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Xenical May Have Role In Long-Term Management of Obesity
CANCUN, MEXICO November 11, 1997
Clinical data presented today at the North American Association for the
Study of Obesity (NAASO) Annual Meeting show that Hoffman-La Roche’s Xenical(R)
(orlistat) may be effective for the long-term management of obesity.
Researchers presented results from several abstracts on Xenical, which
is being investigated to promote weight loss, weight maintenance and reduction
in the risk of weight regain and to improve obesity-related disease factors
when compared to diet alone.
Approximately 58 million, or one-third of American adults are overweight
or obese. Among adults, the incidence of obesity has increased from 25
to 32 percent in the last 10 years. Obesity is second only to smoking as
a cause of preventable death in the US, and is a major contributing factor
to serious medical conditions such as diabetes, hypertension and other
cardiovascular diseases.
Xenical is the first of a new class of non-systemic anti-obesity drugs
called lipase inhibitors which act in the gastrointestinal tract to prevent
the absorption of fat by about 30 percent. Drugs in this class do not achieve
their effect through brain chemistry. Roche originally submitted a New
Drug Application (NDA) for Xenical in 1996. An FDA Advisory Committee unanimously
recommended approval of Xenical on May 14, 1997. Roche later withdrew its
original NDA to conduct further analyses of data at the request of the
FDA. Hoffmann-La Roche expects to resubmit the NDA for Xenical within a
few days.
In a poster presentation, John Foreyt, PhD, Baylor College of Medicine
reported that after one year, patients taking Xenical 120 mg in conjunction
with a mildly hypocaloric diet lost significantly more weight than those
taking placebo in conjunction with a similar diet (57 percent of patients
treated with Xenical lost more than five percent of their initial weight
vs. 34 percent of patients taking placebo).
During the second year, significantly less weight was regained in those
patients who continued taking Xenical than in patients who switched to
placebo (35 percent vs. 63 percent regain of lost weight). Xenical also
reduced total cholesterol and LDL cholesterol levels, as well as mean systolic
and diastolic blood pressure, compared to diet alone.
The clinical trial showed that Xenical was well-tolerated. The most
common side effects reported were non-systemic and primarily gastrointestinal.
These effects generally occurred early in treatment and were self-limited
and of short duration in most cases.
In a poster presented by James Anderson, MD, chief of the endocrine-metabolic
section at the VA Medical Center, Lexington, KY, 729 obese patients who
had lost more than eight percent of their initial body weight after 24
weeks on a hypocaloric diet, were randomized to receive Xenical 120 mg
tid, 60 mg tid, 30 mg tid or placebo in conjunction with a diet designed
to help prevent weight regain rather than promote weight loss.
After one year of treatment the amount of weight regain was significantly
less in the Xenical 120 mg group than in the placebo (32 percent regain
vs. 56 percent with placebo). Furthermore, patients taking Xenical 120
mg experienced significant reductions in total cholesterol and LDL-cholesterol
levels compared to diet alone.
The clinical trial showed that Xenical was well-tolerated. The most
common side effects reported were non-systemic and primarily gastrointestinal.
These effects generally occurred early in treatment and were self-limited
and of short duration in most cases.
A one-year study of weight loss and glycemic control in type 2 diabetics
following orlistat (xenical) treatment, was presented by David Kelley,
MD, associate director of the metabolism and body composition research
core at the University of Pittsburgh Obesity and Nutrition Research Center.
This study examined the efficacy of Xenical in patients with Type 2 diabetes
taking sulfonylureas (medications used to control glucose levels) -- a
patient group in which it is typically difficult to achieve sustained weight
loss.
Results show that patients taking Xenical lost significantly more weight
than in those treated with placebo. After one year of treatment, HbA1c
levels decreased in the Xenical group but increased in the placebo group.
Sulfonylurea doses were reduced 23 percent in the Xenical group versus
nine percent in placebo. In addition, more than twice as many Xenical patients
lost greater than five percent of initial body weight (49 percent on Xenical
versus 23 percent on placebo).
Patients treated with Xenical also showed a significant decrease in
total cholesterol and LDL cholesterol compared to diet alone. The clinical
trial showed that Xenical was well-tolerated. The most common side effects
reported were non-systemic and primarily gastrointestinal. These effects
generally occurred early in treatment and were self-limited and of short
duration in most cases.
The impact of Xenical treatment on quality of life was examined in research
presented by Susan Mathias, MPH, senior analyst at the Technology Assessment
Research Group. Results of this study show patients taking Xenical 120mg
tid for up to two years reported a greater decline in overweight distress,
more satisfaction with treatment and slightly improved depression than
patients receiving placebo. Data was obtained through a new health-related
quality of life (HRQoL) measure and an obesity-specific health state preference
assessment.
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