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Clinical Trial Summary

The current study is designed to test the efficacy, safety and tolerability of LCP-AtorFen, a combination of atorvastatin and fenofibrate.


Clinical Trial Description

This is a multicenter, randomized, double-blind, 12 week study with a 52-week open-label follow-up to evaluate the safety and efficacy of LCP-AtorFen (the combination of atorvastatin and fenofibrate) in the treatment of hyperlipidemia.

After a wash-out phase, eligible patients will be randomized on a 1:1:1 ratio to either LCP-AtorFen, atorvastatin or fenofibrate for 12 weeks. After the completion of the 12-week phase, all eligible patients will be offered to receive open-label LCP-AtorFen for another 52 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00504829
Study type Interventional
Source Veloxis Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date July 2007
Completion date July 2008

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