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New Case Series Demonstrates Potential of Aquadex Therapy for End-Stage Liver Disease Patients with Fluid Overload Early findings suggest Aquadex as a potential solution to safely and effectively remove fluid volume for

Key Takeaway: Nuwellis, Inc. has published new findings on the Aquadex SmartFlow system, revealing its potential benefits for end-stage liver disease patients experiencing fluid overload. The therapy, showcased in a case series involving 14 patients, can effectively remove excess fluid when conventional diuretics fail. This advancement may enhance patient mobility and prepare them for liver transplants more efficiently. Additionally, Aquadex is already approved for clinical use, requiring no further regulatory action, thus opening new market opportunities for the company.

Market Sentiment Analysis

POSITIVE FACTORS

  • Aquadex therapy shows promise for safely removing fluid from liver disease patients.
  • The study establishes Aquadex as a potential new treatment option without requiring additional FDA clearance.
  • Data indicates that Aquadex can improve patient mobility and enhance physical therapy effectiveness.

Full Press Release Details

New Case Series Demonstrates Potential of Aquadex Therapy for End-Stage Liver Disease Patients with Fluid Overload
Early findings suggest Aquadex as a potential solution to safely and effectively remove fluid volume for liver disease patients who
don't respond to diuretics
MINNEAPOLIS - Feb. 6, 2024 - Nuwellis, Inc. (Nasdaq: NUWE), a medical technology company focused on
transforming the lives of people with fluid overload, today announced the publication of new data demonstrating the potential value of the Aquadex SmartFlow system's aquapheresis therapy when treating patients with fluid overload as a
result of end-stage liver disease. The publication, "Utilization of Aquapheresis Among Hospitalized Patients with End-Stage Liver Disease: A Case Series and Literature Review," is a single-center retrospective case series featured in Clinical Transplantation.
"This study presents an exciting new market opportunity for Nuwellis, and we look forward to gathering additional data demonstrating how Aquadex can benefit
these patients," said Nestor Jaramillo, Jr., president and chief executive officer of Nuwellis. "Four and a half million adults in the U.S. have been diagnosed with liver disease.1 To date,
there has been little to no clinical evidence gathered demonstrating the benefits of aquapheresis for patients with liver disease. This publication lays the foundation for a new clinical application already within our current labeling that requires no additional regulatory clearances from the FDA."
The case series assessed the utilization of aquapheresis therapy with Aquadex in the
intensive care unit (ICU) setting at Mount Sinai Hospital between January 2020 and July 2023. Fourteen severely ill patients with end-stage liver disease were
treated with aquapheresis during this period. The most common cause of liver disease was alcohol-related, with nine of the 14 patients presenting with alcohol-associated cirrhosis. Key findings from the case series include:
"For clinicians treating patients with end-stage liver disease, it can be an enormous challenge to safely and effectively remove fluid when patients don't
respond to or can't tolerate diuretic therapy," said John Jefferies, M.D., chief medical officer of Nuwellis. "In such cases, fluid removal via aquapheresis can enhance patients' mobility and allow them to receive more effective physical therapy.
This can reduce cirrhosis-related frailty and enhance their ability to receive a life-saving liver transplant in a more timely manner."
Patients with end-stage liver disease are currently treated with diuretics, but studies show that the longer a patient is on diuretics, the less effective
they become.2,3 End-stage liver disease patients are also prone to developing ascites, which requires paracentesis - a painful procedure
using a needle to remove fluid from the peritoneal cavity. In this case series, Aquadex was shown to provide a potential additional solution to mitigate these clinical gaps.
1 CDC. Chronic Liver
2 Felker MG and Mentz
RJ. J Am Coll Cardiol. 2012;59(24):2145-53.
3 Doering A, et al. Int
J Emerg Med. 2017;10(17).
Aquadex is proven to simply, safely, and precisely remove excess fluid from patients suffering from fluid overload who have not responded to
conventional medical management, including diuretics. Providers can specify and adjust the rate of fluid removed for each individual patient, resulting in a gradual reduction of excess fluid. The device's built-in, customizable hematocrit
monitoring technology provides real-time measurement of percent blood volume changes that can be tailored to individual patients' needs. A customizable fluid removal rate is particularly important for pediatric patients who have a small amount
of blood in their bodies. The Aquadex system is cleared by the U.S. Food and Drug Administration (FDA) for use in adults and pediatric patients weighing 20 kg (44 lbs.) or more.
Nuwellis, Inc. (Nasdaq: NUWE) is a medical technology company dedicated to transforming the lives of patients suffering from fluid overload through
science, collaboration, and innovation. The company is focused on commercializing the Aquadex SmartFlow system for ultrafiltration therapy. Nuwellis is headquartered in Minneapolis, with a wholly owned subsidiary in Ireland. For
more information visit www.nuwellis.com or visit us on LinkedIn or X.
Forward-Looking Statements
Certain statements in this release may be considered forward-looking statements within the meaning of the Private Securities Litigation Reform Act of
1995, including without limitation, statements regarding the new market opportunities and anticipated growth in 2024 and beyond. Forward-looking statements are predictions, projections and other statements about future events that are based on
current expectations and assumptions and, as a result, are subject to risks and uncertainties. Many factors could cause actual future events to differ materially from the forward-looking statements in this release, including, without
limitation, those risks associated with our ability to execute on our commercialization strategy, the possibility that we may be unable to raise sufficient funds necessary for our anticipated operations, our post-market clinical data collection
activities, benefits of our products to patients, our expectations with respect to product development and commercialization efforts, our ability to increase market and physician acceptance of our products, potentially competitive product
offerings, intellectual property protection, our ability to integrate acquired businesses, our expectations regarding anticipated synergies with and benefits from acquired businesses, and other risks and uncertainties described in our filings
with the SEC. Forward-looking statements speak only as of the date when made. Nuwellis does not assume any obligation to publicly update or revise any forward-looking statements, whether due to new information, future events or otherwise.

Frequently Asked Questions

What is the potential of Aquadex therapy for liver disease?

Aquadex therapy may safely and effectively remove excess fluid from liver disease patients who don't respond to diuretics.

What does the case series reveal about Aquadex's efficacy?

The case series highlights Aquadex's effectiveness in managing fluid overload in patients with end-stage liver disease.

How many patients were involved in the Aquadex case series?

Fourteen patients with severe end-stage liver disease were treated with Aquadex in the case series.

What challenges do clinicians face with diuretics in liver disease?

Diuretics can become less effective over time, making fluid removal challenging for clinicians.

Is Aquadex FDA-approved for all patients?

Yes, Aquadex is FDA-cleared for adults and pediatric patients weighing 20 kg or more.

Last updated: Feb 6, 2024