New Study Shows LEVITRA Successfully Treats Erectile Dysfunction (ED) In Men With Dyslipidemia, Including High Cholesterol
(December 11, 2007) -- Results of the first prospective trial
specifically designed to evaluate erectile function in
erectile dysfunction (ED) patients with dyslipidemia show that
LEVITRA(R) (vardenafil HCl), used in
treating ED, significantly improves the ability of men with ED and
dyslipidemia to achieve and maintain an erection for successful sexual
intercourse. These data were presented at the Sexual Medicine Society of
North America (SMSNA) Fall Meeting held in Chicago, IL.
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The double-blind, placebo-controlled study is the first study to measure
the safety and efficacy of a PDE 5 inhibitor in a cohort of men who all had
ED and dyslipidemia. Results from the study of 395 men show that LEVITRA
significantly increased rates of penetration (as measured by SEP2 scores)
and the ability to maintain an erection (as measured by SEP3 scores)
compared to placebo.
"ED is associated with high cholesterol, yet many physicians are not
treating ED, a life-changing condition," said Dr. Martin Miner, Clinical
Associate Professor of Family Medicine at Brown University's Warren Alpert
School of Medicine. "This study provides further support that LEVITRA can
successfully treat ED, even in men with a serious common condition like high
cholesterol."
Nearly 70 percent of the estimated 30 million men in the United States
who have ED also have other common conditions such as dyslipidemia
(including high cholesterol), hypertension, or diabetes, which may lead to
erectile dysfunction. Previous studies have demonstrated the efficacy and
safety of LEVITRA in men with ED who also have high blood pressure or
diabetes.
About the Study
In the double-blind, placebo-controlled study, 395 men ages 18 to 64 that
had ED and dyslipidemia were randomized to treatment with LEVITRA or placebo
for 12 weeks.
Men treated with LEVITRA had statistically significant and clinically
relevant improvements in SEP2 scores (a rating system that measures
penetration) and SEP3 scores (a rating system that measures maintenance of
erection) versus placebo (79.1% and 66.7%, respectively, for LEVITRA, vs.
51.9% and 33.8%, respectively, for placebo). IIEF-EF (International Index of
Erectile Function) scores also were significantly higher for the LEVITRA
group compared to the placebo group. These scores are evaluated based on a
patient questionnaire and their daily diary response to specific questions
about sexual performance.
LEVITRA was well tolerated. Treatment-emergent adverse effects (occurring
in = 5% of patients) included headaches (9% for LEVITRA, 1% for placebo) and
upper respiratory tract infections (5% for LEVITRA, 3% for placebo).
Source: Medical News Today
Last updated: 12/07
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