familial partial lipodystrophy | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Efficacy and Safety of Mibavademab in Adult and Pediatric Patients With Generalized Lipodystrophy	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, Skin Diseases, Metabolic, Skin and Connective Tissue Diseases, congenital generalized lipodystrophy, familial partial lipodystrophy, hereditary disease, inborn errors of metabolism, laminopathy, lipodystrophy, metabolic disease, skin disorder	Recruiting	Phase 3	2026-09-11		NCT07220785
Sexual Quality of Life in Female Patients With Lipodystrophy Syndromes or Turner's Syndrome: a Case-control Study	Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Sex Chromosome Disorders, Skin Diseases, Metabolic, Skin and Connective Tissue Diseases, Turner syndrome, Urogenital Abnormalities, Urogenital Diseases, cardiovascular disorder, chromosomal disorder, congenital heart disease, disorder of sexual differentiation, endocrine system disorder, familial partial lipodystrophy, gonadal disorder, gonadal dysgenesis, heart disorder, hereditary disease, laminopathy, lipodystrophy, metabolic disease, sex chromosome disorder of sex development, skin disorder	Not yet recruiting	Not stated	2026-09-02		NCT07799012
Identification of Women With Severe Insulin Resistant Syndromes of Genetic Origin Among Patients With "Classic" Polycystic Ovary Syndrome (PCOS)	Adnexal Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cysts, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Genital Diseases, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, Skin Diseases, Metabolic, Skin and Connective Tissue Diseases, Urogenital Diseases, endocrine system disorder, familial partial lipodystrophy, female reproductive system disorder, gonadal disorder, hereditary disease, laminopathy, lipodystrophy, metabolic disease, neoplasm, ovarian cyst, ovarian disorder, polycystic ovary syndrome, skin disorder	Recruiting	Not applicable	2026-08-10		NCT07412028
Open-label Extension Study to Evaluate Metreleptin in Patients With Partial Lipodystrophy	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, Skin Diseases, Metabolic, Skin and Connective Tissue Diseases, familial partial lipodystrophy, hereditary disease, laminopathy, lipodystrophy, metabolic disease, skin disorder	Recruiting	Phase 3	2026-07-16		NCT06679270
Registry for Patients With Lipodystrophy	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, Skin Diseases, Metabolic, Skin and Connective Tissue Diseases, familial partial lipodystrophy, hereditary disease, laminopathy, lipodystrophy, metabolic disease, skin disorder	Recruiting	Not stated	2025-12-02		NCT03553420
Low Energy Diet and Familial Partial Lipodystrophy	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, Skin Diseases, Metabolic, Skin and Connective Tissue Diseases, diabetes mellitus, endocrine system disorder, familial partial lipodystrophy, glucose metabolism disease, hereditary disease, laminopathy, lipodystrophy, metabolic disease, skin disorder	Recruiting	Not applicable	2024-12-05		NCT03900286