This study will evaluate the lipid-lowering effect and safety of colesevelam therapy administered to heterozygous familial pediatric patients 10 through 17 years of age who are on a stable dose of a pediatric-approved statin monotherapy (atorvastatin, lovastatin, simvastatin or pravastatin), or who are treatment naive to lipid-lowering therapy.
Official Title
Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Colesevelam HCl Administered to Pediatric Patients With Heterozygous Familial Hypercholesterolemia on a Stable Dose of Statins or Treatment Naive to Lipid-Lowering Therapy
Conditions
Hypercholesterolemia
Study Type
Interventional
Study Design
Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Further Details
Primary Outcome Measures:
- Percent change in plasma LDL-C from study baseline (Day 1)to Week 8.
Secondary Outcome Measures:
- Percent change in LDL-C from Week 8 to Week 26 and from study baseline (Day 1) to Week 26.
Study Start
November 2005
Eligibility & Criteria
- Ages Eligible for Study: 10 Years – 17 Years
- Genders Eligible for Study: Both
Inclusion Criteria:
- Male or female patients
- Ages 10 to 17 years inclusive
- Diagnosis of heterozygous familial hypercholesterolemia
- On a stable dose of statin monotherapy or are treatment naive to lipid- lowering agents
- On a low-cholesterol diet
Exclusion Criteria:
- Patients should not have serious concomitant conditions that could interfere with the analysis of the results or that could interfere with the well-being of the patients
Total Enrolment
144
Contact Details
Camperdown NSW, Australia; Recruiting
- Contact Daiichi Sankyo for more information
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