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Lipid Metabolism, Inborn Errors

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Lipid Metabolism, Inborn Errors

Explore clinical trials studying Lipid Metabolism, Inborn Errors. Study availability and eligibility vary by location and protocol.

834 public trials 155 recruiting studies

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Lipid Metabolism, Inborn Errors trial results

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Care Pathway for Patients With Fabry's Disease (Fabry-PATH)

NCT07485660

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations: Service de Cardiologie - 1 Avenue du Professeur Jean Poulhès Toulouse, Occitanie, France

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Translational Potential of ex Vivo Gene Therapy in GM2 Gangliosidosis

NCT07445490

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +16 more
Locations: Département de Neurologie Paris, France

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QLC7401 in the Treatment of Primary Hypercholesterolemia or Mixed Hyperlipidemia With Elevated Low Density Lipoprotein Cholesterol (LDL-C)

NCT07441317

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +9 more
Locations: Not specified

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QLC7401 Monotherapy in Non-familial Hypercholesterolemia or Mixed Dyslipidemia

NCT07444086

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +9 more
Locations: Not specified

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A Study to Evaluate the Safety, Efficacy of SYH2053 in Chinese Participants With Non-familial Hypercholesterolemia and Mixed Hyperlipidemia on a Background of Lipid-lowering Therapy

NCT07421284

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +9 more
Locations: Affiliation: Peking University Third Hospital Beijing, Beijing Municipality, China

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Identification of Women With Severe Insulin Resistant Syndromes of Genetic Origin Among Patients With "Classic" Polycystic Ovary Syndrome (PCOS)

NCT07412028

Conditions: Adnexal Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cysts, +24 more
Locations: Service Endocrinologie, Hôpital St Antoine Paris, France

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Novel Diagnostic and Prognostic Predictors in Fabry Cardiomyopathy: Proof of Concept in a Rare Disease

NCT07351136

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations: Not specified

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Pediatric Arthropathy Beyond Inflammation: Clinical Spectrum and Diagnostic Approach at Assiut University Children Hospital

NCT07173010

Conditions: Arthropathy, progressive pseudorheumatoid, of childhood, Bone Diseases, Bone Diseases, Developmental, +36 more
Locations: Not specified

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Evaluate the Long-term Efficacy and Safety of SHR-1918 in Patients With Homozygous Familial Hypercholesterolemia

NCT07133815

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Genetic Diseases, Inborn, +9 more
Locations: Xiangya Second Hospital of Central South University Changsha, Hunan, China

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National Multicentre Study of the Natural History of Acid Sphingo-myelinase Deficiency in Adults and Children

NCT06985212

Conditions: Acid Sphingomyelinase Deficiency (ASMD), Brain Diseases, Brain Diseases, Metabolic, +20 more
Locations: Groupe Hospitalier Diaconesses Croix Saint-Simon Paris, France

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Lipid Metabolism, Inborn Errors

Lipid Metabolism, Inborn Errors trial results

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