drugset / Trial / NCT00794664

Safety and Efficacy of Mipomersen in Patients With Severe Hypercholesterolemia on a Maximally Tolerated Lipid-Lowering Regimen and Who Are Not on Apheresis

NCT00794664

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to evaluate the safety and efficacy of dosing with mipomersen for 26 weeks in treating severely hypercholesterolemic patients who are on a maximally tolerated lipid-lowering regimen and who are not on apheresis.

Timeline

Start
2009-01
Primary completion
2010-05
Completion
2010-10

Drugs

EvaluationDrugModalityDoseRoute
Subject mipomersen Antisense oligonucleotide 200 mg Subcutaneous