CompletedPhase 3NCT00943306

Long Term, Follow-on Study of Lomitapide in Patients With Homozygous Familial Hypercholesterolemia

Studying Rare hypercholesterolemia

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Key facts

Sponsor
Aegerion Pharmaceuticals, Inc.
Principal Investigator
Marina Cuchel, MD, PhD
University of Pennsylvania
Intervention
lomitapide(drug)
Enrollment
19 enrolled
Eligibility
18 years · All sexes
Timeline
20092014

Study locations (10)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT00943306 on ClinicalTrials.gov

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