Breaking Medical Technology
News: Aethlon Medical (NASDAQ: $AEMD) Publishes Preclinical Data on the
Hemopurifier® in Transplant Immunology Journal
Preclinical Data
Suggests Expanded Therapeutic Potential of the Hemopurifier® Beyond Virology
and Oncology
Results Support
Further Evaluation of the Hemopurifier® as Part of a Machine Perfusion Circuit
to Further Assess its Impact on the Function of Retrieved Kidneys
SAN DIEGO, CA - March 10, 2025 (Investorideas.com Newswire) Aethlon Medical, Inc. (Nasdaq: AEMD), a medical therapeutic company focused on developing products to treat cancer and life-threatening infectious diseases and for use in organ transplantation, today announced the publication of a pre-clinical study in the peer-reviewed journal Transplant Immunology (https://doi.org/10.1016/j.trim.2025.102215) on February 28, 2025, entitled, "A lectin affinity plasmapheresis device removes extracellular vesicles and microRNAs from renal perfusates following controlled oxygenated rewarming of discarded donor kidneys."
Aethlon Medical's Hemopurifier® is a
therapeutic blood filtration system designed to bind and remove harmful
extracellular vesicles and life-threatening viruses from blood and other
biological fluids. Its capabilities have potential applications in oncology and
infectious diseases, and organ transplantation.
Paid News Dissemination of behalf of AEMD.
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"Kidney transplantation provides
the highest quality of life for those afflicted with end stage renal disease,
yet there is a shortage of organs available, and for those who do receive
organs, complications may include delayed function and organ rejection,"
stated Steven LaRosa, MD, Senior Author of the publication and Chief Medical
Officer of Aethlon Medical.
"The use of machine perfusion of
recovered organs as opposed to cold storage has helped but there is still room
for improvement. The release of extracellular vesicles (EVs) and microRNAs from
the donor kidney are hypothesized to play a role in these complications.
With that in mind, we specifically
examined the ability of the Hemopurifier to remove EVs and noxious microRNAs
from the perfusion fluid from discarded kidneys that had undergone Controlled
Oxygenated Rewarming. We demonstrated significant reductions in EVs as well as
microRNAs implicated in renal dysfunction."
"While the company's funding and
focus are dedicated to the Australian and India Oncology trials, the data
generated from this pre-clinical study demonstrates that extracellular vesicle
removal as a therapeutic target for the Hemopurifier extends beyond virology
and oncology. We believe there exists a "pipeline within a
device"," added James Frakes, Chief Executive Officer and Chief
Financial Officer of Aethlon Medical. However, we acknowledge that further
evaluation is needed, including incorporating the Hemopurifier into a machine
perfusion circuit with discarded kidneys followed by a clinical trial. Our
technology could be potentially "bolted on" to existing organ
preservation technology.
About Aethlon and the Hemopurifier®
Aethlon Medical is a medical
therapeutic company focused on developing the Hemopurifier, a clinical stage
immunotherapeutic device which is designed to combat cancer and
life-threatening viral infections and for use in organ transplantation. In
human studies, the Hemopurifier has demonstrated the removal of
life-threatening viruses and in pre-clinical studies, the Hemopurifier has
demonstrated the removal of harmful exosomes from biological fluids, utilizing
its proprietary lectin-based technology. This action has potential applications
in cancer, where exosomes may promote immune suppression and metastasis, and in
life-threatening infectious diseases. The Hemopurifier is a U.S. Food and Drug
Administration (FDA) designated Breakthrough Device indicated for the treatment
of individuals with advanced or metastatic cancer who are either unresponsive to
or intolerant of standard of care therapy, and with cancer types in which
exosomes have been shown to participate in the development or severity of the
disease. The Hemopurifier also holds an FDA Breakthrough Device designation and
an open Investigational Device Exemption (IDE) application related to the
treatment of life-threatening viruses that are not addressed with approved
therapies.
Forward-Looking Statements
This press release contains
forward-looking statements within the meaning of Section 27A of the Securities
Act of 1933 and Section 21E of the Securities Exchange Act of 1934 that involve
risks and uncertainties. Statements containing words such as "may,"
"believe," "anticipate," "expect," "intend,"
"plan," "project," "will,"
"projections," "estimate," "potentially" or
similar expressions constitute forward-looking statements. Such forward-looking
statements are subject to significant risks and uncertainties and actual
results may differ materially from the results anticipated in the forward-looking
statements. These forward-looking statements are based upon Aethlon's current
expectations and involve assumptions that may never materialize or may prove to
be incorrect. Factors that may contribute to such differences include, without
limitation, the Company's ability to raise additional capital and to
successfully complete development of the Hemopurifier; the Company's ability to
successfully demonstrate the utility of the Hemopurifier in removing EVs and
microRNAs from renal perfusates; the Company's ability to conduct its planned
oncology clinical trials in Australia and India; the Company's ability to
manage and successfully complete its current and future clinical trials, if
initiated; the Company's ability to conduct clinical trial(s) designed to
demonstrate benefits of the incorporation of the Hemopurifier® into renal
perfusion; the Company's ability to successfully manufacture the Hemopurifier
in sufficient quantities for its clinical trials, and other potential risks.
The foregoing list of risks and uncertainties is illustrative, but is not
exhaustive. Additional factors that could cause results to differ materially
from those anticipated in forward-looking statements can be found under the
caption "Risk Factors" in the Company's Annual Report on Form 10-K
for the year ended March 31, 2024, and in the Company's other filings with the
Securities and Exchange Commission, including its quarterly Reports on Form
10-Q. All forward-looking statements contained in this press release speak only
as of the date on which they were made. Except as may be required by law, the
Company does not intend, nor does it undertake any duty, to update this
information to reflect future events or circumstances
.
Additional information can be found
at www.AethlonMedical.com.
Company Contact:
Jim Frakes
Chief Executive Officer and Chief Financial Officer
Aethlon Medical, Inc.
Jfrakes@aethlonmedical.com
Investor Contact:
Susan Noonan
S.A. Noonan Communications, LLC
susan@sanoonan.com
SOURCE Aethlon Medical, Inc.
Aethlon
Medical Inc. (Nasdaq:AEMD) is a featured biotech stock on Investorideas.com
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