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Familial Chylomicronemia Syndrome Clinical Trials

A listing of Familial Chylomicronemia Syndrome medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.


Found (2) clinical trials

Biomarker for Homozygous Familial Hypercholesterolemia

Homozygous familial hypercholesterolemia (HoFH) is a rare hereditary disorder of lipoprotein metabolism characterized by exceptionally high levels of low-density lipoprotein cholesterol (LDL-C). Clinical manifestations may vary but often include markedly premature coronary artery disease, supravalvular aortic stenosis due to aortic root atheroma, and cutaneous manifestations such as tendon xanthomata. Although ...

Phase N/A

GENIALL Lipoprotein Lipase Deficiency (LPLD) Disease Registry

The LPLD Registry is an observational, longitudinal, pharmaco-epidemiologic study in lipoprotein lipase deficient (LPLD) patients, either treated or not treated with Glybera to assess the long-term safety and efficacy of the drug, as well as the epidemiology of the disease. Data from a dietary questionnaire to be completed over a ...

Phase N/A