Evaluation of Safety and Efficacy of AVE5530 as add-on to Ongoing Statins in Patients With Primary Hypercholesterolemia
Status:
Terminated
Trial end date:
2009-06-01
Target enrollment:
Participant gender:
Summary
The present study is assessing the efficacy and safety of AVE5530 (25 mg and 50 mg) in add-on
to ongoing statin treatment in a double-blind manner in comparison with placebo, in the
management of patients with primary hypercholesterolemia considered as inadequately
controlled despite their ongoing statin treatment.
The main objective is to evaluate the effects of the association AVE5530+statin on LDL-C
level reduction after 12 weeks of treatment. The effects of AVE5530 on other lipid parameters
will be assessed as secondary objectives.