European Trial About Effect of RimoNabant on Abdominal Obese Patients With dysLipidemia

Official Title: “A European Randomized, Parallel Group, Two-arm Placebo-controlled, Double-blind Multicenter Study of Rimonabant 20mg Once Daily in the Treatment of Abdominally Obese Patients With Dyslipidemia With or Without Other Comorbidities”

Primary :

To determine the effect of Rimonabant 20 mg on changes in, HDL-Cholesterol (HDL-C), triglyceride levels over a period of 12 months when prescribed with a mild hypocaloric diet in abdominally obese patients with dyslipidemia with or without other associated comorbidities.

Main Secondary :

To determine the effect of 12 months Rimonabant treatment versus placebo on changes in waist circumference (WC), body weight, glycemic and lipid parameters.

To assess the safety of 12 months Rimonabant treatment versus placebo in these patients.

In selected sites, a sub study will be conducted to determine the effect of 12 months of Rimonabant on additional lipoprotein and inflammatory parameters.

Intervention(s) in this Clinical Trial

• Drug: rimonabant
  • Administration of one tablet containing 20 mg of active rimonabantonce daily in the morning. White film-coated tablets, for oral administration containing 20 mg of active rimonabant
• Drug: Placebo
  • Administration of one rimonabant placebo tablet once daily in the morning. Undistinguishable placebo tablets.

Arms, Groups and Cohorts in this Clinical Trial

• Experimental: 1
• Placebo Comparator: 2

Primary Measures

• Change in HDL-C and triglyceride levels
  • Time Frame: From baseline to end of treatment
    Safety Issue?: No

Secondary Measures

• Waist circumference and body weight
  • Time Frame: At each visit
    Safety Issue?: No
• Glycemic parameters : FPG, fasting insulinemia, HbA1c,
  • Time Frame: Prior to baseline, month 3, month 6 and month 12.
    Safety Issue?: No
• Lipid parameters : Total Cholesterol, HDL-C, LDL-C, triglyceride levels
  • Time Frame: Prior to baseline, month 3, month 6 and month 12.
    Safety Issue?: No
• Inflammatory parameter : Hs-CRP
  • Time Frame: Prior to baseline, month 3, month 6 and month 12.
    Safety Issue?: No
• Quality of life : IWQOL questionnaire completed
  • Time Frame: At baseline, month 3, month 6, month 9 and month 12.
    Safety Issue?: No
• Incidence of adverse events in each group, including neuro-psychiatric adverse events
  • Time Frame: Prior to baseline, month 3, month 6 and month 12.
    Safety Issue?: Yes
• Standard laboratory assessments
  • Time Frame: Prior to baseline and month 12
    Safety Issue?: No
• In selected sites, a sub study will be conducted in which additional Lipid parameters will be measured: HDL subfractions, Apo A1, Apo A2, Apo B and Apo C3, Lp A1, LpA1/A2, Lp(a), Oxidized-LDL and LDL size
  • Time Frame: Prior to baseline and at month 12
    Safety Issue?: No
• In selected sites, a sub study will be conducted in which additional Inflammatory parameters will be measured: Adiponectin-High Molecular Weight, Intracellular adhesion molecule 1(ICAM-I) and TNFalpha.
  • Time Frame: Prior to baseline and at month 12
    Safety Issue?: No

Inclusion Criteria:

• BMI > 27 kg/m² and < 40 kg/m²,
• Waist Circumference > 88 cm in women; > 102 cm in men,
• HDL cholesterol < 40 mg/dL (1.03 mmol/L) for men; < 50 mg/dL (1.29 mmol/L) for women, and/or Triglycerides ≥ 150 mg/dL (1.69 mmol/L),
• LDL cholesterol up to 155 mg/dl (4.00 mmol/L) including patients on a stable dose of statins and/or Ezetimibe therapy for at least 8 weeks prior to screening

Concomitant medications:

• Current treatment with statins and/or ezetimibe and/or antihypertensive therapy must be at fixed and stable dose for at least 8 weeks prior to screening visit,
• Patients, who are willing and in the opinion of the Investigator safely assumed to remain on stable and fixed doses of antihypertensive, and/or statins and/or ezetimibe without adding additional medications or changing current treatment for the duration of the trial.

Exclusion Criteria:

• Pregnant or breast-feeding women, or women planning to become pregnant or breastfeed (excluded by pregnancy test),
• Absence of medically approved contraceptive methods for female of childbearing potential,
• History of very low-calorie diet within 3 months prior to screening visit (lower than 1200 Kcal/day),
• Weight change > 5 kg within 3 months prior to screening visit,
• History of surgical procedures for weight loss (e.g., stomach stapling, bypass),
• History of bulimia or anorexia nervosa as per DSM-IV criteria
• Presence of any clinically significant endocrine disease according to the investigator, in particular known abnormal TSH and free T4 blood level (Patients treated with thyroid replacement therapy must be on fixed and stable dose for at least 3 months prior to screening and must be in euthyroïd status),
• Established type 1 or 2 diabetes treated, or with at least 2 measures of fasting blood glucose ≥ 126 mg/dl,
• Triglyceride level > 400 mg/dL (4.52 mmol/L),
• Systolic blood pressure > 160 mm Hg or diastolic blood pressure >100 mmHg at screening visit,
• Known severe renal dysfunction (creatinine clearance < 30 ml/min) or nephrotic syndrome or urinalysis (performed at screening by dipstick) showing 2+ or more protein,
• Known severe hepatic impairment or AST and/or ALT > 3 times the upper limit of normal at screening,
• Presence of any condition (medical, including clinically significant abnormal laboratory tests, psychological, social or geographical) actual or anticipated that the investigator feels would compromise the patient's safety or limit his/her successful participation to the study. In particular :
• Cardiac abnormalities: cardiac failure status NYHA III or IV, relevant acute abnormal finding seen on ECG at screening or within 6 months before screening,
• Any current malignancy or any cancer within the past five years (except adequately treated basal cell skin cancer or cervix carcinoma in situ),
• Significant haematology abnormalities (haemoglobin < 100 g/L and/or neutrophils
• < 1.5 G/L and/or platelets < 100 G/L),
• Acute psychiatric disorders, or mental condition which could interfere with the patient's compliance or safe participation in the study,
• Patient treated for epilepsy
• Ongoing major depressive illness,
• Uncontrolled psychiatric illness,
• History of alcohol or other substance abuse,
• Hypersensitivity /intolerance to the active substance or to any of the excipients such as lactose,

Concomitant medications prior to study entry::

• Administration of any investigational treatment (drug or device) within 30 days prior to screening,
• Previous participation in a Rimonabant study or previous administration of Rimonabant,
• 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,
• nicotinic acid, fibrates or bile acid sequestrants,
• Prolonged use (more than one week) of systemic corticosteroids, neuroleptics,
• Omega-3 fatty acid approved medication
• Ongoing antidepressive treatment (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: 18 Years

Maximum Age for this Clinical Trial: 75 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/NCT00412698

Study ID Number: RIMON_R_00962

ClinicalTrials.gov Identifier: NCT00412698

Health Authority: Portugal: National Pharmacy and Medicines Institute