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Liponex names Kenneth Sokoll Vice
President of Drug Development
Ottawa, ON, Canada – October 18,
2005 – Liponex Inc. (LPX-T), a biopharmaceutical company specializing in
developing advanced products related to High Density Lipoprotein (HDL), often
called "good cholesterol," today announced the appointment of Kenneth Sokoll to
the position of Vice President of Drug Development, effective November 1.
Mr. Sokoll has eleven years of experience in the pharmaceutical/vaccine
development, quality control, quality assurance, manufacturing and regulatory
fields. His work has been published in multiple peer-reviewed publications and
he holds a number of patents in the drug delivery area. In addition, Mr. Sokoll
has received prestigious awards, scholarships and has been the principal
investigator (P.I.) or co-P.I. on several grants for his work in life sciences,
including the Marie Curie Fellowship grant and an NIH development contract for
the development of an HIV vaccine.
"This position will enable me to put to use my many years of experience in the
life sciences and biopharmaceuticals sectors," said Kenneth Sokoll, about his
new position. "The company’s primary drug candidate shows great promise for
having tremendous effects on heart disease and I am excited to be a part of
that. Liponex’s novel mechanism of drug delivery is also an area I look forward
to working on."
Liponex recently announced an improved formulation for its primary drug
candidate, CRD5, on which Liponex’s drug development team will be focused for
the coming months.
CRD5 is being developed to treat and prevent heart disease by increasing the
level of HDL in the blood and controlling the actions of HDL in the body. It was
demonstrated to be safe and showed indications of efficacy in raising HDL in
three completed Phase I clinical trials.
Through ongoing clinical research and development it was discovered that the
addition of an excipient to the formulation of CRD5 resulted in increased
efficacy at a lower dosage. The new CRD5 formulation demonstrated a significant
increase in bioavailability and efficacy in animal models, which will translate
into considerably lower doses for evaluation in future human clinical trials,
including the Phase II clinical trials, scheduled to begin in early 2006.
"I congratulate Ken on his new position and welcome him to the Liponex team,"
said Bill Dickie, President and CEO of Liponex Inc. "The addition of Ken will
enable faster development of CRD5 and undoubtedly move products along our
pipeline more quickly. Ken and his team have an exciting time ahead of them."
Prior to joining Liponex Inc., Mr. Sokoll spent four years at United Biomedical
Inc., where he began as management of the formulations group, and then moved on
to management of the formulation and API/adjuvant development group, ultimately
holding the position of vice president of vaccine product development where he
was responsible head of regulatory affairs. Throughout his career Mr. Sokoll has
gained a wealth of experience in the life sciences sector, holding positions as
a research scientist, and management positions with companies such as PMC-Canada
and Rhodia/Aventis Pasteur–France. Mr. Sokoll has a B. Sc. from the University
of Toronto and a Ph.D. in Organic Chemistry from the University of Waterloo.
About Liponex
Liponex is a biopharmaceutical company specializing in developing products
related to High Density Lipoprotein (HDL), often called "good cholesterol." Its
drug candidates relate to the various roles of HDL as a transport vehicle,
including removing excess cholesterol from the body, delivering molecules to
cells and removing unwanted materials from the body. Liponex recently completed
its IPO and is listed on the TSX under the ticker "LPX". For more information on
Liponex, visit www.liponex.ca .
Certain of the statements contained in this press release contain
forward-looking statements which involve known and unknown risks, uncertainties
and other factors which may cause the actual results, performance or
achievements of the Company, or industry results, to be materially different
from any future results, performance or achievements expressed or implied by
such forward-looking statements. The Company does not expect to update
forward-looking statements continually as conditions change. Investors are
referred to the full discussion of risk factors associated with the Company's
business contained in the Company's periodic regulatory filings, which can be
found in the SEDAR database at www.sedar.com
.
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For further information, or to arrange for interviews, contact:
Liponex Inc.
Linda Woods
inmedia Public Relations
(613) 234-7227 ext 234
lwoods@inmedia.com
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