NCT04227678
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +9 more
- Locations
-
- Centre de recherche du CHUS Sherbrooke, Quebec, Canada
Clinical trial condition
Hyperlipoproteinemia Type I
Explore clinical trials studying Hyperlipoproteinemia Type I. Study availability and eligibility vary by location and protocol.
13 public trials
2 recruiting studies
Hyperlipoproteinemia Type I trial results
NCT07371767
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Dyslipidemias, +12 more
- Locations
-
- Shanghai Children's Medical Center Shanghai, Shanghai Municipality, China
NCT05089084
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Familial Chylomicronemia, +9 more
- Locations
-
- Clinical Site 1 Boca Raton, Florida, United States
- Clinical Site 2 Suwanee, Georgia, United States
- Clinical Site 3 Indianapolis, Indiana, United States
- Clinical Site 4 Elkridge, Maryland, United States
NCT03783377
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Familial Chylomicronemia, +10 more
- Locations
-
- Research Site 2 Camperdown, New South Wales, Australia
- Research Site 5 Sippy Downs, Queensland, Australia
- Research Site 3 Adelaide, South Australia, Australia
- Research Site 4 Perth, Washington, Australia
Completed
Baby Detect : Genomic Newborn Screening
NCT05687474
- Conditions
- 3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency, +368 more
- Locations
-
- CRMN, Hôpital La Citadelle Liège, Wallonia, Belgium
NCT03293810
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Familial Hyperchylomicronemia, +11 more
- Locations
-
- Interdisciplinary Metabolism Center, Lipid Out-Patient-Clinic, Lipid Apheresis, Charité, University of Berlin Berlin, Germany
NCT02767531
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +9 more
- Locations
-
- UT Southwestern Medical Center 5323 Harry Hines Blvd Dallas, Texas, United States
NCT02658175
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Familial Chylomicronemia Syndrome, +12 more
- Locations
-
- IONIS Investigative Site Huntington Beach, California, United States
- IONIS Investigative Site San Francisco, California, United States
- IONIS Investigative Site Boca Raton, Florida, United States
- IONIS Investigative Site Boston, Massachusetts, United States
NCT03360747
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Familial Chylomicronemia Syndrome, +12 more
- Locations
-
- Investigative Site Montreal, Quebec, Canada
NCT01146522
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +10 more
- Locations
-
- Novartis Investigative Site Québec, Canada