Lecithin Cholesterol Acyltransferase Deficiency

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Single and Multiple Dose Study to Evaluate Safety and Pharmacokinetics of BMS-986533 in Healthy Participants and Assessments of Food and pH Effects on Relative Bioavailability, and Drug-Drug Interaction Potential in Healthy Participants	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Lecithin Cholesterol Acyltransferase Deficiency, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, hereditary disease, hypoalphalipoproteinemia, hypolipoproteinemia, inborn errors of metabolism, metabolic disease	Recruiting	Phase 1	2026-07-24		NCT07629999
LCAT (Lecithin Cholesterol Acyl Transferase) Natural History Study	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Lecithin Cholesterol Acyltransferase Deficiency, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Urogenital Diseases, cardiovascular disorder, hereditary disease, hypoalphalipoproteinemia, hypolipoproteinemia, inborn errors of metabolism, kidney disorder, metabolic disease, urinary system disorder	Recruiting	Not stated	2026-05-06		NCT06217588

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