Familial Chylomicronemia

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

3 public trials 0 recruiting studies

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Familial Chylomicronemia trial results

Completed

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

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Completed

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

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