Communicating The Risk For Developing Alzheimer's Disease

As part of the A4 Study Team, Great Lakes Clinical Trials is proud to contribute to an important article released in the peer-reviewed Journal of the American Medical Association (JAMA) Neurology. The article entitled, “Short-term Psychological Outcomes of Disclosing Amyloid Imaging Results to Research Participants Who Do Not Have Cognitive Impairment” was published on August 10, 2020 and a link to the article can be found by clicking the image below.

“The key question posed in this publication is whether information about a person’s increased risk for developing Alzheimer’s disease can be safely shared,'“ commented Steve Satek, President of Great Lakes Clinical Trials. “Through innovative PET Scan technology, researchers now have the ability to look inside a living human’s brain and see if there are silent changes going on that may be a precursor to Alzheimer’s disease. These changes can happen decades before memory loss starts to take hold and can determine a person’s future risk for progressing to Alzheimer’s disease.”

Study Conclusion: In this observational preclinical AD study, participants who learned they had elevated amyloid levels and a great risk for developing Alzheimer’s, did not experience short-term negative psychological issues compared with persons who learned they did not have elevated amyloid levels.

The questions we often get asked about learning these risk results are:

  • Why would someone want to know their risk of developing Alzheimer’s?

  • if I have an increased risk, what can I do about it?

There are steps you can take today to support a healthier brain and potentially slow down the effects of normal aging. These include things like eating a Mediterranean diet, getting a full night’s sleep, and socializing with family and friends. Great Lakes Clinical Trials has promoted these activities through their Brain Health Video Series, which can be found here.

In addition, people at higher risk for developing Alzheimer’s can join clinical research studies to assess whether new innovative treatments can minimize or eliminate that risk. A list of studies being conducted by Great Lakes Clinical Trials can be found here.

“One thing we know for certain, is that doing nothing will not help alter the course of the memory loss,” commented Satek. “Taking simple brain-healthy steps in your day to day life is important - and joining a clinical trial may not only help change your risk, but the information gained in the study will help in the development of therapies for future generations.”





Study Conducted at Great Lakes Clinical Trials Shows Positive Results for Atopic Dermatitis

Preliminary Data Shows Promise in Helping Individuals with Moderate to Severe Eczema

Atopic Dermatitis (AD), the most common form of Eczema, currently affects more than 9.6 million children and 16.5 million adults in the United States, according to The National Eczema Association. Although treatable, symptoms of the condition—including rashes, itching, and redness—can be extremely painful to live with both physically and emotionally.

These symptoms, often referred to as flare ups, aren’t just limited to rashes, itching, and redness. Acute to severe dryness, peeling, flakiness, bumps, and fissures may also follow; and can occur almost anywhere on the skin including hands, behind the knees, or on the face.

However, there is new hope on the horizon. A medication labeled RINVOQ (upadacitinib) has been used to help treat patients with moderate to severe rheumatoid arthritis since August 2019. But now, preliminary data from a clinical trial being conducted at Great Lakes, shows that RINVOQ Monotherapy has significantly improved skin clearance and reduced itching in adult and adolescent patients with moderate to severe atopic dermatitis. Since the drug has been effective in helping treat those with rheumatoid arthritis, doctors believe it is a promising future treatment for those who have eczema, as both conditions are overactive immune system occurrences.

“We are very pleased to be given the opportunity to research this drug here at our own facility,” says Steve Satek, President & Founder of Great Lakes Clinical Trials. “Great Lakes has always been passionate about the care of others, and we look forward to continue helping them find the best treatments possible for their medical conditions.”

Great Lakes Clinical Trials is continuing their clinical trials of RINVOQ with adults, and currently enrolling child participants between the ages of 12-17. With this research, Great Lakes hopes to not just provide relief, but physical and mental clarity for those living with eczema.

You can read the full Abbvie press release here. For more information on Great Lakes Clinical Trials Atopic Dermatitis study, please visit our website, or call our office at 773-275-3500.

PBS Features Great Lakes Clinical Trials In News Report

We are proud to announce that Great Lakes Clinical Trials’ President, Steve Satek, was recently featured in a Public Broadcasting Service’s news article addressing how COVID-19 has affected Alzheimer’s disease clinical trials.

Steve Satek, President and Founder of Great Lakes Clinical Trials

Steve Satek, President and Founder of Great Lakes Clinical Trials

“It is humbling to have the important work we do at Great Lakes Clinical Trials, be recognized alongside renown institutions like the Alzheimer’s Therapeutic Research Institute (ATRI) at the University of Southern California and the Global Alzheimer’s Platform,” commented Mr. Satek. “As a research center embedded with a residential community on the northside of Chicago and on the campus of the Lutheran Home in Arlington Heights, we intentionally brought convenient access to research studies to communities that otherwise have limited access to innovative and cutting-edge medications to treat this disease.”

Great Lakes Clinical Trials has remained open as an essential business during the COVID-19 pandemic, and is currently enrolling participants in multiple trials — including individuals experiencing mild memory loss and those already diagnosed with Alzheimer’s disease. “We have taken great care to protect both our patients and our staff during these challenging times,” added Mr. Satek. “A person who is experiencing memory loss cannot put that decline on hold while we wait to address COVID. Our team is dedicated to continuing to fight to save people’s memory.“

Full text of the article can be found below or to view this article on PBS’ Next Avenue website, click here.


How Alzheimer’s Clinical Trials Have Become COVID-19 Victims

What the pandemic means for Alzheimer's treatment prospects

By Stephenie Overman
July 9, 2020

After a frustrating 2019, Alzheimer’s researchers had reason to look forward to 2020 as a year of promise. Then the pandemic struck.

“Last year, seven Alzheimer’s clinical trials were stopped. The portfolio was more than halved,” said John R. Dwyer, Jr., president of the Global Alzheimer’s Platform (GAP) foundation, a network for clinical trials in North America.

Clinical trials with human participants are needed to test the safety and effectiveness of any new Alzheimer’s drugs or treatments to prevent, slow or cure the disease.

Alzheimer’s studies take a long time to conclude. There hasn’t been a successful treatment approved since 2003,” Dwyer said.

Setting Back Alzheimer’s Research

Private clinical trial sites have been particularly hard hit because of COVID-19 restrictions. “If sites fail, that loss of research capacity could set back Alzheimer’s research for years,” Dwyer noted.

The disruption in clinical trials might have an irreversible effect on the health and wellbeing of Alzheimer’s patients and their caregivers.

Before the pandemic, Alzheimer’s researchers were hopeful that 2020 could have been a breakthrough year for the nearly 6 million Americans living with the disease and for their caregivers. The National Institutes of Health was set to allocate $2.8 billion for dementia research, a nearly threefold increase over 2016.

But the disruption in clinical trials might have an irreversible effect on the health and wellbeing of Alzheimer’s patients and their caregivers, said Steve Satek, president of Great Lakes Clinical Trials in Chicago.

“The greatest hope for treating this disease lies in clinical trials. That is where the most cutting-edge, innovative medicines can be found,” he noted. “A person who is experiencing gradual memory loss cannot put that decline on hold while we wait to start up or reactivate trials. Their disease moves on.”

Our Commitment to Covering the Coronavirus

We are committed to reliable reporting on the risks of the coronavirus and steps you can take to benefit you, your loved ones and others in your community. Read Next Avenue’s Coronavirus Coverage.

As of the beginning of April, only 12% of research centers were enrolling in any clinical trials, according to reports to GAP. Some said they could be closing their doors in the next few months; more than half said they may need to lay off staff.

Workarounds to Keep Alzheimer’s Clinical Trials Going

In some cases, Alzheimer’s researchers have been devising alternatives to lower the number of required visits vulnerable older participants must make to health care facilities for the trials. Home visits and telemedicine are taking up some of the slack. But these workarounds add another degree of difficulty to an already complex process, according to Dwyer.

Observational studies, which don’t involve the introduction of an actual drug or treatment, are not considered essential to participants’ health. So, they “have pretty much shut down,” according to Dr. Paul Aisen, director of the Alzheimer’s Therapeutic Research Institute (ATRI) at the University of Southern California.

But interventional or therapeutic trials where participants receive some type of treatment are more likely to be considered essential. That has allowed some of them to continue, albeit with difficulties. But “at many sites, we have had to put a hiatus in place. It’s very disruptive,” said Aisen.

These tests are rigorous, Aisen noted, adding that “when you already have a study underway, it’s critical to try to maintain it, to try to keep the dosing on schedule” at home or in a setting that does not put participants at risk.

A Major Clinical Trial Pushed Back

One major Alzheimer’s study ATRI is participating in is known as the AHEAD 3-45. It’s a global multicenter clinical trial aimed at preventing memory loss due to Alzheimer’s disease. This study was poised to launch in May but had to be pushed back until at least mid-July.

“For a number of reasons, participation in AHEAD 3-45 cannot be done at home. The screening process requires in-person cognitive and clinical assessment, as well as MRI and PET brain imaging,” said Aisen. “In addition, the study medication is administered intravenously.”

Despite the delays, many Alzheimer’s clinical trial participants remain committed. “We’re confident we are going to be able to complete studies,” said Aisen. “There will be delays, it will require adjustments, but we will complete and evaluate therapies.”

However, Li-Huei Tsai, director of the Picower Institute for Learning and Memory at the Massachusetts Institute of Technology, is much less confident that her institute will be able to complete trials to test non-invasive brain simulation.

“We will still have useful data, but there may be limits on some outcome measures compared to what we would have had without the pandemic.”

“We had tested animals with light and sound, and this reduced Alzheimer’s pathology and improved cognitive function,” according to Tsai. Based on that research, “we designed a study to have human subjects receive light and sound one hour a day for a year.”

‘Completely Disrupted’

A device consisting of a 2’x2′ panel designed to produce the gamma frequency light and a speaker producing the gamma frequency sound was installed in each participant’s home. One group had been receiving treatment and the second group got a placebo. Caregivers were instructed how to monitor the treatment.

Although use of the device has not been much affected by the pandemic, “our ability to bring subjects back for evaluation is completely disrupted,” said Tsai. “I don’t see any time soon that we will be able to evaluate them.”

The pandemic is requiring Tsai and her team to make changes to a painstakingly designed protocol, setting research back by at least six months.

“We will still have useful data, but there may be limits on some outcome measures compared to what we would have had without the pandemic,” Tsai said.

Many participants had agreed to sign on to the trial with the understanding that even if they were initially given the placebo they’d later be switched to the actual treatment. With that possibility indefinitely on hold, Tsai said, “I feel bad.”

She’s also concerned about the ability to expand the light/sound study and to begin other trials.

The Pandemic’s Biggest Impact on Alzheimer’s Research

Satek sees the inability to screen new patients for trials as “probably the biggest impact” of the pandemic for Alzheimer’s research.

That’s because it takes years of working within a community to convince people to participate in clinical trials.

Said Satek: “Normally we bring in ten to fifteen people a week for free memory tests. That doesn’t mean they will join a trial, but a lot do” once they’re educated about how trials work. Now, few people are coming in for free tests.

And although Great Lake Clinical Trials has remained open during the coronavirus outbreak, the nearby hospital that provides MRI and PET scans closed its imaging center for weeks, along with other services, to prevent the spread of COVID-19.

As a result, some people temporarily couldn’t get the brain scans they needed to enter the program and the clinic had to postpone follow-up scans for trial participants who’d already enrolled.

Challenges for Doing the Tests at Home

Since most Alzheimer’s medications under study haven’t been approved for prescription by the Food and Drug Administration, having patients take the medicine at home and report the results makes the assessment more challenging, Satek said.

“We still need to assess the patient’s safety via physical exam, ECG and  lab tests and perform standardized cognitive and quality of life assessments. This could possibly be done in the home setting as long as it is approved by our ethics board and study sponsor. But it would require assembling a traveling research team,” he added.

And entering homes opens the door to questions about COVID-19 safety for the patients as well as the researchers.

For people visiting his clinic, Satek said, numerous steps have been taken to protect against the coronavirus.

Patients are reminded to stay home if they show any COVID-19 symptoms. And for social distancing, “we don’t have two people coming to the waiting area at the same time,” said Satek.

Also, interviews with new patients and memory assessments have been moved from small rooms to larger conference rooms and offices.

How to Attract New Clinical Trial Participants

In an effort to keep the pipeline of new trial participants from drying up, Satek has been conducting Zoom meetings and virtual memory assessments.

“It’s going pretty well. We ask them: ‘Do you want to be called when things open again?’ We keep them on the list,” Satek noted.

In the past, he often spoke to groups in person about the importance of volunteering for clinical trials. Those talks have moved online, too.

“It takes years to build up a presence in the community. We’re doing our best to keep the momentum going. We’re focused on trying to keep the information river flowing,” said Satek.

Still, Dwyer worries about the pipeline of participants drying up. “Healthy folks are needed, sick people are needed,” he said.

He encourages people concerned about getting Alzheimer’s to enter clinical trials. “You’re going to get the best neurological workups. A complete review of your cognitive situation. Even if you don’t go into a study, you get information,” Dwyer said.

These days, he’s especially concerned that small, family-owned private clinics won’t survive the current economic crisis.

More than half of Alzheimer’s studies are done in what Dwyer calls this “capillary system.” Getting financial relief to them “is more of a challenge. There’s not a natural mechanism to get them help,” Dwyer noted.

If these small clinics don’t get some type of small-business relief from the government, Dwyer said, their capacity will be reduced 20% to 30%.

“That means that one full Alzheimer’s trial will not get done. We lose one more big shot on goal,” said Dwyer.

Stephenie Overman writes about workplace and health issues. She is the author of Next-Generation Wellness at Work.

Clinical Trials Press Forward in the Age of COVID

Attracting experimental subjects for Alzheimer's research is never easy. COVID made it harder.

Chicago Sun-Times
By Neil Steinberg
Jun 14, 2020, 11:27am CDT

Jim Butler is receiving his monthly 45-minute infusion of drugs.

What kind of drugs? He doesn't know. Nor do the nurses administering them. Could be an experimental medicine that will help his brain fight Alzheimer's disease. Or could be a placebo that does nothing.

Only one doctor conducting the medical research at Great Lakes Clinical Trials knows what drug Butler is getting, and even he doesn't know what the effect will be.

None of this influences Butler's determination to be here.

Jim Butler, a Chicago retiree, arrives at Great Lakes Clinical Trials in Andersonville for his monthly infusion, part of a study evaluating potential new Alzheimer's treatments. He also performs cognitive tests to gauge his memory and brain function…

Jim Butler, a Chicago retiree, arrives at Great Lakes Clinical Trials in Andersonville for his monthly infusion, part of a study evaluating potential new Alzheimer's treatments. He also performs cognitive tests to gauge his memory and brain function. I Photo by Neil Steinberg

"I got an Alzheimer's diagnosis four years ago," said Butler, 71, who describes the disease as causing "multiple times a day, cognitive hiccups, confusion."

One thing he is not confused about is the importance of participating in research.

 "The simplest reason is I like to be very proactive about my diagnosis," he said. "My game plan is not to get overwhelmed and unsettled at these things. To try to smile at them, dismiss them, let them go. A clinical trial is an enormously great way to do that."

Clinical trials are the minor leagues of medicine. Before drug companies can sign up a star cure to wow the public, they need to know if it can deliver. To do that, they spend billions of dollars and commission hundreds of small clinics like Great Lakes Clinical Trials, which opened in Andersonville in 2014. There is a second location in Arlington Heights.

Clinical trials must be run like clockwork, with drugs administered and tests - in between infusions, Butler takes cognitive tests to see how his brain is functioning - done on a set schedule. A certain pandemic has upended Alzheimer's research along with everything else. 

"COVID is substantially impairing our research efforts for two reasons," said John Dwyer, president of Global Alzheimer's Platform Foundation based in Washington, D.C. "First, older folks are saying, 'I'm really worried about Alzheimer's and want to fight it. I know it can kill me in 10 or 15 years. But COVID can kill me right now.'"

Second, some research partners had to stop participating. Great Lakes had to stop using the MRI at Swedish Covenant, for instance, while the hospital fought COVID. Revenue at Great Lakes is down 50% over the past three months.

Jim Butler receives an infusion as part of an Alzheimer's study at Great Lakes Clinical Trials in Andersonville. The COVID-19 crisis has made such trials even more difficult to run than they already are. I Photo by Neil Steinberg

Jim Butler receives an infusion as part of an Alzheimer's study at Great Lakes Clinical Trials in Andersonville. The COVID-19 crisis has made such trials even more difficult to run than they already are. I Photo by Neil Steinberg

"Most of our patients have still continued to come in," said Steve Satek, president and founder of Great Lakes. "It's just a little bit slower process, spreading out visits. Not letting patients come in at the same time."

 Arriving at the clinic, I thought Alzheimer's could only be confirmed after death. But I was behind the times.

"That's radically changed in the last five years," said Dr. Jeffrey Ross, lead investigator at Great Lakes. "It used to be we could only detect Alzheimer's from brain tissue. Now we can see that in the living brain in a PET scan, using special radioactive isotopes. That has helped us to make earlier diagnoses. We see the presence of amyloids" (protein plaques that builds up in the brain due to Alzheimer's, disrupting its function) 20 years before the onset of symptoms."

Dwyer said medical research is a collaboration between massive pharmaceutical companies and famous hospitals joined by the need for a steady stream of test patients with small clinical trial sites.

"It's a wonderful amalgamation of great brand names - Harvard and Washington University and Northwestern, the Mayo Clinic and the Cleveland Clinic, and these committed mom and pop institutions," he said.

"The discovery process for new therapies, from Alzheimer's to cancer, is largely done on the backs of little enterprises they hire to conduct the trials. Billion dollar companies rely on primary care physicians to organize and enroll and monitor the care of patients in trials to see whether therapies work or not. It's a little understood and highly critical part of finding solutions to disease."

Before the effects of Alzheimer's drugs on the brains of Alzheimer's patients can be studied, those patients have to come through the door.

"You can't just take anybody," Dwyer said. "To get a pristine, rigorous collection of people who will give you a clear signal the drug is working, you have to screen a lot of people. This is not a trivial commitment. You're signing up for a one-year run, most are longer. Every month, like clockwork, you gotta go back to Great Lakes for another drug in your veins. Rain, sleet, snow."

Or pandemic coupled with recession and civil unrest.

"A number of high-profile studies were canceled," Ross said. "COVID put us on hold for starting new studies. But once this thing subsides, we're going to hit the ground running." 

Dwyer wishes clinical trial volunteers could be nudged into the ever-expanding hero class.

"The first responders - the cops, the firemen, doctors, nurses - we celebrate all these people," he said. "But first responders come in many forms. These people who participate in trials, they are first responders, too.

"If we don't get them into studies, we don't have therapies for cystic fibrosis, sickle cell anemia, cancer, Alzheimer's. We're dealing with older people, the most vulnerable population for COVID, asking them to get into trials, disrupt their lives. Not just for themselves but to possibly find a solution to terrible, terrible diseases."

That's what keeps Jim Butler coming back, despite the masks and the elaborate cleaning precautions now being taken.

"I'd hate to have to interrupt it," he said. Why?

"This is yet one more way to be positive and on top of my diagnosis," he said. "I could be helping myself if this proves to be a real home run; then great, I got lucky. I want to get lucky. I also want to contribute."

Those interested in participating can contact Great Lakes Clinical Trials at (773) 275- 3500 or go to greatlakesclinicaltrials.com.

Great Lakes Clinical Trials Needs Your Help to Support Swedish Hospital in Fighting COVID-19

banner_novel_coronavirus_2.png

As healthcare partners on the north side of Chicago, Great Lakes Clinical Trials is helping Swedish Hospital in the fight to keep our community healthy and safe. 

Our community is seeing an increased incidence of COVID-19 infection. We need everyone’s help to spread the word about COVID-19 prevention and be vigilant if they or their families have COVID-19 symptoms. It is critically important that we continue to follow public health requirements, including social distancing and wearing face coverings in public. We know from recent studies that a significant portion of individuals with COVID-19 lack symptoms and these individuals could spread the virus when they are in close proximity to others.

We are asking for your support and assistance to help personally reach out to your friends and families so any individuals with symptoms can be evaluated by an expert who may recommend testing. Below are some ways you can help.

Swedish Hospital Neighborhood Update 5.8.20 Multilingual.jpg

Multilingual Flier for Help Line and Screening Assistance

This flier can be shared with the community to encourage anyone who is experiencing COVID-19 symptoms, or has had contact with a person confirmed or tested for COVID-19, to call the help line today. Our clinicians will screen your symptoms and advise next steps which may include testing for COVID-19. If they require testing, it will be at no cost to them. The flier provides a simple message in English, Spanish, Korean, Arabic, Vietnamese, Assyrian and Polish.

Click here to download a copy

 

Personal Calls to Your Family and Friends

We are asking for your help to call your friends, family members and other community contacts as soon as possible and ask them if they are experiencing COVID-19 symptoms, or if any members of their households are experiencing any of these symptoms.

○      Fever – temperature of 100 or higher

○      Cough

○      Congestion

○      Sore throat

○      Runny nose

○      Shortness of breath

○      Loss or decrease of smell or taste

○      Muscle aches with flu-like symptoms

○      Loss of appetite

○      Chills or shaking chills

○      Headache

○      Diarrhea, nausea or other gastrointestinal symptoms

It is also important to remember than a significant number of people with COVID-19 infection, especially younger patients, may exhibit none of these symptoms, but can pass it to those they come in contact with. That is why it is essential to practice the public health measures of social distancing, frequent hand washing and wearing a mask in public

If a person replies “yes” to these symptoms, please strongly urge them to contact Swedish Hospital’s COVID-19 Help Line at 773-907-7700 for immediate screening and possible testing. Online screening is also available by clicking here.

If the answer is “no,” we still remind people to be alert for the virus’s symptoms and to follow the key safety measures on the Swedish Hospital website at  SwedishCovenant.org/covid.

Costs

If a test is recommended at Swedish Hospital, it will come at no cost to patients. Uninsured will be offered free testing and follow up care will be managed through their financial assistance and charity program. Those who are insured will not be responsible for any out-of-pocket costs related to being tested for COVID-19.

Reminders

  • For information about COVID-19 safety behaviors, temporary operations at Swedish Hospital, and more please visit SwedishCovenant.org/covid

  • To begin a COVID-19 self-assessment online, please visit SwedishCovenant.org/tent

  • Call Swedish Hospital’s COVID-19 Help Line at 773-907-7700 if you are experiencing COVID-19 symptoms, or have had contact with a person confirmed or tested for COVID-19. Certified medical interpreters are ready to help in many languages.

  • Printable COVID-19 resources are available on the Swedish website.

Great Lakes Clinical Trials Contributes to FDA Approval of Vyepti™ for the Prevention of Migraines

Great Lakes Clinical Trials is proud to share in the announcement of the FDA’s approval of Lundbeck’s Vyepti™ – the first and only intravenous preventive treatment for migraines.

“We are pleased to see this important advancement of medicine, and improvement in our nation’s healthcare as a result of the important work we are doing at Great Lakes Clinical Trials,” commented Steve Satek, President of Great Lakes Clinical Trials. “First and foremost, we recognize and acknowledge the sincere commitment and dedication of our amazing volunteers who participated in this research. Without the contributions of our Chicagoland community in joining clinical trials, we would not have such important advances in our healthcare.”

Full Press Release

To review the full press release from Lundback, click here

About Migraines

Migraines are a complex and incapacitating neurological disease characterized by recurrent episodes of severe headaches typically accompanied by an array of symptoms, including nausea, vomiting, and sensitivity to light or sound. It is estimated to affect approximately 39 million people in the U.S. and more than 1.3 billion worldwide. Migraines have a profound impact on patients’ lives, their relationships, as well as their ability to carry out activities of daily living. More than 157 million work days are lost each year in the U.S. due to migraine

About Great Lakes Clinical Trials

Great Lakes Clinical Trials is an independent, phase I-IV clinical trials center, specializing in the study of investigational medications, food products, devices and supplements for the treatment of chronic diseases, notably in Mental Health, Memory Disorders, Pain Management, Vaccines, Nutrition and Dermatology. All medical services at  Great Lakes Clinical Trials are provided free-of-charge, and are led by board-certified physicians.  We do not bill insurance and health information is kept confidential, unless you ask us to collaborate with your personal physician. Stipends are provided for your participation - amounts vary based on each study.  Free transportation is also provided for some of our trials.  The Great Lakes team have managed more than 450 clinical trials over the past 25 years and are committed to providing quality services for both study volunteers & the research industry.

Leucine Added to Plant Based Protein Supplements Research Study

Leucine Added to Plant Based Protein Supplements Research Study

We are looking for healthy adults between the ages of 40 and 64 to participate in this study which requires one, one-hour screening visit and then five, four-and-a-half-hour study visits.

The objective of this study is to assess the effects of leucine, added to soy and pea rice proteins, in both crisp and ready-to-mix drink formulations compared to a whey protein ready-to-mix drink blend. This is determined by blood samples which are analyzed for their plasma amino acid, glucose, and insulin responses after consuming the products.

Matinas BioPharma Announces Pre-Screening of Patients to Determine Eligibility for Phase 2 ENHANCE-IT Study Against Vascepa®

BEDMINSTER, N.J., Sept. 25, 2019 (GLOBE NEWSWIRE) -- Matinas BioPharma Holdings, Inc. (NYSE AMER: MTNB), a clinical stage biopharmaceutical company, today announced that it has commenced pre-screening patients to determine eligibility for ENHANCE-IT, its Phase 2 head-to-head pharmacodynamic (PD) study of MAT9001 against Vascepa in patients with elevated triglycerides (150-499 mg/dL).

“Our second head-to-head trial against Vascepa is an important milestone for our Company, and pre-screening patients for eligibility will facilitate rapid enrollment in the first quarter of 2020,” commented Jerome D. Jabbour, Chief Executive Officer of Matinas. “Topline data from this study, which we expect in the second half of 2020, will be another opportunity to distinguish MAT9001 from the market leading therapy in this emerging prescription omega-3 space.”

The “ENHANCE-IT trial (Pharmacodynamic effects of a free fatty acid formulation of omega-3 pentaenoic acids to enhance efficacy in adults with elevated triglycerides) will be led by Kevin C. Maki, Ph.D., President and Chief Scientist of Midwest Biomedical Research, and is expected to involve approximately six sites in the United States. “I am very excited about this clinical study,” stated Dr. Maki. “The world of prescription omega-3 therapies changed significantly after the results of REDUCE-IT, but there is still more to learn about this emerging class of medications regarding effects on cardiometabolic risk factors. ENHANCE-IT gives us an opportunity to confirm prior compelling data about the efficacy of MAT9001 compared to Vascepa.”

James J. Ferguson, M.D., Chief Medical Officer of Matinas, commenting on recent developments in omega-3 therapy and hypertriglyceridemia, said, “Momentum and excitement around the prescription omega-3 class continues to build as we enter a new era in the treatment of patients with elevated triglycerides (TGs). The recent Scientific Advisory document from the American Heart Association (AHA), which mentions MAT9001 favorably, the new European Society of Cardiology/European Atherosclerosis Society (ESC/EAS) Lipid Guidelines and a new National Lipid Association (NLA) Position Statement all recommend omega-3 therapy for treating higher-risk patients with elevated TGs, not just those with severe hypertriglyceridemia (≥500 mg/dL). This additional head-to-head efficacy study in a greater number of patients over a longer period of time will allow us to further highlight MAT9001 and support its potential to benefit patients.”

About Matinas BioPharma

Matinas BioPharma is a clinical-stage biopharmaceutical company focused on development of its lead product candidate, MAT9001, for the treatment of cardiovascular and metabolic conditions. MAT9001 is a prescription-only omega-3 fatty acid-based composition, comprised primarily of EPA and DPA, under development for hypertriglyceridemia, that was specifically designed to overcome the shortcomings seen with other agents in the omega-3 class. Company leadership has a deep history and knowledge of cardiovascular drug development and is supported by a world-class team of scientific advisors.

In addition, the Company is developing MAT2203, an oral, encochleated formulation of Amphotericin B, to treat serious invasive fungal infections. The drug is based on Matinas’ proprietary lipid nano-crystal (“LNC”) platform technology which can help solve complex challenges relating to the safe and effective delivery of potent medicines, potentially making them more targeted, less toxic and orally bioavailable. 

Forward-Looking Statements

This release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including those relating to the Company's anticipated capital and liquidity needs, strategic focus and the future development of its product candidates, including MAT9001 and MAT2203, the anticipated timing of regulatory submissions, the anticipated timing of clinical studies, the anticipated timing of regulatory interactions, the Company’s ability to identify and pursue development and partnership opportunities for its products or platform delivery technology on favorable terms, if at all, and the ability to obtain required regulatory approval and other statements that are predictive in nature, that depend upon or refer to future events or conditions. All statements other than statements of historical fact are statements that could be forward-looking statements. Forward-looking statements include words such as "expects," "anticipates," "intends," "plans," "could," "believes," "estimates" and similar expressions. These statements involve known and unknown risks, uncertainties and other factors which may cause actual results to be materially different from any future results expressed or implied by the forward-looking statements. Forward-looking statements are subject to a number of risks and uncertainties, including, but not limited to, our ability to obtain additional capital to meet our liquidity needs on acceptable terms, or at all, including the additional capital which will be necessary to complete the clinical trials of our product candidates; our ability to successfully complete research and further development and commercialization of our product candidates; the uncertainties inherent in clinical testing; the timing, cost and uncertainty of obtaining regulatory approvals; our ability to protect the Company's intellectual property; the loss of any executive officers or key personnel or consultants; competition; changes in the regulatory landscape or the imposition of regulations that affect the Company's products; and the other factors listed under "Risk Factors" in our filings with the SEC, including Forms 10-K, 10-Q and 8-K. Investors are cautioned not to place undue reliance on such forward-looking statements, which speak only as of the date of this release. Except as may be required by law, the Company does not undertake any obligation to release publicly any revisions to such forward-looking statements to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events. Matinas BioPharma's product candidates are all in a development stage and are not available for sale or use.

Download PDF

Investor and Media Contacts Peter Vozzo
Westwicke
443-213-0505
peter.vozzo@westwicke.com
Ian Cooney
Director – Investor Relations & Corporate Development
Matinas Biopharma, Inc.
(415) 722-4563
icooney@matinasbiopharma.com

Source: Matinas BioPharma Holdings, Inc.

Released September 25, 2019