lasting partner we have been serving during those several years with extensive medicinal chemistry and SAR efforts.

About Enamine Ltd. http://www.enamine.net

Established in Kyiv in 1991, Enamine is a leading global designer and largest producer of building blocks (285,000+), fragments (172,000+) and screening libraries (3M+ compounds). Enamine provides expertise in advanced organic synthesis, library synthesis, and medicinal chemistry. In 2011 Enamine established a pre-clinical service unit including ADME, in-vivo PK studies and High Throughput Screening under the brand name Bienta, allowing the company to tackle since that time fully integrated or -la-carte research programs.

About Endogena AG http://www.endogena.com

Endogena Therapeutics Inc. is a clinical-stage biotech company that discovers and develops first-in-class endogenous regenerative medicines to repair and regenerate tissues and organs. Its approach has the potential to change the way degenerative conditions related to aging and genetic disorders are treated. The concept is based on selective regulation of endogenous adult stem- and progenitor cells for controlled tissue repair by small molecules. Endogenas most advanced programs target degenerative diseases of the eye, including retinitis pigmentosa and geographic atrophy secondary to AMD. Endogena is registered in San Francisco, USA, with a Head office in Zrich, Switzerland, and holds a research facility at JLABS in Toronto, Canada.

View source version on businesswire.com: https://www.businesswire.com/news/home/20230419005115/en/

Enamine Ltd.Michael Bossert[emailprotected]

Endogena Therapeutics[emailprotected]

Source: Enamine Ltd. and Endogena Therapeutics AG

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Enamine and Endogena Therapeutics a successful, multi-year ... - StreetInsider.com

Ask the doctors: Non-hodgkin lymphoma considered very treatable – The Spokesman Review

By Eve Glazier, M.D., and Elizabeth Ko, M.D. Andrews McMeel Syndication

Dear Doctors: My grandfather is 72 years old and has been diagnosed with non-Hodgkin lymphoma. I would like to know more about this type of cancer and what kind of treatment may be involved. Is it unusual for someone his age to get this kind of a diagnosis?

Dear Reader: Lymphoma is a type of cancer that originates in the lymphatic system, most often in the lymph nodes. These are small pea- or bean-sized tissues that, along with a network of vessels, ducts and other structures, make up the lymphatic system. They work together to circulate a specialized fluid known as lymph. You know when you have a scrape and theres a layer of clear, watery fluid oozing from the wound? Thats lymph.

Just as the job of the circulatory system is to transport blood, the lymphatic system carries lymph throughout most of the tissues of the body. It carries away cellular waste and helps maintain optimal fluid balance in the tissues. The lymphatic system is also part of the immune system and plays an important role in fighting infection and disease.

When someone has lymphoma, it means that certain types of white blood cells found in lymph, known as lymphocytes, have begun to grow out of control. Their abnormal behavior leads to the formation of tumors. These not only interfere with the workings of the lymphatic system, but cancer cells from the tumors can spread to other parts of the body.

Lymphoma is divided into two types. One is non-Hodgkin lymphoma, which is your grandfathers diagnosis. This type of cancer is more common in men than in women. Although it can occur at any age, most cases are diagnosed in people 60 and older. A family history of the disease increases someones risk. Certain chemicals and drugs, including insecticides and some types of chemotherapy, are also suspected to play a role.

The other type of lymphoma, known as Hodgkin lymphoma, is not as common. It involves a different subset of lymphocytes and is treated differently from non-Hodgkin lymphoma.

Both types of lymphoma have similar symptoms. These include fatigue; unexplained weight loss; enlarged lymph nodes in the neck, armpits or groin; night sweats; and itching that can become severe.

Non-Hodgkin lymphoma can progress at different rates. A slow-growing cancer that has few symptoms is known as indolent. With this diagnosis, a treatment approach known as watchful waiting is sometimes recommended. Its just as it sounds keeping a close eye on disease progress and not starting treatment unless symptoms begin to change.

When lymphoma spreads quickly and has signs and symptoms that can be severe, it is characterized as aggressive. Aggressive lymphoma requires immediate treatment. The approach depends on the stage at which the cancer is diagnosed, the patients medical history and their general health. Treatment can include chemotherapy, immunotherapy, radiation and targeted drug therapy. In some cases, stem cell or bone marrow transplants may be recommended. These are arduous treatments and can have serious side effects.

Still, although it depends on the type and stage of the cancer, with a five-year survival rate of 74%, non-Hodgkin lymphoma is considered very treatable.

Send your questions to askthedoctors@mednet.ucla.edu.

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Ask the doctors: Non-hodgkin lymphoma considered very treatable - The Spokesman Review

Liskeard teen given second chance at life thanks to complete stranger from Germany who donated stem cells – Cornwall Live

A boxer from Cornwall with a rare condition has been given a second chance at life thanks to a complete stranger who donated stem cells. Charlie Dugdale, aged 17, had just qualified to become a chef in Winchester and was waiting to go to Plymouth to start his submarine training in the Royal Navy when he was diagnosed with aplastic anaemia - a type of blood disorder where your bone marrow doesnt make enough blood cells - at the end of last year.

Charlie underwent multiple blood transfusions as well as a platelet transfusion but was informed by doctors that a stem cell transplant was needed to give him a second chance at life. So, his family teamed up with blood cancer charity, Anthony Nolan, to help find Charlie a donor and to encourage people from all backgrounds to sign up to become potential donors.

After a number of stem cell donation rallies were held across Liskeard, Charlie was able to find a match on the Anthony Nolan stem cell register - which came from a donor in Germany - and successfully received a stem cell transplant last month. Following an initial recovery period in hospital, Charlie is now back home and continues to recover well from his transplant.

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His father, Thomas Dugdale, has described the success of the transplant as being 'a miracle' and said his family couldn't be more grateful for the support they received from the community and those who donated stem cells to help save Charlie's life. "It's amazing and it's a miracle we found a perfect match for him," Thomas told CornwallLive.

"The transplant went really well and aside from an infection he got just after, he is doing well now. He's also gained 10 kilograms since and aside from the odd days, he's almost back to himself, which means the world to us."

Despite the fact that the stem cells came from a donor in Germany, Thomas said his family is still grateful for the donor days that were held and wanted to thank everyone who donated. "The stem cell donation actually came from Germany and it was a perfect 12/12 match for Charlie," he said.

"But I don't want to take away from the donor days we held because those donations could still help others in need. It was still lovely to know that all these people came forward to help Charlie and we can't thank everyone enough."

He said he also hopes to meet the stranger who saved Charlie's life in the future and thank them in person. "We have to wait about two years before we're able to have the opportunity to meet the person who the donated stem cells that helped give Charlie a second chance at life," he said. "I'm really looking forward to it, I'll never be able to thank them enough."

Now Thomas, who is an Officer and Engineer in the Royal Navy, is set to run the London Marathon this weekend to help raise money for Anthony Nolan. The 39-year-old previously ran the New York Marathon in 2018, but was keen to run the London Marathon this year to raise money and bring awareness to the charity that has had a significant impact on Charlies life.

"Whilst I had heard of Anthony Nolan before, I wasnt really aware of exactly what they did until what happened to our family," he said. "Its incredible work, and Im really glad Ive got the opportunity to share how important they are and the work they do. It's also really important to encourage more people to come forward to donate stem cells, so that it can help save other people's lives."

Thomas has had to overcome a few challenges during training, including multiple work trips abroad and battling a chest infection. However, throughout these difficulties, he said he has taken inspiration from Charlies attitude towards overcoming barriers, which has helped him push forward with his training.

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"There were days Charlie didnt want to do his chemotherapy or have his treatment, but he never moaned once and was incredibly strong throughout his treatment," he said. "On the days I didnt want to go for a run, I take strength from what Charlie has overcome and realise that if he can go through what he went through, then I can make it through a 26-mile run. I want to show my gratitude towards his strength."

So far, Thomas has smashed his fundraising target and has already raised 6,927 of the 5,000 goal. However, he hopes to continue raising more funds for the vital charity in the days leading up to and after the marathon and has set himself a new fundraising target of 7,000.

You can view his fundraising page, here.

Anthony Nolan are calling for more people between the ages of 16 and 30 to join the register, specifically young men as research shows that they have the most success donating. Currently just 18% of the UK Anthony Nolan stem cell register is made up of young men, but they account for 55% of people called upon to donate, and potentially save the lives of people like Charlie.

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Liskeard teen given second chance at life thanks to complete stranger from Germany who donated stem cells - Cornwall Live

CDC allows second covid booster: Who should get it and when – The Washington Post

Federal health officials this week updated their recommendations for coronavirus vaccinations to allow people who are at least 65 years old or immunocompromised to receive a second updated booster shot to strengthen protection for the most vulnerable Americans, even as the virus recedes.

The Food and Drug Administration authorized the additional shot for those high-risk groups, and Rochelle Walensky, director of the Centers for Disease Control and Prevention, signed off Wednesday after the agencys vaccine advisers met to discuss its benefits. People who are eligible for additional boosters should be able to get them later this week.

Federal health officials also simplified coronavirus vaccinations for everyone going forward. Anyone getting a Pfizer-BioNTech or Moderna shot whether a booster or first-ever vaccination will now get an updated vaccine, known as a bivalent shot, not the original vaccines, called monovalents. Health officials say the bivalent shots more closely match the circulating virus. For unvaccinated adults, that means one shot instead of several doses of the original vaccine.

Many people are likely to have questions about who should get a second booster, the best timing and what the recommendations mean for younger age groups. The changes for young children are more complicated. The recommendations will vary by age, vaccine and which shots they received previously. The CDC plans to post a detailed chart with recommendations for children under 6.

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CDC allows second covid booster: Who should get it and when - The Washington Post

Immunotherapy Regenerative Medicine: Advanced Care With … – Wealth Of Geeks

Medical science has witnessed remarkable advancements in recent years, moving beyond traditional medicine toward the field of regenerative and proteomics medicine. While conventional methods focus on treating symptoms and managing diseases, regenerative medicine promotes the body's natural healing mechanisms to repair damaged tissues and organs.

This approach has become increasingly popular due to its potential to offer long-term benefits and reduce the need for invasive procedures or medications.

Immunotherapy Regenerative Medicine is a clinic that champions the power of natural healing to treat chronic degenerative diseases, autoimmune disorders, or neurological problems. Harnessing the power of high-level stem cell therapy, they enable the body's own regeneration and healing process.

As a leader in stem cell research based in Puerto Vallarta, Mexico, Immunotherapy Regenerative Medicine holds over 20 years of experience under the leadership of regenerative medicine expert Dr. Ernesto Romero.

Dr. Romero's visionary leadership at the forefront of regenerative medicine began over 17 years ago with the belief that Stromal Cell Precursors, a type of stem cell, were the next step in advancing people's health. Since then, he has advocated for this innovative approach as a potential solution for many suffering patients to improve their quality of life, far surpassing the results of traditional medicinal methods.

Regenerative medicine uses various techniques such as Mesenchymal stem cell therapy, gene therapy, and immunotherapy, to stimulate tissue regeneration and promote healing. At its core, regenerative medicine relies on preparing a correct environment and then using stem cells, which can segment into different types of cells in the body depending on the signals they receive.

Mesenchymal stem cells (MSCs) are one of the most researched cells for regenerative therapies. MSCs are adult stem cells with self-renewal, immunomodulatory, anti-inflammatory, signaling, and differentiation properties. Depending on the environment created for them, they can be used to regenerate or replace damaged tissues, allowing the body to heal itself in a way that was previously impossible.

Dr. Romero explains, By using the body's own healing mechanisms, regenerative medicine offers a safe, effective, and minimally invasive way to treat these conditions and improve patient outcomes.

Immunotherapy Regenerative Medicine is at the forefront of the regenerative field, offering patients comprehensive and innovative medical care through the most advanced regenerative and proteomics medicine techniques.

One of the techniques employed by Immunotherapy Regenerative Medicine is stem cell therapy. Their treatment methods use high-quality MSCs spanning a vitality of 95% to 98% to repair and regenerate damaged tissues, with the potential to treat a wide range of conditions, including chronic degenerative diseases, autoimmune diseases, aging conditions, and neurological and musculoskeletal disorders, such as stroke and heart problem.

Due to its high compatibility, mesenchymal stem cells develop into many cell types to help regenerate tissue and regulate the immune system.

At Immunotherapy Regenerative Medicine, patients can be assured that their regenerative medicine treatments are carefully planned and monitored for the best possible outcomes. Led by Dr. Romero and a team of professionals composed of doctors, biologists, biophysicists, biochemists, and nutritionists, the clinic recognizes that regenerative medicine is a significant investment for every that might be looking to improve their quality of life and used traditional medicine but failed to help them completely recuperate. So to ensure undeniable success results, the team takes a personalized approach to every treatment.

Rather than simply administering stem cells and hoping for the best, they take the time to get to know each patient's unique needs and body. By doing so, they can adequately prepare patients for therapy and recommend ways to improve their overall health and healing. With every treatment closely monitored and planned, patients can have the utmost confidence in its quality and compatibility. Patients can trust that their investment in regenerative medicine will result in long-lasting benefits for their health and well-being.

Dr. Romero believes that by combining these advanced techniques and personalized approaches, Immunotherapy Regenerative Medicine is pushing the boundaries of medical care, offering patients a new paradigm in healing and recovery.

Immunotherapy Regenerative Medicine takes pride as a pioneer in medical innovation and research. They are the first to adopt immunotherapy treatments and stem cell therapy in Mexico. By catering to medical tourism, they continually pursue excellence through their commitment to research and development. The team is constantly unlocking new ways and methods of treatment. They offer hope to patients and their families, allowing them to look forward to improved health and better quality of life now and in the years to come.

This article was produced and syndicated byWealth of Geeks.

Sam Allcock is thefounder of PR Fire. His team help small to medium-sized businesses achieve coverage in publications like Yahoo Finance, Daily Mail, Metro, USA Today, MSN News, The Huffington Post, and The Telegraph through smart press release distribution.

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Immunotherapy Regenerative Medicine: Advanced Care With ... - Wealth Of Geeks

Scots Football hosting "Be the Match" registry event – WQKT

The College of Wooster is among the latest college football teams to join forces with Be The Match and get in the game with a blood stem cell registry drive. Woosters drive will take place on Friday, April 28 from 10 a.m. 3 p.m. inside the Lowry Student Center at the student tabling tables.

Hundreds of college athletic teams have registered thousands of their team members, peers, and local community members for the Be The Match Registry. Wooster football players will run tables to assist students, faculty, staff, and local community members with their Be The Match process, which includes a registration, filling out a health history form, and providing a swab inside your cheek. The registry drive is open to people ages 18 to 40 years old, and the event is open to the local community.

More young people of diverse racial and ethnic heritage are needed to help patients searching for a match. People between the ages of 18 and 35 are most urgently needed since they are requested by transplant doctors most often, and research shows that these donors provide the greatest chance for transplant success.

Every year, 12,000 patients are diagnosed with life-threatening blood cancers or other diseases like sickle cell, for which a blood stem cell transplant from an unrelated donor may be their best or only hope for a cure. Be The Match connects patients with a matching donor for a life-saving blood stem cell transplant. A blood stem cell transplant can cure or treat more than 75 difference diseases, including leukemia and lymphoma, aplastic anemia, and sickle cell and immune-deficiency disorders. Be The Match has facilitated more than 120,000 transplants since 1987 and continues to impact more lives every year. Be The Match is a global leader in bone marrow transplantation and conducts research to improve transplant outcomes, provides support and resources for patients, and partners with a global network.

Football teams, especially small college teams within Ohio, can help effectively communicate signing up for Be The Match, added junior defensive back Andrew Armile, who is helping spearhead Woosters registry event. Through community involvement and with the large number of football programs in the country, we can help by spreading the important message of registering for blood and marrow donations and hopefully save lives.

Those unable to make Woosters football teams registry drive can join the Be The Match donor registry online, order a free cheek swab kit from Be The Match, and return it to the organization.

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Scots Football hosting "Be the Match" registry event - WQKT