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The Induced Pluripotent Stem Cell (IPSC) Market Growth Is Driven By The Rising Prevalence Of Genetic Diseases – PR Newswire

Posted: August 14, 2022 at 1:52 am

The Business Research Company's induced pluripotent stem cell (IPSC) market research report expands on key drivers, trends, and growth opportunities in the market.

LONDON, Aug. 9, 2022 /PRNewswire/ --The increasing prevalence of genetic diseases is expected to drive the induced pluripotent stem cell market in the forecast period. To reveal the pathogenesis of genetic diseases, various patient-derived iPSCs were developed. These genetic abnormality-harboring iPSCs can be repaired, and the genetically repaired iPSC can be differentiated into normal-functioning cells. In the future, these patient-derived normal cells can be used in a patient-tailored therapy to replace the damaged cells due to the disease. iPSCs for various genetic diseases have been developed, such as for certain types of Parkinson's disease, spinal muscular atrophy, lentigines, electrocardiographic abnormalities, and other genetic disorders.For instance, in the case of albinism, which is a genetic disorder, an estimated 1 in 20,000 people worldwide are born with oculocutaneous albinism. Also, nearly one million people were living with Parkinson's disease (PD) in the U.S. by 2020.

The global induced pluripotent stem cell (iPSC) market size is expected to grow from $ 2.43 billion in 2021 to $ 2.64 billion in 2022 at a compound annual growth rate (CAGR) of 8.6%. The induced pluripotent stem cell (iPSC) technology market is expected to reach $ 3.57 billion in 2026 at a CAGR of 7.8%.

Request a free sample of the Induced Pluripotent Stem Cell (IPSC) Market Report

Induced Pluripotent Stem Cells Market Overview

The induced pluripotent stem cell (iPSC) market consists of sales of induced pluripotent stem cells and related services. Induced pluripotent stem cells are the regenerated form of stem cells, which are produced from an existing adult cell, such as hepatocytes, fibroblasts, keratinocytes, and neurons. The various applications include academic research, drug development and discovery, toxicity screening, and regenerative medicine and are used in several sectors such as hospitals and research laboratories.

Induced Pluripotent Stem Cells Are Increasingly Being Used To Treat Type 1 Diabetes

As per the induced pluripotent stem cell (iPSC) market report, players in the industry are extensively developing pluripotent cells to treat type 1 diabetes. Cellular therapy has recently been started for type 1 diabetes (T1D) to replace islet cells, which are insulin-producing cells that are lost in T1D patients. These problems could be at least partially resolved by producing pancreatic islet cells from PSCs, and significant advancements have been made by imitating how the human pancreas naturally develops. Recently, two biotech companies, Semma Therapeutics and Viacyte, produced cells that were found to be capable of functional insulin secretion upon exposure to high-glucose or high-potassium stimuli.

In 2021, Fujifilm Holdings Corporation Held The Largest Market Share

Fujifilm Holdings Corporation was the largest competitor in the induced pluripotent stem cell market in 2021, with a 10.46% share of the market. FUJIFILM Cellular Dynamics's growth strategy focuses on strengthening its cell therapy business through expanding its operational capabilities. For instance, in March 2020, the company began the operation of its new cGMP-compliant-1 iPSC production at the Innovation Facility for Advanced Cell Therapy (i-FACT). The new facility is involved in manufacturing and developing induced pluripotent stem cells for therapeutic applications.

See more on the Induced Pluripotent Stem Cell (IPSC) Market Report

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Therapeutic Solutions International Reports Superior Efficacy of ApoptoCyte on Chronic Obstructive Pulmonary Disease Model Compared to Conventional…

Posted: August 14, 2022 at 1:52 am

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Phase III Clinical Stage Company Demonstrates Superior Efficacy of Proprietary Stem Cell Apoptotic Body Based Drug

ELK CITY, Idaho--(BUSINESS WIRE)--Therapeutic Solutions International announced today new data demonstrating superior effects of the Companys ApoptoCyte procedure treated JadiCell product compared to other stem cells in treating an animal model of Chronic Obstructive Pulmonary Disease (COPD).

In a series of experiments, mice were administered the enzyme elastase to mimic COPD. It was shown that untreated JadiCell stem cells, as well as stem cells from sources conventionally utilized, specifically fat and bone marrow, had some therapeutic activity including reduction of inflammation, stimulation of regenerative growth factors, and preservation of alveoli structure1. All cell types had improved therapeutic activity when processed using the ApoptoCyte procedure, with JadiCell possessing the highest activity.

In May of this year we announced and filed a patent on the ApoptoCyte procedure which involves the induction of cellular suicide in the stem cell, extraction of small vesicles called apoptotic bodies and co-administration with specific drugs such as certain histone deacetylase (HDAC) inhibitors. Leveraging this technology, we have filed a new patent on COPD which contains the data disclosed today, said Dr. James Veltmeyer, Chief Medical Officer of the Company, and co-inventor of both patents. The demonstration that the ApoptoCyte Procedure is applicable to COPD, which is one of the major causes of death in the world, is extremely exciting.

The Company possesses IND #28508 for using non-modified JadiCells for COPD, however the clinical trial is expected to initiate following further discussions between the Company and the FDA. Additionally, the Company currently is running a Phase III clinical trial using JadiCells for treatment of advanced COVID-19 infection.

COPD represents a significant unmet medical need for which no curative approaches exist, said Timothy Dixon, President, and CEO of the Company and co-inventor of the patents. We are grateful to have a team of cellular and COPD experts who have assisted us in creating what we believe is a first in class approach to treating COPD. We hope to continue exploring the applicability of the ApoptoCyte Procedure in other therapeutics in the regenerative medicine space.

About Therapeutic Solutions International, Inc.

Therapeutic Solutions International is focused on immune modulation for the treatment of several specific diseases. The Company's corporate website is http://www.therapeuticsolutionsint.com.

1 Therapeutic Solutions International Announces ApoptoCyte Procedure for Enhancing Stem Cell Activity | BioSpace

View source version on businesswire.com: https://www.businesswire.com/news/home/20220812005201/en/

Timothy G. Dixon[emailprotected]

Source: Therapeutic Solutions International, Inc.

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Ethical perils lie ahead after the creation of ‘synthetic embryos’ – MercatorNet

Posted: August 14, 2022 at 1:52 am

Israeli scientists have created the worlds first synthetic embryos. They used mouse stem cells to create embryos, nurtured them in an artificial womb, and grew them for 8 days roughly the equivalent of three weeks of a human pregnancy.

Their research, which was published in the journal Cell last week, is being acclaimed by scientists as a ground-breaking development. Inside the tiny mouse embryos, the researchers can see organs developing. We view the embryo as the best 3D bio printer, says Jacob Hanna, a biologist at the Weizmann Institute of Science, told MIT Technology Review. Its the best entity to make organs and proper tissue.

The mouse embryos developed beating hearts, flowing blood, intestinal tracts and cranial folds in the brain even though they were created from scratch in a Petri dish.

This experiment has huge implications, says Bernard Siegel, of the World Stem Cell Summit, a group which lobbies for regenerative medicine. One wonders what mammal could be next in line.

All going well, the next mammal is going to be homo sapiens.

Dr Hannas ambitions are immense. The ultimate goal of his start-up company, Renewal Bio, is to make humanity younger and healthier by leveraging the power of the new stem cell technology to solve ailments such as infertility, genetic diseases, and longevity.

He believes that there will be a huge market for products derived from synthetic human embryos.

Since the turn of the century, developed nations have seen a clear trend: declining birth rates and fast aging populations. With significant socioeconomic implications, this trend threatens to upend health systems, retirement programs, and workforces across the globe. At the beginning of life, this is shown by a 5-10% increase in infertility treatments by U.S. couples each year. Towards the end of life, these issues are manifesting in fast-aging populations that balloon healthcare costs. In the U.S., the aging population is driving national health expenditures to increase at a rate of 5.5% per year, and are expected to reach more than $6 trillion annually by 2027.

The vision of the company is Can we use these organized embryo entities that have early organs to get cells that can be used for transplantation? We view it as perhaps a universal starting point, Dr Hanna says.

What he has in mind is projects like rebooting the immune system for the elderly by creating blood from an embryo. Or growing a female embryo until the gonads form and the eggs can be harvested. In other words, Dr Hanna and his colleagues want to strip-mine human embryos which have been custom-made for their clients.

They also claim that their method of producing synthetic embryos creates the placenta and yolk sac surrounding the embryo. This suggests that perhaps a baby could reach full term in an artificial womb with no need for a mother at all.

But would these synthetic embryos really be human? Hanna dismisses the idea. We are not trying to make human beings. That is not what we are trying to do, he told MIT Technology Review. To call a day-40 embryo a mini-me is just not true.

However, Dr Hanna is not a philosopher. He is just a talented technician tinkering with biological structures. Whether or not it is human is not his to decide. Even though the embryo has not been conceived naturally, it might grow into a human being if it were transferred into a womb.

At the moment scientists quoted in the media are insisting that synthetic embryos are definitely not embryos. As Australian stem cell scientist Megan Munsie wrote in The Conversation: They replicate only some aspects of development, but not fully reproduce the cellular architecture and developmental potential of embryos derived after fertilisation of eggs by sperm so-called natural embryos.

But even if this is true, Dr Hannas ultimate goal seems to be to create synthetic embryos which are as close as possible to natural embryos. If they are not human initially, might they become human later on, as the field advances?

With so many unknowns, the need for regulation of this new technology is urgent. And the ones writing the law should not be the same entrepreneurs who stand to become billionaires if their dreams come true. If the brief history of stem cell science has taught us anything, it is that scientists lust for power always outruns their interest in ethics.

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Aesthetics Biomedical Inc. Announces Issuance of its Third U.S. Patent for Biological Preserving Composition and Methods of Use for its SoME Skincare…

Posted: August 14, 2022 at 1:52 am

This latest, additional patent for preserving biologics marks a paradigm shift for skincare and adds additional protection to Aesthetics Biomedicals product portfolio, Shaun Wootten, Director of Innovation and Design.

PHOENIX (PRWEB) August 10, 2022

Aesthetics Biomedical Inc (ABM), a leader in regenerative medicine and advanced aesthetics committed to the development and distribution of breakthrough, novel, and personalized aesthetic devices and products announces the issuance of its third US patent for Biological Preserving Composition and Methods of Use from the United States Patent Trademark Office. The newly issued [third] patent continues the protection of its innovation in the proprietary topical compositions of its SoME Skincare product which combines with physician infused biologics and presents the future of personalized skincare.

Founder & Chief Executive Officer, MaryAnn Guerra says of the issuance Once again, I am excited to see that Aesthetics Biomedicals innovations have been validated by the issuance of a new patent, further strengthening our SoME Skincare brand and patent portfolio. Our SoME Skincare product line will be expanded to fully utilize the broader patent coverage, under the leadership of our Director of Innovation & Design, Shaun Wootten.

SoME Skincare, medically dispensed through professional offices, with its unique technology platform combines the bodys own regenerative cytokines within skincare. Proven in skin renewal and regeneration, SoME Skincare is clinically shown to improve both visual and cellular facial aging. This latest, additional patent for preserving biologics marks a paradigm shift for skincare and adds additional protection to Aesthetics Biomedicals product portfolio, said Shaun Wootten, Director of Innovation and Design. This is Aesthetics Biomedicals broadest patent yet on the matter and cements the ingenuity of our Center of Aesthetic Innovation.

The growth factors, derived from Platelet Rich Plasma [PRP] infused within its advanced formula signals the biochemical receptors on the cell surface to stimulate new collagen and new elastin critical for regeneration and repair of photodamaged skin to produce a personalized, autologous skincare treatment. Aesthetics Biomedical Inc. is continuing to build its pipeline of regenerative products with a focus on skin, hair, and nail personalized products. The patents cover multiple delivery systems including, gel, cream, ointment, and spray. This is coupled with the PRP serving as a rich source of exosomes that provide a natural comprehensive means for regeneration. According to Lawrence A Rheins PhD, Chief Scientific Officer, The additional patent protection offered for SoME Skincare, will continue to provide Aesthetics Biomedical with a unique technology platform consisting of stabilized platelet rich plasma, permitting Aesthetics Biomedical to develop a multitude of topical products for various skin conditions including facial anti-aging.

ABOUT AESTHETICS BIOMEDICAL: Aesthetics Biomedical Inc., headquartered in Phoenix, Ariz., is committed to the development and distribution of novel aesthetic devices, products, and services in the global market. Aesthetics Biomedicals innovation center is a leader in breakthrough technologies and combination therapies for its clients, physician network, and the aesthetic arena, creating novel and unique patient experiences that benefit from ongoing research, approved clinical indications for use, as well as a personalized approach designed for consumer benefit. For more information, please visit [AestheticsBiomedical.com.

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Panacell Biotech to conduct toxicity tests for NK cells, exosomes, and brown adipose-derived stem cells to treat patients with long COVID – PR…

Posted: August 14, 2022 at 1:52 am

SEOUL, South Korea, Aug. 10, 2022 /PRNewswire/ --Panacell Biotech Co., Ltd. said that NK cells, exosomes, and brown adipose-derived stem cells are effective to treat patients with long COVID conditions, or post COVID-19 conditions, as well as those with terminal illness.

Seung-Ho Choi, CEO of Panacell Biotech

Panacell Biotech is South Korea's research institute specializing in advanced regenerative medical cell therapy using adipose-derived stem cells (ADSC).

The company announced on August 10 that it will soon conduct those cells' toxicity tests through clinical trials and laboratory animals.

Currently, in South Korea, there are guidelines for plasma treatment that administers plasma from patients who have recovered from COVID-19 to other patients. Although there already exist COVID-19 treatments, such as Paxrovid, a clear therapeutic effect has not been confirmed yet.

There are over 60 long COVID conditions, including decreased libido and hair loss.

According to the Mayo Clinic, a nonprofit American academic medical center, "A whopping one in four people aged 65 or above suffer from aftereffects of COVID-19"

The Guardian also reported that people with long COVID often experience and an "extremely broad" variety of symptoms, including less well-known side effects such as amnesia, and an inability to perform familiar movements or commands."

According to the TIME magazine said about four million people or 2.4% of the U.S. employed population have reduced ability to work because of Long COVID.

Associate Professor Gwenalle Douaud at the Nuffield Department of Clinical Neurosciences (NDCN), University of Oxford, and her team observed a "greater reduction in grey matter thickness and tissue contract in the orbitofrontal cortex and parahippocampal gyrus" and "greater changes in markers of tissue damage in regions that are functionally connected to primary olfactory cortex." While the long-term effects of COVID-19 on smell remain inconclusive, the study suggests a possible connection between brain changes by COVID-19 and memory.

However, there have been many clinical results in which the coronavirus causes inflammation in various organs, including the respiratory system, and chronic symptoms persist.

While research on a treatment for COVID-19 is underway around the world, Chinese researchers said they are researching ways to treat COVID-19 patients using stem cells.

Sun Yanrong, Deputy Director of China Biotechnology Development Center, asserted, "We are continuing to monitor the treatment using stem cells. In Wuhan, over 200 patients have already been treated with stem cells."

He continued explaining, "The clinical treatment results show that the stem cell therapy has good safety and has also been confirmed to have a therapeutic effect. It was also effective in recovering the lungs."

Seung-Ho Choi, CEO of Panacell Biotech, affirmed, "We expect that this clinical trial will reveal therapeutic effects of stem cell therapy along with these treatments."

Panacell Biotech is a leading bio institute in advanced regenerative medicine and cell therapy, widely recognized for its contributions to the development of biotechnology by researching stem cell culture and cell banking, focusing on the development of treatments for various cancers and incurable diseases.

The Ministry of Food and Drug Safety of South Korea approved Panacell Biotech on April 1 this year as one of the 21 licensed cell treatment facilities.

It received the K-ESG Management Innovation Award in June 2022, and is scheduled to receive the 2022 Global Clean Environment Award in the healthcare category in this upcoming October 18.

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Source: Panacell Biotech Co., Ltd.

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PAINWeek 2022 Announces the Return of the ASIPP and Interventional Pain Management Tracks – PR Web

Posted: August 14, 2022 at 1:52 am

The PAINWeek National Conference, September 6-9

MONTCLAIR, N.J. (PRWEB) August 11, 2022

The statistics are alarming: At least a fifth of the US population has chronic pain.[1] Costs to society, ranging from direct costs to lost work, is over $630 billion a year.[2] Something needs to change, and education will help. At the PAINWeek National Conference, September 6-9 at The Cosmopolitan of Las Vegas, attendees will experience stellar pain management education, including the ASIPPAmerican Society of Interventional Pain Physiciansand the Interventional Pain Management Tracks.

The ASIPP Track will include Nick Knezevic, MD, PhD, presenting Atomic Secrets: Regenerative Medicine in Managing Chronic Pain. He commented, ASIPP has a long-standing relationship with PAINWeek. Together, theyve organized a series of lectures with ASIPP key leaders as speakers to help explain the importance of interventional pain management procedures in managing pain conditions.

The ASIPP Track will also feature the following courses and presenters:

Sean Li, MD, who will present during the Interventional Pain Management Track, stated, PAINWeek has always been one of my favorite meetings because of its diversity and inclusion: it is the only meeting where I can join clinicians from all specialties who treat pain patients. Dr. Li's sessions: The Petrified Forest: Sacroiliac Joint Dysfunction and Treatment Update; and When Stars Align: The New Era of Peripheral Nerve Stimulation. He continued, Attendees will experience an emersion of emotional and intellectual experiences into the world of pain management. Dont miss out!

Johnathan Goree, MD, who will co-present East v. West: Who Should Hold the Needle First?, commented, I am excited to again take part in PAINWeek, this time discussing back pain and Whats next? I will debate Carrie Hyde, MD, a physician medical acupuncturist, and discuss our approaches to the low back pain patient, treatment philosophies, cost benefit analysis. Wholl win the debate? Both attendees and patients!

The Interventional Pain Management Track will also feature:

PAINWeek will present over 75 CME/CE credit hours in tracks such as Behavioral Pain Management, Chronic Pain Syndromes, Health Coaching, Integrative Pain Management, Medical/Legal, Neurology, Physical Therapy, Pharmacotherapy, and Psychedelics. Master Classes, Special Interest Sessions, and sponsored courses complement the agenda, along with tracks presented by the International Pelvic Pain Society.

For more information, click PAINWeek or go to painweek.org.

Dr. Goree: Associate Professor and Director of Chronic Pain Division, University of Arkansas for Medical Sciences, Little Rock. Dr. Knezevic: Clinical Professor of Anesthesiology & Surgery, College of Medicine, University of Illinois, Chicago. Dr. Li: Regional Medical Director, National Spine and Pain Centers, Lincroft, New Jersey.

PAINWeek accreditation provided by Global Education Group:

Global Education Group focuses on producing partnership-based CME for healthcare practitioners. The Global team works with a select group of medical education companies, associations, academic institutions, and healthcare facilities to develop and accredit live healthcare conferences and workshops as well as online activities. With each partnership or joint providership, Global brings accreditation expertise, project management excellence and grant funding intelligence. Based in Littleton, Colo., Global has accreditation with commendation from the ACCME and accredited with distinction from the ANCC. Global also holds accreditations to offer continuing education for nurse practitioners, pharmacists, dietitians, dentists, and psychologists. Global is a division of Ultimate Medical Academy.

1. National Center for Health Statistics, National Health Interview Survey, 2019.2. https://nationalpain.org/fast-facts-about-pain

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CEL-SCI Appoints Dr. Gail Naughton to Its Board of Directors – Business Wire

Posted: August 14, 2022 at 1:52 am

VIENNA, Va.--(BUSINESS WIRE)--CEL-SCI Corporation (NYSE American: CVM) today announced the appointment of Dr. Gail K. Naughton to its Board of Directors.

Dr. Naughton has been a pioneer in the field of regenerative medicine for over 35 years. She was the founder of Advanced Tissue Sciences (NASDAQ:ATIS) where she oversaw the design and development of the worlds first up-scaled manufacturing facility for cell-based products, established corporate development and marketing partnerships with companies including Smith & Nephew, Medtronic, and Inamed Corporation, was pivotal in raising over $350 million from the public market and corporate partnerships, and brought four human cell-based products from concept through FDA approval and market launch. She founded Histogen (NASDAQ:HSTO) in 2007 and holds more than 125 U.S. and foreign patents and has been extensively published in the field. Dr. Naughton served as Dean of the College of Business Administration at San Diego State University from 2002 until 2011 where she helped to make SDSU the first US campus to establish a Ph.D./MBA in life sciences. In 2000, Dr. Naughton received the 27th Annual National Inventor of the Year award by the Intellectual Property Owners Association in honor of her pioneering work in the field of tissue engineering and regenerative medicine. Dr. Naughton received her Ph.D. and M.S. from NYU Medical Center and an MBA from UCLA. She currently sits on the Board of directors of Therapeutics MD (NASDAQ: TXMD) and is the Chair of the Board of the La Jolla Institute for Immunology.

A highly accomplished visionary in biotechnology, Dr. Naughton has brought several FDA approved products to market, and we are very pleased to welcome her to our board. Her unparalleled expertise will be very helpful to CEL-SCI, stated CEL-SCI CEO Geert Kersten.

Dr. Naughton commented, Based on the results of the largest study of its kind, Multikine can significantly improve outcomes for patients with newly diagnosed head and neck cancer. CEL-SCIs management team and board have been tenacious in advancing an immune therapy that can have the greatest beneficial impact on patientswhen they are first diagnosed with cancer. I look forward to contributing my guidance as the company transitions through regulatory approval and into delivering treatments that can help extend patient lives.

About CEL-SCI Corporation

CEL-SCI believes that boosting a patients immune system while it is still intact should provide the greatest possible impact on survival. Therefore, in the Phase 3 study CEL-SCI treated patients who are newly diagnosed with advanced primary squamous cell carcinoma of the head and neck with the investigational product Multikine* first, BEFORE they received surgery and radiotherapy or surgery plus concurrent radiochemotherapy (the current standard of care for these patients). This approach is unique. Most other cancer immunotherapies are administered only after conventional therapies have been tried and/or failed. Multikine (Leukocyte Interleukin, Injection) received Orphan Drug designation from the FDA for neoadjuvant therapy in patients with squamous cell carcinoma (cancer) of the head and neck. CEL-SCI believes that this Phase 3 study is the largest Phase 3 study in the world for the treatment of advanced primary head and neck cancer.

Multikine is designed to help the immune system see the tumor at a time when the immune system is still relatively intact and thereby thought to be better able to mount an attack on the tumor. The Phase 3 study was started in early 2011 and was fully enrolled with 928 patients in September 2016. To prove an overall survival benefit, the study required CEL-SCI to wait until at least 298 (deaths) events had occurred among the two main comparator groups. The study results announced in June 2021 showed excellent survival benefit for those patients who received Multikine treatment regimen plus surgery and radiation. When chemotherapy was added to radiotherapy following surgery the survival benefit was negated.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. When used in this press release, the words "intends," "believes," "anticipated," "plans" and "expects," and similar expressions, are intended to identify forward-looking statements. Such statements are subject to risks and uncertainties that could cause actual results to differ materially from those projected. Such statements include, but are not limited to, statements about the terms, expected proceeds, use of proceeds and closing of the offering. Factors that could cause or contribute to such differences include an inability to duplicate the clinical results demonstrated in clinical studies, timely development of any potential products that can be shown to be safe and effective, receiving necessary regulatory approvals, difficulties in manufacturing any of the Company's potential products, inability to raise the necessary capital and the risk factors set forth from time to time in CEL-SCI's filings with the Securities and Exchange Commission, including but not limited to its report on Form 10-K for the year ended September 30, 2021. The Company undertakes no obligation to publicly release the result of any revision to these forward-looking statements which may be made to reflect the events or circumstances after the date hereof or to reflect the occurrence of unanticipated events.

* Multikine (Leukocyte Interleukin, Injection) is the trademark that CEL-SCI has registered for this investigational therapy, and this proprietary name is subject to FDA review in connection with the Company's future anticipated regulatory submission for approval. Multikine has not been licensed or approved for sale, barter or exchange by the FDA or any other regulatory agency. Similarly, its safety or efficacy has not been established for any use.

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What Is Minoxidil? A Complete Guide to the Product – Mane Addicts

Posted: August 14, 2022 at 1:52 am

Minoxidil, or the active ingredient in Rogaine, has been billed as a miracle cure for hair loss. But what is it, really? And more importantly, who does it help? Hair thinning can be a painful process so we take special notice when we find something that can stop or reverse it. While weve tried the natural route (hello, rosemary oil) its not every day we find an actually clinically proven solution to hair loss. So, to learn more about this ingredient, we checked in with an expert for a guide on what it is, its side effects, benefits, and how to use it.

About the Expert

Azza Halim, M.D., is a board-certified aesthetic medicine, anti-aging, and regenerative medicine physician.

Minoxidil was originally developed to lower blood pressure in the 1960s, with a happy side effect being hair growth. It was then formulated into a topical treatment to treat hair loss in men as Rogaine, followed by a female-specific product. Board-certified physician Azza Halim, M.D. explains, It is a vasodilator medicationthat canbe taken as a pill or applied topically. This means it expandsbloodvesselsto increase flow, circulation, and add nutrients to the follicles, she continues.

The main benefit of minoxidil is restoring haireven a little bit back can be a huge confidence booster. According to Dr. Halim, minoxidil may expand the hair follicles, especially those that shrunk over time or in response to hormonal changes, which translates to more sustained growth. It also prolongs the growth phase of the hair cycle, aka the anagen phase, she notes. Minoxidil can increase hair thickness, density, and treat hair disorders like androgenetic alopecia and female pattern hair loss.

Ideal candidates are those in early stages of hair loss or thinning, says Dr. Halim. All hair types can take minoxidil, though it may be less effective on women with natural hair who have scarring from alopecia. Pregnant women cant take minoxidil, and it isnt safe for nursing mothers either. It can cause irritation when mixed with hair dye, though it can be used on color-treated hair.

As with everything there are pros and cons/side effects, Dr. Halim tells us. Side effects include scalp dryness, irritation, low blood pressure, allergic reaction, and rarelybut it is possibleto trigger interim hair loss before stimulating hair growth. Other side effects include unwanted hair growth, lightheadedness, and scalp irritation.

Minoxidil must be applied topically twice a day, says Dr. Halim. Dont expect instant gratification, however, as results take three to four months. If you stop minoxidil, be warned that hair will revert to the thickness it would have been if you didnt take it at all, not where it was when you startedthis can be a shocker. The downside is once discontinued, hair then reverts to baseline and new growth will be lost within few months, therefore, it needs maintained use, she continues. Minoxidil giveth and minoxidil taketh away.

This 2% solution is clinically proven to help fight hair loss by activating hair follicles at the scalp and extending your hairs natural growth cycle. You can even subscribe to get this product delivered to your door every month so you wont miss out on a treatment.

With a 4.2 star review from nearly 200 reviews on Ulta, its no wonder this treatment is recommended by so many. Yes, it does take about three to six months for results to show, but once they do, youll realize why it was worth the wait.

A 5% topical treatment, Rogaines four-month supply will take you to the first stages of hair regrowth.

Promote hair growth with minoxidil and refresh follicles naturally with biotin, thanks to this hair growth oil. Youll be happy to know its free of parabens, gluten, sulfates, and any other nasty ingredients that may irritate your scalp. Translation? You likely wont experience any minoxidil side effects.

Minoxidil meets DHT blocker Finasteride and Spironolactone, which slows the production of hair loss-causing hormones. People who have used this treatment have said they noticed hair regrowth in as little as one month.

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The Mugglehead technology roundup: biotechnology edition – Mugglehead

Posted: August 14, 2022 at 1:50 am

Theres usually some confusion over just what biotechnology is. For the sake of brevity, we can think of biotechnology as a broad term that applies to all practical uses of living organisms, from microorganisms like yeast used in fermentation of beer to sophisticated gene therapies.

Biotechnology involves the connection point of the natural and engineering related sciences to achieve the select application of organisms, cells, molecular analogues, and more in terms of putting together products and services. The four types of biotechnology are human, environmental, industrial, animal and plant, which we leverage to help fight hunger and disease, produce more safely, cleanly and efficiently, and work to save the environment by reducing our ecological footprint.

Here are five companies operating somewhere within the biotechnology framework.

Amgen (NASDAQ:AMGN) produced new data from its phase 1 dose exploration and expansion clinical trial for the safety and efficacy of its investigational drug tarlatamab.

Tarlatamab is a bispecific T-cell engager molecule targeting delta-like ligand3 (DLL3) in small cell lung cancer. The updated data from the ongoing trial was presented originally at the International Association for the Study of Lung Cancer 2022 World Conference on Lung Cancer in Vienna, Austria.

Small cell lung cancer is one of the most devastating and aggressive solid tumor cancers. The disease has lacked effective treatments with no therapies specifically approved to treat patients in the third-line setting. Our Phase 1 data for tarlatamab presented earlier today at WCLC continues to demonstrate exciting antitumor activity with remarkable response durability in heavily pre-treated patients. We are encouraged by the overall survival of 13.2 months, said David M. Reese, M.D., executive vice president of research and development at Amgen.

Amgen is one of the biggest pharmaceutical companies in the world. Its working on discovering, developing, manufacturing and delivering human therapeutics using tools like advanced human genetics to unravel diseases and understand the fundamentals of human biology. The companys specific focus is unmet medical needs and it uses its expertise to find solutions to improve health outcomes. The company has been in the biotech game since 1980 and has since grown to be recognized as one of the worlds leading and largest independent biotech companies with millions of patients around the world and a substantial medicine pipeline.

Its also one of the 30 companies that make up the Dow Jones Industrial Average and part of the NASDAQ 100 index.

What is Tarlatamab?

Tarlatamab is an investigational half-life extended bispecific T-cell engager (BiTE) molecule designed to target delta-like ligand 3 in neuroendrocrine cancers, like small cell lung cancer, and neuroendrocrine prostate cancer, both of which have neither treatments nor cures. In standard English, its a powerful cancer fighter with a lot of potential that uses BiTE technology. BiTE technoloy is a targeted immuno-oncology platform designed to engage the patients own T-cells to any tumor-specific antigen, basically getting the patients T-cells to turn on and attack the cancer.

Shares rose $0.04 to close at $248.39.

Cumberland Pharmaceuticals (NASDAQ:CPIX) released its ESG and sustainability report earlier this week.

Over the past few years as the public has started to place a lot more scrutiny on the acts and actions of companies in terms of mitigating negative externalities, ESG has become a hot button topic. For Cumberland, though, the numbers tell the tale. The company provided 2.43 million patient doses of its products in 2021 and safely disposed of 6,200 pounds of expired and damaged goods, following all the necessary waste guidelines. Beyond the numbers, though, the company had no product recalls, no products listed on the FDAs MedWatch Safety Alerts for Human Medical Products list, and no product issues singled out by the FDA from its Adverse Event Reporting System. Also, none of Cumberlands clinical trials were terminated because of failure to practice good clinical standards.

Good deal.

As the largest biopharmaceutical company founded and headquartered in the Mid-South, we understand the importance of recognizing and addressing our impact on the environment, our team members and the community. We are proud to release our third annual sustainability report, and we remain committed to building on the positive actions weve taken in these areas, said Caroline Young, Cumberland Pharmaceuticals sustainability board director.

Cumberland Pharmaceuticals is a biotechnology cum pharma-company working on the delivery of high-quality prescription brands designed to help with patient care. The company is in the business of developing, acquiring and commercializing products for the hospital acute care, gasteroenterology, rheumatology and oncology sub-sectors. The companys portfolio includes eight brands approved by the FDA. The company also has a number of Phase II clinical trials presently underway to evaluate its ifetroban product candidate in patients with cardiomyopathy associated with Duchenne Muscular Dystrophy, Aspirin-Exacerbated Respiratory Disease and Systemic Sclerosis.

The company is focused on providing medications to improve quality of care for patients and address medical needs that have since gone unmet. Cumberland is creating solutions to help reduce costs for both healthcare providers and patients. Also, in 2021, Cumberland ate up to 60 per cent of patient prescription costs for its gastrointestinal products through a coupon program.

The company invested an average of $4,000 per full-time employee in training and development, including educational programs, initiatives for employee development and awards. Cumberlands workforce is 44 per cent women and 15 per cent of its employees are minorities. The organization also has a philanthropic arm called Cumberland Pharmaceuticals Foundation, which has donated over $33,000 to non-profit organizations in 2021.

Shares rose a penny to close at $2.45.

DNA sequencing and array-based biotechnology company, Illumina (NASDAQ:ILMN), announced that its Illumina Genomics Forum (IGF) will feature Bill Gates, who will deliver a keynote address on the potential of genomics to change global health, and then host a panel called Making Genomics for All more than a mantra, on whats needed to get genomic health out there for everyone.

Bill Gates probably doesnt need an introduction, but in the rare case he does and youve been living in a shack in Montana for the past thirty years, hes the founder and former CEO of Microsoft. After his retirement, he and his wife started the Bill and Melinda Gates Foundation, which is a nonprofit fighting inequity, disease and poverty throughout the world.

Genomics should be available to the many, not the few, and even though the genomic health era has already led to breakthrough discoveries that are advancing medical care, the benefits have not yet had a true global impact,. Through sessions led by Bill Gates and expert panelists, Illumina Genomics Forum will help attendees see and understand the path toward global health equity, said Kathryne Reeves, chief marketing officer for Illumina.

Illuminas deal is in improving human health by unlocking the power inherent in the human genome. The companys focus has been on DNA sequencing in service to customers in the research, clinical and applied markets. Its products are used in applications for the life sciences, oncology, reproductive health, agriculture and other emerging sectors.

The company previously announced that former United States President Barack Obama would be headlining the inaugural forum in a fireside chat on Wednesday, Sept. 28. Hell discuss the continued need for equity, accessibility and smart healthcare to help improve upon the human condition some twelve years after the passage of the Affordable Care Act. There will be more speakers announced in the coming weeks.

Other IGF key themes include:

IGF will take place in San Diego from September 28 through October 1.

Shares dipped $19.11 to close at $208.32.

Zynex (NASDAQ:ZYXI) announced that The Healthcare Technology Report has recognized Zynex as 33 in the Top 100 Healthcare Technology Companies of 2022.

The report provides market research, business news, updates on investment activity, as well as important corporate developments related to the healthcare technology sector. Its based in New York City and run by a team of editors, writers and media professionals embedded deep in the sector, who provide knowledgeable analysis on healthcare technology and the various companies, executives and investors that comprise the scene.

The inclusion in the Top 100 Healthcare Technology Companies of 2022 list is a testament to the focus on our mission of improving the quality of life of our patients. We are honored to be included in the ranks among some of the worlds most well-respected healthcare companies. This years list represents a wide portfolio of products and solutions, and we are humbled to know that Zynexs emphasis on innovation and patient care is being acknowledged in the life sciences community, said Thomas Sandgaard, CEO of Zynex.

Zynex has been around since 1996, and its been involved in the development, marketing and sales of medical devices for pain management and rehab, as well as a non-invasive fluid, sepsis and laser-based pulse oximetry monitoring systems for hospital use. A few of the companys other offerings, and what actually managed to land them the listing, was its pain management devices and more specifically electrotherapy, bracing, hot/cold therapy, and cervical traction. These devices are primarily used in rehabilitation or orthopedic settings, helping patients recover from chronic or acute pain.

The years top 100 companies include a significant range of specialties, from genomics to pharmaceuticals, lab testing, biotechnology, therapeutics, data analysis and more.

Shares of Zynex were flat today, and closed at $9.83.

Its hard to tell whether or not Monkeypox is real or if its a media-hyped health scare. Without the data its both hard (and irresponsible) to speculate and maybe its in our best interests to treat it like it is. Kind of like COVID-19, the original strain. Deadly for some but not widely distributed. Treat it as such until proven otherwise. But you have to admit, when you follow the money there are folks out there who stand to profit from the fear the media pumps out about these diseases.

Regardless, WeTrade Group (NASDAQ:WETG), itself a tech company offering software-as-a-service (SaaS) cloud-based systems, and Jiqing Biomedical Technology decided to sign an official contract that would have WeTrade taking on the sales for Jiqings monkeypox virus test kits.

Jiqing is a Chinese medical company thats expanded its development strategy to include overseas markets, generally by offering COVID-19 antigen tests and now monkeypox kits. The company anticipates being able to benefit from the advanced tech and international market channels it picks up with WeTrade.

Working with Jiqing is not only for the profit, but it is a prominent occasion for customer base expansion. We are looking forward to attracting more customers from different industry to use our channel and private domain marketing promotion, to help them avoid the domestic competitiveness and develop overseas markets with differentiated thinking, said Pijun Liu, CEO of Wetrade.

As a global-oriented biotechnology development enterprise, Wetrade has been working on discovering overseas business for domestic companies. Wetrade believes that building its own private domain traffic would help Chinese companies carry out business operations in overseas markets easier. In the meantime, it would empower those companies to increase product awareness rapidly, find targeted audiences accurately and accumulate customers efficiently.

WeTrade Group is a technical service provider of SaaS and cloud intelligence system for micro-businesses, with a hand in the research and development for innovations and promotion for said technology. The company also developed the cloud intelligent system for micro-businesses called Ycloud. Ycloud helps with marketing and increases the payment scenario to increase customers revenue by multi-channel data statistics, AI fission and management as well as improved supply chain systems. Ycloud is presently only available in China and Hong Kong.

Shares dipped 22 per cent today and closed at $11.23.

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The Mugglehead technology roundup: biotechnology edition - Mugglehead

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The 9th ARDD: Longevity Biotechnology Is Gaining Prominence And Credibility In The Pharmaceutical Industry – Forbes

Posted: August 14, 2022 at 1:50 am

9th ARDD: Mindjourney AI-generated image depicting a convention of scientists at the University of ... [+] Copenhagen

About eighteen years ago, when I was still a computer scientist, very few credible scientists, and entrepreneurs were interested in aging research or longevity. There were very few conferences and meetings on the topic of longevity. Venture capitalists and pharmaceutical companies were also not too keen in investing in drugs intended to increase healthy productive lifespan. The first significant conference on aging I helped organize was 2008 GTCBios New Applications of Aging Research in San Diego and it was very small less than 80 people showed up. That was one of the first high-level academia meets industry conferences. It was very difficult to find credible startup companies and there were very few credible scientists. At that conference Michael West (now at AgeX), the founder of Geron, presented his vision for BioTime (now Lineage Cell Therapeutics), Michael Rose and his team presented their work on long-lived flies, Lenny Guarente of MIT and Olivier Boss of Sirtris (later acquired by GSK) presented on sirtuin biology. So 4-5 startup companies focusing on longevity in total.

But in eighteen years, since I transitioned from IT to biotech, all of that has changed. Now, not only are there multiple conferences and meetings on longevity and aging research around the world, there is also growing interest from venture capitalists and biotechnology companies to pursue the noble cause of prolonging healthy human lifespan. Four out of the top thirty pharmaceutical companies supported by Insilico Medicine have prioritized aging research in their early-stage R&D efforts, and the more visionary and agile pharmaceutical companies have made significant progress in addressing cellular senescence. Conferences and meetings allow key opinion leaders and industry veterans to share ideas and technologies, compare research ideas, and inspire the next generation of scientists. These are just a few reasons why it is important to have conferences and meetings regularly. With coronavirus lockdowns finally coming to a halt, people are beginning to ditch virtual meetings for in-person interactions. This has led to a surge in events and conferences around the world, and scientists are finally able to meet in-person to share ideas and have open discussions. From a longevity point of view, the industry now has multiple conferences and meetings around the world, especially when compared to eighteen years ago. This years in person GRC Systems Aging conference was a major success.

AI-generated Midjourney representation of a group of scientists convening at the University of ... [+] Copenhagen

But One of the largest conferences on longevity will take place this year at the University of Copenhagen from August 29 to September 2. It is called the 9th Aging Research and Drug Discovery (ARDD) Meeting.

The ARDD meeting will feature well-known scientists and researchers from some of the biggest biotechnology companies in the world, as well as leading experts from the top academic institutions. The conference will include a longevity medicine workshop, discussions on various topics like the power of artificial intelligence, and aging of specific organs, and much, much more.

The first ARDD meeting took place in 2014, the year I founded Insilico Medicine. It started when I brought together a group of aging researchers and pharmaceutical company executives at the Aging Forum as part of the Miptec/BaselLife conference in Basel, Switzerland. The first ARDD meeting was highly successful because a lot of companies that were going to the BaselLife conference also participated in the ARDD meeting. We co-organized it with Bhupinder Bhullar or Novartis, and Brian Kennedy of the Buck Institute for several years and it was pretty successful with the many big pharmaceutical companies and startups presenting their cutting-edge research. High-level of academic speakers, interesting program, and the proximity to Roche and Novartis as well as the Basel Life conference ensured steady participation from Big Pharma and brought credibility to the conference.

But it was not until Morten Scheibye-Knudsen took over the conference and moved it to Copenhagen that the conference took off and became the largest event in aging research in the biopharmaceutical industry globally. During COVID-19 in 2020 and 2021, we arranged hybrid ARDD events, with social distancing and masks in place, and also so that people could join the event virtually. Specifically in 2021, over 160 scientists participated in the hybrid event with more than 2,000 dialing-in virtually. Within a span of 9 years, the ARDD has become the largest conference in the world on aging research and longevity. The conference costs a lot of money to arrange and we hire programmers to record the conference so that people are able to follow on YouTube. Videos from the 8th ARRD meeting can be viewed here. All the lectures from ARDD 2021 are also available online.

Group picture and statistics from the 8th Aging Research and Drug Discovery (ARDD) meeting organized ... [+] by the University of Copenhagen, Insilico Medicine, and Columbia University in 2021

This year, the ARDD is expecting over 400 people on-site, making 9th ARRD meeting one of the largest conferences in the world on longevity.

What to Expect from the 9th ARDD Meeting

Day 1: The event will begin on August 29 with a Longevity Medicine Workshop. This workshop will be the first in history to bring together health care providers involved in longevity to discuss the status quo and the future of the field, as well as related challenges, perspectives, and actionable items. The workshop is organized by Dr. Evelyne Bischof of Human Longevity Inc., with Dr. Sebastien Thuault, chief editor of Nature Aging, helping as co-organizer. Evelyn is an expert in internal medicine and oncology. Early in her career, she spent time practicing medicine and performing translational research in Switzerland, US, and China. She is the author of over 40 peer-reviewed papers. Sebastian is the launch editor of Nature Aging. He obtained his PhD from the University of Bristol and performed postdoctoral research in neuroscience at Columbia University. He joined Nature Research in 2011 and served as a senior editor at Nature Neuroscience until 2019. Following this, he transitioned to Nature Communications to steer the Neuroscience and Psychology team. In 2018, he worked as a publishing manager focusing on the proposal to launch Nature Aging and took over direction of the journal in March 2020.

Some of the other talented scientists who will be involved in this workshop include Tornado Therapeutics CEO Joan Mannick, Human Longevity CEO Wei-Wu He, Gameto CEO Dina Radenkovic, and Hevolution Foundation CEO Mehmood Khan, to name a few. I have written about Dina and Joan as part of my Women in Longevity series and also recently covered the Hevolution Foundation.

The scientists taking part in this workshop will speak on such topics as what is needed to translate geroscience into the clinic, longevity medicine therapeutics, and longevity medicine diagnostics and innovations.

Another workshop that will also take place this day is called the Emerging Tech Workshop. In this first-of-its kind workshop, we will explore the interplay between technologies that are transforming the future of biotechnology, drug discovery and aging research. This hands-on workshop will take you through the realms of blockchain, artificial intelligence, and rapid prototyping with robotics. You will also experience the power of AI and robotics to accelerate, enhance and scale scientific experiments. The Emerging Tech Workshop will be organized by Maximilan Unfried of VitaDAO. Michael Petr of Tracked.bio, Tim Peterson, co-founder of Healthspan Technologies and BIOIO, and Garri Zmudze, general partner at LongeVC will be there to lead the workshop.

The first day will also be divided into three lecture tracks, each focused on a specific area of aging research. These lecture tracks will also include time for strategic debates and open discussions.

Day 2: August 30 will begin with a talk on drugging the nutrient-sensing network by Dr. Linda Partridge of the Max Planck Institute for Biology of Aging. This will be followed by a series of talks on topics including chemical interventions in aging promoting healthspan, an update on geroscience approached to treat age-related diseases, and regulation of stem cell biology by interferons independent of antiviral function. Some of the speakers include Gordon Lithgow, Tyler Golato, Carles Canto, and Vishwa Dixit. The day will end with a talk on quantifying aging and rejuvenation by Judith Campisi of the Buck Institute. In total, there are 18 lectures scheduled just in the first day giving you an idea of what to expect next! Participants will also be able to set-up posters on this day.

Day 3: On the third day of the conference, delegates will learn about genome stability and aging, and genome maintenance mechanisms in aging by Dr. Bjorn Schumacher and Morten, respectively. These will be followed by more sessions on human biological aging. We will also learn about aging through the lens of reproductive longevity. This will also be the only time when a venture capital panel will be present to talk about investing in longevity biotechnology. Alexandra Bause, co-founder of Apollo Health Ventures, will be there to guide folks on how to get more involved in investing in longevity. Alexandra is leading the venture creation programs that aim at founding new biotech startups targeting the aging process at a molecular level. She is also a trained pharmacist with expertise in pharmaceutics and pharmacology. Before joining Apollo, Alexandra worked with The Boston Consulting Group, specializing in biopharma strategy so if you want to start your journey as a longevity investor, you simply cannot afford to miss this one!

Day 4: The fourth day will start with new methods of target identification, biomarkers, and muscle stem cells in age and disease. We will be joined by Anders Malarstig, director at Pfizer, as well. Anders is a medical researcher and manager with experience in clinical and experimental human genetics, epidemiology and vascular biology. He is also an expert in population research and functional genomics strategies to inform drug development from preclinical phase to phase III.

Following more lectures on telomeres and circadian clocks, we will conclude the day with discussing what reprogramming, parabiosis, and autophagy have in common. Some of the speakers include Joris Deelen, Nir Barzilai, Sarah Mitchell, and Sara Hagg.

Day 5: The last day of the event will kick-off with a poster award ceremony, followed by presentations on bringing geroscience into clinical practice, predicting mortality in old age, and quantifying age and rejuvenation. The final presentation will be made by Vera Gorbunova on the topic of mechanisms of longevity and epigenome stability. The event will wrap up after this however, this is not all, theres way more!

The ARDD is Completely Non-Profit and has several unique features:

Inspire Longevity High School Students Engaging in Longevity Research

To help nurture the next generation of biogerontologists from the very early years, we are piloting the Student Ambassador Program called "Inspire Longevity". Becoming a student ambassador for the ARDD Meeting is an excellent way for students to meet with leading academic and industrial researchers and practitioners in the fields of aging and drug discovery. The student ambassador program is also an excellent way of interacting with other students from all over the world and enjoy the ARDD sessions together. PandaOmics is a platform that allows researchers a unique opportunity to both explore the unknown of OMICs data and interpret it in the context of all the scientific data generated by the scientific community. This platform will not only be showcased at ARDD 2022, but students and scientists will get a chance to explore how it works through a detailed demonstration.

Interview with the members of Inspire Longevity program - high school students planning their ... [+] careers in longevity biotechnology

The student ambassador program will be coordinated by Andrea Olsen, Zachary Harpaz, and Nina Khera. Andrea is an aspiring neurobiologist and a former intern at Insilico Medicine, while Zachary is passionate about applying AI and computer science in ways that can impact the world. Nina is currently working on a startup called Biotein, that has raised $65,000 to increase access to tools to prevent aging-related diseases. These teenagers already have impressive CVs and will be happy to guide applicants through the Inspire Longevity program.

Transparency

The two primary sources of funding for ARDD are corporate sponsorship and ticket sales for the event. Sponsorship is important to make the conferences more accessible and affordable. The finances are managed by the University of Copenhagen. The funding is distributed in three broad categories: academic speakers expense (travel expenses and overnight accommodation), on-site costs (catering, etc), and venue costs. ARDD is a non-profit with a sole aim of bringing the longevity field to the forefront of scientific research.

Supporting Ukrainian Scientists

Mindjourney AI-generated post-war recovery of Ukraine

Due to the ongoing war in Ukraine, Ukrainian scientists and researchers are invited to participate in the ARDD 2022 for free. If they cannot travel physically to the venue, they can dial-in for free and join virtually.

A screenshot of the Zoom interview with Professors Morten Scheibye-Knudsen, MD, PhD and Daniela ... [+] Bakula, MD, PhD

What To Expect from the 9th ARDD in 2022: Interview with Dr. Morten Scheibye-Knudsen and Dr. Daniela Bakula

Alex: Since you two took over the ARDD as the executive chairs and took charge of the program and organization the conference transformed into the worlds largest event in aging research in the biopharmaceutical industry. In your opinion, what were the main factors for such spectacular success?

Morten: I think we were very fortunate to be able to get leading scientist to join the meetings. We have always focused on having stellar academic speakers, including great speakers from a bit outside the field. With a great academic lineup, companies are interested in the event and this then also brings in venture capitalists.

Alex: What should we expect to see at ARDD this year? What are the hottest topics?

Daniela: I think the growing clinical focus is a very hot topic in the field. But for clinical trials to happen we need good biomarkers, so called biological clocks, and this is also a very hot topic that will be discussed by the leaders in the field. We also have the best basic scientists in the world giving us the latest on the breakthroughs in aging research that will shape the field in the coming years. I am also extremely excited about all the companies joining and the growing interest from VCs.

Alex: Most of the speakers will be on site this year. But there will be many delegates dialing in from all over the world. How would you recommend watching the lectures?

Morten: The event is streamed via a University of Copenhagen service. When you register, you will receive a link that will get you to the streaming website. BUT, if you have the possibility of coming to Copenhagen, then watching them in person is a whole other experience.

Alex: You are spending enormous amount of time and energy every week for 50 weeks in a row to get the best speakers, get the conference funded, and ensure that the people interested in aging are aware of this conference. Do you think the resulting event is worth this effort?

Daniela: This is a lot of work but also very exciting and rewarding. We hope that with this event we can contribute to foster new collaborations by bringing people from different areas and perspectives together. Also seeing that we provide a valuable knowledge and networking platform for young people with an interest in aging research makes the conference worth the effort.

Alex: Last year, around 25% of all delegates were from biopharmaceutical companies, what should we expect this year?

Morten: We currently have about 40% non-academic so the proportion of people from the industry has grown over the last years. This perhaps reflects the increasing commercial interest we have in this field.

Alex: One of the crown jewels of the pharmaceutical industry in Denmark is Novo Nordisk. In fact, it is majority-owned by a non-profit foundation. But Novo Nordisk never supported the ARDD even after it turned into the worlds largest event in its field and moved to Copenhagen. Do you know why are they ignoring it?

Morten: I think Novo Nordisk is still opening their eyes towards aging as a pharmacological target. Every year we have more and more speakers from big pharma so the field is definitely becoming very interesting for these companies and we actually do have many participants from Novo, Pfizer, Roche, and others. Hopefully we can get their support in the future.

Morten Scheibye-Knudsen, MD, PhD

Morten Scheibye-Knudsen, MD, PhD, executive chair, Aging Research and Drug Discovery (ARDD) meeting. ... [+] 8th ARDD, September, 2021

Morten Scheibye-Knudsen did his medical training at the University of Copenhagen including a short scholarship investigating mitochondrial physiology. During medical school he founded his first company, Forsoegsperson.dk, which has grown to be the largest provider of volunteers for clinical trials in Denmark. After medical school he worked as a medical doctor in Denmark and Greenland before moving to basic science as a post doctoral fellow at the National Institute on Aging, NIH, in Baltimore. Here, he utilized computational and wet lab science to investigate how DNA damage contributes to the complex phenotypes seen in premature and normal aging. In 2016 he returned to Copenhagen as an assistant professor to start his own research program focusing on aging. In 2018, he received tenure and was promoted to associate professor. His team (~20 people) utilizes computational science, animal models, gene editing, and high-throughput approaches such as high-content microscopy and omics investigations to understand the molecular basis of aging and age-associated phenotypes. Lab generated data is routinely analyzed through AI-assisted pipelines such as novel cellular senescence classifiers and fully automated animal tracking (www.tracked.bio). He has published his research in some of the best journals in the world including Cell, Cell Metabolism, New England Journal of Medicine and many others. In addition to his core research, he has been lecturing at Johns Hopkins School of Public Health for 8 years; He is a chief editor at Frontiers in Aging running the Aging Interventions section; He is an advisor to Deep Longevity, the Longevity Vision Fund and Vitexia; He has given invited presentations at top institutions (NIH, MIT, Harvard, NUS, Karolinska and others); and received several awards for his research. In addition, he has been organizing the Aging Research and Drug Discovery meeting.

Daniela Bakula, PhD

Daniela Bakula, PhD, co-chair of the Aging Research and Drug Discovery (ARDD) conference in ... [+] Copenhagen

Daniela Bakula graduated in Biology from the University of Tbingen, Germany in 2012. She obtained her PhD with the highest honors in 2017 from the University of Tbingen within the International Max-Planck Research School From Molecules to Organisms. Her PhD work focused on molecular mechanisms regulating autophagy and was awarded with highly competitive dissertation prizes. Daniela Bakula moved to Denmark in 2016, where she did her postdoc in the lab of Morten Scheibye-Knudsen at the Center for Healthy Aging, University of Copenhagen before transitioning into an assistant professorship. Her work focuses on understanding how DNA damage may impact aging. Based on her work she received a DFG fellowship as well as a Lundbeck foundation fellowship and several other grants to fund her research. She is an associate editor with Frontiers in Aging and is co-organizing ARDD since 2020.

AI-generated Midjourney representation of a group of scientists convening at the University of ... [+] Copenhagen

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The 9th ARDD: Longevity Biotechnology Is Gaining Prominence And Credibility In The Pharmaceutical Industry - Forbes

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