Welcome to: Rimonabant Information Source (rimonabant and fda and today)

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Effective weight loss with Rimonabant
- rimonabant smoking
- rimonabant
- rimonabant and fda and today
- rimonabant fda june 2007
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- issue rimonabant clarification
- rimonabant sanofi aventis
Rimonabant Pricelist
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Early Phase 2 data published in April 2004 showed that inhibiting CETP with torcetrapib at 120 mg per day produced significant increases in HDL-C when given alone (46%), as well as in combination with Lipitor (61%). When the dosage of torcetrapib was increased to 240 mg per day, HDL-C increased by over 100%. However, patients taking 60 mg of torcetrapib with Lipitor also experienced an increase in systolic blood pressure, a drawback which may outweigh the benefit of raised HDL-C. It is currently estimated that Torcetrapib will be in the U. S.market in 2008. Rimonabant-Acomplia (discovered and developed by Sanofi-Aventis) is a CB1 endocannabinoid receptor antagonist. CB1 blockers act on the endocannabinoid system, a system controlling energy and nicotine dependence, reducing the overstimulation thought to lead to obesity and nicotine addiction.
The information was clear to conclude that the drug which can control the action of CB-1 receptor can also have control over appetite and urge for tobacco. Sanofi-Aventis of France the prominent drug manufacturer realized the significance of this fact and started its research with Rimonabant. These clinical trials with Rimonabant were basically focused on using Rimonabant as medication for cessation of smoking. During clinical trials the drug developers came across to know about the high efficacy of the Rimonabant as an appetite suppressor. Then rigorous clinical trials were conducted with the view of checking the feasibility and suitability of Rimonabant as an anti-obesity drug. The medication set the high standard and evolved a ray of hope for millions of obese across the globe.
