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Health Enhancement Products Announced the Long Awaited Discovery of a Class of "Orally Active Agents" in Its Primary Product, ProAlgaZyme
Company Describes the as "Unusual Proteins" Still Under Development
| Source: Health Enhancement Products, Inc.
SCOTTSDALE, AZ--(Marketwire - November 14, 2007) - Health Enhancement Products, Inc. (OTCBB : HEPI ),
announced today that the company has captured the active agents from it
primary product ProAlgaZyme, and described it as a class of orally active
agents which are responsible for the clinical activity. The company stated
that the unusual proteins agents are still under development and that they
are now determining the individual components responsible for these
observed positive clinical activities. The company plans to begin active
discussions with large pharmaceutical and veterinary medicine companies in
earnest in early 2008, to exploit the attractive drug development
opportunities offered by the orally active unusual protein agents.
The company also announced that one of its key patent applications covering
the composition of ProAlgaZyme has been published by the US patent office.
About Health Enhancement Products, Inc. and ProAlgaZyme
Health Enhancement Products Inc. is a nutraceutical company engaged in the
development of a Dietary Supplement product using only pure, all-natural
ingredients. The company's sole product is ProAlgaZyme, a liquid product
produced from algae grown in 100% distilled water. The liquid in which the
algae are grown is drawn off, filtered, tested and bottled as ProAlgaZyme.
HEPI Pharmaceuticals, Inc. is exploring the development of the potential
pharmaceutical applications of ProAlgaZyme.
Except for any historical information, the matters discussed in this press
release contain 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. These forward-looking statements involve risks and
uncertainties. A number of factors could cause actual results to differ
from those indicated in the forward-looking statements, including the
timing of completion of a trial, actual future clinical trial results being
different than the results the company has obtained to date, our inability
to obtain regulatory approvals necessary to market and sell PAZ as a
pharmaceutical, and the company's ability to secure funding, including for
the subsidiary's pharmaceutical development of PAZ. Such statements are
subject to a number of assumptions, risks and uncertainties. Readers are
cautioned that such statements are not guarantees of future performance and
that actual results or developments may differ materially from those set
forth in the forward-looking statements. The company undertakes no
obligation to publicly update or revise forward-looking statements, whether
as a result of new information or otherwise.