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Health Enhancement Products Reports Results in the Second Testing of the ProAlgaZyme Clinical Lot Used in the Suspended Clinical Trial
Second Test Also Confirmed That the Clinical Materials That Had Partially Frozen Showed Loss of Active Components, Compared to the Original Product
| Source: Health Enhancement Products, Inc.
SCOTTSDALE, AZ--(Marketwire - November 6, 2007) - Health Enhancement Products, Inc. (OTCBB : HEPI ) announced today that they have received the second, independent test
results of the clinical lot of ProAlgaZyme that was used in the recently
suspended clinical trial. This test was designed to detect potential
degradation of the active protein components in ProAlgaZyme. Dr. Michael
Tempesta, Chairman of the Scientific Advisory Board stated: This second
round of tests further confirms our belief that the key protein-based
components of ProAlgaZyme are sensitive to freezing, and that the original
clinical ProAlgaZyme product lot was degraded during shipment to Minnesota
during last winter. As stated in our earlier announcement, all bottles
will now be marked "Do not Freeze."
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.
For more information, please visit www.heponline.com.