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Humacyte Announces the Appointments of Three Surgical and Cardiovascular Opinion Leaders to Advisory Roles

DURHAM, N.C., Dec. 31, 2021 (GLOBE NEWSWIRE) -- Humacyte, Inc. (Nasdaq: HUMA), a clinical-stage biotechnology platform company developing universally implantable bioengineered human tissue at commercial scale, today announced the appointment of Surgical Key Opinion Leaders (KOLs) Alan P. Kypson, M.D., FACS; Luigi Pascarella, M.D., FACS; and Todd E. Rasmussen, M.D., FACS, (Col, ret. USAF MC), to new advisory positions. In these roles, the KOLs will lend their expertise and support to guide the education and clinical advancement efforts of the Human Acellular VesselTM (HAV) and help identify opportunities to advance the Company's early stage complex tissue constructs pipeline and platform.

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Humacyte Announces the Appointments of Three Surgical and Cardiovascular Opinion Leaders to Advisory Roles

Nuvectis Pharma Initiates Phase 1 Clinical Trial of NXP800

The Phase 1 Study Will be Comprised of Two Parts: Phase 1a Dose-escalation that will Evaluate the Safety and Tolerability of NXP800 in Patients with Advanced Solid Tumors, Followed by a Phase 1b to Evaluate Preliminary Efficacy in Specific Populations The Phase 1 Study Will be Comprised of Two Parts: Phase 1a Dose-escalation that will Evaluate the Safety and Tolerability of NXP800 in Patients with Advanced Solid Tumors, Followed by a Phase 1b to Evaluate Preliminary Efficacy in Specific Populations

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Nuvectis Pharma Initiates Phase 1 Clinical Trial of NXP800

Lui Franciosi Tracking Published Fall Numbers of Seniors During this COVID-19 Pandemic

VANCOUVER, British Columbia, Dec. 31, 2021 (GLOBE NEWSWIRE) -- Franciosi Consulting Ltd. is currently tracking the number of falls involving seniors and that have been reported in the public domain during this COVID-19 pandemic. In particular, government sites such as the Canadian Institute for Health Information, online media reports and survey portals from various countries are being searched to determine these numbers as well as the nature and location of the falls in designated senior housing such as long term care, assisted living and independent living. Lui Franciosi states, “During this pandemic, seniors have likely not had the same level of exercise and therefore their body core strength is not as optimal to prevent injury. It is known that falls are the leading cause of injuries among seniors, accounting for 61 per cent of injury-related deaths and 81 per cent of injury-related hospitalizations in Canada. There are close to 5,000 deaths each year linked to seniors’ falls and nearly 100,000 hospitalizations.” The aim of this work is to better understand how many of these falls are actually predictable and whether an algorithm could be developed to help healthcare staff and families prevent falls, especially in frequent fallers.

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Lui Franciosi Tracking Published Fall Numbers of Seniors During this COVID-19 Pandemic

Baudax Bio Reports Inducement Grant Under Nasdaq Listing Rule 5635(c)(4)

MALVERN, Pa., Dec. 31, 2021 (GLOBE NEWSWIRE) -- Baudax Bio, Inc. (NASDAQ:BXRX) (the “Company”), a pharmaceutical company focused on commercializing and developing innovative products for acute care settings, today announced that the Compensation Committee of Baudax Bio’s Board of Directors approved inducement grants of stock options to purchase an aggregate of 109,250 shares of Baudax Bio’s common stock and restricted stock units covering 31,900 shares of Baudax Bio’s common stock to 14 newly-hired employees, with a grant date of December 29, 2021. The equity awards were granted pursuant to the Nasdaq Rule 5635(c)(4) inducement grant exception as a component of each individual’s employment compensation and were granted as an inducement material to his or her acceptance of employment with Baudax Bio.

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Baudax Bio Reports Inducement Grant Under Nasdaq Listing Rule 5635(c)(4)

Unproved Stem Cell Clinics Proliferate in the U.S …

Patients seeking stem cell therapies for achy joints or shoulder injuries no longer need to hop a plane to Mexico or China. More than 550 clinics around the U.S. offer unproved interventions for sports injuries and conditions including autism, multiple sclerosis and Alzheimers disease. In cities like Beverly Hills or New York a prospective patient may only need to drive some 20 or 30 minutes from the center of town to find such a treatment.

This vast stem cell market has boomed in recent years, particularly for orthopedic applications such as easing joint pain or for facelifts and other cosmetic procedures. In one frequently advertised regimen a patient might have adult stem cells harvested from his own fat tissue and injected at an injury site, purportedly to speed recovery. Professional athletes including football stars Peyton Manning and Chris Johnson have reportedly used stem cell injections to help them get back onto the field.

Yet there is a darker side to the promise of these treatments. There is little systematic data about patients long-term outcomespositive or negativeand in most cases there is no scientific evidence that these costly procedures work. Many of these cellular therapies may not do much of anything but there is also the serious risk that recipients of cell injections could develop serious complications including blood clots or dangerous immune reactions, says Paul Knoepfler, a stem cell researcher at the University of California, Davis, School of Medicine and co-author of a new analysis, published Thursday in Cell Stem Cell.*

One U.S. patient traveled to China, Mexico and Argentina for stem cell therapies following a stroke and went on to develop a huge mass in his lower spinereplete with someone elses cells, according to a recent account in The New England Journal of Medicine. Without clear evidence that these procedures are safe, effective and actually tap the type of cells they claim to use, they should be avoided, Knoepfler says. (Bone marrow stem cell therapies used for cancer and blood disorder treatments, however, are widely accepted medical procedures.)

Armed with new data about the proliferation of stem cell clinics, Knoepfler and co-author, University of Minnesota bioethicist Leigh Turner, are seeking to correct the widespread belief that such procedures only happen overseas: Patients wishing to engage in stem cell tourism need only drive minutes from metropolitan areas across the U.S., not to a foreign country, they note.

Such clinics have often sidestepped heavy regulatory scrutiny, claiming they are eligible for a U.S. Food and Drug Administration exemption that applies to minimally manipulated cells. Some claim to extract a patients cells found in fat, bones or other tissues and inject them back into the same patient at a different sitesuch as a joint or a saggy chinwithin the same operation, all without substantially altering the cells. But many of these clinics also offer myriad types of stem cell treatment that would suggest they are not compliant with federal regulations, the authors wrote.

Amid this stem cell therapy explosion, the FDA recently issued draft guidance that would clarify and tighten its regulation of this area. The FDA is concerned that the hope patients have for treatments not yet proven to be safe and effective may leave them vulnerable to unscrupulous providers of stem cell treatments that are illegal and potentially harmful, FDA spokesperson Andrea Fischer said in a statement. If the proposed guidelines are enacted, the FDA would likely bring more of these clinics under its purview and regulate offerings in the same way as biological drugs. Public interest in this contentious area is undeniable: The FDA is holding a delayed public hearing on stem cell regulation this fall, after it was overwhelmed by audience sign-ups for its scheduled hearing in April.

This all should still be in the research phase without question, says Peter Rubin, a stem cell researcher who chairs the Department of Plastic Surgery at the University of Pittsburgh Medical Center and runs a clinical trial to test the use of stem cells to repair severe facial wounds and limb injuries in soldiers. We need to establish credible data around these therapies before bringing them to patients, he adds. Rubin, who was not involved in Knoepfler and Turners latest research, plans to testify at the hearing this fall.

Currently, hundreds of U.S. clinics61 percent of the businesses in the new analysismarket therapies that use fat stem cells. Although details vary between clinics, that often means the clinic gives a patient liposuction then chemically separates stem cells from the fat and centrifuges them before injecting them into an injury site to purportedly help a patient heal faster or to alleviate pain. Fat is a structural tissue, and if you break down its biological properties so it can no longer provide padding or cushioning, then it has been manipulated, Rubin says. Such procedures, he says, would likely require FDA regulation under the new proposed guidelines.

To get a new count showing exactly how widespread stem cell clinics have become, Knoepfler and Turner scoured the internet for Web sites marketing stem cell interventions. They found 351 U.S. businesses engaged in direct-to-consumer marketing of such services offered at 570 clinics. Most of the clinics were concentrated in California, Florida, Texas, Colorado, Arizona and New York, but most states had at least one. There were also certain hot spot cities with a dozen or more clinics such as Beverly Hills, New York, San Antonio and Los Angeles. The authors could not verify that the clinics truly offer what is advertised on their Web sites, the sources of their stem cells or their interactions with the FDA.

Yet what they did find, Knoepfler says, was very concerningparticularly because some of the ads targeted conditions that affect particularly vulnerable populations, including children. Nine clinics promoted stem cell treatments for autism and cerebral palsy and another 33 advertised therapies for muscular dystrophy, a disease that primarily afflicts kids. Alzheimers disease treatments were offered by 27 clinics. These are the conditions that most concern me because there is the most striking gap between the marketing claims being made and the actual evidence that is available, Turner says. In effect [the patients] are participants in unapproved human-subjects research without even realizing it.

*Editor's Note (7/11/16): This sentence was edited after posting to clarify information about the authorship of the study.

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Unproved Stem Cell Clinics Proliferate in the U.S ...

Exploring the potential of stem cell-based therapy for aesthetic and plastic surgery – Newswise

Abstract:

Over the last decade, stem cell-associated therapies are widely used because of their potential in self-renewable and multipotent differentiation ability. Stem cells have become more attractive for aesthetic uses and plastic surgery, including scar reduction, breast augmentation, facial contouring, hand rejuvenation, and anti-aging. The current preclinical and clinical studies of stem cells on aesthetic uses also showed promising outcomes. Adipose-derived stem cells are commonly used for fat grafting that demonstrated scar improvement, anti-aging, skin rejuvenation properties, etc. While stem cell-based products have yet to receive approval from the FDA for aesthetic medicine and plastic surgery. Moving forward, the review on the efficacy and potential of stem cell-based therapy for aesthetic and plastic surgery is limited. In the present review, we discuss the current status and recent advances of using stem cells for aesthetic and plastic surgery. The potential of cell-free therapy and tissue engineering in this field is also highlighted. The clinical applications, advantages, and limitations are also discussed. This review also provides further works that need to be investigated to widely apply stem cells in the clinic, especially in aesthetic and plastic contexts.

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Exploring the potential of stem cell-based therapy for aesthetic and plastic surgery - Newswise