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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Theophylline for Treatment of PseudohypoparathyroidismBone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, bone disorder, calcium metabolic disease, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, pseudohypoparathyroidism, pseudohypoparathyroidism type 1AEnrolling by invitationPhase 22026-09-02NCT04240821
Setmelanotide to Treat Obesity in a Patient With Pseudohypoparathyroidism Type 1a (PHP1a)Body Weight, Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Overweight, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, bone disorder, calcium metabolic disease, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, nutritional disorder, obesity disorder, overnutrition, pseudohypoparathyroidism, pseudohypoparathyroidism type 1AEnrolling by invitationPhase 22026-07-23NCT07496463
Albright Hereditary Osteodystrophy: Natural History, Growth, and Cognitive/Behavioral AssessmentsBone Diseases, Developmental, Bone Diseases, Endocrine, Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dwarfism, Nutritional and Metabolic Diseases, bone disorder, brain disorder, calcium metabolic disease, central nervous system disorder, endocrine system disorder, hereditary disease, hypopituitarism, hypothalamic disorder, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, nervous system disorder, pituitary dwarfism, pituitary gland disorder, pseudohypoparathyroidism, pseudohypoparathyroidism type 1A, pseudopseudohypoparathyroidismActive, not recruitingNot applicable2026-06-02NCT00209235
Theophylline Treatment for Pseudohypoparathyroidism - Children 2-12 Years OldBone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, bone disorder, calcium metabolic disease, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, pseudohypoparathyroidism, pseudohypoparathyroidism type 1AActive, not recruitingPhase 22026-04-29NCT04551170