Nuwellis’ Strategic Partner, SeaStar Medical, Receives FDA Approvable Letter for Its Pediatric Selective Cytopheretic Device
October 31 2023 - 8:00AM
Nuwellis, Inc. (Nasdaq: NUWE), a medical technology company focused
on transforming the lives of people with fluid overload, today
announced its strategic partner, SeaStar Medical Holding
Corporation (Nasdaq: ICU) (SeaStar Medical), received an Approvable
Letter from the U.S. Food and Drug Administration (FDA) for its
pediatric Selective Cytopheretic Device (SCD-PED). The SCD-PED will
provide a new therapy option for children weighing 10 kilograms or
more who have acute kidney injury (AKI) and sepsis or a septic
condition requiring continuous kidney replacement therapy (CKRT) in
a hospital intensive care unit.
The Approvable Letter indicates that SeaStar
Medical’s Humanitarian Device Exemption (HDE) application
substantially meets the requirements for an Approval Order and
outlines remaining administrative steps that must be finalized
before the HDE can be active for commercialization. For the
SCD-PED, these include revisions to product labeling and minor
modifications to the post-approval study plan.
Nuwellis and SeaStar Medical previously announced an exclusive
U.S. license and distribution agreement for Nuwellis to distribute
the SCD-PED. “We’re excited to collaborate with SeaStar Medical to
bring this innovative product to market, which, upon FDA approval,
will represent a new revenue stream for Nuwellis,” said Nestor
Jaramillo, Jr., President and Chief Executive Officer of Nuwellis.
“Most importantly, the clinical data used for the approval in
support of the HDE application showed a 77% reduction in mortality
rate and no dialysis dependency at Day 601,2.”
“Receipt of this Approvable Letter is a major accomplishment
indicating that the FDA supports SeaStar Medical’s application and
acknowledges the potential of our device to save lives and
eliminate dialysis dependency in critically ill children with AKI
and sepsis,” said Kevin Chung, MD, Chief Medical Officer of SeaStar
Medical. “SeaStar intends to work closely with the FDA to complete
the final steps outlined in the Letter and anticipate the
much-needed availability of the product in pediatric intensive care
units by early next year.”
SeaStar Medical’s SCD-PED therapy is a patented, cell-directed
extracorporeal tool for managing cytokine storm-induced
hyperinflammation. The therapy precisely targets and neutralizes
activated toxic immune cells that drive cytokine storms (an
overreaction of the immune system) that can ultimately cause organ
damage and failure for critically ill patients. Clinical studies
have demonstrated the SCD-PED’s potential to eliminate dialysis
dependency, shorten intensive care unit time, and restore the lives
of critically ill pediatric patients.1,2,3
About Nuwellis 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 Twitter.
About SeaStar Medical, Inc.Denver-based SeaStar
Medical is a medical technology company that is redefining how
extracorporeal therapies may reduce the consequences of excessive
inflammation on vital organs. SeaStar Medical’s novel technologies
rely on science and innovation to provide life-saving solutions to
critically ill patients. The company is developing and
commercializing extracorporeal therapies that target the effector
cells that drive systemic inflammation, causing direct tissue
damage and secreting a range of pro-inflammatory cytokines that
initiate and propagate imbalanced immune responses. For more
information visit http://www.seastarmedical.com/ or visit us on
LinkedIn or Twitter.
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 2023 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
impact of the COVID-19 pandemic, 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.
1 Goldstein, Stuart L., et al. “Use of the Selective
Cytopheretic Device in Critically Ill Children.” Kidney
International Reports, vol. 6, no. 3, 18 Dec. 2020, pp. 775–784.,
https://doi.org/10.1016/j.ekir.2020.12.010. 2 Tumlin, James A., et
al. “A Multi-Center, Randomized, Controlled, Pivotal Study to
Assess the Safety and Efficacy of a Selective Cytopheretic Device
in Patients with Acute Kidney Injury.” PLOS ONE, vol. 10, no. 8,
2015, https://doi.org/10.1371/journal.pone.0132482. 3 Yessayan,
Lenar T., et al. “Extracorporeal Immunomodulation Treatment and
Clinical Outcomes in ICU COVID-19 Patients.” Critical Care
Explorations, vol. 4, no. 5, 19 May 2022,
https://doi.org/10.1097/cce.0000000000000694.
CONTACTS
INVESTORS: Vivian Cervantes Gilmartin Group
ir@nuwellis.com
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