Stem Cell Clinics: Effective or Pricey False Hope?

Second in a two-part series about stem cells. See the first entry here.

Aug. 13, 2019 -- Beverly Hills plastic surgeon Mark Berman says he can offer 12,000 reasons people should consider getting stem cell therapy at one of the clinics he co-founded across the country. Thats the number of patients he says his 100-plus affiliated clinics have treated for conditions like knee pain, erectile dysfunction, asthma, congestive heart failure, stroke, and Parkinsons disease. Sports figures have also publicized the therapies.

But a number of stem cell scientists say that these and other self-described stem cell clinics are misleading the public. The treatments, which often cost $5,000 to $20,000, have no proof of safety or effectiveness. In many cases, theres no logical scientific reason to think they might work, they say. And the procedures, which involve moving cells from one part of the body to another, arent really even stem cell therapies, according to scientists at Harvard University, New York University, the University of California, Davis, Arizona State University, the University of Minnesota, and others.

Stem cell therapies often involve taking cells from one area, like the abdomen, spinning them in a centrifuge to concentrate the cells, and then reinjecting them into another part of the body, like the knee.

Offering these procedures violates the standards of medical practice, says Insoo Hyun, PhD, a bioethicist at Harvard and Case Western Reserve University School of Medicine in Cleveland, OH.

Berman says the procedures that he offers are safe but adds that his clinics stopped providing stem cell shots into the eyeball after a woman treated for macular degeneration, a cause of age-related vision loss, had retinal detachments and went blind. Several other women treated elsewhere for macular degeneration were also blinded. Other reports blame stem cell procedures, mostly performed outside the United States, for tumors, infections, and brain inflammation.

Hyun says it may sound harmless to move your own cells around, but not all cells are the same. Your bodys stem cells -- theyre found, they work, and they live in a very particular system, he says. When you transfer them out of that system, theres no evidence theyre going to do anything except maybe cause harm because theyre in unfamiliar territory.

Hyun says theres no rational reason to try a stem cell therapy offered by one of these clinics, which are thought to number more than 700 across the country -- though he understands why desperate patients and families might be willing to take a risk for the promise of effective treatment. Some mainstream hospitals also offer stem cell and similar procedures, sometimes in the context of a research trial, sometimes not -- earning them the same criticisms as the clinics.

Hyun and others are quick to note that genuine treatments based on stem cells -- cells that can transform into different cell types -- have tremendous potential to eventually help patients with a wide range of ailments. But except for bone marrow transplants, which have been used for decades, and some research trials, which should be free to patients who volunteer, those treatments are not yet ready for patients, and certainly not for clinics in strip malls, Hyun says.

If they would actually cure a devastating disease, we would all know about it, he says.

The federal government has begun to crack down on these clinics, after largely ignoring them for years. The FDA has charged some clinics, including Bermans, with selling drugs without appropriate approvals and with unsafe manufacturing practices.

In late June, a federal judge in Florida sided with the FDA against two clinics there. In a statement at the time, the government said: Court decisions like this reaffirm the FDAs compliance and enforcement efforts in the ongoing fight to protect the public from individuals and clinics who mislead patients with unapproved and potentially harmful medical products.

Berman, who was not involved in the Florida case, has been sued by the FDA as co-founder of the California Stem Cell Treatment Center and the Cell Surgical Network. He argues that the federal government is overstepping its bounds by trying to regulate the procedures he offers.

He says hes just giving patients back their own cells, not making a drug, so the FDA has no jurisdiction. A procedure like skin grafting, for instance, where skin from one part of the body is moved to cover a wound elsewhere, isnt FDA-regulated.

All Im doing is giving you back your own stuff, Berman says. You own it.

But the FDA says that when a product is created from a persons own body, manipulated, and put back into the body, but for a different purpose, it could be considered a new product subject to FDA approval.

Stem cell products can create unique and serious risks depending on how theyre manipulated once theyre taken from the body and how they are used once theyre reinserted in the body, then-FDA Commissioner Scott Gottlieb, MD, and FDA Biologics Center Director Peter Marks, MD, said in April. When a product undergoes more than minimal manipulation, its characteristics may be changed in a way that are novel, and its risks and potential benefits unique.

Berman says that his procedures are very safe, and that the handful of injury lawsuits against stem cell clinics come from rare bad apples, or procedures that are no longer done.

Leigh Turner, PhD, a bioethicist at the University of Minnesota, says theres no way to know how patients have fared, because no one has been keeping track. Do we have a clear understanding of the number of people harmed by such procedures? I think the answer is: We probably dont, he says.

Stem cell clinics cloak their marketing in science, Turner and other scientists say. For example, they use proper scientific terms and fill their websites with explanations and links to scientific studies. Some clinics have patients sign waivers suggesting that their treatment is part of research. But most of these clinics have done little or no legitimate research, Turner says. Instead of publishing their findings in reputable, peer-reviewed journals where studies routinely change medical practice, these clinics publish in junk journals, if at all, he says.

Berman dismisses such scientific criticism. These are misinformed PhDs working in their labs who have their own special interests, he says.

The condition that Bermans clinics treat most often is knee pain, and stem cell therapies may someday become the first line of treatment for patients with mild knee arthritis, says Philipp Leucht, MD, an orthopedic surgeon with NYU Langone Health in New York.

Injecting cells from the fat or bone marrow into the knee is generally safe, says Leucht, also a member of the American Academy of Orthopaedic Surgeons Biologics and Regenerative Medicine Committee. The main thing that could go wrong is an infection where you get the shot.

Its a low-risk procedure, he says. Its expensive -- thats the highest risk, probably, that you have to pay for it.

But whether such shots are useful remains an open question. The science is still weak, Leucht says. There has never been a large, well-designed research trial, with patients getting the treatment compared to those receiving a placebo.

Some people with early-stage arthritis do seem to get pain relief with cell therapy, he says. (Leucht doesnt believe in calling the procedures stem cell therapies because so few actual stem cells are in the fat or bone marrow thats withdrawn and then injected into the knee. He prefers to call them cell therapies.) Its not clear why some patients report improvements and others dont, or how to target those most likely to benefit, he says.

Plus, Leucht says, any pain relief from cell therapy will likely be short-lived, because the relocated cells die off in a few days, and thus wont stop arthritis from getting worse over time.

This will be part of the future treatment for osteoarthritis, but we just have to understand it first, says Leucht, adding that weight loss, exercise, and treating inflammation with over-the-counter medications and a healthy diet are already proven ways to reduce knee pain. We cant trial it on patients first and then figure it out [scientifically].

The International Society for Stem Cell Research, a scientific group, publishes guidelines on its website to help patients decide what to consider when theyre thinking of getting treated at a stem cell clinic. Hyun co-wrote the most recent guidelines in 2016.

Before agreeing to treatments at stem cell clinics, you should ask questions about the procedure and the doctor performing it, say Emma Frow and David Brafman, both PhDs and assistant professors at Arizona State University. The pair helped co-author a study on the stem cell industry, published this month, that offered details about nearly 170 stem cell businesses in the Southwestern United States.

At those businesses, many specialists in orthopedics, sports medicine, and rehabilitation focused their stem cell treatments on conditions related to their specialty, according to the study, while specialists in cosmetic or alternative medicine were more likely to use cell therapies to treat a wide range of medical conditions. Next, the two say they want to examine the boards that are certifying some of these doctors as qualified.

But the lack of regulation and certification puts more pressure on patients to carefully consider the procedure and their doctors credentials, the pair says. Currently, Frow and Brafman say, the system is stacked against patients.

Theyre assuming all of the risk -- theyre assuming the personal risk, the physical risk, the financial risk, Frow says. We have a system at the moment really weighted toward benefiting the clinics, without a clear mechanism for benefiting patients and making sure they have recourse if things dont go well.

Turner agrees and thinks government regulators need to play more of a role. We put too much on shoulders of individual patients, and we ought to be expecting a lot more from regulatory bodies, he says.

Berman says he and others in the industry will continue to fight against tighter government regulations.

Were doing some amazing things, and were getting treated like were the scum of the earth, he says. Im sick of it, and we will beat the FDA in the court as long as the judge is willing to listen to the law.

But if the courts continue to uphold the FDAs right to regulate stem cell clinics, many of the procedures that Berman and his peers perform today wont be permitted.

That would transform the stem cell clinic industry, says Paul Knoepfler, PhD, a stem cell scientist at the University of California, Davis, School of Medicine, who tracks the field.

Some clinics might shut down, dropping out entirely, he says. For others, the temptation to continue doing some kind of stem cell stuff might be too great.

Knoepfler, a frequent critic of these clinics, thinks any reduction in their numbers would be good. I think fewer people will be put at risk.

Original post:
Stem Cell Clinics: Effective or Pricey False Hope?

FDA Warns About Stem Cell Therapies | FDA

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Researchers hope stem cells will one day be effective in the treatment of many medical conditions and diseases. But unproven stem cell treatments can be unsafeso get all of the facts if youre considering any treatment.

Stem cells have been called everything from cure-alls to miracle treatments. But dont believe the hype. Some unscrupulous providers offer stem cell products that are both unapproved and unproven. So beware of potentially dangerous proceduresand confirm whats really being offered before you consider any treatment.

The facts: Stem cell therapies may offer the potential to treat diseases or conditions for which few treatments exist. Sometimes called the bodys master cells, stem cells are the cells that develop into blood, brain, bones, and all of the bodys organs. They have the potential to repair, restore, replace, and regenerate cells, and could possibly be used to treat many medical conditions and diseases.

But the U.S. Food and Drug Administration is concerned that some patients seeking cures and remedies are vulnerable to stem cell treatments that are illegal and potentially harmful. And the FDA is increasing its oversight and enforcement to protect people from dishonest and unscrupulous stem cell clinics, while continuing to encourage innovation so that the medical industry can properly harness the potential of stem cell products.

To do your part to stay safe, make sure that any stem cell treatment you are considering is either:

And see the boxed section below for more advice.

The FDA has the authority to regulate stem cell products in the United States.

Today, doctors routinely use stem cells that come from bone marrow or blood in transplant procedures to treat patients with cancer and disorders of the blood and immune system.

With limited exceptions, investigational products must also go through a thorough FDA review process as investigators prepare to determine the safety and effectiveness of products in well-controlled human studies, called clinical trials. The FDA has reviewed many stem cell products for use in these studies.

As part of the FDAs review, investigators must show how each product will be manufactured so the FDA can make sure appropriate steps are being taken to help assure the products safety, purity, and strength (potency). The FDA also requires sufficient data from animal studies to help evaluate any potential risks associated with product use. (You can learn more about clinical trials on the FDAs website.)

That said, some clinics may inappropriately advertise stem cell clinical trials without submitting an IND. Some clinics also may falsely advertise that FDA review and approval of the stem cell therapy is unnecessary. But when clinical trials are not conducted under an IND, it means that the FDA has not reviewed the experimental therapy to help make sure it is reasonably safe. So be cautious about these treatments.

About FDA-approved Products Derived from Stem Cells

The only stem cell-based products that are FDA-approved for use in the United States consist of blood-forming stem cells (hematopoietic progenitor cells) derived from cord blood.

These products are approved for limited use in patients with disorders that affect the body system that is involved in the production of blood (called the hematopoietic system). These FDA-approved stem cell products are listed on the FDA website. Bone marrow also is used for these treatments but is generally not regulated by the FDA for this use.

All medical treatments have benefits and risks. But unproven stem cell therapies can be particularly unsafe.

For instance, attendees at a 2016 FDA public workshop discussed several cases of severe adverse events. One patient became blind due to an injection of stem cells into the eye. Another patient received a spinal cord injection that caused the growth of a spinal tumor.

Other potential safety concerns for unproven treatments include:

Note: Even if stem cells are your own cells, there are still safety risks such as those noted above. In addition, if cells are manipulated after removal, there is a risk of contamination of the cells.

When stem cell products are used in unapproved waysor when they are processed in ways that are more than minimally manipulated, which relates to the nature and degree of processingthe FDA may take (and has already taken) a variety of administrative and judicial actions, including criminal enforcement, depending on the violations involved.

In August 2017, the FDA announced increased enforcement of regulations and oversight of stem cell clinics. To learn more, see the statement from FDA Commissioner Scott Gottlieb, M.D., on the FDA website.

And in March 2017, to further clarify the benefits and risks of stem cell therapy, the FDA published a perspective article in the New England Journal of Medicine.

The FDA will continue to help with the development and licensing of new stem cell therapies where the scientific evidence supports the products safety and effectiveness.

Know that the FDA plays a role in stem cell treatment oversight. You may be told that because these are your cells, the FDA does not need to review or approve the treatment. That is not true.

Stem cell products have the potential to treat many medical conditions and diseases. But for almost all of these products, it is not yet known whether the product has any benefitor if the product is safe to use.

If you're considering treatment in the United States:

If you're considering treatment in another country:

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FDA Warns About Stem Cell Therapies | FDA

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NK Cell Therapy Stem Cell Therapy

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3) Asia Pacific- (China, Japan, Korea, India, Australia, Indonesia, Thailand, Philippines, Vietnam)

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Chapter 1 NK Cell Therapy and Stem Cell Therapy Introduction and Market Overview

Chapter 2 Executive Summary

Chapter 3 Industry Chain Analysis

Chapter 4 Global NK Cell Therapy and Stem Cell Therapy Market, by Type

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Chapter 6 Global NK Cell Therapy and Stem Cell Therapy Market Analysis by Regions

Chapter 7 North America NK Cell Therapy and Stem Cell Therapy Market Analysis by Countries

Chapter 8 Europe NK Cell Therapy and Stem Cell Therapy Market Analysis by Countries

Chapter 9 Asia Pacific NK Cell Therapy and Stem Cell Therapy Market Analysis by Countries

Chapter 10 Middle East and Africa NK Cell Therapy and Stem Cell Therapy Market Analysis by Countries

Chapter 11 South America NK Cell Therapy and Stem Cell Therapy Market Analysis by Countries

Chapter 12 Competitive Landscape

Chapter 13 Industry Outlook

Chapter 14 Global NK Cell Therapy and Stem Cell Therapy Market Forecast

Chapter 15 New Project Feasibility Analysis

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Global NK Cell Therapy and Stem Cell Therapy Market: Development, Current Analysis and Estimated Forecast to 2025 - The Courier

ADMA Biologics Adopts Limited Duration Stockholder Rights Plan

RAMSEY, N.J. and BOCA RATON, Fla., Dec. 16, 2020 (GLOBE NEWSWIRE) -- ADMA Biologics, Inc. (Nasdaq: ADMA), an end-to-end commercial biopharmaceutical company dedicated to manufacturing, marketing and developing specialty plasma-derived biologics, today announced that its Board of Directors has approved the adoption of a limited duration stockholder rights plan and declared a dividend distribution of one right for each outstanding share of common stock. The record date for such dividend distribution is December 30, 2020. The rights plan expires, without any further action being required to be taken by ADMA’s Board of Directors, on December 15, 2021.

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ADMA Biologics Adopts Limited Duration Stockholder Rights Plan

SCYNEXIS Announces Launch of $50 Million Public Offering of Common Stock and Warrants

JERSEY CITY, N.J., Dec. 16, 2020 (GLOBE NEWSWIRE) -- SCYNEXIS, Inc. (Nasdaq:SCYX) today announced that it has commenced an underwritten public offering of shares of its common stock and warrants to purchase shares of its common stock, including pre-funded warrants to purchase common stock in lieu of common stock for certain purchasers. All of the shares of common stock and warrants in the offering will be sold by SCYNEXIS. The offering is subject to market conditions, and there can be no assurance as to whether or when the offering may be completed or as to the actual size or terms of the offering.

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SCYNEXIS Announces Launch of $50 Million Public Offering of Common Stock and Warrants

MacroGenics Announces FDA Approval of MARGENZA™ for Patients with Pretreated Metastatic HER2-Positive Breast Cancer

ROCKVILLE, MD, Dec. 16, 2020 (GLOBE NEWSWIRE) --  MacroGenics, Inc. (Nasdaq: MGNX), a biopharmaceutical company focused on developing and commercializing innovative monoclonal antibody-based therapeutics for the treatment of cancer, today announced that the U.S. Food and Drug Administration (FDA) has approved MARGENZA, in combination with chemotherapy, for the treatment of adult patients with metastatic HER2-positive breast cancer who have received two or more prior anti-HER2 regimens, at least one of which was for metastatic disease. MARGENZA is the first product approved from MacroGenics’ promising pipeline. The approval was based on safety and efficacy results from the pivotal Phase 3 SOPHIA trial.

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MacroGenics Announces FDA Approval of MARGENZA™ for Patients with Pretreated Metastatic HER2-Positive Breast Cancer

Phathom Pharmaceuticals Announces Pricing of Public Offering of Common Stock

FLORHAM PARK, N.J., Dec. 16, 2020 (GLOBE NEWSWIRE) -- Phathom Pharmaceuticals, Inc. (Nasdaq: PHAT), a late clinical-stage biopharmaceutical company focused on developing and commercializing novel treatments for gastrointestinal diseases, announced today the pricing of its underwritten public offering of 2,250,000 shares of its common stock at a price to the public of $42.00 per share. All of the shares to be sold in the offering are being sold by Phathom. The gross proceeds to Phathom from the offering, before deducting the underwriting discounts and commissions and other offering expenses, are expected to be $94.5 million. In addition, Phathom has granted the underwriters a 30-day option to purchase up to an additional 337,500 shares of common stock at the public offering price, less underwriting discounts and commissions. The offering is expected to close on or about December 21, 2020.

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Phathom Pharmaceuticals Announces Pricing of Public Offering of Common Stock

Drone X Pro Reviews – Evergreen Drone worth it? – Product Review by Mike Vaughn

The Drone X Pro is an interesting drone that can help you with your shots and bring you photos which you can't imagine. With its long battery life and flight time it's a great beginner drone. The Drone X Pro is an interesting drone that can help you with your shots and bring you photos which you can't imagine. With its long battery life and flight time it's a great beginner drone.

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Drone X Pro Reviews - Evergreen Drone worth it? - Product Review by Mike Vaughn