Medical Technology Breaking News: Aethlon Medical, Inc.
(OTCBB: AEMD) - The Launch of a Clinical Program That Re-Thinks the Treatment
of Viral Pathogens
SAN
DIEGO - February 5, 2015 (Investorideas.com newswire) Aethlon Medical, Inc. (OTCBB:AEMD),
today published an article on The Chairman's Blog, written by the Company's
Chairman and CEO, Jim Joyce. TheChairmansBlog.com is an exclusive online media
publication that enables key executive officers a unique platform to share
insights about their company and industry trends.
In
the article, entitled "The Launch of a Clinical Program That Re-Thinks the
Treatment of Viral Pathogens," Mr. Joyce discusses the increasing
incidence of viral epidemics as well as patient enrollment and the launch of
the Company's first FDA approved study. Read the full article from Mr. Joyce on
TheChairmansBlog.com (http://www.thechairmansblog.com/aethlon-medical/james-joyce/launch-clinical-program-re-thinks-treatment-viral-pathogens).
About Aethlon Medical, Inc.
Aethlon
Medical creates medical devices that target unmet therapeutic needs in
infectious disease, cancer and neurodegenerative disorders. The company's lead
product is the Aethlon Hemopurifier®, a first-in-class device that selectively
targets the rapid 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. Additional
information can be found online at 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.
Contacts:
David
Zazoff
MDM Worldwide Solutions
646-403-3554
MDM Worldwide Solutions
646-403-3554
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