Welcome to: Rimonabant Information Source (rimonabant and fda)

1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 |
Effective weight loss with Rimonabant
- generic accomplia rimonabant order
- rimonabant and caffiene
- kaufen rimonabant
- rimonabant hydrochloride
- rimonabant a stimulant
- buying rimonabant
- rimonabant and fda
Rimonabant Pricelist
Please wait while we load the price list
RIO-Europe is a seven-nation study involving patients with a mean body mass index of 36 kg/[m.sup. 2] and an average waist circumference of 110 cm. As is typical of obesity clinical trials, 80% were women. Participants were encouraged by dietitians and counselors to modify their lifestyle by increasing physical activity and adopting a diet with a 600-cal/day deficit. One-fifth of subjects were randomized to placebo, while the remainder received either 5 mg or 20 mg of rimonabant daily. The placebo response was high, which Dr. Van Gaal attributed to the counselors' dedication. Thirty-one percent of patients who completed 1 year of placebo therapy lost more than 5% of their initial body weight, and although that's an impressive figure, it is well below those of the rimonabant groups: 44% in the patients receiving 5 mg/day and a 67% rate in those receiving 20 mg/day.
S.and European regulators are expected to act on Sanofi-Aventis' application to bring the drug to market. In this trial, researchers compared weight-loss, improvements in metabolic variables, and reduction in cardiovascular risk factors for obese diabetics who took Acomplia compared to those on a placebo. Announcement of the results of the RIO-Diabetes trial is slated for a symposium on "Late-Breaking Clinical Trials" set for 2 p.m. PDT June 12th. Researchers have hinted privately to reporters that the results are consistent with the highly encouraging results from their three studies reported earlier -- RIO-North America, RIO-Europe and RIO-Lipids. The fact that the results are being presented at the highest-profile symposium at the American Diabetes Association meeting -- only weeks after Sanofi filed for approval of the drug with the U.
