VIsceral Fat Reduction Assessed by CT-scan On RImonabAnt

Official Title: “A Randomized, Double Blind, Two-arm Placebo Controlled, 12-Month Study of the Effects of Rimonabant 20mg Once Daily on the Amount and the Activity of Visceral Fat in Abdominally Obese Patients With Metabolic Syndrome.”

Primary objective:

To assess the effect of rimonabant on visceral fat area over a period of 12 months when prescribed with a mild hypocaloric diet in abdominally obese patients with metabolic syndrome

Secondary objectives: - To assess the effect of rimonabant over a period of 12 months on: - Liver fat content using CT scan (Computed Tomography scan) - Anthropometric measures (weight, waist circumference, body composition using Dual Energy X-ray Absorptiometry (DEXA)) - Lipid, lipoprotein profile - Glycemia, insulinemia and HbA1c - Adipokines, inflammatory and hemostatic markers - To evaluate the percentage of patients with metabolic syndrome at 12 months - To evaluate the safety and tolerability of rimonabant in these patients

In four selected US sites the effect of rimonabant at 12 months will be also assessed on: - Basal lipolysis and insulin suppressed lipolysis (euglycemic hyperinsulinemic clamp). - Resting metabolic rate and substrate oxidation at rest using indirect calorimetry. - Adipose tissue histology and expression of genes involved in glucose and lipid metabolism (superficial adipose tissue biopsy).

Intervention(s) in this Clinical Trial

• Drug: Rimonabant
  • White-opaque tablets, for oral administration containing 20 mg of active rimonabant
• Drug: Placebo
  • Undistinguishable placebo tablets

Arms, Groups and Cohorts in this Clinical Trial

• Experimental: 1
  • Once daily in the morning
• Placebo Comparator: 2
  • Once daily in the morning

Primary Measures

• Relative change in visceral fat area assessed by CT scan
  • Time Frame: From baseline to Month 12
    Safety Issue?: No

Secondary Measures

• Absolute change in visceral fat area assessed by CT scan
  • Time Frame: From baseline to Month 12
    Safety Issue?: No
• Relative and absolute changes in: Liver fat content measured using CT scan, Anthropometric measures, Specific lipid parameters, Glucose control parameters, Adipokines, inflammatory and hemostatic markers
  • Time Frame: From baseline to Month 12
    Safety Issue?: No
• Percentages of patients with a metabolic syndrome
  • Time Frame: At 12 months
    Safety Issue?: No
• Adverse events
  • Time Frame: From the beginning to the end of the study
    Safety Issue?: Yes
• Standard laboratory blood test
  • Time Frame: At baseline, 3 months, 7 months and 12 months
    Safety Issue?: No

Inclusion criteria :

• Waist circumference > 102 cm in men and > 88 cm in women
• Two other components of the metabolic syndrome (NCEP/ATPIII definition) among the following :
• Triglyceridemia ≥ 150 mg/dl (or 1.69 mmol/L)
• HDL cholesterol < 50 mg/dL (or 1.29 mmol/L) in women or < 40 mg/dL (or 1.04 mmol/L) in men
• Blood pressure ≥ 130/85 mmHg (systolic blood pressure ≥ 130 mmHg and/or diastolic blood pressure ≥ 85 mmHg) or Treatment with antihypertensive agent(s) for this condition
• Fasting blood glucose > 110 mg/dl (or 6.1 mmol/L)

Exclusion criteria :

• Positive pregnancy test, pregnant or breast-feeding women, or women planning to become pregnant or breastfeed
• Absence of medically approved contraceptive methods for female of childbearing potential
• History of very low-calorie diet (≤ 800 kcal/day) within 3 months prior to screening visit
• History of surgical procedures for weight loss (eg, stomach stapling, bypass).
• Presence of any clinically significant endocrine disease according to the investigator.
• Weight change > 5 kg within 3 months prior to screening visit
• Obese patients (BMI> 40 kg/m²)
• Established type 1 or 2 diabetes (treated or untreated): at least 2 measures of fasting blood glucose ≥ 126 mg/dl
• Severe renal dysfunction (creatinine clearance < 30 ml/min) or nephrotic syndrome
• Chronic hepatitis or clinically significant hepatic disease
• Positive test for hepatitis B or C
• Marijuana or hashish users
• Significant haematology abnormalities (haemoglobin < 100 g/L and/or neutrophils < 1.5
• G/L and/or platelets < 100 G/L).
• Presence or history of cancer within the past 5 years with the exception of adequately treated basal cell skin cancer or in situ uterine cervical cancer
• Presence or history of severe depression that can be defined as depression which necessitated the patient to be hospitalised, or patient with 2 or more recurrent episodes of depression or an history of suicide attempt
• Presence or history of bulimia or anorexia nervosa (DSM-IV (Diagnostic and Statistical Manual of Mental Disorders) criteria) or binge eating disorders
• Presence of any other condition (eg geographical, social…) current or anticipated that the Investigator feels that would restrict or limit the subject's participation for the duration of the studyRelated to previous or concomitant drugs that could interfere with the evaluation of study drug effects
• Administration of any investigational treatment (drug or device) within 30 days prior to screening
• Previous participation in a rimonabant study
• Administration of any of the following within 3 months prior to screening visit:
• anti obesity drugs (eg, sibutramine, orlistat)
• other drugs for weight reduction (phentermine, amphetamines)
• herbal preparations for weight reduction
• thyroid preparations or thyroxin treatment (except in patients on replacement therapy on a stable dose)
• Patient treated within the last 3 months with nicotinic acid, fibrates, bile acid sequestrants or ezetimibe (patients treated with statins can be included if the dose received is stable since at least 3 months and should not be modified during the whole study period).
• Patient treated with antidiabetic drug(s).
• Prolonged use (more than one week) within the last 3 months of systemic corticosteroids, neuroleptics, or antidepressants (including bupropion).
• The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 35 Years

Maximum Age for this Clinical Trial: 70 Years

Are Healthy Volunteers Accepted for this Clinical Trial?: No

Lead Investigator: Sanofi-Aventis Industry

Overall Clinical Trial Officials and Contacts

Valérie Pilorget, MD Study Director Sanofi-Aventis  

Information obtained from ClinicalTrials.gov on February 12, 2012

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00299325

Study ID Number: PM_C_0172

ClinicalTrials.gov Identifier: NCT00299325

Health Authority: United States: Food and Drug Administration