Medicure Announces Presentation of Phase II Matched Results at Cardiovascular Conference
April 16 2008 - 6:00AM
Marketwired
WINNIPEG, MANITOBA (AMEX: MCU), a cardiovascular-focused
biopharmaceutical company, today announced that the positive
results from the Phase II MATCHED study, which evaluated the
combination of MC-1 and lisinopril in patients with coexisting type
II diabetes and hypertension, will be presented today at the
Arteriosclerosis, Thrombosis and Vascular Biology (ATVB) Annual
Conference 2008 in Atlanta, GA.
Data presented from the poster titled, "MC-1 and Angiotension
Converting Enzyme Therapeutic Combination for Hypertensive
Diabetics (MATCHED): An Evaluation of Ambulatory Blood pressure and
Metabolic Function", included previously released metabolic and
cardiovascular results:
- The combination of MC-1 300mg and lisinopril 20mg had a
reduction in fasting serum glucose of 1.45 mmol/L (p equals 0.026)
versus placebo.
- In patients with elevated baseline triglycerides (greater than
1.7mmol/L), the combination of MC-1 300mg and lisinopril 20mg had a
reduction of 0.7 mmol/L (p equals 0.040) versus baseline.
- In patients with elevated baseline LDL (greater than 2.6
mmol/L), the combination of MC-1 300mg and lisinopril 20mg had a
reduction of 0.4 mmol/L (p equals 0.045) versus baseline.
- The combination of MC-1 300mg and lisinopril 20mg had a
reduction in mean daytime ambulatory systolic blood pressure
(MDASBP) of 12.0 mmHg (p less than 0.0001) from baseline after 8
weeks of therapy as compared to 7.5 mmHg with 20mg lisinopril
monotherapy, equating to an additional 4.5 mmHg reduction (p equals
0.130).
- The combination of MC-1 300mg and lisinopril 20mg had a
reduction in mean daytime ambulatory diastolic blood pressure
(MDADBP) of 7.5 mmHg (p less than 0.0001) from baseline after 8
weeks of therapy as compared to a 4.1 mmHg reduction with 20mg
lisinopril monotherapy, equating to an additional 3.4 mmHg
reduction (p equals 0.060).
"The data from MATCHED demonstrate the potential for the chronic
application of MC-1 in patients with metabolic and cardiovascular
disease," commented Medicure's President and CEO, Albert D.
Friesen, PhD. "We are currently working with our clinical and
scientific advisors to develop an appropriate study design to
further confirm MC-1's chronic application efficacy."
Medicure completed the Phase II MATCHED study (MC-1 and ACE
Therapeutic Combination for Hypertensive Diabetics) in September
2005. MATCHED was a randomized, parallel group, cross-over,
double-blind, placebo-controlled comparison of 100, 300 or 1000 mg
of MC-1 alone and in combination with 20 mg of lisinopril. The
study results are based on a population of 120 patients with
coexisting type II diabetes and hypertension from 12 sites across
Canada.
About Medicure Inc.
Medicure Inc. is a biopharmaceutical company focused on the
research, development and commercialization of novel compounds to
treat cardiovascular disorders.
Cardiovascular medicine represents the largest pharmaceutical
sector, with annual global sales of over US $70 billion. Medicure
aims to make a global impact on cardiovascular disease and stroke
by reducing deaths, improving the quality of life and serving the
unmet needs of people who suffer from cardiovascular disease and
stroke.
This press release contains forward-looking statements, as
defined under applicable securities legislation, that involve
risks, which may cause actual results to differ materially from the
statements made, and accordingly may be deemed to be
forward-looking statements made pursuant to the safe harbor
provisions of the Private Securities Litigation Reform Act of 1995.
The forward-looking statements are made as of the date hereof, and
the Company disclaims any intention and has no obligation or
responsibility to update or revise any forward-looking statements,
whether as a result of new information, future events, or otherwise
except as required by law. Such forward-looking statements involve
known and unknown risks, uncertainties and other factors that may
cause the actual results, events or developments to be materially
different from any future results, events or developments expressed
or implied by such forward-looking statements. Such factors
include, among others, the Company's stage of development, lack of
product revenues, additional capital requirements, risks associated
with the completion of clinical trials and obtaining regulatory
approval to market the Company's products, the ability to protect
its intellectual property, dependence on collaborative partners and
the ability to meet its debt obligations. These factors should be
considered carefully and readers are cautioned not to place undue
reliance on such forward-looking statements. Additional risks and
uncertainties relating to the Company and its business can be found
in the "Risk Factors" section of its Form 20F for the year ended
May 31, 2007 and the Company's MD&A for the third quarter ended
February 29, 2008.
Contacts: Medicure Inc. Derek Reimer Chief Financial Officer
1-888-435-2220 (204) 488-9823 (FAX) Email: info@medicure.com
Website: www.medicure.com
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