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Clinical trial condition

Homozygous Familial Hypercholesterolemia

Explore clinical trials studying Homozygous Familial Hypercholesterolemia. Study availability and eligibility vary by location and protocol.

57 public trials 10 recruiting studies
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Homozygous Familial Hypercholesterolemia trial results

Completed

Trial Evaluating PCSK9 Antibody in Subjects With LDL Receptor Abnormalities

NCT01588496

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +10 more
Locations
  • Research Site New York, United States
  • Research Site Cincinnati, Ohio, United States
  • Research Site Brussels, Belgium
  • Research Site La Louvière, Belgium
View all 21 locations
View Trial Details
Completed

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

NCT00943306

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Familial Hypercholesterolemia, +11 more
Locations
  • Cedars-Sinai Medical Center Los Angeles, California, United States
  • University of Pennsylvania Philadelphia, Pennsylvania, United States
  • Robarts Research Institute London, Ontario, Canada
  • Lipid Clinic and University of Montreal Community Genomic Medicine Center Chicoutimi, Quebec, Canada
View Trial Details
Completed

A Safety and Efficacy Study of AEGR-733 to Treat Homozygous Familial Hypercholesterolemia (FH)

NCT00730236

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +9 more
Locations
  • Cedars-Sinai Medical Center Los Angeles, California, United States
  • University of Pennsylvania Philadelphia, Pennsylvania, United States
  • Robarts Research Institute London, Ontario, Canada
  • Lipid Clinic and University of Montreal Community Genomic Medicine Center Chicoutimi, Quebec, Canada
View Trial Details
Completed

A Study to Evaluate the Safety of Rosuvastatin in Children and Adolescents With Homozygous Familial Hypercholesterolemia

NCT02434497

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +10 more
Locations
  • Research Site Brussels (Woluwé-St-Lambert), Belgium
  • Research Site Chicoutimi, Quebec, Canada
  • Research Site Copenhagen, Denmark
  • Research Site Halfa, Israel
View Trial Details

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