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Clinical Trial Summary

The objective of the study is to evaluate the effect of Rimonabant 20mg in comparison to placebo, on HDL and VLDL lipoprotein kinetics, over a 12 months period.

Primary objectives:

- To assess effect of Rimonabant on HDL ApoA-I fractional catabolic rate (FCR).

Secondary objectives:

- To assess effect of Rimonabant on HDL ApoA-I production rate (PR) and on other lipoprotein kinetics.

- To assess effect of Rimonabant on lipids, glycemic and inflammatory parameters

- To assess effect of Rimonabant on body composition

- To assess safety of Rimonabant


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00408148
Study type Interventional
Source Sanofi
Contact
Status Terminated
Phase Phase 3
Start date October 2006
Completion date December 2008

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