Breaking Medical Technology News: Aethlon
Medical (NASDAQ: $AEMD) Provides Update on the Ability of Its Hemopurifier® to
Capture H5N1 Bird Flu
SAN
DIEGO - December 20, 2024 (Investorideas.com Newswire) Aethlon Medical, Inc. (Nasdaq: AEMD), a medical therapeutic company focused on developing products to treat
cancer and life-threatening infectious diseases, today provided a statement of
its investigational medical device with respect to H5N1 avian influenza
"Bird Flu."
Aethlon has recently received a
number of inquiries regarding the potential utility of its Hemopurifier device
in the treatment of Bird Flu. These inquiries come on the heels of the reporting
of isolation of Bird Flu in dairy cows, 60 human cases in eight states
including a case of severe infection in Louisiana, and yesterday's declaration
of a state of emergency in California.
Paid News Dissemination of behalf of AEMD.
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The Aethlon Hemopurifier is an
investigational extracorporeal medical device designed to remove enveloped
viruses and extracellular vesicles from the bloodstream. The device
incorporates plasma separation, size exclusion, and affinity binding to a
proprietary resin containing the plant lectin Galanthus nivalis agglutinin
(GNA) bound to a medical grade diatomaceous earth. Enveloped viruses and
extracellular vesicles contain the sugar mannose on their surface, which is the
therapeutic target of the GNA.
Aethlon has previously contracted
Battelle labs to examine the in vitro removal of influenza viruses including
H5N1 by a scaled down version of the Aethlon Hemopurifier. In this experiment,
cell culture media was spiked with the H5N1 virus and continuously circulated
over the device. Samples were taken periodically to examine viral removal by
the device. In this study, a miniature version of the device removed 99% of
H5N1 following 6 hours of treatment.
While the Aethlon Hemopurifier has
not yet been used to treat patients with severe influenza, including those
infected with H5N1, it has been used in 38 patients across 164 distinct
treatment sessions, targeting diseases such as hepatitis C, HIV, and in
patients critically ill due to COVID-19 and Ebola. The Hemopurifier has a
"breakthrough device" designation with the FDA for life-threatening
viruses for which there is no effective treatment.
Current treatment guidelines from the
Center for Disease Control and Prevention (https://www.cdc.gov/bird-flu/hcp/novel-av-treatment-guidance/),
for hospitalized patients with suspected Bird Flu (H5N1), are to initiate
antiviral therapy as soon as possible with Oseltamivir, with or without
combination therapy with Baloxavir. Clinical failures during Oseltamavir
therapy due to the development of antiviral resistance have been observed in
hospitalized patients with H5N1. This phenomenon raises the possibility that
novel treatment strategies may be required. Aethlon Medical will monitor this
situation closely and interact with hospitals, the state of California, and the
FDA as appropriate if cases mount and currently available treatments are not
effective.
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.
Additional information can be found
at www.AethlonMedical.com.
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 on terms favorable to the Company, or at all; the
Company's ability to successfully complete development of the Hemopurifier; the
Company's ability to successfully demonstrate the utility of the Hemopurifier
in patients with solid tumors in our oncology clinical trials; the Company's
ability to achieve and realize the anticipated benefits from potential
milestones; the Company's ability to obtain approval from the Ethics Committee
of its third location in Australia, including on the timeline expected by the
Company; the Company's ability to enroll additional patients in its oncology
clinical trials in Australia and India, including on the timeline expected by
the Company; whether or not patients that are enrolled in the Company's
clinical trials will respond to PD-1 antibody monotherapy; the number of
patients that are enrolled in the Company's clinical trials that will
ultimately be treated with the Company's Hemopurifier; the Company's ability to
manage and successfully complete its clinical trials; 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, 2023, 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.
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
917-513-5303
Aethlon
Medical Inc. (Nasdaq:AEMD) is a featured biotech stock on Investorideas.com
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