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Erschienen in: Drugs 16/2006

01.11.2006 | Adis Drug Profile

Rimonabant

verfasst von: Sheridan Henness, Dean M. Robinson, Katherine A. Lyseng-Williamson

Erschienen in: Drugs | Ausgabe 16/2006

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Abstract

  • ▴ Rimonabant is the first of a new class of selective cannabinoid receptor-1 blockers. It reduces the overactivity of the endocannabinoid system, improving lipid and glucose metabolism and regulating food intake and energy balance.
  • ▴ In four randomised, double-blind clinical trials in overweight or obese adults with or without type 2 diabetes and/or dyslipidaemia, oral rimonabant 20mg once daily reduced weight and waist circumference to a significantly greater extent than placebo.
  • ▴ A significantly greater proportion of rimonabant than placebo recipients achieved the clinically significant weight-loss target of ≥5% or ≥10% of initial weight.
  • ▴ Rimonabant was associated with significant improvements in glycaemic control relative to placebo, with ≈57% of the reduction in glycosylated haemoglobin being independent of the effects of weight loss in one trial.
  • ▴ Improvements in other cardiometabolic risk factors (i.e. increases in high-density lipoprotein-cholesterol [HDL-C] and decreases in triglyceride [TG] levels) were significantly greater with rimonabant than with placebo.
  • ▴ The improvement in lipid profile also demonstrated a weight-independent effect, with ≈47–58% of the mprovement in HDL-C and TG being beyond that expected through weight loss alone.
  • ▴ Rimonabant was generally well tolerated, with most adverse events considered mild to moderate in severity.
Fußnoten
1
The use of trade names is for product identification purposes only and does not imply endorsement.
 
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Metadaten
Titel
Rimonabant
verfasst von
Sheridan Henness
Dean M. Robinson
Katherine A. Lyseng-Williamson
Publikationsdatum
01.11.2006
Verlag
Springer International Publishing
Erschienen in
Drugs / Ausgabe 16/2006
Print ISSN: 0012-6667
Elektronische ISSN: 1179-1950
DOI
https://doi.org/10.2165/00003495-200666160-00006

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