This study was a 12-month multicenter open-label randomized, comparative study. The protocol was approved by the institutional review board. All patients provided written informed consent. The study included hypercholesterolemic patients with type
This study was a 12-month multicenter open-label randomized,comparative study. The protocol was approved by the institutionalreview board. All patients provided written informedconsent.The study included hypercholesterolemic patients with type