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Clinical Trial Summary

The primary objective was to evaluate the effect of 12 weeks of subcutaneous (SC) evolocumab every 2 weeks (Q2W) and monthly (QM), compared with ezetimibe, on percent change from baseline in low-density lipoprotein cholesterol (LDL-C) in hypercholesterolemic adults unable to tolerate an effective dose of a statin (HMG-CoA (5-hydroxy-3-methylglutaryl-coenzyme A) reductase inhibitors).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01763905
Study type Interventional
Source Amgen
Contact
Status Completed
Phase Phase 3
Start date January 24, 2013
Completion date November 19, 2013

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