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Clinical Trial Summary

The primary objective of this study was to evaluate the effect of 12 weeks of subcutaneous evolocumab (AMG 145), compared with placebo, on percent change from baseline in LDL-C in adults with heterozygous familial hypercholesterolemia (HeFH).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01375751
Study type Interventional
Source Amgen
Contact
Status Completed
Phase Phase 2
Start date August 2, 2011
Completion date May 16, 2012

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