Medical Technology Breaking News: Time Magazine Names The
Aethlon Hemopurifier® (OTCBB: AEMD) One of the 25 Best Inventions of 2014
SAN DIEGO - November 21, 2014 (Investorideas.com newswire)
Aethlon Medical, Inc. (OTCBB:AEMD),
the pioneer in developing targeted therapeutic devices to address infectious
disease and cancer, announced today that the Aethlon Hemopurifier® has been
named one of the 25 best inventions of 2014 by Time Magazine. The article can
be found on-line at the following link: http://time.com/3594971/the-25-best-inventions-of-2014
The Aethlon Hemopurifier® is a first-in-class bio-filtration
device that targets the rapid elimination of viruses and immunosuppressive
proteins from the circulatory system of infected individuals. To date, the
device has been utilized in the treatment of Ebola, HIV and Hepatitis C virus.
Time previously reported on the successful use of Hemopurifier® therapy in an
Ebola patient with multiple organ failure. The article can be found on-line at
the following link: http://time.com/3586271/ebola-treatment-dialysis-blood
About Aethlon Medical, Inc.
Aethlon
Medical creates targeted therapeutic devices to address infectious disease,
cancer and neurodegenerative disorders. The company's lead product is the
Aethlon Hemopurifier®, a first-in-class antiviral and immunotherapeutic device
that selectively targets the broad-spectrum elimination of circulating viruses
and tumor-secreted exosomes that promote cancer progression. Exosome Sciences,
Inc. is a majority owned subsidiary that is advancing exosome-based products to
diagnose and monitor cancer, infectious disease and neurological disorders. For
more information, please visit http://www.aethlonmedical.com and connect with
the Company on Twitter, LinkedIn,
Facebook and Google+.
Certain statements herein may be forward-looking and involve
risks and uncertainties. Such forward-looking statements involve assumptions,
known and unknown risks, uncertainties and other factors which may cause the
actual results, performance or achievements of Aethlon Medical, Inc. to be
materially different from any future results, performance, or achievements
expressed or implied by the forward-looking statements. Such potential risks
and uncertainties include, without limitation, that the ESI will not be able to
commercialize its future products, that the FDA will not approve the initiation
of the Company's clinical programs or provide market clearance of the company's
products, future human studies whether revenue or non-revenue generating of the
Aethlon ADAPT™ system or the Aethlon Hemopurifier® as an adjunct therapy to
improve patient responsiveness to established cancer or hepatitis C therapies
or as a standalone cancer or hepatitis C therapy or as a broad spectrum defense
against viral pathogens, including ebola, the Company's ability to raise
capital when needed, the Company's ability to complete the development of its
planned products, the Company's ability to manufacture its products either
internally or through outside companies and provide its services, the impact of
government regulations, patent protection on the Company's proprietary
technology, the ability of the Company to meet the milestones contemplated in
the DARPA contract, product liability exposure, uncertainty of market acceptance,
competition, technological change, and other risk factors. In such instances,
actual results could differ materially as a result of a variety of factors,
including the risks associated with the effect of changing economic conditions
and other risk factors detailed in the Company's Securities and Exchange
Commission filings. The Company undertakes no obligation to publicly update or
revise any forward-looking statements, whether as a result of new information,
future events, or otherwise.
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